A. Estop
Impact in
- Reproductive Medicine top 2%
- Sperm and Testicular Function
-
- Prenatal Screening and Diagnostics
- Assisted Reproductive Technology and Twin Pregnancy
Papers in
- Genetics 28
- Genomic variations and chromosomal abnormalities 10
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 9
- Animal Genetics and Reproduction 7
-
- Chromosomal and Genetic Variations 21
- Co-authors
- S. Munné (12 shared papers)C. Templado (6 shared papers)Kathleen Cieply (10 shared papers)Kathy Cieply (5 shared papers)Eleanor Feingold (4 shared papers)Francesca Vidal (1 shared paper)Jesús Giraldo (2 shared papers)Harry Fisch (1 shared paper)
- Journals
- Human Genetics (5 papers)Cytogenetic and Genome Research (3 papers)Human Reproduction (3 papers)European Journal of Human Genetics (2 papers)Genetica (2 papers)
- Partner nations
- United StatesSpainNetherlands
In The Last Decade
A. Estop
38 papers receiving 973 citations
Peers
Comparison fields: 5 of 47
- Reproductive Medicine 376
- Pediatrics, Perinatology and Child Health 428
- Genetics 622
- Public Health, Environmental and Occupational Health 304
- Plant Science 335
Countries citing papers authored by A. Estop
This map shows the geographic impact of A. Estop'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. Estop with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A. Estop more than expected).
Fields of papers citing papers by A. Estop
This network shows the impact of papers produced by A. Estop. 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. Estop. The network helps show where A. Estop may publish in the future.
Co-authors
The 25 scholars most cited alongside A. Estop, 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 43 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1998 | 118 | |
| 2 | 2011 | 91 | |
| 3 | 2000 | 88 | |
| 4 | 2013 | 82 | |
| 5 | 2010 | 69 | |
| 6 | 2008 | 63 | |
| 7 | 1999 | 52 | |
| 8 | 1989 | 49 | |
| 9 | 1986 | 43 | |
| 10 | Mechanisms of small ring formation suggested by the molecular characterization of two small accessory ring chromosomes derived from chromosome 4. | 1995 | 37 |
| 11 | An analysis of human sperm chromosome breakpoints. | 1995 | 36 |
| 12 | 1991 | 34 | |
| 13 | 2016 | 29 | |
| 14 | The meiotic segregation pattern of a reciprocal translocation t(10;12)(q26.1;p13.3) by fluorescence in situ hybridization sperm analysis. | 1997 | 29 |
| 15 | 1992 | 28 | |
| 16 | 1991 | 27 | |
| 17 | 1993 | 26 | |
| 18 | 1993 | 26 | |
| 19 | 2008 | 25 | |
| 20 | 1983 | 22 |
About A. Estop
A. Estop is a scholar working on Genetics, Plant Science, Molecular Biology, Pediatrics, Perinatology and Child Health and Public Health, Environmental and Occupational Health, having authored 43 papers that have together received 1.1k indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (21 papers), Prenatal Screening and Diagnostics (11 papers), Genomic variations and chromosomal abnormalities (10 papers), Reproductive Biology and Fertility (10 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers), Sperm and Testicular Function (8 papers), Animal Genetics and Reproduction (7 papers) and Genomics and Chromatin Dynamics (4 papers). The work is most often cited by research in Reproductive Medicine (376 citations), Pediatrics, Perinatology and Child Health (428 citations), Genetics (622 citations), Public Health, Environmental and Occupational Health (304 citations) and Plant Science (335 citations). A. Estop has collaborated with scholars based in United States, Spain and Netherlands. Frequent co-authors include S. Munné, C. Templado, Kathleen Cieply, Kathy Cieply, Eleanor Feingold, Francesca Vidal, Jesús Giraldo, Harry Fisch, Allen N. Lamb and J. Egozcue. Their work appears in journals such as Human Genetics, Cytogenetic and Genome Research, Human Reproduction, European Journal of Human Genetics and Genetica.
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.