Author details

Full Name

Hung-Hsin Chen

Affiliation

ORCID

Career Start Year

2010

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37163006	Detection of distant familial relatedness in biobanks for identification of undiagnosed carriers of a Mendelian disease variant: application to Long QT syndrome.	medRxiv	2023
36413071	IMMerge: merging imputation data at scale.	Bioinformatics	2023
37653519	Sex-specific associations between adipokine profiles and carotid-intima media thickness in the Cameron County Hispanic Cohort (CCHC).	Cardiovasc Diabetol	2023
38049589	Genetic risk converges on regulatory networks mediating early type 2 diabetes.	Nature	2023
35157052	Novel diabetes gene discovery through comprehensive characterization and integrative analysis of longitudinal gene expression changes.	Hum Mol Genet	2022
36088317	Genetic pleiotropy underpinning adiposity and inflammation in self-identified Hispanic/Latino populations.	BMC Med Genomics	2022
35379992	New insights into the genetic etiology of Alzheimer's disease and related dementias.	Nat Genet	2022
36268164	Erratum: Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium.	HGG Adv	2022
34873149	Genetically regulated expression in late-onset Alzheimer's disease implicates risk genes within known and novel loci.	Transl Psychiatry	2021
33894541	Identifying developmental stuttering and associated comorbidities in electronic health records and creating a phenome risk classifier.	J Fluency Disord	2021
33357513	Host genetic effects in pneumonia.	Am J Hum Genet	2021
35047858	Population-based genetic effects for developmental stuttering.	HGG Adv	2021
34861174	Phenome risk classification enables phenotypic imputation and gene discovery in developmental stuttering.	American Journal of Human Genetics	2021
32873181	Optimizing Genetic Analyses of Serum Lipids in Longitudinal Data.	Circ Res	2020
30624610	Functionally oriented analysis of cardiometabolic traits in a trans-ethnic sample.	Hum Mol Genet	2019
33312764	GWAS and Beyond: Using Omics Approaches to Interpret SNP Associations.	Curr Genet Med Rep	2019
29535820	The hypoxia-responsive lncRNA promotes NDRG1 degradation via ubiquitin-mediated proteolysis in breast cancer cells.	Oncotarget	2018
25907313	The metabolome profiling and pathway analysis in metabolic healthy and abnormal obesity.	International Journal of Obesity	2015
23820878	Developing comprehensive and Brief ICF core sets for morbid obesity for disability assessment in Taiwan: a preliminary study.	European Journal of Physical and Rehabilitation Medicine	2014
23641141	A Tool Preference Choice Method for RNA Secondary Structure Prediction by SVM with Statistical Tests.	Evolutionary Bioinformatics	2013
22771481	Stroke risk in poliomyelitis survivors: a nationwide population-based study.	Archives of Physical Medicine and Rehabilitation	2012
21703553	Efficacy of creamatocrit technique in evaluation of premature infants fed with breast milk.	Pediatrics and Neonatology	2011
21445159	Localized shape resonance on silver film perforated by H-shaped and more complex shaped hole arrays.	Optics Express	2011
21186990	A business model analysis of telecardiology service.	Telemedicine Journal and e-Health	2010