Edwin Reyniers

Researcher Next ID · RN-023254

Researcher · Biochemistry, Genetics and Molecular Biology

Reykjavik, Iceland

Not currently recruitingFunding unknown

Research interests

Biochemistry, Genetics and Molecular Biology

Neuroscience

Genetics and Neurodevelopmental Disorders

Genomic variations and chromosomal abnormalities

Autism Spectrum Disorder Research

Genomics and Rare Diseases

Congenital heart defects research

Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome
European Journal of Medical Genetics · 2009 · https://doi.org/10.1016/j.ejmg.2009.02.006
A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism
Nature Genetics · 2006 · https://doi.org/10.1038/ng1853
Mildly impaired water maze performance in maleFmr1 knockout mice
Neuroscience · 1997 · https://doi.org/10.1016/s0306-4522(96)00224-2
Transgenic mouse model for the fragile X syndrome
American Journal of Medical Genetics · 1996 · https://doi.org/10.1002/(sici)1096-8628(19960809)64:2<241::aid-ajmg1>3.0.co;2-x
FMR1 Knockout mice: A model to study fragile X mental retardation
The American Journal of Human Genetics · 1994
The full mutation in the FMR–1 gene of male fragile X patients is absent in their sperm
Nature Genetics · 1993 · https://doi.org/10.1038/ng0693-143
A point mutation in the FMR-1 gene associated with fragile X mental retardation
Nature Genetics · 1993 · https://doi.org/10.1038/ng0193-31

No projects listed.