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Negligible impact of rare autoimmune-locus coding-region variants on missing heritability
Karen A. Hunt, Vanisha Mistry, Nicholas A. Bockett, Tariq Ahmad, Maria Ban, Jonathan N. Barker, Jeffrey C. Barrett, Hannah Blackburn, Oliver Brand, Oliver Burren, Francesca Capon, Alastair Compston, Stephen C. L. Gough, Luke Jostins, Yong Kong, James C. Lee, Monkol Lek, Daniel G. MacArthur, John C. Mansfield, Christopher G. Mathew
*Corresponding author for this work
- Queen Mary University of London
- University of Exeter
- University of Cambridge
- Wellcome Sanger Institute
- University of Oxford
- Wellcome Trust Ctr Human Genet
- Yale University
- Massachusetts General Hospital, Harvard University
- Newcastle University
- University of Virginia
- Kings Coll London, Guy's & St Thomas' NHS Foundation Trust, Kings College London, University of London, Sch Med, Div Genet & Mol Med, Guys Hosp
- University of Edinburgh
- UCL University College London
Research output: Contribution to journal › Letter › peer-review
161
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(Scopus)