Holger Prokisch

Also affiliated with LMU Klinikum, German Center for Pediatric and Adolescent Rheumatology, Institute of Human Genetics, German Centre for Cardiovascular Research, Technical University of Munich, Ludwig-Maximilians-Universität München

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 5%percentile

0.382Author 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.

Aberrant splicing prediction across human tissues

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.06.13.495326

Top 47%

0.382DataRank

Top 47%8 citations

Nils Wagner, Florian R. Hölzlwimmer, Vicente A. Yépez, Christian Mertes, Holger Prokisch +2 more

Papers

Driven by 29 papers — median percentile 26. Top paper: “Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression”.

Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression

Nature Genetics(2021)10.1038/s41588-021-00913-z

N/A

11.2DataRank · unranked

2226 citations

Annique Claringbould, Harm-Jan Westra, Marc Jan Bonder, Patrick Deelen, Biao Zeng +89 more

Multi-omic signature of body weight change: results from a population-based cohort study

BMC Medicine(2015)10.1186/s12916-015-0282-y

N/A

2.9DataRank · unranked

81 citations

Susanne Vogt, Ferdinand Stückler, Jan Krumsiek, Jörg Bartel, Tim Kacprowski +27 more

OTTERS: a powerful TWAS framework leveraging summary-level reference data

Nature Communications(2023)10.1038/s41467-023-36862-w

N/A

1.1DataRank · unranked

56 citations

Geyu Zhou, Luca Pinello, Urmo Võsa, Lude Franke, Alexis Battle +81 more

Epigenome-wide association study of whole blood gene expression in Framingham Heart Study participants provides molecular insight into the potential role of CHRNA5 in cigarette smoking-related lung diseases

Clinical Epigenetics(2021)10.1186/s13148-021-01041-5

N/A

0.865DataRank · unranked

28 citations

Roby Joehanes, Rory Wilson, Toshiko Tanaka, Luigi Ferrucci, Anja Kretschmer +9 more

Detection of aberrant splicing events in RNA-seq data using FRASER

Nature Communications(2021)10.1038/s41467-020-20573-7

N/A

0.781DataRank · unranked

182 citations

Ines F. Scheller, Vicente A. Yépez, Muhammed Hasan Çelik, Yingjiqiong Liang, Laura S. Kremer +4 more

Impaired complex I repair causes recessive Leber’s hereditary optic neuropathy

Journal of Clinical Investigation(2021)10.1172/jci138267

N/A

0.756DataRank · unranked

153 citations

Natalia L. Sheremet, Claudia B. Catarino, Natalia A. Andreeva, Zahra Assouline, Piero Barboni +49 more

Blood DNA methylation sites predict death risk in a longitudinal study of 12, 300 individuals

Aging(2020)10.18632/aging.103408

N/A

0.574DataRank · unranked

45 citations

Riccardo E. Marioni, Cavin Ward‐Caviness, Rahul Gondalia, Weihua Guan, Brian Chen +44 more

Systematic analysis of NDUFAF6 in complex I assembly and mitochondrial disease

Nature Metabolism(2024)10.1038/s42255-024-01039-2

N/A

0.470DataRank · unranked

22 citations

Rachel M. Guerra, Laura Steenberge, Charlotte L. Alston, Kei Murayama, Yasushi Okazaki +10 more

Single cell spatial transcriptomics integration deciphers the morphological heterogeneity of atherosclerotic carotid arteries

Nature Communications(2025)10.1038/s41467-025-67679-4

N/A

0.464DataRank · unranked

21 citations

Dániel Garger, Fatemeh Peymani, Justus Wettich, Nadja Sachs, Johannes Wirth +12 more

Network reconstruction for trans acting genetic loci using multi-omics data and prior information

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.05.19.101592

N/A

0.408DataRank · unranked

6 citations

Ashis Saha, Mélanie Waldenberger, Sonja Kunze, Simone Wahl, Martina Müller‐Nurasyid +11 more

Aberrant splicing prediction across human tissues

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.06.13.495326

Top 47%

0.382DataRank

Top 47%8 citations

Nils Wagner, Florian R. Hölzlwimmer, Vicente A. Yépez, Christian Mertes, Holger Prokisch +2 more

Network reconstruction for trans acting genetic loci using multi-omics data and prior information

Genome Medicine(2022)10.1186/s13073-022-01124-9

N/A

0.269DataRank · unranked

5 citations

Ashis Saha, Melanie Waldenberger, Sonja Kunze, Simone Wahl, Martina Müller-Nurasyid +14 more

Blood cis-eQTL Analysis Fails to Identify Novel Association Signals among Sub-Threshold Candidates from Genome-Wide Association Studies in Restless Legs Syndrome

PLoS ONE(2014)10.1371/journal.pone.0098092

N/A

0.183DataRank · unranked

2 citations

Katharina Schramm, Claudia Schurmann, Peter Lichtner, Christian Herder, Michael Roden +22 more

Biallelic USP14 variants cause a syndromic neurodevelopmental disorder

Genetics in Medicine(2024)10.1016/j.gim.2024.101120

N/A

0.170DataRank · unranked

2 citations

Xénia Latypova, Ka Ying Sharon Hung, Miguel A. Prado, Byung‐Hoon Lee, Sophie Möller +19 more

Biallelic variants in DAP3 result in reduced assembly of the mitoribosomal small subunit with altered intrinsic and extrinsic apoptosis and a Perrault syndrome-spectrum phenotype

medRxiv(2024)10.1101/2024.08.19.24312079

N/A

0.165DataRank · unranked

2 citations

Robert Kopajtich, Leigh Demain, Alessandro Rea, Huw B. Thomas, Manuel Schiff +35 more

Protonation-Dependent Sequencing of 5-Formylcytidine in RNA

Biochemistry(2022)10.1021/acs.biochem.1c00761

N/A

0DataRank · unranked

21 citations

Supuni Thalalla Gamage, Diamond Gallimore, Robert Kopajtich, Christine N. Evans, Samantha Nance +7 more

Aberrant splicing prediction across human tissues

Nature Genetics(2023)10.1038/s41588-023-01373-3

N/A

0DataRank · unranked

95 citations

Muhammed Hasan Çelik, Florian R. Hölzlwimmer, Christian Mertes, Holger Prokisch, Vicente A. Yépez +2 more

Protonation-Dependent Sequencing of 5-Formylcytidine in RNA

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.11.23.469744

N/A

0DataRank · unranked

1 citations

Supuni Thalalla Gamage, Diamond A. Gallimore, Robert Kopajtich, Christine N. Evans, Samantha R. Nance +7 more

Systematic analysis of NDUFAF6 in complex I assembly and mitochondrial disease

Research Square(2023)10.21203/rs.3.rs-3332602/v1

N/A

0DataRank · unranked

0 citations

Andrew Y. Sung, Rachel M. Guerra, Laura Steenberge, Charlotte L. Alston, Kei Murayama +10 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

Loss‐of‐Function Variants in CUL3 Cause a Syndromic Neurodevelopmental Disorder

Annals of Neurology(2024)10.1002/ana.27077

N/A

0DataRank · unranked

10 citations

Frédéric Ebstein, Tzung‐Chien Hsieh, Marialetizia Motta, Francesca Clementina Radio, Johanna C. Herkert +74 more

Bi-allelic variants in DAP3 result in reduced assembly of the mitoribosomal small subunit with altered apoptosis and a Perrault-syndrome-spectrum phenotype

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.11.007

N/A

0DataRank · unranked

7 citations

Robert Kopajtich, Leigh Demain, Alessandro Rea, Huw B. Thomas, Manuel Schiff +34 more

Associations of carotid intima media thickness with gene expression in whole blood and genetically predicted gene expression across 48 tissues

Human Molecular Genetics(2021)10.1093/hmg/ddab236

N/A

0DataRank · unranked

10 citations

Lauren E. Petty, Markus Scholz, Rick Jansen, Stefan Weiß, Xiaoling Zhang +41 more

Bi-allelic mutations in FASTKD5 are associated with cytochrome c oxidase deficiency and early- to late-onset Leigh syndrome

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.05.007

N/A

0DataRank · unranked

2 citations

Woranontee Weraarpachai, Katherine M. Szigety, Robert Kopajtich, James B. Gibson, Johan L.K. Van Hove +13 more

Single cell spatial transcriptomics integration deciphers the morphological heterogeneity of atherosclerotic carotid arteries

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.04.16.649077

N/A

0DataRank · unranked

4 citations

Dániel Garger, Fatemeh Peymani, Justus Wettich, Nadja Sachs, Johannes Wirth +11 more

Genotypic diversity and phenotypic spectrum of infantile liver failure syndrome type 1 due to variants in LARS1

Genetics in Medicine(2020)10.1038/s41436-020-0904-4

N/A

0DataRank · unranked

50 citations

Desirée E.C. Smith, Ellen Crushell, Ralf A. Husain, Gajja S. Salomons, Bader Alhaddad +35 more

Genotypic and phenotypic spectrum of infantile liver failure due to pathogenic TRMU variants

Genetics in Medicine(2022)10.1016/j.gim.2022.09.015

N/A

0DataRank · unranked

17 citations

Yael Mozer‐Glassberg, Yuval E. Landau, Lea D. Schlieben, Holger Prokisch, René G. Feichtinger +56 more

Additional file 2 of Network reconstruction for trans acting genetic loci using multi-omics data and prior information

Open MIND(2022)10.6084/m9.figshare.21520295

Top 100%

0DataRank

Top 100%0 citations

Ashis Saha, Mélanie Waldenberger, Sonja Kunze, Simone Wahl, Martina Müller‐Nurasyid +11 more

Protonation‐Dependent Sequencing of 5‐Formylcytidine in RNA

The FASEB Journal(2022)10.1096/fasebj.2022.36.s1.r5310

N/A

0DataRank · unranked

1 citations

Supuni Thalalla Gamage, Diamond A. Gallimore, Robert Kopajtich, Christine N. Evans, Samantha R. Nance +7 more

Holger Prokisch

Indexed papers

Top data-sharing exemplar

Papers