Peter N�rnberg

513 total citations
15 papers, 362 citations indexed

About

Peter N�rnberg is a scholar working on Molecular Biology, Neurology and Rheumatology. According to data from OpenAlex, Peter N�rnberg has authored 15 papers receiving a total of 362 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 4 papers in Neurology and 3 papers in Rheumatology. Recurrent topics in Peter N�rnberg's work include Neurofibromatosis and Schwannoma Cases (4 papers), Mitochondrial Function and Pathology (2 papers) and Forensic and Genetic Research (2 papers). Peter N�rnberg is often cited by papers focused on Neurofibromatosis and Schwannoma Cases (4 papers), Mitochondrial Function and Pathology (2 papers) and Forensic and Genetic Research (2 papers). Peter N�rnberg collaborates with scholars based in Germany, United States and Hungary. Peter N�rnberg's co-authors include Jörg T. Epplen, J. Hundrieser, Lutz Roewer, Sigrid Tinschert, Gundula Thiel, Frank Weber, Annegret Buske, Hans Zischler, Karl Sperling and Jörg Schmidtke and has published in prestigious journals such as Glia, Human Mutation and Human Genetics.

In The Last Decade

Peter N�rnberg

15 papers receiving 349 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Peter N�rnberg Germany 9 133 107 75 54 51 15 362
Keiichi Kawamoto Japan 14 99 0.7× 47 0.4× 58 0.8× 28 0.5× 85 1.7× 49 567
Margot A. Cousin United States 14 304 2.3× 223 2.1× 21 0.3× 29 0.5× 25 0.5× 42 660
Christopher W. Whelan United States 8 214 1.6× 78 0.7× 49 0.7× 11 0.2× 14 0.3× 13 504
Leonard Prouty United States 11 191 1.4× 157 1.5× 12 0.2× 14 0.3× 39 0.8× 17 401
Maika Onishi United States 10 106 0.8× 43 0.4× 14 0.2× 10 0.2× 12 0.2× 19 435
Ashley N. Sigafoos United States 9 188 1.4× 63 0.6× 11 0.1× 22 0.4× 11 0.2× 15 330
Kim Moorwood United Kingdom 13 599 4.5× 257 2.4× 13 0.2× 51 0.9× 28 0.5× 18 719
A Castenholz Germany 10 78 0.6× 11 0.1× 23 0.3× 35 0.6× 22 0.4× 39 340
Selby Chen United States 9 69 0.5× 158 1.5× 12 0.2× 31 0.6× 17 0.3× 23 563
Gianfranco Bellipanni United States 15 409 3.1× 71 0.7× 10 0.1× 29 0.5× 22 0.4× 26 590

Countries citing papers authored by Peter N�rnberg

Since Specialization
Citations

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

Fields of papers citing papers by Peter N�rnberg

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peter N�rnberg. 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 Peter N�rnberg. The network helps show where Peter N�rnberg may publish in the future.

Co-authorship network of co-authors of Peter N�rnberg

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

All Works

15 of 15 papers shown
1.
Pusch, Carsten M., Birgit Meyer, Susan Kupka, et al.. (2004). Refinement of the DFNA4 locus to a 1.44�Mb region in 19q13.33. Journal of Molecular Medicine. 82(6). 398–402. 3 indexed citations
2.
Bercovitch, Fred B., Anja Widdig, Andrea Trefilov, et al.. (2003). A longitudinal study of age-specific reproductive output and body condition among male rhesus macaques, Macaca mulatta. Die Naturwissenschaften. 90(7). 309–312. 65 indexed citations
3.
N�rnberg, Peter, et al.. (2001). Metaphyseal dysplasia: A new autosomal dominant type in a large German kindred. American Journal of Medical Genetics. 101(1). 74–77. 5 indexed citations
4.
Harder, Anja, K. Jendroska, Friedmar R. Kreuz, et al.. (1999). Novel twelve-generation kindred of fatal familial insomnia from Germany representing the entire spectrum of disease expression. American Journal of Medical Genetics. 87(4). 311–316. 27 indexed citations
5.
Buske, Annegret, et al.. (1999). RecurrentNF1 gene mutation in a patient with oligosymptomatic neurofibromatosis type 1 (NF1). American Journal of Medical Genetics. 86(4). 328–330. 11 indexed citations
6.
Harder, Anja, Hartmut Peters, Sven Hoffmeyer, et al.. (1999). Two independent mutations in a family with neurofibromatosis type 1 (NF1). American Journal of Medical Genetics. 83(1). 6–12. 22 indexed citations
7.
Harder, Anja, et al.. (1999). A novel 5-bp deletion in exon 30 of the neurofibromatosis type 1 (NF1) gene. Human Mutation. 13(3). 259–259. 1 indexed citations
8.
Tinschert, Sigrid, et al.. (1999). McCune-Albright syndrome: Clinical and molecular evidence of mosaicism in an unusual giant patient. American Journal of Medical Genetics. 83(2). 100–108. 17 indexed citations
9.
10.
Robinson, Peter N., et al.. (1995). Two recurrent nonsense mutations and a 4 bp deletion in a quasi-symmetric element in exon 37 of the NF1 gene. Human Genetics. 96(1). 95–98. 40 indexed citations
11.
Gomolka, Maria, J. Hundrieser, Peter N�rnberg, et al.. (1994). Selected di- and tetranucleotide microsatellites from chromosomes 7, 12, 14, and Y in various Eurasian populations. Human Genetics. 93(5). 592–6. 35 indexed citations
12.
N�rnberg, Peter, Gundula Thiel, Frank Weber, & Jörg T. Epplen. (1993). Changes of telomere lengths in human intracranial tumours. Human Genetics. 91(2). 190–2. 44 indexed citations
13.
14.
Rieß, Olaf, et al.. (1989). RELP-discordance within the human phenylalanine hydroxylase locus. Human Genetics. 83(2). 199–201. 3 indexed citations
15.
N�rnberg, Peter, Lutz Roewer, Heidemarie Neitzel, et al.. (1989). DNA Fingerprinting with the oligonucleotide probe (CAC)5/(GTG)5: somatic stability and germline mutations. Human Genetics. 84(1). 75–78. 77 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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