Leif Groop

Also affiliated with University of Helsinki, Lund University, Institute for Molecular Medicine Finland

MedicineBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 1%percentile

9.3Author DataRank

Indexed papers

4in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 4 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

A structural variation reference for medical and population genetics

Nature(2020)10.1038/s41586-020-2287-8

Top 3%

6.7DataRank

Top 3%1180 citations

Harrison Brand, Konrad J. Karczewski, Xuefang Zhao, Jessica Alföldi, Laurent C. Francioli +201 more

Papers

Driven by 31 papers — median percentile 73. Top paper: “A structural variation reference for medical and population genetics”.

A structural variation reference for medical and population genetics

Nature(2020)10.1038/s41586-020-2287-8

Top 3%

6.7DataRank

Top 3%1180 citations

Harrison Brand, Konrad J. Karczewski, Xuefang Zhao, Jessica Alföldi, Laurent C. Francioli +201 more

Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes

Nature Communications(2020)10.1038/s41467-019-12438-5

N/A

5.6DataRank · unranked

143 citations

James Zou, Beryl B. Cummings, Jessica Alföldi, Laurent C. Francioli, Laura D. Gauthier +174 more

Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals

Nature Communications(2020)10.1038/s41467-019-10717-9

N/A

5.2DataRank · unranked

191 citations

Konrad J. Karczewski, Xiaolei Zhang, Sonia Chothani, Miriam J. Smith, D. Gareth Evans +181 more

The effect of LRRK2 loss-of-function variants in humans

Nature Medicine(2020)10.1038/s41591-020-0893-5

N/A

4.9DataRank · unranked

114 citations

Irina M. Armean, Aaron Kleinman, Jamie L. Marshall, Eric V. Minikel, Julia K. Goodrich +214 more

Underlying Genetic Models of Inheritance in Established Type 2 Diabetes Associations

American Journal of Epidemiology(2009)10.1093/aje/kwp145

N/A

4.0DataRank · unranked

67 citations

Lorraine Southam, David Altshuler, Kristin G. Ardlie, Inês Barroso, Michael Boehnke +27 more

Genetic variant effects on gene expression in human pancreatic islets and their implications for T2D

Nature Communications(2020)10.1038/s41467-020-18581-8

N/A

2.4DataRank · unranked

164 citations

Arushi Varshney, Martijn van de Bunt, Rashmi B. Prasad, Olof Asplund, Amanda J. Bennett +31 more

TIGER: The gene expression regulatory variation landscape of human pancreatic islets

Cell Reports(2021)10.1016/j.celrep.2021.109807

Top 10%

2.2DataRank

Top 10%103 citations

Anthony Piron, Ignasi Morán, Marta Guindo-Martínez, Sílvia Bonàs‐Guarch, Goutham Atla +24 more

Distinct Molecular Signatures of Clinical Clusters in People With Type 2 Diabetes: An IMI-RHAPSODY Study

Diabetes(2021)10.2337/db20-1281

N/A

1.5DataRank · unranked

55 citations

Louise A. Donnelly, Hugo Fitipaldi, Gerard A. Bouland, Giuseppe N. Giordano, Mikael Åkerlund +30 more

PGC-1α-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes

Nature Genetics(2003)10.1038/ng1180

N/A

1.4DataRank · unranked

10534 citations

Cecilia M. Lindgren, Karl-Fredrik Eriksson, Aravind Subramanian, Smita Sihag, Joseph Lehar +19 more

The mutational constraint spectrum quantified from variation in 141,456 humans

Nature(2020)10.1038/s41586-020-2308-7

N/A

1.4DataRank · unranked

9958 citations

Laurent C. Francioli, Grace Tiao, Beryl B. Cummings, Jessica Alföldi, Qingbo S. Wang +187 more

The genetic architecture of type 2 diabetes

Nature(2016)10.1038/nature18642

N/A

1.1DataRank · unranked

1106 citations

Menachem Fromer, Tanya M. Teslovich, Anubha Mahajan, Vineeta Agarwala, Kyle J. Gaulton +334 more

Transcript expression-aware annotation improves rare variant interpretation

Nature(2020)10.1038/s41586-020-2329-2

N/A

0.796DataRank · unranked

201 citations

Konrad J. Karczewski, Ditte Demontis, Eleanor G. Seaby, Nicholas A. Watts, Moriel Singer-Berk +177 more

Evaluating drug targets through human loss-of-function genetic variation

Nature(2020)10.1038/s41586-020-2267-z

N/A

0.779DataRank · unranked

179 citations

Konrad J. Karczewski, Hilary C. Martin, Beryl B. Cummings, Nicola Whiffin, Daniel R. Rhodes +150 more

TIGER: The gene expression regulatory variation landscape of human pancreatic islets

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.05.26.445616

Top 45%

0.415DataRank

Top 45%8 citations

Anthony Piron, Ignasi Morán, Marta Guindo-Martínez, Sílvia Bonàs‐Guarch, Goutham Atla +25 more

The type 1 diabetes gene TYK2 regulates β-cell development and its responses to interferon-α

Nature Communications(2022)10.1038/s41467-022-34069-z

N/A

0DataRank · unranked

53 citations

Hazem Ibrahim, Clémentine Halliez, Rashmi B. Prasad, Federica Vecchio, Om Prakash Dwivedi +13 more

Smoking, use of smokeless tobacco, HLA genotypes and incidence of latent autoimmune diabetes in adults

Diabetologia(2022)10.1007/s00125-022-05763-w

N/A

0DataRank · unranked

14 citations

Yuxia Wei, Emma Ahlqvist, Lars Alfredsson, Valdemar Grill, Leif Groop +7 more

The type 1 diabetes gene TYK2 regulates β-cell development and its responses to interferon-α

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.02.22.481272

N/A

0DataRank · unranked

0 citations

Hazem Ibrahim, Clémentine Halliez, Rashmi B. Prasad, Federica Vecchio, Om Prakash Dwivedi +13 more

Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake

Nature Genetics(2023)10.1038/s41588-023-01408-9

N/A

0DataRank · unranked

76 citations

Dougall M. Norris, Xianyong Yin, K. Alaine Broadaway, Anne H. Moxley, Swarooparani Vadlamudi +94 more

Physical Activity, Genetic Susceptibility, and the Risk of Latent Autoimmune Diabetes in Adults and Type 2 Diabetes

The Journal of Clinical Endocrinology & Metabolism(2020)10.1210/clinem/dgaa549

N/A

0DataRank · unranked

19 citations

Emma Ahlqvist, Tomas Andersson, Lars Alfredsson, Per-Ola Carlsson, Valdemar Grill +7 more

Metabolic and Genetic Determinants of Glucose Shape After Oral Challenge in Obese Youths: A Longitudinal Study

The Journal of Clinical Endocrinology & Metabolism(2020)10.1210/clinem/dgz207

N/A

0DataRank · unranked

12 citations

Domenico Tricò, Chiara Dalla Man, Nicola Santoro, Bridget Pierpont, Leif Groop +3 more

Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci

Oxford University Research Archive (ORA) (University of Oxford)(2020)10.17615/gc55-0r45

N/A

0DataRank · unranked

2 citations

Sonsoles Morcillo, Nicholas J. Wareham, Richard A. Jensen, Allan Linnenberg, Josée Dupuis +74 more

Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes

medRxiv(2020)10.1101/2020.09.22.20195529

N/A

0DataRank · unranked

11 citations

Moriel Singer‐Berk, Rachel G. Son, Abigail Sveden, Jordan C. Wood, Eleina England +95 more

Rare coding variants in 35 genes associate with circulating lipid levels – a multi-ancestry analysis of 170,000 exomes

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.12.22.423783

N/A

0DataRank · unranked

11 citations

Peter Dornbos, Mark Chaffin, Dajiang J. Liu, Minxian X. Wang, Margaret Sunitha Selvaraj +95 more

The Genetic Structure of the Swedish Population

UNC Libraries(2020)10.17615/fvdj-e024

Top 100%

0DataRank

Top 100%0 citations

Jianjun Liu, Per Hall, Pamela Sklar, Samuli Ripatti, Henrik Grönberg +18 more

Loss-of-function mutations in SLC30A8 protect against type 2 diabetes

UNC Libraries(2020)10.17615/p2f9-t736

N/A

0DataRank · unranked

0 citations

Jeff K. Trimmer, Pål R. Njølstad, Allan Linneberg, Kāri Stefánsson, David R. Cox +16 more

Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes

Nature Communications(2021)10.1038/s41467-021-23556-4

N/A

0DataRank · unranked

110 citations

Moriel Singer‐Berk, Rachel G. Son, Abigail Sveden, Jordan C. Wood, Eleina England +95 more

Genome-Wide Association Study of Peripheral Artery Disease

Circulation Genomic and Precision Medicine(2021)10.1161/circgen.119.002862

N/A

0DataRank · unranked

86 citations

Alexander Stiby, Moustafa Abdalla, Erin Austin, Stela McLachlan, Efthymia Vlachopoulou +50 more

Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.11.021

N/A

0DataRank · unranked

70 citations

Peter Dornbos, Mark Chaffin, Dajiang J. Liu, Minxian Wang, Margaret Sunitha Selvaraj +95 more

Absence of islet autoantibodies and modestly raised glucose values at diabetes diagnosis should Lead to testing for MODY: lessons from a 5-year pediatric Swedish National Cohort study

Yearbook of pediatric endocrinology(2021)10.1530/ey.18.10.8

N/A

0DataRank · unranked

1 citations

Maggie Shepherd, Sian Ellard, Michael N. Weedon, Åke Lernmark, Gun Forsander +12 more

Identification of ten loci associated with height highlights new biological pathways in human growth

UNC Libraries(2021)10.17615/jwbr-0w10

N/A

0DataRank · unranked

0 citations

Frank B. Hu, Peter Kraft, S. Eyheramendy, Candace Guiducci, H.‐Erich Wichmann +26 more

Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes

Human Molecular Genetics(2022)10.1093/hmg/ddac050

N/A

0DataRank · unranked

128 citations

Gunn-Helen Moen, Maria Carolina Borges, Teresa Ferreira, James P. Cook, Catherine Allard +68 more

Leif Groop

Indexed papers

Top data-sharing exemplar

Papers