Ethan M. Lange mainly investigates Genetics, Prostate cancer, Single-nucleotide polymorphism, Genome-wide association study and Genetic linkage. His Locus, Allele frequency, Genotype, Gene and Haplotype study are his primary interests in Genetics. Ethan M. Lange interconnects Germline mutation and Prostate in the investigation of issues within Prostate cancer.
Ethan M. Lange has researched Single-nucleotide polymorphism in several fields, including Myocardial infarction, Allele and Bioinformatics. His Genome-wide association study research incorporates elements of Imputation, Genotyping and Chronic periodontitis. His Genetic linkage research incorporates themes from Genetic marker, Asthma, Allergy, Gene–environment interaction and Linkage.
His primary areas of investigation include Genetics, Prostate cancer, Genome-wide association study, Internal medicine and Single-nucleotide polymorphism. Genetic linkage, Genotype, Haplotype, Locus and Gene are among the areas of Genetics where he concentrates his study. Ethan M. Lange focuses mostly in the field of Prostate cancer, narrowing it down to matters related to Missense mutation and, in some cases, Germline mutation.
His Genome-wide association study study integrates concerns from other disciplines, such as SNP, Imputation, Genetic association and Human genetics. The concepts of his Internal medicine study are interwoven with issues in Diabetes mellitus, Endocrinology and Oncology. His Single-nucleotide polymorphism study combines topics in areas such as Adiponectin, Cohort and Allele frequency.
Ethan M. Lange focuses on Genetics, Internal medicine, Genome-wide association study, Obesity and Endocrinology. His work is connected to Exome, Minor allele frequency, Allele frequency, Gene and Genome, as a part of Genetics. His Internal medicine research includes elements of Diabetes mellitus and Oncology.
His Genome-wide association study study is associated with Single-nucleotide polymorphism. His biological study deals with issues like Genotype, which deal with fields such as Phenotype, Mitral valve prolapse, Mitral valve, Genetic linkage and Mendelian inheritance. His Risk factor study combines topics from a wide range of disciplines, such as Prostate cancer, Blood pressure and Forest plot.
His primary areas of study are Genetics, Genome-wide association study, Genetic association, Exome and Allele frequency. Minor allele frequency and Single-nucleotide polymorphism are among the areas of Genetics where the researcher is concentrating his efforts. His Single-nucleotide polymorphism research is multidisciplinary, incorporating elements of LDL receptor and Haplotype.
His work carried out in the field of Genome-wide association study brings together such families of science as Immunology, Quantitative trait locus, Allele, Locus and Lipoprotein. The study incorporates disciplines such as Imputation, Statistics, Confounding and Econometrics in addition to Genetic association. His studies in Exome integrate themes in fields like Acquired immune system, Hematopoietic stem cell differentiation, White blood cell and Myeloid.
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Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction
Ron Do;Ron Do;Nathan O. Stitziel;Hong Hee Won;Hong Hee Won;Anders Berg Jørgensen.
Germline Mutations in HOXB13 and Prostate-Cancer Risk
Charles M. Ewing;Anna M. Ray;Ethan M. Lange;Kimberly A. Zuhlke.
The New England Journal of Medicine (2012)
Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array
Rosalind A. Eeles;Ali Amin Al Olama;Sara Benlloch;Edward J. Saunders.
Nature Genetics (2013)
Identification of seven new prostate cancer susceptibility loci through a genome-wide association study
Rosalind A. Eeles;Zsofia Kote-Jarai;Ali Amin Al Olama;Graham G. Giles;Graham G. Giles.
Nature Genetics (2009)
REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants
Nilah M M. Ioannidis;Joseph H H. Rothstein;Joseph H H. Rothstein;Vikas Pejaver;Sumit Middha.
American Journal of Human Genetics (2016)
Germline mutations and sequence variants of the macrophage scavenger receptor 1 gene are associated with prostate cancer risk
Jianfeng Xu;S. Lilly Zheng;Akira Komiya;Josyf C. Mychaleckyj.
Nature Genetics (2002)
Association of polymorphisms in the CRP gene with circulating C-reactive protein levels and cardiovascular events.
Leslie A. Lange;Christopher S. Carlson;Lucia A. Hindorff;Ethan M. Lange.
The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. I. An autosomal genome scan for genes that predispose to type 2 diabetes.
Soumitra Ghosh;Richard M. Watanabe;Timo T. Valle;Elizabeth R. Hauser.
American Journal of Human Genetics (2000)
Prostate Cancer Susceptibility Locus on Chromosome 1q: a Confirmatory Study
K.A. Cooney;J.D. McCarthy;E. Lange;L. Huang.
Journal of the National Cancer Institute (1997)
Genetic modifiers of liver disease in cystic fibrosis.
Jaclyn R. Bartlett;Kenneth J. Friedman;Simon C. Ling;Rhonda G. Pace.
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