H.P. Klinger
- Genetics top 1%
- Genomic variations and chromosomal abnormalities 10
- Animal Genetics and Reproduction 9
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 8
- Virus-based gene therapy research 6
- Developmental Biology top 5%
- Molecular Biology top 5%
- Genomics and Chromatin Dynamics 10
- DNA and Nucleic Acid Chemistry 7
- Virology top 5%
- Cancer Research top 10%
- Cancer Genomics and Diagnostics 7
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- Chromosomal and Genetic Variations 16
- Co-authors
- Kurt S. LudwigM. KaelblingD.G. HarndenHj. MüllerMichael MullokandovBrian J. O’HaraD. G. BlairM. Fraccaro
- Journals
- Cytogenetic and Genome Research (36 papers)Proceedings of the National Academy of Sciences (4 papers)Annals of Human Genetics (2 papers)
- Partner nations
- United StatesSwitzerlandSweden
In The Last Decade
H.P. Klinger
80 papers receiving 2.6k citations
Peers
Comparison fields: 5 of 116
- Genetics 1.3k
- Developmental Biology 48
- Molecular Biology 1.5k
- Virology 102
- Cancer Research 285
Countries citing papers authored by H.P. Klinger
This map shows the geographic impact of H.P. Klinger'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.P. Klinger with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites H.P. Klinger more than expected).
Fields of papers citing papers by H.P. Klinger
This network shows the impact of papers produced by H.P. Klinger. 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.P. Klinger. The network helps show where H.P. Klinger may publish in the future.
Co-authorship network
The 25 scholars most cited alongside H.P. Klinger, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2001 | 16 | |
| 2 | 2000 | 46 | |
| 3 | 1997 | 117 | |
| 4 | 1997 | 3 | |
| 5 | Human gene mapping 9 : Paris Conference (1987) : Ninth International Workshop on Human Gene Mapping : at the University of Paris, Faculté de Médecine, France, September 6-11, 1987 | 1987 | 1 |
| 6 | 1987 | 1 | |
| 7 | 1987 | 9 | |
| 8 | 1986 | 25 | |
| 9 | 1986 | 18 | |
| 10 | 1986 | 5 | |
| 11 | ISCN 1985 : an international system for human cytogenetic nomenclature (1985) : report of the Standing Committee on Human Cytogenetic Nomenclature | 1985 | 118 |
| 12 | 1984 | 25 | |
| 13 | 1978 | 18 | |
| 14 | 1975 | 12 | |
| 15 | 1970 | 49 | |
| 16 | The 13q-deletion syndrome. | 1969 | 133 |
| 17 | 1968 | 13 | |
| 18 | 1965 | 29 | |
| 19 | 1963 | 47 | |
| 20 | 1958 | 38 |
About H.P. Klinger
H.P. Klinger is a scholar working on Genetics, Molecular Biology, Cancer Research, Immunology and Allergy and Developmental Biology, having authored 81 papers that have together received 2.9k indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (16 papers), Genomics and Chromatin Dynamics (10 papers), Genomic variations and chromosomal abnormalities (10 papers), Animal Genetics and Reproduction (9 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), DNA and Nucleic Acid Chemistry (7 papers), Cancer Genomics and Diagnostics (7 papers) and Virus-based gene therapy research (6 papers). The work is most often cited by research in Genetics (1.3k citations), Developmental Biology (48 citations), Molecular Biology (1.5k citations), Virology (102 citations) and Cancer Research (285 citations). H.P. Klinger has collaborated with scholars based in United States, Switzerland and Sweden. Frequent co-authors include Kurt S. Ludwig, M. Kaelbling, D.G. Harnden, Hj. Müller, Michael Mullokandov, Brian J. O’Hara, D. G. Blair, M. Fraccaro, Kathleen Dunn and T. Robins. Their work appears in journals such as Cytogenetic and Genome Research, Proceedings of the National Academy of Sciences, Annals of Human Genetics, Nature and Experimental Cell Research.
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.