A Mayerová
Impact in
- Genetics top 10%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Animal Genetics and Reproduction
- 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
- Co-authors
- U. Wolf (5 shared papers)Eberhard Nieschlag (1 shared paper)H. Sperling (1 shared paper)C. Aulehla‐Scholz (1 shared paper)Hans-Jürgen Pander (1 shared paper)Eberhard Passarge (1 shared paper)Dagmar Wieczorek (1 shared paper)Thilo Dörk (1 shared paper)
- Journals
- Human Genetics (3 papers)Journal of Medical Genetics (3 papers)International Journal of Immunogenetics (2 papers)Differentiation (2 papers)Human Heredity (2 papers)
- Partner nations
- GermanyFranceSwitzerland
In The Last Decade
A Mayerová
28 papers receiving 497 citations
Peers
Comparison fields: 5 of 74
- Genetics 185
- Reproductive Medicine 53
- Pulmonary and Respiratory Medicine 141
- Biological Psychiatry 8
- Pediatrics, Perinatology and Child Health 50
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 | 1983 | 33 | |
| 4 | 1982 | 33 | |
| 5 | Assignment of the gene coding for human catalase to the short arm of chromosome 11. | 1980 | 28 |
| 6 | 1983 | 23 | |
| 7 | 1988 | 21 | |
| 8 | 1976 | 17 | |
| 9 | 1987 | 13 | |
| 10 | 1987 | 13 | |
| 11 | 1969 | 11 | |
| 12 | 1997 | 10 | |
| 13 | 1985 | 9 | |
| 14 | 1983 | 9 | |
| 15 | 1996 | 8 | |
| 16 | 1983 | 8 | |
| 17 | 1995 | 8 | |
| 18 | 1984 | 6 | |
| 19 | 1985 | 5 | |
| 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 524 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), Immunodeficiency and Autoimmune Disorders (3 papers), Sperm and Testicular Function (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Chromosomal and Genetic Variations (3 papers), Cellular transport and secretion (2 papers) and Neonatal Health and Biochemistry (2 papers). The work is most often cited by research in Genetics (185 citations), Reproductive Medicine (53 citations), Pulmonary and Respiratory Medicine (141 citations), Biological Psychiatry (8 citations) and Pediatrics, Perinatology and Child Health (50 citations). A Mayerová has collaborated with scholars based in Germany, France and Switzerland. Frequent co-authors include U. Wolf, Eberhard Nieschlag, H. Sperling, C. Aulehla‐Scholz, Hans-Jürgen Pander, Eberhard Passarge, Dagmar Wieczorek, Thilo Dörk, Bernd Dworniczak and Dieter Meschede. Their work appears in journals such as Human Genetics, Journal of Medical Genetics, International Journal of Immunogenetics, Differentiation 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.