A Mayerová
Impact in
- Genetics top 10%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Reproductive Medicine top 10%
- Sperm and Testicular Function
Papers in
- Genetics 15
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 9
- Genomic variations and chromosomal abnormalities 3
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- Sexual Differentiation and Disorders 3
- CRISPR and Genetic Engineering 2
- Co-authors
- U. Wolf (5 shared papers)K. Bender (5 shared papers)Dieter Meschede (1 shared paper)Manfred Stuhrmann (1 shared paper)Jürgen Horst (1 shared paper)Félix Ratjen (1 shared paper)Hans-Jürgen Pander (1 shared paper)Bernd Dworniczak (1 shared paper)
- Journals
- Journal of Medical Genetics (3 papers)Human Genetics (3 papers)Differentiation (2 papers)International Journal of Immunogenetics (2 papers)Human Heredity (2 papers)
- Partner nations
- GermanyFranceUnited States
In The Last Decade
A Mayerová
29 papers receiving 517 citations
Peers
Comparison fields: 5 of 78
- Genetics 199
- Reproductive Medicine 60
- Pulmonary and Respiratory Medicine 149
- Biological Psychiatry 9
- Psychiatry and Mental health 52
Countries citing papers authored by A Mayerová
This map shows the geographic impact of A Mayerová'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 A Mayerová with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A Mayerová more than expected).
Fields of papers citing papers by A Mayerová
This network shows the impact of papers produced by A Mayerová. 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 A Mayerová. The network helps show where A Mayerová may publish in the future.
Co-authors
The 25 scholars most cited alongside A Mayerová, 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 33 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1997 | 190 | |
| 2 | 1996 | 59 | |
| 3 | 1982 | 34 | |
| 4 | 1983 | 33 | |
| 5 | Assignment of the gene coding for human catalase to the short arm of chromosome 11. | 1980 | 28 |
| 6 | 1983 | 24 | |
| 7 | 1988 | 21 | |
| 8 | 1978 | 19 | |
| 9 | 1976 | 17 | |
| 10 | 1987 | 13 | |
| 11 | 1987 | 13 | |
| 12 | 1969 | 11 | |
| 13 | 1997 | 10 | |
| 14 | 1985 | 9 | |
| 15 | 1983 | 9 | |
| 16 | 1996 | 8 | |
| 17 | 1995 | 8 | |
| 18 | 1983 | 8 | |
| 19 | 1984 | 6 | |
| 20 | [Prenatal virus infections and orofacial clefts]. | 1992 | 5 |
About A Mayerová
A Mayerová is a scholar working on Genetics, Molecular Biology, Immunology, Plant Science and Cellular and Molecular Neuroscience, having authored 33 papers that have together received 545 indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers), Sexual Differentiation and Disorders (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Immunodeficiency and Autoimmune Disorders (3 papers), Chromosomal and Genetic Variations (3 papers), Sperm and Testicular Function (3 papers), CRISPR and Genetic Engineering (2 papers) and Viral Infections and Immunology Research (2 papers). The work is most often cited by research in Genetics (199 citations), Reproductive Medicine (60 citations), Pulmonary and Respiratory Medicine (149 citations), Biological Psychiatry (9 citations) and Psychiatry and Mental health (52 citations). A Mayerová has collaborated with scholars based in Germany, France and United States. Frequent co-authors include U. Wolf, K. Bender, Dieter Meschede, Manfred Stuhrmann, Jürgen Horst, Félix Ratjen, Hans-Jürgen Pander, Bernd Dworniczak, H. H. Seydewitz and C. Aulehla‐Scholz. Their work appears in journals such as Journal of Medical Genetics, Human Genetics, Differentiation, International Journal of Immunogenetics and Human Heredity.
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.