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Francesca Vitelli
Observed names:
F Vitelli,
F. VITELLI,
F. Vitelli,
VITELLI F,
Vitelli, F,
Vitelli, Francesca
show all 6
Observed institutions:
University of Siena,
Texas A&M Health Science Center,
Baylor College of Medicine,
Istituto Giannina Gaslini,
Yale University,
University of Florence,
Texas A&M University
show all 7
OpenAlex ID:
A5003825780
Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice
2001
·
Elizabeth A. Lindsay
, Francesca Vitelli
, et al.
·
Nature
·
1,019
Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways
2002
·
F. Vitelli
·
Human Molecular Genetics
·
330
A genetic link betweenTbx1and fibroblast growth factor signaling
2002
·
Francesca Vitelli
, Ilaria Taddei
, et al.
·
Development
·
281
Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice
2009
·
Victoria Randall
, Karen McCue
, et al.
·
Journal of Clinical Investigation
·
149
PDF
FACL4, a New Gene Encoding Long-Chain Acyl-CoA Synthetase 4, Is Deleted in a Family with Alport Syndrome, Elliptocytosis, and Mental Retardation
1998
·
Monica Piccini
, Francesca Vitelli
, et al.
·
Genomics
·
130
PDF
Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development
2005
·
Zhen Zhang
, Fabiana Cerrato
, et al.
·
Development
·
129
Preserved speech variant is allelic of classic Rett syndrome
2000
·
Cristina De Bona
, Michele Zappella
, et al.
·
European Journal of Human Genetics
·
127
PDF
TBX1 is required for inner ear morphogenesis
2003
·
F. Vitelli
·
Human Molecular Genetics
·
119
Microsatellite instability in sporadic mucinous colorectal carcinomas: relationship to clinico-pathological variables
1997
·
Luca Messerini
, Francesca Vitelli
, et al.
·
The Journal of Pathology
·
88
Screening for mutations in the neurofibromatosis type 2 (NF2) gene in sporadic meningiomas
1996
·
Lucia Rosaria De Vitis
, Andrea Tedde
, et al.
·
Human Genetics
·
79
Somatic mutations in the neurofibromatosis type 2 gene in sporadic meningiomas
1995
·
Laura Papi
, Lucia Rosaria De Vitis
, et al.
·
Human Genetics
·
76
KCNE1-like Gene Is Deleted in AMME Contiguous Gene Syndrome: Identification and Characterization of the Human and Mouse Homologs
1999
·
Monica Piccini
, Francesca Vitelli
, et al.
·
Genomics
·
75
Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis: a new X linked contiguous gene deletion syndrome?
1998
·
J J Jonsson
, A Renieri
, et al.
·
Journal of Medical Genetics
·
62
PDF
Fgf8 expression in the Tbx1 domain causes skeletal abnormalities and modifies the aortic arch but not the outflow tract phenotype of Tbx1 mutants
2006
·
Francesca Vitelli
, Zhen Zhang
, et al.
·
Developmental Biology
·
52
PDF
Early thyroid development requires a Tbx1–Fgf8 pathway
2009
·
Gabriella Lania
, Zhen Zhang
, et al.
·
Developmental Biology
·
51
PDF
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)
1999
·
Francesca Vitelli
, Monica Piccini
, et al.
·
Genomics
·
42
Gain of function of Tbx1 affects pharyngeal and heart development in the mouse
2009
·
Francesca Vitelli
, Tuong Huynh
, et al.
·
genesis
·
37
Analysis of the neurofibromatosis type 2 gene in different human tumors of neuroectodermal origin
1996
·
Lucia Rosaria De Vitis
, Andrea Tedde
, et al.
·
Human Genetics
·
35
Partial rescue of the Tbx1 mutant heart phenotype by Fgf8: Genetic evidence of impaired tissue response to Fgf8
2010
·
Francesca Vitelli
, Gabriella Lania
, et al.
·
Journal of Molecular and Cellular Cardiology
·
25
Inheritance of a 38-kb fragment in apparently sporadic facioscapulohumeral muscular dystrophy
1999
·
Francesca Vitelli
, Marcello Villanova
, et al.
·
Muscle & Nerve
·
22
Establishment of a scalable manufacturing platform for in-silico-derived ancestral adeno-associated virus vectors
2018
·
Bingnan Gu
, Vijetha Bhat
, et al.
·
Cell and Gene Therapy Insights
·
19
Generating and modifying DiGeorge syndrome-like phenotypes in model organisms: is there a common genetic pathway?
2003
·
Francesca Vitelli
, Antonio Baldini
·
Trends in Genetics
·
18
Genetic Dissection of the DiGeorge Syndrome Phenotype
2002
·
F. VITELLI
, E.A. LINDSAY
, et al.
·
Cold Spring Harbor Symposia on Quantitative Biology
·
16
Identification and characterization of mouse orthologs of the AMMECR1 and FACL4 genes deleted in AMME syndrome: orthology of Xq22.3 and MmuXF1–F3
2000
·
F. Vitelli
, I. Meloni
, et al.
·
Cytogenetic and Genome Research
·
13
Gene Therapy
2017
·
Barb Thorne
, Ryan Takeya
, et al.
·
Advances in biochemical engineering, biotechnology
·
11
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Works count:
38
Citation count:
3,009
H-index:
20
I10-index:
25
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