GJB2 mutations and degree of hearing loss: a multicenter study RL Snoeckx, PLM Huygen, D Feldmann, S Marlin, F Denoyelle, ... The American Journal of Human Genetics 77 (6), 945-957, 2005 | 700 | 2005 |
Occupational noise, smoking, and a high body mass index are risk factors for age-related hearing impairment and moderate alcohol consumption is protective: a European … E Fransen, V Topsakal, JJ Hendrickx, L Van Laer, JR Huyghe, ... Journal of the Association for Research in Otolaryngology 9, 264-276, 2008 | 405 | 2008 |
A genotype-phenotype correlation for GJB2 (connexin 26) deafness K Cryns, E Orzan, A Murgia, PLM Huygen, F Moreno, I Del Castillo, ... Journal of medical genetics 41 (3), 147-154, 2004 | 322 | 2004 |
GRM7 variants confer susceptibility to age-related hearing impairment RA Friedman, L Van Laer, MJ Huentelman, SS Sheth, E Van Eyken, ... Human molecular genetics 18 (4), 785-796, 2009 | 259 | 2009 |
Cx26 deafness: mutation analysis and clinical variability A Murgia, E Orzan, R Polli, M Martella, C Vinanzi, E Leonardi, E Arslan, ... Journal of medical genetics 36 (11), 829-832, 1999 | 212 | 1999 |
The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment L Van Laer, E Van Eyken, E Fransen, JR Huyghe, V Topsakal, ... Human molecular genetics 17 (2), 159-169, 2008 | 188 | 2008 |
Early primary cytomegalovirus infection in pregnancy: maternal hyperimmunoglobulin therapy improves outcomes among infants at 1 year of age S Visentin, R Manara, L Milanese, A Da Roit, G Forner, E Salviato, ... Clinical infectious diseases 55 (4), 497-503, 2012 | 180 | 2012 |
Global problem of drug‐induced hearing loss E Arslan, E Orzan, R Santarelli Annals of the New York Academy of Sciences 884 (1), 1-14, 1999 | 124 | 1999 |
Contribution of the N-acetyltransferase 2 polymorphism NAT2* 6A to age-related hearing impairment E Van Eyken, G Van Camp, E Fransen, V Topsakal, JJ Hendrickx, ... Journal of medical genetics 44 (9), 570-578, 2007 | 117 | 2007 |
Reliability of hearing screening in high-risk neonates: comparative study of otoacoustic emission, automated and conventional auditory brainstem response A Suppiej, E Rizzardi, V Zanardo, M Franzoi, M Ermani, E Orzan Clinical Neurophysiology 118 (4), 869-876, 2007 | 95 | 2007 |
Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait JR Huyghe, L Van Laer, JJ Hendrickx, E Fransen, K Demeester, ... The American Journal of Human Genetics 83 (3), 401-407, 2008 | 79 | 2008 |
The contribution of GJB2 (Connexin 26) 35delG to age-related hearing impairment and noise-induced hearing loss E Van Eyken, L Van Laer, E Fransen, V Topsakal, JJ Hendrickx, ... Otology & Neurotology 28 (7), 970-975, 2007 | 77 | 2007 |
Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene N Hilgert, MJ Huentelman, AQ Thorburn, E Fransen, N Dieltjens, ... European journal of human genetics 17 (4), 517-524, 2009 | 65 | 2009 |
Molecular genetics applied to clinical practice: the Cx26 hearing impairment E Orzan, R Polli, M Martella, C Vinanzi, M Leonardi, A Murgia British journal of audiology 33 (5), 291-295, 1999 | 51 | 1999 |
Short report on the effects of SARS-CoV-2 face protective equipment on verbal communication E Muzzi, C Chermaz, V Castro, M Zaninoni, A Saksida, E Orzan European Archives of Oto-rhino-laryngology 278, 3565-3570, 2021 | 46 | 2021 |
Familial aggregation of tinnitus, a European multicentre study. JJ Hendrickx, JR Huyghe, K Demeester, V Topsakal, E Van Eyken, ... B ENT 2, 51-60, 2007 | 39 | 2007 |
A multicenter clinical evaluation of data logging in cochlear implant recipients using automated scene classification technologies E Cristofari, D Cuda, A Martini, F Forli, D Zanetti, D Di Lisi, P Marsella, ... Audiology and Neurotology 22 (4-5), 226-235, 2018 | 36 | 2018 |
Connexin 26 deafness is not always congenital E Orzan, A Murgia International journal of pediatric otorhinolaryngology 71 (3), 501-507, 2007 | 36 | 2007 |
Monitoring protocols for cochlear toxicity SG Lord Seminars in hearing 40 (02), 122-143, 2019 | 31 | 2019 |
Genomic studies in a large cohort of hearing impaired Italian patients revealed several new alleles, a rare case of uniparental disomy (UPD) and the importance to search for … A Morgan, S Lenarduzzi, S Cappellani, V Pecile, M Morgutti, E Orzan, ... Frontiers in Genetics 9, 681, 2018 | 29 | 2018 |