H.-H. Ropers - Concepedia

Author

H.-H. Ropers

Also Known As

H H Ropers, H Hilger Ropers, H Ropers, H. -H. Ropers, H. H. Ropers, H.-H. Ropers, H.-Hilger Ropers, H.H Ropers, H.H. Ropers, Hans-Hilger Ropers

Publications

2.7K

Citations

H-Index

Concepts

All Affiliations

Radboud University Nijmegen Max Planck Institute for Molecular Genetics Women's and Children's Hospital Inserm Combined Ophthalmic Research Rotterdam

About

H.-H. Ropers is an author at Radboud University Nijmegen specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	14	1.6K
2	Cell Biology	3	3	447
3	Health Sciences	1	1	49
4	Natural Sciences	1	1	381
5	Public Health	1	1	356

H.-H. Ropers

Publications

2.3K

Citations

H-Index

Page 1

	Year	Citations
Positional cloning of the gene for X-linked retinitis pigmentosa 2 Uwe Schwahn, Steffen Lenzner, Juan Dong, Nature Genetics Natural SciencesGeneticsGenomic MechanismMolecular BiologyDna Replication	1998	381
Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia George Kirov, Dilihan Gumus, Wei Chen, Human Molecular Genetics	2007	380
Report of the committee on the genetic constitution of the X and Y chromosomes P.N. Goodfellow, Kay E. Davies, H.-H. Ropers Cytogenetic and Genome Research Developmental BiologyY ChromosomesGenetic DisorderGeneticsGenetic Mechanism	1985	366
Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene Hannie Kremer, Robert Kraaij, S. P. A. Toledo, Nature Genetics Male PseudohermaphroditismInfertilityAndrologyMendelian DisorderHormonal Receptor	1995	356
Localization of the gene for X-linked Alport's syndrome Han G. Brunner, C.H. Schröder, Cor van Bennekom, Kidney International X-linked AlportMendelian DisorderGenetic DisorderGeneticsHistopathology	1988	80
A duplication/paracentric inversion associated with familial X-linked deafness (DFN3) suggests the presence of a regulatory element more than 400 kb upstream of the POU3F4 gene Y J de Kok, Gerard Merkx, Silvère M. van der Maarel, Human Molecular Genetics CytogeneticsGeneticsMolecular BiologyMolecular GeneticsDisease Gene Identification	1995	79
Presymptomatic diagnosis of myotonic dystrophy. Han G. Brunner, W Nillesen, Bernard A. van Oost, Journal of Medical Genetics Ctg Triplet NumberMendelian DisorderGenetic DisorderMedicineGenetics	1992	75
Submicroscopic interstitial deletion of the X chromosome explains a complex genetic syndrome dominated by Norrie disease A. Gal, B. Wieringa, D F Smeets, Cytogenetic and Genome Research GeneticsPathologyMolecular GeneticsDisease Gene IdentificationEpigenetics	1986	74
Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines. Graeme Suthers, V.J. Hyland, David F. Callen, PubMed	1990	61
Molecular analysis of male-viable deletions and duplications allows ordering of 52 DNA probes on proximal Xq. Frans P.M. Cremers, T J van de Pol, B. Wieringa, PubMed	1988	56

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