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Brunella Franco, MD
Brunella Franco, MD
Federico II University and Telethon Institute of Genetics and Medicine TIGEM, Naples Italy
Verified email at tigem.it
Title
Cited by
Cited by
Year
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
DJ Klionsky, AK Abdel-Aziz, S Abdelfatah, M Abdellatif, A Abdoli, S Abel, ...
autophagy 17 (1), 1-382, 2021
12554*2021
A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules
B Franco, S Guioli, A Pragliola, B Incerti, B Bardoni, R Tonlorenzi, ...
Nature 353 (6344), 529-536, 1991
9601991
Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene
AJ Coffey, RA Brooksbank, O Brandau, T Oohashi, GR Howell, JM Bye, ...
Nature genetics 20 (2), 129-135, 1998
8581998
Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiency
V Tiranti, K Hoertnagel, R Carrozzo, C Galimberti, M Munaro, ...
The American Journal of Human Genetics 63 (6), 1609-1621, 1998
6301998
Mutation analysis of the HLA-H gene in Italian hemochromatosis patients.
M Carella, L D'ambrosio, A Totaro, A Grifa, MA Valentino, A Piperno, ...
American journal of human genetics 60 (4), 828, 1997
4351997
Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22
NA Quaderi, S Schweiger, K Gaudenz, B Franco, EI Rugarli, W Berger, ...
Nature genetics 17 (3), 285-291, 1997
4051997
Autophagy promotes primary ciliogenesis by removing OFD1 from centriolar satellites
Z Tang, MG Lin, TR Stowe, S Chen, M Zhu, T Stearns, B Franco, Q Zhong
Nature 502 (7470), 254-257, 2013
3922013
Identification of the gene for oral-facial-digital type I syndrome
MI Ferrante, SA Feather, A Bulfone, V Wright, M Ghiani, A Selicorni, ...
The American Journal of Human Genetics 68 (3), 569-576, 2001
3782001
Oral-facial-digital type I protein is required for primary cilia formation and left-right axis specification
MI Ferrante, A Zullo, A Barra, S Bimonte, N Messaddeq, M Studer, P Dollé, ...
Nature genetics 38 (1), 112-117, 2006
3592006
A cluster of sulfatase genes on Xp22. 3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy
B Franco, G Meroni, G Parenti, J Levilliers, L Bernard, M Gebbia, L Cox, ...
Cell 81 (1), 15-25, 1995
3291995
Intragenic deletion of the KALIG-1 gene in Kallmann's syndrome
D Bick, B Franco, RJ Sherins, B Heye, L Pike, J Crawford, A Maddalena, ...
New England Journal of Medicine 326 (26), 1752-1755, 1992
2421992
An organelle-specific protein landscape identifies novel diseases and molecular mechanisms
K Boldt, J Van Reeuwijk, Q Lu, K Koutroumpas, TMT Nguyen, Y Texier, ...
Nature communications 7 (1), 11491, 2016
2342016
Oral–facial–digital syndromes: review and diagnostic guidelines
F Gurrieri, B Franco, H Toriello, G Neri
American Journal of Medical Genetics Part A 143 (24), 3314-3323, 2007
1772007
Activation of autophagy, observed in liver tissues from patients with Wilson disease and from ATP7B-deficient animals, protects hepatocytes from copper-induced apoptosis
EV Polishchuk, A Merolla, J Lichtmannegger, A Romano, A Indrieri, ...
Gastroenterology 156 (4), 1173-1189. e5, 2019
1752019
Identification and characterization of a novel serine–threonine kinase gene from the Xp22 region
E Montini, G Andolfi, A Caruso, G Buchner, SM Walpole, M Mariani, ...
Genomics 51 (3), 427-433, 1998
1671998
CDKL5/Stk9 kinase inactivation is associated with neuronal developmental disorders
C Lin, B Franco, MR Rosner
Human molecular genetics 14 (24), 3775-3786, 2005
1472005
The oral-facial-digital syndrome gene C2CD3 encodes a positive regulator of centriole elongation
C Thauvin-Robinet, JS Lee, E Lopez, V Herranz-Pérez, T Shida, B Franco, ...
Nature genetics 46 (8), 905-911, 2014
1392014
The ciliopathy-associated CPLANE proteins direct basal body recruitment of intraflagellar transport machinery
M Toriyama, C Lee, SP Taylor, I Duran, DH Cohn, AL Bruel, JM Tabler, ...
Nature genetics 48 (6), 648-656, 2016
1342016
Mutations in COX7B cause microphthalmia with linear skin lesions, an unconventional mitochondrial disease
A Indrieri, VA Van Rahden, V Tiranti, M Morleo, D Iaconis, R Tammaro, ...
The American Journal of Human Genetics 91 (5), 942-949, 2012
1342012
A gene from the Xp22. 3 region shares homology with voltage-gated chloride channels
MA Slegtenhorst, M T. Bassl, G Borsanil, MC Wapenaar, GB Ferrero, ...
Human molecular genetics 3 (4), 547-552, 1994
1291994
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