William G. Newman

Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes

Nasim Mavaddat, Kyriaki Michailidou, Joe Dennis et al. · The American Journal of Human Genetics · 2018 · 1.2K citations · Full text

Life Sciences, Biostatistics, Genetics +17

Whole-genome sequencing of patients with rare diseases in a national health system

Ernest Turro, Karyn Mégy, Olga Shamardina et al. · Nature · 2020 · 582 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Heterozygous Mutations in TREX1 Cause Familial Chilblain Lupus and Dominant Aicardi-Goutières Syndrome

Gillian Rice, William G. Newman, John Dean et al. · The American Journal of Human Genetics · 2007 · 408 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9

Germline Mutations in <i>SUFU</i> Cause Gorlin Syndrome–Associated Childhood Medulloblastoma and Redefine the Risk Associated With <i>PTCH1</i> Mutations

Miriam J. Smith, Christian Beetz, Simon G. Williams et al. · Journal of Clinical Oncology · 2014 · 296 citations

Life Sciences, Genetics, Oncology +17

Dominant Mutations in the Autoimmune Regulator AIRE Are Associated with Common Organ-Specific Autoimmune Diseases

Bergithe E Oftedal, Alexander Hellesen, Martina M. Erichsen et al. · Immunity · 2015 · 283 citations

Life Sciences, Genetics, Immunology +14