Gábor Marth

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 1%percentile

32.0Author DataRank

Indexed papers

5in 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 5 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 global reference for human genetic variation

Nature(2015)10.1038/nature15393

Top 1%

10.6DataRank

Top 1%20166 citations

Gonçalo R. Abecasis, Richard M. Durbin, Panagiotis Deloukas, Aravinda Chakravarti, Peter Donnelly +516 more

Papers

Driven by 33 papers — median percentile 98. Top paper: “A global reference for human genetic variation”.

A global reference for human genetic variation

Nature(2015)10.1038/nature15393

Top 1%

10.6DataRank

Top 1%20166 citations

Gonçalo R. Abecasis, Richard M. Durbin, Panagiotis Deloukas, Aravinda Chakravarti, Peter Donnelly +516 more

An integrated map of structural variation in 2,504 human genomes

Nature(2015)10.1038/nature15394

Top 2%

9.1DataRank

Top 2%2686 citations

Tobias Rausch, Marianne K. DeGorter, Robert E. Handsaker, Alexej Abyzov, Joanna M. M. Howson +75 more

Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel

Nature Communications(2014)10.1038/ncomms4934

Top 2%

8.3DataRank

Top 2%460 citations

Jonathan Marchini, Peter Donnelly, Gerton Lunter, Jonathan L. Marchini, Simon Myers +364 more

A human breast cancer-derived xenograft and organoid platform for drug discovery and precision oncology

Nature Cancer(2022)10.1038/s43018-022-00337-6

Top 6%

3.9DataRank

Top 6%400 citations

Maihi Fujita, Andrew Butterfield, Sandra D. Scherer, Matthew H. Bailey, Zhengtao Chu +37 more

The Sequence Alignment/Map format and SAMtools

Bioinformatics(2009)10.1093/bioinformatics/btp352

N/A

1.7DataRank · unranked

66179 citations

Alec Wysoker, Tim Fennell, Jue Ruan, Nils Homer, Richard Durbin +5 more

The variant call format and VCFtools

Bioinformatics(2011)10.1093/bioinformatics/btr330

N/A

1.5DataRank · unranked

17436 citations

Joanna M. M. Howson, University of Michigan, Iain Mathieson, Mark A. DePristo, Robert E. Handsaker +8 more

Genomic analyses implicate noncoding de novo variants in congenital heart disease

Nature Genetics(2020)10.1038/s41588-020-0652-z

N/A

0.779DataRank · unranked

179 citations

Sarah U. Morton, Seong Won Kim, Alexander Kitaygorodsky, Lauren K. Wasson, Kathleen Chen +30 more

The Somatic Mosaicism across Human Tissues Network

Nature(2025)10.1038/s41586-025-09096-7

N/A

0.672DataRank · unranked

43 citations

Ji Won Oh, Yujin Angelina Choi, Nam Seop Lim, Boxun Zhao, Adam Voshall +365 more

Archetype tasks link intratumoral heterogeneity to plasticity and cancer hallmarks in small cell lung cancer

Cell Systems(2022)10.1016/j.cels.2022.07.006

N/A

0.614DataRank · unranked

59 citations

Geena V. Ildefonso, Caitlin O. McAtee, Patricia Midori Murobushi Ozawa, Abbie S. Ireland, Philip E. Stauffer +21 more

Differences in molecular sampling and data processing explain variation among single-cell and single-nucleus RNA-seq experiments

Genome Research(2024)10.1101/gr.278253.123

N/A

0.406DataRank · unranked

14 citations

YOUNGHEE LEE, Gábor Marth, Aaron R. Quinlan, John Chamberlin

The stochastic nature of errors in next-generation sequencing of circulating cell-free DNA

PLoS ONE(2020)10.1371/journal.pone.0229063

N/A

0.406DataRank · unranked

14 citations

Sabine Hellwig, Christopher J. Conley, Alun Thomas, Carrie L. Fuertes, Cindy Hamil +6 more

Mobile element insertions and associated structural variants in longitudinal breast cancer samples

Scientific Reports(2021)10.1038/s41598-021-92444-0

N/A

0.345DataRank · unranked

9 citations

Kristi Russell, Julie Feusier, 義行高橋, Sean V. Tavtigian, Gábor Marth +2 more

Comprehensive variant calling from whole‐genome sequencing identifies a complex inversion that disrupts ZFPM2 in familial congenital diaphragmatic hernia

Molecular Genetics & Genomic Medicine(2022)10.1002/mgg3.1888

N/A

0.345DataRank · unranked

9 citations

Najla Al‐Sweel, Andrew Farrell, Rong Mao, Pınar Bayrak‐Toydemir, Christine E. Miller +22 more

Long-read single-cell RNA sequencing enables the study of cancer subclone-specific genotypes and phenotypes in chronic lymphocytic leukemia

Genome Research(2025)10.1101/gr.279049.124

N/A

0.331DataRank · unranked

6 citations

Xiaomeng Huang, Yi Qiao, Philip J. Moos, Deepa Sampath, Deborah M. Stephens +3 more

Comprehensive benchmarking of somatic single-nucleotide variant and indel detection at ultra-low allele fractions using short- and long-read data

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.10.13.681545

Top 70%

0.165DataRank

Top 70%2 citations

Dominika Maziec, Julia Markowski, Stephanie Georges, Nancy L. Parmalee, Michele Berselli +41 more

A precision oncology-focused deep learning framework for personalized selection of cancer therapy

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.12.12.628190

N/A

0.145DataRank · unranked

1 citations

Chieh‐Hsiang Yang, Emilio Cortes-Sanchez, Tony Di Sera, Xiaomeng Huang, Sandra D. Scherer +12 more

The extracellular milieu of Toxoplasma ’s lytic cycle drives lab-adaptation and promotes changes in lipid metabolism primarily driven by transcriptional reprogramming

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.03.09.434570

N/A

0.104DataRank · unranked

1 citations

Yasaman Rezvani, Andrew Farrell, Amir Vajdi, Gábor Marth, Kourosh Zarringhalam +2 more

Novel temporal and spatial patterns of metastatic colonization from rapid-autopsy tumor biopsies

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.06.03.446803

N/A

0DataRank · unranked

0 citations

義行高橋, Samuel W. Brady, Rachel E. Factor, Erinn Downs‐Kelly, Andrew Farrell +8 more

quickBAM: a parallelized BAM file access API for high throughput sequence analysis informatics

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.10.05.463280

N/A

0DataRank · unranked

0 citations

Xiaomeng Huang, Gábor Marth, 義行高橋, T. Anders Pitman

A breast cancer patient-derived xenograft and organoid platform for drug discovery and precision oncology

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.02.28.433268

N/A

0DataRank · unranked

20 citations

Maihi Fujita, Andrew Butterfield, Sandra D. Scherer, Matthew H. Bailey, Zhengtao Chu +37 more

OncoGEMINI: software for investigating tumor variants from multiple biopsies with integrated cancer annotations

Genome Medicine(2021)10.1186/s13073-021-00854-6

N/A

0DataRank · unranked

2 citations

Michael J. Cormier, Xiaomeng Huang, 義行高橋, Gábor Marth, Aaron R. Quinlan +1 more

Subclonal evolution of CLL driver mutations is associated with relapse in ibrutinib- and acalabrutinib-treated patients

Blood(2022)10.1182/blood.2021015132

N/A

0DataRank · unranked

11 citations

Xiaomeng Huang, 義行高橋, Szabolcs Tarapcsák, Kerry A. Rogers, Shrilekha Misra +5 more

Novel temporal and spatial patterns of metastatic colonization from breast cancer rapid-autopsy tumor biopsies

Genome Medicine(2021)10.1186/s13073-021-00989-6

N/A

0DataRank · unranked

12 citations

義行高橋, Samuel W. Brady, Rachel E. Factor, Erinn Downs‐Kelly, Andrew Farrell +8 more

quickBAM: a parallelized BAM file access API for high-throughput sequence analysis informatics

Bioinformatics(2023)10.1093/bioinformatics/btad463

N/A

0DataRank · unranked

3 citations

Xiaomeng Huang, Gábor Marth, 義行高橋, Anders Pitman

Combating subclonal evolution of resistant cancer phenotypes

UNC Libraries(2020)10.17615/hett-8q86

N/A

0DataRank · unranked

0 citations

Aaron R. Quinlan, Rachel E. Factor, Ryan M. Layer, Layla A. Anderson, David F. Jenkins +23 more

A Bayesian framework to study tumor subclone–specific expression by combining bulk DNA and single-cell RNA sequencing data

Genome Research(2024)10.1101/gr.278234.123

N/A

0DataRank · unranked

4 citations

Xiaomeng Huang, Philip J. Moos, Jonathan M. Ahmann, Anthony D. Pomicter, Michael W. Deininger +5 more

Deep whole genome sequencing of multiple proband tissues and parental blood reveals the complex genetic etiology of congenital diaphragmatic hernias

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.04.03.024398

N/A

0DataRank · unranked

6 citations

ZD Fox, Andrew Farrell, Julia Wynn, Barry Moore, Lun Yu +7 more

Long-read single-cell RNA sequencing enables the study of cancer subclone-specific genotype and phenotype in chronic lymphocytic leukemia

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.03.15.585298

N/A

0DataRank · unranked

0 citations

Xiaomeng Huang, Yi Qiao, Philip J. Moos, Deepa Sampath, Deborah M. Stephens +3 more

Clonal dynamics of aggressive systemic mastocytosis on avapritinib therapy

Blood Cancer Journal(2024)10.1038/s41408-024-01157-w

N/A

0DataRank · unranked

0 citations

Anthony D. Pomicter, Jonathan M. Ahmann, Yi Qiao, Opal S. Chen, Tracy I. George +5 more

Deep whole-genome sequencing of multiple proband tissues and parental blood reveals the complex genetic etiology of congenital diaphragmatic hernias

Human Genetics and Genomics Advances(2020)10.1016/j.xhgg.2020.100008

N/A

0DataRank · unranked

10 citations

Zac D Fox, Andrew Farrell, Julia Wynn, Barry Moore, Lan Yu +7 more

An optimized variant prioritization process for rare disease diagnostics: recommendations for Exomiser and Genomiser

medRxiv(2025)10.1101/2025.04.18.25326061

N/A

0DataRank · unranked

2 citations

Shruti Marwaha, Alistair Ward, Shilpa N. Kobren, Jennefer N. Carter, Undiagnosed Diseases Network +3 more

Somalier: rapid relatedness estimation for cancer and germline studies using efficient genome sketches

Genome Medicine(2020)10.1186/s13073-020-00761-2

N/A

0DataRank · unranked

150 citations

Preetida J. Bhetariya, Joe Brown, Stephanie N. Kravitz, Gábor Marth, Randy L. Jensen +4 more

Single-cell RNA sequencing in Hirschsprung’s disease tissues reveals lack of neuronal differentiation in the aganglionic colon segment

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.07.01.662516

N/A

0DataRank · unranked

0 citations

Xiaomeng Huang, Yi Qiao, Andrew Farrell, Lija Mammen, Amy Lovichik +7 more

Gábor Marth

Indexed papers

Top data-sharing exemplar

Papers