Nele Cosemans

3PUBLICATIONS
1CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Cell and nuclear divisionGene expression (incl. microarray and other genome-wide approaches)
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Publications (3)

|Mar 08, 2021
8p21.3 deletions are rare causes of non-syndromic autism spectrum disorder.

Nele Cosemans, Jarymke Maljaars, Annick Vogels

|Jan 15, 2020
The clinical relevance of intragenic NRXN1 deletions.

Nele Cosemans, Laura Vandenhove, Annick Vogels

|May 01, 2018
Noise-robust assessment of SNP array based CNV calls through local noise estimation of log R ratios.

Nele Cosemans, Peter Claes, Nathalie Brison

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Frequent Collaborators

1 joint publications

Hilde Peeters