Michael B. Petersen
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
- Genetics 85
- Genomic variations and chromosomal abnormalities 67
- Genetics and Neurodevelopmental Disorders 11
- Genetic Syndromes and Imprinting 10
- Genomics and Rare Diseases 10
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- Connexins and lens biology 10
- Co-authors
- Margareta Mikkelsen (14 shared papers)Morten Krogh Herlin (7 shared papers)Stylianos E. Antonarakis (22 shared papers)Maria Grigoriadou (34 shared papers)Haris Kokotas (27 shared papers)Mats Brännström (1 shared paper)Stephanie L. Sherman (3 shared papers)Albert Schinzel (8 shared papers)
- 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
- GreeceDenmarkUnited States
In The Last Decade
Michael B. Petersen
171 papers receiving 3.9k citations
Peers
Comparison fields: 5 of 130
- Genetics 1.9k
- Sensory Systems 296
- Pediatrics, Perinatology and Child Health 1.1k
- Obstetrics and Gynecology 316
- Molecular Biology 1.7k
Countries citing papers authored by Michael B. Petersen
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
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-authors
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.
All Works
Showing the 20 most-cited of 172 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1996 | 290 | |
| 2 | 1992 | 150 | |
| 3 | 1994 | 141 | |
| 4 | 2020 | 127 | |
| 5 | 2016 | 99 | |
| 6 | Mechanisms of ring chromosome formation in 11 cases of human ring chromosome 21. | 1992 | 86 |
| 7 | 1991 | 75 | |
| 8 | 1991 | 68 | |
| 9 | 2000 | 67 | |
| 10 | 2002 | 63 | |
| 11 | 2013 | 62 | |
| 12 | 2007 | 61 | |
| 13 | 1999 | 59 | |
| 14 | 2007 | 58 | |
| 15 | 2002 | 56 | |
| 16 | 1998 | 56 | |
| 17 | 1993 | 55 | |
| 18 | 2014 | 52 | |
| 19 | 2014 | 50 | |
| 20 | 1992 | 50 |
About Michael B. Petersen
Michael B. Petersen is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Sensory Systems, 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, Morten Krogh Herlin, Stylianos E. Antonarakis, Maria Grigoriadou, Haris Kokotas, Mats Brännström, Stephanie L. Sherman, Albert Schinzel, Aravinda Chakravarti and Terry Hassold. 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.