MB Petersen

936 total citations
10 papers, 645 citations indexed

About

MB Petersen is a scholar working on Molecular Biology, Sensory Systems and Neurology. According to data from OpenAlex, MB Petersen has authored 10 papers receiving a total of 645 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Sensory Systems and 4 papers in Neurology. Recurrent topics in MB Petersen's work include Hearing, Cochlea, Tinnitus, Genetics (4 papers), Vestibular and auditory disorders (3 papers) and Genetic Syndromes and Imprinting (2 papers). MB Petersen is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (4 papers), Vestibular and auditory disorders (3 papers) and Genetic Syndromes and Imprinting (2 papers). MB Petersen collaborates with scholars based in Greece, Denmark and France. MB Petersen's co-authors include PJ Willems, Haris Kokotas, Sofia Douzgou, Carlo Carcassi, Sandro Orrù, Emmanouil Manolakos, Etienne Danis, Dominique Weil, Sedigheh Delmaghani and Barbara Pawlik and has published in prestigious journals such as Acta Paediatrica and Clinical Genetics.

In The Last Decade

MB Petersen

10 papers receiving 629 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
MB Petersen Greece	8	369	361	148	96	89	10	645
Heping Yu United States	19	376 1.0×	518 1.4×	220 1.5×	82 0.9×	123 1.4×	37	909
Mariette Wagenaar Netherlands	11	749 2.0×	612 1.7×	184 1.2×	92 1.0×	89 1.0×	12	1.1k
Haris Kokotas Greece	14	363 1.0×	197 0.5×	101 0.7×	107 1.1×	32 0.4×	31	637
Asadollah Aghaie France	13	641 1.7×	403 1.1×	153 1.0×	76 0.8×	97 1.1×	16	904
Hideki Mutai Japan	20	663 1.8×	626 1.7×	195 1.3×	91 0.9×	125 1.4×	63	1.2k
Tenesha N. Smith United States	7	534 1.4×	456 1.3×	351 2.4×	88 0.9×	85 1.0×	7	857
Nele Hilgert Belgium	11	410 1.1×	585 1.6×	237 1.6×	125 1.3×	144 1.6×	12	847
Judith S. Kempfle United States	13	178 0.5×	380 1.1×	113 0.8×	24 0.3×	131 1.5×	26	653
Suoqiang Zhai China	17	411 1.1×	441 1.2×	146 1.0×	30 0.3×	115 1.3×	42	781
Tzy-Wen L. Gong United States	14	219 0.6×	292 0.8×	108 0.7×	51 0.5×	84 0.9×	17	568

Countries citing papers authored by MB Petersen

Since Specialization

Citations

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

Fields of papers citing papers by MB Petersen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of MB Petersen

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

All Works

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10 of 10 papers shown

1.

Orrù, Sandro, et al.. (2011). High frequency of the TARDBP p.Ala382Thr mutation in Sardinian patients with amyotrophic lateral sclerosis. Clinical Genetics. 81(2). 172–178. 40 indexed citations

2.

Douzgou, Sofia & MB Petersen. (2011). Clinical variability of genetic isolates of Cohen syndrome. Clinical Genetics. 79(6). 501–506. 38 indexed citations

3.

Kokotas, Haris & MB Petersen. (2010). Clinical and molecular aspects of aniridia. Clinical Genetics. 77(5). 409–420. 88 indexed citations

4.

Hilgert, Nele, Fatemeh Alasti, Nele Dieltjens, et al.. (2008). Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11. Clinical Genetics. 74(3). 223–232. 55 indexed citations

5.

Petersen, MB, et al.. (2007). Sex‐linked deafness. Clinical Genetics. 73(1). 14–23. 57 indexed citations

6.

Kokotas, Haris, MB Petersen, & PJ Willems. (2007). Mitochondrial deafness. Clinical Genetics. 71(5). 379–391. 154 indexed citations

7.

Petersen, MB & PJ Willems. (2006). Non‐syndromic, autosomal‐recessive deafness. Clinical Genetics. 69(5). 371–392. 153 indexed citations

8.

Petersen, MB. (2002). Non‐syndromic autosomal‐dominant deafness. Clinical Genetics. 62(1). 1–13. 52 indexed citations

9.

Gyftodimou, Jolanda, et al.. (1999). Angelman syndrome with uniparental disomy due to paternal meiosis II nondisjunction. Clinical Genetics. 55(6). 483–486. 6 indexed citations

10.

Hansen, Claus Thustrup, et al.. (1997). Clinical features and molecular genetic analysis of a boy with Prader‐Willi syndrome caused by an imprinting defect. Acta Paediatrica. 86(8). 906–910. 2 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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