2022 - Research.com Best Scientist Award
His primary areas of investigation include Genetics, Genome-wide association study, Internal medicine, Single-nucleotide polymorphism and Genetic association. His research combines Body mass index and Genetics. His Genome-wide association study study integrates concerns from other disciplines, such as Bioinformatics, Medical genetics, Quantitative trait locus, Genetic architecture and Type 2 diabetes.
His Internal medicine research is multidisciplinary, relying on both Endocrinology and Oncology. Harry Campbell has researched Single-nucleotide polymorphism in several fields, including Meta-analysis, Genetic linkage, Polymorphism and Heritability. The study incorporates disciplines such as HNF1A, Genetic variation, Pulse pressure and Glucose homeostasis in addition to Genetic association.
Harry Campbell focuses on Genetics, Genome-wide association study, Internal medicine, Genetic association and Single-nucleotide polymorphism. His research related to Locus, Allele, Gene, SNP and Quantitative trait locus might be considered part of Genetics. His Genome-wide association study research includes elements of Meta-analysis, Imputation, Bioinformatics and Candidate gene.
His Internal medicine study combines topics from a wide range of disciplines, such as Endocrinology and Oncology. Colorectal cancer is a subfield of Cancer that he explores. His research links Obesity with Body mass index.
His primary scientific interests are in Genome-wide association study, Genetics, Internal medicine, Genetic association and Colorectal cancer. His Genome-wide association study research is within the category of Single-nucleotide polymorphism. Genetic architecture, Gene, Imputation, Allele and Heritability are the primary areas of interest in his Genetics study.
His research integrates issues of Endocrinology and Cardiology in his study of Internal medicine. The study of Genetic association is intertwined with the study of SNP in a number of ways. His Colorectal cancer research is multidisciplinary, incorporating elements of Observational study, Case-control study, Oncology and Genetic variation.
Genome-wide association study, Genetics, Internal medicine, Genetic association and Single-nucleotide polymorphism are his primary areas of study. The various areas that Harry Campbell examines in his Genome-wide association study study include Quantitative trait locus, Genetic architecture, Bioinformatics and Medical genetics. Imputation, 1000 Genomes Project, SNP, Heritability and Locus are among the areas of Genetics where Harry Campbell concentrates his study.
As a part of the same scientific family, he mostly works in the field of SNP, focusing on Meta-analysis and, on occasion, Body mass index. Harry Campbell interconnects Candidate gene and Cardiology in the investigation of issues within Locus. His work in Internal medicine is not limited to one particular discipline; it also encompasses Endocrinology.
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Global, regional, and national causes of child mortality: An updated systematic analysis for 2010 with time trends since 2000
Li Liu;Hope L Johnson;Simon Cousens;Jamie Perin.
The Lancet (2012)
Global, regional, and national causes of child mortality in 2008: a systematic analysis
Robert E Black;Simon Cousens;Hope L Johnson;Joy E Lawn.
The Lancet (2010)
Biological, clinical and population relevance of 95 loci for blood lipids
Tanya M. Teslovich;Kiran Musunuru;Albert V. Smith;Andrew C. Edmondson.
Nature (2010)
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
Elizabeth K. Speliotes;Elizabeth K. Speliotes;Cristen J. Willer;Sonja I. Berndt;Keri L. Monda.
Nature Genetics (2010)
Global burden of acute lower respiratory infections due to respiratory syncytial virus in young children: a systematic review and meta-analysis
Harish Nair;Harish Nair;D James Nokes;D James Nokes;Bradford D. Gessner;Mukesh K Dherani.
The Lancet (2010)
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
Josée Dupuis;Josée Dupuis;Claudia Langenberg;Inga Prokopenko;Richa Saxena;Richa Saxena.
Nature Genetics (2010)
Global burden of childhood pneumonia and diarrhoea
Christa L Fischer Walker;Igor Rudan;Li Liu;Harish Nair;Harish Nair.
The Lancet (2013)
Hundreds of variants clustered in genomic loci and biological pathways affect human height
Hana Lango Allen;Karol Estrada;Guillaume Lettre;Sonja I. Berndt.
Nature (2010)
Epidemiology and etiology of childhood pneumonia
Igor Rudan;Cynthia Boschi-Pinto;Zrinka Biloglav;Kim Mulholland.
Bulletin of The World Health Organization (2008)
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
Benjamin F. Voight;Benjamin F. Voight;Laura J. Scott;Valgerdur Steinthorsdottir;Andrew P. Morris.
Nature Genetics (2010)
Journal of Global Health
(Impact Factor: 7.664)
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