Peter Branney

Gain-of-Function Mutations of ARHGAP31, a Cdc42/Rac1 GTPase Regulator, Cause Syndromic Cutis Aplasia and Limb Anomalies

Laura Southgate, Rajiv D. Machado, Katie Snape et al. · The American Journal of Human Genetics · 2011 · 119 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and Mice

Joe Rainger, Ellen van Beusekom, Jacqueline Ramsay et al. · PLoS Genetics · 2011 · 93 citations · Full text

Medicine, Genetics, Molecular Genetics +15

Miller (Genee-Wiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODH

Joe Rainger, Hemant Bengani, Lauren Campbell et al. · Human Molecular Genetics · 2012 · 69 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Characterisation of the Fibroblast Growth Factor Dependent Transcriptome in Early Development

Peter Branney, Laura Faas, Sarah E. Steane et al. · PLoS ONE · 2009 · 50 citations · Full text

Life Sciences, Developmental Biology, Molecular Biology +17

Bilateral Renal Agenesis/Hypoplasia/Dysplasia (BRAHD): Postmortem Analysis of 45 Cases with Breakpoint Mapping of Two De Novo Translocations

Louise Harewood, Monica Liu, Jean W. Keeling et al. · PLoS ONE · 2010 · 38 citations · Full text

Medicine, Endocrinology, Pathology +17