Roberto Coco
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
- Reproductive Medicine top 5%
- Sperm and Testicular Function
Papers in
- Genetics 29
- Genomic variations and chromosomal abnormalities 16
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 10
- Genetics and Neurodevelopmental Disorders 4
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- Prenatal Screening and Diagnostics 16
- Co-authors
- Víctor B. Penchaszadeh (4 shared papers)M.I. Rahn (3 shared papers)Alberto J. Solari (3 shared papers)Roberta B. Sciurano (2 shared papers)C Bergadá (7 shared papers)S. Brugo Olmedo (1 shared paper)Marco A. Rivarola (3 shared papers)John M. Opitz (1 shared paper)
In The Last Decade
Roberto Coco
41 papers receiving 507 citations
Peers
Comparison fields: 5 of 49
- Genetics 364
- Reproductive Medicine 104
- Pediatrics, Perinatology and Child Health 139
- Developmental Biology 15
- Plant Science 130
Countries citing papers authored by Roberto Coco
This map shows the geographic impact of Roberto Coco'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 Roberto Coco with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Roberto Coco more than expected).
Fields of papers citing papers by Roberto Coco
This network shows the impact of papers produced by Roberto Coco. 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 Roberto Coco. The network helps show where Roberto Coco may publish in the future.
Co-authors
The 25 scholars most cited alongside Roberto Coco, 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 45 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2009 | 104 | |
| 2 | 1978 | 53 | |
| 3 | 1987 | 42 | |
| 4 | 1982 | 33 | |
| 5 | 2011 | 32 | |
| 6 | 2004 | 30 | |
| 7 | 1975 | 29 | |
| 8 | Partial trisomy 14q and familial translocation (2;14) (q12;q13). | 1977 | 21 |
| 9 | 1975 | 20 | |
| 10 | 1980 | 14 | |
| 11 | Inherited parital duplication deficiency of chromosome 15 (p12;q22). | 1978 | 13 |
| 12 | A child with recombinant of chromosome 8 inherited from a carrier mother with a pericentric inversion. | 1982 | 11 |
| 13 | 1995 | 8 | |
| 14 | 2016 | 8 | |
| 15 | 1976 | 8 | |
| 16 | 1987 | 7 | |
| 17 | 2024 | 7 | |
| 18 | 2024 | 7 | |
| 19 | Cytogenetic findings in 125 patients with Turner's syndrome and abnormal karyotypes. | 1977 | 7 |
| 20 | Partial trisomy 13q inherited from balanced translocation (5;13) (p14;q13). | 1978 | 7 |
About Roberto Coco
Roberto Coco is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Plant Science and Surgery, having authored 45 papers that have together received 536 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (16 papers), Prenatal Screening and Diagnostics (16 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers), Chromosomal and Genetic Variations (8 papers), Sexual Differentiation and Disorders (7 papers), Genetics and Neurodevelopmental Disorders (4 papers), Sperm and Testicular Function (4 papers) and Congenital limb and hand anomalies (3 papers). The work is most often cited by research in Genetics (364 citations), Reproductive Medicine (104 citations), Pediatrics, Perinatology and Child Health (139 citations), Developmental Biology (15 citations) and Plant Science (130 citations). Roberto Coco has collaborated with scholars based in Argentina, Italy and Romania. Frequent co-authors include Víctor B. Penchaszadeh, M.I. Rahn, Alberto J. Solari, Roberta B. Sciurano, C Bergadá, S. Brugo Olmedo, Marco A. Rivarola, John M. Opitz, S Iorcansky and G. Antonioli. Their work appears in journals such as Pediatric Research, The Journal of Pediatrics, International Journal of Andrology, Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis and Frontiers in Endocrinology.
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.