Rita Teek

Biallelic <i>CACNA1A</i> mutations cause early onset epileptic encephalopathy with progressive cerebral, cerebellar, and optic nerve atrophy

Karit Reinson, Eve Õiglane‐Shlik, Inga Talvik et al. · American Journal of Medical Genetics Part A · 2016 · 84 citations

Life Sciences, Genetics, Neurology +17

Monosomy 1p36 – A multifaceted and still enigmatic syndrome: Four clinically diverse cases with shared white matter abnormalities

Eve Õiglane‐Shlik, Sanna Puusepp, Inga Talvik et al. · European Journal of Paediatric Neurology · 2014 · 42 citations

Life Sciences, Genetics, Molecular Genetics +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 · 42 citations · Full text

Medicine, Psychiatry, Human Genetics +8

Evaluation of the 124-plex SNP typing microarray for forensic testing

Kaarel Krjutškov, Triin Viltrop, Priit Palta et al. · Forensic Science International Genetics · 2009 · 35 citations

Life Sciences, Genetics, Molecular Genetics +14

Natural history of KBG syndrome in a large European cohort

Lorenzo Loberti, Lucia Pia Bruno, Stefania Granata et al. · Human Molecular Genetics · 2022 · 30 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17