Emmanouil Athanasakis
Emmanouil Athanasakis
University of Trieste
Verified email at burlo.trieste.it - Homepage
Cited by
Cited by
A 3′ UTR SNP in NLRP3 gene is associated with susceptibility to HIV-1 infection
A Pontillo, LA Brandão, RL Guimarães, L Segat, E Athanasakis, ...
JAIDS Journal of Acquired Immune Deficiency Syndromes 54 (3), 236-240, 2010
Ex vivo molecular rejuvenation improves the therapeutic activity of senescent human cardiac stem cells in a mouse model of myocardial infarction
E Avolio, G Gianfranceschi, D Cesselli, A Caragnano, E Athanasakis, ...
Stem Cells 32 (9), 2373-2385, 2014
Genetics of food preferences: a first view from silk road populations
N Pirastu, A Robino, C Lanzara, E Athanasakis, L Esposito, BJ Tepper, ...
Journal of food science 77 (12), S413-S418, 2012
Autosomal recessive stickler syndrome due to a loss of function mutation in the COL9A3 gene
F Faletra, AP D'Adamo, I Bruno, E Athanasakis, S Biskup, L Esposito, ...
American Journal of Medical Genetics Part A 164 (1), 42-47, 2014
Molecular diagnosis of Usher syndrome: application of two different next generation sequencing-based procedures
D Licastro, M Mutarelli, I Peluso, K Neveling, N Wieskamp, R Rispoli, ...
PLoS One 7 (8), e43799, 2012
Molecular epidemiology of Usher syndrome in Italy
D Vozzi, A Aaspõllu, E Athanasakis, A Berto, A Fabretto, D Licastro, ...
Molecular vision 17, 1662, 2011
Next generation sequencing in nonsyndromic intellectual disability: from a negative molecular karyotype to a possible causative mutation detection
E Athanasakis, D Licastro, F Faletra, A Fabretto, S Dipresa, D Vozzi, ...
American Journal of Medical Genetics Part A 164 (1), 170-176, 2014
Phospholipase C-β3 is a key modulator of IL-8 expression in cystic fibrosis bronchial epithelial cells
V Bezzerri, P d’Adamo, A Rimessi, C Lanzara, S Crovella, E Nicolis, ...
The Journal of Immunology 186 (8), 4946-4958, 2011
Genetic profiling of autoinflammatory disorders in patients with periodic fever: a prospective study
C De Pieri, J Vuch, E De Martino, AM Bianco, L Ronfani, E Athanasakis, ...
Pediatric Rheumatology 13 (1), 1-8, 2015
Congenital hyperinsulinism: clinical and molecular analysis of a large Italian cohort
F Faletra, E Athanasakis, A Morgan, X Biarnés, F Fornasier, R Parini, ...
Gene 521 (1), 160-165, 2013
F402L variant in NLRP12 in subjects with undiagnosed periodic fevers and in healthy controls.
C De Pieri, J Vuch, E Athanasakis, GM Severini, S Crovella, AM Bianco, ...
Clinical and experimental rheumatology 32 (6), 993-994, 2014
High-throughput genotyping robot-assisted method for mutation detection in patients with hypertrophic cardiomyopathy
B Bortot, E Athanasakis, F Brun, D Rizzotti, L Mestroni, G Sinagra, ...
Diagnostic Molecular Pathology 20 (3), 175-179, 2011
Association of a variant in the CHRNA5-A3-B4 gene cluster region to heavy smoking in the Italian population
R Sorice, S Bione, S Sansanelli, S Ulivi, E Athanasakis, C Lanzara, ...
European Journal of Human Genetics 19 (5), 593-596, 2011
A technical application of quantitative next generation sequencing for chimerism evaluation
M Aloisio, D Licastro, L Caenazzo, V Torboli, A D'eustacchio, GM Severini, ...
Molecular medicine reports 14 (4), 2967-2974, 2016
Polymorphisms in innate immunity genes and patients response to dendritic cell-based HIV immuno-treatment
L Segat, LAC Brandão, RL Guimarães, A Pontillo, E Athanasakis, ...
Vaccine 28 (10), 2201-2206, 2010
Complex rearrangement of the exon 6 genomic region among Opitz G/BBB Syndrome MID1 alterations
C Migliore, E Athanasakis, S Dahoun, A Wonkam, M Lees, O Calabrese, ...
European journal of medical genetics 56 (8), 404-410, 2013
A novel CRYBB2 missense mutation causing congenital autosomal dominant cataract in an Italian family
F Faletra, AP d’Adamo, S Pensiero, E Athanasakis, D Catalano, I Bruno, ...
Ophthalmic genetics 34 (1-2), 115-117, 2013
The γ-secretase inhibitors enhance the anti-leukemic activity of ibrutinib in B-CLL cells
P Secchiero, R Voltan, E Rimondi, E Melloni, E Athanasakis, V Tisato, ...
Oncotarget 8 (35), 59235, 2017
Vertebral defects in patients with Peters plus syndrome and mutations in B3GALTL
F Faletra, E Athanasakis, F Minen, F Fornasier, F Marchetti, P Gasparini
Ophthalmic genetics 32 (4), 256-258, 2011
Co-inheritance of two ABCC8 mutations causing an unresponsive congenital hyperinsulinism: clinical and functional characterization of two novel ABCC8 mutations
F Faletra, K Snider, SL Shyng, I Bruno, E Athanasakis, P Gasparini, ...
Gene 516 (1), 122-125, 2013
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