Francesco Vetrini, Ph.D.
Francesco Vetrini, Ph.D.
Indiana University School of Medicine
Verified email at
Cited by
Cited by
TFEB links autophagy to lysosomal biogenesis
C Settembre, C Di Malta, VA Polito, MG Arencibia, F Vetrini, S Erdin, ...
science 332 (6036), 1429-1433, 2011
A lysosome‐to‐nucleus signalling mechanism senses and regulates the lysosome via mTOR and TFEB
C Settembre, R Zoncu, DL Medina, F Vetrini, S Erdin, SU Erdin, T Huynh, ...
The EMBO journal 31 (5), 1095-1108, 2012
TFEB controls cellular lipid metabolism through a starvation-induced autoregulatory loop
C Settembre, R De Cegli, G Mansueto, PK Saha, F Vetrini, O Visvikis, ...
Nature cell biology 15 (6), 647-658, 2013
Use of exome sequencing for infants in intensive care units: ascertainment of severe single-gene disorders and effect on medical management
L Meng, M Pammi, A Saronwala, P Magoulas, AR Ghazi, F Vetrini, ...
JAMA pediatrics 171 (12), e173438-e173438, 2017
Reanalysis of clinical exome sequencing data
P Liu, L Meng, EA Normand, F Xia, X Song, A Ghazi, J Rosenfeld, ...
New England Journal of Medicine 380 (25), 2478-2480, 2019
Gene transfer of master autophagy regulator TFEB results in clearance of toxic protein and correction of hepatic disease in alpha‐1‐anti‐trypsin deficiency
N Pastore, K Blomenkamp, F Annunziata, P Piccolo, P Mithbaokar, ...
EMBO molecular medicine 5 (3), 397-412, 2013
Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder
EA Normand, A Braxton, S Nassef, PA Ward, F Vetrini, W He, V Patel, ...
Genome medicine 10, 1-14, 2018
Recurrent muscle weakness with rhabdomyolysis, metabolic crises, and cardiac arrhythmia due to bi-allelic TANGO2 mutations
SR Lalani, P Liu, JA Rosenfeld, LB Watkin, T Chiang, MS Leduc, W Zhu, ...
The American Journal of Human Genetics 98 (2), 347-357, 2016
Generation of a Kupffer cell-evading adenovirus for systemic and liver-directed gene transfer
R Khare, SM May, F Vetrini, EA Weaver, D Palmer, A Rosewell, N Grove, ...
Molecular Therapy 19 (7), 1254-1262, 2011
Complex compound inheritance of lethal lung developmental disorders due to disruption of the TBX-FGF pathway
JA Karolak, M Vincent, G Deutsch, T Gambin, B Cogné, O Pichon, ...
The American Journal of Human Genetics 104 (2), 213-228, 2019
Modifications of adenovirus hexon allow for either hepatocyte detargeting or targeting with potential evasion from Kupffer cells
JM Prill, S Espenlaub, U Samen, T Engler, E Schmidt, F Vetrini, ...
Molecular Therapy 19 (1), 83-92, 2011
Gene therapy with helper-dependent adenoviral vectors: current advances and future perspectives
F Vetrini, P Ng
Viruses 2 (9), 1886, 2010
Haploinsufficiency of the chromatin remodeler BPTF causes syndromic developmental and speech delay, postnatal microcephaly, and dysmorphic features
P Stankiewicz, TN Khan, P Szafranski, L Slattery, H Streff, F Vetrini, ...
The American Journal of Human Genetics 101 (4), 503-515, 2017
The microphthalmia transcription factor (Mitf) controls expression of the ocular albinism type 1 gene: link between melanin synthesis and melanosome biogenesis
F Vetrini, A Auricchio, J Du, B Angeletti, DE Fisher, A Ballabio, V Marigo
Molecular and cellular biology, 2004
Phenotypic expansion in DDX3X – a common cause of intellectual disability in females
X Wang, JE Posey, JA Rosenfeld, CA Bacino, F Scaglia, LD Immken, ...
Annals of clinical and translational neurology 5 (10), 1277-1285, 2018
Bi-allelic mutations in PKD1L1 are associated with laterality defects in humans
F Vetrini, LCA D’Alessandro, ZC Akdemir, A Braxton, MS Azamian, ...
The American Journal of Human Genetics 99 (4), 886-893, 2016
SR-A and SREC-I are Kupffer and endothelial cell receptors for helper-dependent adenoviral vectors
P Piccolo, F Vetrini, P Mithbaokar, NC Grove, T Bertin, D Palmer, P Ng, ...
Molecular Therapy 21 (4), 767-774, 2013
Sustained reduction of hyperbilirubinemia in Gunn rats after adeno-associated virus-mediated gene transfer of bilirubin UDP-glucuronosyltransferase isozyme 1A1 to skeletal muscle
N Pastore, E Nusco, J Vaníkova, RM Sepe, F Vetrini, A McDonagh, ...
Human gene therapy 23 (10), 1082-1089, 2012
Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases
AV Dharmadhikari, R Ghosh, BO Yuan, P Liu, H Dai, S Al Masri, J Scull, ...
Genome medicine 11, 1-17, 2019
FGF and EGF differently affect differentiation of murine retinal stem cells in vitro
F Giordano, A De Marzo, F Vetrini, V Marigo
Molecular vision 13, 1842-1850, 2007
The system can't perform the operation now. Try again later.
Articles 1–20