Intragenic and extragenic disruptions of FOXL2 mapped by whole genome low-coverage sequencing in two BPES families with chromosome reciprocal translocation

Highly Conserved Non-Coding Sequences Are Associated with Vertebrate Development

Adam Woolfe, Martin Goodson, Debbie K. Goode et al. · PLoS Biology · 2004 · 987 citations · Full text

Life Sciences, Developmental Biology, Genetics +16

The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome

Laura Crisponi, Manila Deiana, Angela Loi et al. · Nature Genetics · 2001 · 977 citations

Life Sciences, Genetics, Molecular Genetics +5

Somatic Sex Reprogramming of Adult Ovaries to Testes by FOXL2 Ablation

N. Henriette Uhlenhaut, Susanne Jakob, Katrin Anlag et al. · Cell · 2009 · 952 citations · Full text

Medicine, Endocrinology, Genetics +11

Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype-phenotype correlation

Human Molecular Genetics · 2001 · 280 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

FOXL2 and BPES: Mutational Hotspots, Phenotypic Variability, and Revision of the Genotype-Phenotype Correlation

Diane Beysen, Christine Oley, Birgit Lorenz et al. · The American Journal of Human Genetics · 2003 · 243 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14