His scientific interests lie mostly in Genetics, Genome-wide association study, Genetic association, Immunology and Single-nucleotide polymorphism. His study in Genetics is interdisciplinary in nature, drawing from both Obesity and Renal function. The Genome-wide association study study combines topics in areas such as Body mass index, Polymorphism, Diabetes mellitus, Type 2 diabetes and Case-control study.
As part of the same scientific family, he usually focuses on Genetic association, concentrating on Medical genetics and intersecting with Imputation and Genetic architecture. In his research on the topic of Immunology, Copy-number variation is strongly related with Disease. His studies deal with areas such as Lithium, Genome and Lithium therapy as well as Single-nucleotide polymorphism.
His primary areas of investigation include Genetics, Genome-wide association study, Single-nucleotide polymorphism, Internal medicine and Immunology. His work in Gene, Allele, Polymorphism, Haplotype and SNP is related to Genetics. His Genome-wide association study research is multidisciplinary, relying on both Body mass index, Case-control study, Genetic association, Locus and Type 2 diabetes.
His studies in Single-nucleotide polymorphism integrate themes in fields like Human genome, Genetic predisposition and Candidate gene. His work carried out in the field of Internal medicine brings together such families of science as Endocrinology and Gene polymorphism, Genotype. His research in Immunology intersects with topics in Kawasaki disease and Disease.
Jer-Yuarn Wu mainly focuses on Genome-wide association study, Genetics, Genetic association, Single-nucleotide polymorphism and Locus. Jer-Yuarn Wu has included themes like Antibody, Immunology and Allele in his Genome-wide association study study. Immunology is closely attributed to Genetic marker in his work.
His Genetics research integrates issues from Meta-analysis and Type 2 diabetes. His biological study spans a wide range of topics, including Odds ratio, Han chinese, Disease, Small vessel and Imputation. His Single-nucleotide polymorphism study integrates concerns from other disciplines, such as Internal medicine, Short stature, Ischemic stroke and Bioinformatics.
The scientist’s investigation covers issues in Genome-wide association study, Locus, Genetics, Genetic association and Allele. His Genome-wide association study research is multidisciplinary, incorporating perspectives in Immunoglobulin G, Immunology, Immunoglobulin heavy chain and Immunogenicity. Jer-Yuarn Wu combines subjects such as Genetic marker, Antibody, Immunoglobulin M and Meta-analysis with his study of Locus.
Jer-Yuarn Wu regularly ties together related areas like Glycemic in his Genetics studies. His Genetic association research includes elements of Diabetes mellitus, Glycated hemoglobin, Type 2 diabetes, Human genetics and Medical genetics. Many of his research projects under Allele are closely connected to RBPMS with RBPMS, tying the diverse disciplines of science together.
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Medical genetics: A marker for Stevens-Johnson syndrome
Wen-Hung Chung;Shuen-Iu Hung;Hong-Shang Hong;Mo-Song Hsih.
HLA-B*5801 allele as a genetic marker for severe cutaneous adverse reactions caused by allopurinol
Shuen Lu Hung;Wen Hung Chung;Wen Hung Chung;Wen Hung Chung;Lieh Bang Liou;Chen Chung Chu.
Proceedings of the National Academy of Sciences of the United States of America (2005)
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.
Anubha Mahajan;Min Jin Go;Weihua Zhang;Jennifer E. Below.
Nature Genetics (2014)
Granulysin is a key mediator for disseminated keratinocyte death in Stevens-Johnson syndrome and toxic epidermal necrolysis
Wen-Hung Chung;Wen-Hung Chung;Shuen-Iu Hung;Shuen-Iu Hung;Jui-Yung Yang;Shih-Chi Su.
Nature Medicine (2008)
Carbamazepine-Induced Toxic Effects and HLA-B*1502 Screening in Taiwan
Pei Chen;Juei-Jueng Lin;Chin-Song Lu;Chin-Song Lu;Cheung-Ter Ong.
The New England Journal of Medicine (2011)
A novel functional VKORC1 promoter polymorphism is associated with inter-individual and inter-ethnic differences in warfarin sensitivity
Hsiang-Yu Yuan;Jin-Jer Chen;M.T. Michael Lee;Ju-Chieh Wung.
Human Molecular Genetics (2005)
Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians
Yoon Shin Cho;Chien Hsiun Chen;Chien Hsiun Chen;Cheng Hu;Jirong Long.
Nature Genetics (2012)
Mapping human genetic diversity in Asia
Mahmood Ameen Abdulla;Ikhlak Ahmed;Anunchai Assawamakin;Anunchai Assawamakin;Jong Bhak.
Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians
Norihiro Kato;Fumihiko Takeuchi;Yasuharu Tabara;Tanika N. Kelly.
Nature Genetics (2011)
PSORS2 Is Due to Mutations in CARD14
Catherine T. Jordan;Li Cao;Elisha D.O. Roberson;Katherine C. Pierson.
American Journal of Human Genetics (2012)
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