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Journal of Public Health (Oxford, England)|March 1, 2008
High-prevalence and high-estimated incidence of HIV infection among new injecting drug users in Estonia: need for large scale prevention programsAnneli Uusküla, Mart Kals, Kristiina Rajaleid, et al.European Journal of Human Genetics : EJHG|February 27, 2014
Coffin-Siris Syndrome with obesity, macrocephaly, hepatomegaly and hyperinsulinism caused by a mutation in the ARID1B geneMari-Anne Vals, Eve Õiglane-Shlik, Margit Nõukas, et al.Arrhythmia & Electrophysiology Review|March 2, 2026
Long-term Outcomes of Atrioventricular Node Ablation and Pacemaker Therapy for Rate Control in Atrial Fibrillation: Insights from a 10-year Nationwide AnalysisAnette Caroline Kõre, Martin Serg, Tuljo Ööbik, et al.European Journal of Human Genetics : EJHG|November 24, 2020
Genotype-first approach to the detection of hereditary breast and ovarian cancer risk, and effects of risk disclosure to biobank participantsLiis Leitsalu, Marili Palover, Timo Tõnis Sikka, et al.European Journal of Human Genetics : EJHG|November 14, 2018
Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health recordsTõnis Tasa, Kristi Krebs, Mart Kals, 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.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.European Journal of Medical Genetics|March 22, 2022
Spectrum and frequency of CHEK2 variants in breast cancer affected and general population in the Baltic states region, initial results and literature reviewKristine Pavlovica, Arvids Irmejs, Margit Noukas, et al.HGG Advances|August 29, 2022
Omics-informed CNV calls reduce false-positive rates and improve power for CNV-trait associationsMaarja Lepamets, Chiara Auwerx, Margit Nõukas, et al.Eclinicalmedicine|December 25, 2024
Genetic vulnerability and adverse mental health outcomes following mild traumatic brain injury: a meta-analysis of CENTER-TBI and TRACK-TBI cohortsMart Kals, Lindsay Wilson, Daniel F Levey, et al.Pageof 7