Pinella Failla
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Gastroenterology top 2%
- Celiac Disease Research and Management
Papers in
- Genetics 31
- Genetics and Neurodevelopmental Disorders 12
- Genomic variations and chromosomal abnormalities 11
- Genomics and Rare Diseases 7
- Genetic and rare skin diseases. 5
- Genetic Syndromes and Imprinting 3
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- Celiac Disease Research and Management 8
- Co-authors
- Corrado Romano (25 shared papers)Marco Fichera (11 shared papers)Carmelo Schepis (10 shared papers)Lucia Castiglia (7 shared papers)Maddalena Siragusa (7 shared papers)Rosa Pettinato (5 shared papers)Concetta Barone (5 shared papers)Ornella Galesi (6 shared papers)
- Journals
- The American Journal of Human Genetics (4 papers)Journal of Pediatric Gastroenterology and Nutrition (2 papers)International Journal of Molecular Sciences (2 papers)Journal of Medical Genetics (2 papers)Acta Paediatrica (2 papers)
- Partner nations
- ItalyUnited StatesNetherlands
In The Last Decade
Pinella Failla
46 papers receiving 1.8k citations
Pinella Failla's Hit Papers
Peers
Comparison fields: 5 of 65
- Genetics 977
- Gastroenterology 204
- Cognitive Neuroscience 364
- Developmental Neuroscience 34
- Psychiatry and Mental health 146
Countries citing papers authored by Pinella Failla
This map shows the geographic impact of Pinella Failla'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 Pinella Failla with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Pinella Failla more than expected).
Fields of papers citing papers by Pinella Failla
This network shows the impact of papers produced by Pinella Failla. 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 Pinella Failla. The network helps show where Pinella Failla may publish in the future.
Co-authors
The 25 scholars most cited alongside Pinella Failla, 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 49 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Disruptive CHD8 Mutations Define a Subtype of Autism Early in Development Hit paper breakdown → | 2014 | 602 |
| 2 | 2008 | 476 | |
| 3 | 2001 | 124 | |
| 4 | 2015 | 114 | |
| 5 | 2013 | 90 | |
| 6 | 2009 | 63 | |
| 7 | 1999 | 43 | |
| 8 | 2015 | 36 | |
| 9 | 2007 | 33 | |
| 10 | 2016 | 29 | |
| 11 | 1996 | 28 | |
| 12 | 1993 | 23 | |
| 13 | 2001 | 22 | |
| 14 | 2015 | 21 | |
| 15 | 2009 | 19 | |
| 16 | 2005 | 17 | |
| 17 | 1994 | 16 | |
| 18 | Comparison of three probiotics in the treatment of acute diarrhea in mentally retarded children. | 2000 | 16 |
| 19 | New mutations in XNP/ATR-X gene: a further contribution to genotype/phenotype relationship in ATR/X syndrome. Mutations in brief no. 176. Online. | 1998 | 14 |
| 20 | 2019 | 14 |
About Pinella Failla
Pinella Failla is a scholar working on Genetics, Gastroenterology, Immunology and Allergy, Dermatology and Cognitive Neuroscience, having authored 49 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (12 papers), Genomic variations and chromosomal abnormalities (11 papers), Celiac Disease Research and Management (8 papers), Genomics and Rare Diseases (7 papers), Genetic and rare skin diseases. (5 papers), Down syndrome and intellectual disability research (3 papers), Genetic Syndromes and Imprinting (3 papers) and Autism Spectrum Disorder Research (3 papers). The work is most often cited by research in Genetics (977 citations), Gastroenterology (204 citations), Cognitive Neuroscience (364 citations), Developmental Neuroscience (34 citations) and Psychiatry and Mental health (146 citations). Pinella Failla has collaborated with scholars based in Italy, United States and Netherlands. Frequent co-authors include Corrado Romano, Marco Fichera, Carmelo Schepis, Lucia Castiglia, Maddalena Siragusa, Rosa Pettinato, Concetta Barone, Ornella Galesi, A Alberti and Gaetano Bottaro. Their work appears in journals such as The American Journal of Human Genetics, Journal of Pediatric Gastroenterology and Nutrition, International Journal of Molecular Sciences, Journal of Medical Genetics and Acta Paediatrica.
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.