# Frank Baas

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/frank-baas/

## Facts

| Field | Value |
| --- | --- |
| Citations | 35,633 |
| Field | Hereditary Neurological Disorders |
| h-index | 98 |
| i10-index | 330 |
| Last Known Institution | Leiden University Medical Center |
| OpenAlex ID | https://openalex.org/A5032625076 |
| ORCID iD | https://orcid.org/0000-0003-3912-5428 |
| Works | 551 |

## Researcher papers

- [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/)
- [TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13A](https://scholariq.org/papers/tdp-43-loss-and-als-risk-snps-drive-mis-splicing-and-depletion-of-unc13a/)
- [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/)
- [Postmortem Cortex Samples Identify Distinct Molecular Subtypes of ALS: Retrotransposon Activation, Oxidative Stress, and Activated Glia](https://scholariq.org/papers/postmortem-cortex-samples-identify-distinct-molecular-subtypes-of-als/)
- [NEK1 variants confer susceptibility to amyotrophic lateral sclerosis](https://scholariq.org/papers/nek1-variants-confer-susceptibility-to-amyotrophic-lateral-sclerosis/)
- [CLP1 Founder Mutation Links tRNA Splicing and Maturation to Cerebellar Development and Neurodegeneration](https://scholariq.org/papers/clp1-founder-mutation-links-trna-splicing-and-maturation-to-cerebellar/)
- [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/)
- [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/)

## Researcher topics

- [Hereditary Neurological Disorders](https://scholariq.org/topics/hereditary-neurological-disorders/)
- [Neurological diseases and metabolism](https://scholariq.org/topics/neurological-diseases-and-metabolism/)
- [Amyotrophic Lateral Sclerosis Research](https://scholariq.org/topics/amyotrophic-lateral-sclerosis-research/)
- [RNA modifications and cancer](https://scholariq.org/topics/rna-modifications-and-cancer/)
- [Genetic Neurodegenerative Diseases](https://scholariq.org/topics/genetic-neurodegenerative-diseases/)

## Researcher university

- [Leiden University Medical Center](https://scholariq.org/institutions/leiden-university-medical-center/)

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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.