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Author: Leif Groop

  • ORCiD: http://orcid.org/0000-0002-0187-3263
  • Most recently observed institution: Lund University Diabetes Centre, Malmo, Sweden, Finnish Institute for Molecular Medicine, Helsinki University; Folkhalsan Research Centre, Helsinki, Finland

Rankings

  • All-time downloads: 24,370 (rank: 5,283 out of 511,089)
  • Categories:
    • cell biology: 1,866 (rank: 2,566 (tie) out of 33,954)
    • endocrinology: 146 (rank: 657 (tie) out of 1,067)
    • genetic and genomic medicine: 1,373 (rank: 706 (tie) out of 6,821)
    • genetics: 13,589 (rank: 971 out of 38,712)
    • genomics: 5,736 (rank: 3,419 out of 45,704)
    • infectious diseases: 499 (rank: 21,855 (tie) out of 32,281)
    • molecular biology: 678 (rank: 7,183 (tie) out of 24,245)
    • systems biology: 483 (rank: 7,304 (tie) out of 12,894)

Downloads per author, site-wide

Preprints

A reference panel of 64,976 haplotypes for genotype imputation

genetics more details view paper
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Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

genomics more details view paper
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TCF7L2 is a master regulator of insulin production and processing

cell biology more details view paper
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Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

genetics more details view paper
  • Downloaded 1,814 times
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Genetic discovery and translational decision support from exome sequencing of 20,791 type 2 diabetes cases and 24,440 controls from five ancestries

genetics more details view paper
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Influence of genetic variants on gene expression in human pancreatic islets – implications for type 2 diabetes

genomics more details view paper
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Narrow-sense heritability estimation of complex traits using identity-by-descent information.

genetics more details view paper
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Haplotype sharing provides insights into fine-scale population history and disease in Finland

genetics more details view paper
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Loss of ZnT8 function protects against diabetes by enhanced insulin secretion

genetics more details view paper
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    • In genetics: 925 out of 5,140
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    • Site-wide: 42,679 out of 118,476

Heterozygous RFX6 protein truncating variants cause Maturity-Onset Diabetes of the Young (MODY) with reduced penetrance

genetics more details view paper
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Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation

genetics more details view paper
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    • In genetics: 1,434 out of 5,140
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Trans-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

genetic and genomic medicine more details view paper
  • Downloaded 706 times
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    • In genetic and genomic medicine: 60 out of 488
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Islet Gene View - a tool to facilitate islet research

molecular biology more details view paper
  • Downloaded 678 times
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    • In molecular biology: 846 out of 3,620
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Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes

genetic and genomic medicine more details view paper
  • Downloaded 667 times
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Turning vice into virtue: Using Batch-Effects to Detect Errors in Large Genomic Datasets

genomics more details view paper
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The Trans-Ancestral Genomic Architecture of Glycaemic Traits

genetics more details view paper
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Serology assessment of antibody response to SARS-CoV-2 in patients with COVID-19 by rapid IgM/IgG antibody test

infectious diseases more details view paper
  • Downloaded 499 times
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Controllability in an islet specific regulatory network identifies the transcriptional factor NFATC4, which regulates Type 2 Diabetes associated genes

systems biology more details view paper
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    • Site-wide: 106,737 out of 118,476

Human pancreatic β cell lncRNAs control cell-specific regulatory networks

genomics more details view paper
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Exome-wide association study on Albuminuria identifies a novel rare variant in CUBN and additional genes, in 33,985 Europeans with and without diabetes

genetics more details view paper
  • Downloaded 240 times
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Genetic analysis of obstructive sleep apnoea discovers a strong association with cardiometabolic health

genetics more details view paper
  • Downloaded 187 times
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    • In genetics: 4,367 out of 5,140
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Aetiological differences between novel subtypes of diabetes derived from genetic associations

endocrinology more details view paper
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