Eve Vaidla

Chromosomal microarray analysis as a first‐tier clinical diagnostic test: <scp>E</scp>stonian experience

Olga Žilina, Rita Teek, Pille Tammur et al. · Molecular Genetics & Genomic Medicine · 2014 · 27 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Neonatal Spinal Muscular Atrophy Type 1 With Bone Fractures and Heart Defect

Eve Vaidla, Inga Talvik, Andres Kulla et al. · Journal of Child Neurology · 2007 · 24 citations

Medicine, Cardiology, Pediatrics +15

Descriptive Epidemiology of Spinal Muscular Atrophy Type I in Estonia

Eve Vaidla, Inga Talvik, Andres Kulla et al. · Neuroepidemiology · 2006 · 14 citations

Medicine, Genetics, Neurology +17

A prenatally diagnosed case of Meckel–Gruber syndrome with novel compound heterozygous pathogenic variants in the <i>TXNDC15</i> gene

Konstantin Ridnõi, Marek Šois, Eve Vaidla et al. · Molecular Genetics & Genomic Medicine · 2019 · 13 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

The Birth Prevalence of Spinal Muscular Atrophy: A Population Specific Approach in Estonia

Siiri Sarv, Tiina Kahre, Eve Vaidla et al. · Frontiers in Genetics · 2021 · 12 citations · Full text

Life Sciences, Genetics, Pediatrics +17