121
TÍTULO: Duplication 17q24.3q25.1, inserted on 17p13, encompassing SOX9: the impact on the phenotype
AUTORES: Matoso, E; Louro, P; Estevinho, A; Ferreira, SI; Paiva, P; Melo, JB; Mirante, A; Melo, US; Mundlos, S; Sousa, SB; Ramos, L; Saraiva, J; Carreira, IM;
PUBLICAÇÃO: 2019, FONTE: 52nd Conference of the European-Society-of-Human-Genetics (ESHG) in EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 27
INDEXADO EM: WOS
NO MEU: ORCID
122
TÍTULO: Laryngeal metastasis and relapse development predicted by a (epi)genomic signature
AUTORES: Carreira, IM; Ribeiro, IP; Caramelo, F; Ribeiro, M; Migueis, J; Marques, F; Melo, JB;
PUBLICAÇÃO: 2019, FONTE: 52nd Conference of the European-Society-of-Human-Genetics (ESHG) in EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 27
INDEXADO EM: WOS
NO MEU: ORCID
123
TÍTULO: Genomic Profiling of two distinct morphological portions of a Uveal Melanoma by Array-CGH
AUTORES: Pires, LM; Fonseca, C; Val, M; Fernandes, J; Cachulo, ML; Melo, JB; Proenca, R; Carreira, IM;
PUBLICAÇÃO: 2019, FONTE: 52nd Conference of the European-Society-of-Human-Genetics (ESHG) in EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 27
INDEXADO EM: WOS
NO MEU: ORCID
124
TÍTULO: Array-CGH cohort of 1500 patients with Neurodevelopmental Disorders: Copy Number Variation in 16p13.11
AUTORES: Val, M; Carreira, IM; Pires, LM; Ribeiro, J; Lavoura, N; Ferreira, SI; Venancio, M; Ramos, F; Melo, JB;
PUBLICAÇÃO: 2019, FONTE: 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) in EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 27
INDEXADO EM: WOS
NO MEU: ORCID
125
TÍTULO: Predictive model for metastasis and recurrence in head and neck cancer using amplified genes of tumor samples
AUTORES: Ribeiro, IP; Esteves, L; Marques, F; Barroso, L; Baptista, IP; Caramelo, F; Melo, JB; Carreira, IM;
PUBLICAÇÃO: 2019, FONTE: 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) in EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 27
INDEXADO EM: WOS
NO MEU: ORCID
126
TÍTULO: p11.2 CNVs detected by Array-CGH in a cohort of patients with intellectual disability, autism spectrum and obesity
AUTORES: Carreira, IM; Rosmaninho Salgado, J; Pires, LM; Saraiva, JM; Sousa, SB; Melo, JB;
PUBLICAÇÃO: 2019, FONTE: 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) in EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 27
INDEXADO EM: WOS
NO MEU: ORCID
127
TÍTULO: UPF3B gene deletion in a patient with severe intellectual disability, epilepsy, absent speech: problematic of array-CGH coverage
AUTORES: Melo, JB; Ferreira, SI; Ramos, L; Pinto, M; Jardim, A; Carreira, IM;
PUBLICAÇÃO: 2019, FONTE: 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) in EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 27
INDEXADO EM: WOS
NO MEU: ORCID
128
TÍTULO: Cytogenetic, genomic, and epigenetic characterization of the HSC-3 tongue cell line with lymph node metastasis  Full Text
AUTORES: Ribeiro, IP; Rodrigues, JM; Mascarenhas, A; Kosyakova, N; Caramelo, F; Liehr, T; Melo, JB; Carreira, IM;
PUBLICAÇÃO: 2018, FONTE: JOURNAL OF ORAL SCIENCE, VOLUME: 60, NÚMERO: 1
INDEXADO EM: Scopus WOS CrossRef: 7
NO MEU: ORCID
129
TÍTULO: Molecular approaches identify a cryptic MECOM rearrangement in a child with a rapidly progressive myeloid neoplasm  Full Text
AUTORES: de Matos, RRC; Othman, MAK; Ferreira, GM; Costa, ES; Melo, JB; Carreira, IM; de Souza, MT; Lopes, BA; Emerenciano, M; Land, MGP; Liehr, T; Ribeiro, RC; Silva, MLM;
PUBLICAÇÃO: 2018, FONTE: CANCER GENETICS, VOLUME: 221
INDEXADO EM: Scopus WOS CrossRef: 7
NO MEU: ORCID
130
TÍTULO: Genomic and epigenetic signatures associated with survival rate in oral squamous cell carcinoma patients
AUTORES: Ribeiro, IP; Caramelo, F; Esteves, L; Oliveira, C; Marques, F; Barroso, L; Melo, JB; Carreira, IM;
PUBLICAÇÃO: 2018, FONTE: JOURNAL OF CANCER, VOLUME: 9, NÚMERO: 11
INDEXADO EM: Scopus WOS CrossRef: 21
NO MEU: ORCID
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