H.-H. Ropers
Impact in
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Immunology and Allergy top 5%
- Cell Adhesion Molecules Research
Papers in
-
- Retinal Development and Disorders 4
- CRISPR and Genetic Engineering 3
- Advanced biosensing and bioanalysis techniques 2
- Fungal and yeast genetics research 2
- Genetics 10
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
- Genomic variations and chromosomal abnormalities 3
- Co-authors
- P.N. Goodfellow (1 shared paper)Kay E. Davies (1 shared paper)Han G. Brunner (7 shared papers)Frans P.M. Cremers (6 shared papers)B. Wieringa (5 shared papers)Reinhard Ullmann (1 shared paper)Michael J. Owen (1 shared paper)George Kirov (1 shared paper)
- Journals
- Cytogenetic and Genome Research (6 papers)Nature Genetics (2 papers)Human Molecular Genetics (2 papers)Kidney International (2 papers)Human Genetics (2 papers)
- Partner nations
- NetherlandsGermanyAustralia
In The Last Decade
H.-H. Ropers
23 papers receiving 1.7k citations
Peers
Comparison fields: 5 of 91
- Genetics 764
- Immunology and Allergy 111
- Molecular Biology 1.2k
- Reproductive Medicine 138
- Cellular and Molecular Neuroscience 246
Countries citing papers authored by H.-H. Ropers
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
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-authors
The 25 scholars most cited alongside H.-H. Ropers, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 25 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1985 | 311 | |
| 2 | 1998 | 297 | |
| 3 | 2007 | 271 | |
| 4 | 1995 | 223 | |
| 5 | 1988 | 72 | |
| 6 | 1986 | 64 | |
| 7 | 1995 | 60 | |
| 8 | Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines. | 1990 | 55 |
| 9 | 1992 | 53 | |
| 10 | Molecular analysis of male-viable deletions and duplications allows ordering of 52 DNA probes on proximal Xq. | 1988 | 52 |
| 11 | 1989 | 47 | |
| 12 | 1992 | 43 | |
| 13 | 1989 | 43 | |
| 14 | 1988 | 38 | |
| 15 | 1986 | 30 | |
| 16 | 1989 | 17 | |
| 17 | 1990 | 13 | |
| 18 | 1978 | 12 | |
| 19 | 1991 | 10 | |
| 20 | 1992 | 8 |
About H.-H. Ropers
H.-H. Ropers is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Immunology and Allergy and Surgery, having authored 25 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (5 papers), Retinal Development and Disorders (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), CRISPR and Genetic Engineering (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Advanced biosensing and bioanalysis techniques (2 papers), Cell Adhesion Molecules Research (2 papers) and Fungal and yeast genetics research (2 papers). The work is most often cited by research in Genetics (764 citations), Immunology and Allergy (111 citations), Molecular Biology (1.2k citations), Reproductive Medicine (138 citations) and Cellular and Molecular Neuroscience (246 citations). H.-H. Ropers has collaborated with scholars based in Netherlands, Germany and Australia. Frequent co-authors include P.N. Goodfellow, Kay E. Davies, Han G. Brunner, Frans P.M. Cremers, B. Wieringa, Reinhard Ullmann, Michael J. Owen, George Kirov, Murat Sarı and Wei Chen. Their work appears in journals such as Cytogenetic and Genome Research, Nature Genetics, Human Molecular Genetics, Kidney International and Human Genetics.
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.