D-Index & Metrics Best Publications
Research.com 2022 Best Scientist Award Badge

D-Index & Metrics

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 and Molecular Biology D-index 142 Citations 95,803 620 World Ranking 79 National Ranking 53
Medicine D-index 140 Citations 78,111 722 World Ranking 647 National Ranking 388
Best Scientists D-index 178 Citations 133,989 1,069 World Ranking 458 National Ranking 308

Research.com Recognitions

Awards & Achievements

2022 - Research.com Best Scientist Award

Member of the Association of American Physicians

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Internal medicine
  • Genetics

His primary areas of investigation include Genetics, Genome-wide association study, Single-nucleotide polymorphism, Genetic association and Copy-number variation. Gene, Locus, Allele frequency, Genotype and Genetic variation are among the areas of Genetics where he concentrates his study. His Genome-wide association study study combines topics in areas such as SNP, Case-control study, Immunology, Allele and Candidate gene.

His Single-nucleotide polymorphism study integrates concerns from other disciplines, such as Odds ratio, Body mass index, Genotyping and Neuroblastoma. He has included themes like Genetic model, International HapMap Project, Meta-analysis, Quantitative trait locus and Minor allele frequency in his Genetic association study. His studies in Copy-number variation integrate themes in fields like Structural variation, Schizophrenia, Bioinformatics, Autism and Gene duplication.

His most cited work include:

  • ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data (6749 citations)
  • Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease (3117 citations)
  • Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease (2614 citations)

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

Hakon Hakonarson mainly investigates Genetics, Genome-wide association study, Single-nucleotide polymorphism, Internal medicine and Gene. His Genetics study is mostly concerned with Locus, Copy-number variation, Allele, Candidate gene and Genotype. His Genome-wide association study study incorporates themes from Bioinformatics, Case-control study, Immunology, Linkage disequilibrium and Genetic association.

His Immunology research is multidisciplinary, relying on both Disease and Inflammatory bowel disease. His Single-nucleotide polymorphism research includes themes of Odds ratio, Genotyping, Genetic variation and Cohort. Hakon Hakonarson interconnects Endocrinology and Oncology in the investigation of issues within Internal medicine.

He most often published in these fields:

  • Genetics (63.21%)
  • Genome-wide association study (54.85%)
  • Single-nucleotide polymorphism (31.16%)

What were the highlights of his more recent work (between 2019-2021)?

  • Genetics (63.21%)
  • Genome-wide association study (54.85%)
  • Internal medicine (20.36%)

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

His primary scientific interests are in Genetics, Genome-wide association study, Internal medicine, Gene and Phenotype. His Genetics study frequently links to adjacent areas such as Asthma. Genome-wide association study is the subject of his research, which falls under Single-nucleotide polymorphism.

His Internal medicine research is multidisciplinary, incorporating perspectives in Endocrinology and Oncology. His Gene research is multidisciplinary, incorporating elements of Machine learning and Artificial intelligence. His Genetic association study combines topics in areas such as Linkage disequilibrium and Immunology.

Between 2019 and 2021, his most popular works were:

  • Distinct features of SARS-CoV-2-specific IgA response in COVID-19 patients. (115 citations)
  • Distinct features of SARS-CoV-2-specific IgA response in COVID-19 patients. (115 citations)
  • Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic Groups (14 citations)

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

  • Gene
  • Internal medicine
  • Mutation

The scientist’s investigation covers issues in Genome-wide association study, Genetics, Internal medicine, Phenotype and Immunology. His Genome-wide association study study results in a more complete grasp of Single-nucleotide polymorphism. His Single-nucleotide polymorphism study deals with Rheumatoid arthritis intersecting with Genetic association.

His study on Genetics is mostly dedicated to connecting different topics, such as Asthma. His Internal medicine study incorporates themes from Endocrinology, Oncology and Cardiology. His work on Neuroinflammation and Immune system as part of general Immunology research is frequently linked to 2019-20 coronavirus outbreak and Pandemic, bridging the gap between disciplines.

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

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

Kai Wang;Mingyao Li;Hakon Hakonarson.
Nucleic Acids Research (2010)

7070 Citations

Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease

Luke Jostins;Stephan Ripke;Rinse K Weersma;Richard H Duerr.
Nature (2012)

3671 Citations

Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

Jean-Charles Lambert;Jean-Charles Lambert;Jean-Charles Lambert;Carla A Ibrahim-Verbaas;Denise Harold;Adam C Naj.
Nature Genetics (2013)

2605 Citations

Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci

Andre Franke;Dermot P B McGovern;Jeffrey C. Barrett;Kai Wang.
Nature Genetics (2010)

2549 Citations

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

Stephen Sawcer;Garrett Hellenthal;Matti Pirinen;Chris C. A. Spencer.
Nature (2011)

2262 Citations

Functional impact of global rare copy number variation in autism spectrum disorders

Dalila Pinto;Alistair T. Pagnamenta;Lambertus Klei;Richard Anney.
Nature (2010)

1898 Citations

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

S. Hong Lee;Stephan Ripke;Stephan Ripke;Benjamin M. Neale;Benjamin M. Neale;Stephen V. Faraone.
Nature Genetics (2013)

1708 Citations

PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

Kai Wang;Mingyao Li;Dexter Hadley;Rui Liu.
Genome Research (2007)

1606 Citations

Common variants at MS4A4/MS4A6E , CD2AP , CD33 and EPHA1 are associated with late-onset Alzheimer's disease

Adam C. Naj;Gyungah Jun;Gary W. Beecham;Li-San Wang.
Nature Genetics (2011)

1580 Citations

Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.

Carl A. Anderson;Gabrielle Boucher;Charlie W. Lees;Andre Franke.
Nature Genetics (2011)

1359 Citations

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