# Margaret A. Pericak‐Vance

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/margaret-a-pericak-vance/

## Facts

| Field | Value |
| --- | --- |
| Citations | 78,045 |
| Field | Genetic Associations and Epidemiology |
| h-index | 111 |
| i10-index | 387 |
| Last Known Institution | University of Miami |
| OpenAlex ID | https://openalex.org/A5069324665 |
| ORCID iD | https://orcid.org/0000-0001-7283-8804 |
| Works | 915 |

## Researcher papers

Showing 12 of 13.

- [Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease](https://scholariq.org/papers/cloning-of-a-gene-bearing-missense-mutations-in-early-onset-familial-alzheimer-s/)
- [Mutations in the <i>FUS/TLS</i> Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis](https://scholariq.org/papers/mutations-in-the-i-fus-tls-i-gene-on-chromosome-16-cause-familial-amyotrophic/)
- [Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism](https://scholariq.org/papers/large-scale-exome-sequencing-study-implicates-both-developmental-and-functional/)
- [Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia](https://scholariq.org/papers/mutations-in-ubqln2-cause-dominant-x-linked-juvenile-and-adult-onset-als-and-als/)
- [Seven new loci associated with age-related macular degeneration](https://scholariq.org/papers/seven-new-loci-associated-with-age-related-macular-degeneration/)
- [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/)
- [Genetic variants near <i>TIMP3</i> and high-density lipoprotein–associated loci influence susceptibility to age-related macular degeneration](https://scholariq.org/papers/genetic-variants-near-i-timp3-i-and-high-density-lipoprotein-associated-loci/)
- [Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries](https://scholariq.org/papers/genome-wide-meta-analysis-identifies-127-open-angle-glaucoma-loci-with/)
- [Exceptionally low likelihood of Alzheimer’s dementia in APOE2 homozygotes from a 5,000-person neuropathological study](https://scholariq.org/papers/exceptionally-low-likelihood-of-alzheimer-s-dementia-in-apoe2-homozygotes-from-a/)
- [Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma](https://scholariq.org/papers/genome-wide-association-analysis-identifies-txnrd2-atxn2-and-foxc1-as/)
- [Locus for severity implicates CNS resilience in progression of multiple sclerosis](https://scholariq.org/papers/locus-for-severity-implicates-cns-resilience-in-progression-of-multiple/)
- [Age-Related Maculopathy: A Genomewide Scan with Continued Evidence of Susceptibility Loci within the 1q31, 10q26, and 17q25 Regions](https://scholariq.org/papers/age-related-maculopathy-a-genomewide-scan-with-continued-evidence-of/)

## Researcher topics

- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Alzheimer's disease research and treatments](https://scholariq.org/topics/alzheimer-s-disease-research-and-treatments/)
- [Retinal Diseases and Treatments](https://scholariq.org/topics/retinal-diseases-and-treatments/)
- [Bioinformatics and Genomic Networks](https://scholariq.org/topics/bioinformatics-and-genomic-networks/)
- [Dementia and Cognitive Impairment Research](https://scholariq.org/topics/dementia-and-cognitive-impairment-research/)

## Researcher university

- [University of Miami](https://scholariq.org/institutions/university-of-miami/)

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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.
