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American Journal of Human Genetics|August 2, 2007
New perspectives for the elucidation of genetic disordersHans-Hilger RopersDialogues in Clinical Neuroscience|April 9, 2010
Single gene disorders come into focus--againHans-Hilger RopersJournal of Community Genetics|April 3, 2012
On the future of genetic risk assessmentHans-Hilger RopersCurrent Opinion in Genetics & Development|May 2, 2006
X-linked mental retardation: many genes for a complex disorderHans-Hilger RopersAnnual Review of Genomics and Human Genetics|September 9, 2010
Genetics of early onset cognitive impairmentHans Hilger RopersCold Spring Harbor Molecular Case Studies|March 25, 2022
Rare diseases: human genome research is coming homeHans-Hilger Ropers, Clara D van KarnebeekGene|May 18, 2004
cDNA cloning and characterization of the human THRAP2 gene which maps to chromosome 12q24, and its mouse ortholog Thrap2Luciana Musante, Oliver Bartsch, Hans-Hilger Ropers, et al.Biochimica Et Biophysica Acta|November 10, 2005
Characterization of FBX25, encoding a novel brain-expressed F-box proteinOlivier Hagens, Eleonora Minina, Susann Schweiger, et al.European Journal of Pediatrics|July 28, 2010
Brachyphalangy, polydactyly and tibial aplasia/hypoplasia syndrome (OMIM 609945): case report and review of the literatureYousef Shafeghati, Kimia Kahrizi, Hossein Najmabadi, et al.European Journal of Human Genetics : EJHG|August 10, 2006
Ulnar-mammary syndrome with dysmorphic facies and mental retardation caused by a novel 1.28 Mb deletion encompassing the TBX3 geneEva Klopocki, Luitgard M Neumann, Holger Tönnies, et al.Pageof 13