H.-H. Ropers

2.7k total citations
25 papers, 1.7k citations indexed

About

H.-H. Ropers is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, H.-H. Ropers has authored 25 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 10 papers in Genetics and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in H.-H. Ropers's work include Genetic Neurodegenerative Diseases (5 papers), Retinal Development and Disorders (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). H.-H. Ropers is often cited by papers focused on Genetic Neurodegenerative Diseases (5 papers), Retinal Development and Disorders (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). H.-H. Ropers collaborates with scholars based in Netherlands, Germany and Australia. H.-H. Ropers's co-authors include P.N. Goodfellow, Kay E. Davies, Han G. Brunner, Frans P.M. Cremers, B. Wieringa, George Kirov, Wei Chen, Fikret Erdogan, Reinhard Ullmann and Murat Sarı and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Genetics.

In The Last Decade

H.-H. Ropers

23 papers receiving 1.7k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
H.-H. Ropers Netherlands 16 1.2k 764 246 171 142 25 1.7k
Steven H. Laval United Kingdom 25 1.2k 1.0× 510 0.7× 161 0.7× 57 0.3× 267 1.9× 51 2.0k
Anne Seawright United Kingdom 18 1.6k 1.4× 580 0.8× 145 0.6× 85 0.5× 111 0.8× 22 1.9k
Kirsten Kuhlbrodt Germany 10 1.4k 1.2× 645 0.8× 386 1.6× 47 0.3× 353 2.5× 11 2.3k
Hope O. Sweet United States 21 1.0k 0.9× 440 0.6× 264 1.1× 111 0.6× 398 2.8× 32 1.9k
Véronique Pingault France 26 1.7k 1.5× 818 1.1× 131 0.5× 62 0.4× 765 5.4× 52 3.2k
Dorien Lugtenberg Netherlands 18 1.0k 0.9× 920 1.2× 70 0.3× 97 0.6× 121 0.9× 34 1.6k
Tanja Vogel Germany 22 1.1k 1.0× 512 0.7× 277 1.1× 68 0.4× 106 0.7× 52 1.8k
Yasuko Matsumura Japan 9 2.2k 1.9× 489 0.6× 297 1.2× 37 0.2× 100 0.7× 15 2.6k
Andreas Tzschach Germany 30 2.1k 1.9× 1.8k 2.4× 238 1.0× 206 1.2× 266 1.9× 104 3.3k
Kathleen A. Williamson United Kingdom 21 1.2k 1.0× 836 1.1× 87 0.4× 27 0.2× 134 0.9× 35 1.8k

Countries citing papers authored by H.-H. Ropers

Since Specialization
Citations

This map shows the geographic impact of H.-H. Ropers's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by H.-H. Ropers with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites H.-H. Ropers more than expected).

Fields of papers citing papers by H.-H. Ropers

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by H.-H. Ropers. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by H.-H. Ropers. The network helps show where H.-H. Ropers may publish in the future.

Co-authorship network of co-authors of H.-H. Ropers

This figure shows the co-authorship network connecting the top 25 collaborators of H.-H. Ropers. A scholar is included among the top collaborators of H.-H. Ropers based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with H.-H. Ropers. H.-H. Ropers is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Ropers, H.-H.. (2008). Neue Perspektiven für die Aufklärung von genetischen Kranheiten. Journal of Consumer Protection and Food Safety. 3(S1). 18–24.
2.
Kirov, George, Wei Chen, Nadine Norton, et al.. (2007). Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia. Human Molecular Genetics. 17(3). 458–465. 271 indexed citations
3.
Schwahn, Uwe, Steffen Lenzner, Silke Feil, et al.. (1998). Positional cloning of the gene for X-linked retinitis pigmentosa 2. Nature Genetics. 19(4). 327–332. 297 indexed citations
4.
Merkx, Gerard, Silvère M. van der Maarel, I Huber, et al.. (1995). 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. Human Molecular Genetics. 4(11). 2145–2150. 60 indexed citations
5.
Kremer, Hannie, Robert Kraaij, S. P. A. Toledo, et al.. (1995). Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene. Nature Genetics. 9(2). 160–164. 223 indexed citations
6.
Berger, Wolfgang, A Meindl, B. de Leeuw, et al.. (1992). Generation and characterization of radiation reduced cell hybrids and isolation of probes from the proximal short arm of the human X chromosome. Human Genetics. 90(3). 243–246. 8 indexed citations
7.
Smeets, H.J.M., Jos Melenhorst, Henny H. Lemmink, et al.. (1992). Different mutations in the COL4A5 collagen gene in two patients with different features of Alport syndrome. Kidney International. 42(1). 83–88. 43 indexed citations
8.
Brunner, Han G., Bernard A. van Oost, Gert Jansen, et al.. (1992). Presymptomatic diagnosis of myotonic dystrophy.. Journal of Medical Genetics. 29(11). 780–784. 53 indexed citations
9.
Brunner, Han G., Frank Spaans, H. Smeets, et al.. (1991). Genetic linkage with chromosome 19 but not chromosome 17 in a family with myotonic dystrophy associated with hereditary motor and sensory neuropathy. Neurology. 41(1). 80–80. 10 indexed citations
10.
Pol, T.J.R. van de, Frans P.M. Cremers, Richard M. Brohet, Bé Wieringa, & H.-H. Ropers. (1990). Derivation of clones from the choroideremia locus by preparative field inversion gel electrophoresis. Nucleic Acids Research. 18(4). 725–731. 13 indexed citations
11.
Suthers, Graeme, V.J. Hyland, David F. Callen, et al.. (1990). Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines.. PubMed. 47(2). 187–95. 55 indexed citations
12.
Smeets, H., Jan Schepens, M. Coerwinkel, et al.. (1989). TaqI RFLP at 19q13.1 identified by the anonymous DNA sequence p5B18 [D19S28]. Nucleic Acids Research. 17(8). 3325–3325. 3 indexed citations
13.
Brunner, Han G., Robert G. Korneluk, Alex MacKenzie, et al.. (1989). Myotonic dystrophy is closely linked to the gene for muscle-type creatine kinase (CKMM). Human Genetics. 81(4). 308–310. 43 indexed citations
14.
Brunner, Han G., H.J.M. Smeets, Jan Schepens, et al.. (1989). Definition of subchromosomal intervals around the myotonic dystrophy locus at 19q.. PubMed. 306. 107–14. 5 indexed citations
15.
Cremers, Frans P.M., B. Wieringa, FS Collins, et al.. (1989). Chromosomal jumping from the DXS165 locus allows molecular characterization of four microdeletions and a de novo chromosome X/13 translocation associated with choroideremia.. Proceedings of the National Academy of Sciences. 86(19). 7510–7514. 17 indexed citations
16.
Brunner, Han G., C.H. Schröder, J.H.A.M. Tuerlings, et al.. (1988). Localization of the gene for X-linked Alport's syndrome. Kidney International. 34(4). 507–510. 72 indexed citations
17.
Hulsebos, Theo J.M., et al.. (1988). Isolation and characterization of alphoid DNA sequences specific for the pericentric regions of chromosomes 4, 5, 9, and 19. Cytogenetic and Genome Research. 47(3). 144–148. 38 indexed citations
18.
Hulsebos, Theo J.M., B. Wieringa, Ron Hochstenbach, et al.. (1986). Toward early diagnosis of myotonic dystrophy:construction and characterization of a somatic cell hybrid with a single human der(19) chromosome. Cytogenetic and Genome Research. 43(1-2). 47–56. 30 indexed citations
19.
Goodfellow, P.N., Kay E. Davies, & H.-H. Ropers. (1985). Report of the committee on the genetic constitution of the X and Y chromosomes. Cytogenetic and Genome Research. 40(1-4). 296–352. 311 indexed citations
20.
Hameister, H., H.-H. Ropers, & Karl‐Heinz Grzeschik. (1978). Assignment of the gene for human glucose dehydrogenase (E.C. 1.1.1.47) to chromosome 1 using somatic cell hybrids. Cytogenetic and Genome Research. 22(1-6). 200–202. 12 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Steven H. Laval Breakdown of academic impact, for papers by Anne Seawright Breakdown of academic impact, for papers by Kirsten Kuhlbrodt Breakdown of academic impact, for papers by Hope O. Sweet Breakdown of academic impact, for papers by Véronique Pingault Breakdown of academic impact, for papers by Dorien Lugtenberg Breakdown of academic impact, for papers by Tanja Vogel Breakdown of academic impact, for papers by Yasuko Matsumura Breakdown of academic impact, for papers by Andreas Tzschach Breakdown of academic impact, for papers by Kathleen A. Williamson
Rankless by CCL
2026