P. K�hnl

609 total citations
19 papers, 508 citations indexed

About

P. K�hnl is a scholar working on Molecular Biology, Hematology and Genetics. According to data from OpenAlex, P. K�hnl has authored 19 papers receiving a total of 508 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Hematology and 5 papers in Genetics. Recurrent topics in P. K�hnl's work include Blood groups and transfusion (4 papers), Blood properties and coagulation (2 papers) and Molecular Biology Techniques and Applications (2 papers). P. K�hnl is often cited by papers focused on Blood groups and transfusion (4 papers), Blood properties and coagulation (2 papers) and Molecular Biology Techniques and Applications (2 papers). P. K�hnl collaborates with scholars based in Germany, United States and United Kingdom. P. K�hnl's co-authors include W. Spielmann, J. Constans, M. Viau, W. Weber, S. Seidl, E. Schifferdecker, L. Nowicki, Burkhard Manfras, James Lee and K. H. Usadel and has published in prestigious journals such as Human Genetics, Journal of Molecular Medicine and International Journal of Legal Medicine.

In The Last Decade

P. K�hnl

19 papers receiving 474 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
P. K�hnl Germany	13	190	172	105	73	66	19	508
H. van Someren Netherlands	10	326 1.7×	185 1.1×	38 0.4×	80 1.1×	129 2.0×	20	574
Mei‐Chi Cheung United States	8	298 1.6×	139 0.8×	75 0.7×	50 0.7×	25 0.4×	8	597
L.L. Deaven United States	9	399 2.1×	162 0.9×	95 0.9×	15 0.2×	123 1.9×	14	648
Glynis McCray United States	8	309 1.6×	76 0.4×	89 0.8×	26 0.4×	55 0.8×	8	504
Joel S. Trupin United States	14	388 2.0×	121 0.7×	29 0.3×	38 0.5×	29 0.4×	17	828
Marion R. Fung Canada	11	389 2.0×	252 1.5×	170 1.6×	48 0.7×	159 2.4×	14	788
Janet Stiernberg United States	8	226 1.2×	33 0.2×	166 1.6×	37 0.5×	95 1.4×	9	507
Guiqing Huang United States	10	396 2.1×	132 0.8×	68 0.6×	54 0.7×	86 1.3×	14	639
Walter L. Henley United States	13	199 1.0×	49 0.3×	31 0.3×	34 0.5×	190 2.9×	46	574
Lorraine Caruccio United States	10	147 0.8×	83 0.5×	80 0.8×	39 0.5×	121 1.8×	16	363

Countries citing papers authored by P. K�hnl

Since Specialization

Citations

This map shows the geographic impact of P. K�hnl'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 P. K�hnl with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites P. K�hnl more than expected).

Fields of papers citing papers by P. K�hnl

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by P. K�hnl. 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 P. K�hnl. The network helps show where P. K�hnl may publish in the future.

Co-authorship network of co-authors of P. K�hnl

This figure shows the co-authorship network connecting the top 25 collaborators of P. K�hnl. A scholar is included among the top collaborators of P. K�hnl 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 P. K�hnl. P. K�hnl is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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19 of 19 papers shown

Boehm, Bernhard O., et al.. (1993). HLA-DR3 and HLA-DR5 confer risk for autoantibody positivity against the thyroperoxidase (mic-TPO) antigen in healthy blood donors. Journal of Molecular Medicine. 71(3). 221–5. 19 indexed citations

Manfras, Burkhard, Michael Swinyard, Edward J. Ball, et al.. (1993). Altered CYP21 genes in HLA-haplotypes associated with congenital adrenal hyperplasia (CAH): a family study. Human Genetics. 92(1). 33–39. 2 indexed citations

Boehm, B. O., P. K�hnl, Burkhard Manfras, et al.. (1992). HLA-DRB3 gene alleles in Caucasian patients with Graves' disease. Journal of Molecular Medicine. 70(10). 956–60. 36 indexed citations

Schwanitz, Gesa, Max P. Baur, Carol M. Black, et al.. (1988). Family studies in scleroderma (systemic sclerosis) demonstrating an HLA-linked increased chromosomal breakage rate in cultured lymphocytes. Human Genetics. 81(1). 64–70. 22 indexed citations

K�hnl, P., et al.. (1982). Improved coagulation factor XIII B (FXIIIB) phenotyping after neuraminidase treatment of plasma and first description of the FXIIIB 2 phenotype. Annals of Hematology. 45(5). 337–345. 6 indexed citations

K�hnl, P., et al.. (1982). Human coagulation factor XIIIA (FXIIIA) phenotyping by immunofixation agarose gel electrophoresis (IAGE). Annals of Hematology. 44(5). 309–314. 8 indexed citations

Constans, J., P. K�hnl, M. Viau, & W. Spielmann. (1980). A new procedure for the determination of transferrinC (TfC) subtypes by isoelectric focusing. Human Genetics. 55(1). 111–114. 58 indexed citations

K�hnl, P., W. Spielmann, & W. Weber. (1979). Isoelectric focusing of rare transferrin (Tf) variants and common TfC subtypes. Human Genetics. 46(1). 83–87. 21 indexed citations

K�hnl, P. & W. Spielmann. (1979). A third common allele in the transferrin system, Tf C3 , detected by isoelectric focusing. Human Genetics. 50(2). 193–198. 52 indexed citations

10.

K�hnl, P., et al.. (1979). PiT: A new allele in the alpha1-antitrypsin system. Human Genetics. 50(2). 221–223. 9 indexed citations

11.

K�hnl, P. & W. Spielmann. (1978). Properdin factor B-polymorphism in the population of Hessen, Germany. International Journal of Legal Medicine. 81(2). 125–31. 4 indexed citations

12.

K�hnl, P. & W. Spielmann. (1978). Transferrin: Evidence for two common subtypes of the TfC allele. Human Genetics. 43(1). 91–95. 70 indexed citations

13.

K�hnl, P., et al.. (1977). Investigations on the polymorphism of sperm diaphorase in man. Human Genetics. 40(1). 79–86. 14 indexed citations

14.

K�hnl, P., et al.. (1977). Investigations on the polymorphism of glyoxalase I (EC 4.4.1.5) in the population of Hessen, Germany. Human Genetics. 38(1). 99–106. 29 indexed citations

15.

K�hnl, P., et al.. (1977). Evidence for two additional common alleles at the PGM1 locus (Phosphoglucomutase-E.C.:2.7.5.1). Human Genetics. 35(2). 219–223. 94 indexed citations

16.

K�hnl, P., L. Nowicki, & W. Spielmann. (1974). Untersuchungen zum Polymorphismus der Galaktose-1-Phosphat-Uridyltransferase (EC: 2.7.7.12) mittels Agarosegelelektrophorese. Human Genetics. 24(3). 227–30. 19 indexed citations

17.

Spielmann, W., et al.. (1973). Untersuchungen zum GPT-System unter besonderer Ber�cksichtigung des stummen Allels GPT0. Human Genetics. 18(4). 341–348. 20 indexed citations

18.

K�hnl, P. & W. Spielmann. (1972). Untersuchungen zum C?3-Polymorphismus (? 1c-Globulin): Genfrequenzen und Familienuntersuchungen an hessischen Blutspendern und einer Bantupopulation. Human Genetics. 15(1). 7–13. 2 indexed citations

19.

K�hnl, P. & W. Spielmann. (1972). Untersuchungen zum C?3-Polymorphismus (? 1c-Globulin). Human Genetics. 15(1). 7–13. 23 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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