His main research concerns Internal medicine, Genome-wide association study, Genetics, Endocrinology and Single-nucleotide polymorphism. Alan R. Shuldiner interconnects Allele and Cardiology in the investigation of issues within Internal medicine. Alan R. Shuldiner combines subjects such as Kidney disease, Renal function, Quantitative trait locus, Genetic architecture and Genotyping with his study of Genome-wide association study.
His Genetics study deals with Body mass index intersecting with FTO gene and Glucose homeostasis. Endocrinology is a component of his Insulin resistance, Diabetes mellitus, Obesity, Type 2 diabetes and Insulin studies. Medical genetics is closely connected to Mendelian randomization in his research, which is encompassed under the umbrella topic of Cholesterol.
Internal medicine, Endocrinology, Genetics, Genome-wide association study and Single-nucleotide polymorphism are his primary areas of study. In Internal medicine, Alan R. Shuldiner works on issues like Old Order Amish, which are connected to Heritability. His biological study spans a wide range of topics, including Allele and Allele frequency.
His Genetic association, Gene, Candidate gene, Locus and Genetic variation investigations are all subjects of Genetics research. His study in Genome-wide association study is interdisciplinary in nature, drawing from both Quantitative trait locus and Bioinformatics. His work is connected to SNP, Linkage disequilibrium and Minor allele frequency, as a part of Single-nucleotide polymorphism.
His scientific interests lie mostly in Internal medicine, Genetics, Genome-wide association study, Endocrinology and Exome sequencing. His research in Internal medicine intersects with topics in Diabetes mellitus, CYP2C19 and Cardiology. His work in Genome-wide association study addresses subjects such as Locus, which are connected to disciplines such as Single-nucleotide polymorphism.
His Endocrinology research focuses on Old Order Amish and how it connects with Clinical psychology. His Exome sequencing research incorporates themes from Disease, Computational biology, Allele and Cohort. His Type 2 diabetes research integrates issues from Obesity and Insulin.
His primary areas of investigation include Internal medicine, Genetics, Genome-wide association study, Endocrinology and Exome sequencing. In his study, Pathological and ABCC8 is inextricably linked to Cardiology, which falls within the broad field of Internal medicine. His Genome-wide association study research is multidisciplinary, incorporating perspectives in Kidney disease, Renal function, Medical genetics, Quantitative trait locus and Locus.
His study explores the link between Locus and topics such as Single-nucleotide polymorphism that cross with problems in Waist, Waist–hip ratio and Meta-analysis. The concepts of his Endocrinology study are interwoven with issues in Old Order Amish and Genotype. His work carried out in the field of Exome sequencing brings together such families of science as Disease, Human genetics and Cohort.
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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)
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)
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)
Hundreds of variants clustered in genomic loci and biological pathways affect human height
Hana Lango Allen;Karol Estrada;Guillaume Lettre;Sonja I. Berndt.
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.
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
Andrew P Morris;Benjamin F Voight;Benjamin F Voight;Tanya M Teslovich;Teresa Ferreira.
Nature Genetics (2012)
Defining the role of common variation in the genomic and biological architecture of adult human height
Andrew R. Wood;Tonu Esko;Jian Yang;Sailaja Vedantam.
Nature Genetics (2014)
Newly identified loci that influence lipid concentrations and risk of coronary artery disease
Cristen J. Willer;Serena Sanna;Anne U. Jackson;Angelo Scuteri.
Nature Genetics (2008)
A genome-wide association search for type 2 diabetes genes in African Americans.
N D Palmer;C W McDonough;P J Hicks;B H Roh.
PLOS ONE (2012)
Genetic studies of body mass index yield new insights for obesity biology
Adam E. Locke;Bratati Kahali;Sonja I. Berndt;Anne E. Justice.
Faculty of Health; Institute of Health and Biomedical Innovation (2015)
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