| Screening of genetic alterations related to non-syndromic hearing loss using MassARRAY iPLEX® technology MCCCCM Svidnicki, SM Silva-Costa, PZ Ramos, NZP Dos Santos, ... BMC medical genetics 16, 1-11, 2015 | 34 | 2015 |
| Optimization of simultaneous screening of the main mutations involved in non-syndromic deafness using the TaqMan® OpenArray™ Genotyping platform FTA Martins, PZ Ramos, MCCM Svidnicki, AM Castilho, EL Sartorato BMC medical genetics 14, 1-9, 2013 | 31 | 2013 |
| Molecular analysis of SLC26A4 gene in patients with nonsyndromic hearing loss and EVA: identification of two novel mutations in Brazilian patients VCS de Moraes, NZP dos Santos, PZ Ramos, MCCM Svidnicki, ... International journal of pediatric otorhinolaryngology 77 (3), 410-413, 2013 | 25 | 2013 |
| Targeted next-generation sequencing identified novel mutations associated with hereditary anemias in Brazil M Svidnicki, GK Zanetta, A Congrains-Castillo, FF Costa, STO Saad Annals of hematology 99, 955-962, 2020 | 23 | 2020 |
| Etiologic and diagnostic evaluation: algorithm for severe to profound sensorineural hearing loss in Brazil PZ Ramos, VCS de Moraes, MCCM Svidnicki, MN Soki, AM Castilho, ... International journal of audiology 52 (11), 746-752, 2013 | 21 | 2013 |
| Novel mutations associated with pyruvate kinase deficiency in Brazil MCCM Svidnicki, A Santos, JAA Fernandez, APH Yokoyama, ... Hematology, Transfusion and Cell Therapy 40 (1), 5-11, 2018 | 17 | 2018 |
| Karyotypic variability in Iheringichthys lahrosus(Teleostei, Pimelodidae) from the Tibagi River basin(Parana State, Brazil) LB Ribeiro, DA Matoso, MC Almeida, MR Vicari, A Moraes-Neto, ... Genetics and Molecular Research 7 (3), 718-724, 2008 | 17 | 2008 |
| Study of candidate genes for dyslexia in Brazilian individuals M Svidnicki, CA Salgado, RF Lima, SM Ciasca, R Secolin, MCA Pomilio, ... Genetics and Molecular Research 12 (4), 5356-5364, 2013 | 15 | 2013 |
| New germline GATA1 variant in females with anemia and thrombocytopenia MCCM Svidnicki, MA Ferreira Filho, MM Brandão, M Dos Santos, ... Blood Cells, Molecules, and Diseases 88, 102545, 2021 | 9 | 2021 |
| Mutations in triple-negative patients with myeloproliferative neoplasms MCCM Svidnicki, PDM Campos, MA Ferreira Filho, CAL Fujiura, ... Blood 134, 5395, 2019 | 4 | 2019 |
| Estudo de genes candidatos em indivíduos brasileiros com dislexia MCCM Svidnicki [sn], 2011 | 2 | 2011 |
| Desenvolvimento de painel diagnóstico para rastreamento simultâneo das principais mutações envolvidas na perda auditiva MCCM Svidnicki [sn], 2015 | 1 | 2015 |
| Mutations in Triple-Negative Patients with Myeloproliferative Neoplasms T Yoshizato, MCCM Svidnicki, STO Saad, H Makishima, S Ogawa, ... Blood 134, 5395-5395, 2019 | | 2019 |
| Screening of Mutations Related to Hereditary Anemias Using NGS-Targeted Sequencing Panel MCCM Svidnicki, FF Costa, STO Saad Blood 130, 2209, 2017 | | 2017 |
| Associação entre fenótipo, desempenho com próteses auditivas e genótipo da deficiência auditiva infantil em crianças com e sem alteração genética EPV Biaggio, MF Azevedo, MCM Iório, MCCM Svidnicki, EL Satorato Jornal da Sociedade Brasileira de Fonoaudiologia 24, 327-334, 2012 | | 2012 |
| Association between phenotype, performance with hearing aids, and genotype of childhood hearing loss in children with and without genetic alteration EPV Biaggio, MF Azevedo, MCM Iório, MCCM Svidnicki, EL Satorato Jornal da Sociedade Brasileira de Fonoaudiologia 24, 327-334, 2012 | | 2012 |
| Karyotypic variability in Iheringichthys labrosus (Teleostei, Pimelodidae) from the Tibagi River basin (Paraná State, Brazil) L Braga Ribeiro, DA Matoso, MC Almeida, MR Vicari, A Moraes-Neto, ... Volume 7, Número 3, Pags. 718-724, 2008 | | 2008 |
| Hematology, Transfusion and Cell Therapy MCCM Svidnicki, A Santos, JAA Fernandez, APH Yokoyama, ... | | |
