| Prevalence of GJB2 (connexin-26) and GJB6 (connexin-30) mutations in a cohort of 300 Brazilian hearing-impaired individuals: implications for diagnosis and genetic counseling AC Batissoco, RS Abreu-Silva, MCC Braga, K Lezirovitz, V Della-Rosa, ... Ear and hearing 30 (1), 1-7, 2009 | 100 | 2009 |
| Novel OTOF mutations in Brazilian patients with auditory neuropathy J Romanos, L Kimura, ML Fávero, FAR Izarra, MTB de Mello Auricchio, ... Journal of human genetics 54 (7), 382-385, 2009 | 69 | 2009 |
| Unexpected genetic heterogeneity in a large consanguineous Brazilian pedigree presenting deafness K Lezirovitz, E Pardono, MTB de Mello Auricchio, FL de Carvalho e Silva, ... European Journal of Human Genetics 16 (1), 89-96, 2008 | 68 | 2008 |
| Aspectos moleculares do sistema sangüíneo ABO AC Batissoco, MCZ Novaretti Revista Brasileira de Hematologia e Hemoterapia 25, 47-58, 2003 | 55 | 2003 |
| The search of a genetic basis for noise-induced hearing loss (NIHL) RS Abreu-Silva, D Rincon, ARVR Horimoto, AP Sguillar, LAC Ricardo, ... Annals of Human Biology 38 (2), 210-218, 2011 | 52 | 2011 |
| Is autosomal recessive deafness associated with oculocutaneous albinism a “coincidence syndrome”? K Lezirovitz, FS Nicastro, E Pardono, RS Abreu-Silva, AC Batissoco, ... Journal of human genetics 51 (8), 716-720, 2006 | 24 | 2006 |
| Stem-cell therapy for hearing loss: are we there yet? LG Dufner-Almeida, DB Cruz, RC Mingroni, AC Batissoco, J Oiticica, ... Brazilian journal of otorhinolaryngology 85, 520-529, 2019 | 22 | 2019 |
| A cell junctional protein network associated with connexin-26 AC Batissoco, R Salazar-Silva, J Oiticica, RF Bento, RC Mingroni-Netto, ... International journal of molecular sciences 19 (9), 2535, 2018 | 20 | 2018 |
| Retention of progenitor cell phenotype in otospheres from guinea pig and mouse cochlea J Oiticica, LCM Barboza-Junior, AC Batissoco, K Lezirovitz, ... Journal of Translational Medicine 8, 1-10, 2010 | 20 | 2010 |
| Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing-impaired subjects RW Nonose, K Lezirovitz, MTB de Mello Auricchio, AC Batissoco, ... BMC medical genetics 19, 1-10, 2018 | 18 | 2018 |
| NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss R Salazar-Silva, VLG Dantas, LU Alves, AC Batissoco, J Oiticica, ... Human Molecular Genetics 29 (22), 3691-3705, 2020 | 16 | 2020 |
| " In vivo" and" in vitro" demonstration of hemoglobin C crystals in non-splenectomized patients JT De Araujo, AC Batissoco, L Bodemeier Revista do Instituto de Medicina Tropical de São Paulo 41, 235-238, 1999 | 14 | 1999 |
| Exome Sequencing Identifies a Novel Nonsense Mutation of MYO6 as the Cause of Deafness in a Brazilian Family J Sampaio‐Silva, AC Batissoco, R Jesus‐Santos, O Abath‐Neto, ... Annals of human genetics 82 (1), 23-34, 2018 | 13 | 2018 |
| Aberrant transcript produced by a splice donor site deletion in the TECTA gene is associated with autosomal dominant deafness in a Brazilian family K Lezirovitz, AC Batissoco, FT Lima, MTBM Auricchio, RW Nonose, ... Gene 511 (2), 280-284, 2012 | 13 | 2012 |
| A rare genomic duplication in 2p14 underlies autosomal dominant hearing loss DFNA58 K Lezirovitz, GA Vieira-Silva, AC Batissoco, D Levy, JP Kitajima, ... Human molecular genetics 29 (9), 1520-1536, 2020 | 12 | 2020 |
| A novel missense mutation p. L76P in the GJB2 gene causing nonsyndromic recessive deafness in a Brazilian family AC Batissoco, MTBM Auricchio, L Kimura, A Tabith-Junior, ... Brazilian Journal of Medical and Biological Research 42, 168-171, 2009 | 12 | 2009 |
| Molecular and genetic characterization of a large Brazilian cohort presenting hearing loss AC Batissoco, V Pedroso-Campos, E Pardono, J Sampaio-Silva, ... Human genetics 141 (3), 519-538, 2022 | 9 | 2022 |
| Easy method for determining the frequency of O^ 1 and O^ 2 alleles in Brazilian blood donors by PCR-RFLP analysis AC Batissoco, MC Zago-Novaretti, VJ Bueno, PE Dorlhiac-Llacer, ... IMMUNOHEMATOLOGY-WASHINGTON DC- 17 (4), 111-116, 2001 | 7 | 2001 |
| Correspondence regarding Ballana et al.,“Mitochondrial 12S rRNA gene mutations affect RNA secondary structure and lead to variable penetrance in hearing impairment” RS Abreu-Silva, AC Batissoco, K Lezirovitz, J Romanos, D Rincon, ... Biochemical and biophysical research communications 343 (3), 675-676, 2006 | 6 | 2006 |
| Molecular aspects of ABO blood group system AC Batissoco, MCZ Novaretti Revista Brasileira de Hematologia e Hemoterapia 25, 47-58, 2003 | 5 | 2003 |
Karina Lezirovitz MandelbaumUniversidade de São Paulo - Faculdade de Medicina - Hospital das Clínicas - Otolaringology Lab/LIM32在 hc.fm.usp.br 的电子邮件经过验证
