| Factor V Leiden and prothrombin 21210G> A mutation and paediatric ischaemic stroke: a case–control study and two meta‐analyses R Laugesaar, T Kahre, A Kolk, Ü Uustalu, P Kool, T Talvik Acta paediatrica 99 (8), 1168-1174, 2010 | 55 | 2010 |
| Presumed perinatal stroke: risk factors, clinical and radiological findings P Ilves, R Laugesaar, D Loorits, A Kolk, T Tomberg, S Lõo, I Talvik, ... Journal of child neurology 31 (5), 621-628, 2016 | 44 | 2016 |
| Cystic fibrosis in Estonia T Kahre Tartu University Press, 2004 | 44 | 2004 |
| Prevalence of Angelman syndrome and Prader–Willi syndrome in Estonian children: Sister syndromes not equally represented E Õiglane‐Shlik, T Talvik, R Žordania, H Poder, T Kahre, E Raukas, T Ilus, ... American Journal of Medical Genetics Part A 140 (18), 1936-1943, 2006 | 41 | 2006 |
| Large gene panel sequencing in clinical diagnostics—results from 501 consecutive cases S Pajusalu, T Kahre, H Roomere, Ü Murumets, L Roht, K Simenson, ... Clinical genetics 93 (1), 78-83, 2018 | 39 | 2018 |
| The number of CAG and GGN triplet repeats in the Androgen Receptor gene exert combinatorial effect on hormonal and sperm parameters in young men M Grigorova, M Punab, T Kahre, M Ivandi, N Tõnisson, O Poolamets, ... Andrology 5 (3), 495-504, 2017 | 36 | 2017 |
| Overview of hereditary breast and ovarian cancer (HBOC) guidelines across Europe DH Marmolejo, MYZ Wong, S Bajalica-Lagercrantz, M Tischkowitz, ... European Journal of Medical Genetics 64 (12), 104350, 2021 | 35 | 2021 |
| Prevalence of c. 35delG and p. M34T mutations in the GJB2 gene in Estonia R Teek, K Kruustük, R Zordania, K Joost, T Reimand, T Möls, E Oitmaa, ... International journal of pediatric otorhinolaryngology 74 (9), 1007-1012, 2010 | 31 | 2010 |
| A retrospective analysis of the prevalence of imprinting disorders in Estonia from 1998 to 2016 M Yakoreva, T Kahre, R Žordania, K Reinson, R Teek, V Tillmann, A Peet, ... European Journal of Human Genetics 27 (11), 1649-1658, 2019 | 30 | 2019 |
| Prevalence of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency in Estonia K Joost, K Ounap, R Žordania, ML Uudelepp, RK Olsen, K Kall, K Kilk, ... JIMD Reports-Case and Research Reports, 2011/2, 79-85, 2012 | 21 | 2012 |
| Prevalence of the fragile X syndrome among Estonian mentally retarded and the entire children's population H Puusepp, T Kahre, H Sibul, V Soo, I Lind, E Raukas, K Õunap Journal of child neurology 23 (12), 1400-1405, 2008 | 21 | 2008 |
| Familial 1.3-Mb 11p15. 5p15. 4 duplication in three generations causing Silver-Russell and Beckwith-Wiedemann syndromes MA Vals, T Kahre, P Mee, K Muru, E Kallas, O Žilina, V Tillmann, K Õunap Molecular Syndromology 6 (3), 147-151, 2015 | 20 | 2015 |
| A descriptive epidemiological study of Duchenne muscular dystrophy in childhood in Estonia ÜA Talkop, T Kahre, A Napa, I Talvik, A Sööt, A Piirsoo, V Sander, T Talvik European Journal of Paediatric Neurology 7 (5), 221-226, 2003 | 20 | 2003 |
| Are Methylenetetrahydrofolate Reductase (MTHFR) Gene Polymorphisms C677T and A1298C Associated with Higher Risk of Pediatric Migraine in Boys and Girls? AL Lorenz, T Kahre, E Mihailov, T Nikopensius, EM Lotman, A Metspalu, ... Journal of Biomedical Science and Engineering 2014, 2014 | 19 | 2014 |
| Hearing impairment in Estonia: an algorithm to investigate genetic causes in pediatric patients R Teek, K Kruustük, R Žordania, K Joost, T Kahre, N Tonisson, M Nelis, ... Advances in Medical Sciences 58 (2), 419-428, 2013 | 18 | 2013 |
| Descriptive epidemiology of spinal muscular atrophy type I in Estonia E Vaidla, I Talvik, A Kulla, T Kahre, M Hamarik, A Napa, T Metsvaht, ... Neuroepidemiology 27 (3), 164-168, 2006 | 18 | 2006 |
| Aortic arch thrombosis in a neonate with heterozygous carrier status of factor V Leiden mutation T Metsvaht, T Hermlin, H Kern, T Kahre, J Starkopf Congenital heart disease 1 (1‐2), 40-45, 2006 | 18 | 2006 |
| The estimated prevalence of N-linked congenital disorders of glycosylation across various populations based on allele frequencies in general population databases S Pajusalu, MA Vals, L Mihkla, U Šamarina, T Kahre, K Õunap Frontiers in genetics 12, 719437, 2021 | 15 | 2021 |
| A new case of a rare combination of Temple syndrome and mosaic trisomy 14 and a literature review M Yakoreva, T Kahre, S Pajusalu, P Ilisson, O Žilina, V Tillmann, ... Molecular Syndromology 9 (4), 182-189, 2018 | 15 | 2018 |
| The frequency of methylation abnormalities among estonian patients selected by clinical diagnostic scoring systems for Silver–Russell Syndrome and Beckwith–Wiedemann Syndrome MA Vals, M Yakoreva, T Kahre, P Mee, K Muru, K Joost, R Teek, ... Genetic Testing and Molecular Biomarkers 19 (12), 684-691, 2015 | 11 | 2015 |
