# Kym M. Boycott

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/kym-m-boycott/

## Facts

| Field | Value |
| --- | --- |
| Citations | 21,557 |
| Field | Genomics and Rare Diseases |
| h-index | 77 |
| i10-index | 253 |
| Last Known Institution | University of Ottawa |
| OpenAlex ID | https://openalex.org/A5065051535 |
| ORCID iD | https://orcid.org/0000-0003-4186-8052 |
| Works | 427 |

## Researcher papers

- [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/)
- [The Human Phenotype Ontology in 2017](https://scholariq.org/papers/the-human-phenotype-ontology-in-2017/)
- [International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases](https://scholariq.org/papers/international-cooperation-to-enable-the-diagnosis-of-all-rare-genetic-diseases/)

## Researcher topics

- [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/)
- [Genetic Neurodegenerative Diseases](https://scholariq.org/topics/genetic-neurodegenerative-diseases/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Mitochondrial Function and Pathology](https://scholariq.org/topics/mitochondrial-function-and-pathology/)

## Researcher university

- [University of Ottawa](https://scholariq.org/institutions/university-of-ottawa/)

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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.