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Research in Microbiology|April 15, 2015
Complementary seminovaginal microbiome in couplesReet Mändar, Margus Punab, Natalja Borovkova, et al.European Journal of Human Genetics : EJHG|April 13, 2017
Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panelMario Mitt, Mart Kals, Kalle Pärn, et al.Prenatal Diagnosis|October 16, 2010
Molecular diagnosis of Down syndrome using quantitative APEX-2 microarraysEneli Oitmaa, Maire Peters, Kadri Vaidla, et al.The International Journal of Neuropsychopharmacology|June 2, 2005
Analysis of SNP profiles in patients with major depressive disorderSulev Kõks, Tiit Nikopensius, Kati Koido, et al.Frontiers in Genetics|August 5, 2022
Do Biobank Recall Studies Matter? Long-Term Follow-Up of Research Participants With Familial HypercholesterolemiaMiriam Nurm, Anu Reigo, Margit Nõukas, et al.Psychiatric Genetics|February 22, 2005
Association study of 90 candidate gene polymorphisms in panic disorderEduard Maron, Tiit Nikopensius, Sulev Kõks, et al.Human Molecular Genetics|November 19, 2013
Sex- and age-interacting eQTLs in human complex diseasesChen Yao, Roby Joehanes, Andrew D Johnson, et al.Scientific Reports|November 26, 2020
An epigenome-wide association study of metabolic syndrome and its componentsMarja-Liisa Nuotio, Natalia Pervjakova, Anni Joensuu, et al.European Journal of Medical Genetics|November 30, 2010
A parallel SNP array study of genomic aberrations associated with mental retardation in patients and general population in EstoniaKatrin Männik, Sven Parkel, Priit Palta, et al.Journal of Child Neurology|December 20, 2013
De novo SCN8A mutation identified by whole-exome sequencing in a boy with neonatal epileptic encephalopathy, multiple congenital anomalies, and movement disordersUlvi Vaher, Margit Nõukas, Tiit Nikopensius, et al.Pageof 42