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Manuel R. Teixeira was born in Porto in 1967 and received his medical degree from the School of Medicine and Biomedical Sciences (ICBAS) of the University of Porto (UP) in 1992. He obtained his PhD (Dr Med) degree in Medicine (Medical Genetics) at the University of Oslo, Norway, after performing his doctoral studies in the field of cytogenetic heterogeneity of breast cancer at the Department of Medical Genetics of Odense University Hospital in 1993-1994 and then at the Department of Genetics at the Institute for Cancer Research, The Norwegian Radium Hospital (now part of Oslo University Hospital) in 1994-1997, under the supervision of Prof. Sverre Heim. He then obtained a postoctoral research position from the Norwegian Cancer Society for 1998-2000 to work on molecular cytogenetic methods to gather prognostic information from diagnostic biopsies of prostate cancer patients at the Oslo University Hospital. In February 2001 Manuel R. Teixeira was hired as Assistant Researcher at the Portuguese Oncology Institute of Porto (IPO Porto) and was appointed Coordinating Researcher in 2008. He is the Head of the Department of Genetics of this institution since May 2001, where he was responsible for the implementation the areas of molecular cytogenetics diagnosis of hematological diseases and conventional and molecular cytogenetic diagnosis of soft tissue tumors and for genetic counseling of families with inherited cancer predisposition (from June 2004 to 2021). In September 2003 he led the implementation of the IPO Porto Research Center (CI-IPOP), being appointed its Director from 2003 to 2021, in parallel with his diagnostic activities at the Department of Genetics. The CI-IPOP has been recognized as a Research and Development Unit since 2004 by the Portuguese Science and Technology Foundation and was classified as Excellent in the last international evaluation. Besides his main appointment at IPO Porto, Manuel R. Teixeira is a Guest Full Professor at the School of Medicine and Biological Sciences (ICBAS) of the University of Porto, where he is responsible for the curricular unit of Medical Genetics of the integrated master degree in Medicine, as well as of the curricular units of Oncobiology (MSc degree in Oncology), Genes and Cancer (PhD degree in Pathology and Molecular Genetics), and Molecular Cytogenetics (MSc and PhD degrees in Molecular Medicine and Oncology). His research interests are pursued as the coordinator of the Cancer Genetics Group of CI-IPOP, a multidisciplinary research group that includes medical doctors, pharmacists, biochemists and biologists, all specialized in cancer genetics. His research group aims to study the interplay between inherited cancer predisposition and the pattern of acquired genetic alterations that give rise to cancer, in order to understand the mechanisms of tumor initiation and progression and their role in therapy response and resistance. In fact, the fields of germline and somatic genetics are progressively more interconnected, as exemplified by shared mutation signatures that might have similar predictive value for targeted cancer therapy. Over the years his group has discovered several novel gene fusions in different malignant diseases, as well as several founder germline variants associated with cancer predisposition. Recently, his group has discovered PRUNE2 as a novel gene involved in prostate cancer predisposition, especially for early-onset and/or familial disease. He has authored or co-authored more than 330 publications in international peer-reviewed journals and several book chapters and his publications were cited more than 14.000 times (H-index: 61). The updated publication list can be found here: http://publicationslist.org/manuel.r.teixeira
Identificação

Identificação pessoal

Nome completo
Manuel António Rodrigues Teixeira

Nomes de citação

  • Teixeira, Manuel R.

Identificadores de autor

Ciência ID
4D1D-1F29-9100
ORCID iD
0000-0002-4896-5982
Researcher Id
E-4885-2011
Scopus Author Id
7202390422

Endereços de correio eletrónico

  • manuel.teixeira@ipoporto.min-saude.pt (Profissional)
  • mateixeira@icbas.up.pt (Profissional)

Telefones

Telefone
  • 225084000 Ext.: 7916 (Profissional)

Moradas

  • Dpt. Laboratory Genetics, IPO Porto, Rua Dr. António Bernardino Almeida, 4200-072, Porto, Porto, Portugal (Profissional)

Websites

Domínios de atuação

  • Ciências Médicas e da Saúde - Medicina Básica - Genética Humana

Idiomas

Idioma Conversação Leitura Escrita Compreensão Peer-review
Português (Idioma materno)
Inglês Utilizador proficiente (C2) Utilizador proficiente (C2) Utilizador proficiente (C2) Utilizador proficiente (C2) Utilizador proficiente (C2)
Norueguês Utilizador independente (B2) Utilizador proficiente (C1) Utilizador independente (B2) Utilizador proficiente (C1) Utilizador proficiente (C1)
Formação
Grau Classificação
2008
Concluído
Habilitado para funções de coordenação científica (Título de Habilitação de Coordenação Científica)
Especialização em Oncobiology (Cancer Genetics)
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
1994 - 1997
Concluído
Doctor Medicinae (Doctor of Philosophy)
Especialização em Medicine (Medical Genetics)
Universitetet i Oslo Det medisinske fakultet, Noruega
"Intra- and intertumor cytogenetic heterogeneity in breast cancer" (TESE/DISSERTAÇÃO)
1986 - 1992
Concluído
Medicina (Licenciatura)
Universidade do Porto Instituto de Ciências Biomédicas Abel Salazar, Portugal
17
Percurso profissional

Ciência

Categoria Profissional
Instituição de acolhimento
Empregador
2008/11/26 - Atual Investigador Coordenador (carreira) (Investigação) Instituto Português de Oncologia do Porto Francisco Gentil EPE, Portugal
2001 - 2008 Investigador Auxiliar (carreira) (Investigação) Instituto Português de Oncologia do Porto Francisco Gentil EPE, Portugal
1998 - 2000 Pós-doutorado (Investigação) Oslo Universitetssykehus Institutt for kreftforskning, Noruega

Docência no Ensino Superior

Categoria Profissional
Instituição de acolhimento
Empregador
2009 - Atual Professor Catedrático Convidado (Docente Universitário) Universidade do Porto Instituto de Ciências Biomédicas Abel Salazar, Portugal
2007 - 2009 Professor Associado Convidado (Docente Universitário) Universidade do Porto Instituto de Ciências Biomédicas Abel Salazar, Portugal
2002 - 2007 Professor Auxiliar Convidado (Docente Universitário) Universidade do Porto Instituto de Ciências Biomédicas Abel Salazar, Portugal

Outras Carreiras

Categoria Profissional
Instituição de acolhimento
Empregador
1993 - 1993 Interno (Médica) Centro Hospitalar Universitário do Porto EPE, Portugal

Cargos e Funções

Categoria Profissional
Instituição de acolhimento
Empregador
2001 - Atual Director de Unidade Orgânica Instituto Português de Oncologia do Porto Francisco Gentil EPE, Portugal
2003 - 2021 Director de Unidade Orgânica Instituto Português de Oncologia do Porto Francisco Gentil EPE, Portugal
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Projetos

Bolsa

Designação Financiadores
2019 - 2024 Inherited predisposition to gastric cancer: novel susceptibility genes and a minimally invasive screening strategy in germline mutation carriers
SFRH/BD/138670/2018
Orientador
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Fundação para a Ciência e a Tecnologia
Em curso
2018 - 2023 Germline mutations in genes involved in the chromosome segregation machinery associated with inherited prostate cancer predisposition
SFRH/BD/132441/2017
Orientador
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2017 - 2023 Recurrent germline mutations in patients with early-onset and/or familial prostate cancer
SFRH/BD/116557/2016
Orientador
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2016 - 2021 Detection of cancer specific genetic alterations in circulating free tumor DNA as a tool for early cancer diagnosis and follow up in Lynch syndrome patients
SFRH/BPD/113014/2015
Orientador
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2011 - 2014 Hereditary predisposition to prostate cancer
SFRH/BD/71397/2010
Orientador
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2011 - 2014 Characterization of membrane receptors differentially overexpressed in prostate carcinomas with and without ETS fusion genes
SFRH/BD/73964/2010
Orientador
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2011 - 2014 Phenotypic and genotypic heterogeneity of hereditary breast and ovarian cancer
SFRH/BD/73719/2010
Orientador
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2010 - 2013 Spectrum of somatic mutations in tumors arising in different large bowel locations in patients with hereditary predisposition to colorectal cancer
SFRH/BD/65326/2009
Orientador
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2009 - 2012 Characterization of fusion oncogenes involving the ETS family of transcription factors and their role as diagnostic and prognostic markers in prostate cancer
SFRH/BD/46574/2008
Orientador
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2007 - 2010 Fusion oncogenes involving the ETS family of transcription factors in prostate cancer: target genes and clinical applications
SFRH/BD/27669/2006
Orientador
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2007 - 2010 Expression changes of the ETS family of transcription factors associated with chromosome rearrangements in breast cancer
SFRH/BD/30097/2006
Orientador
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2007 - 2010 Gene targets of 5q copy number gain and mechanisms of resistance to targeted therapy in clear cell renal cell cancer
SFRH/BPD/34085/2006
Orientador
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2006 - 2009 Microarray analyses of prostate cancer: integrating genome-wide DNA copy number changes and RNA expression levels to uncover molecular markers of disease progression
SFRH/BPD/26492/2005
Orientador
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Fundação para a Ciência e a Tecnologia
Concluído

Projeto

Designação Financiadores
2017 - Atual Validation of liquid biopsies for predictive biomarker testing, therapy response monitoring, and resistance mechanism identification in cancer patients
CI-IPOP 54-2017
Investigador responsável
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação
Em curso
2016 - Atual Detection of cancer specific genetic alterations in circulating free tumor DNA as a tool for early cancer diagnosis and follow up in Lynch syndrome patients
CI-IPOP 36-2016
Investigador responsável
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação
Em curso
2016 - Atual Identification of somatic and germline mutations in circulating tumor DNA in ovarian cancer patients and in germline BRCA1/BRCA2 mutation carriers undergoing cancer screening
CI-IPOP 35-2016
Investigador responsável
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação
Em curso
2015 - Atual Inherited predisposition to prostate cancer
CI-IPOP 24-2015
Investigador responsável
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação
Em curso
2021/01/01 - 2025/12/31 Health Research Network: From Lab to Community Health
Investigador
Universidade do Porto Unidade de Investigação e Desenvolvimento Cardiovascular, Portugal

Instituto Português de Oncologia do Porto Francisco Gentil EPE, Portugal

Universidade do Porto Instituto de Ciências Biomédicas Abel Salazar, Portugal

Universidade do Algarve, Portugal

Universidade do Porto Faculdade de Ciências, Portugal

Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal

Universidade da Madeira, Portugal

Universidade de Lisboa Centro Cardiovascular da Universidade de Lisboa, Portugal

Universidade de Aveiro, Portugal

Centro de Investigação em Tecnologias e Serviços de Saúde, Portugal

Associação para a Investigação e Desenvolvimento da Faculdade de Medicina, Portugal

Escola Superior de Enfermagem do Porto, Portugal

Universidade do Porto Faculdade de Medicina, Portugal

Universidade NOVA de Lisboa, Portugal
Fundação para a Ciência e a Tecnologia
Em curso
2017 - 2024 Identification of germline mutations by gene-panel next generation sequencing in familial tubular and mixed tubular-diffuse gastric cancer
CI-IPOP 56-2017
Investigador responsável
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação
Em curso
2020/01/01 - 2023/12/31 IPO Porto Research Center
UIDB/00776/2020
Investigador responsável
Instituto Português de Oncologia do Porto Francisco Gentil EPE, Portugal
Fundação para a Ciência e a Tecnologia
Em curso
2020/01/01 - 2023/12/31 IPO Porto Research Center
UIDP/00776/2020
Investigador responsável
Instituto Português de Oncologia do Porto Francisco Gentil EPE, Portugal
Fundação para a Ciência e a Tecnologia
Em curso
2021/06/01 - 2023/11/30 The Porto Comprehensive Cancer Center
PINFRA03/72678/2020
Investigador
Instituto Português de Oncologia do Porto Francisco Gentil EPE, Portugal

Universidade do Porto Instituto de Biologia Molecular e Celular, Portugal

Universidade do Porto Instituto de Patologia e Imunologia Molecular, Portugal

Instituto Nacional de Engenharia Biomédica, Portugal

Universidade do Porto Instituto de Investigação e Inovação em Saúde, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2018/07/26 - 2021/11/25 The role of chromosome segregation machinery defects in genetic predisposition to prostate cancer.
PTDC/MED-GEN/28245/2017
Co-Investigador Responsável (Co-IR)
Instituto Português de Oncologia do Porto Francisco Gentil EPE, Portugal

Instituto de Biologia Molecular e Celular, Portugal

Rede de Química e Tecnologia Laboratório Associado para a Química Verde, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2019/01/01 - 2019/12/31 Portuguese Oncology Institute - Porto Research Center
UID/DTP/00776/2019
Investigador responsável
Instituto Português de Oncologia do Porto Francisco Gentil EPE, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2016/07/01 - 2019/07/01 Inherited predisposition to prostate cancer: finding the missing heritability by combining exome sequencing and haplotype analyses in a population with strong founder effects
PTDC/DTP-PIC/1308/2014
Investigador responsável
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2015/01/01 - 2018/12/31 Portuguese Oncology Institute - Porto Research Center
UID/DTP/00776/2013
Investigador responsável
Instituto Português de Oncologia do Porto Francisco Gentil EPE, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2014/01/01 - 2014/12/31 Strategic Project - UI 776 - 2014
PEst-OE/SAU/UI0776/2014
Investigador responsável
Instituto Português de Oncologia do Porto Francisco Gentil EPE, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2011 - 2014 Identification of novel fusion genes originated by chromosome rearrangements in hematological malignancies
LPCC-NRN
Investigador responsável
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Liga Portuguesa Contra o Cancro Núcleo Regional do Norte
Concluído
2013/01/01 - 2013/12/31 Incentive - UI 776 - 2013
Incentivo/SAU/UI0776/2013
Investigador responsável
Instituto Português de Oncologia do Porto Francisco Gentil EPE, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2011/01/01 - 2013/12/31 Strategic Project - UI 776 - 2011-2012
PEst-OE/SAU/UI0776/2011
Investigador responsável
Instituto Português de Oncologia do Porto Francisco Gentil EPE, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2009 - 2012 Genetic study of Common Hereditary Bowel Cancers in Hispania and the Americas (CHIBCHA)
CHIBCHA
Investigador
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
European Union
Concluído
2008 - 2011 Fusion oncogenes involving the ETS family of transcription factors in prostate cancer: target genes and clinical applications
CI-IPOP 9-2008
Investigador responsável
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação
Concluído
2007/09 - 2010/08 Characterization of fusion genes involving the ETS family of transcription factors and their role as diagnostic and prognostic markers in prostate cancer
PTDC/SAU-OBD/70543/2006
Investigador responsável
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2006 - 2010 Identification and characterization of novel MLL partner fusion genes in acute leukemia patients
APCL
Investigador responsável
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Associação Portuguesa Contra a Leucemia
Concluído
2005/07/01 - 2008/06/30 In mismatch repair deficiency colorectal cancer are BRAF and KRAS new prognostic and therapeutic tools?
POCI/SAU-OBS/56921/2004
Investigador
Universidade do Porto Instituto de Patologia e Imunologia Molecular, Portugal

Instituto Português de Oncologia do Porto Francisco Gentil EPE, Portugal

Instituto Português de Oncologia de Lisboa Francisco Gentil EPE, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2005/04 - 2008/03 Identification of target genes of genomic deletions and amplifications common to breast and prostate cancer
POCI/SAU-OBS/58357/2004
Investigador responsável
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2002 - 2006 Diagnostic and prognostic value of cytogenetic and molecular genetic analyses of sextant biopsies from prostate cancer suspects
POCTI/CBO/38853/2001
Investigador responsável
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2002 - 2004 Comparative genomic hybridization analysis of sextant biopsies from prostate cancer suspects
219/01
Investigador responsável
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Ministério da Saúde
Concluído
1995/01/01 - 1997/12/31 Cytogenetic Heterogeneity in Breast Cancer
PRAXIS XXI/BD/3109/94
Bolseiro de Doutoramento
Fundação para a Ciência e a Tecnologia
Concluído
Produções

Publicações

Artigo em revista
  1. Pinto, Emilia M.; Fridman, Cintia; Figueiredo, Bonald C.; Salvador, Hector; Teixeira, Manuel R.; Pinto, Carla; Pinheiro, Manuela; et al. "Multiple TP53 p.R337H haplotypes and implications for tumor susceptibility". Human Genetics and Genomics Advances 5 1 (2024): 100244. http://dx.doi.org/10.1016/j.xhgg.2023.100244.
    10.1016/j.xhgg.2023.100244
  2. Wang, Anqi; Shen, Jiayi; Rodriguez, Alex A.; Saunders, Edward J.; Chen, Fei; Janivara, Rohini; Darst, Burcu F.; et al. "Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants". Nature Genetics 55 12 (2023): 2065-2074. http://dx.doi.org/10.1038/s41588-023-01534-4.
    Publicado • 10.1038/s41588-023-01534-4
  3. Moreira, Inês; Ferreira, Marta; Garcia, Sofia; Novais, Pedro; Gama, João; Ferro, Beatriz; Leite-Silva, Pedro; et al. "Practical lessons learned from real-world implementation of the molecular classification for endometrial carcinoma". Gynecologic Oncology 176 (2023): 53-61. http://dx.doi.org/10.1016/j.ygyno.2023.07.005.
    10.1016/j.ygyno.2023.07.005
  4. Pinto, Carla; Guerra, Joana; Pinheiro, Manuela; Escudeiro, Carla; Santos, Catarina; Pinto, Pedro; Porto, Miguel; et al. "Combined germline and tumor mutation signature testing identifies new families with NTHL1 tumor syndrome". Frontiers in Genetics 14 (2023): http://dx.doi.org/10.3389/fgene.2023.1254908.
    10.3389/fgene.2023.1254908
  5. Guerra, Joana; Pinto, Carla; Pinto, Pedro; Pinheiro, Manuela; Santos, Catarina; Peixoto, Ana; Escudeiro, Carla; et al. "Frequency of CDH1, CTNNA1 and CTNND1 Germline Variants in Families with Diffuse and Mixed Gastric Cancer". Cancers 15 17 (2023): 4313. http://dx.doi.org/10.3390/cancers15174313.
    10.3390/cancers15174313
  6. Pinheiro, Manuela; Peixoto, Ana; Rocha, Patrícia; Santos, Catarina; Escudeiro, Carla; Veiga, Isabel; Porto, Miguel; et al. "Implementation of upfront DPYD genotyping with a low-cost and high-throughput assay to guide fluoropyrimidine treatment in cancer patients". Pharmacogenetics and Genomics (2023): http://dx.doi.org/10.1097/fpc.0000000000000505.
    10.1097/fpc.0000000000000505
  7. Paula Paulo; Marta Cardoso; Andreia Brandao; Pinto P; Falconi A; Pinheiro M; Cerveira N; et al. "Genetic landscape of homologous recombination repair genes in early-onset/familial prostate cancer patients.". Genes, chromosomes & cancer (2023): https://doi.org/10.1002/gcc.23190.
    10.1002/gcc.23190
  8. Burcu Darst; Shen J; Madduri RK; Rodriguez AA; Xiao Y; Sheng X; Saunders EJ; et al. "Evaluating approaches for constructing polygenic risk scores for prostate cancer in men of African and European ancestry.". American journal of human genetics (2023): https://doi.org/10.1016/j.ajhg.2023.05.010.
    10.1016/j.ajhg.2023.05.010
  9. Taru Annika Muranen; Morra A; Sofia Khan; Barnes DR; Bolla MK; Joe Dennis; Renske Keeman; et al. "PREDICT validity for prognosis of breast cancer patients with pathogenic BRCA1/2 variants.". NPJ breast cancer (2023): https://europepmc.org/articles/PMC10182045.
    10.1038/s41523-023-00546-x
  10. Denise G. O'Mahony; Susan Ramus; Southey MC; Nicola S Meagher; Hadjisavvas A; John EM; Hamann U; et al. "Ovarian cancer pathology characteristics as predictors of variant pathogenicity in BRCA1 and BRCA2.". British journal of cancer (2023): https://europepmc.org/articles/PMC10241792.
    10.1038/s41416-023-02263-5
  11. Marta Cardoso; Sofia Maia; Andreia Brandão; Ruta Sahasrabudhe; Paul Lott; Natalia Belter; Luis G. Carvajal-Carmona; Paula Paulo; Manuel R. Teixeira. "Exome sequencing of affected duos and trios uncovers PRUNE2 as a novel prostate cancer predisposition gene". British Journal of Cancer (2023): https://doi.org/10.1038/s41416-022-02125-6.
    10.1038/s41416-022-02125-6
  12. Peixoto A; Cirnes L; Carvalho AL; Andrade MJ; Brito MJ; Borralho P; Borralho PM; et al. "Evaluation of PIK3CA mutations in advanced ER+/HER2-breast cancer in Portugal - U-PIK Project.". Frontiers in molecular biosciences (2023): https://europepmc.org/articles/PMC9941536.
    10.3389/fmolb.2023.1082915
  13. Marisa Linhares; Cláudia Marques Pinto; Diogo Libânio; Manuel R. Teixeira; Mário Dinis-Ribeiro; Catarina Brandão. "Gastric Cancer: A Practical Review on Management of Individuals with Hereditary or Familial Risk for Gastric Cancer". GE - Portuguese Journal of Gastroenterology (2023): https://doi.org/10.1159/000527208.
    10.1159/000527208
  14. Garcia-Pelaez J; Barbosa-Matos R; Silvana Lobo; Alexandre Dias; Garrido L; Sergio Castedo; Sousa S; et al. "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.". The Lancet. Oncology (2022): https://europepmc.org/articles/PMC9810541.
    10.1016/s1470-2045(22)00643-x
  15. Hakkaart C; John F Pearson; Marquart L; Joe Dennis; Wiggins GAR; Daniel Barnes; Robinson BA; et al. "Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers.". Communications biology (2022): https://europepmc.org/articles/PMC9537519.
    10.1038/s42003-022-03978-6
  16. Ana Marote; Santos, Diogo J; Mendes-Pinheiro B; Serre-Miranda C; Anjo SI; Vieira J; Ferreira-Antunes F; et al. "Cellular Aging Secretes: a Comparison of Bone-Marrow-Derived and Induced Mesenchymal Stem Cells and Their Secretome Over Long-Term Culture.". Stem cell reviews and reports (2022): https://doi.org/10.1007/s12015-022-10453-6.
    10.1007/s12015-022-10453-6
  17. Inês Moreira; Carla Bartosch; Manuel Teixeira; Marta Ferreira. "Molecular Classification of Endometrial Carcinoma: Protocol for a Cohort Study". JMIR Research Protocols (2022): https://doi.org/10.2196/34461.
    10.2196/34461
  18. Teixeira MR; Oliveira J; Borralho P; O Fernandes MG; Almodovar T; Gabriela Fernandes; Macedo D; et al. "Portuguese Consensus Recommendations for Next-Generation Sequencing of Lung Cancer, Rare Tumors, and Cancers of Unknown Primary Origin in Clinical Practice.". Acta medica portuguesa (2022): https://doi.org/10.20344/amp.17680.
    10.20344/amp.17680
  19. Huynh-Le, M.-P.; Karunamuni, R.; Fan, C.C.; Asona, L.; Thompson, W.K.; Martinez, M.E.; Eeles, R.A.; et al. "Prostate cancer risk stratification improvement across multiple ancestries with new polygenic hazard score.". Prostate cancer and prostatic diseases (2022): https://doi.org/10.1038/s41391-022-00497-7.
    Publicado • 10.1038/s41391-022-00497-7
  20. Costa, C.; Souteiro, P.; Paredes, S.; Bettencourt-Silva, R.; Pedro, J.; Ferreira, M.J.; Salazar, D.; et al. "Male gender as a poor prognostic factor in Medullary Thyroid Carcinoma: behaviour or biological difference?". Minerva Endocrinology (2022): http://dx.doi.org/10.23736/s2724-6507.22.03692-2.
    10.23736/s2724-6507.22.03692-2
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  301. Micci, F.; Teixeira, M.R.; Bjerkehagen, B.; Heim, S.. "Characterization of supernumerary rings and giant marker chromosomes in well-differentiated lipomatous tumors by a combination of G-banding, CGH, M-FISH, and chromosome- and locus-specific FISH". Cytogenetic and Genome Research 97 1-2 (2002): 13-19. http://www.scopus.com/inward/record.url?eid=2-s2.0-0036052032&partnerID=MN8TOARS.
    10.1159/000064038
  302. Teixeira, M.R. "Combined classical and molecular cytogenetic analysis of cancer". European Journal of Cancer 38 12 (2002): 1580-1584. http://www.scopus.com/inward/record.url?eid=2-s2.0-0036342487&partnerID=MN8TOARS.
    10.1016/S0959-8049(02)00117-X
  303. Teixeira, M.R.; Pandis, N.; Heim, S.. "Cytogenetic clues to breast carcinogenesis". Genes Chromosomes and Cancer 33 1 (2002): 1-16. http://www.scopus.com/inward/record.url?eid=2-s2.0-0036131935&partnerID=MN8TOARS.
    10.1002/gcc.1206
  304. Kleivi, K.; Lothe, R.A.; Heim, S.; Tsarouha, H.; Kraggerud, S.M.; Pandis, N.; Papadopoulou, A.; et al. "Genome profiling of breast cancer cells selected against in vitro shows copy number changes". Genes Chromosomes and Cancer 33 3 (2002): 304-309. http://www.scopus.com/inward/record.url?eid=2-s2.0-18244395111&partnerID=MN8TOARS.
    10.1002/gcc.10032
  305. Heim, S.; Teixeira, M.A.R.; Pandis, N.. "Are some breast carcinomas polyclonal in origin?". Journal of Pathology 194 4 (2001): 395-397. http://www.scopus.com/inward/record.url?eid=2-s2.0-0034869244&partnerID=MN8TOARS.
    10.1002/1096-9896(200108)194:4<395::AID-PATH975>3.0.CO;2-4
  306. Micci, F.; Teixeira, M.R.; Heim, S.. "Complete cytogenetic characterization of the human breast cancer cell line MA11 combining G-banding, comparative genomic hybridization, multicolor fluorescence in situ hybridization, RxFISH, and chromosome-specific painting". Cancer Genetics and Cytogenetics 131 1 (2001): 25-30. http://www.scopus.com/inward/record.url?eid=2-s2.0-0035180787&partnerID=MN8TOARS.
    10.1016/S0165-4608(01)00484-8
  307. Teixeira, M.R.; Tsarouha, H.; Kraggerud, S.M.; Pandis, N.; Dimitriadis, E.; Andersen, J.A.; Lothe, R.A.; Heim, S.. "Evaluation of breast cancer polyclonality by combined chromosome banding and comparative genomic hybridization analysis". Neoplasia 3 3 (2001): 204-214. http://www.scopus.com/inward/record.url?eid=2-s2.0-0034880470&partnerID=MN8TOARS.
    10.1038/sj.neo.7900152
  308. Panagopoulos, I.; Teixeira, M.R.; Micci, F.; Hammerstrsm, J.; Isaksson, M.; Johansson, B.; Mitelman, F.; Heim, S.. "Acute Myeloid Leukemia with inv(8)(p11q13)". Leukemia and Lymphoma 39 42130 (2000): 651-656. http://www.scopus.com/inward/record.url?eid=2-s2.0-0034489925&partnerID=MN8TOARS.
    10.3109/10428190009113397
  309. Teixeira, M.R.; Micci, F.; Dietrich, C.U.; Heim, S.. "Detailed genome-wide screening for inter- and intrachromosomal abnormalities by sequential G-banding and RxFISH color banding of the same metaphase cells". Cancer Genetics and Cytogenetics 119 2 (2000): 94-101. http://www.scopus.com/inward/record.url?eid=2-s2.0-0034091604&partnerID=MN8TOARS.
    10.1016/S0165-4608(99)00220-4
  310. Kraggerud, S.M.; Szymanska, J.; Abeler, V.M.; Kærn, J.; Eknæs, M.; Heim, S.; Teixeira, M.R.; et al. "DNA copy number changes in malignant ovarian germ cell tumors". Cancer Research 60 11 (2000): 3025-3030. http://www.scopus.com/inward/record.url?eid=2-s2.0-0034214053&partnerID=MN8TOARS.
  311. Teixeira, M.R.; Wæhre, H.; Lothe, R.A.; Stenwig, A.E.; Pandis, N.; Giercksky, K.E.; Heim, S.. "High frequency of clonal chromosome abnormalities in prostatic neoplasms sampled by prostatectomy or ultrasound-guided needle biopsy". Genes Chromosomes and Cancer 28 2 (2000): 211-219. http://www.scopus.com/inward/record.url?eid=2-s2.0-0034059609&partnerID=MN8TOARS.
    10.1002/(SICI)1098-2264(200006)28:2<211::AID-GCC10>3.0.CO;2-Y
  312. Micci, F.; Teixeira, M.R.; Dietrich, C.U.; Sæter, G.; Bjerkehagen, B.; Heim, S.. "Combined RxFISH/G-banding allows refined karyotyping of solid tumors". Human Genetics 104 5 (1999): 370-375. http://www.scopus.com/inward/record.url?eid=2-s2.0-0033040327&partnerID=MN8TOARS.
    10.1007/s004390050970
  313. Teixeira, M.R.; Micci, F.; Dietrich, C.U.; Heim, S.. "Cross-species color banding characterization of chromosomal rearrangements in leukemias with incomplete G-band karyotypes". Genes Chromosomes and Cancer 26 1 (1999): 13-19. http://www.scopus.com/inward/record.url?eid=2-s2.0-0032839401&partnerID=MN8TOARS.
    10.1002/(SICI)1098-2264(199909)26:1<13::AID-GCC2>3.0.CO;2-1
  314. Tsarouha, H.; Pandis, N.; Bardi, G.; Teixeira, M.R.; Andersen, J.A.; Heim, S.. "Karyotypic E evolution in breast carcinomas with i(1)(q10) and der(1;16)(q10;p10) as the primary chromosome abnormality". Cancer Genetics and Cytogenetics 113 2 (1999): 156-161. http://www.scopus.com/inward/record.url?eid=2-s2.0-0032588199&partnerID=MN8TOARS.
    10.1016/S0165-4608(99)00016-3
  315. Teixeira, M.R.; Kristensen, G.B.; Abeler, V.M.; Heim, S.. "Karyotypic findings in tumors of the vulva and vagina". Cancer Genetics and Cytogenetics 111 1 (1999): 87-91. http://www.scopus.com/inward/record.url?eid=2-s2.0-0032962932&partnerID=MN8TOARS.
    10.1016/S0165-4608(98)00226-X
  316. Teixeira, M.R.; Pandis, N.; Dietrich, C.U.; Reed, W.; Andersen, J.; Qvist, H.; Heim, S.. "Chromosome banding analysis of gynecomastias and breast carcinomas in men". Genes Chromosomes and Cancer 23 1 (1998): 16-20. http://www.scopus.com/inward/record.url?eid=2-s2.0-0031880709&partnerID=MN8TOARS.
    10.1002/(SICI)1098-2264(199809)23:1<16::AID-GCC3>3.0.CO;2-9
  317. Teixeira, M.R.; Qvist, H.; Bøhler, P.J.; Pandis, N.; Heim, S.. "Cytogenetic analysis shows that carcinosarcomas of the breast are of monoclonal origin". Genes Chromosomes and Cancer 22 2 (1998): 145-151. http://www.scopus.com/inward/record.url?eid=2-s2.0-0031979316&partnerID=MN8TOARS.
    10.1002/(SICI)1098-2264(199806)22:2<145::AID-GCC9>3.0.CO;2-X
  318. Pandis, N.; Teixeira, M.R.; Adeyinka, A.; Rizou, H.; Bardi, G.; Mertens, F.; Andersen, J.A.; et al. "Cytogenetic comparison of primary tumors and lymph node metastases in breast cancer patients". Genes Chromosomes and Cancer 22 2 (1998): 122-129. http://www.scopus.com/inward/record.url?eid=2-s2.0-0031979315&partnerID=MN8TOARS.
    10.1002/(SICI)1098-2264(199806)22:2<122::AID-GCC6>3.0.CO;2-Z
  319. Teixeira, M.R.; Giercksky, K.E.; Ikonomou, I.M.; Heim, S.. "Translocation (3;3)(p14;q29) as the primary chromosome abnormality in a peritoneal mesothelioma". Cancer Genetics and Cytogenetics 103 1 (1998): 73-75. http://www.scopus.com/inward/record.url?eid=2-s2.0-0032077363&partnerID=MN8TOARS.
    10.1016/S0165-4608(97)00368-3
  320. Teixeira, M.R.; Qvist, H.; Giercksky, K.E.; Bøhler, P.J.; Heim, S.. "Cytogenetic analysis of several pseudomyxoma peritonei lesions originating from a mucinous cystadenoma of the appendix". Cancer Genetics and Cytogenetics 93 2 (1997): 157-159. http://www.scopus.com/inward/record.url?eid=2-s2.0-0030889238&partnerID=MN8TOARS.
    10.1016/S0165-4608(96)00186-0
  321. Heim, S.; Teixeira, M.R.; Dietrich, C.U.; Pandis, N.. "Cytogenetic polyclonality in tumors of the breast". Cancer Genetics and Cytogenetics 95 1 (1997): 16-19. http://www.scopus.com/inward/record.url?eid=2-s2.0-0030988915&partnerID=MN8TOARS.
    10.1016/S0165-4608(96)00322-6
  322. Teixeira, M.R.; Pandis, N.; Bardi, G.; Andersen, J.A.; Bøhler, P.J.; Qvist, H.; Heim, S.. "Discrimination between multicentric and multifocal breast carcinoma by cytogenetic investigation of macroscopically distinct ipsilateral lesions". Genes Chromosomes and Cancer 18 3 (1997): 170-174. http://www.scopus.com/inward/record.url?eid=2-s2.0-0030897156&partnerID=MN8TOARS.
    10.1002/(SICI)1098-2264(199703)18:3<170::AID-GCC3>3.0.CO;2-Z
  323. Gerdes, A.-M.; Pandis, N.; Bomme, L.; Dietrich, C.U.; Teixeira, M.R.; Bardi, G.; Heim, S.. "Fluorescence in situ hybridization of old G-banded and mounted chromosome preparations". Cancer Genetics and Cytogenetics 98 1 (1997): 9-15. http://www.scopus.com/inward/record.url?eid=2-s2.0-0030768866&partnerID=MN8TOARS.
    10.1016/S0165-4608(96)00407-4
  324. Teixeira, M.R.; Pandis, N.; Gerdes, A.-M.; Dietrich, C.U.; Bardi, G.; Andersen, J.A.; Graversen, H.P.; Mitelman, F.; Heim, S.. "Cytogenetic abnormalities in an in situ ductal carcinoma and five prophylactically removed breasts from members of a family with hereditary breast cancer". Breast Cancer Research and Treatment 38 2 (1996): 177-182. http://www.scopus.com/inward/record.url?eid=2-s2.0-0029998976&partnerID=MN8TOARS.
    10.1007/BF01806672
  325. Teixeira, M.R.; Pandis, N.; Bardi, G.; Andersen, J.A.; Heim, S.. "Karyotypic comparisons of multiple tumorous and macroscopically normal surrounding tissue samples from patients with breast cancer". Cancer Research 56 4 (1996): 855-859. http://www.scopus.com/inward/record.url?eid=2-s2.0-0030020692&partnerID=MN8TOARS.
  326. Cline, J.M.; Teixeira, M.R.; Heim, S.; Pandis, N.; Bardi, G.; Andersen, J.A.. "M. R. Teixeira et al., Karyotypic comparisons of multiple tumorous and macroscopically normal surrounding tissue samples from patients with breast cancer. Cancer Res., 56: 855-859, 1996". Cancer Research 56 21 (1996): http://www.scopus.com/inward/record.url?eid=2-s2.0-0029953487&partnerID=MN8TOARS.
  327. Dietrich, C.U.; Pandis, N.; Teixeira, M.R.; Bardi, G.; Gerdes, A.-M.; Andersen, J.A.; Heim, S.. "Chromosome abnormalities in benign hyperproliferative disorders of epithelial and stromal breast tissue". International Journal of Cancer 60 1 (1995): 49-53. http://www.scopus.com/inward/record.url?eid=2-s2.0-0028966394&partnerID=MN8TOARS.
    10.1002/ijc.2910600107
  328. Pandis, N.; Teixeira, M.R.; Gerdes, A.-M.; Limon, J.; Bardi, G.; Andersen, J.A.; Idvall, I.; et al. "Chromosome abnormalities in bilateral breast carcinomas. Cytogenetic evaluation of the clonal origin of multiple primary tumors". Cancer 76 2 (1995): 250-258. http://www.scopus.com/inward/record.url?eid=2-s2.0-0029042985&partnerID=MN8TOARS.
    10.1002/1097-0142(19950715)76:2<250::AID-CNCR2820760215>3.0.CO;2-W
  329. Teixeira, M.R.; Pandis, N.; Bardi, G.; Andersen, J.A.; Mitelman, F.; Heim, S.. "Clonal heterogeneity in breast cancer: Karyotypic comparisons of multiple intra—and extra—tumorous samples from 3 patients". International Journal of Cancer 63 1 (1995): 63-68. http://www.scopus.com/inward/record.url?eid=2-s2.0-0028848437&partnerID=MN8TOARS.
    10.1002/ijc.2910630113
  330. Teixeira, M.R.; Pandis, N.; Bardi, G.; Andersen, J.A.; Mandahl, N.; Mitelman, F.; Heim, S.. "Cytogenetic analysis of multifocal breast carcinomas: Detection of karyotypically unrelated clones as well as clonal similarities between tumour foci". British Journal of Cancer 70 5 (1994): 922-927. http://www.scopus.com/inward/record.url?eid=2-s2.0-0027973945&partnerID=MN8TOARS.
    10.1038/bjc.1994.421
  331. Dietrich, C.U.; Pandis, N.; Bardi, G.; Teixeira, M.R.; Soukhikh, T.; Petersson, C.; Andersen, J.A.; Heim, S.. "Karyotypic changes in phyllodes tumors of the breast". Cancer Genetics and Cytogenetics 78 2 (1994): 200-206. http://www.scopus.com/inward/record.url?eid=2-s2.0-0028661210&partnerID=MN8TOARS.
    10.1016/0165-4608(94)90090-6
Capítulo de livro
  1. Teixeira, M.R.; Heim, S.. "Tumors of the male genital organs". In Cancer Cytogenetics: Chromosomal and Molecular Genetic Aberrations of Tumor Cells, editado por Sverre Heim, Felix Mitelman. New York, Estados Unidos: Wiley-Liss, 2015.
    Publicado
  2. Teixeira, M.R.; Pandis, N.; Heim, S.. "Tumors of the breast". In Cancer Cytogenetics: Chromosomal and Molecular Genetic Aberrations of Tumor Cells. New York, Estados Unidos: Wiley-Liss, 2015.
    Publicado
  3. Teixeira, M.R.; Heim, S.. "Cytogenetic Analysis of Tumor Clonality". In Advances in Cancer Research, 127-149. Academic Press Inc., 2011.
    Publicado • 10.1016/B978-0-12-387688-1.00005-3
  4. Teixeira, M.R.; Pandis, N.; Heim, S.. "Tumors of the Breast". In Cancer Cytogenetics: Chromosomal and Molecular Genetic Aberrations of Tumor Cells, editado por Sverre Heim, Felix Mitelman. New York, Estados Unidos: Wiley-Liss, 2010.
    Publicado • 10.1002/9781118010136.ch15
  5. Teixeira, M.R.; Heim, S.. "Tumors of the Male Genital Organs". In Cancer Cytogenetics: Chromosomal and Molecular Genetic Aberrations of Tumor Cells, editado por Sverre Heim, Felix Mitelman. New York, Estados Unidos: Wiley-Liss, 2010.
    Publicado • 10.1002/9781118010136.ch17
  6. Ribeiro, F. R.; Skotheim, R. I.; Henrique, R.; Teixeira, M. R.. Autor correspondente: Teixeira, M. R.. "Array-Based Comparative Genomic Hybridization in Prostate Cancer: Research and Clinical Applications". In General Methods and Overviews, Lung Carcinoma and Prostate Carcinoma, 415-429. Estados Unidos: Springer Netherlands, 2008.
    Publicado • 10.1007/978-1-4020-8442-3_30
  7. Teixeira, M. R.; Pandis, N.; Heim, S.. Autor correspondente: Heim, S.. "Genome-wide analysis of breast cancer by chromosome banding and comparative genomic hybridization.". In Focus on Breast Cancer Research, 37-66. New York, Estados Unidos: Nova Biomedical Books, 2004.
    Publicado
  8. Wilkinson, E.J.; Teixeira, M.R.. "Epithelial tumors of the vulva.". In Pathology and Genetics of Tumours of the Breast and Female Genital Organs, editado por P Kleihues; WK Cavenee. Lyon, França: WHO Lyon: IARCPress., 2003.
    Publicado
  9. Kempson, R.L.; Teixeira, M.R.; Hendrickson, M.R.. "Soft tissue tumors of the vulva". In Pathology and Genetics of Tumours of the Breast and Female Genital Organs, editado por P Kleihues; WK Cavenee. Lyon: WHO Lyon: IARCPress., 2003.
    Publicado
  10. Wilkinson, E.J.; Teixeira, M.R.. "Melanocytic tumors of the vulva". In Pathology and Genetics of Tumours of the Breast and Female Genital Organs, editado por P Kleihues; WK Cavenee. Lyon, França: WHO Lyon: IARCPress., 2003.
    Publicado
  11. Teixeira, M.R.; Heim, S.. "Clonal evolution of neoplastic cell populations: lessons from solid tumor cytogenetics". In DNA Alterations in Cancer: Genetic and Epigenetic Changes. Natick, MA: Eaton Publishing, 2000.
    Publicado
  12. Heim, S.; Teixeira, M.R.; Pandis, N.. "Cytogenetic Approaches to Breast Cancer". In Breast Cancer, 373-388. Humana Press, 1999.
    Publicado • 10.1007/978-1-59259-456-6_17
Poster em conferência
  1. Cruz, Pedro; Meneses, Olga; Ramos, Raquel; Brandão, Andreia; Veiga, Isabel; Rocha, Patricia; Henrique, Rui; et al. Autor correspondente: Paulo, Paula. "Eficácia de anti-EGFR em cancro colorretal metastizado é aumentada pela sobreexpressão de EGFR ou ETV4 e reduzida pela de ETV5 ou ETV1". Trabalho apresentado em 3ª Edição do Concurso de Pósteres Científicos Revolution Poster Awards by Pierre Fabre, 2023.
  2. Paiva, Elsa; Orr, Bernard; Teixeira, Manuel R.; Paulo, Paula. Autor correspondente: Paulo, Paula. "Molecular subtypes of prostate carcinomas may identify patients eligible for combined anti-EGFR/STAT3 therapy". Trabalho apresentado em 1st Young Researcher's Day, 2023.
  3. Ramos, Raquel Almeida; Brandão, Andreia; Cruz, Pedro; Meneses, Olga; Veiga, Isabel; Rocha, Patricia; Henrique, Rui; et al. Autor correspondente: Paulo, Paula. "PEA3 transcription factors are prognostic biomarkers of response to anti-EGFR therapy in metastatic colorectal cancer". Trabalho apresentado em 1st Young Researcher's Day, 2023.
  4. Meneses, Olga; Cruz, Pedro; Ramos, Raquel; Brandão, Andreia; Veiga, Isabel; Rocha, Patricia; Henrique, Rui; et al. Autor correspondente: Paulo, Paula. "Determinantes moleculares da eficácia terapêutica anti-EGFR no cancro colorretal metastizado.". Trabalho apresentado em 20º Congresso Nacional de Oncologia, 2023.
  5. Silva, Maria P.; Ferreira, Luisa T; Bras, Natercia F.; Torres, Lurdes; Brandão, Andreia; Pinheiro, Manuela; Cardoso, Marta; et al. Autor correspondente: Paulo, Paula. "Proceedings of the 26th Annual Meeting of the Portuguese Society of Human Genetics (SPGH ¿ Sociedade Portuguesa de Genética Humana) Coimbra, 17¿19 November 2022". 2023.
    10.1097/md.0000000000033154
  6. Silva, Maria P.; Ferreira, Luísa; Brás, Natércia; Torres, Lurdes; Brandão, Andreia; Pinheiro, Manuela; Cardoso, Marta; et al. Autor correspondente: Paulo, Paula. "BUB1B monoallelic germline variants contribute to prostate cancer predisposition by triggering chromosomal instability". Trabalho apresentado em 26ª Reunião Anual da Sociedade Portuguesa de Genética Humana, 2022.
  7. Canário, Rita; Morgado, Inês; Ribeiro, Ana Sofia; Mendes, Nuno; Teixeira, Manuel R.; BARTOSCH, CARLA; Paredes, Joana. "P-cadherin: a promising prognostic biomarker for homologous repair proficient high grade serous ovarian carcinoma". Trabalho apresentado em ESGO 2022 Congress, 2022.
  8. Canário, Rita; Morgado, Inês; Mendes, Nuno; Teixeira, Manuel R.; Ribeiro, Ana Sofia; BARTOSCH, CARLA; Paredes, Joana. Autor correspondente: Canário, Rita. "P-cadherin overexpression is associated with shorter overall survival in high grade serous ovarian cancer". Trabalho apresentado em ASPIC 5th International Congress, 2022.
  9. Silva, Maria P. ((9618-5B5D-E47A); Ferreira, Luisa; Torres, Lurdes; Brandão, Andreia; Pinheiro, Manuela; Palmeira, Carlos; Maiato, Helder; Paulo, Paula; Teixeira, Manuel R.. Autor correspondente: Paulo, Paula. "A recurrent in-frame BUB1B germline variant in prostate cancer predisposition". Trabalho apresentado em EMBO Workshop: Systems Approaches in Cancer, 2021.
  10. Pires-Luis, Ana S.; Bartosch, Carla; Meireles, Catarina; Pinto, Carla; Lopes, Jose M.; Shannon, Kristen M.; Teixeira, Manuel R.; Oliva, Esther; José Manuel Lopes. "Hysterectomy Specimens of Patients with Lynch Syndrome: Clinicopathologic Study of 70 Cases". 2016.
  11. Caldas, Margarida; Polónia, António; Vieira, J; Teixeira, Manuel R.; Leal, C. "A case of secretory carcinoma of the breast expressing gross cystic disease fluid protein-15". Trabalho apresentado em 25th European Congress of Pathology, 2013.
  12. Jerónimo, Carmen; Monteiro, Paula; Henrique, Rui; Dinis-Ribeiro, Mário; Costa, Vera L.; L. Filipe; Carvalho, André L.; et al. "Marcadores epigenéticos aumentam a acuidade diagnostica em citologia aspirativa de lesões mamárias". Trabalho apresentado em 12ªs Jornadas de Oncologia Médica, 2007.
Atividades

Comissão de avaliação

Descrição da atividade
Tipo de assessoria
Instituição / Organização Entidade financiadora
2007 - 2018 External Quality Assessor, European Molecular Genetics Quality Network
2006 - 2012 External Quality Assessor, United Kingdom National External Quality Assessment Scheme in Clinical Cytogenetics
Avaliador

Consultoria / Parecer

Descrição da atividade Instituição / Organização
2008 - 2017 Visiting Professor, Center for Cancer Biomedicine, University of Oslo, Norway

Membro de associação

Nome da associação Tipo de participação
2013 - Atual European Association for Cancer Research
2011 - 2013 Direction of Portuguese Society of Human Genetics (SPGH) - President 2012; Elected 2011; Outgoing 2013

Membro de comissão

Descrição da atividade
Tipo de participação
Instituição / Organização
2013 - 2017 Coordinator of the Scientific Committee of the Portuguese Society of Human Genetics (SPGH)
Coordenador
Distinções

Prémio

1997 Jacinto de Magalhães Medical Genetics Institute’s 1st prize (for the best Portuguese work in genetics)
Centro de Genética Médica Doutor Jacinto Magalhães, Portugal