Carl D. Langefeld mainly focuses on Genetics, Internal medicine, Single-nucleotide polymorphism, Immunology and Genome-wide association study. His work in Linkage disequilibrium, Haplotype, Genetic linkage, Locus and Allele is related to Genetics. Carl D. Langefeld has included themes like Diabetes mellitus, Endocrinology, Nephropathy and Type 2 diabetes in his Internal medicine study.
His research investigates the link between Single-nucleotide polymorphism and topics such as Odds ratio that cross with problems in Case-control study. His Immunology study combines topics in areas such as Systemic lupus erythematosus and Genotype. His Genome-wide association study course of study focuses on Disease and Bioinformatics and Stroke.
His primary areas of study are Internal medicine, Genetics, Single-nucleotide polymorphism, Genome-wide association study and Endocrinology. His research in Internal medicine intersects with topics in Diabetes mellitus, Type 2 diabetes and Cardiology. His research related to Haplotype, Linkage disequilibrium, Locus, Allele and Gene might be considered part of Genetics.
His Single-nucleotide polymorphism research includes elements of Immunology and Allele frequency. Carl D. Langefeld interconnects Imputation, Genotyping, Disease, Genetic variation and Candidate gene in the investigation of issues within Genome-wide association study. His Nephropathy research incorporates themes from Diabetic nephropathy and End stage renal disease.
His main research concerns Internal medicine, Genetics, Single-nucleotide polymorphism, Genome-wide association study and Intracerebral hemorrhage. His Internal medicine research is multidisciplinary, incorporating perspectives in Endocrinology, Type 2 diabetes and Cardiology. His study in Gene, Expression quantitative trait loci, Genotype, Haplotype and Allele falls under the purview of Genetics.
The study incorporates disciplines such as Polymorphism and Arthritis in addition to Single-nucleotide polymorphism. His research investigates the link between Genome-wide association study and topics such as Locus that cross with problems in Candidate gene. His Immunology research integrates issues from Apolipoprotein L1 and Nephropathy.
Carl D. Langefeld focuses on Genome-wide association study, Internal medicine, Genetics, Single-nucleotide polymorphism and Immunology. His Genome-wide association study research includes themes of Cholesterol, Genetic association, Locus and Medical genetics. His work carried out in the field of Internal medicine brings together such families of science as Endocrinology and Type 2 diabetes.
His Genetics study combines topics from a wide range of disciplines, such as Blood lipids and Lipid metabolism. His study in Single-nucleotide polymorphism is interdisciplinary in nature, drawing from both Polymorphism and Allele frequency. His studies in Immunology integrate themes in fields like Systemic lupus erythematosus and Epigenomics.
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Human polymorphism at microRNAs and microRNA target sites.
Liuqing Yang;Chunru Lin;Chunyu Jin;Joy C. Yang.
Frontiers in Genetics (2013)
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.
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)
Association of trypanolytic ApoL1 variants with kidney disease in African Americans.
Giulio Genovese;Giulio Genovese;David J. Friedman;Michael D. Ross;Laurence Lecordier.
Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci.
John B. Harley;John B. Harley;John B. Harley;Marta E. Alarcón-Riquelme;Lindsey A. Criswell;Chaim O. Jacob.
Nature Genetics (2008)
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries
Mary F. Feitosa;Aldi T. Kraja;Daniel I. Chasman;Yun J. Sung.
PLOS ONE (2018)
Genetic association of the R620W polymorphism of protein tyrosine phosphatase PTPN22 with human SLE.
Chieko Kyogoku;Carl D. Langefeld;Ward A. Ortmann;Annette Lee.
American Journal of Human Genetics (2004)
Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data
Hon-Chung Fung;Hon-Chung Fung;Hon-Chung Fung;Sonja Scholz;Mar Matarin;Javier Simón-Sánchez;Javier Simón-Sánchez.
Lancet Neurology (2006)
Insulin Sensitivity, Insulin Secretion, and Abdominal Fat: The Insulin Resistance Atherosclerosis Study (IRAS) Family Study
Lynne E. Wagenknecht;Carl D. Langefeld;Ann L. Scherzinger;Jill M. Norris.
Adiponectin as a novel determinant of bone mineral density and visceral fat
Lenchik L;Register Tc;Hsu Fc;Lohman K.
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