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Paper Details

Rare and common genetic determinants of metabolic individuality and their effects on human health.
Nat Med
34
2022
330, DPYD, SRD5A2, causal genes, genomic regions, human, human plasma, inborn errors of metabolism, variant-
Author NameAffiliation
Praveen SurendranBritish Heart Foundation Cardiovascular Epidemiology Unit, University of Cambridge
Praveen SurendranUniversity of Cambridge
Praveen SurendranWellcome Genome Campus and University of Cambridge
Praveen SurendranBritish Heart Foundation Centre of Research Excellence, School of Clinical Medicine, Addenbrooke's Hospital, University of Cambridge
Nicholas A Watkins
Massimo ManginoKing's College London
Massimo ManginoNIHR Biomedical Research Centre at Guy's and St Thomas' Foundation Trust
Tim D SpectorKing's College London
Tim D SpectorKing's College London
Nicole SoranzoBritish Heart Foundation Centre of Research Excellence, School of Clinical Medicine, Addenbrooke's Hospital, University of Cambridge
Nicole SoranzoUniversity of Cambridge
Nicole SoranzoNIHR Blood and Transplant Research Unit in Donor Health and Genomics, University of Cambridge
Nicole Soranzo
Nicole SoranzoWellcome Sanger Institute
Nicole SoranzoBritish Heart Foundation Centre of Research Excellence, School of Clinical Medicine, Addenbrooke's Hospital, University of Cambridge
Nicole SoranzoWellcome Sanger Institute
Nicole Soranzo
Nicole SoranzoNIHR Blood and Transplant Research Unit in Donor Health and Genomics, University of Cambridge
Nicole SoranzoUniversity of Cambridge
Gregory A Michelotti
Wiebke ArltInstitute of Metabolism and Systems Research, University of Birmingham
Wiebke ArltNIHR Birmingham Biomedical Research Centre, University Hospitals Birmingham NHS Foundation Trust and University of Birmingham
Luca A LottaUniversity of Cambridge
Spiros DenaxasInstitute of Health Informatics, University College London
Spiros Denaxas
Spiros DenaxasBritish Heart Foundation Data Science Centre
Eric R GamazonVanderbilt Genetics Institute, Vanderbilt University Medical Center
Eric R GamazonUniversity of Cambridge
Eric R GamazonVanderbilt Genetics Institute, Vanderbilt University Medical Center
Eric R GamazonUniversity of Cambridge
Joanna M M HowsonBritish Heart Foundation Cardiovascular Epidemiology Unit, University of Cambridge
Joanna M M HowsonNovo Nordisk Research Centre Oxford
John DaneshBritish Heart Foundation Cardiovascular Epidemiology Unit, University of Cambridge
John DaneshNIHR Blood and Transplant Research Unit in Donor Health and Genomics, University of Cambridge
John DaneshWellcome Sanger Institute
John DaneshWellcome Genome Campus and University of Cambridge
John DaneshBritish Heart Foundation Centre of Research Excellence, School of Clinical Medicine, Addenbrooke's Hospital, University of Cambridge
Nicholas J WarehamWellcome Genome Campus and University of Cambridge
Nicholas J WarehamUniversity of Cambridge
Eric B FaumanInternal Medicine Research Unit
Adam S ButterworthBritish Heart Foundation Cardiovascular Epidemiology Unit, University of Cambridge
Adam S ButterworthBritish Heart Foundation Centre of Research Excellence, School of Clinical Medicine, Addenbrooke's Hospital, University of Cambridge
Adam S ButterworthWellcome Genome Campus and University of Cambridge
Adam S ButterworthNIHR Blood and Transplant Research Unit in Donor Health and Genomics, University of Cambridge
Adam S ButterworthBritish Heart Foundation Cardiovascular Epidemiology Unit, University of Cambridge
Adam S ButterworthBritish Heart Foundation Centre of Research Excellence, School of Clinical Medicine, Addenbrooke's Hospital, University of Cambridge
Adam S ButterworthWellcome Genome Campus and University of Cambridge
Adam S ButterworthNIHR Blood and Transplant Research Unit in Donor Health and Genomics, University of Cambridge
Claudia LangenbergUniversity of Cambridge
Claudia LangenbergBerlin Institute of Health at Charite-Universitatsmedizin Berlin
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