Identification of genetic variants affecting vitamin D receptor binding and associations with autoimmune disease

Author:

Gallone Giuseppe123,Haerty Wilfried12,Disanto Giulio2,Ramagopalan Sreeram V.4,Ponting Chris P.125,Berlanga-Taylor Antonio J.678

Affiliation:

1. MRC Functional Genomics Unit

2. Department of Physiology, Anatomy and Genetics, University of Oxford, South Parks Road, Oxford OX1 3PT, UK

3. Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton CB10 1SA, UK

4. Real-World Evidence, Evidera, London W6 8DL, UK

5. MRC Human Genetics Unit, The Institute of Genetics and Molecular Medicine, University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK

6. Wellcome Trust Centre for Human Genetics, Nuffield Department of Clinical Medicine, University of Oxford, Oxford OX3 7BN, UK

7. CGAT, MRC Functional Genomics Unit, Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford OX1 3PT, UK

8. MRC-PHE Centre for Environment and Health, Department of Epidemiology & Biostatistics, School of Public Health, Faculty of Medicine, Imperial College London, St Mary’s Campus, Norfolk Place, London W2 1PG, UK

Funder

Medical Research Council

Wellcome Trust and Genzyme

Multiple Sclerosis Society UK

Council for Science and Technology (CONACyT) Mexico

Research Councils UK (RCUK)

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

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