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
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 80
- Genomic variations and chromosomal abnormalities 64
- Genomics and Rare Diseases 10
- Genetic Syndromes and Imprinting 10
- Genetics and Neurodevelopmental Disorders 8
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- Genomics and Chromatin Dynamics 9
- Co-authors
- Margareta Mikkelsen (16 shared papers)Stylianos E. Antonarakis (24 shared papers)Morten Krogh Herlin (7 shared papers)Maria Grigoriadou (34 shared papers)Haris Kokotas (27 shared papers)Mats Brännström (1 shared paper)Aravinda Chakravarti (10 shared papers)Stephanie L. Sherman (3 shared papers)
- Journals
- Genomics (10 papers)Prenatal Diagnosis (10 papers)Journal of Medical Genetics (7 papers)Human Mutation (7 papers)Human Genetics (6 papers)
- Partner nations
- GreeceDenmarkUnited States
In The Last Decade
Michael B. Petersen
176 papers receiving 4.2k citations
Peers
Comparison fields: 5 of 132
- Genetics 1.9k
- Pediatrics, Perinatology and Child Health 1.1k
- Sensory Systems 279
- Obstetrics and Gynecology 325
- Molecular Biology 1.6k
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 177 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1996 | 309 | |
| 2 | 1994 | 172 | |
| 3 | 1992 | 159 | |
| 4 | 2020 | 140 | |
| 5 | 2016 | 102 | |
| 6 | Mechanisms of ring chromosome formation in 11 cases of human ring chromosome 21. | 1992 | 90 |
| 7 | 1991 | 79 | |
| 8 | 2000 | 77 | |
| 9 | 2013 | 72 | |
| 10 | 1991 | 71 | |
| 11 | 2007 | 68 | |
| 12 | 2002 | 67 | |
| 13 | 1999 | 64 | |
| 14 | 1998 | 63 | |
| 15 | 1986 | 62 | |
| 16 | 2007 | 62 | |
| 17 | 2014 | 60 | |
| 18 | 1990 | 55 | |
| 19 | 2002 | 55 | |
| 20 | 1993 | 55 |
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 177 papers that have together received 4.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (64 papers), Prenatal Screening and Diagnostics (44 papers), Chromosomal and Genetic Variations (32 papers), Hearing, Cochlea, Tinnitus, Genetics (17 papers), Genomics and Rare Diseases (10 papers), Genetic Syndromes and Imprinting (10 papers), Genomics and Chromatin Dynamics (9 papers) and Genetics and Neurodevelopmental Disorders (8 papers). The work is most often cited by research in Genetics (1.9k citations), Pediatrics, Perinatology and Child Health (1.1k citations), Sensory Systems (279 citations), Obstetrics and Gynecology (325 citations) and Molecular Biology (1.6k 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, Aravinda Chakravarti, Stephanie L. Sherman, Albert Schinzel and Terry Hassold. Their work appears in journals such as Genomics, Prenatal Diagnosis, Journal of Medical Genetics, Human Mutation and Human Genetics.
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.