W. Schempp
Impact in
- Genetics top 0.5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
- Animal Genetics and Reproduction
- Reproductive Medicine top 1%
- Sperm and Testicular Function
Papers in
- Genetics 94
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 63
- Genomic variations and chromosomal abnormalities 25
- Animal Genetics and Reproduction 13
-
- Genomics and Chromatin Dynamics 21
- Sexual Differentiation and Disorders 18
- Co-authors
- Gerd Scherer (10 shared papers)U. Wolf (8 shared papers)Juan J. Pasantes (12 shared papers)Jobst Meyer (3 shared papers)Jutta Wirth (3 shared papers)Thomas Wagner (2 shared papers)Niels Tommerup (2 shared papers)Bernhard Zabel (1 shared paper)
- Journals
- Human Genetics (27 papers)Chromosome Research (14 papers)Cytogenetic and Genome Research (12 papers)Chromosoma (7 papers)Genomics (4 papers)
- Partner nations
- GermanyUnited StatesUnited Kingdom
In The Last Decade
W. Schempp
122 papers receiving 4.3k citations
W. Schempp's Hit Papers
Peers
Comparison fields: 5 of 102
- Genetics 3.0k
- Reproductive Medicine 608
- Molecular Biology 2.8k
- Plant Science 1.3k
- Developmental Biology 60
Countries citing papers authored by W. Schempp
This map shows the geographic impact of W. Schempp'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 W. Schempp with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites W. Schempp more than expected).
Fields of papers citing papers by W. Schempp
This network shows the impact of papers produced by W. Schempp. 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 W. Schempp. The network helps show where W. Schempp may publish in the future.
Co-authors
The 25 scholars most cited alongside W. Schempp, 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 126 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9 Hit paper breakdown → | 1994 | 1344 |
| 2 | 1993 | 167 | |
| 3 | 2011 | 142 | |
| 4 | 2013 | 121 | |
| 5 | 2000 | 117 | |
| 6 | 1996 | 112 | |
| 7 | 1981 | 109 | |
| 8 | 1983 | 96 | |
| 9 | 1996 | 82 | |
| 10 | 1995 | 82 | |
| 11 | 1989 | 80 | |
| 12 | Chromosomal localization of the carcinoembryonic antigen gene family and differential expression in various tumors. | 1988 | 79 |
| 13 | 2001 | 63 | |
| 14 | 2009 | 59 | |
| 15 | 1997 | 58 | |
| 16 | 2006 | 58 | |
| 17 | 1990 | 52 | |
| 18 | 1998 | 50 | |
| 19 | 2004 | 46 | |
| 20 | 1998 | 43 |
About W. Schempp
W. Schempp is a scholar working on Genetics, Molecular Biology, Plant Science, Reproductive Medicine and Cancer Research, having authored 126 papers that have together received 4.7k indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (63 papers), Chromosomal and Genetic Variations (63 papers), Genomic variations and chromosomal abnormalities (25 papers), Genomics and Chromatin Dynamics (21 papers), Sexual Differentiation and Disorders (18 papers), Animal Genetics and Reproduction (13 papers), Sperm and Testicular Function (13 papers) and Prenatal Screening and Diagnostics (6 papers). The work is most often cited by research in Genetics (3.0k citations), Reproductive Medicine (608 citations), Molecular Biology (2.8k citations), Plant Science (1.3k citations) and Developmental Biology (60 citations). W. Schempp has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Gerd Scherer, U. Wolf, Juan J. Pasantes, Jobst Meyer, Jutta Wirth, Thomas Wagner, Niels Tommerup, Bernhard Zabel, Elisabeth Hustert and F. Dagna Bricarelli. Their work appears in journals such as Human Genetics, Chromosome Research, Cytogenetic and Genome Research, Chromosoma and Genomics.
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.