Vanessa Suckow
Max Planck Institute for Molecular Genetics(DE)
Publications by Year
Research Areas
Congenital heart defects research, Genetics and Neurodevelopmental Disorders, Genomics and Rare Diseases, RNA modifications and cancer, Genomic variations and chromosomal abnormalities
Most-Cited Works
- → MID1, mutated in Opitz syndrome, encodes an ubiquitin ligase that targets phosphatase 2A for degradation(2001)291 cited
- Elevated levels of Rad51 recombination protein in tumor cells.(2002)
- → Genetics of intellectual disability in consanguineous families(2018)210 cited
- → The Opitz syndrome gene product, MID1, associates with microtubules(1999)137 cited
- → GPR30 estrogen receptor agonists induce mechanical hyperalgesia in the rat(2008)84 cited
- → Redefining the MED13L syndrome(2015)82 cited
- → Effect of inbreeding on intellectual disability revisited by trio sequencing(2018)80 cited
- → Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations(2004)73 cited
- → De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females(2016)68 cited
- → Deleterious de novo variants of X‐linked ZC4H2 in females cause a variable phenotype with neurogenic arthrogryposis multiplex congenita(2019)46 cited