2022 - Research.com Best Scientist Award
Member of the Association of American Physicians
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.
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.
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.
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.
ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
Kai Wang;Mingyao Li;Hakon Hakonarson.
Nucleic Acids Research (2010)
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease
Luke Jostins;Stephan Ripke;Rinse K Weersma;Richard H Duerr.
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)
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)
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Stephen Sawcer;Garrett Hellenthal;Matti Pirinen;Chris C. A. Spencer.
Functional impact of global rare copy number variation in autism spectrum disorders
Dalila Pinto;Alistair T. Pagnamenta;Lambertus Klei;Richard Anney.
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)
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)
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)
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)
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