Han G. Brunner
Radboud University Nijmegen(NL)Maastricht University Medical Centre(NL)University Medical Center(US)Radboud University Medical Center(NL)Maastricht University(NL)Universitätsklinikum Tübingen(DE)University Hospital and Clinics(US)Radboud Institute for Molecular Life Sciences(NL)University Children's Hospital Tübingen(DE)ERN GUARD-Heart(NL)
Publications by Year
Research Areas
Genomics and Rare Diseases, Genomic variations and chromosomal abnormalities, Genetics and Neurodevelopmental Disorders, Congenital heart defects research, Cardiomyopathy and Myosin Studies
Most-Cited Works
- → Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome(2001)1,728 cited
- → Abnormal Behavior Associated with a Point Mutation in the Structural Gene for Monoamine Oxidase A(1993)1,641 cited
- → Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability(2012)1,570 cited
- → Mutations in a new member of the chromodomain gene family cause CHARGE syndrome(2004)1,270 cited
- → Genome sequencing identifies major causes of severe intellectual disability(2014)1,130 cited
- → De novo mutations in human genetic disease(2012)874 cited
- →