Kristof Van Schil

4PUBLICATIONS
57CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Genetic immunologyGene expression (incl. microarray and other genome-wide approaches)
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Publications (4)

|May 23, 2025
Biallelic loss-of-function variants in ZNF142 are associated with a robust DNA methylation signature affecting a limited number of genomic loci.

Mathis Hildonen, Andrea Ciolfi, Marco Ferilli

|Mar 07, 2025
Uncovering the genetic architecture of inherited retinal disease in a consanguineous Iranian cohort.

Lieselot Vincke, Kristof Van Schil, Hamid Ahmadieh

|May 26, 2022
Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder.

Maria B Christensen, Amanda M Levy, Nazanin A Mohammadi

|Sep 09, 2016
arrEYE: a customized platform for high-resolution copy number analysis of coding and noncoding regions of known and candidate retinal dystrophy genes and retinal noncoding RNAs.

Caroline Van Cauwenbergh, Kristof Van Schil, Robrecht Cannoodt

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