Tiina Kahre

Familial 1.3-Mb 11p15.5p15.4 Duplication in Three Generations Causing Silver-Russell and Beckwith-Wiedemann Syndromes

Mari‐Anne Vals, Tiina Kahre, Pille Mee et al. · Molecular Syndromology · 2015 · 49 citations · Full text

Beckwith-wiedemann Syndrome, Developmental Anomaly, Beckwith-wiedemann Syndromes +15

A retrospective analysis of the prevalence of imprinting disorders in Estonia from 1998 to 2016

Maria Yakoreva, Tiina Kahre, Riina Žordania et al. · European Journal of Human Genetics · 2019 · 40 citations · Full text

Retrospective Analysis, Psychiatry

Prevalence of Angelman syndrome and Prader–Willi syndrome in Estonian children: Sister syndromes not equally represented

Eve Õiglane‐Shlik, Tiina Talvik, Riina Žordania et al. · American Journal of Medical Genetics Part A · 2006 · 37 citations

Presumed Perinatal Stroke

Pilvi Ilves, Rael Laugesaar, Dagmar Loorits et al. · Journal of Child Neurology · 2015 · 33 citations

The number of <scp>CAG</scp> and <scp>GGN</scp> triplet repeats in the <i>Androgen Receptor</i> gene exert combinatorial effect on hormonal and sperm parameters in young men

Marina Grigorova, Margus Punab, Tiina Kahre et al. · Andrology · 2017 · 31 citations · Full text