Lina Basel‐Vanagaite

Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible

Bernward Hinkes, Roger C. Wiggins, Rasheed Gbadegesin et al. · Nature Genetics · 2006 · 564 citations

Medicine, Genetics, Molecular Genetics +14

G Protein-Coupled Receptor-Dependent Development of Human Frontal Cortex

Xianhua Piao, R. Sean Hill, Adria Bodell et al. · Science · 2004 · 522 citations

Life Sciences, Developmental Biology, Neuroscience +17

tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia

Birgit Budde, Yasmin Namavar, P. G. Barth et al. · Nature Genetics · 2008 · 256 citations

Life Sciences, Genetics, Molecular Genetics +2

Dominant Mutations in GRHL3 Cause Van der Woude Syndrome and Disrupt Oral Periderm Development

Myriam Peyrard‐Janvid, Elizabeth J. Leslie, Youssef A. Kousa et al. · The American Journal of Human Genetics · 2013 · 230 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Fragile-X Carrier Screening and the Prevalence of Premutation and Full-Mutation Carriers in Israel

Hagit Toledano‐Alhadef, Lina Basel‐Vanagaite, Nurit Magal et al. · The American Journal of Human Genetics · 2001 · 228 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14