H.P. Klinger

3.8k total citations
81 papers, 2.9k citations indexed

About

H.P. Klinger is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, H.P. Klinger has authored 81 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 33 papers in Genetics and 17 papers in Plant Science. Recurrent topics in H.P. Klinger's work include Chromosomal and Genetic Variations (16 papers), Genomics and Chromatin Dynamics (10 papers) and Genomic variations and chromosomal abnormalities (10 papers). H.P. Klinger is often cited by papers focused on Chromosomal and Genetic Variations (16 papers), Genomics and Chromatin Dynamics (10 papers) and Genomic variations and chromosomal abnormalities (10 papers). H.P. Klinger collaborates with scholars based in United States, Switzerland and Sweden. H.P. Klinger's 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 and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

H.P. Klinger

80 papers receiving 2.6k 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.P. Klinger United States 30 1.5k 1.3k 520 369 285 81 2.9k
J. H. Tjio United States 26 1.2k 0.8× 975 0.7× 404 0.8× 325 0.9× 256 0.9× 66 3.4k
J. E. Landegent Netherlands 16 1.4k 0.9× 1.0k 0.8× 793 1.5× 211 0.6× 207 0.7× 22 2.4k
J Couturier France 29 1.6k 1.0× 1.1k 0.8× 645 1.2× 799 2.2× 419 1.5× 110 3.3k
D.G. Harnden United Kingdom 33 2.5k 1.7× 1.6k 1.2× 434 0.8× 723 2.0× 1.0k 3.5× 90 4.8k
Alain Niveleau France 30 3.6k 2.4× 1.3k 1.0× 260 0.5× 286 0.8× 208 0.7× 72 4.3k
Ramana Tantravahi United States 36 2.5k 1.6× 993 0.7× 886 1.7× 664 1.8× 289 1.0× 79 5.8k
Andreas Weith Germany 29 1.7k 1.1× 772 0.6× 238 0.5× 490 1.3× 450 1.6× 59 3.0k
L. Zech Sweden 32 2.3k 1.5× 2.0k 1.5× 1.2k 2.4× 798 2.2× 451 1.6× 105 5.5k
John Barber United Kingdom 30 1.2k 0.8× 1.8k 1.3× 537 1.0× 110 0.3× 82 0.3× 106 3.1k
Orlando J. Miller United States 27 1.8k 1.2× 1.2k 0.9× 682 1.3× 106 0.3× 121 0.4× 69 2.5k

Countries citing papers authored by H.P. Klinger

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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 of co-authors of H.P. Klinger

This figure shows the co-authorship network connecting the top 25 collaborators of H.P. Klinger. A scholar is included among the top collaborators of H.P. Klinger 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.P. Klinger. H.P. Klinger 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.
Cass, Ilana, Rae Lynn Baldwin, Abbie L. Fields, et al.. (2001). Allelotype of Papillary Serous Peritoneal Carcinomas. Gynecologic Oncology. 82(1). 69–76. 16 indexed citations
2.
Jaggernauth, Wainwright, et al.. (2000). Cell lines from the same cervical carcinomabut with different radiosensitivities exhibit different cDNA microarray patterns of gene expression. Cytogenetic and Genome Research. 91(1-4). 39–43. 46 indexed citations
3.
Boldog, Ferenc, Robert M. Gemmill, James West, et al.. (1997). Chromosome 3p14 Homozygous Deletions and Sequence Analysis of FRA3B. Human Molecular Genetics. 6(2). 193–203. 117 indexed citations
4.
Mullokandov, Michael, et al.. (1997). Assignment of ACTBP8 (alias ACTBP2) within or close to human chromosome band 6q13 using a radiation hybrid panel. Cytogenetic and Genome Research. 78(1). 46–47. 3 indexed citations
5.
Frézal, J & H.P. Klinger. (1987). 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. S. Karger eBooks. 1 indexed citations
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Kaelbling, M., et al.. (1986). DNA polymorphisms indicate loss of heterozygosity for chromosome 11 of D98AH2 cells. Cytogenetic and Genome Research. 41(4). 240–244. 18 indexed citations
10.
O’Hara, Brian J., H.P. Klinger, & Donald G. Blair. (1986). Many oncogenes are transcribed in the D98AH2 derivative of the HeLa carcinoma cell line. Cytogenetic and Genome Research. 43(1-2). 97–102. 5 indexed citations
11.
Harnden, D.G. & H.P. Klinger. (1985). ISCN 1985 : an international system for human cytogenetic nomenclature (1985) : report of the Standing Committee on Human Cytogenetic Nomenclature. S. Karger eBooks. 118 indexed citations
12.
Kurnit, David M., et al.. (1984). Recent evolution of DNA sequence homology in the pericentromeric regions of human acrocentric chromosomes. Cytogenetic and Genome Research. 38(2). 99–105. 25 indexed citations
13.
Klinger, H.P., et al.. (1978). Human chromosomes which affect tumorigenicity in hybrids of diploid human with heteroploid human or rodent cells. Cytogenetic and Genome Research. 22(1-6). 245–249. 18 indexed citations
14.
Chapelle, Albert de la, Jim Schröder, H.P. Klinger, et al.. (1975). An (X;3) translocation, balanced, 46 chromosomes. Cytogenetic and Genome Research. 15(6). 404–405. 12 indexed citations
15.
Miller, Orlando J., W. Roy Breg, Dorothy Warburton, et al.. (1970). Partial deletion of the short arm of chromosome No. 4(4p-): Clinical studies in five unrelated patients. The Journal of Pediatrics. 77(5). 792–801. 49 indexed citations
16.
Allderdice, P. W., Jessica G. Davis, O.J. Miller, et al.. (1969). The 13q-deletion syndrome.. PubMed. 21(5). 499–512. 133 indexed citations
17.
Klinger, H.P., et al.. (1968). Secondary Infertility in a Phenotypically Normal 45,X /46,XX Female. Fertility and Sterility. 19(5). 835–838. 13 indexed citations
18.
Lindsten, J., M. Fraccaro, H.P. Klinger, & P Zetterqvist. (1965). Meiotic and Mitotic Studies of a Familial Reciprocal Translocation Between Two Autosomes of Group 6–12. Cytogenetic and Genome Research. 4(1). 45–64. 29 indexed citations
19.
Hamerton, J.L., et al.. (1963). The Somatic Chromosomes of the Hominoidea. Cytogenetic and Genome Research. 2(4-5). 240–263. 47 indexed citations
20.
Klinger, H.P.. (1958). The fine structure of the sex chromatin body. Experimental Cell Research. 14(1). 207–211. 38 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.

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