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
- Genetics and Neurodevelopmental Disorders
Papers in
-
- Prenatal Screening and Diagnostics 55
- Fetal and Pediatric Neurological Disorders 13
- Assisted Reproductive Technology and Twin Pregnancy 10
- Genetics 45
- Genomic variations and chromosomal abnormalities 28
- Genetic Syndromes and Imprinting 7
- Hemoglobinopathies and Related Disorders 6
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
- Co-authors
- Wolfgang Holzgreve (49 shared papers)Isabel Filges (21 shared papers)Sevgi Tercanli (24 shared papers)Karl Heinimann (13 shared papers)Dorothee Gänshirt-Ahlert (4 shared papers)Jürgen Horst (6 shared papers)Benno Röthlisberger (9 shared papers)Henk Garritsen (2 shared papers)
- Journals
- Prenatal Diagnosis (12 papers)Clinical Genetics (4 papers)Human Genetics (3 papers)Ultraschall in der Medizin - European Journal of Ultrasound (3 papers)Child s Nervous System (2 papers)
- Partner nations
- GermanySwitzerlandUnited States
In The Last Decade
Peter Miny
90 papers receiving 1.5k citations
Peers
Comparison fields: 5 of 84
- Pediatrics, Perinatology and Child Health 820
- Genetics 616
- Developmental Biology 28
- Obstetrics and Gynecology 69
- Infectious Diseases 158
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 97 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1993 | 169 | |
| 2 | 1992 | 119 | |
| 3 | 2000 | 70 | |
| 4 | 2013 | 70 | |
| 5 | 2006 | 70 | |
| 6 | 2010 | 63 | |
| 7 | 2019 | 49 | |
| 8 | 2009 | 47 | |
| 9 | 1991 | 43 | |
| 10 | 2011 | 43 | |
| 11 | 2010 | 41 | |
| 12 | 1992 | 40 | |
| 13 | 2013 | 40 | |
| 14 | 1998 | 36 | |
| 15 | 2008 | 33 | |
| 16 | 2016 | 29 | |
| 17 | 1993 | 28 | |
| 18 | 1990 | 28 | |
| 19 | 1987 | 27 | |
| 20 | 1990 | 27 |
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 97 papers that have together received 1.7k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (55 papers), Genomic variations and chromosomal abnormalities (28 papers), Fetal and Pediatric Neurological Disorders (13 papers), Assisted Reproductive Technology and Twin Pregnancy (10 papers), Congenital Anomalies and Fetal Surgery (8 papers), Genetic Syndromes and Imprinting (7 papers), Hemoglobinopathies and Related Disorders (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (820 citations), Genetics (616 citations), Developmental Biology (28 citations), Obstetrics and Gynecology (69 citations) and Infectious Diseases (158 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, Dorothee Gänshirt-Ahlert, Jürgen Horst, Benno Röthlisberger, Henk Garritsen, Friedel Wenzel and J. Horst. Their work appears in journals such as Prenatal Diagnosis, Clinical Genetics, Human Genetics, Ultraschall in der Medizin - European Journal of Ultrasound and Child s Nervous System.
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.