Steven A. Wall

Factors influencing success of clinical genome sequencing across a broad spectrum of disorders

Jenny C. Taylor, Hilary C. Martin, Stefano Lise et al. · Nature Genetics · 2015 · 388 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Mutations of ephrin-B1 ( <i>EFNB1</i> ), a marker of tissue boundary formation, cause craniofrontonasal syndrome

Stephen R.F. Twigg, Rui Kan, Christian Babbs et al. · Proceedings of the National Academy of Sciences · 2004 · 340 citations · Full text

Dentistry, Genetics, Molecular Genetics +17

Exclusive paternal origin of new mutations in Apert syndrome

Dominique M. Moloney, Sarah R Slaney, Michael Oldridge et al. · Nature Genetics · 1996 · 321 citations

Life Sciences, Genetics, Molecular Genetics +14

Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification

Andrew O.M. Wilkie, Zequn Tang, Navaratnam Elanko et al. · Nature Genetics · 2000 · 318 citations

Dentistry, Genetics, Molecular Genetics +16

Prevalence and Complications of Single-Gene and Chromosomal Disorders in Craniosynostosis

Andrew O.M. Wilkie, Jo C. Byren, Jane A. Hurst et al. · PEDIATRICS · 2010 · 287 citations · Full text

Medicine, Genetics, Molecular Genetics +17