Hugh Watkins - Concepedia

Author

Hugh Watkins

Also Known As

Adrian Thrasher, Arcturus Wang, Bruce M. Psaty, C E Seidman, Chakravarti, Aravinda, Cheng-Hock Toh, Chris Thornborough, Christoph Tillmanns, David S. Siscovick, Dawn M Waterworth

909

Publications

121K

Citations

144

H-Index

167

Concepts

All Affiliations

University of Oxford Centre for Human Genetics Harvard University John Radcliffe Hospital Brigham and Women's Hospital

About

Hugh Watkins is an author at University of Oxford specializing in medicine, genetics, and cardiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	60	102	31.7K
2	Engineering	8	8	966
3	Health Sciences	8	8	763
4	Natural Sciences	5	5	1.4K
5	Language Studies	1	1	14

Hugh Watkins

276

Publications

63.7K

Citations

H-Index

Page 1

	Year	Citations
Analysis of protein-coding genetic variation in 60,706 humans Monkol Lek, Konrad J. Karczewski, Eric Vallabh Minikel, Nature Phenotypic VariationProtein-coding Genetic VariationGeneticsHuman PolymorphismGenomics	2016	10.1K
The mutational constraint spectrum quantified from variation in 141,456 humans Konrad J. Karczewski, Laurent C. Francioli, Grace Tiao, Nature	2020	9.6K
Hundreds of variants clustered in genomic loci and biological pathways affect human height Hana Lango Allen, Karol Estrada, Guillaume Lettre, Nature Genome-wide Association StudyGenetic AnalysisAllelic VariantQuantitative GeneticsGenotype-phenotype Association	2010	2K
Large-scale association analysis identifies new risk loci for coronary artery disease Panos Deloukas, Stavroula Kanoni, Christina Willenborg, Nature Genetics Genome-wide Association StudyLarge-scale Association AnalysisEpidemiologyCardiovascular EpidemiologyCardiovascular Disease	2012	1.7K
Genetic Variants Associated with Lp(a) Lipoprotein Level and Coronary Disease Robert Clarke, John F. Peden, Jemma C. Hopewell, New England Journal of Medicine	2009	1.6K
HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies Michael J. Ackerman, Silvia G. Priori, Stephan Willems, Heart Rhythm ChannelopathiesGenetic TestingCardiomyopathyGeneticsCongenital Heart Anomaly	2011	1.5K
Genome-wide association study identifies eight loci associated with blood pressure Christopher Newton‐Cheh, Toby Johnson, Vesela Gateva, Nature Genetics Genome-wide Association StudyEpidemiologyGenetic DeterminantBlood PressureGenotype-phenotype Association	2009	1.2K
Left Ventricular Non-Compaction Steffen E. Petersen, Joseph B. Selvanayagam, Frank Wiesmann, Journal of the American College of Cardiology Heart FailureDevice TherapyCardiac MechanicElectrophysiologyLeft Ventricular Non-compaction	2005	1.2K
A genomic mutational constraint map using variation in 76,156 human genomes Siwei Chen, Laurent C. Francioli, Julia K. Goodrich, Nature MedicineGeneticsEvolutionary BiologyNatural SciencesGenome Analysis	2023	1.1K
α-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere Ludwig Thierfelder, Hugh Watkins, Calum A. MacRae, Cell Cardiac MuscleCardiomyopathyFamilial Hypertrophic CardiomyopathyPathologyMedicine	1994	1K

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