Coviello Domenico
Coviello Domenico
IRCCS Giannina Gaslini Research Institute, Genova
Verified email at unige.it - Homepage
Title
Cited by
Cited by
Year
A mutant tropomyosin that causes hypertrophic cardiomyopathy is expressed in vivo and associated with an increased calcium sensitivity
R Bottinelli, DA Coviello, CS Redwood, MA Pellegrino, BJ Maron, ...
Circulation Research 82 (1), 106-115, 1998
1921998
The interface between assisted reproductive technologies and genetics: technical, social, ethical and legal issues
S Soini, D Ibarreta, V Anastasiadou, S Aymé, S Braga, M Cornel, ...
European Journal of Human Genetics 14 (5), 588-645, 2006
1902006
Clinical features of hypertrophic cardiomyopathy caused by mutation of a “hot spot” in the alpha-tropomyosin gene
DA Coviello, BJ Maron, P Spirito, H Watkins, HP Vosberg, L Thierfelder, ...
Journal of the American College of Cardiology 29 (3), 635-640, 1997
1611997
Androgen and estrogen receptors are present in primary cultures of human synovial macrophages
M Cutolo, S Accardo, B Villaggio, A Barone, A Sulli, DA Coviello, ...
The Journal of Clinical Endocrinology & Metabolism 81 (2), 820-827, 1996
1491996
Genetic education and the challenge of genomic medicine: development of core competences to support preparation of health professionals in Europe
H Skirton, C Lewis, A Kent, DA Coviello
European Journal of Human Genetics 18 (9), 972-977, 2010
1362010
Genotype and phenotype characterization in a large dystrophinopathic cohort with extended follow-up
F Magri, A Govoni, MG D’Angelo, R Del Bo, S Ghezzi, G Sandra, ...
Journal of neurology 258 (9), 1610-1623, 2011
1342011
R990G polymorphism of calcium-sensing receptor does produce a gain-of-function and predispose to primary hypercalciuria
G Vezzoli, A Terranegra, T Arcidiacono, R Biasion, D Coviello, ML Syren, ...
Kidney international 71 (11), 1155-1162, 2007
1302007
Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance
F Zara, N Specchio, P Striano, A Robbiano, E Gennaro, R Paravidino, ...
Epilepsia 54 (3), 425-436, 2013
1192013
Banking together: a unified model of informed consent for biobanking
E Salvaterra, L Lecchi, S Giovanelli, B Butti, MT Bardella, PA Bertazzi, ...
EMBO reports 9 (4), 307-313, 2008
1182008
Presence of estrogen‐binding sites on macrophage‐like synoviocytes and CD8+, CD29+, CD45RO+ T lymphocytes in normal and rheumatoid synovium
M Cutolo, S Accardo, B Villaggio, P Clerico, M Bagnasco, DA Coviello, ...
Arthritis & Rheumatism: Official Journal of the American College of …, 1993
991993
Provision of genetic services in Europe: current practices and issues
B Godard, H Kääriäinen, U Kristoffersson, L Tranebjaerg, D Coviello, ...
European Journal of Human Genetics 11 (2), S13-S48, 2003
982003
Estradiol inhibits growth of hormone-nonresponsive PC3 human prostate cancer cells
G Carruba, U Pfeffer, E Fecarotta, DA Coviello, E D'Amato, ML Casto, ...
Cancer research 54 (5), 1190-1193, 1994
981994
Mutation frequencies of GNAQ, GNA11, BAP1, SF3B1, EIF1AX and TERT in uveal melanoma: detection of an activating mutation in the TERT gene promoter …
M Dono, G Angelini, M Cecconi, A Amaro, AI Esposito, V Mirisola, I Maric, ...
British journal of cancer 110 (4), 1058-1065, 2014
902014
Molecular characterization and structural implications of 25 new ABCB4 mutations in progressive familial intrahepatic cholestasis type 3 (PFIC3)
D Degiorgio, C Colombo, M Seia, L Porcaro, L Costantino, L Zazzeron, ...
European Journal of Human Genetics 15 (12), 1230-1238, 2007
892007
First characterization of human amniotic fluid stem cell extracellular vesicles as a powerful paracrine tool endowed with regenerative potential
C Balbi, M Piccoli, L Barile, A Papait, A Armirotti, E Principi, D Reverberi, ...
Stem cells translational medicine 6 (5), 1340-1355, 2017
822017
A de novo mutation in α-tropomyosin that causes hypertrophic cardiomyopathy
H Watkins, R Anan, DA Coviello, P Spirito, JG Seidman, CE Seidman
Circulation 91 (9), 2302-2305, 1995
821995
ELOVL5 mutations cause spinocerebellar ataxia 38
E Di Gregorio, B Borroni, E Giorgio, D Lacerenza, M Ferrero, NL Buono, ...
The American Journal of Human Genetics 95 (2), 209-217, 2014
812014
Clinical significance of rare copy number variations in epilepsy: a case-control survey using microarray-based comparative genomic hybridization
P Striano, A Coppola, R Paravidino, M Malacarne, S Gimelli, A Robbiano, ...
Archives of neurology 69 (3), 322-330, 2012
752012
De novo balanced chromosome rearrangements in prenatal diagnosis
D Giardino, C Corti, L Ballarati, D Colombo, E Sala, N Villa, G Piombo, ...
Prenatal diagnosis 29 (3), 257-265, 2009
732009
Clinical features and genotype-phenotype correlations in children with progressive familial intrahepatic cholestasis type 3 related to ABCB4 mutations
C Colombo, P Vajro, D Degiorgio, DA Coviello, L Costantino, L Tornillo, ...
Journal of pediatric gastroenterology and nutrition 52 (1), 73-83, 2011
642011
The system can't perform the operation now. Try again later.
Articles 1–20