Felicity Payne - Concepedia

Author

Felicity Payne

Also Known As

Alexandros Onoufriadis, Chines, Peter S., F B Payne, F Payne, F. PAYNE, F. Payne, Felicity Payne, Finley Payne, Hannah M. Mitchison, Karola Rehnström

Publications

19.7K

Citations

H-Index

Concepts

All Affiliations

University of Cambridge Wellcome Trust Wellcome Sanger Institute Addenbrooke's Hospital Wellcome/MRC Institute of Metabolic Science

About

Felicity Payne is an author at University of Cambridge specializing in medicine, genetics, and diabetes.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	20	5.8K
2	Public Health	4	4	573
3	Health Sciences	3	3	794
4	Natural Sciences	1	1	128
5	Allergy	1	1	66

Felicity Payne

Publications

8.6K

Citations

H-Index

Page 1

	Year	Citations
Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease Hironori Ueda, Joanna M. M. Howson, Laura Esposito, Nature ImmunogeneticsAutoimmune DiseaseT-regulatory CellImmunologyPathology	2003	2.2K
Haplotype tagging for the identification of common disease genes Gillian C.L. Johnson, Laura Esposito, Bryan J. Barratt, Nature Genetics Haplotype DeterminationGeneticsComplex DiseaseDisease Gene IdentificationGenomics	2001	1.2K
Integrative genomic analysis implicates limited peripheral adipose storage capacity in the pathogenesis of human insulin resistance Luca A. Lotta, Pawan Gulati, Felix R. Day, Nature Genetics Insulin ResistanceMetabolic SyndromeObesityMetabolic DisorderGenetics	2016	594
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel Jie Huang, Bryan Howie, Shane McCarthy, Nature Communications	2015	374
Genome-Wide Association Identifies Nine Common Variants Associated With Fasting Proinsulin Levels and Provides New Insights Into the Pathophysiology of Type 2 Diabetes Rona J. Strawbridge, Josée Dupuis, Inga Prokopenko, Diabetes	2011	366
Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes Amélie Bonnefond, Nathalie Clément, Katherine A. Fawcett, Nature Genetics Metabolic SyndromeSleepRare Mtnr1b VariantsMedicineDiabetes	2012	361
Mosaic overgrowth with fibroadipose hyperplasia is caused by somatic activating mutations in PIK3CA Marjorie J. Lindhurst, Victoria E R Parker, Felicity Payne, Nature Genetics Genome InstabilitySomatic VariantCell DivisionGenetic DisorderGenetics	2012	313
The UK10K project identifies rare variants in health and disease Klaudia Walter, Josine L. Min, Jie Huang, Kölner Universitäts PublikationsServer (Universität zu Köln)	2015	299
Detailed Physiologic Characterization Reveals Diverse Mechanisms for Novel Genetic Loci Regulating Glucose and Insulin Metabolism in Humans Erik Ingelsson, Claudia Langenberg, Marie‐France Hivert, Diabetes	2010	255
Replication and extension of genome-wide association study results for obesity in 4923 adults from northern Sweden Frida Renström, Felicity Payne, Anna Nordström, Human Molecular Genetics	2009	228

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