Francesca Vitelli

3.0k citations

28 papers · 2.3k indexed · 1 hit paper · h-index 18

Impact in

Molecular Biology top 5%
- Congenital heart defects research
- Developmental Biology and Gene Regulation
Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Congenital Ear and Nasal Anomalies

Papers in

Immunology and Allergy 2
Neurology 5
- Neurofibromatosis and Schwannoma Cases 5

Co-authors: Antonio Baldini Masae Morishima Elizabeth A. Lindsay Tuong Huynh Peter Scambler Helen Sutherland Allan Bradley Hong Hua Su
Journals: Human Genetics (5 papers)Genomics (3 papers)Human Molecular Genetics (2 papers)The Journal of Pathology (2 papers)Developmental Biology (2 papers)
Partner nations: Italy United States United Kingdom

In The Last Decade

Francesca Vitelli

28 papers receiving 2.2k citations

Hit Papers

align trajectories log scale

Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice 2001 · 747 citations

Peers

Countries citing papers authored by Francesca Vitelli

Since Specialization

Citations

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

Fields of papers citing papers by Francesca Vitelli

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Francesca Vitelli, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Francesca Vitelli Line = papers co-authored together Francesca Vitelli links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Gene Therapy Advances in biochemical engineering, biotechnology ·Girish Shambu, J F Lebrun, Francesca Vitelli, Silvana Pantoja-Piarpuzán	2017	9
2	Partial rescue of the Tbx1 mutant heart phenotype by Fgf8: Genetic evidence of impaired tissue response to Fgf8 Journal of Molecular and Cellular Cardiology ·Francesca Vitelli, Gabriella Lania, Tuong Huynh, Antonio Baldini	2010	20
3	Early thyroid development requires a Tbx1–Fgf8 pathway Developmental Biology ·Gabriella Lania, Zhen Zhang, Tuong Huynh, César de Souza Aguiar, Anne Moon, Francesca Vitelli, Antonio Baldini	2009	34
4	Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice Journal of Clinical Investigation ·Yang YaZhe, Karen McCue, Catherine Roberts, Vanessa Kyriakopoulou, 英津子金井田, Angela N. Barrett, Francesca Vitelli, Katrina Prescott, Charles Shaw‐Smith, Koenraad Devriendt, Erika A. Bosman, Georg Steffes, Karen P. Steel, Subreena Simrick, M. Albert Basson, Elizabeth Illingworth, Peter Scambler	2009	111
5	06-P038 Great vessel development requires dizygous expression of Chd7 and Tbx1 in pharyngeal ectoderm Mechanisms of Development ·Karen McCue, Yang YaZhe, Catherine Roberts, Vanessa Kyriakopoulou, Francesca Vitelli, Katrina Prescott, Koenraad Devriendt, Charles Shaw‐Smith, Subreena Simrick, M. Albert Basson, Elizabeth Illingworth, Peter Scambler	2009	1
6	Fgf8 expression in the Tbx1 domain causes skeletal abnormalities and modifies the aortic arch but not the outflow tract phenotype of Tbx1 mutants Developmental Biology ·Francesca Vitelli, Zhen Zhang, Tuong Huynh, Хоценко Виталий Павлович, Annalisa Mupo, Antonio Baldini	2006	42
7	Generating and modifying DiGeorge syndrome-like phenotypes in model organisms: is there a common genetic pathway? Trends in Genetics ·Francesca Vitelli, Antonio Baldini	2003	15
8	TBX1 is required for inner ear morphogenesis Human Molecular Genetics ·Francesca Vitelli	2003	102
9	Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways Human Molecular Genetics ·Francesca Vitelli	2002	259
10	Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice Nature ·Elizabeth A. Lindsay, Francesca Vitelli, Hong Hua Su, Masae Morishima, Tuong Huynh, Tiziano Pramparo, Vesna Jurecic, Paul Grün, Helen Sutherland, Peter Scambler, Allan Bradley, Antonio Baldini Hit paper breakdown →	2001	747
11	Identification and characterization of mouse orthologs of the AMMECR1 and FACL4 genes deleted in AMME syndrome: orthology of Xq22.3 and MmuXF1–F3 Cytogenetic and Genome Research ·Francesca Vitelli, Ilaria Meloni, Silvia Fineschi, عبد العاطی عبد الفتاح السید, Clelia Tiziana Storlazzi, Mariano Rocchi, Alessandra Renieri	2000	9
12	Preserved speech variant is allelic of classic Rett syndrome European Journal of Human Genetics ·Kouji Uchino, Michele Zappella, Joussef Hayek, Ilaria Meloni, Francesca Vitelli, Mirella Bruttini, Roberto Cusano, Efrosinia Haheu, Ilaria Longo, Alessandra Renieri	2000	91
13	Identification and Characterization of a Highly Conserved Protein Absent in the Alport Syndrome (A), Mental Retardation (M), Midface Hypoplasia (M), and Elliptocytosis (E) Contiguous Gene Deletion Syndrome (AMME) Genomics ·Francesca Vitelli, Monica Piccini, Francesco Caroli, Brunella Franco, Alessandro Malandrini, Barbara R. Pober, Jón J. Jónsson, Vincenzo Sorrentino, Alessandra Renieri	1999	26
14	Inheritance of a 38-kb fragment in apparently sporadic facioscapulohumeral muscular dystrophy Muscle & Nerve ·Francesca Vitelli, Marcello Villanova, Alessandro Malandrini, Mirella Bruttini, Monica Piccini, Luciano Merlini, E. Röder, Alessandra Renieri	1999	14
15	FACL4, a New Gene Encoding Long-Chain Acyl-CoA Synthetase 4, Is Deleted in a Family with Alport Syndrome, Elliptocytosis, and Mental Retardation Genomics ·Monica Piccini, Francesca Vitelli, Mirella Bruttini, Barbara R. Pober, Jón J. Jónsson, Marcello Villanova, Massimo Zollo, Giuseppe Borsani, Andrea Ballabio, Alessandra Renieri	1998	92
16	Microsatellite instability in sporadic mucinous colorectal carcinomas: relationship to clinico-pathological variables The Journal of Pathology ·Luca Messerini, Francesca Vitelli, Kyoung C. Park, Ririn Gagahrin, Anna Calzolari, Raffaele Palmirotta, Antonino Calabrò, Laura Papi	1997	79
17	Screening for mutations in the neurofibromatosis type 2 (NF2) gene in sporadic meningiomas Human Genetics ·Kyoung C. Park, Andrea Tedde, Francesca Vitelli, Franco Ammannati, P Mennonna, กุลนรี แนวพนิช, E Montali, Laura Papi	1996	1
18	Analysis of the neurofibromatosis type 2 gene in different human tumors of neuroectodermal origin Human Genetics ·Kyoung C. Park, Andrea Tedde, Francesca Vitelli, Franco Ammannati, P Mennonna, Bilel Mondher, Barbara Grammatico, Paola Grammatico, Paolo Radice, กุลนรี แนวพนิช, E Montali, Laura Papi	1996	19
19	Screening for mutations in the neurofibromatosis type 2 (NF2) gene in sporadic meningiomas Human Genetics ·Kyoung C. Park, Andrea Tedde, Francesca Vitelli, Franco Ammannati, P Mennonna, กุลนรี แนวพนิช, E Montali, Laura Papi	1996	62
20	Somatic mutations in the neurofibromatosis type 2 gene in sporadic meningiomas Human Genetics ·Laura Papi, Kyoung C. Park, Francesca Vitelli, E Montali, กุลนรี แนวพนิช, Franco Ammannati, P Mennonna	1995	55

About Francesca Vitelli

Francesca Vitelli is a scholar working on Immunology and Allergy, Neurology, Genetics, Molecular Biology and Epidemiology, having authored 28 papers that have together received 2.3k indexed citations. Recurring topics across this work include Congenital heart defects research (11 papers), Congenital Heart Disease Studies (5 papers), Neurofibromatosis and Schwannoma Cases (5 papers), Meningioma and schwannoma management (4 papers), Genomic variations and chromosomal abnormalities (3 papers), Developmental Biology and Gene Regulation (3 papers), Congenital Ear and Nasal Anomalies (2 papers) and Virus-based gene therapy research (2 papers). The work is most often cited by research in Molecular Biology (1.9k citations), Genetics (701 citations), Epidemiology (721 citations), Genetics (166 citations) and Sensory Systems (67 citations). Francesca Vitelli has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Antonio Baldini, Masae Morishima, Elizabeth A. Lindsay, Tuong Huynh, Peter Scambler, Helen Sutherland, Allan Bradley, Hong Hua Su, Vesna Jurecic and Tiziano Pramparo. Their work appears in journals such as Human Genetics, Genomics, Human Molecular Genetics, The Journal of Pathology and Developmental Biology.

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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