# James F. Gusella

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/james-f-gusella/

## Facts

| Field | Value |
| --- | --- |
| Citations | 74,278 |
| Field | Genetic Neurodegenerative Diseases |
| h-index | 132 |
| i10-index | 499 |
| Last Known Institution | Broad Institute |
| OpenAlex ID | https://openalex.org/A5044329623 |
| ORCID iD | https://orcid.org/0000-0003-0681-9263 |
| Works | 721 |

## Researcher papers

- [A polymorphic DNA marker genetically linked to Huntington's disease](https://scholariq.org/papers/a-polymorphic-dna-marker-genetically-linked-to-huntington-s-disease/)
- [Association between Microdeletion and Microduplication at 16p11.2 and Autism](https://scholariq.org/papers/association-between-microdeletion-and-microduplication-at-16p11-2-and-autism/)
- [Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders](https://scholariq.org/papers/microdeletion-duplication-at-15q13-2q13-3-among-individuals-with-features-of/)
- [Clinical Genetic Testing for Patients With Autism Spectrum Disorders](https://scholariq.org/papers/clinical-genetic-testing-for-patients-with-autism-spectrum-disorders/)
- [CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion](https://scholariq.org/papers/cag-repeat-expansion-in-huntington-disease-determines-age-at-onset-in-a-fully/)
- [Deletions of <i>NRXN1</i> (neurexin‐1) predispose to a wide spectrum of developmental disorders](https://scholariq.org/papers/deletions-of-i-nrxn1-i-neurexin-1-predispose-to-a-wide-spectrum-of-developmental/)
- [Human Chromosome 7: DNA Sequence and Biology](https://scholariq.org/papers/human-chromosome-7-dna-sequence-and-biology/)
- [Exonic Deletions in AUTS2 Cause a Syndromic Form of Intellectual Disability and Suggest a Critical Role for the C Terminus](https://scholariq.org/papers/exonic-deletions-in-auts2-cause-a-syndromic-form-of-intellectual-disability-and/)

## Researcher topics

- [Genetic Neurodegenerative Diseases](https://scholariq.org/topics/genetic-neurodegenerative-diseases/)
- [Mitochondrial Function and Pathology](https://scholariq.org/topics/mitochondrial-function-and-pathology/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Neurofibromatosis and Schwannoma Cases](https://scholariq.org/topics/neurofibromatosis-and-schwannoma-cases/)
- [Neurological disorders and treatments](https://scholariq.org/topics/neurological-disorders-and-treatments/)

## 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.