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Publications: Kõks, Sulev

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Journal Article

Kulkarni, P., Kõks, S., Harsulkar, A. and Martson, A. (2019) AB1323 Osteophytosis process suggest involvement of mast cells, revealed by whole transcriptome analysis of osteophytes from knee osteoarthritis patients. Annals of the Rheumatic Diseases, 78 (Suppl 2).

Asser, A., Kõks, S., Soomets, U., Terasmaa, A., Sauk, M., Eltermaa, M., Piip, P., Ubhayasekera, K., Bergquist, J. and Taba, P. (2019) Acute effects of methcathinone and manganese in mice: A dose response study. Heliyon, 5 (9).

Kõks, S., Ho, X.D., Maasalu, K., Wood, D. and Martson, A. (2019) Analysis of alternative spicing in the transcriptome of osteosarcoma. Asia-Pacific Journal of Clinical Oncology, 15 (S9). pp. 56-102.

Billingsley, K.J., Lättekivi, F., Planken, A., Reimann, E., Kurvits, L., Kadastik-Eerme, L., Kasterpalu, K.M., Bubb, V.J., Quinn, J.P., Kõks, S. and Taba, P. (2019) Analysis of repetitive element expression in the blood and skin of patients with Parkinson’s disease identifies differential expression of satellite elements. Scientific Reports, 9 (1).

Tätte, K., Pagani, L., Pathak, A.K., Kõks, S., Ho Duy, B., Ho, X.D., Sultana, G.N.N., Sharif, M.I., Asaduzzaman, Md, Behar, D.M., Hadid, Y., Villems, R., Chaubey, G., Kivisild, T. and Metspalu, M. (2019) Author Correction: The genetic legacy of continental scale admixture in Indian Austroasiatic speakers. Scientific Reports, 9 (1).

Zhytnik, L., Maasalu, K., Pashenko, A., Khmyzov, S., Reimann, E., Prans, E., Kõks, S. and Märtson, A. (2019) COL1A1/2 Pathogenic Variants and Phenotype Characteristics in Ukrainian Osteogenesis Imperfecta Patients. Frontiers in Genetics, 10 .

Kõks, G., Tran, H.D.T., Ngo, N.B.T., Hoang, L.N.N., Tran, H.M.T., Ngoc, T.C., Phuoc, T.D., Dung Ho, X., Duy, B.H., Lättekivi, F. and Kõks, S. (2019) Cross-Sectional study to characterise nicotine dependence in central Vietnamese men. Substance Abuse: Research and Treatment, 13 .

Zhytnik, L., Maasalu, K., Duy, B.H., Pashenko, A., Khmyzov, S., Reimann, E., Prans, E., Kõks, S. and Märtson, A. (2019) De novo and inherited pathogenic variants in collagen-related osteogenesis imperfecta. Molecular Genetics & Genomic Medicine, 7 (3). e559.

Eltermaa, M., Jakobson, M., Utt, M., Kõks, S., Mägi, R. and Starkopf, J. (2019) Genetic variants in humanin nuclear isoform gene regions show no association with coronary artery disease. BMC Research Notes, 12 (1).

Zhytnik, L., Maasalu, K., Duy, B.H., Pashenko, A., Khmyzov, S., Reimann, E., Prans, E., Kõks, S. and Märtson, A. (2019) IFITM5 pathogenic variant causes osteogenesis imperfecta V with various phenotype severity in Ukrainian and Vietnamese patients. Human Genomics, 13 (1).

Nõmm, M., Porosk, R., Pärn, P., Kilk, K., Soomets, U., Kõks, S. and Jaakma, Ü. (2019) In vitro culture and non-invasive metabolic profiling of single bovine embryos. Reproduction, Fertility and Development, 31 (2). pp. 306-314.

Zamani Esteki, M., Viltrop, T., Tšuiko, O., Tiirats, A., Koel, M., Nõukas, M., Žilina, O., Teearu, K., Marjonen, H., Kahila, H., Meekels, J., Söderström-Anttila, V., Suikkari, A-M, Tiitinen, A., Mägi, R., Kõks, S., Kaminen-Ahola, N., Kurg, A., Voet, T., Vermeesch, J.R. and Salumets, A. (2019) In vitro fertilization does not increase the incidence of de novo copy number alterations in fetal and placental lineages. Nature Medicine, 25 (11). pp. 1699-1705.

Billingsley, K.J., Barbosa, I.A., Bandrés-Ciga, S., Quinn, J.P., Bubb, V.J., Deshpande, C., Botia, J.A., Reynolds, R.H., Zhang, D., Simpson, M.A., Blauwendraat, C., Gan-Or, Z., Gibbs, J.R., Nalls, M.A., Singleton, A., Ryten, M. and Kõks, S. (2019) Mitochondria function associated genes contribute to Parkinson’s Disease risk and later age at onset. npj Parkinson's Disease, 5 (1).

Traks, T., Keermann, M., Karelson, M., Rätsep, R., Reimann, E., Silm, H., Vasar, E., Kõks, S. and Kingo, K. (2019) Polymorphisms in Corticotrophin-releasing Hormone-proopiomelanocortin (CRH-POMC) system genes are associated with plaque psoriasis. Acta Dermato Venereologica, 99 (4). pp. 444-445.

Traks, T., Keermann, M., Prans, E., Karelson, M., Loite, U., Kõks, G., Silm, H., Kõks, S. and Kingo, K. (2019) Polymorphisms in IL36G gene are associated with plaque psoriasis. BMC Medical Genetics, 20 (1).

Kurvits, L., Reimann, E., Kadastik-Eerme, L., Truu, L., Kingo, K., Erm, T., Kõks, S., Taba, P. and Planken, A. (2019) Serum Amyloid Alpha Is Downregulated in Peripheral Tissues of Parkinson’s Disease Patients. Frontiers in Neuroscience, 13 . Article number 13.

Vollstedt, E‐J, Kasten, M., Klein, C., Aasly, J., Adler, C., Ahmad‐Annuar, A., Albanese, A., Alcalay, R., Al‐Mubarak, B., Alvarez, V., Andree‐Muñoz, B., Annesi, G., Appel‐Cresswell, S., Arkadir, D., Armasu, S., Barber, T.R., Bardien, S., Barkhuizen, M., Barrett, M.J., BaŞak, A.N., Beach, T., Benitez, B.A., Berg, D., Bhatia, K., Binkofski, F., Blauwendraat, C., Bonifati, V., Borges, V., Bozi, M., Brice, A., Brighina, L., Brockmann, K., Brüggemann, N., Camacho, M., Cardoso, F., Belin, A.C., Carr, J., Chan, P., Chang‐Castello, J., Chase, B., Chen‐Plotkin, A., Chung, S.J., Cilia, R., Clarimon, J., Clark, L., Cornejo‐Olivas, M., Corvol, J‐C, Cosentino, C., Cras, P., Crosiers, D., Damásio, J., Das, P., Carvalho Aguiar, P., De Michele, G., De Rosa, A., Dieguez, E., Dorszewska, J., Erer, S., Ertan, S., Farrer, M., Fedotova, E., Ferese, R., Ferrarese, C., Ferraz, H., Fiala, O., Foroud, T., Friedman, A., Frigerio, R., Funayama, M., Gambardella, S., Garraux, G., Gatto, E.M., Genç, G., Goldwurm, S., Gomez‐Esteban, J.C., Gómez‐Garre, P., Gorostidi, A., Grosset, D., Hanagasi, H., Hardy, J., Hassan, A., Hattori, N., Hauser, R.A., Hedera, P., Hentati, F., Hertz, J.M., Holton, J.L., Houlden, H., Hutz, M.H., Ikeuchi, T., Illarioshkin, S., Inca‐Martinez, M., Infante, J., Jankovic, J., Jeon, B.S., Jesús, S., Jimenez‐Del‐Rio, M., Kasten, M., Kataoka, H., Kawakami, H., Kim, Y.J., Klein, C., Klivényi, P., Kõks, S., König, I.R., KostiĆ, V., Koziorowski, D., Krüger, R., Krygowska‐Wajs, A., Kulisevsky, J., Lang, A., LeDoux, M., Lesage, S., Lim, S‐Y, Lin, C‐H, Lohmann, K., Lopera, F., Lopez, G., Lu, C‐S, Lynch, T., Machaczka, M., Madoev, H., Magalhães, M., Majamaa, K., Maraganore, D., Marder, K., Markopoulou, K., Martikainen, M.H., Mata, I., Mazzetti, P., Mellick, G., Menéndez‐González, M., Micheli, F., Mirelman, A., Mir, P., Morino, H., Morris, H., Munhoz, R.P., Naito, A., Olszewska, D.A., Ozelius, L.J., Padmanabhan, S., Paisán‐Ruiz, C., Payami, H., Peluso, S., Petkovic, S., Petrucci, S., Pezzoli, G., Pimentel, M., Pirker, W., Pramstaller, P.P., Pulkes, T., Puschmann, A., Quattrone, A., Raggio, V., Ransmayr, G., Rieder, C., Riess, O., Rodriguez‐Porcel, F., Rogaeva, E., Ross, O.A., Ruiz‐Martinez, J., Sammler, E., Luciano, M.S., Satake, W., Saunders‐Pullman, R., Sazci, A., Scherzer, C., Schrag, A., Schumacher‐Schuh, A., Sharma, M., Sidransky, E., Singleton, A.B., Petersen, M.S., Smolders, S., Spitz, M., Stefanis, L., Struhal, W., Sue, C., Swan, M., Swanberg, M., Taba, P., Taipa, R., Tan, M., Tan, A.H., Tan, E‐K, Tang, B., Tayebi, N., Thaler, A., Thomas, A., Toda, T., Toft, M., Torres, L., Tumas, V., Valente, E.M., Van Broeckhoven, C., Vecsei, L., Velez‐Pardo, C., Vidailhet, M., Vollstedt, E‐J, Warner, T.T., Williams‐Gray, C.H., Winkelmann, J., Woitalla, D., Wood, N.W., Wszolek, Z.K., Wu, R‐M, Wu, Y‐R, Xie, T., Yoshino, H., Zhang, B. and Zimprich, A. (2019) Using global team science to identify genetic Parkinson's disease worldwide. Annals of Neurology, 86 (2). pp. 153-157.

Bandrés-Ciga, S., Saez-Atienzar, S., Bonet-Ponce, L., Billingsley, K., Vitale, D., Blauwendraat, C., Gibbs, J.R., Pihlstrøm, L., Gan-Or, Z., Cookson, M.R., Nalls, M.A., Singleton, A.B. and Kõks, S. (2019) The endocytic membrane trafficking pathway plays a major role in the risk of Parkinson's disease. Movement Disorders, 34 (4). pp. 460-468.

Tätte, K., Pagani, L., Pathak, A.K., Kõks, S., Ho Duy, B., Ho, X.D., Sultana, G.N.N., Sharif, M.I., Asaduzzaman, Md, Behar, D.M., Hadid, Y., Villems, R., Chaubey, G., Kivisild, T. and Metspalu, M. (2019) The genetic legacy of continental scale admixture in Indian Austroasiatic speakers. Scientific Reports, 9 (1).

Nõmm, M., Ivask, M., Pärn, P., Jaakma, Ü. and Kõks, S. (2018) 36 transgenic somatic cell nuclear transfer blastocyst selection with embryo biopsying. Reproduction, Fertility and Development, 30 (1). p. 157.

Tankov, S., Lavrits, A., Lättekivi, F., Krjutskov, K., Sikut, A., Kõks, S., Andronowska, A., Salumets, A. and Fazeli, A. (2018) Characterization of extracellular vesicles produced by single human embryos at early stages of development. Journal of Extracellular Vesicles, 7 (Supp. 1). p. 37.

Blunder, S., Kõks, S., Kõks, G., Reimann, E., Hackl, H., Gruber, R., Moosbrugger-Martinz, V., Schmuth, M. and Dubrac, S. (2018) Enhanced expression of genes related to xenobiotic metabolism in the skin of patients with atopic dermatitis but not with ichthyosis vulgaris. Journal of Investigative Dermatology, 138 (1). pp. 98-108.

Kõks, G., Prans, E., Tran, H.D.T., Ngo, N.B.T., Hoang, L.N.N., Tran, H.M.T., Cao Ngoc, T., Doan Phuoc, T., Ho, X.D., Ho Duy, B., Lättekivi, F., Quinn, J. and Kõks, S. (2018) Genetic interaction between Two VNTRs in the SLC6A4 gene regulates nicotine dependence in Vietnamese Men. Frontiers in Pharmacology, 9 .

Ivask, M., Pajusalu, S., Reimann, E. and Kõks, S. (2018) Hippocampus and Hypothalamus RNA-sequencing of WFS1-deficient Mice. Neuroscience, 374 . pp. 91-103.

Eimre, M., Paju, K., Peet, N., Kadaja, L., Tarrend, M., Kasvandik, S., Seppet, J., Ivask, M., Orlova, E. and Kõks, S. (2018) Increased mitochondrial protein levels and bioenergetics in the musculus rectus femoris of Wfs1-deficient mice. Oxidative Medicine and Cellular Longevity, 2018 . pp. 1-12.

Kurvits, L., Planken, A., Kadastik-Eerme, L., Reimann, E., Kingo, K., Kõks, S. and Taba, P. (2018) Parkinson’s disease as a multisystem disorder: Whole transcriptome study in Parkinson’s disease patients’ skin and blood–finding the pathomechanistic link. European Journal of Neurology, 25 . p. 126.

Traks, T., Keermann, M., Karelson, M., Rätsep, R., Reimann, E., Silm, H., Vasar, E., Kõks, S. and Kingo, K. (2018) Polymorphisms in melanocortin system and MYG1 genes are associated with vitiligo. Journal of the European Academy of Dermatology and Venereology, 33 (2). e65-e67.

Eimre, M., Kasvandik, S., Ivask, M. and Kõks, S. (2018) Proteomic dataset of wolframin-deficient mouse heart and skeletal muscles. Data in Brief, 21 . pp. 616-619.

Kõks, G., Fischer, K. and Kõks, S. (2018) Smoking-related general and cause-specific mortality in Estonia. BMC Public Health, 18 (1).

Es-haghi, M., Haling, A., Lättekivi, F., Tankov, S., James, V., Nafee, T., Kõks, S. and Fazeli, A. (2018) Tracking and capturing of bioorthogonal labelled RNA carried by extracellular vesicles during maternal–embryo communication. Journal of Extracellular Vesicles, 7 (Supp. 1). p. 203.

Lättekivi, F., Kõks, S., Keermann, M., Reimann, E., Prans, E., Abram, K., Silm, H., Kõks, G. and Kingo, K. (2018) Transcriptional landscape of human endogenous retroviruses (HERVs) and other repetitive elements in psoriatic skin. Scientific Reports, 8 (1).

Laius, O., Pisarev, H., Volmer, D., Kõks, S., Märtson, A. and Maasalu, K. (2018) Use of a national database as a tool to identify primary medication non-adherence: The Estonian ePrescription system. Research in Social and Administrative Pharmacy, 14 (8). pp. 776-783.

Mössner, R., Wilsmann-Theis, D., Oji, V., Gkogkolou, P., Löhr, S., Schulz, P., Körber, A., Prinz, J.C., Renner, R., Schäkel, K., Vogelsang, L., Peters, K.-P., Philipp, S., Reich, K., Ständer, H., Jacobi, A., Weyergraf, A., Kingo, K., Kõks, S., Gerdes, S., Steinz, K., Schill, T., Griewank, K. G., Müller, M., Frey, S., Ebertsch, L., Uebe, S., Sticherling, M., Sticht, H. and Hüffmeier, U. (2018) The genetic basis for most patients with pustular skin disease remains elusive. British Journal of Dermatology, 178 (3). pp. 740-748.

Carreras-Badosa, G., Runnel, T., Plaas, M., Kärner, J., Rückert, B., Lättekivi, F., Kõks, S., Akdis, C.A., Kingo, K. and Rebane, A. (2018) microRNA-146a is linked to the production of IgE in mice but not in atopic dermatitis patients. Allergy, 73 (12). pp. 2400-2403.

Carreras-Badosa, G., Runnel, T., Plaas, M., Kärner, J., Rückert, B., Lättekivi, F., Kõks, S., Cezmi, A.A., Kingo, K. and Rebane, A. (2018) microRNA-146a is linked to the production of IgE in mice but not in atopic dermatitis patients. Allergy, 73 . pp. 126-127.

Marjonen, H., Auvinen, P., Kahila, H., Tšuiko, O., Kõks, S., Tiirats, A., Viltrop, T., Tuuri, T., Söderström-Anttila, V., Suikkari, A-M, Salumets, A., Tiitinen, A. and Kaminen-Ahola, N. (2018) rs10732516 polymorphism at the IGF2/H19 locus associates with genotype-specific effects on placental DNA methylation and birth weight of newborns conceived by assisted reproductive technology. Clinical Epigenetics, 10 (1).

Ounpuu, L., Klepinin, A., Pook, M., Teino, I., Peet, N., Paju, K., Tepp, K., Chekulayev, V., Shevchuk, I., Kõks, S., Maimets, T. and Kaambre, T. (2017) 2102Ep embryonal carcinoma cells have compromised respiration and shifted bioenergetic profile distinct from H9 human embryonic stem cells. Biochimica et Biophysica Acta (BBA) - General Subjects, 1861 (8). pp. 2146-2154.

Kõks, S. and Kõks, G. (2017) Activation of GPR15 and its involvement in the biological effects of smoking. Experimental Biology and Medicine, 242 (11). pp. 1207-1212.

Laius, O., Pisarev, H., Maasalu, K., Kõks, S. and Märtson, A. (2017) Adherence to osteoporosis medicines in Estonia—a comprehensive 15-year retrospective prescriptions database study. Archives of Osteoporosis, 12 (1).

Hamel, C., Jagodzinska, J., Bonner-Wersinger, D., Kõks, S., Seveno, M. and Delettre, C. (2017) Advances in gene therapy for Wolfram syndrome. Acta Ophthalmologica, 95 .

Ho, X.D., Nguyen, H.G., Trinh, L.H., Reimann, E., Prans, E., Kõks, G., Maasalu, K., Le, V.Q., Nguyen, V.H., Le, N.T.N., Phung, P., Märtson, A., Lättekivi, F. and Kõks, S. (2017) Analysis of the expression of repetitive DNA elements in Osteosarcoma. Frontiers in Genetics, 8 .

Eimre, M., Peet, N., Kadaja, L., Tarrend, M., Kasvandik, S., Orlova, E., Ivask, M. and Kõks, S. (2017) Changes in intracellular energy transfer enzymes in muscles of mice with deleted wolframin (wfs1) gene. Acta Physiologica, 219 . pp. 17-18.

Ehrlich, M., Ivask, M. and Kõks, S. (2017) Cold induced Ucp1 expression in brown and white adipose tissue of WFS1-deficient mice. The FASEB Journal, 31 (1 Supp).

Reemann, P., Reimann, E., Ilmjärv, S., Porosaar, O., Silm, H., Jaks, V., Vasar, E., Kingo, K. and Kõks, S. (2017) Correction: Melanocytes in the Skin – Comparative Whole Transcriptome Analysis of Main Skin Cell Types. PLoS ONE, 12 (3).

Zhytnik, L., Maasalu, K., Duy, B.H., Reimann, E., Prans, E., Kõks, S. and Märtson, A. (2017) Correlation of the first fracture time and COL1A1/2 mutations in patients with Osteogenesis Imperfecta. Bone Abstracts, 6 .

Eimre, M., Paju, K., Peet, N., Kasvandik, S., Orlova, E., Ivask, M. and Kõks, S. (2017) Energy production and transfer in oxidative muscles of mice with deleted wolframin (wfs1) gene. Acta Physiologica, 221 . p. 112.

Orlova, E., Eimre, M., Paju, K., Peet, N., Kadaja, L., Tarrend, M., Kasvandik, S., Ivask, M. and Kõks, S. (2017) Expression of mitochondrial proteins and respiration in muscles of mice with deleted wolframin (wfs1) gene. Acta Physiologica, 219 (S710). pp. 27-28.

Maasalu, K., Laius, O., Zhytnik, L., Kõks, S., Prans, E., Reimann, E. and Märtson, A. (2017) Featured Article: Transcriptional landscape analysis identifies differently expressed genes involved in follicle-stimulating hormone induced postmenopausal osteoporosis. Experimental Biology and Medicine, 242 (2). pp. 203-213.

Mägi, A., Unt, E., Prans, E. and Kõks, S. (2017) Genes’ Polymorphisms Related To Athletic Physical Performance. Medicine & Science in Sports & Exercise, 49 . pp. 86-87.

Kroon, H., Eltermaa, M., Reigo, A., Karu, I., Ruusalepp, A., Starkopf, J. and Kõks, S. (2017) Humaniin – väike peptiid, suured ülesanded? Ülevaateartikkel humaniini-nimelisest peptiidist. Eesti Arst, 96 (6). pp. 328-334.

Orlova, E., Eimre, M., Paju, K., Peet, N., Kadaja, L., Tarrend, M., Kasvandik, S., Ivask, M. and Kõks, S. (2017) Increased proton leak and expression of mitochondria! proteins in white skeletal muscle of mice with deleted wolframin (wfs1) gene. Acta Physiologica, 221 . p. 113.

Galimova, E., Rätsep, R., Traks, T., Kingo, K., Escott-Price, V. and Kõks, S. (2017) Interleukin-10 family cytokines pathway: genetic variants and psoriasis. British Journal of Dermatology, 176 (6). pp. 1577-1587.

Kõks, S., Kõks, G., Ho, X.D., Maasalu, K. and Märtson, A. (2017) Intrinsic reactivation of human endogenous retroviruses in the osteosarcoma. The FASEB Journal, 31 (1 Supp).

Tsoi, L.C., Stuart, P.E., Tian, C., Gudjonsson, J.E., Das, S., Zawistowski, M., Ellinghaus, E., Barker, J.N., Chandran, V., Dand, N., Duffin, K.C., Enerbäck, C., Esko, T., Franke, A., Gladman, D.D., Hoffmann, P., Kingo, K., Kõks, S., Krueger, G.G., Lim, H.W., Metspalu, A., Mrowietz, U., Mucha, S., Rahman, P., Reis, A., Tejasvi, T., Trembath, R., Voorhees, J.J., Weidinger, S., Weichenthal, M., Wen, X., Eriksson, N., Kang, H.M., Hinds, D.A., Nair, R.P., Abecasis, G.R. and Elder, J.T. (2017) Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants. Nature Communications, 8 (1).

Planken, A., Kurvits, L., Reimann, E., Kadastik-Eerme, L., Kingo, K., Kõks, S. and Taba, P. (2017) Looking beyond the brain to improve the pathogenic understanding of Parkinson’s disease: Implications of whole transcriptome profiling of Patients’ skin. BMC Neurology, 17 (1).

Lättekivi, F., Reimann, E., Keermann, M., Abram, K., Kõks, S., Kingo, K. and Fazeli, A. (2017) Multicomponent biomarkers: A novel method for accurate diagnosis of psoriasis. British Journal of Dermatology, 177 (5). e294-e295.

Zhytnik, L., Maasalu, K., Reimann, E., Prans, E., Kõks, S. and Märtson, A. (2017) Mutational analysis of COL1A1 and COL1A2 genes among Estonian osteogenesis imperfecta patients. Human Genomics, 11 (1).

Nguyen, M.S., Binh, H.D., Nguyen, K.M., Maasalu, K., Kõks, S., Märtson, A., Saag, M. and Jagomägi, T. (2017) Occlusal features and need for orthodontic treatment in persons with osteogenesis imperfecta. Clinical and Experimental Dental Research, 3 (1). pp. 19-24.

Lindholm, D., Korhonen, L., Eriksson, O. and Kõks, S. (2017) Recent insights into the role of unfolded protein response in ER stress in health and disease. Frontiers in Cell and Developmental Biology, 5 .

Galimova, E.S., Kingo, K. and Kõks, S. (2017) Toll-like receptor 7 gene Gln11Leu missensemutation and susceptibility to psoriasis. Medical Immunology (Russia), 19 (3). pp. 267-274.

Laius, O., Pisarev, H., Maasalu, K., Kõks, S. and Märtson, A. (2017) Trends in and relation between hip fracture incidence and osteoporosis medication utilization and prices in Estonia in 2004–2015. Archives of Osteoporosis, 12 (1).

Ho, X.D., Phung, P., Le, V.Q., Nguyen, V.H., Reimann, E., Prans, E., Kõks, G., Maasalu, K., Le, N.T.N., Trinh, L.H., Nguyen, H.G., Märtson, A. and Kõks, S. (2017) Whole transcriptome analysis identifies differentially regulated networks between osteosarcoma and normal bone samples. Experimental Biology and Medicine, 242 (18). pp. 1802-1811.

Binh, H.D., Maasalu, K., Dung, V.C., Ngoc, C.T. Bich, Hung, T.T., Nam, T.V., Nhan, L.N.T., Prans, E., Reimann, E., Zhytnik, L., Kõks, S. and Märtson, A. (2017) The clinical features of osteogenesis imperfecta in Vietnam. International Orthopaedics, 41 (1). pp. 21-29.

Nõmm, M., Mark, E., Sarv, O., Kõks, S. and Jaakma, Ü. (2016) 193 Improved post-thaw survival of bovine embryos produced in serum-free In-vitro production system. Reproduction, Fertility and Development, 28 (2). pp. 227-228.

Ehrlich, M., Ivask, M., Raasmaja, A. and Kõks, S. (2016) Analysis of metabolic effects of menthol on WFS1-deficient mice. Physiological Reports, 4 (1).

Traks, T., Karelson, M., Reimann, E., Rätsep, R., Silm, H., Vasar, E., Kõks, S. and Kingo, K. (2016) Association analysis of class II cytokine and receptor genes in vitiligo patients. Human Immunology, 77 (5). pp. 375-381.

Tiirats, A., Viltrop, T., Noukas, M., Reimann, E., Salumets, A. and Kõks, S. (2016) C14orf132 gene is possibly related to extremely low birth weight. BMC Genetics, 17 (1).

Howe, A.S., Buttenschøn, H.N., Bani-Fatemi, A., Maron, E., Otowa, T., Erhardt, A., Binder, E.B., Gregersen, N.O., Mors, O., Woldbye, D.P., Domschke, K., Reif, A., Shlik, J., Kõks, S., Kawamura, Y., Miyashita, A., Kuwano, R., Tokunaga, K., Tanii, H., Smoller, J.W., Sasaki, T., Koszycki, D. and De Luca, V. (2016) Candidate genes in panic disorder: Meta-analyses of 23 common variants in major anxiogenic pathways. Molecular Psychiatry, 21 (5). pp. 665-679.

Lantto, T., Laakso, I., Dorman, H., Mauriala, T., Hiltunen, R., Kõks, S. and Raasmaja, A. (2016) Cellular stress and p53-Associated apoptosis by Juniperus communis L. berry extract treatment in the human SH-SY5Y neuroblastoma cells. International Journal of Molecular Sciences, 17 (7).

Jin, Y., Andersen, G., Yorgov, D., Ferrara, T.M., Ben, S., Brownson, K.M., Holland, P.J., Birlea, S.A., Siebert, J., Hartmann, A., Lienert, A., van Geel, N., Lambert, J., Luiten, R.M., Wolkerstorfer, A., Wietze van der Veen, J.P., Bennett, D.C., Taïeb, A., Ezzedine, K., Kemp, E.H., Gawkrodger, D.J., Weetman, A.P., Kõks, S., Prans, E., Kingo, K., Karelson, M., Wallace, M.R., McCormack, W.T., Overbeck, A., Moretti, S., Colucci, R., Picardo, M., Silverberg, N.B., Olsson, M., Valle, Y., Korobko, I., Bohm, M., Lim, H.W., Hamzavi, I., Zhou, L., Mi, Q-S, Fain, P.R., Santorico, S.A. and Spritz, R.A. (2016) Genome-wide association studies of autoimmune vitiligo identify 23 new risk loci and highlight key pathways and regulatory variants. Nature Genetics, 48 (11). pp. 1418-1424.

Asser, A., Kõks, S., Snellman, A., Haaparanta-Solin, M., Arponen, E., Grönroos, T., Nairismägi, J., Bergquist, J., Soomets, U., Piip, P., Eltermaa, M., Sauk, M., Lindmäe, H., Rinne, J.O. and Taba, P. (2016) Increased striatal VMAT2 binding in mice after chronic administration of methcathinone and manganese. Brain Research, 1652 . pp. 97-102.

Ehrlich, M., Ivask, M., Raasmaja, A. and Kõks, S. (2016) Metabolic effects of menthol on WFS1-deficient mice. The FASEB Journal, 30 (1 Supp).

Rakitin, A., Kõks, S. and Haldre, S. (2016) Metabolic syndrome and anticonvulsants: A comparative study of valproic acid and carbamazepine. Seizure, 38 . pp. 11-16.

Kõks, S., Dogan, S., Tuna, B.G., González-Navarro, H., Potter, P. and Vandenbroucke, R.E. (2016) Mouse models of ageing and their relevance to disease. Mechanisms of Ageing and Development, 160 . pp. 41-53.

Ho Duy, B., Zhytnik, L., Maasalu, K., Kändla, I., Prans, E., Reimann, E., Märtson, A. and Kõks, S. (2016) Mutation analysis of the COL1A1 and COL1A2 genes in Vietnamese patients with osteogenesis imperfecta. Human Genomics, 10 (1).

Kõks, S., Keermann, M., Reimann, E., Prans, E., Abram, K., Silm, H., Kõks, G. and Kingo, K. (2016) Psoriasis-Specific RNA Isoforms Identified by RNA-Seq Analysis of 173,446 Transcripts. Frontiers in Medicine, 3 .

Ivask, M., Hugill, A. and Kõks, S. (2016) RNA-sequencing of WFS1-deficient pancreatic islets. Physiological Reports, 4 (7).

Laius, O., Maasalu, K., Kõks, S. and Märtson, A. (2016) Use of drugs against osteoporosis in the Baltic countries during 2010–2014. Medicina, 52 (5). pp. 315-320.

Kõks, S., Reimann, E., Maasalu, K., Kõks, G., Xuan, D.H., Prans, E. and Märtson, A. (2016) Whole transcriptome analysis of osteosarcoma. The FASEB Journal, 30 (1 Supp).

Ho, X.D., Phung, P., LE, V.Q.., Nguyen, V.H., Reimann, E., Prans, E., Kõks, G., Maasalu, K., Märtson, A., Le, N.T.N., Trinh, L.H., Nguyen, H.G. and Kõks, S. (2016) Whole transcriptome analysis to reveal differentially expressed genes between paired osteosarcoma and normal bone samples. Journal of Clinical Oncology, 34 (15_suppl). e22508-e22508.

Jagodzinska, J.M., Bonnet-Wersinger, D., Kõks, S., Delprat, B., Hamel, C.P. and Delettre-Cirballet, C. (2016) Wolfram Syndrome murine models: Phenotyping and gene therapy. iovs - investigative opthamology & visual science, 57 (12). p. 4040.

Mägi, A., Unt, E., Prans, E., Raus, L., Eha, J., Veraksits, A., Kingo, K. and Kõks, S. (2016) The association analysis between ACE and ACTN3 genes polymorphisms and endurance capacity in Young Cross-Country Skiers: Longitudinal Study. Journal of Sports Science & Medicine, 15 (2). pp. 287-294.

Nõmm, M., Mark, E., Kilk, K., Kõks, S. and Jaakma, Ü. (2015) 85 Low-Molecular-Weight metabolites in bovine In Vitro production culture media as embryo quality markers. Reproduction, Fertility and Development, 27 (1). pp. 135-136.

Mägi, A., Unt, E., Prans, E., Veraksits, A., Raus, L., Eha, J. and Kõks, S. (2015) ACE and ACTN3 Genes Polymorphisms and Endurance Performance: Association Analysis in Young Estonian Male Skiers1401 Board# 194 May 28, 900 AM-1030 AM. Medicine & Science in Sports & Exercise, 47 (5S). p. 375.

Kasvandik, S., Sillaste, G., Velthut-Meikas, A., Mikelsaar, A-V, Hallap, T., Padrik, P., Tenson, T., Jaakma, Ü., Kõks, S. and Salumets, A. (2015) Bovine sperm plasma membrane proteomics through biotinylation and subcellular enrichment. Proteomics, 15 (11). pp. 1906-1920.

Rakitin, A., Kõks, S., Reimann, E., Prans, E. and Haldre, S. (2015) Changes in the peripheral blood gene expression profile induced by 3 Months of valproate treatment in patients with newly diagnosed epilepsy. Frontiers in Neurology, 6 .

Eimre, M., Paju, K., Orlova, E., Peet, N., Ivask, M. and Kõks, S. (2015) Changes of mitochondrial function and energy transfer enzymes in muscles of mice with deleted wolframin (wfs1) gene. Acta Physiologica, 215 (S705). pp. 128-129.

Puschmann, A., Brighina, L., Markopoulou, K., Aasly, J., Chung, S.J., Frigerio, R., Hadjigeorgiou, G., Kõks, S., Krüger, R., Siuda, J., Wider, C., Zesiewicz, T.A. and Maraganore, D.M. (2015) Clinically meaningful parameters of progression and long-term outcome of Parkinson disease: An international consensus statement. Parkinsonism & Related Disorders, 21 (7). pp. 675-682.

Tsoi, L.C., Spain, S.L., Ellinghaus, E., Stuart, P.E., Capon, F., Knight, J., Tejasvi, T., Kang, H.M., Allen, M.H., Lambert, S., Stoll, S.W., Weidinger, S., Gudjonsson, J.E., Kõks, S., Kingo, K., Esko, T., Das, S., Metspalu, A., Weichenthal, M., Enerbäck, C., Krueger, G.G., Voorhees, J.J., Chandran, V., Rosen, C.F., Rahman, P., Gladman, D.D., Reis, A., Nair, R.P., Franke, A., Barker, J.N.W.N., Abecasis, G.R., Trembath, R.C. and Elder, J.T. (2015) Enhanced meta-analysis and replication studies identify five new psoriasis susceptibility loci. Nature Communications, 6 (1).

Kõks, S. (2015) Experimental models on effects of psychostimulants. International Review of Neurobiology, 120 . pp. 107-129.

Karu, I., Tahepold, P., Ruusalepp, A., Reimann, E., Kõks, S. and Starkopf, J. (2015) Exposure to sixty minutes of hyperoxia upregulates myocardial humanins in patients with coronary artery disease - A pilot study. Journal of Physiology and Pharmacology, 66 (6). pp. 899-906.

Keermann, M., Kõks, S., Reimann, E., Abram, K., Erm, T., Silm, H. and Kingo, K. (2015) Expression of IL-36 family cytokines and IL-37 but not IL-38 is altered in psoriatic skin. Journal of Dermatological Science, 80 (2). pp. 150-152.

Stuart, P.E., Nair, R.P., Tsoi, L.C., Tejasvi, T., Das, S., Kang, H.M., Ellinghaus, E., Chandran, V., Callis-Duffin, K., Ike, R., Li, Y., Wen, X., Enerbäck, C., Gudjonsson, J.E., Kõks, S., Kingo, K., Esko, T., Mrowietz, U., Reis, A., Wichmann, H.E., Gieger, C., Hoffmann, P., Nöthen, M.M., Winkelmann, J., Kunz, M., Moreta, E.G., Mease, P.J., Ritchlin, C.T., Bowcock, A.M., Krueger, G.G., Lim, H.W., Weidinger, S., Weichenthal, M., Voorhees, J.J., Rahman, P., Gregersen, P.K., Franke, A., Gladman, D.D., Abecasis, G.R. and Elder, J.T. (2015) Genome-wide association analysis of psoriatic arthritis and cutaneous psoriasis reveals differences in their genetic architecture. The American Journal of Human Genetics, 97 (6). pp. 816-836.

Magi, A., Kõks, S. and Unt, E. (2015) Maximal oxygen uptake in estonian young cross-country skiers: a longitudinal study. Sănătate Publică, Economie şi Management în Medicină, 64 (7).

Mössner, R., Frambach, Y., Wilsmann-Theis, D., Löhr, S., Jacobi, A., Weyergraf, A., Müller, M., Philipp, S., Renner, R., Traupe, H., Burkhardt, H., Kingo, K., Kõks, S., Uebe, S., Sticherling, M., Sticht, H., Oji, V. and Hüffmeier, U. (2015) Palmoplantar pustular psoriasis is associated with missense variants in CARD14 , but not with loss-of-function mutations in IL36RN in European patients. Journal of Investigative Dermatology, 135 (10). pp. 2538-2541.

Traks, T., Keermann, M., Karelson, M., Rätsep, R., Reimann, E., Silm, H., Vasar, E., Kõks, S. and Kingo, K. (2015) Polymorphisms in Toll-like receptor genes are associated with vitiligo. Frontiers in Genetics, 6 .

Traks, T., Koido, K., Balõtšev, R., Eller, T.., Kõks, S., Maron, E., Tõru, I., Shlik, J., Vasar, E. and Vasar, V. (2015) Polymorphisms of IKBKE gene are associated with major depressive disorder and panic disorder. Brain and Behavior, 5 (4).

Maasalu, K., Laius, O., Zhytnik, L., Kõks, S., Prans, E., Reimann, E. and Maertson, A. (2015) Potential osteoporosis MRNA biomarkers discovered in transcriptome study of Estonian postmenopausal female patients. Osteoporosis International, 26 (S1). S306-S307.

Tein, K., Kasvandik, S., Kõks, S., Vasar, E. and Terasmaa, A. (2015) Prohormone convertase 2 activity is increased in the hippocampus of WFS1 knockout mice. Frontiers in Molecular Neuroscience, 8 .

Kõks, G., Uudelepp, M-L, Limbach, M., Peterson, P., Reimann, E. and Kõks, S. (2015) Smoking-induced expression of the GPR15 gene indicates its potential role in chronic inflammatory pathologies. The American Journal of Pathology, 185 (11). pp. 2898-2906.

Keermann, M., Kõks, S., Reimann, E., Prans, E., Abram, K. and Kingo, K. (2015) Transcriptional landscape of psoriasis identifies the involvement of IL36 and IL36RN. BMC Genomics, 16 (1).

Rakitin, A., Kõks, S. and Haldre, S. (2015) Valproate modulates glucose metabolism in patients with epilepsy after first exposure. Epilepsia, 56 (11). e172-e175.

Maasalu, K., Nikopensius, T., Kõks, S., Nõukas, M., Kals, M., Prans, E., Zhytnik, L., Metspalu, A. and Märtson, A. (2015) Whole-exome sequencing identifies de novo mutation in the COL1A1 gene to underlie the severe osteogenesis imperfecta. Human Genomics, 9 (1).

Gareeva, A.E., Traks, T., Kõks, S. and Khusnutdinova, E.K. (2015) The role of neurotrophins and neurexins genes in the risk of paranoid schizophrenia in Russians and Tatars. Russian Journal of Genetics, 51 (7). pp. 683-694.

Kõks, G., Kõks, S., Raag, M., Fischer, K. and Parna, K. (2014) Analysis of smoking prevalence and smoking-related diseases in the Estonian Genome Bank data (834.10). The FASEB Journal, 28 (1 Supp).

Gimalova, G.F., Karunas, A.S., Fedorova, Y.Y., Gumennaya, E.R., Levashova, S.V., Khismatullina, Z.R., Prans, E., Kõks, S., Etkina, E.I. and Khusnutdinova, E.K. (2014) Association of polymorphisms in the toll-like receptor genes with atopic dermatitis in the Republic of Bashkortostan. Molecular Biology, 48 (2). pp. 227-237.

Rakitin, A., Eglit, T., Kõks, S., Lember, M. and Haldre, S. (2014) Comparison of the metabolic syndrome risk in Valproate-Treated patients with epilepsy and the general population in Estonia. PLoS ONE, 9 (7).

Punapart, M., Eltermaa, M., Oflijan, J., Sütt, S., Must, A., Kõks, S., Schalkwyk, L.C., Fernandes, C., Vasar, E., Soomets, U. and Terasmaa, A. (2014) Effect of chronic valproic acid treatment on hepatic gene expression profile in Wfs1 knockout mouse. PPAR Research, 2014 . pp. 1-11.

Noormets, K., Kõks, S., Ivask, M., Aunapuu, M., Arend, A., Vasar, E. and Tillmann, V. (2014) Energy metabolism and thyroid function of mice with deleted Wolframin (Wfs1) gene. Experimental and Clinical Endocrinology & Diabetes, 122 (05). pp. 281-286.

Reemann, P., Reimann, E., Suutre, S., Paavo, M., Loite, U., Porosaar, O., Abram, K., Silm, H., Vasar, E., Kõks, S. and Kingo, K. (2014) Expression of Class II Cytokine Genes in Children’s Skin. Acta Dermato Venereologica, 94 (4). pp. 386-392.

Viltrop, T., Metsalu, T., Tiirats, A., Rajashekar, B., Reimann, E., Kõks, S., Rull, K., Milani, L., Vilo, J., Magi, R., Metspalu, A., Peters, M., Haller-Kikkatalo, K. and Salumets, A. (2014) Imprinting landscape of human placenta as discovered by whole transcriptome RNA-sequencing and exome variant data analysis. Human Reproduction, 29 (Supp. 1). i72.

Reemann, P., Reimann, E., Ilmjärv, S., Porosaar, O., Silm, H., Jaks, V., Vasar, E., Kingo, K. and Kõks, S. (2014) Melanocytes in the Skin – Comparative Whole Transcriptome Analysis of Main Skin Cell Types. PLoS ONE, 9 (12).

Kutlumbetova, Y., Kazantseva, A., Malykh, S., Traks, T., Kõks, S. and Khusnutdinova, E. (2014) P.1.020 The role of tachykinin receptor 1 gene (TACR1), estrogen alpha and oxytocin receptor genes (ESR1, OXTR) in variation of personality traits. European Neuropsychopharmacology, 24 . S19-S20.

Mencacci, N.E., Isaias, I.U., Reich, M.M., Ganos, C., Plagnol, V., Polke, J.M., Bras, J., Hersheson, J., Stamelou, M., Pittman, A.M., Noyce, A.J., Mok, K.Y., Opladen, T., Kunstmann, E., Hodecker, S., Münchau, A., Volkmann, J., Samnick, S., Sidle, K., Nanji, T., Sweeney, M.G., Houlden, H., Batla, A., Zecchinelli, A.L., Pezzoli, G., Marotta, G., Lees, A., Alegria, P., Krack, P., Cormier-Dequaire, F., Lesage, S., Brice, A., Heutink, P., Gasser, T., Lubbe, S.J., Morris, H.R., Taba, P., Kõks, S., Majounie, E., Raphael Gibbs, J., Singleton, A., Hardy, J., Klebe, S., Bhatia, K.P. and Wood, N.W. (2014) Parkinson’s disease in GTP cyclohydrolase 1 mutation carriers. Brain, 137 (9). pp. 2480-2492.

Rakitin, A., Eglit, T., Kõks, S., Lember, M. and Haldre, S. (2014) Prevalence of metabolic syndrome in valproate-treated adult patients with epilepsy. Neurology, 82 (Supp. 10).

Kõks, S., Reimann, E., Lilleoja, R., Lättekivi, F., Salumets, A., Reemann, P. and Jaakma, Ü. (2014) Sequencing and annotated analysis of full genome of Holstein breed bull. Mammalian Genome, 25 (7-8). pp. 363-373.

Kõks, S., Keermann, M., Reimann, E., Prans, E., Abram, K. and Kingo, K. (2014) Transcriptional landscape of psoriasis provides further details for the pathophysiology. British Journal of Dermatology, 171 (6). e124.

Hashimoto, K., Örd, T., Innos, J., Lilleväli, K., Tekko, T., Sütt, S., Örd, D., Kõks, S., Vasar, E. and Örd, T. (2014) Trib3 is developmentally and nutritionally regulated in the brain but is dispensable for spatial memory, fear conditioning and sensing of amino acid-imbalanced diet. PLoS ONE, 9 (4).

Metsalu, T., Viltrop, T., Tiirats, A., Rajashekar, B., Reimann, E., Kõks, S., Rull, K., Milani, L., Acharya, G., Basnet, P., Vilo, J., Magi, R., Metspalu, A., Peters, M., Haller-Kikkatalo, K. and Salumets, A. (2014) Using RNA sequencing for identifying gene imprinting and random monoallelic expression in human placenta. Epigenetics, 9 (10). pp. 1397-1409.

Delettre, C., Hamel, C.P., Kõks, S., Seveno, M., Lenaers, G. and Bonnet-Wersinger, D.M. (2014) Visual phenotyping of Wfs1 mutant mice, models of Wolfram syndrome neuronal and diabetic symptoms. Investigative Ophthalmology and Visual Science, 55 (13).

Kõks, S., Ivask, M. and Ehrlich, M. (2014) WFS1-deficient mice have alterations in energy metabolism: role of TRPM8 receptors (1126.17). The FASEB Journal, 28 (1 Supp).

Reimann, E., Kõks, S., Ho, X.D., Maasalu, K. and Märtson, A. (2014) Whole exome sequencing of a single osteosarcoma case—integrative analysis with whole transcriptome RNA-seq data. Human Genomics, 8 (1).

Reimann, E., Kingo, K., Karelson, M., Reemann, P., Vasar, E., Silm, H. and Kõks, S. (2014) Whole transcriptome analysis (RNA Sequencing) of peripheral blood mononuclear cells of vitiligo patients. Dermatopathology, 1 (1). pp. 11-23.

Pärn, P., Plaas, M., Nõmm, M., Jaakma, Ü. and Kõks, S. (2013) 49 Effects of culture conditions and gene transfection on the development of bovine somatic cell nuclear transfer embryos. Reproduction, Fertility and Development, 25 (1). p. 172.

Prans, E., Kingo, K., Traks, T., Silm, H., Vasar, E. and Kõks, S. (2013) Copy number variations in IL22 gene are associated with Psoriasis vulgaris. Human Immunology, 74 (6). pp. 792-795.

Visnapuu, T., Plaas, M., Reimets, R., Raud, S., Terasmaa, A., Kõks, S., Sütt, S., Luuk, H., Hundahl, C.A., Eskla, K-L, Altpere, A., Alttoa, A., Harro, J. and Vasar, E. (2013) Evidence for impaired function of dopaminergic system in Wfs1-deficient mice. Behavioural Brain Research, 244 . pp. 90-99.

Reemann, P., Kangur, T., Pook, M., Paalo, M., Nurmis, L., Kink, I., Porosaar, O., Kingo, K., Vasar, E., Kõks, S., Jaks, V. and Järvekülg, M. (2013) Fibroblast growth on micro- and nanopatterned surfaces prepared by a novel sol–gel phase separation method. Journal of Materials Science: Materials in Medicine, 24 (3). pp. 783-792.

Loite, U., Kingo, K., Reimann, E., Reemann, P., Vasar, E., Silm, H. and Kõks, S. (2013) Gene expression analysis of the corticotrophin-releasing Hormone-proopiomelanocortin system in psoriasis skin biopsies. Acta Dermato Venereologica, 93 (4). pp. 400-405.

Planken, A., Kadastik-Eerme, L., Kurvits, L., Rinken, S., Pilv, J., Reimann, E., Kingo, K., Kõks, S. and Taba, P. (2013) Gene expression in skin of Parkinson’s disease patients. Movement Disorders, 28 (S1). S376-S377.

Ho, B.D., Märtson, A., Maasalu, K., Kõks, S. and Le, N.N.T. (2013) Hip fractures at the Hue Medical University Hospital, Vietnam. Osteoporosis International, 24 (S4). S593-S594.

Binh, H.D., Nhan, L.N.T., Maasalu, K., Kõks, S. and Märtson, A. (2013) Hip fractures in 5 years at the Hue University Hospital. Tạp chí Y Dược học: Journal of Medicine Pharmacy, 3 (6). pp. 47-50.

Rull, K., Tomberg, K., Kõks, S., Männik, J., Möls, M., Sirotkina, M., Värv, S. and Laan, M. (2013) Increased placental expression and maternal serum levels of apoptosis-inducing TRAIL in recurrent miscarriage. Placenta, 34 (2). pp. 141-148.

Innos, J., Leidmaa, E., Philips, M-A, Sütt, S., Alttoa, A., Harro, J., Kõks, S. and Vasar, E. (2013) Lsamp–/– mice display lower sensitivity to amphetamine and have elevated 5-HT turnover. Biochemical and Biophysical Research Communications, 430 (1). pp. 413-418.

Lill, M., Kõks, S., Soomets, U., Schalkwyk, L.C., Fernandes, C., Lutsar, I. and Taba, P. (2013) Peripheral blood RNA gene expression profiling in patients with bacterial meningitis. Frontiers in Neuroscience, 7 .

Kõks, S., Lilleoja, R., Reimann, E., Salumets, A., Reemann, P. and Jaakma, Ü. (2013) Sequencing and annotated analysis of the Holstein cow genome. Mammalian Genome, 24 (7-8). pp. 309-321.

Kõks, S., Overall, R.W., Ivask, M., Soomets, U., Guha, M., Vasar, E., Fernandes, C. and Schalkwyk, L.C. (2013) Silencing of the WFS1 gene in HEK cells induces pathways related to neurodegeneration and mitochondrial damage. Physiological Genomics, 45 (5). pp. 182-190.

Gimalova, G., Prans, E., Karunas, A., Fedorova, Y., Gumennaya, E., Levashova, S., Etkina, E., Kõks, S. and Khusnutdinova, E. (2013) Toll-like receptor gene polymorphisms are associated with atopic dermatitis in Volga-Ural region of Russia. Allergy, 68 . p. 437.

Märtson, A., Kõks, S., Reimann, E., Prans, E., Erm, T. and Maasalu, K. (2013) Transcriptome analysis of osteosarcoma identifies suppression of wnt pathway and up-regulation of adiponectin as potential biomarker. Genomics Discovery, 1 (1). p. 3.

Kõks, S., Ivask, M., Hugill, A., Terasmaa, A., Plaas, M. and Vasar, E. (2013) Valproic acid does not affect decreased insulin secretion in WFS1-deficient pancreatic islets. The FASEB Journal, 27 (1 Supp).

Visnapuu, T., Raud, S., Loomets, M., Reimets, R., Sütt, S., Luuk, H., Plaas, M., Kõks, S., Volke, V., Alttoa, A., Harro, J. and Vasar, E. (2013) Wfs1-deficient mice display altered function of serotonergic system and increased behavioral response to antidepressants. Frontiers in Neuroscience, 7 .

Galimova, E., Akhmetova, V., Latipov, B., Kingo, K., Rätsep, R., Traks, T., Kõks, S. and Khusnutdinova, E. (2012) Analysis of genetic variants of class II cytokine and their receptor genes in psoriasis patients of two ethnic groups from the Volga-Ural region of Russia. Journal of Dermatological Science, 68 (1). pp. 9-18.

Koido, K., Traks, T., Balõtšev, R., Eller, T., Must, A., Kõks, S., Maron, E., Tõru, I., Shlik, J., Vasar, V. and Vasar, E. (2012) Associations between LSAMP gene polymorphisms and major depressive disorder and panic disorder. Translational Psychiatry, 2 (8). e152-e152.

Philips, M-A, Vikeså, J., Luuk, H., Jønson, L., Lilleväli, K., Rehfeld, J.F., Vasar, E., Kõks, S. and Nielsen, F.C. (2012) Characterization of MYG1 gene and protein: Subcellular distribution and function. Biology of the Cell, 101 (6). pp. 361-377.

Ellinghaus, D., Ellinghaus, E., Nair, R.P., Stuart, P.E., Esko, T., Metspalu, A., Debrus, S., Raelson, J.V., Tejasvi, T., Belouchi, M., West, S.L., Barker, J.N., Kõks, S., Kingo, K., Balschun, T., Palmieri, O., Annese, V., Gieger, C., Wichmann, H.E., Kabesch, M., Trembath, R.C., Mathew, C.G., Abecasis, G.R., Weidinger, S., Nikolaus, S., Schreiber, S., Elder, J.T., Weichenthal, M., Nothnagel, M. and Franke, A. (2012) Combined analysis of Genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci. The American Journal of Human Genetics, 90 (4). pp. 636-647.

Innos, J., Philips, M-A, Raud, S., Lilleväli, K., Kõks, S. and Vasar, E. (2012) Deletion of the Lsamp gene lowers sensitivity to stressful environmental manipulations in mice. Behavioural Brain Research, 228 (1). pp. 74-81.

Reimann, E., Kingo, K., Karelson, M., Reemann, P., Loite, U., Keermann, M., Abram, K., Vasar, E., Silm, H. and Kõks, S. (2012) Expression profile of genes associated with the dopamine pathway in vitiligo skin biopsies and blood sera. Dermatology, 224 (2). pp. 168-176.

Ellinghaus, E., Stuart, P.E., Ellinghaus, D., Nair, R.P., Debrus, S., Raelson, J.V., Belouchi, M., Tejasvi, T., Li, Y., Tsoi, L.C., Onken, A.T., Esko, T., Metspalu, A., Rahman, P., Gladman, D.D., Bowcock, A.M., Helms, C., Krueger, G.G., Kõks, S., Kingo, K., Gieger, C., Erich Wichmann, H., Mrowietz, U., Weidinger, S., Schreiber, S., Abecasis, G.R., Elder, J.T., Weichenthal, M. and Franke, A. (2012) Genome-wide Meta-analysis of psoriatic arthritis identifies susceptibility locus at REL. Journal of Investigative Dermatology, 132 (4). pp. 1133-1140.

Kõks, S., Unt, E., Tillmann, V., Fischer, K., Alaver, M., Kiudma, T. and Terasmaa, A. (2012) Growth hormone response to the strenuous training in professional skiers has longer recovery time than expected. The FASEB Journal, 26 (1 Supp).

Dalle, S., Parmentier, L., Moscarella, E., Phan, A., Argenziano, G., Demiriz, M., Reimann, E., Kingo, K., Karelson, M., Reemann, P., Loite, U., Keermann, M., Abram, K., Vasar, E., Silm, H., Kõks, S., Vaienti, L., Zilio, D., Di Matteo, A., Riccio, M., Marchesi, A., Tang, L., Li, J., Lin, X., Wu, W., Kang, K., Fu, W., Patrizi, A., Tabanelli, M., Grzeschik, K-H, Misciali, C., Neri, I., Happle, R., Ivanova, K., Itin, P., Haeusermann, P., Granström, S., Langenbruch, A., Augustin, M., Mautner, V-F, Köse, O., Huseynov, S., Cavalli, R., Buffon, R.B., de Souza, M., Colli, A.M., Gelmetti, C., Le Saché-de Peufeilhoux, L., Ingen-Housz-Oro, S., Hue, S., Sbidian, E., Valeyrie-Allanore, L., Ortonne, N., Roujeau, J.C., Wolkenstein, P., Chosidow, O., André, C., Rashtak, S., Gamble, G.L., Gibson, L.E., Pittelkow, M.R., Shi, T-W, Ren, X-K, Yu, H-X, Tang, Y-B, Gutierrez-Salmeron, M.T., Aneiros-Cachaza, J., Naranjo-Sintes, R., Thomas, L., Skov, P.S., Jensen, L.B., Maurer, M., Bindslev-Jensen, C., Tannert, L.K., Husein-ElAhmed, H., Seneschal, J., Guillet, S., Ezzedine, K., Taïeb, A., Milpied, B. and Aneiros-Fernandez, J. (2012) ILDS Newsletter No. 24. Dermatology, 224 (2). pp. 189-192.

Tsoi, L.C., Spain, S.L., Knight, J., Ellinghaus, E., Stuart, P.E., Capon, F., Ding, J., Li, Y., Tejasvi, T., Gudjonsson, J.E., Kang, H.M., Allen, M.H., McManus, R., Novelli, G., Samuelsson, L., Schalkwijk, J., Ståhle, M., Burden, A.D., Smith, C.H., Cork, M.J., Estivill, X., Bowcock, A.M., Krueger, G.G., Weger, W., Worthington, J., Tazi-Ahnini, R., Nestle, F.O., Hayday, A., Hoffmann, P., Winkelmann, J., Wijmenga, C., Langford, C., Edkins, S., Andrews, R., Blackburn, H., Strange, A., Band, G., Pearson, R.D., Vukcevic, D., Spencer, C.C.A., Deloukas, P., Mrowietz, U., Schreiber, S., Weidinger, S., Kõks, S., Kingo, K., Esko, T., Metspalu, A., Lim, H.W., Voorhees, J.J., Weichenthal, M., Wichmann, H.E., Chandran, V., Rosen, C.F., Rahman, P., Gladman, D.D., Griffiths, C.E.M., Reis, A., Kere, J., Nair, R.P., Franke, A., Barker, J.N.W.N., Abecasis, G.R., Elder, J.T. and Trembath, R.C. (2012) Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. Nature Genetics, 44 (12). pp. 1341-1348.

Asser, A., Raki, M., Juurmaa, J., Krispin, V., Muldmaa, M., Raetsep, H., Poldsepp, S., Maennistoe, P., Kõks, S., Bergstroem, K. and Taba, P. (2012) Methcathinone (ephedrone) and manganese both reduce D2-receptor function: An animal SPECT study. Movement Disorders, 27 (S1). S430.

Uusküla, L., Männik, J., Rull, K., Minajeva, A., Kõks, S., Vaas, P., Teesalu, P., Reimand, J. and Laan, M. (2012) Mid-Gestational gene expression profile in placenta and link to pregnancy complications. PLoS ONE, 7 (11). e49248.

Douroudis, K., Kingo, K., Traks, T., Reimann, E., Raud, K., Rätsep, R., Mössner, R., Silm, H., Vasar, E. and Kõks, S. (2012) Polymorphisms in the ATG16L1 Gene are associated with psoriasis vulgaris. Acta Dermato Venereologica, 92 (1). pp. 85-87.

Rünkorg, K., Orav, L., Kõks, S., Matsui, T., Volke, V. and Vasar, E. (2012) Rimonabant attenuates amphetamine sensitisation in a CCK2 receptor-dependent manner. Behavioural Brain Research, 226 (1). pp. 335-339.

Lilleoja, R., Sarapik, A., Reimann, E., Reemann, P., Jaakma, Ü., Vasar, E. and Kõks, S. (2012) Sequencing and annotated analysis of an Estonian human genome. Gene, 493 (1). pp. 69-76.

Rull, K., Tomberg, K., Kõks, S., Männik, J., Möls, M., Sirotkina, M., Värv, S. and Laan, M. (2012) WITHDRAWN: TNF-Related Apoptosis-Inducing Ligand TRAIL as a Potential Biomarker for Early Pregnancy Complications. Journal of Clinical Endocrinology & Metabolism, 97 . p. 1210.

Reimann, E., Kingo, K., Karelson, M., Reemann, P., Loite, U., Sulakatko, H., Keermann, M., Raud, K., Abram, K., Vasar, E., Silm, H. and Kõks, S. (2012) The mRNA expression profile of cytokines connected to the regulation of melanocyte functioning in vitiligo skin biopsy samples and peripheral blood mononuclear cells. Human Immunology, 73 (4). pp. 393-398.

Kõks, S., Velthut, A., Sarapik, A., Altmäe, S., Reinmaa, E., Schalkwyk, L.C., Fernandes, C., Lad, H., Soomets, U., Jaakma, Ü.W. and Salumets, A. (2011) 166 The differential transcriptome and ontology profiles of mural and cumulus granulosa cells in stimulated human antral follicles. Reproduction, Fertility and Development, 23 (1). pp. 185-186.

Douroudis, K., Kingo, K., Traks, T., Rätsep, R., Silm, H., Vasar, E. and Kõks, S. (2011) ATG16L1 gene polymorphisms are associated with palmoplantar pustulosis. Human Immunology, 72 (7). pp. 613-615.

Soomets, U., Kingo, K., Mahlapuu, R. and Kõks, S. (2011) Antioxidants have possible therapeutic activity for psoriasis. British Journal of Dermatology, 165 (6). e28.

Karelson, M., Silm, H., Salum, T., Kõks, S. and Kingo, K. (2011) Differences between familial and sporadic cases of vitiligo. Journal of the European Academy of Dermatology and Venereology, 26 (7). pp. 915-918.

Kõks, S., Soomets, U., Plaas, M., Terasmaa, A., Noormets, K., Tillmann, V., Vasar, E., Fernandes, C. and Schalkwyk, L.C. (2011) Hypothalamic gene expression profile indicates a reduction in G protein signaling in the Wfs1 mutant mice. Physiological Genomics, 43 (24). pp. 1351-1358.

Douroudis, K., Sirotkina, M., Kingo, K., Mössner, R. and Kõks, S. (2011) Immunohistochemical expression of the PRO2268 protein in psoriasis vulgaris skin. Human Immunology, 72 (6). pp. 522-524.

Matto, V., Terasmaa, A., Vasar, E. and Kõks, S. (2011) Impaired striatal dopamine output of homozygous Wfs1 mutant mice in response to [K+] challenge. Journal of Physiology and Biochemistry, 67 (1). pp. 53-60.

Vasar, E., Visnapuu, T., Luuk, H., Terasmaa, A., Raud, S., Innos, J., Plaas, M., Philips, M-A and Kõks, S. (2011) Limbic system associated membrane protein (LSAMP) and wolframin (WFS1) as the potential targets for influencing emotional disorders. Basic & Clinical Pharmacology & Toxicology, 109 (S1). p. 5.

Innos, J., Philips, M-A, Leidmaa, E., Heinla, I., Raud, S., Reemann, P., Plaas, M., Nurk, K., Kurrikoff, K., Matto, V., Visnapuu, T., Mardi, P., Kõks, S. and Vasar, E. (2011) Lower anxiety and a decrease in agonistic behaviour in Lsamp-deficient mice. Behavioural Brain Research, 217 (1). pp. 21-31.

Douroudis, K., Kingo, K., Karelson, M., Silm, H., Reimann, E., Traks, T., Vasar, E. and Kõks, S. (2011) The PRO2268 Gene as a Novel Susceptibility Locus for Vitiligo. Acta Dermato Venereologica, 91 (2). pp. 189-191.

Sikk, K., Kõks, S., Soomets, U., Schalkwyk, L., Fernandes, C., Haldre, S., Aquilonius, S-M and Taba, P. (2011) Peripheral blood RNA expression profiling in illicit methcathinone users reveals effect on immune system. Frontiers in Genetics, 2 .

Douroudis, K., Prans, E., Ivask, M., Visnapuu, T., Vasar, E. and Kõks, S. (2011) Wfs1 deficiency impairs glucose metabolism and induces XBP1 (s) gene expression levels in mice with a diabetes related phenotype. Diabetologia, 54 (S1). S191.

Terasmaa, A., Soomets, U., Oflijan, J., Punapart, M., Hansen, M., Matto, V., Ehrlich, K., Must, A., Kõks, S. and Vasar, E. (2011) Wfs1 mutation makes mice sensitive to insulin-like effect of acute valproic acid and resistant to streptozocin. Journal of Physiology and Biochemistry, 67 (3). pp. 381-390.

Kõks, S., Silm, H., Mössner, R., Traks, T. and Kingo, K. (2011) The association between endoplasmic reticulum stress genes and psoriasis. British Journal of Dermatology, 165 (6). e12.

Asser, A., Kõks, S., Soomets, U., Terasmaa, A., Sauk, M., Eltermaa, M., Piip, P. and Taba, P. (2010) Acute effects of methcathinone and manganese in mice: A dose response study. Movement Disorders, 25 (S2). S226.

Reimann, E., Kingo, K., Karelson, M., Salum, T., Aunin, E., Reemann, P., Abram, K., Vasar, E., Silm, H. and Kõks, S. (2010) Analysis of the expression profile of CRH–POMC system genes in vitiligo skin biopsies. Journal of Dermatological Science, 60 (2). pp. 125-128.

Kingo, K., Reimann, E., Karelson, M., Rätsep, R., Raud, K., Vasar, E., Silm, H. and Kõks, S. (2010) Association analysis of genes of the IL19 cluster and their receptors in vitiligo patients. Dermatology, 221 (3). pp. 261-266.

Douroudis, K., Kingo, K., Silm, H., Reimann, E., Traks, T., Vasar, E. and Kõks, S. (2010) The CD226 Gly307Ser gene polymorphism is associated with severity of psoriasis. Journal of Dermatological Science, 58 (2). pp. 160-161.

Kingo, K., Mössner, R., Traks, T., Rätsep, R., Raud, K., Reimann, E., Krüger, U., Silm, H., Vasar, E., Reich, K. and Kõks, S. (2010) Further association analysis of chr 6q22-24 suggests a role of IL-20RA polymorphisms in psoriasis. Journal of Dermatological Science, 57 (1). pp. 71-73.

Koido, K., Eller, T., Kingo, K., Kõks, S., Traks, T., Shlik, J., Vasar, V., Vasar, E. and Maron, E. (2010) Interleukin 10 family gene polymorphisms are not associated with major depressive disorder and panic disorder phenotypes. Journal of Psychiatric Research, 44 (5). pp. 275-277.

Philips, M-A, Abramov, U., Lilleväli, K., Luuk, H., Kurrikoff, K., Raud, S., Plaas, M., Innos, J., Puussaar, T. and Kõks, S. (2010) Myg1-deficient mice display alterations in stress-induced responses and reduction of sex-dependent behavioural differences. Behavioural Brain Research, 207 (1). pp. 182-195.

Kazantseva, A., Khannanova, A., Traks, T., Kõks, S. and Khusnutdinova, E. (2010) P.1.a.007 Neurotrophin family genes (BDNF and NTRK2) and personality traits in healthy individuals. European Neuropsychopharmacology, 20 . S216-S217.

Lill, M., Kõks, S., Soomets, U., Schalkwyk, L., Fernandes, C., Lutsar, I. and Taba, P. (2010) Peripheral blood RNA gene expression profiling in the patients with community-acquired bacterial meningitis. Clinical Microbiology and Infection, 16 . S517-S518.

Philips, M-A, Kingo, K., Karelson, M., Rätsep, R., Aunin, E., Reimann, E., Reemann, P., Porosaar, O., Vikeså, J., Nielsen, F.C., Vasar, E., Silm, H. and Kõks, S. (2010) Promoter polymorphism -119C/G in MYG1 (C12orf10) gene is related to vitiligo susceptibility and Arg4Gln affects mitochondrial entrance of Myg1. BMC Medical Genetics, 11 (1).

Sütt, S., Raud, S., Abramov, U., Innos, J., Luuk, H., Plaas, M., Kõks, S., Zilmer, K., Mahlapuu, R., Zilmer, M. and Vasar, E. (2010) Relation of exploratory behaviour to plasma corticosterone and Wfs1 gene expression in Wistar rats. Journal of Psychopharmacology, 24 (6). pp. 905-913.

Noormets, K., Kõks, S., Muldmaa, M., Mauring, L., Vasar, E. and Tillmann, V. (2010) Sex differences in the development of diabetes in mice with deleted Wolframin (Wfs1) gene-an animal model for Wolfram syndrome: O/5/FRI/03. Pediatric Diabetes, 11 . pp. 29-30.

Noormets, K., Kõks, S., Muldmaa, M., Mauring, L., Vasar, E. and Tillmann, V. (2010) Sex differences in the development of diabetes in mice with deleted wolframin (Wfs1) gene. Experimental and Clinical Endocrinology & Diabetes, 119 (5). pp. 271-275.

Salum, T., Kõks, S., Kairane, C., Mahlapuu, R., Zilmer, M. and Vasar, E. (2010) Temperature dependence of the sodium pump is altered in the cerebral cortex of CCK2 receptor-deficient mice. Neurochemical Research, 35 (5). pp. 688-692.

Kõks, S., Mehevits, K., Terasmaa, A., Matto, V. and Vasar, E. (2010) Wfs1 deficient mice have altered response to the morphine and decreased release of striatal dopamine: P-14. Genes, Brain and Behavior, 9 (4). pp. 419-447.

Karelson, M., Kingo, K., Salum, T., Kõks, S. and Silm, H. (2009) An Adult`s Vitiligo in Estonia: Study of 155 Patients. The Open Dermatology Journal, 3 (1). pp. 68-72.

Must, A., Kõks, S., Vasar, E., Tasa, G., Lang, A., Maron, E. and Väli, M. (2009) Common variations in 4p locus are related to male completed suicide. NeuroMolecular Medicine, 11 (1). pp. 13-19.

Noormets, K., Kõks, S., Kavak, A., Arend, A., Aunapuu, M., Keldrimaa, A., Vasar, E. and Tillmann, V. (2009) Male mice with deleted Wolframin (Wfs1) gene have reduced fertility. Reproductive Biology and Endocrinology, 7 (1).

Raud, S., Sütt, S., Luuk, H., Plaas, M., Innos, J., Kõks, S. and Vasar, E. (2009) Relation between increased anxiety and reduced expression of alpha1 and alpha2 subunits of GABAA receptors in Wfs1-deficient mice. Neuroscience Letters, 460 (2). pp. 138-142.

Vasar, E., Kõks, S., Luuk, H., Plaas, M., Sütt, S., Raud, S., Kurrikoff, K., Abramov, U. and Innos, J. (2009) S.2.05 Wolframin (WFS1) deficient mice display increased anxiety and reduced adaptation in a novel environment. European Neuropsychopharmacology, 19 (Supp. 2). S117-S119.

Kõks, S., Soomets, U., Paya-Cano, J.L., Fernandes, C., Luuk, H., Plaas, M., Terasmaa, A., Tillmann, V., Noormets, K., Vasar, E. and Schalkwyk, L.C. (2009) Wfs1 gene deletion causes growth retardation in mice and interferes with the growth hormone pathway. Physiological Genomics, 37 (3). pp. 249-259.

Kõks, S., Velthut, A., Sarapik, A., Altmäe, S., Reinmaa, E., Schalkwyk, L.C., Fernandes, C., Lad, H.V., Soomets, U., Jaakma, Ü. and Salumets, A. (2009) The differential transcriptome and ontology profiles of floating and cumulus granulosa cells in stimulated human antral follicles. MHR: Basic science of reproductive medicine, 16 (4). pp. 229-240.

Asser, A., Kõks, S., Haaparanta-Solin, M., Grönroos, T., Pakkanen, A., Nairismägi, J., Plaas, M., Soomets, U., Sauk, M., Piip, P., Eltermaa, M., Lindmäe, H. and Taba, P. (2009) The effects of chronic administration of ephedrone (methcathinone) and manganese in mice. Movement Disorders, 24 (S1). S48-S49.

Plaas, M., Karis, A., Innos, J., Rebane, E., Baekelandt, V., Vaarmann, A., Luuk, H., Vasar, E. and Kõks, S. (2008) Alpha-synuclein A30P point-mutation generates age-dependent nigrostriatal deficiency in mice. Journal of Physiology and Pharmacology, 59 (2). pp. 205-216.

Aunapuu, M., Roosaar, P., Järveots, T., Kurrikoff, K., Kõks, S., Vasar, E. and Arend, A. (2008) Altered renal morphology in transgenic mice with cholecystokinin overexpression. Transgenic Research, 17 (6). pp. 1079-1089.

Kingo, K., Mössner, R., Rätsep, R., Raud, K., Krüger, U., Silm, H., Vasar, E., Reich, K. and Kõks, S. (2008) Association analysis of IL20RA and IL20RB genes in psoriasis. Genes & Immunity, 9 (5). pp. 445-451.

Must, A., Tasa, G., Lang, A., Vasar, E., Kõks, S., Maron, E. and Väli, M. (2008) Association of limbic system-associated membrane protein (LSAMP) to male completed suicide. BMC Medical Genetics, 9 (1).

Sütt, S., Raud, S., Areda, T., Reimets, A., Kõks, S. and Vasar, E. (2008) Cat odour-induced anxiety—a study of the involvement of the endocannabinoid system. Psychopharmacology, 198 (4). pp. 509-520.

Luuk, H., Kõks, S., Plaas, M., Hannibal, J., Rehfeld, J.F. and Vasar, E. (2008) Distribution of Wfs1 protein in the central nervous system of the mouse and its relation to clinical symptoms of the Wolfram syndrome. The Journal of Comparative Neurology, 509 (6). pp. 642-660.

Kingo, K., Aunin, E., Karelson, M., Rätsep, R., Silm, H., Vasar, E. and Kõks, S. (2008) Expressional changes in the intracellular melanogenesis pathways and their possible role the pathogenesis of vitiligo. Journal of Dermatological Science, 52 (1). pp. 39-46.

Kõks, S., Fernandes, C., Kurrikoff, K., Vasar, E. and Schalkwyk, L.C. (2008) Gene expression profiling reveals upregulation of Tlr4 receptors in Cckb receptor deficient mice. Behavioural Brain Research, 188 (1). pp. 62-70.

Rätsep, R., Kingo, K., Karelson, M., Reimann, E., Raud, K., Silm, H., Vasar, E. and Kõks, S. (2008) Gene expression study of IL10 family genes in vitiligo skin biopsies, peripheral blood mononuclear cells and sera. British Journal of Dermatology, 159 (6). pp. 1275-1281.

Traks, T., Koido, K., Eller, T., Maron, E., Kingo, K., Vasar, V., Vasar, E. and Kõks, S. (2008) Polymorphisms in the interleukin-10 gene cluster are possibly involved in the increased risk for major depressive disorder. BMC Medical Genetics, 9 (1).

Kingo, K., Mössner, R., Kõks, S., Rätsep, R., Krüger, U., Vasar, E., Reich, K. and Silm, H. (2007) Association analysis of IL19, IL20 and IL24 genes in palmoplantar pustulosis. British Journal of Dermatology, 156 (4). pp. 646-652.

Raud, S., Sütt, S., Plaas, M., Luuk, H., Innos, J., Philips, M-A, Kõks, S. and Vasar, E. (2007) Cat odor exposure induces distinct changes in the exploratory behavior and Wfs1 gene expression in C57Bl/6 and 129Sv mice. Neuroscience Letters, 426 (2). pp. 87-90.

Kingo, K., Aunin, E., Karelson, M., Philips, M-A, Rätsep, R., Silm, H., Vasar, E., Soomets, U. and Kõks, S. (2007) Gene expression analysis of melanocortin system in vitiligo. Journal of Dermatological Science, 48 (2). pp. 113-122.

Schalkwyk, L.C., Fernandes, C., Nash, M.W., Kurrikoff, K., Vasar, E. and Kõks, S. (2007) Interpretation of knockout experiments: the congenic footprint. Genes, Brain and Behavior, 6 (3). pp. 299-303.

Nelovkov, A., Sütt, S., Raud, S., Vasar, E. and Kõks, S. (2007) Screen for genes in periaqueductal grey of male Wistar rats related to reduced exploratory activity in the elevated plus-maze. Behavioural Brain Research, 183 (1). pp. 8-17.

Koido, K., Kõks, S., Must, A., Reimets, A., Maron, E., Shlik, J., Vasar, V. and Vasar, E. (2006) Association analysis of limbic system-associated membrane protein gene polymorphisms in mood and anxiety disorders. European Neuropsychopharmacology, 16 (Supp. 1). S9.

Areda, T., Raud, S., Philips, M-A, Innos, J., Matsui, T., Kõks, S., Vasar, E., Karis, A. and Asser, T. (2006) Cat odour exposure decreases exploratory activity and alters neuropeptide gene expression in CCK2 receptor deficient mice, but not in their wild-type littermates. Behavioural Brain Research, 169 (2). pp. 212-219.

Rünkorg, K., Värv, S., Matsui, T., Kõks, S. and Vasar, E. (2006) Differences in behavioural effects of amphetamine and dopamine-related gene expression in wild-type and homozygous CCK2 receptor deficient mice. Neuroscience Letters, 406 (1-2). pp. 17-22.

Abramov, U., Raud, S., Innos, J., Kõks, S., Matsui, T. and Vasar, E. (2006) Gender specific effects of ethanol in mice, lacking CCK2 receptors. Behavioural Brain Research, 175 (1). pp. 149-156.

Tõnissoo, T., Kõks, S., Meier, R., Raud, S., Plaas, M., Vasar, E. and Karis, A. (2006) Heterozygous mice with Ric-8 mutation exhibit impaired spatial memory and decreased anxiety. Behavioural Brain Research, 167 (1). pp. 42-48.

Kingo, K., Philips, M-A, Aunin, E., Luuk, H., Karelson, M., Rätsep, R., Silm, H., Vasar, E. and Kõks, S. (2006) MYG1, novel melanocyte related gene, has elevated expression in vitiligo. Journal of Dermatological Science, 44 (2). pp. 119-122.

Nelovkov, A., Areda, T., Innos, J., Kõks, S. and Vasar, E. (2006) Rats displaying distinct exploratory activity also have different expression patterns of γ-aminobutyric acid- and cholecystokinin-related genes in brain regions. Brain Research, 1100 (1). pp. 21-31.

Roots, K., Kairane, C., Salum, T., Kõks, S., Karelson, E., Vasar, E. and Zilmer, M. (2006) Very low levels of cholecystokinin octapeptide activate Na-pump in the cerebral cortex of CCK2 receptor-deficient mice. International Journal of Developmental Neuroscience, 24 (6). pp. 395-400.

Areda, T., Kõks, S., Philips, M-A, Vasar, E., Karis, A. and Asser, T. (2005) Alterations in opioid system of the rat brain after cat odor exposure. Neuroscience Letters, 377 (2). pp. 136-139.

Abramov, U., Vasar, E. and Kõks, S. (2005) Altered behavioural effects of ethanol and increased voluntary ethanol comsumption in mice lacking CCK2 receptors. Behavioural Pharmacology, 16 . S19.

Kõks, S., Nikopensius, T., Koido, K., Maron, E., Altmäe, S., Heinaste, E., Vabrit, K., Tammekivi, V., Hallast, P., Kurg, A., Shlik, J., Vasar, V., Metspalu, A. and Vasar, E. (2005) Analysis of SNP profiles in patients with major depressive disorder. The International Journal of Neuropsychopharmacology, 9 (2). pp. 167-174.

Maron, E., Nikopensius, T., Kõks, S., Altmäe, S., Heinaste, E., Vabrit, K., Tammekivi, V., Hallast, P., Koido, K., Kurg, A., Metspalu, A., Vasar, E., Vasar, V. and Shlik, J. (2005) Association study of 90 candidate gene polymorphisms in panic disorder. Psychiatric Genetics, 15 (1). pp. 17-24.

Kingo, K., Rätsep, R., Kõks, S., Karelson, M., Silm, H. and Vasar, E. (2005) Influence of genetic polymorphisms on interleukin-10 mRNA expression and psoriasis susceptibility. Journal of Dermatological Science, 37 (2). pp. 111-113.

Luuk, H., Tools, U., Kõks, S. and Vasar, E. (2005) P.1.03 N-terminal domain of Wolframin interacts with carboxypeptidase E. European Neuropsychopharmacology, 15 . S5-S6.

Maron, E., Kõks, S., Nikopensius, T., Ahmäe, S., Heinaste, E., Vabrit, K., Tammekivi, V., Hallast, E., Koido, K., Kurg, A., Shlik, J., Vasar, V., Metspalu, A. and Vasar, E. (2005) P.3.05 Association and haplotype analaysis of 90 single-nucleotide polymorphisms in mood disorders. European Neuropsychopharmacology, 15 . S55-S56.

Shlik, J., Koido, K., Nikopensius, T., Maron, E. and Kõks, S. (2005) P.8.028 Associations between genetic polymorphisms of cholecystokinin and its receptors and personality traits. European Neuropsychopharmacology, 15 (Supp. 3). S618.

Koido, K., Kõks, S., Nikopensius, T., Maron, E., Altmäe, S., Heinaste, E., Vabrit, K., Tammekivi, V., Hallast, P., Kurg, A., Shlik, J., Vasar, V., Metspalu, A. and Vasar, E. (2005) Polymorphisms in wolframin (WFS1) gene are possibly related to increased risk for mood disorders. The International Journal of Neuropsychopharmacology, 8 (2). pp. 235-244.

Kõks, S., Kingo, K., Vabrit, K., Rätsep, R., Karelson, M., Silm, H. and Vasar, E. (2005) Possible relations between the polymorphisms of the cytokines IL-19, IL-20 and IL-24 and plaque-type psoriasis. Genes & Immunity, 6 (5). pp. 407-415.

Raud, S., Innos, J., Abramov, U., Reimets, A., Kõks, S., Soosaar, A., Matsui, T. and Vasar, E. (2005) Targeted invalidation of CCK2 receptor gene induces anxiolytic-like action in light–dark exploration, but not in fear conditioning test. Psychopharmacology, 181 (2). pp. 347-357.

Kingo, K., Rätsep, R., Kõks, S., Silm, H. and Vasar, E. (2005) The potential functional influence of polymorphisms of IL-20 gene in plaque psoriasis. Journal of the European Academy of Dermatology and Venereology, 19 (s2). pp. 176-177.

Vasar, E., Abramov, U., Raud, S., Kurrikoff, K., Volke, V., Matsui, T. and Kõks, S. (2004) CCK2 receptor deficient mice: Evidence for changes in anxiety. Regulatory Peptides, 122 (1). pp. 45-46.

Kõks, S., Kingo, K., Rätsep, R., Karelson, M., Silm, H. and Vasar, E. (2004) Combined haplotype analysis of the interleukin-19 and -20 genes: Relationship to plaque-type psoriasis. Genes & Immunity, 5 (8). pp. 662-667.

Kõks, S., Kurrikoff, K., Matsui, T., Bourin, M. and Vasar, E. (2004) Deletion of the CCK2 receptor abolishes the development of hyperalgesia in mononeuropathic mice. Regulatory Peptides, 122 (1). p. 26.

Kurrikoff, K., Kõks, S., Matsui, T., Bourin, M., Arend, A., Aunapuu, M. and Vasar, E. (2004) Deletion of the CCK2 receptor gene reduces mechanical sensitivity and abolishes the development of hyperalgesia in mononeuropathic mice. European Journal of Neuroscience, 20 (6). pp. 1577-1586.

Maron, E., Nkopensius, T., Kõks, S., Altmäe, S., Heinaste, E., Vabrit, K., Tammekivi, V., Hallast, P., Koido, K., Kurg, A., Metspalu, A., Vasar, E., Vasar, V. and Shlik, J. (2004) P.3.031 Association study of 90 candidate genetic polymorphisms in panic disorder: Positive findings with SNPs in serotonin, cholecystokinin and dopamine related genes. European Neuropsychopharmacology, 14 (Supp. 3). S317.

Kingo, K., Kõks, S., Nikopensius, T., Silm, H. and Vasar, E. (2004) Polymorphisms in the interleukin-20 gene: relationships to plaque-type psoriasis. Genes & Immunity, 5 (2). pp. 117-121.

Abramov, U., Raud, S., Kõks, S., Innos, J., Kurrikoff, K., Matsui, T. and Vasar, E. (2004) Targeted mutation of CCK2 receptor gene antagonises behavioural changes induced by social isolation in female, but not in male mice. Behavioural Brain Research, 155 (1). pp. 1-11.

Kõks, S., Luuk, H., Nelovkov, A., Areda, T. and Vasar, E. (2004) A screen for genes induced in the amygdaloid area during cat odor exposure. Genes, Brain and Behavior, 3 (2). pp. 80-89.

Kingo, K., Mössner, R. and Kõks, S. (2003) 10. Inflammatory Dermatoses. Journal of Cutaneous Medicine and Surgery: Incorporating Medical and Surgical Dermatology, 7 (6). p. 493.

Veraksits, A., Rünkorg, K., Kurrikoff, K., Raud, S., Abramov, U., Matsui, T., Bourin, M., Kõks, S. and Vasar, E. (2003) Altered pain sensitivity and morphine-induced anti-nociception in mice lacking CCK2 receptors. Psychopharmacology, 166 (2). pp. 168-175.

Kõks, S., Koido, K., Maron, E., Nikopensius, T., Kurg, A., Slik, J., Vasar, E. and Metspalu, A. (2003) Analysis of single nucleotide polymorphisms in patients with mood disorders. Behavior Genetics, 33 (6). p. 709.

Kõks, S., Abramov, U., Veraksits, A., Bourin, M., Matsui, T. and Vasar, E. (2003) CCK2 receptor-deficient mice have increased sensitivity of dopamine D2 receptors. Neuropeptides, 37 (1). pp. 25-29.

Rünkorg, K., Veraksits, A., Kurrikoff, K., Luuk, H., Raud, S., Abramov, U., Matsui, T., Bourin, M., Kõks, S. and Vasar, E. (2003) Distinct changes in the behavioural effects of morphine and naloxone in CCK2 receptor-deficient mice. Behavioural Brain Research, 144 (1-2). pp. 125-135.

Kingo, K., Kõks, S., Silm, H. and Vasar, E. (2003) IL-10 promoter polymorphisms influence disease severity and course in psoriasis. Genes & Immunity, 4 (6). pp. 455-457.

Roots, K., Kõks, S., Kairane, C., Salum, T., Karelson, E., Vasar, E. and Zilmer, M. (2003) Na-Pump kinetic properties are differently altered in the brain regions of the Cholecystokinin2 Receptor-Deficient Mice. Annals of the New York Academy of Sciences, 986 (1). pp. 644-645.

Kõks, S. (2003) P.3.020 A screen for genes induced in the amygdaloid area of rats during cat odor exposure. European Neuropsychopharmacology, 13 (Supp. 4). S362.

Vasar, E., Kõks, S., Abramov, U., Innos, J., Raud, S., Kurrikoff, K., Volke, V., Bourin, M. and Matsui, T. (2003) P.3.070 CCK2 receptor deficient mice: Changes in anxiety and pain sensitivity. European Neuropsychopharmacology, 13 . S384.

Nelovkov, A., Philips, M-A, Kõks, S. and Vasar, E. (2003) Rats with low exploratory activity in the elevated plus-maze have the increased expression of limbic system-associated membrane protein gene in the periaqueductal grey. Neuroscience Letters, 352 (3). pp. 179-182.

Raud, S., Rünkorg, K., Veraksits, A., Reimets, A., Nelovkov, A., Abramov, U., Matsui, T., Bourin, M., Volke, V., Kõks, S. and Vasar, E. (2003) Targeted mutation of CCK2 receptor gene modifies the behavioural effects of diazepam in female mice. Psychopharmacology, 168 (4). pp. 417-425.

Luuk, H., Kõks, S., Nelovkov, A. and Vasar, E. (2003) A screen for genes induced in the amygdaloid area during cat odor Exposure. Behavior Genetics, 33 (6). pp. 710-711.

Kõks, S., Planken, A., Luuk, H. and Vasar, E. (2002) Cat odour exposure increases the expression of wolframin gene in the amygdaloid area of rat. Neuroscience Letters, 322 (2). pp. 116-120.

Kõks, S. and Vasar, E. (2002) Deramciclane (Egis). Current Opinion in Investigational Drugs, 3 (2). pp. 289-294.

Kurg, A., Nikopensius, T., Hallast, P., Laan, M., Kõks, S., Slik, J., Maron, E., Vasar, E. and Metspalu, A. (2002) Possible association of serotonin 1B receptor and cholecystolkinin 1 receptor gene polymorphisms in bipolar and unipolar affective disorder cases in Estonia. American Journal of Human Genetics, 71 (4).

Kingo, K., Kõks, S., Karelson, M., Silm, H. and Vasar, E. (2002) Promoter polymorphism at position –592 of the interleukin-10 is not associated with early and late-onset psoriasis. Journal of the European Academy of Dermatology and Venereology, 16 (s1). p. 291.

Kairane, C., Roots, K., Uusma, T., Bogdanovic, N., Karelson, E., Kõks, S. and Zilmer, M. (2002) Regulation of the frontocortical sodium pump by Na+ in Alzheimer's disease: Difference from the age-matched control but similarity to the rat model. FEBS Letters, 531 (2). pp. 241-244.

Kõks, S., Beljajev, S., Koovit, I., Abramov, U., Bourin, M. and Vasar, E. (2001) 8-OH-DPAT, but not deramciclane, antagonizes the anxiogenic-like action of paroxetine in an elevated plus-maze. Psychopharmacology, 153 (3). pp. 365-372.

Kõks, S., Volke, V., Veraksits, A., Rünkorg, K., Sillat, T., Abramov, U., Bourin, M., Huotari, M., Männistö, P., Matsui, T. and Vasar, E. (2001) Cholecystokinin 2 receptor-deficient mice display altered function of brain dopaminergic system. Psychopharmacology, 158 (2). pp. 198-204.

Võikar, V., Kõks, S., Vasar, E. and Rauvala, H. (2001) Strain and gender differences in the behavior of mouse lines commonly used in transgenic studies. Physiology & Behavior, 72 (1-2). pp. 271-281.

Raasmaja, A., Soosaar, A., Lampela, P., Kõks, S., Mannik, A., Volke, V., Huotari, M., Joki, S., Ustav, E. and Vasar, E. (2001) Tyrosine hydroxylase gene transfer to rat striatum using Bovine Papilloma Virus-1 expression plasmids in the experimental model of Parkinson's disease. Pharmaceutical and Pharmacological Letters, 11 (2). pp. 83-86.

Kõks, S., Männistö, P.T., Bourin, M., Shlik, J., Vasar, V. and Vasar, E. (2000) Cholecystokinin-induced anxiety in rats: relevance of pre-experimental stress and seasonal variations. Journal of Psychiatry and Neuroscience, 25 (1). pp. 33-42.

Võikar, V., Soosaar, A., Volke, V., Kõks, S., Bourin, M., Männistö, P.T. and Vasar, E. (1999) Apomorphine-induced behavioural sensitization in rats: Individual differences, role of dopamine and NMDA receptors. European Neuropsychopharmacology, 9 (6). pp. 507-514.

Kõks, S., Soosaar, A., Võikar, V., Bourin, M. and Vasar, E. (1999) BOC-CCK-4, CCKB receptor agonist, antagonizes anxiolytic-like action of morphine in elevated plus-maze. Neuropeptides, 33 (1). pp. 63-69.

Bourin, M., Vasar, E., Kõks, S. and Völkar, V. (1999) A CCKB receptor antagonist LY288513 reverses the anti-exploratory action of paroxetine, a selective serotonin reuptake inhibitor. European Neuropsychopharmacology, 9 (Supp. 5). p. 310.

Kõks, S., Bourin, M., Võikar, V., Soosaar, A. and Vasar, E. (1999) Role of CCK in anti-exploratory action of paroxetine, 5-HT reuptake inhibitor. The International Journal of Neuropsychopharmacology, 2 (1). pp. 9-16.

Kõks, S., Soosaar, A., Võikar, V., Volke, V., Ustav, M., Männistö, P.T., Bourin, M. and Vasar, E. (1998) Opioid antagonist naloxone potentiates anxiogenic-like action of cholecystokinin agonists in elevated plus-maze. Neuropeptides, 32 (3). pp. 235-240.

Volke, V., Soosaar, A., Kõks, S., Vasar, E. and Männistö, P.T. (1998) l-Arginine abolishes the anxiolytic-like effect of diazepam in the elevated plus-maze test in rats. European Journal of Pharmacology, 351 (3). pp. 287-290.

Vasar, E., Kõks, S., Volke, V. and Võikar, V. (1997) Cholecystokinin in animal models of anxiety. Biological Psychiatry, 42 (1). 196S-197S.

Kõks, S., Vasar, E., Soosaar, A., Lang, A., Volke, V., Võikar, V., Bourin, M. and Männistö, P.T. (1997) Relation of exploratory behavior of rats in elevated plus-maze to brain receptor binding properties and serum growth hormone levels. European Neuropsychopharmacology, 7 (4). pp. 289-294.

Volke, V., Soosaar, A., Kõks, S., Bourin, M., Männistö, P.T. and Vasar, E. (1996) Nitric oxide mediates caeruleininduced suppression of locomotor activity. Neuropeptides, 30 (4). pp. 323-326.

Kõks, S., Volke, V., Vasar, E. and Maennistoe, P.T. (1995) Anxiolytic-like effect of L-NAME, nitric oxide synthase inhibitor, in elevated plus-maze. Pharmacology & Toxicology, 76 . p. 35.

Vasar, E., Volke, V., Kõks, S. and Bradwejn, J. (1995) Cholecystokinin and regulation of emotional behaviour in rats. Pharmacology & Toxicology, 76 . p. 85.

Peuranen, E., Vasar, E., Kõks, S., Volke, V., Lang, A., Rauhala, P. and Männistö, P.T. (1995) Further studies on the role of cholecystokinin-A and B receptors in secretion of anterior pituitary hormones in male rats. Neuropeptides, 28 (1). pp. 1-11.

Volke, V., Kõks, S., Vasar, E., Bourin, M., Bradwejn, J. and Männistö, P.T. (1995) Inhibition of nitric oxide synthase causes anxiolytic-like behaviour in an elevated plus-maze. Neuroreport, 6 (10). pp. 1413-1416.

Lang, A., Harro, J., Soosaar, A., Kõks, S., Volke, V., Oreland, L., Bourin, M., Vasar, E., Bradwejn, J. and Männistö, P.T. (1995) Role of N-methyl-d-aspartic acid and cholecystokinin receptors in apomorphine-induced aggressive behaviour in rats. Naunyn-Schmiedeberg's Archives of Pharmacology, 351 (4). pp. 363-370.

Lang, A., Soosaar, A., Kõks, S., Volke, K., Bourin, M., Bradwejn, J. and Vasar, E. (1994) Pharmacological comparison of antipsychotic drugs and σ-Antagonists in rodents. Pharmacology & Toxicology, 75 (3-4). pp. 222-227.

Vasar, E., Lang, A., Harro, J., Kõks, S., Volke, V., Sihver, S., Bourin, M., Bradwejn, J. and Männistö, P.T. (1994) Subdiaphragmatic vagotomy does not prevent the anti-exploratory effect of caerulein in the elevated plus-maze. Neuropeptides, 26 (1). pp. 39-45.

Vasar, E., Harro, J., Lang, A., Soosaar, A., Ööpik, T., Kõks, S., Sihver, S. and Volke, V. (1993) Anti-exploratory effect of N-methyl-d-aspartate in elevated plus-maze. Involvement of NMDA and CCK receptors. European Neuropsychopharmacology, 3 (1). pp. 63-73.

Non-refereed Article

Fang, L.T., Zhu, B., Zhao, Y., Chen, W., Yang, Z., Kerrigan, L., Langenbach, K., de Mars, M., Lu, C., Idler, K., Jacob, H., Yu, Y., Ren, L., Zheng, Y., Jaeger, E., Schroth, G., Abaan, O.D., Lack, J., Shen, T-W, Talsania, K., Chen, Z., Stanbouly, S., Shetty, J., Tran, B., Meerzaman, D., Nguyen, C., Petitjean, V., Sultan, M., Cam, M., Hung, T., Peters, E., Kalamegham, R., Ebrahim Sahraeian, S.M., Mohiyuddin, M., Guo, Y., Yao, L., Song, L., Lam, H.Y.K., Drabek, J., Maestro, R., Gasparotto, D., Kõks, S., Reimann, E., Scherer, A., Nordlund, J., Liljedahl, U., Jensen, R.V., Pirooznia, M., Li, Z., Xiao, C., Sherry, S., Kusko, R., Moos, M., Donaldson, E., Tezak, Z., Ning, B., Li, J., Duerken-Hughes, P., Hong, H., Shi, L., Wang, C. and Xiao, W. (2019) Establishing reference samples for detection of somatic mutations and germline variants with NGS technologies. bioRxiv .

Billingsley, K.J., Barbosa, I.A., Bandrés-Ciga, S., Quinn, J.P., Bubb, V.J., Deshpande, C., Botia, J.A., Reynolds, R.H., Zhang, D.ORCID: 0000-0002-9847-1403, Simpson, M.A., Blauwendraat, C., Gan-Or, Z., Gibbs, J.R., Nalls, M.A., Singleton, A., Ryten, M. and Kõks, S. (2018) Genetic variation within genes associated with mitochondrial function is significantly associated with later age at onset of Parkinson disease and contributes to disease risk. bioRxiv .

Conference Paper

Lilleoja, R., Reimann, E., Nõmm, M., Plaas, M., Ivask, M., Pärn, P., Häling, A., Jaakma, Ü. and Kõks, S. (2016) Kloonembrüote ja in vitro viljastatud embrüote RNA sünteesi erinevused. In: Healthy Animal and Healthy Food 2016, 2 - 3 March 2016, Estonian University of Life Sciences

Conference Item

Zamani Esteki, M., Viltrop, T., Tiirats, A., Tsuiko, O., Koel, M., Noukas, M., Zilina, O., Magi, R., Kõks, S., Kurg, A., Voet, T., Vermeesch, J. and Salumets, A. (2017) In vitro fertilization has no effect on prevalence of mosaic copy-number alterations in fetal and placental lineages. In: European Human Genetics Conference (ESHG) 2017, 27 - 30 May 2017, Copenhagen, Denmark.

Rull, K., Tomberg, K., Kõks, S., Männik, J., Möls, M., Sirotkina, M., Värv, S. and Laan, M. (2012) Aberrant expression of TRAIL in placenta and maternal serum in early pregancy complications. In: 15th International & 14th European Congress of Endocrinology, 05 - 09 May 2012, Florence, Italy.

Abramov, U., Kõks, S. and Vasar, E. (2006) Altered behavioural effects of ethanol in mice lacking CCK-2 receptors. In: FENS Forum 2006, 8 - 12 July 2006, Vienna, Austria.

Sütt, S., Areda, T., Raud, S., Kõks, S. and Vasar, E. (2006) CB1 receptors and anandamide expression is increased in mesolimbic structure after exposure to cat odour. In: FENS Forum 2006, 8 - 12 July 2006, Vienna, Austria.

Innos, J., Kõks, S. and Vasar, E. (2006) CCK2 receptor deficient mice display normal memory but impaired pain sensitivity. In: FENS Forum 2006, 8 - 12 July 2006, Vienna, Austria.

Vasar, E., Kõks, S., Kurrikoff, K., Sütt, S., Raud, S. and Areda, T. (2006) Cat odour induced anxiety in rodents: changes in expression of neuropeptide genes in brain structures. In: FENS Forum 2006, 8 - 12 July 2006, Vienna, Austria.

Philips, M-A, Kingo, K., Kõks, S., Aunin, E., Karelson, M., Silm, H. and Vasar, E. (2006) Myg1 protein is functionally important in both brain and skin. In: FENS Forum 2006, 8 - 12 July 2006, Vienna, Austria.

Book Chapter

Kõks, S. and Kõks, G. (2018) The Role of Human Endogenous Retroviruses (HERVs) in the Pathologies of the Nervous System. In: Gerlai, R.T., (ed.) Molecular-Genetic and Statistical Techniques for Behavioral and Neural Research. Academic Press, pp. 519-533.

Book

Kavak, A., Kärt, O., Ernits, E., Padrik, P., Hallap, T., Nahkur, E., Jalakas, M., Kask, K., Jaakma, Ü, Nõmm, M., Kurõkin, J., Kõks, S. and Mark, E. (2018) Veise sigimine: kõrgkooliõpik. Estonian University of Life Sciences.

Bekaer, S., Blancke, S., Bols, P.E.J., Boullart, K., Braeckman, J., Burvenich, C., Deceuninck, B., Dedobbeleer, W., De porte, H.F.M., Ediers, T., Hanzen, C., Jaakma, Ü., Knight, C.H., Kõks, S., Leman, M., Rubens, R., Segers, D. and Rijckeghem, C.V. (2015) Historia Physiologiae. Ghent University. Department of Comparative Physiology and Biometrics.

Working Paper

Nõmm, M., Porosk, R., Pärn, P., Soomets, U., Jaakma, Ü., Kõks, S. and Kilk, K. (2017) Low molecular weight metabolites as possible new non-invasive tool for selecting bovine in vitro produced embryos. Estonian University of Life Sciences.

This list was generated on Sun Dec 15 12:41:31 2019 UTC.