Peter Wieacker
Impact in
- Genetics top 1%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
- Reproductive Medicine top 2%
- Sperm and Testicular Function
Papers in
-
- Sexual Differentiation and Disorders 39
- Genetics 72
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 48
- Genomic variations and chromosomal abnormalities 15
- Co-authors
- Susanne Ledig (23 shared papers)Hans‐Hilger Ropers (13 shared papers)Sibylle Jakubiczka (28 shared papers)Ilse Wieland (14 shared papers)Albrecht Röpke (19 shared papers)Thomas F. Wienker (8 shared papers)Markus Stümm (21 shared papers)Petra Muschke (8 shared papers)
- Journals
- Human Genetics (12 papers)Cytogenetic and Genome Research (7 papers)Clinical Genetics (7 papers)Sexual Development (7 papers)Human Mutation (5 papers)
- Partner nations
- GermanyUnited StatesPoland
In The Last Decade
Peter Wieacker
134 papers receiving 3.6k citations
Peers
Comparison fields: 5 of 107
- Genetics 1.6k
- Reproductive Medicine 393
- Molecular Biology 2.4k
- Obstetrics and Gynecology 267
- Urology 206
Countries citing papers authored by Peter Wieacker
This map shows the geographic impact of Peter Wieacker'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 Wieacker with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter Wieacker more than expected).
Fields of papers citing papers by Peter Wieacker
This network shows the impact of papers produced by Peter Wieacker. 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 Wieacker. The network helps show where Peter Wieacker may publish in the future.
Co-authors
The 25 scholars most cited alongside Peter Wieacker, 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 141 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2004 | 178 | |
| 2 | 1995 | 172 | |
| 3 | 2009 | 156 | |
| 4 | 1997 | 150 | |
| 5 | Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids. | 1984 | 137 |
| 6 | 2018 | 121 | |
| 7 | 2007 | 106 | |
| 8 | 2011 | 105 | |
| 9 | 2010 | 103 | |
| 10 | 1985 | 102 | |
| 11 | 2000 | 92 | |
| 12 | 2012 | 74 | |
| 13 | 2012 | 73 | |
| 14 | 2010 | 72 | |
| 15 | 2013 | 69 | |
| 16 | 2001 | 54 | |
| 17 | 2005 | 53 | |
| 18 | 2005 | 52 | |
| 19 | 2018 | 51 | |
| 20 | 2012 | 48 |
About Peter Wieacker
Peter Wieacker is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Reproductive Medicine and Public Health, Environmental and Occupational Health, having authored 141 papers that have together received 3.8k indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (48 papers), Sexual Differentiation and Disorders (39 papers), Prenatal Screening and Diagnostics (17 papers), Genomic variations and chromosomal abnormalities (15 papers), Reproductive Biology and Fertility (13 papers), Hormonal and reproductive studies (12 papers), Sperm and Testicular Function (12 papers) and Chromosomal and Genetic Variations (10 papers). The work is most often cited by research in Genetics (1.6k citations), Reproductive Medicine (393 citations), Molecular Biology (2.4k citations), Obstetrics and Gynecology (267 citations) and Urology (206 citations). Peter Wieacker has collaborated with scholars based in Germany, United States and Poland. Frequent co-authors include Susanne Ledig, Hans‐Hilger Ropers, Sibylle Jakubiczka, Ilse Wieland, Albrecht Röpke, Thomas F. Wienker, Markus Stümm, Petra Muschke, Sabine Kliesch and Kay E. Davies. Their work appears in journals such as Human Genetics, Cytogenetic and Genome Research, Clinical Genetics, Sexual Development and Human Mutation.
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.