Han G. Brunner
Researcher Next ID · RN-003359
Researcher · Biochemistry, Genetics and Molecular Biology
Nijmegen, Netherlands
- Works count
- 498
- Citation count
- 51,015
- H-index
- 104
- i10-index
- 344
Research interests
Publications
Genome sequencing identifies major causes of severe intellectual disability
Nature · 2014 · https://doi.org/10.1038/nature13394
Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability
New England Journal of Medicine · 2012 · https://doi.org/10.1056/nejmoa1206524
Mutations in a new member of the chromodomain gene family cause CHARGE syndrome
Nature Genetics · 2004 · https://doi.org/10.1038/ng1407
Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome
Nature Genetics · 2001 · https://doi.org/10.1038/ng772
Abnormal Behavior Associated with a Point Mutation in the Structural Gene for Monoamine Oxidase A
Science · 1993 · https://doi.org/10.1126/science.8211186
Current projects
No projects listed.