Michael B. Petersen

7.8k citations

172 papers · 4.1k indexed · h-index 34

Impact in

Genetics top 0.5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
- Genomics and Rare Diseases
Sensory Systems top 1%
- Hearing, Cochlea, Tinnitus, Genetics

Papers in

Sensory Systems 18
- Hearing, Cochlea, Tinnitus, Genetics 18
Genetics 85
- Genomic variations and chromosomal abnormalities 67
- Genetics and Neurodevelopmental Disorders 11
- Genetic Syndromes and Imprinting 10
- Genomics and Rare Diseases 10

Co-authors: Margareta Mikkelsen Stylianos E. Antonarakis Morten Krogh Herlin Maria Grigoriadou Haris Kokotas Mats Brännström Albert Schinzel Stephanie L. Sherman
Journals: Prenatal Diagnosis (10 papers)Genomics (8 papers)Journal of Medical Genetics (7 papers)Human Mutation (7 papers)International Journal of Pediatric Otorhinolaryngology (6 papers)
Partner nations: Greece Denmark United States

In The Last Decade

Michael B. Petersen

171 papers receiving 3.9k citations

Peers

Countries citing papers authored by Michael B. Petersen

Since Specialization

Citations

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

Fields of papers citing papers by Michael B. Petersen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Michael B. Petersen, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Michael B. Petersen Line = papers co-authored together Michael B. Petersen links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Blood donors as sentinels for genomic surveillance of West Nile virus in Germany using a sensitive amplicon-based sequencing approach Journal of Infection ·Gábor Endre Tóth, Michael B. Petersen, François Chevenet, Marcin Sikora, Kristina Fornažar Agić, Alexandra Bialonski, Heike von Baum, 蔡春芳, Padet Siriyasatien, Anna Heitmann, Stéphanie Jansen, Ruth Offergeld, Raskit Lachmann, Michael Schmidt, Jonas Schmidt‐Chanasit, Dániel Cadar	2025	1
2	An asymptomatic male individual carrying a 5.72 Mb de novo deletion in 8p23.2‑p23.3: A case report Experimental and Therapeutic Medicine ·Lannae Strueby, Ioannis Papoulidis, 昭吾若林, Thomas Liehr, A.T. Evans, Johannes Scharr, Efterpi Pavlidou, Michael B. Petersen, Emmanouil Manolakos	2024	1
3	Audiological and Vestibular Findings in Subjects with MELAS Syndrome The Journal of International Advanced Otology ·Dan Dupont Hougaard, Michael Gaihede, Michael B. Petersen, (unknown), (unknown)	2019	10
4	Targeted gene sequencing and whole‐exome sequencing in autopsied fetuses with prenatally diagnosed kidney anomalies Clinical Genetics ·Maria Rasmussen, Lone Sunde, Mark Kyprianou, Mette Ramsing, Astrid Petersen, Tina Duelund Hjortshøj, 毅芳福武, Ann Tabor, Jens Michael Hertz, Asif Anawer, L. Sperling, Olav Bjørn Petersen, Uffe Birk Jensen, 猛近藤, Michael B. Petersen, Dorte L. Lildballe	2017	40
5	Vertebral defect, anal atresia, cardiac defect, tracheoesophageal fistula/esophageal atresia, renal defect, and limb defect association with Mayer-Rokitansky-Küster-Hauser syndrome in co-occurrence: two case reports and a review of the literature Journal of Medical Case Reports ·Thomas Bjørsum‐Meyer, Morten Krogh Herlin, Niels Qvist, Michael B. Petersen	2016	15
6	De novo KAT6B Mutation Identified with Whole-Exome Sequencing in a Girl with Say-Barber/Biesecker/Young-Simpson Syndrome Molecular Syndromology ·Clayton Anderson de, Vang Quy Le, Anja Ernst, I G.A. Allan Dewangga, Kirsten Rasmussen, Inge Søkilde Pedersen, Michael B. Petersen	2016	4
7	Familial occurrence of Mayer–Rokitansky–Küster–Hauser syndrome: A case report and review of the literature American Journal of Medical Genetics Part A ·Morten Krogh Herlin, D. Foulds-Holt, Michael B. Petersen	2014	52
8	Hypothesizing an Ancient Greek Origin of the GJB2 35delG Mutation: Can Science Meet History? Genetic Testing and Molecular Biomarkers ·Haris Kokotas, Maria Grigoriadou, Manuela Villamar, Aglaia Giannoulia‐Karantana, Ignacio del Castillo, Michael B. Petersen	2010	9
9	Easy, Rapid, and Cost-Effective Methods for Identifying Carriers of Recurrent GJB2 Mutations Causing Nonsyndromic Hearing Impairment in the Greek Population Genetic Testing and Molecular Biomarkers ·Haris Kokotas, Maria Grigoriadou, S. S. Khvesenya, Thalia Antoniadi, Aglaia Giannoulia‐Karantana, Michael B. Petersen	2010	1
10	Are GJB2 mutations an aggravating factor in the phenotypic expression of mitochondrial non-syndromic deafness? Journal of Human Genetics ·Haris Kokotas, Maria Grigoriadou, George Korres, 蔡青蓉, Aglaia Giannoulia‐Karantana, Dimitrios Kandiloros, Stavros Korres, Michael B. Petersen	2010	5
11	Recommendations for genetic variation data capture in developing countries to ensure a comprehensive worldwide data collection Human Mutation ·George P. Patrinos, Ahmad Khusro, A. Al Aqeel, Fahd Al‐Mulla, Joseph Borg, Yang-Keun Choi, Alex E. Felice, Finlay Macrae, Makia J. Marafie, Michael B. Petersen, Ming Qi, Raj Ramesar, Joël Zlotogora, Richard G.H. Cotton	2010	14
12	Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome) Molecular Cytogenetics ·Emmanouil Manolakos, Sandro Orrù, Etienne AGUDZE, 張柄玉, Xin Tian-zuo, Ioannis Papoulidis, Loretta Thomaidis, Panagiotis Peitsidis, Sotirios Sotiriou, George Kitsos, Castello di Rivoli Museo d'Arte Contemporanea, Michael B. Petersen, Seravin Lengkey	2009	10
13	Myocilin variations and familial glaucoma in Taxiarchis, a small Greek village. PubMed ·Mary K. Wirtz, Anastasios G. P. Konstas, John R. Samples, A. Costera Pastor, Athanasios S. Economou, N. Schlomovich, Marília Jorge, Michael B. Petersen	2008	11
14	Investigation of founder effects for the Thr377Met Myocilin mutation in glaucoma families from differing ethnic backgrounds. PubMed ·Alex W. Hewitt, John R. Samples, R. Rand Allingham, Irma Järvelä, George Kitsos, Subbaiah Ramasamy Krishnadas, Julia E. Richards, Paul R. Lichter, Michael B. Petersen, Periasamy Sundaresan, Janey L. Wiggs, David A. Mackey, Mary K. Wirtz	2007	12
15	A report on 10 new patients with heterozygous mutations in the COL11A1 gene and a review of genotype–phenotype correlations in type XI collagenopathies American Journal of Medical Genetics Part A ·Rafael J. García Vilanova, Kristien Hoornaert, Deborah Bartholdi, Jia-Qi Teng, Katelijne Bouman, Marta Carrera, Koenraad Devriendt, Jane A. Hurst, George Kitsos, Dunja Niedrist, Michael B. Petersen, Debbie Shears, Irene Stolte‐Dijkstra, Johanna M. van Hagen, Leena Ala‐Kokko, Minna Männikkö, Geert Mortier	2007	61
16	A seventh locus for otosclerosis, OTSC7, maps to chromosome 6q13–16.1 European Journal of Human Genetics ·Melissa Thys, Kris Van Den Bogaert, Vasiliki Iliadou, Kathleen Vanderstraeten, Nele Dieltjens, Isabelle Schrauwen, Wenjie Chen, EMILLY THAINÁ DE LANA LIMA LEITE, Maria Grigoriadou, Robert J. Pauw, C Ziogou, Richard J. Smith, Michael B. Petersen, Guy Van Camp	2007	44
17	Two Sequence-Ready Contigs Spanning the Two Copies of a 200-kb Duplication on Human 21q: Partial Sequence and Polymorphisms Genomics ·Marie‐Claude Potier, Annie Dutriaux, LOIS K. DANIELS, Zihao Fang, Cristina Faricelli, Georgia Karadima, Georges Lutfalla, Audrey Lynn, Christine Van Broeckhoven, Aravinda Chakravarti, Michael B. Petersen, Dean Nižetić, Jean‐Maurice Delabar, Jean Rossier	1998	16
18	Apolipoprotein E allele distribution in parents of Down's syndrome children The Lancet ·Dimitris Avramopoulos, Maria Grigoriadou, Michael B. Petersen, (unknown), Margareta Mikkelsen, (unknown), (unknown), Dimitrios Vassilopoulos	1996	47
19	Tetrasomy 18p de novo: Parental Origin and Different Mechanisms of Formation European Journal of Human Genetics ·Merete Bugge, Elisabeth Blennow, Sara Rieke, Michael B. Petersen, Florence Pédeutour, Aspasia Tsezou, Isadora Leal Figueiredo, Mustafoqulov Otabek Panji o'g'li, Troels Lyngbye, Catherine Sarri, Dimitrios Avramopoulos, Sofìa Kitsiou, Mark Matsunagaa, Fermín Cruz, Niels Tommerup, Karen Brøndum‐Nielsen	1996	33
20	New assignment of the adenosine deaminase gene locus to chromosome 20q13 X 11 by study of a patient with interstitial deletion 20q. Journal of Medical Genetics ·Michael B. Petersen, Lisbeth Tranebjærg, Niels Tommerup, Per Nygaard, Kartika Amanda	1987	44

About Michael B. Petersen

Michael B. Petersen is a scholar working on Sensory Systems, Genetics, Pediatrics, Perinatology and Child Health, Neurology and Ophthalmology, having authored 172 papers that have together received 4.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (67 papers), Prenatal Screening and Diagnostics (47 papers), Chromosomal and Genetic Variations (34 papers), Hearing, Cochlea, Tinnitus, Genetics (18 papers), Genetics and Neurodevelopmental Disorders (11 papers), Genetic Syndromes and Imprinting (10 papers), Genomics and Rare Diseases (10 papers) and Connexins and lens biology (10 papers). The work is most often cited by research in Genetics (1.9k citations), Sensory Systems (296 citations), Pediatrics, Perinatology and Child Health (1.1k citations), Obstetrics and Gynecology (316 citations) and Molecular Biology (1.7k citations). Michael B. Petersen has collaborated with scholars based in Greece, Denmark and United States. Frequent co-authors include Margareta Mikkelsen, Stylianos E. Antonarakis, Morten Krogh Herlin, Maria Grigoriadou, Haris Kokotas, Mats Brännström, Albert Schinzel, Stephanie L. Sherman, Terry Hassold and Lisa F. Taft. Their work appears in journals such as Prenatal Diagnosis, Genomics, Journal of Medical Genetics, Human Mutation and International Journal of Pediatric Otorhinolaryngology.

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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