Roberto Quadrelli
Impact in
- Sensory Systems top 5%
- Ion Channels and Receptors
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 16
- Genomic variations and chromosomal abnormalities 10
- Genetics and Neurodevelopmental Disorders 2
- Cleft Lip and Palate Research 2
- Congenital Ear and Nasal Anomalies 2
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- Congenital heart defects research 3
- Sexual Differentiation and Disorders 2
- Co-authors
- Alicia Vaglio (20 shared papers)Taosheng Huang (3 shared papers)Craig T. Basson (1 shared paper)Giovanni Romeo (1 shared paper)David R. Bachinsky (1 shared paper)Christine E. Seidman (1 shared paper)Alexandre C. Pereira (1 shared paper)Robert C. Lin (1 shared paper)
- Journals
- Prenatal Diagnosis (4 papers)European Journal of Medical Genetics (2 papers)Pediatric Dermatology (2 papers)Journal of Inherited Metabolic Disease (1 paper)Diseases of the Colon & Rectum (1 paper)
- Partner nations
- United StatesUruguayArgentina
In The Last Decade
Roberto Quadrelli
26 papers receiving 601 citations
Peers
Comparison fields: 5 of 66
- Sensory Systems 124
- Genetics 186
- Developmental Biology 14
- Molecular Biology 349
- Pediatrics, Perinatology and Child Health 70
Countries citing papers authored by Roberto Quadrelli
This map shows the geographic impact of Roberto Quadrelli'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 Quadrelli with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Roberto Quadrelli more than expected).
Fields of papers citing papers by Roberto Quadrelli
This network shows the impact of papers produced by Roberto Quadrelli. 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 Quadrelli. The network helps show where Roberto Quadrelli may publish in the future.
Co-authors
The 25 scholars most cited alongside Roberto Quadrelli, 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 26 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1999 | 273 | |
| 2 | 2008 | 186 | |
| 3 | 2010 | 40 | |
| 4 | 2006 | 32 | |
| 5 | 2001 | 18 | |
| 6 | [Familial colonic cancer]. | 1978 | 17 |
| 7 | 2007 | 11 | |
| 8 | 2006 | 11 | |
| 9 | 2000 | 11 | |
| 10 | 1998 | 10 | |
| 11 | 2006 | 7 | |
| 12 | 2007 | 6 | |
| 13 | 2016 | 6 | |
| 14 | 2007 | 5 | |
| 15 | Síndrome de feminización testicular completa | 1980 | 4 |
| 16 | 2010 | 4 | |
| 17 | 2009 | 3 | |
| 18 | 1998 | 3 | |
| 19 | Síndrome de trisomía 9p: características clínico-evolutivas y citogenéticas. Seguimiento de doce años | 2007 | 3 |
| 20 | 2006 | 2 |
About Roberto Quadrelli
Roberto Quadrelli is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Surgery, having authored 26 papers that have together received 661 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (8 papers), Chromosomal and Genetic Variations (6 papers), Congenital heart defects research (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Cleft Lip and Palate Research (2 papers), Sexual Differentiation and Disorders (2 papers) and Congenital Ear and Nasal Anomalies (2 papers). The work is most often cited by research in Sensory Systems (124 citations), Genetics (186 citations), Developmental Biology (14 citations), Molecular Biology (349 citations) and Pediatrics, Perinatology and Child Health (70 citations). Roberto Quadrelli has collaborated with scholars based in United States, Uruguay and Argentina. Frequent co-authors include Alicia Vaglio, Taosheng Huang, Craig T. Basson, Giovanni Romeo, David R. Bachinsky, Christine E. Seidman, Alexandre C. Pereira, Robert C. Lin, Mary Ella Pierpont and Margherita Silengo. Their work appears in journals such as Prenatal Diagnosis, European Journal of Medical Genetics, Pediatric Dermatology, Journal of Inherited Metabolic Disease and Diseases of the Colon & Rectum.
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.