Laura Donker Kaat

7PUBLICATIONS

129CO-AUTHORS

Testing, assessment and psychometricsNeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Cell and nuclear divisionNeurology and neuromuscular diseases

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Publications (7)

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|Jun 12, 2026

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

|Feb 16, 2026

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

Charlotte H Graafland, Harro Seelaar, Jessica L Panman

|Dec 13, 2025

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

Charlotte H Graafland, Eline M Bunnik, Barbara Borroni

|Oct 20, 2025

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

Daphne J Smits, Federico Ferraro, Mark Drost

|Jul 16, 2025

Missense variants in TUBA4A cause myo-tubulinopathies.

Mridul Johari, Chiara Folland, Yoshihiko Saito

|Mar 08, 2025

Copy Number Variation and Haplotype Analysis of 17q21.31 Reveals Increased Risk Associated with Progressive Supranuclear Palsy and Gene Expression Changes in Neuronal Cells.

Hui Wang, Timothy S Chang, Beth A Dombroski

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Frequent Collaborators

John C van Swieten

Harro Seelaar

Julie F H De Houwer

Elise G P Dopper

Ana Rajicic

Eline M Bunnik

Martina Wilke

Charlotte H Graafland

2 joint publications

Lize C Jiskoot

1 joint publications

Olaiya A Aro

Frequent Collaborators

John C van Swieten

Harro Seelaar

Julie F H De Houwer

Elise G P Dopper