Eric Banks
Impact in
- Genetics top 0.01%
- Genomics and Rare Diseases
- Genetic Associations and Epidemiology
- Genetic diversity and population structure
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic Mapping and Diversity in Plants and Animals
- Cancer Research top 0.1%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 46
- Genomics and Rare Diseases 33
- Genomic variations and chromosomal abnormalities 18
- Genetic Associations and Epidemiology 18
- Genetics and Neurodevelopmental Disorders 5
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- Genomics and Phylogenetic Studies 12
- Genomics and Chromatin Dynamics 4
- RNA modifications and cancer 4
- Co-authors
- Mark A. DePristo (5 shared papers)Robert E. Handsaker (2 shared papers)Gonçalo R. Abecasis (2 shared papers)Gábor Marth (2 shared papers)Cornelis A. Albers (1 shared paper)Richard M. Durbin (1 shared paper)Gerton A. Lunter (1 shared paper)Stephen T. Sherry (1 shared paper)
- Journals
- Nature (15 papers)Nature Communications (7 papers)Nature Genetics (5 papers)Bioinformatics (3 papers)Genome biology (2 papers)
- Partner nations
- United StatesUnited KingdomFinland
In The Last Decade
Eric Banks
71 papers receiving 77.3k citations
Eric Banks's Hit Papers
Peers
Comparison fields: 5 of 214
- Genetics 34.6k
- Cancer Research 7.2k
- Molecular Biology 31.8k
- Aging 325
- Genetics 1.8k
Countries citing papers authored by Eric Banks
This map shows the geographic impact of Eric Banks'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 Eric Banks with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eric Banks more than expected).
Fields of papers citing papers by Eric Banks
This network shows the impact of papers produced by Eric Banks. 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 Eric Banks. The network helps show where Eric Banks may publish in the future.
Co-authors
The 25 scholars most cited alongside Eric Banks, 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 72 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A global reference for human genetic variation Hit paper breakdown → | 2015 | 12573 |
| 2 | The variant call format and VCFtools Hit paper breakdown → | 2011 | 11412 |
| 3 | A framework for variation discovery and genotyping using next-generation DNA sequencing data Hit paper breakdown → | 2011 | 8747 |
| 4 | Analysis of protein-coding genetic variation in 60,706 humans Hit paper breakdown → | 2016 | 7751 |
| 5 | The mutational constraint spectrum quantified from variation in 141,456 humans Hit paper breakdown → | 2020 | 6616 |
| 6 | A map of human genome variation from population-scale sequencing Hit paper breakdown → | 2010 | 6317 |
| 7 | An integrated map of genetic variation from 1,092 human genomes Hit paper breakdown → | 2012 | 6211 |
| 8 | From FastQ Data to High‐Confidence Variant Calls: The Genome Analysis Toolkit Best Practices Pipeline Hit paper breakdown → | 2013 | 5095 |
| 9 | Patterns and rates of exonic de novo mutations in autism spectrum disorders Hit paper breakdown → | 2012 | 1378 |
| 10 | De novo mutations in schizophrenia implicate synaptic networks Hit paper breakdown → | 2014 | 1284 |
| 11 | A polygenic burden of rare disruptive mutations in schizophrenia Hit paper breakdown → | 2014 | 1092 |
| 12 | A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes Hit paper breakdown → | 2012 | 923 |
| 13 | The genetic architecture of type 2 diabetes Hit paper breakdown → | 2016 | 839 |
| 14 | A genomic mutational constraint map using variation in 76,156 human genomes Hit paper breakdown → | 2023 | 736 |
| 15 | A structural variation reference for medical and population genetics Hit paper breakdown → | 2020 | 636 |
| 16 | Exome Sequencing, ANGPTL3 Mutations, and Familial Combined Hypolipidemia Hit paper breakdown → | 2010 | 621 |
| 17 | A global reference for human genetic variation Hit paper breakdown → | 2015 | 476 |
| 18 | Demographic history and rare allele sharing among human populations Hit paper breakdown → | 2011 | 475 |
| 19 | 2012 | 461 | |
| 20 | 2012 | 425 |
About Eric Banks
Eric Banks is a scholar working on Genetics, Molecular Biology, Cancer Research, Information Systems and Management and Cognitive Neuroscience, having authored 72 papers that have together received 78.4k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (33 papers), Genomic variations and chromosomal abnormalities (18 papers), Genetic Associations and Epidemiology (18 papers), Genomics and Phylogenetic Studies (12 papers), Cancer Genomics and Diagnostics (6 papers), Genetics and Neurodevelopmental Disorders (5 papers), Genomics and Chromatin Dynamics (4 papers) and RNA modifications and cancer (4 papers). The work is most often cited by research in Genetics (34.6k citations), Cancer Research (7.2k citations), Molecular Biology (31.8k citations), Aging (325 citations) and Genetics (1.8k citations). Eric Banks has collaborated with scholars based in United States, United Kingdom and Finland. Frequent co-authors include Mark A. DePristo, Robert E. Handsaker, Gonçalo R. Abecasis, Gábor Marth, Cornelis A. Albers, Richard M. Durbin, Gerton A. Lunter, Stephen T. Sherry, Petr Danecek and Gil McVean. Their work appears in journals such as Nature, Nature Communications, Nature Genetics, Bioinformatics and Genome biology.
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.