Laura L. Kaat-Donker

Dr. Molewaterplein 40
Rotterdam, ZH 3015GD, Netherlands

Last Updated: 09/26/2026

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Found 41 publications

Impact of awareness of genetic status on cognitive, behavioral, and neuropsychiatric outcomes in genetic frontotemporal dementia.

Impact of awareness of genetic status on cognitive, behavioral, and neuropsychiatric outcomes in genetic frontotemporal dementia.

Journal: Journal of neurology

Published: February 18, 2026

Disclosure of onset-predictive biomarker results to research participants at risk of genetic frontotemporal dementia: a European perspective.

Disclosure of onset-predictive biomarker results to research participants at risk of genetic frontotemporal dementia: a European perspective.

Journal: Alzheimer's research & therapy

Published: September 24, 2025

HiFi long-read RNA sequencing enhances clinical diagnostics in rare disorders.

HiFi long-read RNA sequencing enhances clinical diagnostics in rare disorders.

Journal: European journal of human genetics : EJHG

Published: July 04, 2025

Missense variants in TUBA4A cause myo-tubulinopathies.

Missense variants in TUBA4A cause myo-tubulinopathies.

Journal: Brain : a journal of neurology

Published: June 26, 2025

Reasons for and against presymptomatic genetic testing in frontotemporal dementia: a qualitative study.

Reasons for and against presymptomatic genetic testing in frontotemporal dementia: a qualitative study.

Journal: Human genetics

Published: June 20, 2025

Nanopore long-read sequencing for the critically ill facilitates ultrarapid diagnostics and urgent clinical decision making.

Nanopore long-read sequencing for the critically ill facilitates ultrarapid diagnostics and urgent clinical decision making.

Journal: European journal of human genetics : EJHG

Published: March 24, 2025

Routine RNA-based analysis of potential splicing variants facilitates genomic diagnostics and reveals limitations of in silico prediction tools.

Routine RNA-based analysis of potential splicing variants facilitates genomic diagnostics and reveals limitations of in silico prediction tools.

Journal: HGG advances

Published: February 27, 2025

Clinical utility of DNA-methylation signatures in routine diagnostics for neurodevelopmental disorders.

Clinical utility of DNA-methylation signatures in routine diagnostics for neurodevelopmental disorders.

Journal: European journal of human genetics : EJHG

Published: February 13, 2025

Ethics of disclosure of onset-predictive biomarker test results for genetic frontotemporal dementia in the research context.

Ethics of disclosure of onset-predictive biomarker test results for genetic frontotemporal dementia in the research context.

Journal: Alzheimer's & dementia (Amsterdam, Netherlands)

Published: December 19, 2024

Assessing the Big Five personality traits in presymptomatic and symptomatic C9orf72-related frontotemporal dementia using the Dutch Personality Inventory for DSM-5 (PID-5-NL).

Assessing the Big Five personality traits in presymptomatic and symptomatic C9orf72-related frontotemporal dementia using the Dutch Personality Inventory for DSM-5 (PID-5-NL).

Journal: Journal of the neurological sciences

Published: November 25, 2024

"It seems enormously valuable to me." Perspectives of Dutch (potential) carriers of genetic FTD on onset-predictive biomarker testing.

"It seems enormously valuable to me." Perspectives of Dutch (potential) carriers of genetic FTD on onset-predictive biomarker testing.

Journal: Alzheimer's research & therapy

Published: October 28, 2024

UNC13A Polymorphism Influences Survival in Patients with Frontotemporal Dementia.

UNC13A Polymorphism Influences Survival in Patients with Frontotemporal Dementia.

Journal: Annals of neurology

Published: October 16, 2024

Showing 1-12 of 41

Last Updated: 09/26/2026