Gábor Marth
Impact in
- Genetics top 0.01%
- Genetic diversity and population structure
- Genetic Associations and Epidemiology
- Genetic Mapping and Diversity in Plants and Animals
- Genomics and Rare Diseases
- Genetic and phenotypic traits in livestock
- Molecular Biology top 0.02%
- Genomics and Phylogenetic Studies
- RNA modifications and cancer
Papers in
- Genetics 44
- Genomics and Rare Diseases 29
- Genomic variations and chromosomal abnormalities 10
- Genetic Associations and Epidemiology 10
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- Genomics and Phylogenetic Studies 27
- RNA and protein synthesis mechanisms 11
- Co-authors
- Richard M. Durbin (3 shared papers)Gonçalo R. Abecasis (2 shared papers)Heng Li (1 shared paper)Tim J. Fennell (1 shared paper)Jue Ruan (1 shared paper)Nils Homer (1 shared paper)Alec Wysoker (1 shared paper)Stephen T. Sherry (3 shared papers)
- Journals
- Genetics in Medicine (11 papers)The American Journal of Human Genetics (10 papers)Bioinformatics (7 papers)BMC Genomics (7 papers)Nature (7 papers)
- Partner nations
- United StatesUnited KingdomChina
In The Last Decade
Gábor Marth
126 papers receiving 89.5k citations
Gábor Marth's Hit Papers
Peers
Comparison fields: 5 of 216
- Genetics 31.5k
- Molecular Biology 41.0k
- Cancer Research 7.7k
- Plant Science 14.3k
- Aging 563
Countries citing papers authored by Gábor Marth
This map shows the geographic impact of Gábor Marth's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Gábor Marth with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gábor Marth more than expected).
Fields of papers citing papers by Gábor Marth
This network shows the impact of papers produced by Gábor Marth. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Gábor Marth. The network helps show where Gábor Marth may publish in the future.
Co-authors
The 25 scholars most cited alongside Gábor Marth, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 130 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The Sequence Alignment/Map format and SAMtools Hit paper breakdown → | 2009 | 44810 |
| 2 | A global reference for human genetic variation Hit paper breakdown → | 2015 | 12574 |
| 3 | The variant call format and VCFtools Hit paper breakdown → | 2011 | 11414 |
| 4 | An integrated map of genetic variation from 1,092 human genomes Hit paper breakdown → | 2012 | 6211 |
| 5 | A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms Hit paper breakdown → | 2001 | 2299 |
| 6 | An integrated map of structural variation in 2,504 human genomes Hit paper breakdown → | 2015 | 1624 |
| 7 | ART: a next-generation sequencing read simulator Hit paper breakdown → | 2011 | 1012 |
| 8 | Mapping copy number variation by population-scale genome sequencing Hit paper breakdown → | 2011 | 854 |
| 9 | BamTools: a C++ API and toolkit for analyzing and managing BAM files Hit paper breakdown → | 2011 | 714 |
| 10 | Multi-platform discovery of haplotype-resolved structural variation in human genomes Hit paper breakdown → | 2019 | 563 |
| 11 | A global reference for human genetic variation Hit paper breakdown → | 2015 | 476 |
| 12 | Demographic history and rare allele sharing among human populations Hit paper breakdown → | 2011 | 475 |
| 13 | 1999 | 458 | |
| 14 | 2010 | 416 | |
| 15 | 2015 | 408 | |
| 16 | MYC Drives Temporal Evolution of Small Cell Lung Cancer Subtypes by Reprogramming Neuroendocrine Fate Hit paper breakdown → | 2020 | 369 |
| 17 | 2008 | 322 | |
| 18 | 2014 | 321 | |
| 19 | 2013 | 289 | |
| 20 | A human breast cancer-derived xenograft and organoid platform for drug discovery and precision oncology Hit paper breakdown → | 2022 | 285 |
About Gábor Marth
Gábor Marth is a scholar working on Genetics, Molecular Biology, Cancer Research, Parasitology and Genetics, having authored 130 papers that have together received 90.7k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (29 papers), Genomics and Phylogenetic Studies (27 papers), Cancer Genomics and Diagnostics (12 papers), RNA and protein synthesis mechanisms (11 papers), Genomic variations and chromosomal abnormalities (10 papers), Genetic Associations and Epidemiology (10 papers), Chromosomal and Genetic Variations (7 papers) and Genetic factors in colorectal cancer (6 papers). The work is most often cited by research in Genetics (31.5k citations), Molecular Biology (41.0k citations), Cancer Research (7.7k citations), Plant Science (14.3k citations) and Aging (563 citations). Gábor Marth has collaborated with scholars based in United States, United Kingdom and China. Frequent co-authors include Richard M. Durbin, Gonçalo R. Abecasis, Heng Li, Tim J. Fennell, Jue Ruan, Nils Homer, Alec Wysoker, Stephen T. Sherry, Eric Banks and Petr Danecek. Their work appears in journals such as Genetics in Medicine, The American Journal of Human Genetics, Bioinformatics, BMC Genomics and Nature.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.