Leif Groop
Genetics · 1986–2020
A researcher in the Science corpus: 42 papers; trusts 1 researcher and is trusted by 1 researcher here, as inferred from the citation graph.
Subfields
- Genetics — 470 citations into it
- Molecular Biology — 368 citations into it; #15,597 of 17,773 by trust here, #425 by citations
- Pediatrics, Perinatology and Child Health — 30 citations into it
Whom Leif Groop trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Leif Groop overall
Papers from Leif Groop's perspective
Ordered by how strongly the researchers Leif Groop trusts endorse each paper. Same corpus, a different order for every researcher.
- The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm (Nature Genetics)
- Common variants at 30 loci contribute to polygenic dyslipidemia (Nature Genetics)
- Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus (Nature Genetics)
- Reactome knowledgebase of human biological pathways and processes (Nucleic Acids Res.)
- The PANTHER database of protein families, subfamilies, functions and pathways (Nucleic Acids Res.)
- Common variant in MTNR1B associated with increased risk of type 2 diabetes and impaired early insulin secretion (Nature Genetics)
- Genetic Loci Influencing C-reactive Protein Levels and Risk of Coronary Heart Disease (Journal of the American Medical Association (JAMA))
- Characterization of ADAMTS-9 and ADAMTS-20 as a Distinct ADAMTS Subfamily Related to Caenorhabditis elegans GON-1*
- Measuring inconsistency in meta-analyses (British medical journal)
- Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
Their papers
- Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (2012) — 1,982 citations
- PGC-1α-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes (2003) — 8,321 citations
- Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (2008) — 1,910 citations
- Genome-Wide Association Analysis Identifies Loci for Type 2 Diabetes and Triglyceride Levels (2007) — 2,928 citations
- Identification of ten loci associated with height highlights new biological pathways in human growth (2008) — 644 citations
- Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus (2008) — 768 citations
- Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2010) — 1,860 citations
- The genetic architecture of type 2 diabetes (2016) — 1,066 citations
- A Six Months Exercise Intervention Influences the Genome-wide DNA Methylation Pattern in Human Adipose Tissue (2013) — 600 citations
- Large-scale association analysis identifies new risk loci for coronary artery disease (2012) — 1,642 citations
- Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus (2000) — 1,471 citations
- Cardiovascular morbidity and mortality associated with the metabolic syndrome. (2001) — 4,989 citations
- The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes (2000) — 1,189 citations
- Genome-wide meta-analyses identify multiple loci associated with smoking behavior (2010) — 1,140 citations
- Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population (2014) — 412 citations
- Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2019) — 162 citations
- Type 2 diabetes mellitus (2015) — 2,875 citations
- A structural variation reference for medical and population genetics (2020) — 876 citations
- Evaluating drug targets through human loss-of-function genetic variation (2019) — 168 citations
- Associations of autozygosity with a broad range of human phenotypes (2019) — 112 citations