William Allen

Loss-of-function mutations in the human <i>GLI2</i> gene are associated with pituitary anomalies and holoprosencephaly-like features

Erich Roessler, Yangzhu Du, José L. Mullor et al. · Proceedings of the National Academy of Sciences · 2003 · 344 citations · Full text

Life Sciences, Developmental Biology, Genetics +17

5,10 Methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects

C Y Ou, Roger E. Stevenson, Vicid K. Brown et al. · American Journal of Medical Genetics · 1996 · 228 citations

Life Sciences, Genetics, Molecular Genetics +17

Decline in Prevalence of Neural Tube Defects in a High-Risk Region of the United States

Roger E. Stevenson, William Allen, G. Shashidhar Pai et al. · PEDIATRICS · 2000 · 211 citations

Public Health, Maternal Health, Obstetrics +17

NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease

Paige Martin, Yu Kigoshi-Tansho, Roger B. Sher et al. · Nature Communications · 2020 · 100 citations · Full text

Life Sciences, Genetics, Molecular Biology +17

Mutations in TOP3A Cause a Bloom Syndrome-like Disorder

Carol-Anne Martin, Kata Sarlós, Clare V. Logan et al. · The American Journal of Human Genetics · 2018 · 99 citations · Full text

Life Sciences, Genetics, Molecular Genetics +7