Sérgio Manuel Madeira Jorge Castedo
AuthID: R-000-GF9
1
TITLE: Novel Insights Into Lifetime Risk In HDGC: Lower Cancer Risk For The Most Recurrent <i>CDH1</i> Variant In Europe
AUTHORS: Barbosa Matos, Rita; Fonseca, Joao; Garrido, Luzia; Seixas, Susana; Freixo, Joao Parente; Oliveira, Renata; Hueneburg, Robert; Benusiglio, Patrick; Dahan, Karin; Feret, Damien; Spier, Isabel; Aretz, Stefan; Desseignes, Camille; Quental, Ana Rita Ferreira Pacheco; Fernandes, Susana; Costa, Susy Cabral; Vilarinho, Lucia; Castedo, Sergio; Grangeia, Ana; Vasconcelos, Alice Porto Guerra; ...More
PUBLISHED: 2024, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 32
AUTHORS: Barbosa Matos, Rita; Fonseca, Joao; Garrido, Luzia; Seixas, Susana; Freixo, Joao Parente; Oliveira, Renata; Hueneburg, Robert; Benusiglio, Patrick; Dahan, Karin; Feret, Damien; Spier, Isabel; Aretz, Stefan; Desseignes, Camille; Quental, Ana Rita Ferreira Pacheco; Fernandes, Susana; Costa, Susy Cabral; Vilarinho, Lucia; Castedo, Sergio; Grangeia, Ana; Vasconcelos, Alice Porto Guerra; ...More
PUBLISHED: 2024, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 32
INDEXED IN: 
WOS
WOS2
TITLE: Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes Full Text
AUTHORS: Garcia Pelaez, Jose; Barbosa Matos, Rita; Lobo, Silvana; Dias, Alexandre; Garrido, Luzia; Castedo, Sergio; Sousa, Sonia; Pinheiro, Hugo; Sousa, Liliana ; Monteiro, Rita; Maqueda, Joaquin J.; Fernandes, Susana; Carneiro, Fatima ; Pinto, Nadia ; Lemos, Carolina ; Pinto, Carla; Teixeira, Manuel R. ; Aretz, Stefan; Bajalica Lagercrantz, Svetlana; Balmana, Judith; ...More
PUBLISHED: 2023, SOURCE: LANCET ONCOLOGY, VOLUME: 24, ISSUE: 1
AUTHORS: Garcia Pelaez, Jose; Barbosa Matos, Rita; Lobo, Silvana; Dias, Alexandre; Garrido, Luzia; Castedo, Sergio; Sousa, Sonia; Pinheiro, Hugo; Sousa, Liliana ; Monteiro, Rita; Maqueda, Joaquin J.; Fernandes, Susana; Carneiro, Fatima ; Pinto, Nadia ; Lemos, Carolina ; Pinto, Carla; Teixeira, Manuel R. ; Aretz, Stefan; Bajalica Lagercrantz, Svetlana; Balmana, Judith; ...More
PUBLISHED: 2023, SOURCE: LANCET ONCOLOGY, VOLUME: 24, ISSUE: 1
3
TITLE: Feingold syndrome type 1: a rare cause of fetal microcephaly (prenatal diagnosis)
AUTHORS: Gouveia, Ines; Geraldo, Ana Filipa ; Godinho, Cristina; Castedo, Sergio;
PUBLISHED: 2023, SOURCE: BMJ CASE REPORTS, VOLUME: 16, ISSUE: 3
AUTHORS: Gouveia, Ines; Geraldo, Ana Filipa ; Godinho, Cristina; Castedo, Sergio;
PUBLISHED: 2023, SOURCE: BMJ CASE REPORTS, VOLUME: 16, ISSUE: 3
4
TITLE: Combined loss of CDH1 and downstream regulatory sequences drive early-onset diffuse gastric cancer and increase penetrance of hereditary diffuse gastric cancer
AUTHORS: Celina São José; José Garcia Pelaez; Marta Ferreira; Oscar Arrieta; Ana André; Nelson Martins; Samantha Solís; Braulio Martínez Benítez; María Luisa Ordóñez Sánchez; Maribel Rodríguez Torres; Anna Sommer; Iris A W te Paske; Carlos Caldas; Marc Tischkowitz; Maria Teresa Tusié; Stefan Aretz; Gabriel Capella; Sérgio Castedo; Richarda de Voer; Gareth Evans; ...More
PUBLISHED: 2023, SOURCE: Gastric Cancer, VOLUME: 26, ISSUE: 5
AUTHORS: Celina São José; José Garcia Pelaez; Marta Ferreira; Oscar Arrieta; Ana André; Nelson Martins; Samantha Solís; Braulio Martínez Benítez; María Luisa Ordóñez Sánchez; Maribel Rodríguez Torres; Anna Sommer; Iris A W te Paske; Carlos Caldas; Marc Tischkowitz; Maria Teresa Tusié; Stefan Aretz; Gabriel Capella; Sérgio Castedo; Richarda de Voer; Gareth Evans; ...More
PUBLISHED: 2023, SOURCE: Gastric Cancer, VOLUME: 26, ISSUE: 5
5
TITLE: Congenital Coronary Artery Fistulas, a Polish single-center computed tomographic registry Full Text
AUTHORS: Madeira, Sergio; Almeida, Antonio Rocha; Domingues, Miguel;
PUBLISHED: 2023, SOURCE: KARDIOLOGIA POLSKA, VOLUME: 81, ISSUE: 12
AUTHORS: Madeira, Sergio; Almeida, Antonio Rocha; Domingues, Miguel;
PUBLISHED: 2023, SOURCE: KARDIOLOGIA POLSKA, VOLUME: 81, ISSUE: 12
INDEXED IN: 
Scopus WOS
Scopus WOS6
TITLE: A Comprehensive Study on Surveillance Outcomes of a Male Population Carrying Pathogenic/Likely pathogenic Variants associated with Hereditary Breast Cancer Syndromes at a Portuguese Tertiary Hospital
AUTHORS: Maria João Oliveira; Susy Costa; André Magalhães; Luzia Garrido; Bárbara Peleteiro; José Luís Fougo; Sérgio Castedo;
PUBLISHED: 2023
AUTHORS: Maria João Oliveira; Susy Costa; André Magalhães; Luzia Garrido; Bárbara Peleteiro; José Luís Fougo; Sérgio Castedo;
PUBLISHED: 2023
7
TITLE: Extracolonic tumours in a pedigree with EPCAM-related Lynch Syndrome
AUTHORS: Alves da Silva, J; Castedo, S; Pedroto, I; Marcos Pinto, R;
PUBLISHED: 2022, SOURCE: European Journal of Medical Genetics, VOLUME: 65, ISSUE: 5
AUTHORS: Alves da Silva, J; Castedo, S; Pedroto, I; Marcos Pinto, R;
PUBLISHED: 2022, SOURCE: European Journal of Medical Genetics, VOLUME: 65, ISSUE: 5
8
TITLE: Whole-Exome Sequencing Targeting a Gene Panel for Sensorineural Hearing Loss: The First Portuguese Cohort Study
AUTHORS: Reis, Claudia Sousa; Quental, Sofia; Fernandes, Susana; Castedo, Sergio; Carla Pinto Moura ;
PUBLISHED: 2022, SOURCE: CYTOGENETIC AND GENOME RESEARCH, VOLUME: 162, ISSUE: 1-2
AUTHORS: Reis, Claudia Sousa; Quental, Sofia; Fernandes, Susana; Castedo, Sergio; Carla Pinto Moura ;
PUBLISHED: 2022, SOURCE: CYTOGENETIC AND GENOME RESEARCH, VOLUME: 162, ISSUE: 1-2
9
TITLE: Eleven novel APC mutations identified in Portuguese FAP families.
AUTHORS: Isidro, G; Matos, P ; Almeida, S; Claudino, S; Marshall, B; Soares, J; Leite, J; Regateiro, F; Brito, MJ; Giria, J; Castro, C; Ramos, J; Novais, L; Morna, H; Medeira, A; Castedo, S; Boavida, MG;
PUBLISHED: 2000, SOURCE: Human mutation, VOLUME: 16, ISSUE: 2
AUTHORS: Isidro, G; Matos, P ; Almeida, S; Claudino, S; Marshall, B; Soares, J; Leite, J; Regateiro, F; Brito, MJ; Giria, J; Castro, C; Ramos, J; Novais, L; Morna, H; Medeira, A; Castedo, S; Boavida, MG;
PUBLISHED: 2000, SOURCE: Human mutation, VOLUME: 16, ISSUE: 2
10
TITLE: Molecular cytogenetic characterization of a small, familial supernumerary ring chromosome 7 associated with mental retardation and an abnormal phenotype
AUTHORS: Gita Tan-Sindhunata; Sérgio Castedo; Beike Leegte; Irma Mulder; Anneke Y vd Veen; Annemieke H vd Hout; Titte J Wiersma; Anthonie J Van Essen;
PUBLISHED: 2000, SOURCE: American Journal of Medical Genetics, VOLUME: 92, ISSUE: 2
AUTHORS: Gita Tan-Sindhunata; Sérgio Castedo; Beike Leegte; Irma Mulder; Anneke Y vd Veen; Annemieke H vd Hout; Titte J Wiersma; Anthonie J Van Essen;
PUBLISHED: 2000, SOURCE: American Journal of Medical Genetics, VOLUME: 92, ISSUE: 2
