Peter Miny
Impact in
-
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genomics and Rare Diseases
Papers in
-
- Prenatal Screening and Diagnostics 54
- Fetal and Pediatric Neurological Disorders 14
- Assisted Reproductive Technology and Twin Pregnancy 11
- Genetics 46
- Genomic variations and chromosomal abnormalities 29
- Genetic Syndromes and Imprinting 7
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 6
- Co-authors
- Wolfgang Holzgreve (42 shared papers)Isabel Filges (21 shared papers)Sevgi Tercanli (20 shared papers)Dorothee Gänshirt-Ahlert (4 shared papers)Karl Heinimann (13 shared papers)Jürgen Horst (5 shared papers)Henk Garritsen (2 shared papers)Benno Röthlisberger (9 shared papers)
- Journals
- Prenatal Diagnosis (12 papers)Clinical Genetics (4 papers)Human Genetics (3 papers)Fertility and Sterility (2 papers)American Journal of Obstetrics and Gynecology (2 papers)
- Partner nations
- GermanySwitzerlandUnited States
In The Last Decade
Peter Miny
85 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 82
- Pediatrics, Perinatology and Child Health 844
- Genetics 629
- Developmental Biology 26
- Obstetrics and Gynecology 84
- Infectious Diseases 187
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 88 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1993 | 169 | |
| 2 | 1992 | 110 | |
| 3 | 2013 | 64 | |
| 4 | 2010 | 63 | |
| 5 | 2000 | 60 | |
| 6 | 2006 | 53 | |
| 7 | 2019 | 49 | |
| 8 | 1991 | 43 | |
| 9 | 1992 | 40 | |
| 10 | 2009 | 39 | |
| 11 | 2013 | 37 | |
| 12 | 2010 | 36 | |
| 13 | 1998 | 29 | |
| 14 | 1990 | 27 | |
| 15 | 2016 | 27 | |
| 16 | 2011 | 26 | |
| 17 | 1990 | 26 | |
| 18 | 2001 | 24 | |
| 19 | 1993 | 23 | |
| 20 | 1995 | 23 |
About Peter Miny
Peter Miny is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Molecular Biology, Surgery and Public Health, Environmental and Occupational Health, having authored 88 papers that have together received 1.5k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (54 papers), Genomic variations and chromosomal abnormalities (29 papers), Fetal and Pediatric Neurological Disorders (14 papers), Assisted Reproductive Technology and Twin Pregnancy (11 papers), Chromosomal and Genetic Variations (8 papers), Congenital Anomalies and Fetal Surgery (8 papers), Genetic Syndromes and Imprinting (7 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (844 citations), Genetics (629 citations), Developmental Biology (26 citations), Obstetrics and Gynecology (84 citations) and Infectious Diseases (187 citations). Peter Miny has collaborated with scholars based in Germany, Switzerland and United States. Frequent co-authors include Wolfgang Holzgreve, Isabel Filges, Sevgi Tercanli, Dorothee Gänshirt-Ahlert, Karl Heinimann, Jürgen Horst, Henk Garritsen, Benno Röthlisberger, J. Horst and Friedel Wenzel. Their work appears in journals such as Prenatal Diagnosis, Clinical Genetics, Human Genetics, Fertility and Sterility and American Journal of Obstetrics and Gynecology.
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.