# Steven A. McCarroll

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/steven-a-mccarroll/

## Facts

| Field | Value |
| --- | --- |
| Citations | 201,039 |
| Field | Genetic Associations and Epidemiology |
| h-index | 129 |
| i10-index | 256 |
| Last Known Institution | Broad Institute |
| OpenAlex ID | https://openalex.org/A5072347906 |
| ORCID iD | https://orcid.org/0000-0002-6954-8184 |
| Works | 401 |

## Researcher papers

Showing 12 of 13.

- [Clonal Hematopoiesis and Blood-Cancer Risk Inferred from Blood DNA Sequence](https://scholariq.org/papers/clonal-hematopoiesis-and-blood-cancer-risk-inferred-from-blood-dna-sequence/)
- [An integrated map of structural variation in 2,504 human genomes](https://scholariq.org/papers/an-integrated-map-of-structural-variation-in-2-504-human-genomes/)
- [Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs](https://scholariq.org/papers/genetic-relationship-between-five-psychiatric-disorders-estimated-from-genome/)
- [Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection](https://scholariq.org/papers/common-schizophrenia-alleles-are-enriched-in-mutation-intolerant-genes-and-in/)
- [Genome-wide association analysis identifies 13 new risk loci for schizophrenia](https://scholariq.org/papers/genome-wide-association-analysis-identifies-13-new-risk-loci-for-schizophrenia/)
- [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/)
- [Mapping copy number variation by population-scale genome sequencing](https://scholariq.org/papers/mapping-copy-number-variation-by-population-scale-genome-sequencing/)
- [Whole-genome sequence variation, population structure and demographic history of the Dutch population](https://scholariq.org/papers/whole-genome-sequence-variation-population-structure-and-demographic-history-of/)
- [A multimodal cell census and atlas of the mammalian primary motor cortex](https://scholariq.org/papers/a-multimodal-cell-census-and-atlas-of-the-mammalian-primary-motor-cortex/)
- [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/)
- [Genetic predisposition to mosaic Y chromosome loss in blood](https://scholariq.org/papers/genetic-predisposition-to-mosaic-y-chromosome-loss-in-blood/)
- [Copy number variation in schizophrenia in Sweden](https://scholariq.org/papers/copy-number-variation-in-schizophrenia-in-sweden/)

## Researcher topics

- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Single-cell and spatial transcriptomics](https://scholariq.org/topics/single-cell-and-spatial-transcriptomics/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)

## 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.