Merel O Mol

19PUBLICATIONS
352CO-AUTHORS
Neurology and neuromuscular diseasesNeurogeneticsLexicography and semanticsCell and nuclear divisionEpigenetics (incl. genome methylation and epigenomics)
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Publications (19)

|Oct 01, 2026
Targeted single-nucleus sequencing of 39,800 neurons reveals extensive low-frequency somatic variants.

|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

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Frequent Collaborators

8 joint publications

Harro Seelaar

5 joint publications

Rosa Rademakers

5 joint publications

Melissa E Murray

5 joint publications

Charles L White