Hans‐Hilger Ropers

Max Planck Institute for Molecular Genetics

Publishes on Genetics and Neurodevelopmental Disorders, Genomic variations and chromosomal abnormalities, Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities. 373 papers and 25.8k citations.

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373Publications

25.8kTotal Citations

First publication: 1969First senior author: 1969

Genetics and Neurodevelopmental Disorders Genomic variations and chromosomal abnormalities Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities RNA modifications and cancer Genomics and Rare Diseases

Top publicationsby citations

Abnormal Behavior Associated with a Point Mutation in the Structural Gene for Monoamine Oxidase A

Han G. Brunner, Bernard A. van Oost, Marcel Nelen et al.|Science|1993

Cited by 1.6k

Deep sequencing reveals 50 novel genes for recessive cognitive disorders

Hossein Najmabadi, Hans‐Hilger Ropers, Hao Hu et al.|Nature|2011

Cited by 987

X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family

Frédéric Laumonnier, Sylvain Briault, Martine Raynaud et al.|The American Journal of Human Genetics|2004

Cited by 760

Localization of the gene for Cowden disease to chromosome 10q22–23

Marcel Nelen, Charis Eng, G.W. Padberg et al.|Nature Genetics|1996

Cited by 670

A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation

Patrick Tarpey, Anand K. Srivastava, Raffaella Smith et al.|Nature Genetics|2009

Cited by 617