Merel O Mol

18PUBLICATIONS
349CO-AUTHORS
NeurogeneticsLexicography and semanticsCell and nuclear divisionEpigenetics (incl. genome methylation and epigenomics)Gene mapping
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Publications (18)

|Mar 13, 2026
A repeat expansion in GOLGA8A is a major risk factor for atypical frontotemporal lobar degeneration with ubiquitin-positive inclusions.

Wouter De Coster, Marleen Van den Broeck, Matt Baker

|Mar 06, 2026
Transcriptomic signature of frontotemporal lobar degeneration with TDP-43 type C pathology.

Ana Rajicic, Merel O Mol, Shamiram Melhem

|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 06, 2025
Methylome analysis of FTLD patients with TDP-43 pathology identifies epigenetic signatures specific to pathological subtypes.

Cristina T Vicente, Tejasvi Niranjan, Elise Coopman

|Apr 25, 2025
Deciphering distinct genetic risk factors for FTLD-TDP pathological subtypes via whole-genome sequencing.

Cyril Pottier, Fahri Küçükali, Matt Baker

|Oct 04, 2024
Biallelic and monoallelic variants in EFEMP1 can cause a severe and distinct subtype of heritable connective tissue disorder.

M O Mol, T J van Ham, N Bannink

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Frequent Collaborators

7 joint publications

Harro Seelaar

5 joint publications

Fahri Küçükali

5 joint publications

Carlos Cruchaga

4 joint publications

Rosa Rademakers