2023 - Research.com Genetics in Germany Leader Award
Norman Klopp mainly focuses on Genome-wide association study, Genetics, Single-nucleotide polymorphism, Internal medicine and Genetic association. His Genome-wide association study research includes elements of Bioinformatics, Immunology, Medical genetics, Type 2 diabetes and Genetic architecture. His Genetics research is multidisciplinary, incorporating elements of Uric acid, Gout and Glucose homeostasis.
His research in Single-nucleotide polymorphism intersects with topics in Apolipoprotein E, Disease and Allele. His study in Internal medicine is interdisciplinary in nature, drawing from both Endocrinology and Oncology. His work in Genetic association covers topics such as Locus which are related to areas like SLC30A8.
Norman Klopp mainly investigates Genetics, Single-nucleotide polymorphism, Genome-wide association study, Immunology and Internal medicine. Genetics is represented through his Gene, Candidate gene, Allele, Locus and Genetic variation research. Norman Klopp has researched Single-nucleotide polymorphism in several fields, including Allele frequency and Haplotype.
His biological study spans a wide range of topics, including Bioinformatics, Coronary artery disease, Medical genetics, Meta-analysis and Genetic association. His studies in Genetic association integrate themes in fields like Proportional hazards model and Genetic architecture. His Internal medicine study deals with Endocrinology intersecting with Polymorphism.
His primary scientific interests are in Genome-wide association study, Genetics, Internal medicine, Single-nucleotide polymorphism and Pathology. The concepts of his Genome-wide association study study are interwoven with issues in SNP, Obesity, Genetic association and Bioinformatics. He interconnects Odds ratio, Coronary artery disease and Blood pressure in the investigation of issues within Genetic association.
Many of his studies involve connections with topics such as Glucose homeostasis and Genetics. Many of his studies involve connections with topics such as Endocrinology and Internal medicine. Norman Klopp usually deals with Single-nucleotide polymorphism and limits it to topics linked to Locus and Linkage disequilibrium and Transcriptional regulation.
Norman Klopp spends much of his time researching Genome-wide association study, Genetics, Single-nucleotide polymorphism, Internal medicine and Regulation of gene expression. Norman Klopp combines subjects such as Haplotype, Obesity, Locus and Bioinformatics with his study of Genome-wide association study. Norman Klopp frequently studies issues relating to Glucose homeostasis and Genetics.
In his research, Norman Klopp performs multidisciplinary study on Single-nucleotide polymorphism and Kexin. His Nephrology, Autosomal Recessive Polycystic Kidney Disease and Clinical trial study, which is part of a larger body of work in Internal medicine, is frequently linked to Congenital hepatic fibrosis, bridging the gap between disciplines. His Genetic architecture research is multidisciplinary, incorporating perspectives in Blood pressure and Genetic association.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease
Denise Harold;Richard Abraham;Paul Hollingworth;Rebecca Sims.
Nature Genetics (2009)
Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease (Nature Genetics (2009) 41 (1088-1093))
D Harold;R Abraham;P Hollingworth;R Sims.
Nature Genetics (2013)
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Stephen Sawcer;Garrett Hellenthal;Matti Pirinen;Chris C. A. Spencer.
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)
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
Benjamin F. Voight;Benjamin F. Voight;Laura J. Scott;Valgerdur Steinthorsdottir;Andrew P. Morris.
Nature Genetics (2010)
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)
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease.
Paul Hollingworth;Denise Harold;Rebecca Sims;Amy Gerrish.
Nature Genetics (2011)
Large-scale association analysis identifies new risk loci for coronary artery disease
Panos Deloukas;Stavroula Kanoni;Christina Willenborg;Martin Farrall.
Nature Genetics (2013)
Modulation of genetic associations with serum urate levels by body-mass-index in humans
Jennifer E. Huffman;Eva Albrecht;Alexander Teumer;Massimo Mangino.
PLOS ONE (2015)
A Mutation in VPS35, Encoding a Subunit of the Retromer Complex, Causes Late-Onset Parkinson Disease
Alexander Zimprich;Anna Benet-Pagès;Walter Struhal;Elisabeth Graf.
American Journal of Human Genetics (2011)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below: