D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Genetics D-index 54 Citations 17,116 200 World Ranking 2838 National Ranking 7

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Mutation
  • Genetics

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 most cited work include:

  • Medical genetics: A marker for Stevens-Johnson syndrome (1335 citations)
  • Medical genetics: A marker for Stevens-Johnson syndrome (1335 citations)
  • HLA-B*5801 allele as a genetic marker for severe cutaneous adverse reactions caused by allopurinol (893 citations)

What are the main themes of his work throughout his whole career to date?

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.

He most often published in these fields:

  • Genetics (71.97%)
  • Genome-wide association study (48.11%)
  • Single-nucleotide polymorphism (37.50%)

What were the highlights of his more recent work (between 2016-2021)?

  • Genome-wide association study (48.11%)
  • Genetics (71.97%)
  • Genetic association (25.76%)

In recent papers he was focusing on the following fields of study:

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.

Between 2016 and 2021, his most popular works were:

  • 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 (188 citations)
  • 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 (188 citations)
  • Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels. (85 citations)

In his most recent research, the most cited papers focused on:

  • Gene
  • Mutation
  • Genetics

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.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

Medical genetics: A marker for Stevens-Johnson syndrome

Wen-Hung Chung;Shuen-Iu Hung;Hong-Shang Hong;Mo-Song Hsih.
Nature (2004)

2291 Citations

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)

1365 Citations

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)

844 Citations

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)

801 Citations

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)

702 Citations

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)

673 Citations

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)

648 Citations

Mapping human genetic diversity in Asia

Mahmood Ameen Abdulla;Ikhlak Ahmed;Anunchai Assawamakin;Anunchai Assawamakin;Jong Bhak.
Science (2009)

624 Citations

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)

569 Citations

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)

404 Citations

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