Barbara Malvestiti

530 citations

5 papers · 143 indexed · h-index 5

Co-authors: Francesca Romana Grati Beatrice Grimi Federico Maggi Giuseppe Simoni Francesca Malvestiti Susan J. Gross José Carlos Ferreira Komal Bajaj
Topics: Prenatal Screening and Diagnostics (4 papers)Genomic variations and chromosomal abnormalities (2 papers)Cancer Genomics and Diagnostics (1 paper)
Cited by: Pediatrics, Perinatology and Child Health Genetics Infectious Diseases
Journals: Prenatal Diagnosis American Journal of Medical Genetics Part A Fetal Diagnosis and Therapy
Partner nations: United States Italy Poland

In The Last Decade

Barbara Malvestiti

5 papers receiving 126 citations

Peers

Countries citing papers authored by Barbara Malvestiti

Since Specialization

Citations

This map shows the geographic impact of Barbara Malvestiti'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 Barbara Malvestiti with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Barbara Malvestiti more than expected).

Fields of papers citing papers by Barbara Malvestiti

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Barbara Malvestiti. 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 Barbara Malvestiti. The network helps show where Barbara Malvestiti may publish in the future.

Co-authorship network of co-authors of Barbara Malvestiti

This figure shows the co-authorship network connecting the top 25 collaborators of Barbara Malvestiti. A scholar is included among the top collaborators of Barbara Malvestiti 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 Barbara Malvestiti. Barbara Malvestiti is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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5 of 5 papers shown

#	Work	Indexed citations
1	First Trimester Screening for Common Trisomies and Microdeletion 22q11.2 Syndrome Using Cell-Free DNA: A Prospective Clinical Study 2020 ·Fetal Diagnosis and Therapy ·Karl Oliver Kagan,Markus Hoopmann,(unknown),Natalia Prodan,Philipp Wagner,(unknown),Andreas Dufke,Ulrike A. Mau‐Holzmann,Sara Y. Brucker,(unknown),Barbara Malvestiti,Francesca Romana Grati	18
2	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
3	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
4	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
5	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

About Barbara Malvestiti

Barbara Malvestiti is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Cancer Research, having authored 5 papers that have together received 143 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (2 papers) and Cancer Genomics and Diagnostics (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (111 citations), Genetics (68 citations) and Infectious Diseases (33 citations). Barbara Malvestiti has collaborated with scholars based in United States, Italy and Poland. Frequent co-authors include Francesca Romana Grati, Beatrice Grimi, Federico Maggi, Giuseppe Simoni, Francesca Malvestiti, Susan J. Gross, José Carlos Ferreira, Komal Bajaj, Cristina Agrati and Eva Pompilii. Their work appears in journals such as Prenatal Diagnosis, American Journal of Medical Genetics Part A and Fetal Diagnosis and Therapy.

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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