Wolfram Demaerel
Leuven, VLG, Belgium
Last Updated: 09/26/2026
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Found 8 publications
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion.
Journal: Molecular psychiatry
Published: June 05, 2019
Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins.
Journal: Human molecular genetics
Published: April 10, 2019
Pathogenic variants in CDC45 on the remaining allele in patients with a chromosome 22q11.2 deletion result in a novel autosomal recessive condition.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: January 31, 2019
The 22q11 low copy repeats are characterized by unprecedented size and structural variability.
Journal: Genome research
Published: January 27, 2019
Retraction Notice to: Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic Rearrangements.
Journal: American journal of human genetics
Published: September 08, 2018
Deletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2.
Journal: Human molecular genetics
Published: October 12, 2017
Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic Rearrangements.
Journal: American journal of human genetics
Published: February 22, 2017
Reciprocal 22q11.2 Deletion and Duplication in Siblings with Karyotypically Normal Parents.
Journal: Cytogenetic and genome research
Published: January 07, 2016
Showing 1-8 of 8
Last Updated: 09/26/2026