Christine Verellen‐Dumoulin
Institute of Pathology and Genetics(BE)
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Congenital Anomalies and Fetal Surgery, Genetic Neurodegenerative Diseases, Prenatal Screening and Diagnostics, Cleft Lip and Palate Research
Most-Cited Works
- → Identification of mutations in the α3(IV) and α4(IV) collagen genes in autosomal recessive Alport syndrome(1994)511 cited
- → Deletion of KDM6A, a Histone Demethylase Interacting with MLL2, in Three Patients with Kabuki Syndrome(2011)376 cited
- → Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study(2017)328 cited
- → CNGA3 Mutations in Hereditary Cone Photoreceptor Disorders(2001)321 cited
- → Long term trends in prevalence of neural tube defects in Europe: population based study(2015)244 cited
- → A Cluster of Mutations in the UMOD Gene Causes Familial Juvenile Hyperuricemic Nephropathy with Abnormal Expression of Uromodulin(2003)220 cited