Frank Baas

Leiden University — Netherlands

Neuroscience · Life Sciences

99h-index36.4kcitations555works4.12yr avg
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Research Topics

Hereditary Neurological Disorders(74), Neurological diseases and metabolism(46), RNA modifications and cancer(43), Amyotrophic Lateral Sclerosis Research(41), RNA Research and Splicing(37)

Publications549 total

Search for Additional Pathogenic Variants to Explain Variation in <i>PMP22</i> -Related Neuropathies
Neurology Genetics·2025Open Access
TDP-43 loss induces cryptic polyadenylation in ALS/FTD
Nature Neuroscience·2025· 10 citedOpen Access
SpliPath enhances disease gene discovery in case-control analyses of rare splice-altering genetic variants
Cell Reports Methods·2025Open Access
The Acute Effects of Morning Bright Light on the Human White Adipose Tissue Transcriptome: Exploratory Post Hoc Analysis
Clocks & Sleep·2025Open Access
Unusual Causes of β Thalassemia Trait: Discovery of another Three Novel <i>SUPT5H</i> Variants
Hemoglobin·2025· 2 citedOpen Access
Neurovascular Decoupling Is Associated With Lobar Intracerebral Hemorrhages and White Matter Hyperintensities
Journal of the American Heart Association·2025· 4 citedOpen Access
Innate Immune Cell Functions Contribute to Spontaneous HIV Control
Current HIV/AIDS Reports·2024· 3 citedOpen Access
Jean Marie Baptiste Vianney de Jong (1937–2024)
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration·2024
Loss-of-Function Variants in SUPT5H as Modifying Factors in Beta-Thalassemia
International Journal of Molecular Sciences·2024· 6 citedOpen Access
Rare variant analyses validate known ALS genes in a multi-ethnic population and identifies ANTXR2 as a candidate in PLS
BMC Genomics·2024· 5 citedOpen Access
Author Correction: TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13A
Nature·2024· 3 citedOpen Access
Moderate–severe beta‐thalassemia intermedia phenotype caused by sextuplicated alpha‐globin gene allele in two beta‐thalassemia carriers
American Journal of Hematology·2024· 2 citedOpen Access
<i>PMP22</i> duplication dysregulates lipid homeostasis and plasma membrane organization in developing human Schwann cells
Brain·2024· 18 citedOpen Access
Bi-allelic NIT1 variants cause a brain small vessel disease characterized by movement disorders, massively dilated perivascular spaces, and intracerebral hemorrhage
Genetics in Medicine·2024· 5 citedOpen Access
Corrigendum: Ldlr-/-.Leiden mice develop neurodegeneration, age-dependent astrogliosis and obesity-induced changes in microglia immunophenotype which are partly reversed by complement component 5 neutralizing antibody
Frontiers in Cellular Neuroscience·2023Open Access
Phenotypic Diversity in GNAO1 Patients: A Comprehensive Overview of Variants and Phenotypes
Human Mutation·2023· 13 citedOpen Access
Editorial: Complement in nervous system disease
Frontiers in Cellular Neuroscience·2023· 2 citedOpen Access
CRB1 is required for recycling by RAB11A+ vesicles in human retinal organoids
Stem Cell Reports·2023· 8 citedOpen Access
Ldlr-/-.Leiden mice develop neurodegeneration, age-dependent astrogliosis and obesity-induced changes in microglia immunophenotype which are partly reversed by complement component 5 neutralizing antibody
Frontiers in Cellular Neuroscience·2023· 3 citedOpen Access
Minocycline for sporadic and hereditary cerebral amyloid angiopathy (BATMAN): study protocol for a placebo-controlled randomized double-blind trial
Trials·2023· 15 citedOpen Access
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Frequent Co-authors

Piet Borst(7), Bradley Smith(6), Ammar Al‐Chalabi(6), Jan H. Veldink(6), Christopher E. Shaw(6), Marcel Kool(6), Pamela J. Shaw(6), Peter C. Sapp(5), Simon Topp(5), Jack W. Miller(5), Vincenzo Silani(5), Nicola Ticozzi(5), John E. Landers(5), Robert H. Brown(5), Marcel de Haas(5), Rik J. Scheper(5), Marianne de Visser(5), Pieter A. Bolhuis(5), Linda J. Valentijn(5), Caroline Vance(5)