Axel Bohring

1.8k total citations
17 papers, 609 citations indexed

About

Axel Bohring is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Axel Bohring has authored 17 papers receiving a total of 609 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 6 papers in Molecular Biology and 3 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Axel Bohring's work include Congenital limb and hand anomalies (3 papers), Connective tissue disorders research (3 papers) and Genomics and Rare Diseases (2 papers). Axel Bohring is often cited by papers focused on Congenital limb and hand anomalies (3 papers), Connective tissue disorders research (3 papers) and Genomics and Rare Diseases (2 papers). Axel Bohring collaborates with scholars based in Germany, United States and Netherlands. Axel Bohring's co-authors include Christiane Spaich, Ute Hehr, Claudia M. Haase, Albrecht Röpke, Susanne Ledig, Peter Wieacker, Thomas Stamm, Saadettin Sel, Anja Harder and Jens Schittenhelm and has published in prestigious journals such as The American Journal of Human Genetics, American Journal Of Pathology and The American Journal of Surgical Pathology.

In The Last Decade

Axel Bohring

17 papers receiving 585 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Axel Bohring Germany 13 361 203 94 88 65 17 609
N S Thomas United Kingdom 15 580 1.6× 257 1.3× 52 0.6× 80 0.9× 32 0.5× 31 768
Eeva‐Mari Jouhilahti Finland 15 507 1.4× 121 0.6× 212 2.3× 89 1.0× 10 0.2× 23 830
Gillian L. Hall United Kingdom 18 304 0.8× 44 0.2× 26 0.3× 48 0.5× 60 0.9× 32 1.0k
Manuela Priolo Italy 18 542 1.5× 404 2.0× 16 0.2× 35 0.4× 90 1.4× 48 882
Fotios D. Vrionis United States 12 213 0.6× 120 0.6× 172 1.8× 28 0.3× 15 0.2× 15 541
Jacqueline Siegel‐Bartelt Canada 8 820 2.3× 477 2.3× 19 0.2× 38 0.4× 36 0.6× 10 1.1k
Miriam Entesarian Sweden 12 295 0.8× 168 0.8× 41 0.4× 16 0.2× 32 0.5× 15 626
Judith Goodship United Kingdom 11 729 2.0× 517 2.5× 50 0.5× 30 0.3× 14 0.2× 13 978
Aleksander Jamsheer Poland 16 433 1.2× 397 2.0× 12 0.1× 84 1.0× 31 0.5× 77 731
Stephanie Spranger Germany 14 509 1.4× 606 3.0× 21 0.2× 35 0.4× 12 0.2× 34 860

Countries citing papers authored by Axel Bohring

Since Specialization
Citations

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

Fields of papers citing papers by Axel Bohring

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Axel Bohring. 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 Axel Bohring. The network helps show where Axel Bohring may publish in the future.

Co-authorship network of co-authors of Axel Bohring

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

All Works

17 of 17 papers shown
1.
Stock, Friedrich, Marcel Hanisch, Sarah Lechner, et al.. (2021). Prepubertal Periodontitis in a Patient with Combined Classical and Periodontal Ehlers–Danlos Syndrome. Biomolecules. 11(2). 149–149. 5 indexed citations
2.
Nagel, Inga, Florian Oyen, Reinhard Schneppenheim, et al.. (2016). Molecular Analysis of Hybrid Neurofibroma/Schwannoma Identifies Common Monosomy 22 and α-T-Catenin/CTNNA3 as a Novel Candidate Tumor Suppressor. American Journal Of Pathology. 186(12). 3285–3296. 25 indexed citations
3.
Zirn, Birgit, Luitgard Graul‐Neumann, M. Suckfüll, et al.. (2013). Spectrum of novel mutations found in Waardenburg syndrome types 1 and 2: implications for molecular genetic diagnostics. BMJ Open. 3(3). e001917–e001917. 38 indexed citations
4.
Harder, Anja, Christian Hagel, Jens Schittenhelm, et al.. (2012). Hybrid Neurofibroma/Schwannoma is Overrepresented Among Schwannomatosis and Neurofibromatosis Patients. The American Journal of Surgical Pathology. 36(5). 702–709. 84 indexed citations
5.
Bohnhorst, Bettina, I. Luhmer, Susanne Morlot, et al.. (2010). Novel CHD7 mutations contributing to the mutation spectrum in patients with CHARGE syndrome. European Journal of Medical Genetics. 53(5). 280–285. 14 indexed citations
6.
Mitter, Diana, Barbara Delle Chiaie, Hermann‐Josef Lüdecke, et al.. (2010). Genotype–phenotype correlation in eight new patients with a deletion encompassing 2q31.1. American Journal of Medical Genetics Part A. 152A(5). 1213–1224. 39 indexed citations
7.
Allanson, Judith, Axel Bohring, Andreas Dufke, et al.. (2010). The face of Noonan syndrome: Does phenotype predict genotype. American Journal of Medical Genetics Part A. 152A(8). 1960–1966. 56 indexed citations
8.
Heinritz, Wolfram, Ulrike Hüffmeier, Bianca Miterski, et al.. (2009). New Mutations of EXT1 and EXT2 Genes in German Patients with Multiple Osteochondromas. Annals of Human Genetics. 73(3). 283–291. 24 indexed citations
9.
Bohring, Axel, Thomas Stamm, Christiane Spaich, et al.. (2009). WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes. The American Journal of Human Genetics. 85(1). 97–105. 156 indexed citations
10.
Frank, Valeska, Nadina Ortiz Brüchle, Suzanna G.M. Frints, et al.. (2007). Aberrant splicing is a common mutational mechanism inMKS1, a key player in Meckel-Gruber syndrome. Human Mutation. 28(6). 638–639. 17 indexed citations
11.
Kaname, Tadashi, Kumiko Yanagi, Yasutsugu Chinen, et al.. (2007). Mutations in CD96, a Member of the Immunoglobulin Superfamily, Cause a Form of the C (Opitz Trigonocephaly) Syndrome. The American Journal of Human Genetics. 81(4). 835–841. 34 indexed citations
12.
Hehr, Ute, Goekhan Uyanik, Claudia Groß, et al.. (2007). Novel POMGnT1 mutations define broader phenotypic spectrum of muscle–eye–brain disease. Neurogenetics. 8(4). 279–288. 41 indexed citations
13.
Bohring, Axel, et al.. (2006). New cases of Bohring–Opitz syndrome, update, and critical review of the literature. American Journal of Medical Genetics Part A. 140A(12). 1257–1263. 22 indexed citations
14.
Bohring, Axel, Margherita Silengo, Margherita Lerone, et al.. (1999). Severe end of Opitz trigonocephaly (C) syndrome or new syndrome?. American Journal of Medical Genetics. 85(5). 438–446. 43 indexed citations
15.
Bohring, Axel, et al.. (1997). A further case of vertical transmission of proximal femoral focal deficiency?. American Journal of Medical Genetics. 71(2). 194–196. 5 indexed citations
16.
Bohring, Axel & Hans Oppermann. (1997). A further case of vertical transmission of proximal femoral focal deficiency?. PubMed. 71(2). 194–6. 5 indexed citations
17.
Bohring, Axel, Josef Sonntag, Heinz C. Schröder, & H. ‐R. Wiedemann. (1996). Unusual complex of ventral midline anomalies: A multiple congenital anomalies/mental retardation syndrome. American Journal of Medical Genetics. 66(4). 453–456. 1 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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