Fellow of The Academy of Medical Sciences, United Kingdom
Nilesh J. Samani mainly focuses on Genome-wide association study, Genetics, Single-nucleotide polymorphism, Internal medicine and Genetic association. His work carried out in the field of Genome-wide association study brings together such families of science as Bioinformatics, Coronary artery disease, Disease, Allele and Genetic architecture. As part of his studies on Genetics, Nilesh J. Samani often connects relevant areas like Body mass index.
His biological study spans a wide range of topics, including Allele frequency and Copy-number variation. His Internal medicine research incorporates elements of Endocrinology and Cardiology. His study explores the link between Genetic association and topics such as Blood pressure that cross with problems in Framingham Risk Score.
His primary scientific interests are in Internal medicine, Genetics, Genome-wide association study, Cardiology and Single-nucleotide polymorphism. His Internal medicine study frequently draws connections to adjacent fields such as Endocrinology. His Genome-wide association study research is multidisciplinary, relying on both Genetic predisposition, Bioinformatics, Allele frequency, Genetic association and Genetic architecture.
His study in the field of Ejection fraction, Atrial fibrillation and Sudden cardiac death also crosses realms of In patient. His Single-nucleotide polymorphism study incorporates themes from Odds ratio and Haplotype. Nilesh J. Samani combines subjects such as Case-control study and Disease with his study of Coronary artery disease.
Nilesh J. Samani mainly investigates Internal medicine, Genome-wide association study, Genetics, Heart failure and Cardiology. Internal medicine is frequently linked to Endocrinology in his study. The study incorporates disciplines such as Genetic predisposition, PR interval, Medical genetics, Genetic association and Genetic architecture in addition to Genome-wide association study.
His research investigates the connection between Medical genetics and topics such as Blood pressure that intersect with problems in Diabetes mellitus. Gene, Locus, Single-nucleotide polymorphism, Minor allele frequency and SNP are the core of his Genetics study. He has included themes like Biomarker and Gastroenterology in his Heart failure study.
His primary areas of study are Genome-wide association study, Internal medicine, Genetics, Heart failure and Genetic association. His Genome-wide association study study improves the overall literature in Single-nucleotide polymorphism. His study focuses on the intersection of Internal medicine and fields such as Cardiology with connections in the field of Pathophysiology.
His Genetics research includes themes of Blood lipids and Lipid metabolism. His Heart failure study combines topics in areas such as Biomarker, Atrial fibrillation, ACE inhibitor and Cohort. His Genetic association study integrates concerns from other disciplines, such as Quantitative trait locus, Minor allele frequency and Biobank, Bioinformatics.
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Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
Paul R. Burton;David G. Clayton;Lon R. Cardon;Nick Craddock.
Biological, clinical and population relevance of 95 loci for blood lipids
Tanya M. Teslovich;Kiran Musunuru;Albert V. Smith;Andrew C. Edmondson.
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)
Genetic studies of body mass index yield new insights for obesity biology
Adam E. Locke;Bratati Kahali;Sonja I. Berndt;Anne E. Justice.
Genomewide association analysis of coronary artery disease.
Nilesh J. Samani;Jeanette Erdmann;Alistair S. Hall;Christian Hengstenberg.
The New England Journal of Medicine (2007)
Hundreds of variants clustered in genomic loci and biological pathways affect human height
Hana Lango Allen;Karol Estrada;Guillaume Lettre;Sonja I. Berndt.
Plasma HDL cholesterol and risk of myocardial infarction: A mendelian randomisation study
Benjamin F. Voight;Benjamin F. Voight;Benjamin F. Voight;Gina M. Peloso;Gina M. Peloso;Marju Orho-Melander;Ruth Frikke-Schmidt.
web science (2012)
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Georg B. Ehret;Georg B. Ehret;Georg B. Ehret;Patricia B. Munroe;Kenneth M. Rice;Murielle Bochud.
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation
Cristen J. Willer;Elizabeth K. Speliotes;Elizabeth K. Speliotes;Ruth J. F. Loos;Shengxu Li.
Nature Genetics (2009)
Discovery and refinement of loci associated with lipid levels
Cristen J. Willer;Ellen M. Schmidt;Sebanti Sengupta;Gina M. Peloso;Gina M. Peloso;Gina M. Peloso.
Nature Genetics (2013)
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