Alfredo Ciccodicola
Alfredo Ciccodicola
CNR, Institute of Genetics and Biophysics "A. Buzzati-Traverso" (IGB), Naples, Italy
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Cited by
Cited by
The DNA sequence of the human X chromosome
MT Ross, DV Grafham, AJ Coffey, S Scherer, K McLay, D Muzny, ...
Nature 434 (7031), 325-337, 2005
Genomic rearrangement in NEMO impairs NF-[kappa] B 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
Uncovering the complexity of transcriptomes with RNA-Seq
V Costa, C Angelini, I De Feis, A Ciccodicola
BioMed Research International 2010, 2010
A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X–linked retinitis pigmentosa (RP3)
A Meindl, K Dry, K Herrmann, E Manson, A Ciccodicola, A Edgar, ...
Nature genetics 13 (1), 35-42, 1996
Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa
R Vervoort, A Lennon, AC Bird, B Tulloch, R Axton, MG Miano, A Meindl, ...
Nature genetics 25 (4), 462-466, 2000
Molecular characterization of a gene of the ‘EGF family’expressed in undifferentiated human NTERA2 teratocarcinoma cells.
A Ciccodicola, R Dono, S Obici, A Simeone, M Zollo, MG Persico
The EMBO journal 8 (7), 1987-1991, 1989
RNA-Seq and human complex diseases: recent accomplishments and future perspectives
V Costa, M Aprile, R Esposito, A Ciccodicola
European Journal of Human Genetics 21 (2), 134-142, 2013
Transcriptome profiling in human diseases: new advances and perspectives
A Casamassimi, A Federico, M Rienzo, S Esposito, A Ciccodicola
International journal of molecular sciences 18 (8), 1652, 2017
Isolation, physical mapping, and northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2
M D’esposito, NA Quaderi, A Ciccodicola, P Bruni, T Esposito, M D’Urso, ...
Mammalian Genome 7, 533-535, 1996
Sequence of human glucose-6-phosphate dehydrogenase cloned in plasmids and a yeast artificial chromosome
EY Chen, A Cheng, A Lee, WJ Kuang, LD Hillier, P Green, D Schlessinger, ...
Genomics 10 (3), 792-800, 1991
Clinical and molecular genetics of Leber's congenital amaurosis: a multicenter study of Italian patients
F Simonelli, C Ziviello, F Testa, S Rossi, E Fazzi, PE Bianchi, M Fossarello, ...
Investigative ophthalmology & visual science 48 (9), 4284-4290, 2007
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
Mapping human chromosomes by walking with sequence-tagged sites from end fragments of yeast artificial chromosome inserts
J Kere, R Nagaraja, S Mumm, A Ciccodicola, M D'Urso, D Schlessinger
Genomics 14 (2), 241-248, 1992
Filamin A is mutated in X-linked chronic idiopathic intestinal pseudo-obstruction with central nervous system involvement
A Gargiulo, R Auricchio, MV Barone, G Cotugno, W Reardon, PJ Milla, ...
The American Journal of Human Genetics 80 (4), 751-758, 2007
Identification of new mutations in the Emery-Dreifuss muscular dystrophy gene and evidence for genetic heterogeneity of the disease
S Blone, K Small, VMA Aksmanovic, M D'Urso, A Ciccodicola, L Merlini, ...
Human molecular genetics 4 (10), 1859-1863, 1995
Klinefelter's syndrome as a model of anomalous cerebral laterality: testing gene dosage in the X chromosome pseudoautosomal region using a DNA microarray
DH Geschwind, J Gregg, K Boone, J Karrim, A Pawlikowska‐Haddal, ...
Developmental Genetics 23 (3), 215-229, 1998
Multiple pathogenic and benign genomic rearrangements occur at a 35 kb duplication involving the NEMO and LAGE2 genes
S Aradhya, T Bardaro, P Galgóczy, T Yamagata, T Esposito, H Patlan, ...
Human molecular genetics 10 (22), 2557-2567, 2001
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
Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families
C Ziviello, F Simonelli, F Testa, M Anastasi, SB Marzoli, B Falsini, ...
Journal of medical genetics 42 (7), e47-e47, 2005
PPARG in Human Adipogenesis: Differential Contribution of Canonical Transcripts and Dominant Negative Isoforms
M Aprile, MR Ambrosio, V D'Esposito, F Beguinot, P Formisano, V Costa, ...
PPAR research 2014, 2014
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