Beatrice Grimi

1.2k total citations
17 papers, 695 citations indexed

About

Beatrice Grimi is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Beatrice Grimi has authored 17 papers receiving a total of 695 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Pediatrics, Perinatology and Child Health, 10 papers in Genetics and 4 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Beatrice Grimi's work include Prenatal Screening and Diagnostics (14 papers), Genomic variations and chromosomal abnormalities (8 papers) and Fetal and Pediatric Neurological Disorders (5 papers). Beatrice Grimi is often cited by papers focused on Prenatal Screening and Diagnostics (14 papers), Genomic variations and chromosomal abnormalities (8 papers) and Fetal and Pediatric Neurological Disorders (5 papers). Beatrice Grimi collaborates with scholars based in Italy, United States and Mozambique. Beatrice Grimi's co-authors include Francesca Romana Grati, Giuseppe Simoni, Federico Maggi, Francesca Malvestiti, Cristina Agrati, Elisa Gaetani, Francesca Dulcetti, Anna Maria Trotta, Simona De Toffol and José Carlos Ferreira and has published in prestigious journals such as SHILAP Revista de lepidopterología, Ultrasound in Obstetrics and Gynecology and Genetics in Medicine.

In The Last Decade

Beatrice Grimi

17 papers receiving 630 citations

Peers

Countries citing papers authored by Beatrice Grimi

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Beatrice Grimi

This figure shows the co-authorship network connecting the top 25 collaborators of Beatrice Grimi. A scholar is included among the top collaborators of Beatrice Grimi based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Beatrice Grimi. Beatrice Grimi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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17 of 17 papers shown

#	Work	Indexed citations
1	Performance of conventional cytogenetic analysis on chorionic villi when only one cell layer, cytotrophoblast or mesenchyme alone, is analyzed 2021 ·Prenatal Diagnosis ·Francesca Romana Grati, Francesca Malvestiti, (unknown), (unknown), Beatrice Grimi, Cristina Agrati, (unknown), (unknown), Anna Maria Trotta, (unknown), Giuseppe Simoni, (unknown), Peter Benn	1
2	Rare autosomal trisomies: comparison of detection through cell‐free DNA analysis and direct chromosome preparation of chorionic villus samples 2019 ·Ultrasound in Obstetrics and Gynecology ·Peter Benn, Francesca Malvestiti, Beatrice Grimi, Federico Maggi, Giuseppe Simoni, Francesca Romana Grati	59
3	Implications of fetoplacental mosaicism on cell‐free DNA testing for sex chromosome aneuploidies 2017 ·Prenatal Diagnosis ·Francesca Romana Grati, Komal Bajaj, (unknown), Francesca Malvestiti, Barbara Malvestiti, (unknown), Beatrice Grimi, Federico Maggi, Giuseppe Simoni, Susan J. Gross, José Carlos Ferreira	34
4	The type of feto‐placental aneuploidy detected by cfDNA testing may influence the choice of confirmatory diagnostic procedure 2015 ·Prenatal Diagnosis ·Francesca Romana Grati, Komal Bajaj, Francesca Malvestiti, Cristina Agrati, Beatrice Grimi, Barbara Malvestiti, Eva Pompilii, Federico Maggi, Susan J. Gross, Giuseppe Simoni, José Carlos Ferreira	64
5	Interpreting mosaicism in chorionic villi: results of a monocentric series of 1001 mosaics in chorionic villi with follow-up amniocentesis 2015 ·Prenatal Diagnosis ·Francesca Malvestiti, Cristina Agrati, Beatrice Grimi, Eva Pompilii, Claudia Izzi, (unknown), Elisa Gaetani, (unknown), Anna Maria Trotta, Federico Maggi, Giuseppe Simoni, Francesca Romana Grati	134
6	Fetoplacental mosaicism: potential implications for false-positive and false-negative noninvasive prenatal screening results 2014 ·Genetics in Medicine ·Francesca Romana Grati, Francesca Malvestiti, José Carlos Ferreira, Komal Bajaj, Elisa Gaetani, Cristina Agrati, Beatrice Grimi, Francesca Dulcetti, Anna Ruggeri, Simona De Toffol, Federico Maggi, Ronald J. Wapner, Susan J. Gross, Giuseppe Simoni	144
7	Complex Variant of Philadelphia Translocation Involving Chromosomes 9, 12, and 22 in a Case with Chronic Myeloid Leukaemia 2014 ·SHILAP Revista de lepidopterología ·Francesca Malvestiti, Cristina Agrati, (unknown), (unknown), Simona Cirrincione, Maria Oggionni, Beatrice Grimi, Federico Maggi, Giuseppe Simoni, Francesca Romana Grati	1
8	De novo small supernumerary marker chromosomes detected on 143 000 consecutive prenatal diagnoses: chromosomal distribution, frequencies, and characterization combining molecular cytogenetics approaches 2014 ·Prenatal Diagnosis ·Francesca Malvestiti, Simona De Toffol, Beatrice Grimi, (unknown), (unknown), Cristina Agrati, (unknown), (unknown), Anna Maria Trotta, Barbara Malvestiti, Anna Ruggeri, Francesca Dulcetti, Federico Maggi, Giuseppe Simoni, Francesca Romana Grati	17
9	QF‐PCR as a substitute for karyotyping of cytotrophoblast for the analysis of chorionic villi: advantages and limitations from a cytogenetic retrospective audit of 44,727 first‐trimester prenatal diagnoses 2013 ·Prenatal Diagnosis ·Francesca Romana Grati, Francesca Malvestiti, Beatrice Grimi, Elisa Gaetani, (unknown), Anna Maria Trotta, (unknown), (unknown), Francesca Dulcetti, Anna Ruggeri, Cristina Agrati, (unknown), Silvia Milani, Simona De Toffol, (unknown), (unknown), (unknown), Federico Maggi, Giuseppe Simoni	14
10	Recombinant Chromosome 4 from a Familial Pericentric Inversion: Prenatal and Adulthood Wolf-Hirschhorn Phenotypes 2013 ·SHILAP Revista de lepidopterología ·Francesca Malvestiti, Francesco Benedicenti, Simona De Toffol, (unknown), (unknown), Beatrice Grimi, (unknown), (unknown), Cristina Agrati, (unknown), Federico Maggi, Giuseppe Simoni, Francesca Romana Grati	4
11	Prenatal BACs‐on‐Beads^TM: the prospective experience of five prenatal diagnosis laboratories 2012 ·Prenatal Diagnosis ·François Vialard, Giuseppe Simoni, D. Molina Gomes, (unknown), Simona De Toffol, (unknown), (unknown), Lucio Nitsch, P. Bouhanna, (unknown), Thomas Popowski, Beatrice Grimi, José Antonio Martínez-Conejero, Brigitte Benzacken, Rita Genesio, Francesca Romana Grati	35
12	Prenatal BACs‐on‐Beads^™: a new technology for rapid detection of aneuploidies and microdeletions in prenatal diagnosis 2011 ·Prenatal Diagnosis ·François Vialard, Giuseppe Simoni, Azzedine Aboura, Simona De Toffol, (unknown), (unknown), Stéphane Serero, Patrice Clément, P. Bouhanna, Étienne Rouleau, Beatrice Grimi, J. Selva, Elisa Gaetani, Federico Maggi, (unknown), Brigitte Benzacken, Francesca Romana Grati	40
13	Chromosome abnormalities investigated by non‐invasive prenatal testing account for approximately 50% of fetal unbalances associated with relevant clinical phenotypes 2010 ·American Journal of Medical Genetics Part A ·Francesca Romana Grati, (unknown), Beatrice Grimi, Silvia Milani, (unknown), (unknown), (unknown), Anna Maria Trotta, (unknown), Francesca Dulcetti, Anna Ruggeri, Simona De Toffol, Maurizio Clementi, Federico Maggi, Giuseppe Simoni	41
14	Pure monosomy and pure trisomy of 13q21.2–31.1 consequent to a familial insertional translocation: Exclusion of PCDH9 as the responsible gene for autosomal dominant auditory neuropathy (AUNA1) 2009 ·American Journal of Medical Genetics Part A ·Francesca Romana Grati, Marci M. Lesperance, Simona De Toffol, (unknown), Angelo Selicorni, Sarah B. Emery, Beatrice Grimi, Francesca Dulcetti, Barbara Malvestiti, (unknown), Silvia Milani, Anna Ruggeri, Federico Maggi, Giuseppe Simoni	10
15	Prenatal detection by subtelomeric FISH and MLPA of unbalanced meiotic recombinants resulting from parental pericentric inversions 2008 ·Molecular and Cellular Probes ·Francesca Romana Grati, (unknown), (unknown), (unknown), Beatrice Grimi, Simona De Toffol, Silvia Milani, Francesca Dulcetti, (unknown), (unknown), (unknown), Anna Maria Trotta, Jordy Coffa, Federico Maggi, Giuseppe Simoni	3
16	Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villi 2006 ·European Journal of Human Genetics ·Francesca Romana Grati, Beatrice Grimi, (unknown), (unknown), (unknown), Silvia Milani, Anna Maria Trotta, Francesca Dulcetti, Enrico Grosso, Monica Miozzo, Federico Maggi, Giuseppe Simoni	61
17	Prenatal search for UPD 14 and UPD 15 in 83 cases of familial and de novo heterologous Robertsonian translocations 2004 ·Prenatal Diagnosis ·Anna Ruggeri, Francesca Dulcetti, Monica Miozzo, Francesca Romana Grati, Beatrice Grimi, (unknown), Federica Natacci, Federico Maggi, Giuseppe Simoni	33

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.

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