Marten H. Hofker focuses on Genetics, Internal medicine, Endocrinology, Genome-wide association study and Single-nucleotide polymorphism. His study looks at the intersection of Genetics and topics like Molecular biology with Facioscapulohumeral muscular dystrophy and Episodic ataxia. His Internal medicine study frequently intersects with other fields, such as Hyperlipidemia.
His work carried out in the field of Endocrinology brings together such families of science as Inflammation and Fatty liver. His Genome-wide association study study incorporates themes from SNP, Genetic variation and Candidate gene. Marten H. Hofker has researched Single-nucleotide polymorphism in several fields, including Regulation of gene expression and Regulatory sequence.
Internal medicine, Endocrinology, Genetics, Inflammation and Immunology are his primary areas of study. His Genetics study frequently involves adjacent topics like Molecular biology. While the research belongs to areas of Inflammation, Marten H. Hofker spends his time largely on the problem of Steatosis, intersecting his research to questions surrounding Nonalcoholic fatty liver disease.
Marten H. Hofker has included themes like Quantitative trait locus, Expression quantitative trait loci and TCF7L2 in his Genome-wide association study study. His studies deal with areas such as Genetic variation and Allele as well as Single-nucleotide polymorphism. His Allele research is multidisciplinary, relying on both Odds ratio and Case-control study.
Marten H. Hofker mainly focuses on Internal medicine, Endocrinology, Inflammation, Genetics and Immunology. His study in Inflammation is interdisciplinary in nature, drawing from both Tumor necrosis factor alpha, Liver disease, Steatosis and Cathepsin D. His work in Genetics covers topics such as Disease which are related to areas like Gut microbiome.
His studies in Immunology integrate themes in fields like Phenotype and Inflammatory bowel disease. The various areas that he examines in his Single-nucleotide polymorphism study include Blood lipids, Allele and Candidate gene. The Immune system study which covers Cohort study that intersects with Odds ratio.
His scientific interests lie mostly in Internal medicine, Endocrinology, Inflammation, Insulin resistance and Metagenomics. He integrates Internal medicine and WASH complex in his studies. His Endocrinology research includes themes of Single-nucleotide polymorphism and Allele.
When carried out as part of a general Inflammation research project, his work on Proinflammatory cytokine is frequently linked to work in Microbial composition, therefore connecting diverse disciplines of study. His Metagenomics research is classified as research in Genetics. His Blood lipids research is multidisciplinary, incorporating perspectives in Body mass index and Case-control study.
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Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4
Roel A. Ophoff;Gisela M. Terwindt;Monique N. Vergouwe;Ronald Van Eijk.
Cell (1996)
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)
A variant in CDKAL1 influences insulin response and risk of type 2 diabetes.
Valgerdur Steinthorsdottir;Gudmar Thorleifsson;Inga Reynisdottir;Rafn Benediktsson.
Nature Genetics (2007)
Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes
Julius Gudmundsson;Patrick Sulem;Valgerdur Steinthorsdottir;Jon T. Bergthorsson.
Nature Genetics (2007)
Population-based metagenomics analysis reveals markers for gut microbiome composition and diversity.
Alexandra Zhernakova;Alexander Kurilshikov;Marc Jan Bonder;Ettje F. Tigchelaar.
Science (2016)
Nuclear factor kappaB signaling in atherogenesis
Menno P.J. de Winther;Edwin Kanters;Georg Kraal;Marten H. Hofker.
Arteriosclerosis, Thrombosis, and Vascular Biology (2005)
Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy.
Cisca Wijmenga;Jane E. Hewitt;Lodewijk A. Sandkuijl;Lorraine N. Clark.
Nature Genetics (1992)
Association between alcohol and cardiovascular disease:Mendelian randomisation analysis based on individual participant data
Michael V Holmes;Michael V Holmes;Caroline E Dale;Luisa Zuccolo;Richard J Silverwood.
BMJ (2014)
Role of ApoCs in Lipoprotein Metabolism Functional Differences Between ApoC1, ApoC2, and ApoC3
Miek C. Jong;Marten H. Hofker;Louis M. Havekes.
Arteriosclerosis, Thrombosis, and Vascular Biology (1999)
Minor Xp21 chromosome deletion in a male associated with expression of duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome
Francke U;Ochs Hd;de Martinville B;Giacalone J.
American Journal of Human Genetics (1985)
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