Alicia R. Martin
Broad Institute
Affiliation Broad Institute Top Publications A global reference for human genetic variation (2015) – 20,527 citations Clinical use of current polygenic risk scores may exacerbate health disparities (2019) – 3,101 citations Mapping genomic loci implicates genes and synaptic biology in schizophrenia (2022) – 2,921 citations Identification of common genetic risk variants for autism spectrum disorder ... <a title="Alicia R. Martin" class="read-more" href="https://journalsworld.com/researchers/alicia-r-martin/" aria-label="Read more about Alicia R. Martin">Read more</a>
Read biography ↓Biography, research & contributions
Affiliation
Broad Institute
Top Publications
- A global reference for human genetic variation (2015) - 20,527 citations
- Clinical use of current polygenic risk scores may exacerbate health disparities (2019) - 3,101 citations
- Mapping genomic loci implicates genes and synaptic biology in schizophrenia (2022) - 2,921 citations
- Identification of common genetic risk variants for autism spectrum disorder (2019) - 2,739 citations
- Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism (2020) - 2,550 citations
At a glance
- Full name
- Alicia R. Martin
- ORCID
- 0000-0003-0241-3522
- OpenAlex ID
- https://openalex.org/A5055040294
Research interests
- Genetic Associations and Epidemiology, Forensic and Genetic Research, Race, Genetics, and Society, Genetic Mapping and Diversity in Plants and Animals, Genetic and phenotypic traits in livestock
Research topics
Education
Not yet documented in this profile.
Selected research & further reading
A curated reading list, not a ranking by citation count. References use DOI metadata, matching public scholarly records or authoritative lecture sources.
See the source-linked reading and original works in the research guide above.
Citation & publication trends
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Source: OpenAlex · Retrieved 2026-10-07. Metrics are database-specific and are not a scientific ranking.
Most-cited linked publications
Publications matched across ORCID and OpenAlex. Citation counts are source-specific.
- A global reference for human genetic variation ↗2015 · Nature20,527OpenAlex citations
- Clinical use of current polygenic risk scores may exacerbate health disparities ↗2019 · Nature Genetics3,101OpenAlex citations
- 2,921OpenAlex citations
- Identification of common genetic risk variants for autism spectrum disorder ↗2019 · Nature Genetics2,739OpenAlex citations
- 2,550OpenAlex citations
Recent linked publications
Publications matched across ORCID and OpenAlex. Citation counts are source-specific.
- A global reference for human genetic variation ↗2015 · Nature
- Clinical use of current polygenic risk scores may exacerbate health disparities ↗2019 · Nature Genetics
- Identification of common genetic risk variants for autism spectrum disorder ↗2019 · Nature Genetics
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Institutions
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Awards & honors
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Career timeline
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Co-authors
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Education & career institution links
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Sign in to claim this profileSources & data information
Editorial review: 2026-10-07 · Last data update: 2026-10-07 23:38:33
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