What is he best known for?
The fields of study he is best known for:
- Gene
- Internal medicine
- Genetics
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.
His most cited work include:
- Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease (2556 citations)
- Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis (1970 citations)
- Discovery and refinement of loci associated with lipid levels (1814 citations)
What are the main themes of his work throughout his whole career to date?
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.
He most often published in these fields:
- Genetics (47.42%)
- Single-nucleotide polymorphism (34.27%)
- Genome-wide association study (32.39%)
What were the highlights of his more recent work (between 2014-2021)?
- Genome-wide association study (32.39%)
- Genetics (47.42%)
- Internal medicine (25.82%)
In recent papers he was focusing on the following fields of study:
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.
Between 2014 and 2021, his most popular works were:
- Modulation of genetic associations with serum urate levels by body-mass-index in humans (1089 citations)
- An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans (374 citations)
- Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci (275 citations)
In his most recent research, the most cited papers focused on:
- Gene
- Internal medicine
- Mutation
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.
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