Wolfram Demaerel

Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion

Isabelle Cleynen, Worrawat Engchuan, Matthew S. Hestand et al. · Molecular Psychiatry · 2020 · 132 citations · Full text

Psychiatry, Risk Prediction, Psychotic Disorder +8

The 22q11 low copy repeats are characterized by unprecedented size and structural variability

Wolfram Demaerel, Yulia Mostovoy, Feyza Yilmaz et al. · Genome Research · 2019 · 61 citations · Full text

Biology, Lcr Variation, Sequence Assembly +14

Reciprocal 22q11.2 Deletion and Duplication in Siblings with Karyotypically Normal Parents

Wolfram Demaerel, Majid Hosseinzadeh, Nayereh Nouri et al. · Cytogenetic and Genome Research · 2016 · 35 citations

Deletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2

Tingwei Guo, Alexander Diacou, Hiroko Nomaru et al. · Human Molecular Genetics · 2018 · 27 citations · Full text

Cytogenetics, Genetics, Molecular Biology +19

Pathogenic variants in CDC45 on the remaining allele in patients with a chromosome 22q11.2 deletion result in a novel autosomal recessive condition

Marta Unolt, Molka Kammoun, Beata Nowakowska et al. · Genetics in Medicine · 2019 · 24 citations · Full text

Allelic Variant, Deletion Result, Genetic Disorder +10