Author details

Full Name

Chien-Hsiun Chen

Affiliation

ORCID

Career Start Year

2001

Papers

102

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
36428003	Levonorgestrel intrauterine devices improve body constitution deviations in the perspective of traditional Chinese medicine and quality of life in patients with chronic pelvic pain and heavy menstrual bleeding.		2022
36303164	Enrichment of Prevotella intermedia in human colorectal cancer and its additive effects with Fusobacterium nucleatum on the malignant transformation of colorectal adenomas.	Journal of Biomedical Science	2022
35385754	Population-based high-throughput toxicity screen of human iPSC-derived cardiomyocytes and neurons.	Cell Reports	2022
35745684	Cardio- and Neurotoxicity of Selected Anti-COVID-19 Drugs.	Pharmaceuticals	2022
35551307	Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.	Nat Genet	2022
34417613	Corrigendum to: Detecting Genetic Ancestry and Adaptation in the Taiwanese Han People.	Molecular Biology and Evolution	2021
34288885	Genetic factors of idiopathic central precocious puberty and their polygenic risk in early puberty.	European Journal of Endocrinology	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
34026292	Rare variants discovery by extensive whole-genome sequencing of the Han Chinese population in Taiwan: Applications to cardiovascular medicine.		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
33170928	Detecting Genetic Ancestry and Adaptation in the Taiwanese Han People.	Molecular Biology and Evolution	2021
33106546	Association of an IGHV3-66 gene variant with Kawasaki disease.	J Hum Genet	2021
34763707	Spatially varying effects of measured confounding variables on disease risk.	International Journal of Health Geographics	2021
32453789	Glucose transporter 10 modulates adipogenesis via an ascorbic acid-mediated pathway to protect mice against diet-induced metabolic dysregulation.	PLoS Genetics	2020
32170311	Genetic Architecture Associated With Familial Short Stature.	Journal of Clinical Endocrinology and Metabolism	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
31852448	Genome-wide association study of morbid obesity in Han Chinese.	BMC Genetics	2019
31879508	Targeted Next Generation Sequencing for Genetic Mutations of Dilated Cardiomyopathy.	Acta Cardiologica Sinica	2019
29866173	Recognizing spatial and temporal clustering patterns of dengue outbreaks in Taiwan.	BMC Infectious Diseases	2018
30487518	Interethnic analyses of blood pressure loci in populations of East Asian and European descent.	Nat Commun	2018
28160554	Pharmacogenetics of dipeptidyl peptidase 4 inhibitors in a Taiwanese population with type 2 diabetes.	Oncotarget	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
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
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
29131869	Assessing current temporal and space-time anomalies of disease incidence.	PLoS ONE	2017
29123153	A genome-wide association study links small-vessel ischemic stroke to autophagy.	Scientific Reports	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
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
26785701	Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference.	Sci Rep	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
27798100	Population structure of Han Chinese in the modern Taiwanese population based on 10,000 participants in the Taiwan Biobank project.	Human Molecular Genetics	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
26389959	Bioinformatic Interrogation of 5p-arm and 3p-arm Specific miRNA Expression Using TCGA Datasets.	Journal of Clinical Medicine	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