Brooke L. Latour
Nijmegen, GE 6525GA, Netherlands
Last Updated: 09/26/2026
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Found 10 publications
Evolutionary hotspots of structural variation drive inter-individual differences in the expression of fusion transcripts in the human brain.
Journal: Nucleic acids research
Published: February 26, 2025
Integrative transcriptomics and electrophysiological profiling of hiPSC-derived neurons identifies novel druggable pathways in Koolen-de Vries Syndrome.
Journal: Molecular psychiatry
Published: November 27, 2024
A microglia-containing cerebral organoid model to study early life immune challenges.
Journal: bioRxiv : the preprint server for biology
Published: June 03, 2024
A microglia-containing cerebral organoid model to study early life immune challenges.
Journal: Brain, behavior, and immunity
Published: May 28, 2024
Dysfunction of the ciliary ARMC9/TOGARAM1 protein module causes Joubert syndrome.
Journal: The Journal of clinical investigation
Published: July 08, 2019
Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish.
Journal: American journal of human genetics
Published: April 10, 2017
Cellular ciliary phenotyping indicates pathogenicity of novel variants in IFT140 and confirms a Mainzer-Saldino syndrome diagnosis.
Journal: Cilia
Published: April 03, 2017
An organelle-specific protein landscape identifies novel diseases and molecular mechanisms.
Journal: Nature communications
Published: February 15, 2016
De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations.
Journal: American journal of human genetics
Published: November 11, 2015
Showing 1-10 of 10
Last Updated: 09/26/2026