# Bradley Smith

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/bradley-smith/

## Facts

| Field | Value |
| --- | --- |
| Citations | 16,682 |
| Field | Amyotrophic Lateral Sclerosis Research |
| h-index | 52 |
| i10-index | 79 |
| OpenAlex ID | https://openalex.org/A5058523077 |
| ORCID iD | https://orcid.org/0000-0002-6980-2453 |
| Works | 117 |

## Researcher papers

- [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/)
- [Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways](https://scholariq.org/papers/exome-sequencing-in-amyotrophic-lateral-sclerosis-identifies-risk-genes-and/)
- [Genome-wide Analyses Identify KIF5A as a Novel ALS Gene](https://scholariq.org/papers/genome-wide-analyses-identify-kif5a-as-a-novel-als-gene/)
- [Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology](https://scholariq.org/papers/common-and-rare-variant-association-analyses-in-amyotrophic-lateral-sclerosis/)
- [Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS](https://scholariq.org/papers/exome-wide-rare-variant-analysis-identifies-tuba4a-mutations-associated-with/)
- [NEK1 variants confer susceptibility to amyotrophic lateral sclerosis](https://scholariq.org/papers/nek1-variants-confer-susceptibility-to-amyotrophic-lateral-sclerosis/)
- [Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis](https://scholariq.org/papers/mutations-in-the-vesicular-trafficking-protein-annexin-a11-are-associated-with/)
- [Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase](https://scholariq.org/papers/familial-amyotrophic-lateral-sclerosis-is-associated-with-a-mutation-in-d-amino/)
- [The C9ORF72 expansion mutation is a common cause of ALS+/−FTD in Europe and has a single founder](https://scholariq.org/papers/the-c9orf72-expansion-mutation-is-a-common-cause-of-als-ftd-in-europe-and-has-a/)
- [CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia](https://scholariq.org/papers/ccnf-mutations-in-amyotrophic-lateral-sclerosis-and-frontotemporal-dementia/)

## 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/)

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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.