Dagmar Wieczorek
Düsseldorf University Hospital(DE)Heinrich Heine University Düsseldorf(DE)
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Genomics and Rare Diseases, Genetics and Neurodevelopmental Disorders, Chromatin Remodeling and Cancer, RNA modifications and cancer
Most-Cited Works
- → Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study(2012)1,063 cited
- → Deep sequencing reveals 50 novel genes for recessive cognitive disorders(2011)982 cited
- → Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome(2006)598 cited
- → SARS ‐CoV‐2 targets neurons of 3D human brain organoids(2020)529 cited
- → Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes(2010)506 cited
- → Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome(2010)366 cited
- → De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome(2011)