Thomas Meitinger

Also affiliated with German Centre for Cardiovascular Research

Biochemistry, 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 7%percentile

0.104Author DataRank

Indexed papers

2in 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 2 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.

Preprocessed IgG Fc glycomics data in four Croatian cohorts (LC-ESI-MS)

Figshare(2017)10.6084/m9.figshare.5335861

Top 78%

0.104DataRank

Top 78%1 citations

Maja Pučić‐Baković, Toma Keser, Annika Wahl, Antti Hassinen, Jeong‐Yeh Yang +26 more

Papers

Driven by 43 papers — median percentile 11. Top paper: “Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants”.

Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

Nature Genetics(2022)10.1038/s41588-022-01233-6

N/A

7.7DataRank · unranked

721 citations

Tao Jiang, Anuj Goel, Stavroula Kanoni, Brooke N. Wolford, Deepak Atri +92 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

2.7DataRank · unranked

110 citations

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

52 Genetic Loci Influencing Myocardial Mass

Journal of the American College of Cardiology(2016)10.1016/j.jacc.2016.07.729

N/A

2.4DataRank · unranked

135 citations

Jessica van Setten, Niek Verweij, Georg Vogler, Matthew T. Maurano, Xinchen Wang +172 more

DeepWAS: Multivariate genotype-phenotype associations by directly integrating regulatory information using deep learning

PLOS Computational Biology(2020)10.1371/journal.pcbi.1007616

N/A

2.3DataRank · unranked

88 citations

Till F. M. Andlauer, Jade Martins, Stella Iurato, Brigitte Kühnel, Melanie Waldenberger +26 more

A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine

Nature Communications(2020)10.1038/s41467-020-17002-0

N/A

2.1DataRank · unranked

76 citations

Pamela M. Rist, Iyas Daghlas, Franco Giulianini, Padhraig Gormley, Verneri Anttila +95 more

Defining the role of common variation in the genomic and biological architecture of adult human height

Nature Genetics(2014)10.1038/ng.3097

N/A

1.1DataRank · unranked

2093 citations

Emilio Rodríguez-Ruiz, The PAGE Consortium, Diana O. Perkins, Tonu Esko, Jian Yang +479 more

A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids

Nature Communications(2021)10.1038/s41467-021-23899-y

N/A

1.1DataRank · unranked

45 citations

Michael Mendelson, Rory Wilson, Rahul Gondalia, Roby Joehanes, Elias Salfati +59 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

Seven new loci associated with age-related macular degeneration

Nature Genetics(2013)10.1038/ng.2578

N/A

1.0DataRank · unranked

798 citations

Lars G. Fritsche, Wei Chen, Brian L. Yaspan, Yi Yu, Guðmar Þorleifsson +141 more

Discovery of Sexual Dimorphisms in Metabolic and Genetic Biomarkers

PLoS Genetics(2011)10.1371/journal.pgen.1002215

N/A

0.899DataRank · unranked

400 citations

Janina S. Ried, Zhonghao Yu, Jan Krumsiek, Christian Gieger, Cornelia Prehn +16 more

Effect of predicted protein-truncating genetic variants on the human transcriptome

Science(2015)10.1126/science.1261877

N/A

0.877DataRank · unranked

345 citations

Matti Pirinen, Donald F. Conrad, Monkol Lek, Emily K. Tsang, Konrad J. Karczewski +206 more

Network inference from glycoproteomics data reveals new reactions in the IgG glycosylation pathway

Nature Communications(2017)10.1038/s41467-017-01525-0

N/A

0.604DataRank · unranked

55 citations

Toma Keser, Annika Wahl, Antti Hassinen, Lin Liu, Genadij Razdorov +26 more

Variants associated with HHIP expression have sex-differential effects on lung function

Wellcome Open Research(2021)10.12688/wellcomeopenres.15846.2

N/A

0.306DataRank · unranked

5 citations

Ma’en Obeidat, Carl Melbourne, Nick Shrine, Anna L. Guyatt, Catherine John +70 more

Publisher Correction: Network inference from glycoproteomics data reveals new reactions in the IgG glycosylation pathway

Nature Communications(2018)10.1038/s41467-017-02379-2

N/A

0.241DataRank · unranked

4 citations

Toma Keser, Annika Wahl, Antti Hassinen, Lin Liu, Genadij Razdorov +26 more

Identification of a novel missense mutation (G314E) in exon 7 of the cystic fibrosis transmembrane conductance regulator gene identified in a CF patient with pancreatic sufficiency

Human Mutation(1994)10.1002/humu.1380030112

N/A

0.208DataRank · unranked

3 citations

Annette Deufel, Christa Aulehla-Scholz, Ingolf Böhm, Bruno Hilz, Thomas Meitinger +2 more

pulver: an R package for parallel ultra-rapid p-value computation for linear regression interaction terms

BMC Bioinformatics(2017)10.1186/s12859-017-1838-y

N/A

0.104DataRank · unranked

1 citations

Clemens Baumbach, Simone Wahl, Martina Müller-Nurasyid, Konstantin Strauch, Rui Wang-Sattler +13 more

Preprocessed IgG Fc glycomics data in four Croatian cohorts (LC-ESI-MS)

Figshare(2017)10.6084/m9.figshare.5335861

Top 78%

0.104DataRank

Top 78%1 citations

Maja Pučić‐Baković, Toma Keser, Annika Wahl, Antti Hassinen, Jeong‐Yeh Yang +26 more

Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies

Kidney International(2022)10.1016/j.kint.2022.05.021

N/A

0DataRank · unranked

54 citations

Humaira Rasheed, Alexander Teumer, Laurent F. Thomas, Sarah E. Graham, Garðar Sveinbjörnsson +94 more

Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways

Nature Communications(2022)10.1038/s41467-022-32821-z

N/A

0DataRank · unranked

52 citations

Najim Lahrouchi, Aaron Isaacs, ThuyVy Duong, Luisa Foco, Farah Ahmed +95 more

Suleiman-El-Hattab syndrome: a histone modification disorder caused by TASP1 deficiency

Human Molecular Genetics(2022)10.1093/hmg/ddac098

N/A

0DataRank · unranked

9 citations

Anna Lena Burgemeister, Vincent Cantagrel, Jeanne Amiel, Karine Siquier-Pernet, Nathalie Boddaert +16 more

Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus

Nature Human Behaviour(2023)10.1038/s41562-023-01528-6

N/A

0DataRank · unranked

58 citations

Felix R. Day, Nicola Barban, Felix C. Tropf, David M. Brazel, Diana van Heemst +92 more

Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)

Kidney International(2023)10.1016/j.kint.2023.11.032

N/A

0DataRank · unranked

9 citations

Thanh-Minh T. Nguyen, Can Koşukçu, Julia Calzada‐Wack, Yong Li, Nurit Assia Batzir +55 more

Implication of FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)

medRxiv(2023)10.1101/2023.03.21.23287206

N/A

0DataRank · unranked

1 citations

Thanh-Minh T. Nguyen, Can Koşukçu, Julia Calzada‐Wack, Yong Li, Seha Saygılı +47 more

Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications

Nature Communications(2024)10.1038/s41467-024-44701-9

N/A

0DataRank · unranked

74 citations

Inga Steinbrenner, Yong Li, Melissa Bujnis, Tatsuhiko Naito, Eirini Marouli +95 more

A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure

UNC Libraries(2024)10.17615/rmgv-6646

N/A

0DataRank · unranked

5 citations

H.J. De Silva, Annette Peters, Matthew Brown, J.D. Faul, Thomas W. Winkler +95 more

Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity

Digital Commons@Becker (Washington University School of Medicine)(2024)10.17615/r2s5-pn26

N/A

0DataRank · unranked

0 citations

J.M. Norris, Evangelos Evangelou, C.E. Lewis, André G. Uitterlinden, M.Y. Tsai +95 more

A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids

UNC Libraries(2024)10.17615/6p9v-ms63

N/A

0DataRank · unranked

0 citations

Themistocles L. Assimes, Alan R. Shuldiner, Min-A Jhun, W. Chen, D. Absher +59 more

Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk

UNC Libraries(2020)10.17615/2bje-6g29

N/A

0DataRank · unranked

0 citations

Deborah J. Thompson, Hannes Helgason, Timothy M. Frayling, Hilary K. Finucane, Patrick Sulem +211 more

Cross-trait analyses with migraine reveal widespread pleiotropy and suggest a vascular component to migraine headache

International Journal of Epidemiology(2020)10.1093/ije/dyaa050

N/A

0DataRank · unranked

83 citations

Derek Klarin, Scott M. Damrauer, Kyong-Mi Chang, Philip S. Tsao, Themistocles L. Assimes +93 more

Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.06.015

N/A

0DataRank · unranked

55 citations

Mona Grimmel, Matias Wagner, J. Christopher Hennings, Christian Marx, René G. Feichtinger +41 more

Multi-ancestry genome-wide association study accounting for gene-psychosocial factor interactions identifies novel loci for blood pressure traits

Human Genetics and Genomics Advances(2020)10.1016/j.xhgg.2020.100013

N/A

0DataRank · unranked

14 citations

Melissa A. Richard, Solomon K. Musani, Yun Ju Sung, Thomas W. Winkler, Karen Schwander +95 more

Variants associated with HHIP expression have sex-differential effects on lung function

Wellcome Open Research(2020)10.12688/wellcomeopenres.15846.1

N/A

0DataRank · unranked

12 citations

Ma’en Obeidat, Carl Melbourne, Nick Shrine, Anna L. Guyatt, Catherine John +70 more

Low-frequency variation near common germline susceptibility loci are associated with risk of Ewing sarcoma

PLoS ONE(2020)10.1371/journal.pone.0237792

N/A

0DataRank · unranked

10 citations

Joshua N. Sampson, Thomas G. P. Grünewald, Didier Surdez, Stéphanie Reynaud, Olivier Mirabeau +51 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

Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.05.29.123505

N/A

0DataRank · unranked

3 citations

Raymond Noordam, Brian E. Cade, Karen Schwander, Thomas W. Winkler, Jiwon Lee +95 more

Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass

UNC Libraries(2020)10.17615/y892-y714

N/A

0DataRank · unranked

0 citations

Wen‐Chi Hsueh, Eric Orwoll, Serkalem Demissie, Liisa Byberg, Arjun Verma +95 more

An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans

UNC Libraries(2020)10.17615/kf29-bk98

Top 100%

0DataRank

Top 100%0 citations

Karl Gertow, Veikko Salomaa, John D. Eicher, Anders Hamsten, Inga Prokopenko +94 more

Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect

Nature Genetics(2021)10.1038/s41588-020-00762-2

N/A

0DataRank · unranked

296 citations

Catherine Francis, Xiao Yun Xu, Alexa M.C. Vermeer, Andrew R. Harper, Roy Huurman +65 more

Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.08.003

N/A

0DataRank · unranked

42 citations

Somayeh Bakhtiari, Ashley P.L. Marsh, Rauan Kaiyrzhanov, Matias Wagner, Sheetal Shetty +95 more

Multi-ancestry genome-wide gene–sleep interactions identify novel loci for blood pressure

Molecular Psychiatry(2021)10.1038/s41380-021-01087-0

N/A

0DataRank · unranked

23 citations

Raymond Noordam, Brian E. Cade, Karen Schwander, Thomas W. Winkler, Jiwon Lee +95 more

Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

medRxiv(2021)10.1101/2021.05.24.21257377

N/A

0DataRank · unranked

69 citations

Tao Jiang, Anuj Goel, Stavroula Kanoni, Brooke N. Wolford, Elle M. Weeks +87 more

Clinical implementation of RNA sequencing for Mendelian disease diagnostics

medRxiv(2021)10.1101/2021.04.01.21254633

N/A

0DataRank · unranked

33 citations

Mirjana Gušić, Robert Kopajtich, Christian Mertes, Nicholas H. Smith, Charlotte L. Alston +48 more

Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility

Nature Genetics(2022)10.1038/s41588-021-01007-6

N/A

0DataRank · unranked

143 citations

Rafik Tadros, Charlotte Glinge, David Y. Chiang, Mariam Jouni, Floriane Simonet +95 more

Thomas Meitinger

Indexed papers

Top data-sharing exemplar

Papers