Yeda Wu

发表

Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes

Luke R. Lloyd-Jones, Sina A. Gharib, P. Visscher, 2018, Nature Communications.

Association of common and rare variants of SCN10A gene with sudden unexplained nocturnal death syndrome in Chinese Han population

Yeda Wu, Jianding Cheng, Liyong Zhang, 2016, International Journal of Legal Medicine.

Polygenic Risk Scores Derived From Varying Definitions of Depression and Risk of Depression.

N. Wray, I. Hickie, N. Martin, 2021, JAMA psychiatry.

Forensic Pathological Study of 1656 Cases of Sudden Cardiac Death in Southern China

Yeda Wu, Jianding Cheng, Liyong Zhang, 2016, Medicine.

Molecular pathological study on LRRC10 in sudden unexplained nocturnal death syndrome in the Chinese Han population

J. Makielski, Yeda Wu, Jianding Cheng, 2017, International Journal of Legal Medicine.

GJA1 gene variations in sudden unexplained nocturnal death syndrome in the Chinese Han population.

Yeda Wu, Jianding Cheng, Liyong Zhang, 2017, Forensic science international.

The biophysical characterization of the first SCN5A mutation R1512W identified in Chinese sudden unexplained nocturnal death syndrome

J. Makielski, Yeda Wu, Jianding Cheng, 2016, Medicine.

The forensic pathological analysis of sport-related sudden cardiac death in Southern China

Yeda Wu, Jianding Cheng, Liyong Zhang, 2017, Forensic sciences research.

The Diagnostic Value of Quantitative Assessment of Diatom Test for Drowning: An Analysis of 128 Water‐related Death Cases using Microwave Digestion‐Vacuum Filtration‐Automated Scanning Electron Microscopy

Yeda Wu, Jianding Cheng, Sun-lin Hu, 2017, Journal of forensic sciences.

Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals

Jonathan P. Beauchamp, Gerardus A. Meddens, Joseph K. Pickrell, 2022, Nature Genetics.

GWAS of peptic ulcer disease implicates Helicobacter pylori infection, other gastrointestinal disorders and depression

P. Visscher, N. Wray, G. Murray, 2021, Nature Communications.

Genetic analyses of medication-use and implications for precision medicine

P. Visscher, N. Wray, Jian Yang, 2018 .

Genome-wide association study of medication-use and associated disease in the UK Biobank

P. Visscher, N. Wray, Jian Yang, 2019, Nature Communications.

Genome-wide association study of gastrointestinal disorders reinforces the link between the digestive tract and the nervous system

P. Visscher, N. Wray, G. Murray, 2019 .

Novel susceptibility loci and genetic regulation mechanisms for type 2 diabetes

Luke R. Lloyd-Jones, P. Visscher, A. McRae, 2018, bioRxiv.

SCN5A mutation R1512W The biophysical characterization of the first identified in Chinese sudden unexplained nocturnal death syndrome

J. Makielski, Yeda Wu, Jianding Cheng, 2016 .

Glucose-Responsive Nanosystem Mimicking the Physiological Insulin Secretion via an Enzyme–Polymer Layer-by-Layer Coating Strategy

Hongwei Zhang, Chengzhong Yu, Yeda Wu, 2017 .

Hexarelin, a Growth Hormone Secretagogue, Improves Lipid Metabolic Aberrations in Nonobese Insulin‐Resistant Male MKR Mice

D. Leroith, Yeda Wu, Li-li Huang, 2017, Endocrinology.

Brugada syndrome: a fatal disease with complex genetic etiologies – still a long way to go

Yeda Wu, Jianding Cheng, Liyong Zhang, 2017, Forensic sciences research.

150 risk variants for diverticular disease of intestine prioritize cell types and enable polygenic prediction of disease susceptibility

N. Wray, L. Davis, M. Gandal, 2023, Cell genomics.

Genome-wide meta-analysis identifies novel loci and improves disease prediction of age-related macular degeneration.

D. Mackey, A. Hewitt, P. Gharahkhani, 2023, Ophthalmology.

Study profile: the Genetics of Glaucoma Study

D. Mackey, A. Hewitt, P. Gharahkhani, 2023, BMJ open.