Author details

Full Name

Jer-Yuarn Wu

Affiliation

ORCID

Career Start Year

1996

Papers

216

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36769350	A Functional Polymorphism Downstream of Vitamin A Regulator Gene Is Associated with Hand Osteoarthritis.		2023
37034649	Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.	medRxiv	2023
35551307	Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.	Nat Genet	2022
34635148	Modifiable factors affecting renal preservation in type I glycogen storage disease after liver transplantation: a single-center propensity-match cohort study.	Orphanet Journal of Rare Diseases	2021
33574314	Genetic profiles of 103,106 individuals in the Taiwan Biobank provide insights into the health and history of Han Chinese.	NPJ Genom Med	2021
33350037	Genetic risk score constructed from common genetic variants is associated with cardiovascular disease risk in type 2 diabetes mellitus.	Journal of Gene Medicine	2021
33276381	Genome-Wide and Candidate Gene Association Analyses Identify a 14-SNP Combination for Hypertension in Patients With Type 2 Diabetes.	American Journal of Hypertension	2021
33106546	Association of an IGHV3-66 gene variant with Kawasaki disease.	J Hum Genet	2021
33127893	Towards a reference genome that captures global genetic diversity.	Nat Commun	2020
32170311	Genetic Architecture Associated With Familial Short Stature.	Journal of Clinical Endocrinology and Metabolism	2020
32887585	Copy number variant hotspots in Han Taiwanese population induced pluripotent stem cell lines - lessons from establishing the Taiwan human disease iPSC Consortium Bank.	Journal of Biomedical Science	2020
30674924	Genome-wide transcriptome analysis to further understand neutrophil activation and lncRNA transcript profiles in Kawasaki disease.	Scientific Reports	2019
31699087	Genomic interrogation of familial short stature contributes to the discovery of the pathophysiological mechanisms and pharmaceutical drug repositioning.	Journal of Biomedical Science	2019
31877813	Both IgM and IgG Antibodies Against Polyethylene Glycol Can Alter the Biological Activity of Methoxy Polyethylene Glycol-Epoetin Beta in Mice.	Pharmaceutics	2019
29771320	Immunoglobulin profiling identifies unique signatures in patients with Kawasaki disease during intravenous immunoglobulin treatment.	Human Molecular Genetics	2018
28952330	Genome-wide association study identifies novel susceptibility loci for migraine in Han Chinese resided in Taiwan.	Cephalalgia	2018
30487518	Interethnic analyses of blood pressure loci in populations of East Asian and European descent.	Nat Commun	2018
29336782	Loss of GPNMB Causes Autosomal-Recessive Amyloidosis Cutis Dyschromica in Humans.	American Journal of Human Genetics	2018
28145000	Filamin B Loss-of-Function Mutation in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies.	Human Mutation	2017
28348047	Genome-Wide Association Study Meta-Analysis of Long-Term Average Blood Pressure in East Asians.	Circ Cardiovasc Genet	2017
28900105	A genome-wide association study identifies a novel susceptibility locus for the immunogenicity of polyethylene glycol.	Nature Communications	2017
28898252	Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis.	PLoS Med	2017
28377241	Genetic epidemiological study doesn't support GLA IVS4+919G>A variant is a significant mutation in Fabry disease.	Molecular Genetics and Metabolism	2017
28334899	Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels.	Hum Mol Genet	2017
28526873	Role of S-Palmitoylation by ZDHHC13 in Mitochondrial function and Metabolism in Liver.	Sci Rep	2017
28744025	Genetic loci associated with an earlier age at onset in multiplex schizophrenia.	Sci Rep	2017
28744006	Association of human height-related genetic variants with familial short stature in Han Chinese in Taiwan.	Scientific Reports	2017
29123153	A genome-wide association study links small-vessel ischemic stroke to autophagy.	Scientific Reports	2017
29121990	Identification of functional single nucleotide polymorphisms in the branchpoint site.	Human Genomics	2017
28017375	Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis.	Am J Hum Genet	2017
28112575	Pharmacogenetic dosing of warfarin in the Han-Chinese population: a randomized trial.	Pharmacogenomics	2017
28160554	Pharmacogenetics of dipeptidyl peptidase 4 inhibitors in a Taiwanese population with type 2 diabetes.	Oncotarget	2017
27726379	Measurement of Pre-Existing IgG and IgM Antibodies against Polyethylene Glycol in Healthy Individuals.	Analytical Chemistry	2016
27025970	Identification of PTCSC3 as a Novel Locus for Large-Vessel Ischemic Stroke: A Genome-Wide Association Study.	Journal of the American Heart Association	2016
26935888	Novel susceptibility gene for nonfamilial hypokalemic periodic paralysis.	Neurology	2016
27391550	Homozygosity Mapping and Whole-Genome Sequencing Links a Missense Mutation in POMGNT1 to Autosomal Recessive Retinitis Pigmentosa.	Investigative Ophthalmology and Visual Science	2016
26976339	Pharmacogenomics for personalized pain medicine.		2016
26785701	Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference.	Sci Rep	2016
27042285	Genome-wide analysis of copy number variations identifies PARK2 as a candidate gene for autism spectrum disorder.	Molecular Autism	2016
27450446	Identification of Susceptible Loci and Enriched Pathways for Bipolar II Disorder Using Genome-Wide Association Studies.	International Journal of Neuropsychopharmacology	2016
27029637	An integrated analysis tool for analyzing hybridization intensities and genotypes using new-generation population-optimized human arrays.	BMC Genomics	2016
27503288	Identification of susceptibility gene associated with female primary SjÃ¶gren's syndrome in Han Chinese by genome-wide association study.	Human Genetics	2016
26121212	Cyclic Alopecia and Abnormal Epidermal Cornification in Zdhhc13-Deficient Mice Reveal the Importance of Palmitoylation in Hair and Skin Differentiation.	J Invest Dermatol	2015
25458913	Immunologic basis for allopurinol-induced severe cutaneous adverse reactions: HLA-B*58:01-restricted activation of drug-specific T cells and molecular interaction.	Journal of Allergy and Clinical Immunology	2015
25789810	Investigation of associations between NR1D1, RORA and RORB genes and bipolar disorder.	PLoS ONE	2015
25605650	CXCL10/IP-10 is a biomarker and mediator for Kawasaki disease.	Circulation Research	2015
26399967	Use of HLA-B*58:01 genotyping to prevent allopurinol induced severe cutaneous adverse reactions in Taiwan: national prospective cohort study.	BMJ, The	2015
26434682	Genetic variants in PLCB4/PLCB1 as susceptibility loci for coronary artery aneurysm formation in Kawasaki disease in Han Chinese in Taiwan.	Sci Rep	2015
26398136	Genome-Wide Association Study for Autism Spectrum Disorder in Taiwanese Han Population.	PLoS ONE	2015
26390057	Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation.	Nat Genet	2015