Michael J. Browning

机构：Oxford Health NHS Foundation Trust, University of Oxford

发表论文 121 篇 · 总被引 6519 次 · h-index 36

代表论文

• Whole-genome sequencing of patients with rare diseases in a national health system (2020 · Nature · 被引 588)
• Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease (2016 · The American Journal of Human Genetics · 被引 490)
• Germline selection shapes human mitochondrial DNA diversity (2019 · Science · 被引 258)
• Whole-genome sequencing of a sporadic primary immunodeficiency cohort (2020 · Nature · 被引 246)
• Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans (2018 · Journal of Allergy and Clinical Immunology · 被引 242)
• Validation of preoperative cardiopulmonary exercise testing-derived variables to predict in-hospital morbidity after major colorectal surgery (2016 · British journal of surgery · 被引 158)