Elisa Merello
Impact in
- Rheumatology top 2%
- Folate and B Vitamins Research
-
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
Papers in
-
- Wnt/β-catenin signaling in development and cancer 11
- Kruppel-like factors research 4
- Surgery 16
- Congenital gastrointestinal and neural anomalies 6
- Co-authors
- Valeria Capra (46 shared papers)Patrizia De Marco (43 shared papers)Zoha Kibar (21 shared papers)Armando Cama (28 shared papers)Philippe Gros (5 shared papers)Maria Grazia Calevo (9 shared papers)Richard H. Finnell (5 shared papers)Samantha Mascelli (12 shared papers)
- Journals
- Birth Defects Research Part A Clinical and Molecular Teratology (10 papers)Human Molecular Genetics (4 papers)Human Mutation (4 papers)European Journal of Medical Genetics (3 papers)European Journal of Human Genetics (2 papers)
- Partner nations
- ItalyCanadaUnited States
In The Last Decade
Elisa Merello
50 papers receiving 1.8k citations
Peers
Comparison fields: 5 of 90
- Rheumatology 474
- Pediatrics, Perinatology and Child Health 327
- Genetics 405
- Molecular Biology 976
- Cell Biology 214
Countries citing papers authored by Elisa Merello
This map shows the geographic impact of Elisa Merello'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 Elisa Merello with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Elisa Merello more than expected).
Fields of papers citing papers by Elisa Merello
This network shows the impact of papers produced by Elisa Merello. 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 Elisa Merello. The network helps show where Elisa Merello may publish in the future.
Co-authors
The 25 scholars most cited alongside Elisa Merello, 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 50 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2007 | 231 | |
| 2 | 2010 | 100 | |
| 3 | 2002 | 97 | |
| 4 | 2009 | 88 | |
| 5 | 2011 | 85 | |
| 6 | 2011 | 79 | |
| 7 | 2003 | 79 | |
| 8 | 2012 | 77 | |
| 9 | 2011 | 66 | |
| 10 | 2005 | 60 | |
| 11 | 2015 | 55 | |
| 12 | 2000 | 49 | |
| 13 | 2001 | 48 | |
| 14 | 2011 | 47 | |
| 15 | 2007 | 46 | |
| 16 | 2012 | 43 | |
| 17 | 2010 | 41 | |
| 18 | 2011 | 40 | |
| 19 | 2006 | 39 | |
| 20 | 2014 | 38 |
About Elisa Merello
Elisa Merello is a scholar working on Molecular Biology, Surgery, Genetics, Pediatrics, Perinatology and Child Health and Rheumatology, having authored 50 papers that have together received 1.9k indexed citations. Recurring topics across this work include Wnt/β-catenin signaling in development and cancer (11 papers), Folate and B Vitamins Research (9 papers), Congenital gastrointestinal and neural anomalies (6 papers), Prenatal Screening and Diagnostics (6 papers), Connective tissue disorders research (5 papers), Kruppel-like factors research (4 papers), Hippo pathway signaling and YAP/TAZ (4 papers) and Fetal and Pediatric Neurological Disorders (4 papers). The work is most often cited by research in Rheumatology (474 citations), Pediatrics, Perinatology and Child Health (327 citations), Genetics (405 citations), Molecular Biology (976 citations) and Cell Biology (214 citations). Elisa Merello has collaborated with scholars based in Italy, Canada and United States. Frequent co-authors include Valeria Capra, Patrizia De Marco, Zoha Kibar, Armando Cama, Philippe Gros, Maria Grazia Calevo, Richard H. Finnell, Samantha Mascelli, Redouane Allache and Gianluca Piatelli. Their work appears in journals such as Birth Defects Research Part A Clinical and Molecular Teratology, Human Molecular Genetics, Human Mutation, European Journal of Medical Genetics and European Journal of Human Genetics.
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.