Laura D. Kaat

Rotterdam, ZH, Netherlands

Last Updated: 09/26/2026

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Found 15 publications

Neuronal Antibodies in Patients With Atypical Parkinsonism.

Neuronal Antibodies in Patients With Atypical Parkinsonism.

Journal: Neurology(R) neuroimmunology & neuroinflammation
Published: August 24, 2026

Missense variants in TUBA4A cause myo-tubulinopathies.

Missense variants in TUBA4A cause myo-tubulinopathies.

Journal: medRxiv : the preprint server for health sciences
Published: July 16, 2025

Targeted plasma proteomics uncover proteins associated with KIF5A-linked SPG10 and ALS spectrum disorders.

Targeted plasma proteomics uncover proteins associated with KIF5A-linked SPG10 and ALS spectrum disorders.

Journal: HGG advances
Published: April 25, 2025

Correction: Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy.

Correction: Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy.

Journal: Molecular neurodegeneration
Published: October 14, 2024

Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy.

Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy.

Journal: Molecular neurodegeneration
Published: January 29, 2024

Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear Palsy.

Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear Palsy.

Journal: medRxiv : the preprint server for health sciences
Published: January 18, 2024

Diagnostic utility and reporting recommendations for clinical DNA methylation episignature testing in genetically undiagnosed rare diseases.

Diagnostic utility and reporting recommendations for clinical DNA methylation episignature testing in genetically undiagnosed rare diseases.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: August 29, 2023

TRAPPC6B biallelic variants cause a neurodevelopmental disorder with TRAPP II and trafficking disruptions.

TRAPPC6B biallelic variants cause a neurodevelopmental disorder with TRAPP II and trafficking disruptions.

Journal: Brain : a journal of neurology
Published: April 18, 2023

Mapping the genetic landscape of early-onset Alzheimer's disease in a cohort of 36 families.

Mapping the genetic landscape of early-onset Alzheimer's disease in a cohort of 36 families.

Journal: Alzheimer's research & therapy
Published: March 04, 2022

Recruitment of trimeric eIF2 by phosphatase non-catalytic subunit PPP1R15B.

Recruitment of trimeric eIF2 by phosphatase non-catalytic subunit PPP1R15B.

Journal: Molecular cell
Published: February 01, 2022

Novel TUBA4A Variant Associated With Familial Frontotemporal Dementia.

Novel TUBA4A Variant Associated With Familial Frontotemporal Dementia.

Journal: Neurology. Genetics
Published: September 28, 2020

Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder.

Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: June 19, 2020
Showing 1-12 of 15

Last Updated: 09/26/2026