# Bryan J. Traynor

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/bryan-j-traynor/

## Facts

| Field | Value |
| --- | --- |
| Citations | 40,757 |
| Field | Amyotrophic Lateral Sclerosis Research |
| h-index | 92 |
| i10-index | 221 |
| Last Known Institution | National Institutes of Health |
| OpenAlex ID | https://openalex.org/A5035072440 |
| ORCID iD | https://orcid.org/0000-0003-0527-2446 |
| Works | 348 |

## Researcher papers

Showing 12 of 16.

- [A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD](https://scholariq.org/papers/a-hexanucleotide-repeat-expansion-in-c9orf72-is-the-cause-of-chromosome-9p21/)
- [State of play in amyotrophic lateral sclerosis genetics](https://scholariq.org/papers/state-of-play-in-amyotrophic-lateral-sclerosis-genetics/)
- [Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS](https://scholariq.org/papers/mutations-in-prion-like-domains-in-hnrnpa2b1-and-hnrnpa1-cause-multisystem/)
- [Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study](https://scholariq.org/papers/frequency-of-the-c9orf72-hexanucleotide-repeat-expansion-in-patients-with/)
- [Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS](https://scholariq.org/papers/exome-sequencing-reveals-vcp-mutations-as-a-cause-of-familial-als/)
- [Global Epidemiology of Amyotrophic Lateral Sclerosis: A Systematic Review of the Published Literature](https://scholariq.org/papers/global-epidemiology-of-amyotrophic-lateral-sclerosis-a-systematic-review-of-the/)
- [Controversies and priorities in amyotrophic lateral sclerosis](https://scholariq.org/papers/controversies-and-priorities-in-amyotrophic-lateral-sclerosis/)
- [Projected increase in amyotrophic lateral sclerosis from 2015 to 2040](https://scholariq.org/papers/projected-increase-in-amyotrophic-lateral-sclerosis-from-2015-to-2040/)
- [Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis](https://scholariq.org/papers/mutations-in-the-matrin-3-gene-cause-familial-amyotrophic-lateral-sclerosis/)
- [Descriptive epidemiology of amyotrophic lateral sclerosis: new evidence and unsolved issues](https://scholariq.org/papers/descriptive-epidemiology-of-amyotrophic-lateral-sclerosis-new-evidence-and/)
- [Poly(GP) proteins are a useful pharmacodynamic marker for <i>C9ORF72</i> -associated amyotrophic lateral sclerosis](https://scholariq.org/papers/poly-gp-proteins-are-a-useful-pharmacodynamic-marker-for-i-c9orf72-i-associated/)
- [A Genome-Wide Association Study of Myasthenia Gravis](https://scholariq.org/papers/a-genome-wide-association-study-of-myasthenia-gravis/)

## Researcher topics

- [Amyotrophic Lateral Sclerosis Research](https://scholariq.org/topics/amyotrophic-lateral-sclerosis-research/)
- [Neurogenetic and Muscular Disorders Research](https://scholariq.org/topics/neurogenetic-and-muscular-disorders-research/)
- [Neurological diseases and metabolism](https://scholariq.org/topics/neurological-diseases-and-metabolism/)
- [Parkinson's Disease Mechanisms and Treatments](https://scholariq.org/topics/parkinson-s-disease-mechanisms-and-treatments/)
- [Genetic Neurodegenerative Diseases](https://scholariq.org/topics/genetic-neurodegenerative-diseases/)

## Researcher university

- [National Institutes of Health](https://scholariq.org/institutions/national-institutes-of-health/)

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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.