Follow
Fernando Gianfrancesco
Fernando Gianfrancesco
Research Director, National Researcher Council of Italy
Verified email at igb.cnr.it
Title
Cited by
Cited by
Year
Genomic rearrangement in NEMO impairs NF-κB activation and is a cause of incontinentia pigmenti.
A Smahi, G Courtois, P Vabres, S Yamaoka, S Heuertz, A Munnich, ...
Nature 405 (6785), 466-473, 2000
8662000
Genome-wide association identifies three new susceptibility loci for Paget's disease of bone
Nature genetics 43 (7), 685-689, 2011
1902011
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region
A Ciccodicola, M D’Esposito, T Esposito, F Gianfrancesco, C Migliaccio, ...
Human Molecular Genetics 9 (3), 395-401, 2000
1372000
A synaptobrevin–like gene in the Xq28 pseudoautosomal region undergoes X inactivation
M D'Esposito, A Ciccodicola, F Gianfrancesco, T Esposito, L Flagiello, ...
Nature genetics 13 (2), 227-229, 1996
1041996
Identification of a novel candidate gene, CASC2, in a region of common allelic loss at chromosome 10q26 in human endometrial cancer
P Baldinu, A Cossu, A Manca, MP Satta, MC Sini, C Rozzo, S Dessole, ...
Human mutation 23 (4), 318-326, 2004
1002004
piR_015520 belongs to Piwi-associated RNAs regulates expression of the human melatonin receptor 1A gene
T Esposito, S Magliocca, D Formicola, F Gianfrancesco
PLoS One 6 (7), e22727, 2011
982011
FSHR gene polymorphisms influence bone mineral density and bone turnover in postmenopausal women
D Rendina, F Gianfrancesco, G De Filippo, D Merlotti, T Esposito, ...
European journal of endocrinology 163 (1), 165-172, 2010
972010
Identification of a novel gene and a common variant associated with uric acid nephrolithiasis in a Sardinian genetic isolate
F Gianfrancesco, T Esposito, MN Ombra, P Forabosco, G Maninchedda, ...
The American Journal of Human Genetics 72 (6), 1479-1491, 2003
942003
SQSTM1 gene analysis and gene‐environment interaction in Paget's disease of bone
L Gennari, F Gianfrancesco, M Di Stefano, D Rendina, D Merlotti, ...
Journal of Bone and Mineral Research 25 (6), 1375-1384, 2010
792010
ZNF687 mutations in severe Paget disease of bone associated with giant cell tumor
G Divisato, D Formicola, T Esposito, D Merlotti, L Pazzaglia, A Del Fattore, ...
The American Journal of Human Genetics 98 (2), 275-286, 2016
752016
Common variants in the regulative regions of GRIA1 and GRIA3 receptor genes are associated with migraine susceptibility
D Formicola, A Aloia, S Sampaolo, O Farina, D Diodato, LR Griffiths, ...
BMC medical genetics 11, 1-12, 2010
702010
Common susceptibility alleles and SQSTM1 mutations predict disease extent and severity in a multinational study of patients with Paget's disease
OME Albagha, MR Visconti, N Alonso, S Wani, K Goodman, WD Fraser, ...
Journal of Bone and Mineral Research 28 (11), 2338-2346, 2013
652013
Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy
T Esposito, S Sampaolo, G Limongelli, A Varone, D Formicola, D Diodato, ...
Orphanet journal of rare diseases 8, 1-13, 2013
522013
Identification of sixteen novel candidate genes for late onset Parkinson’s disease
A Gialluisi, MG Reccia, N Modugno, T Nutile, A Lombardi, ...
Molecular neurodegeneration 16, 1-18, 2021
502021
Differential divergence of three human pseudoautosomal genes and their mouse homologs: implications for sex chromosome evolution
F Gianfrancesco, R Sanges, T Esposito, S Tempesta, E Rao, G Rappold, ...
Genome Research 11 (12), 2095-2100, 2001
502001
Clinical characteristics and evolution of giant cell tumor occurring in Paget's disease of bone
D Rendina, G De Filippo, SH Ralston, D Merlotti, F Gianfrancesco, ...
Journal of Bone and Mineral Research 30 (2), 257-263, 2015
462015
Different spectra of genomic deletions within the CCM genes between Italian and American CCM patient cohorts
CL Liquori, S Penco, J Gault, TP Leedom, L Tassi, T Esposito, IA Awad, ...
Neurogenetics 9, 25-31, 2008
462008
Identification and chromosomal localisation by fluorescence in situ hybridisation of human gene of phosphoinositide-specific phospholipase C β1
D Peruzzi, G Calabrese, I Faenza, L Manzoli, A Matteucci, ...
Biochimica et Biophysica Acta (BBA)-Molecular and Cell Biology of Lipids …, 2000
462000
A novel pseudoautosomal human gene encodes a putative protein similar to Ac-like transposases
T Esposito, F Gianfrancesco, A Ciccodicola, L Montanini, S Mumm, ...
Human molecular genetics 8 (1), 61-67, 1999
451999
A novel pseudoautosomal gene encoding a putative GTP-binding protein resides in the vicinity of the Xp/Yp telomere
F Gianfrancesco, T Esposito, L Montanini, A Ciccodicola, S Mumm, ...
Human molecular genetics 7 (3), 407-414, 1998
441998
The system can't perform the operation now. Try again later.
Articles 1–20