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Journal of Human Genetics|June 21, 2008
Variation of the oxytocin/neurophysin I (OXT) gene in four human populationsYang Xu, Yali Xue, Asan, et al.American Journal of Human Genetics|September 2, 2008
Adaptive evolution of UGT2B17 copy-number variationYali Xue, Donglin Sun, Allan Daly, et al.American Journal of Human Genetics|March 15, 2006
Spread of an inactive form of caspase-12 in humans is due to recent positive selectionYali Xue, Allan Daly, Bryndis Yngvadottir, et al.Diabetes|July 2, 2008
Evaluating the role of LPIN1 variation in insulin resistance, body weight, and human lipodystrophy in U.K. PopulationsKatherine A Fawcett, Neil Grimsey, Ruth J F Loos, et al.Genetics|September 10, 2009
Population differentiation as an indicator of recent positive selection in humans: an empirical evaluationYali Xue, Xuelong Zhang, Ni Huang, et al.Frontiers in Endocrinology|June 2, 2012
Early Diagnosis of Werner's Syndrome Using Exome-Wide Sequencing in a Single, Atypical PatientEleanor Raffan, Liam A Hurst, Saeed Al Turki, et al.Diabetes|December 24, 2009
Detailed investigation of the role of common and low-frequency WFS1 variants in type 2 diabetes riskKatherine A Fawcett, Eleanor Wheeler, Andrew P Morris, et al.Cell Metabolism|June 4, 2020
Exome Sequencing Identifies Genes and Gene Sets Contributing to Severe Childhood Obesity, Linking PHIP Variants to Repressed POMC TranscriptionGaëlle Marenne, Audrey E Hendricks, Aliki Perdikari, et al.JCI Insight|October 22, 2016
Insulin resistance uncoupled from dyslipidemia due to C-terminal PIK3R1 mutationsIsabel Huang-Doran, Patsy Tomlinson, Felicity Payne, et al.Nature Genetics|July 3, 2007
Common variants in WFS1 confer risk of type 2 diabetesManjinder S Sandhu, Michael N Weedon, Katherine A Fawcett, et al.Pageof 2