Georg Klaus Hinkel

1.8k total citations
41 papers, 933 citations indexed

About

Georg Klaus Hinkel is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Georg Klaus Hinkel has authored 41 papers receiving a total of 933 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Genetics, 13 papers in Pediatrics, Perinatology and Child Health and 12 papers in Molecular Biology. Recurrent topics in Georg Klaus Hinkel's work include Genomic variations and chromosomal abnormalities (12 papers), Neonatal Health and Biochemistry (8 papers) and Chromosomal and Genetic Variations (6 papers). Georg Klaus Hinkel is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Neonatal Health and Biochemistry (8 papers) and Chromosomal and Genetic Variations (6 papers). Georg Klaus Hinkel collaborates with scholars based in Germany, United States and Australia. Georg Klaus Hinkel's co-authors include Oliver Bartsch, Frank Majewski, Peter Meinecke, Vera M. Kalscheuer, Jürgen W. Spranger, Fred Zepp, W. Thoenes, David S. Wargowski, H Stöß and Markus Stümm and has published in prestigious journals such as Human Molecular Genetics, The Journal of Pediatrics and Human Genetics.

In The Last Decade

Georg Klaus Hinkel

38 papers receiving 904 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Georg Klaus Hinkel Germany 17 528 498 167 107 90 41 933
B. Le Marec France 19 474 0.9× 506 1.0× 33 0.2× 150 1.4× 115 1.3× 67 1.0k
M. Mannens Netherlands 15 314 0.6× 595 1.2× 78 0.5× 197 1.8× 40 0.4× 30 836
Francesca Romana Lepri Italy 18 429 0.8× 608 1.2× 142 0.9× 64 0.6× 74 0.8× 62 972
Beatrice Sellinger United States 11 293 0.6× 567 1.1× 50 0.3× 41 0.4× 99 1.1× 17 743
Zeynep Coban‐Akdemir United States 18 396 0.8× 544 1.1× 131 0.8× 35 0.3× 66 0.7× 50 965
Nelson A. Arango United States 13 660 1.3× 929 1.9× 243 1.5× 80 0.7× 58 0.6× 17 1.5k
Marga Schepens Netherlands 14 336 0.6× 539 1.1× 83 0.5× 185 1.7× 83 0.9× 20 779
Shalini C. Reshmi United States 20 413 0.8× 1.1k 2.1× 67 0.4× 121 1.1× 87 1.0× 54 1.8k
Jonathan P. Park United States 19 267 0.5× 462 0.9× 98 0.6× 97 0.9× 88 1.0× 36 898
Nadja Bogdanova Germany 18 855 1.6× 823 1.7× 129 0.8× 157 1.5× 54 0.6× 40 1.3k

Countries citing papers authored by Georg Klaus Hinkel

Since Specialization
Citations

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

Fields of papers citing papers by Georg Klaus Hinkel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Georg Klaus Hinkel. 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 Georg Klaus Hinkel. The network helps show where Georg Klaus Hinkel may publish in the future.

Co-authorship network of co-authors of Georg Klaus Hinkel

This figure shows the co-authorship network connecting the top 25 collaborators of Georg Klaus Hinkel. A scholar is included among the top collaborators of Georg Klaus Hinkel 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 Georg Klaus Hinkel. Georg Klaus Hinkel 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.
Hinkel, Georg Klaus, et al.. (2009). Effects of High Doses of Oestrogens and Androgens on Lipoproteins: Observations in the Treatment of Excessive Growth with Sexual Hormones. Experimental and Clinical Endocrinology & Diabetes. 86(4). 17–25.
2.
Sabherwal, Nitin, Fiona Bangs, Rainer Roth, et al.. (2006). Long-range conserved non-coding SHOX sequences regulate expression in developing chicken limb and are associated with short stature phenotypes in human patients. Human Molecular Genetics. 16(2). 210–222. 90 indexed citations
3.
Horn, Denise, Holger Tönnies, Heidemarie Neitzel, et al.. (2004). Minimal clinical expression of the holoprosencephaly spectrum and of Currarino syndrome due to different cytogenetic rearrangements deleting the sonic hedgehog gene and the HLXB9 gene at 7q36.3. American Journal of Medical Genetics Part A. 128A(1). 85–92. 37 indexed citations
4.
Walter, Sabine, Georg Klaus Hinkel, Beate Mitulla, et al.. (2004). Subtelomere FISH in 50 children with mental retardation and minor anomalies, identified by a checklist, detects 10 rearrangements including a de novo balanced translocation of chromosomes 17p13.3 and 20q13.33. American Journal of Medical Genetics Part A. 128A(4). 364–373. 26 indexed citations
5.
Musante, Luciana, Hans-Gerd Kehl, Frank Majewski, et al.. (2003). Spectrum of mutations in PTPN11 and genotype–phenotype correlation in 96 patients with Noonan syndrome and five patients with cardio-facio-cutaneous syndrome. European Journal of Human Genetics. 11(2). 201–206. 111 indexed citations
6.
Horn, Denise, Heidemarie Neitzel, Holger Tönnies, et al.. (2002). Familial MCA/MR syndrome due to inherited submicroscopic translocation t(18;21)(q22.1q21.3) with breakpoint at the Down syndrome critical region. American Journal of Medical Genetics Part A. 117A(3). 236–244. 10 indexed citations
7.
Tiecke, Frank, Patrick Booms, Peter N. Robinson, et al.. (2001). Classic, atypically severe and neonatal Marfan syndrome: twelve mutations and genotype–phenotype correlations in FBN1 exons 24–40. European Journal of Human Genetics. 9(1). 13–21. 98 indexed citations
8.
Bartsch, Oliver, et al.. (1999). FISH studies in 45 patients with Rubinstein-Taybi syndrome: deletions associated with polysplenia, hypoplastic left heart and death in infancy. European Journal of Human Genetics. 7(7). 748–756. 65 indexed citations
9.
Bartsch, Oliver, et al.. (1996). Evidence for a critical region for penoscrotal inversion, hypospadias, and imperforate anus within chromosomal region 13q32.2q34. American Journal of Medical Genetics. 65(3). 218–221. 29 indexed citations
10.
Kuhnle, Ursula, et al.. (1995). Familial pseudohypoaldosteronism: A review on the heterogeneity of the syndrome. Steroids. 60(1). 157–160. 12 indexed citations
11.
Schuffenhauer, Simone, Oliver Bartsch, Markus Stümm, et al.. (1995). DNA, FISH and complementation studies in ICF syndrome: DNA hypomethylation of repetitive and single copy loci and evidence for a trans acting factor. Human Genetics. 96(5). 562–571. 46 indexed citations
12.
Chotai, Kokila, Louise Brueton, Lynne van Herwerden, et al.. (1994). Six cases of 7p deletion: Clinical, cytogenetic, and molecular studies. American Journal of Medical Genetics. 51(3). 270–276. 38 indexed citations
13.
Spranger, Jürgen W., Georg Klaus Hinkel, H Stöß, et al.. (1991). Schimke immuno-osseous dysplasia: A newly recognized multisystem disease. The Journal of Pediatrics. 119(1). 64–72. 78 indexed citations
14.
15.
Lorenz, Peter, et al.. (1990). The craniodigital syndrome of Scott: Report of a second family. American Journal of Medical Genetics. 37(2). 224–226. 6 indexed citations
16.
Hinkel, Georg Klaus, et al.. (1989). A new case of deletion 1q42 syndrome. Clinical Genetics. 35(4). 289–292. 10 indexed citations
17.
Hinkel, Georg Klaus & E Rupprecht. (1989). Hemihypertrophie als Leitsymptom einer Dysplasia epiphysealis hemimelica. Klinische Pädiatrie. 201(1). 58–62. 3 indexed citations
18.
Hinkel, Georg Klaus, et al.. (1970). [Side effects of orotic acid in premature infants].. PubMed. 38(6). 247–52. 1 indexed citations
19.
Rupprecht, E & Georg Klaus Hinkel. (1968). Beitrag zum metaphys�r dysostotischen Minderwuchs. European Journal of Pediatrics. 103(1). 73–80. 4 indexed citations
20.
Hinkel, Georg Klaus, et al.. (1968). Die Ausscheidung von freiem und glucuronosidkonjugiertem Epitestosteron und Testosteron bei Kindern. European Journal of Pediatrics. 102(4). 341–345.

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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