H‐H Ropers
Max Planck Institute for Molecular Genetics(DE)The University of Texas Southwestern Medical Center(US)
Publications by Year
Research Areas
Genomics and Rare Diseases, Microtubule and mitosis dynamics, Genomic variations and chromosomal abnormalities, Genetics and Neurodevelopmental Disorders, Autism Spectrum Disorder Research
Most-Cited Works
- → X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes(2015)302 cited
- → Molecular basis of choroideremia (CHM): Mutations involving the rab escort protein-1 (REP-1) gene(1997)173 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
- → Investigation of primary microcephaly in Bushehr province of Iran: novel STIL and ASPM mutations(2012)18 cited
- → Evidence for X-linkage and non-inactivation of steroid sulphatase locus in wood lemming(1982)17 cited