Beatrice Grimi
Impact in
-
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
Papers in
-
- Prenatal Screening and Diagnostics 12
- Fetal and Pediatric Neurological Disorders 1
- Genetics 4
- Genomic variations and chromosomal abnormalities 3
- Genetic Syndromes and Imprinting 2
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
- Myeloproliferative Neoplasms: Diagnosis and Treatment 1
- Co-authors
- Giuseppe Simoni (17 shared papers)Francesca Romana Grati (17 shared papers)Federico Maggi (15 shared papers)Francesca Malvestiti (10 shared papers)Cristina Agrati (8 shared papers)Elisa Gaetani (4 shared papers)Francesca Dulcetti (8 shared papers)Anna Maria Trotta (7 shared papers)
- Journals
- Prenatal Diagnosis (9 papers)European Journal of Human Genetics (1 paper)Ultrasound in Obstetrics and Gynecology (1 paper)Genetics in Medicine (1 paper)American Journal of Medical Genetics Part A (2 papers)
- Partner nations
- ItalyUnited StatesMozambique
In The Last Decade
Beatrice Grimi
17 papers receiving 643 citations
Peers
Comparison fields: 5 of 35
- Pediatrics, Perinatology and Child Health 605
- Genetics 233
- Infectious Diseases 89
- Cancer Research 29
- Obstetrics and Gynecology 11
Countries citing papers authored by Beatrice Grimi
This map shows the geographic impact of Beatrice Grimi'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 Beatrice Grimi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Beatrice Grimi more than expected).
Fields of papers citing papers by Beatrice Grimi
This network shows the impact of papers produced by Beatrice Grimi. 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 Beatrice Grimi. The network helps show where Beatrice Grimi may publish in the future.
Co-authors
The 25 scholars most cited alongside Beatrice Grimi, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2014 | 146 | |
| 2 | 2015 | 137 | |
| 3 | 2015 | 67 | |
| 4 | 2006 | 63 | |
| 5 | 2019 | 61 | |
| 6 | 2010 | 41 | |
| 7 | 2011 | 40 | |
| 8 | 2012 | 35 | |
| 9 | 2017 | 35 | |
| 10 | 2004 | 33 | |
| 11 | 2014 | 17 | |
| 12 | 2013 | 14 | |
| 13 | 2009 | 10 | |
| 14 | 2013 | 4 | |
| 15 | 2008 | 3 | |
| 16 | 2021 | 1 | |
| 17 | 2014 | 1 |
About Beatrice Grimi
Beatrice Grimi is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Infectious Diseases, Molecular Biology and Genetics, having authored 17 papers that have together received 708 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (12 papers), Genomic variations and chromosomal abnormalities (3 papers), Genetic Syndromes and Imprinting (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper), Chronic Myeloid Leukemia Treatments (1 paper), Myeloproliferative Neoplasms: Diagnosis and Treatment (1 paper), Fetal and Pediatric Neurological Disorders (1 paper) and Eosinophilic Disorders and Syndromes (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (605 citations), Genetics (233 citations), Infectious Diseases (89 citations), Cancer Research (29 citations) and Obstetrics and Gynecology (11 citations). Beatrice Grimi has collaborated with scholars based in Italy, United States and Mozambique. Frequent co-authors include Giuseppe Simoni, Francesca Romana Grati, Federico Maggi, Francesca Malvestiti, Cristina Agrati, Elisa Gaetani, Francesca Dulcetti, Anna Maria Trotta, Simona De Toffol and José Carlos Ferreira. Their work appears in journals such as Prenatal Diagnosis, European Journal of Human Genetics, Ultrasound in Obstetrics and Gynecology, Genetics in Medicine and American Journal of Medical Genetics Part A.
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.