Peter Miny
Impact in
-
- Prenatal Screening and Diagnostics
- Developmental Biology top 5%
- Congenital limb and hand anomalies
Papers in
-
- Prenatal Screening and Diagnostics 63
- Fetal and Pediatric Neurological Disorders 3
- Genetics 36
- Genomic variations and chromosomal abnormalities 12
- Genomics and Rare Diseases 11
- Hemoglobinopathies and Related Disorders 5
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
- Genetic and Kidney Cyst Diseases 4
- Co-authors
- Wolfgang Holzgreve (63 shared papers)Isabel Filges (23 shared papers)Sevgi Tercanli (26 shared papers)Karl Heinimann (13 shared papers)Jürgen Horst (7 shared papers)Dorothee Gänshirt-Ahlert (6 shared papers)J. Horst (11 shared papers)Henk Garritsen (3 shared papers)
- Journals
- Prenatal Diagnosis (15 papers)The Lancet (7 papers)Clinical Genetics (5 papers)Human Genetics (3 papers)Ultraschall in der Medizin - European Journal of Ultrasound (3 papers)
- Partner nations
- GermanySwitzerlandUnited States
In The Last Decade
Peter Miny
114 papers receiving 2k citations
Peers
Comparison fields: 5 of 83
- Pediatrics, Perinatology and Child Health 1k
- Developmental Biology 53
- Genetics 624
- Genetics 55
- Obstetrics and Gynecology 58
Countries citing papers authored by Peter Miny
This map shows the geographic impact of Peter Miny'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 Miny with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter Miny more than expected).
Fields of papers citing papers by Peter Miny
This network shows the impact of papers produced by Peter Miny. 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 Miny. The network helps show where Peter Miny may publish in the future.
Co-authors
The 25 scholars most cited alongside Peter Miny, 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 123 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 178 | |
| 2 | 1993 | 175 | |
| 3 | 1992 | 119 | |
| 4 | 2002 | 83 | |
| 5 | 2013 | 81 | |
| 6 | 2010 | 73 | |
| 7 | 2000 | 72 | |
| 8 | 2006 | 72 | |
| 9 | 2019 | 56 | |
| 10 | 2009 | 51 | |
| 11 | 2010 | 47 | |
| 12 | 1991 | 46 | |
| 13 | 1992 | 45 | |
| 14 | 2011 | 44 | |
| 15 | 1991 | 42 | |
| 16 | 1998 | 42 | |
| 17 | 2013 | 40 | |
| 18 | 2008 | 33 | |
| 19 | 1994 | 32 | |
| 20 | 1992 | 31 |
About Peter Miny
Peter Miny is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Developmental Biology, Genetics and Obstetrics and Gynecology, having authored 123 papers that have together received 2.3k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (63 papers), Genomic variations and chromosomal abnormalities (12 papers), Genomics and Rare Diseases (11 papers), Hemoglobinopathies and Related Disorders (5 papers), Congenital limb and hand anomalies (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers), Genetic and Kidney Cyst Diseases (4 papers) and Fetal and Pediatric Neurological Disorders (3 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (1k citations), Developmental Biology (53 citations), Genetics (624 citations), Genetics (55 citations) and Obstetrics and Gynecology (58 citations). Peter Miny has collaborated with scholars based in Germany, Switzerland and United States. Frequent co-authors include Wolfgang Holzgreve, Isabel Filges, Sevgi Tercanli, Karl Heinimann, Jürgen Horst, Dorothee Gänshirt-Ahlert, J. Horst, Henk Garritsen, Benno Röthlisberger and Friedel Wenzel. Their work appears in journals such as Prenatal Diagnosis, The Lancet, Clinical Genetics, Human Genetics and Ultraschall in der Medizin - European Journal of Ultrasound.
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.