# Eric Banks

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/eric-banks/

## Facts

| Field | Value |
| --- | --- |
| Citations | 174,240 |
| Field | Genomics and Rare Diseases |
| h-index | 59 |
| i10-index | 86 |
| Last Known Institution | Broad Institute |
| OpenAlex ID | https://openalex.org/A5029475781 |
| ORCID iD | https://orcid.org/0000-0001-9615-2372 |
| Works | 123 |

## Researcher papers

- [The mutational constraint spectrum quantified from variation in 141,456 humans](https://scholariq.org/papers/the-mutational-constraint-spectrum-quantified-from-variation-in-141-456-humans/)
- [An integrated map of genetic variation from 1,092 human genomes](https://scholariq.org/papers/an-integrated-map-of-genetic-variation-from-1-092-human-genomes/)
- [A map of human genome variation from population-scale sequencing](https://scholariq.org/papers/a-map-of-human-genome-variation-from-population-scale-sequencing-2/)
- [A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes](https://scholariq.org/papers/a-systematic-survey-of-loss-of-function-variants-in-human-protein-coding-genes/)
- [Rare coding variation provides insight into the genetic architecture and phenotypic context of autism](https://scholariq.org/papers/rare-coding-variation-provides-insight-into-the-genetic-architecture-and/)
- [Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel](https://scholariq.org/papers/integrating-sequence-and-array-data-to-create-an-improved-1000-genomes-project/)
- [Effect of predicted protein-truncating genetic variants on the human transcriptome](https://scholariq.org/papers/effect-of-predicted-protein-truncating-genetic-variants-on-the-human/)

## Researcher topics

- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Genomics and Phylogenetic Studies](https://scholariq.org/topics/genomics-and-phylogenetic-studies/)
- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Cancer Genomics and Diagnostics](https://scholariq.org/topics/cancer-genomics-and-diagnostics/)

## Researcher university

- [Broad Institute](https://scholariq.org/institutions/broad-institute/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.