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 Tecnology 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 his 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 persued as the coordinator of the Cancer Genetic Group of CI-IPOP, which aims to characterize the pattern of germline and somatic genetic alterations that are involved in carcinogenesis, under the assumption that tailor-made therapy specifically directed towards the altered metabolism of tumor cells requires exact knowledge about the inherited and acquired genomic abnormalities of individual patients, not just about diagnostic categories. 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. As PI or Co-PI, he has raised competitive funding at national and European level. He has authored or co-authored more than 300 publications in international peer-reviewed journals and several book chapters and his publications were cited more than 11.000 times (H-index: 56).

Identificação pessoal

Nome completo
Manuel António Rodrigues Teixeira

Nomes de citação

  • Teixeira, Manuel R.

Identificadores de autor

Ciência ID
Researcher Id
Scopus Author Id

Endereços de correio eletrónico

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


  • 225084000 Ext.: 7916 (Profissional)


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


Domínios de atuação

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


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)
Grau Classificação
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
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
Medicina (Licenciatura)
Universidade do Porto Instituto de Ciências Biomédicas Abel Salazar, Portugal
Percurso profissional


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


Designação Financiadores
2017 - Atual Exome sequencing of families with strong cancer incidence of unknown genetic cause
CI-IPOP 57-2017
Investigador responsável
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Em curso
2017 - Atual 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
Em curso
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
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
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
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
Em curso
2020/01/01 - 2023/12/31 IPO Porto Research Center
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
Instituto Português de Oncologia do Porto Francisco Gentil EPE, Portugal
Fundação para a Ciência e a Tecnologia
Em curso
2018/07/26 - 2021/11/25 The role of chromosome segregation machinery defects in genetic predisposition to prostate cancer.
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
2019/01/01 - 2019/12/31 Portuguese Oncology Institute - Porto Research Center
Instituto Português de Oncologia do Porto Francisco Gentil EPE, Portugal
Fundação para a Ciência e a Tecnologia
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
Investigador responsável
Instituto Português de Oncologia do Porto Francisco Gentil EPE, Portugal
Fundação para a Ciência e a Tecnologia
2015/01/01 - 2018/12/31 Portuguese Oncology Institute - Porto Research Center
Instituto Português de Oncologia do Porto Francisco Gentil EPE, Portugal
Fundação para a Ciência e a Tecnologia
2014/01/01 - 2014/12/31 Strategic Project - UI 776 - 2014
Instituto Português de Oncologia do Porto Francisco Gentil EPE, Portugal
Fundação para a Ciência e a Tecnologia
2011 - 2014 Identification of novel fusion genes originated by chromosome rearrangements in hematological malignancies
Investigador responsável
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Liga Portuguesa Contra o Cancro Núcleo Regional do Norte
2013/01/01 - 2013/12/31 Incentive - UI 776 - 2013
Instituto Português de Oncologia do Porto Francisco Gentil EPE, Portugal
Fundação para a Ciência e a Tecnologia
2011/01/01 - 2013/12/31 Strategic Project - UI 776 - 2011-2012
Instituto Português de Oncologia do Porto Francisco Gentil EPE, Portugal
Fundação para a Ciência e a Tecnologia
2009 - 2012 Genetic study of Common Hereditary Bowel Cancers in Hispania and the Americas (CHIBCHA)
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
European Union
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
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
Investigador responsável
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Fundação para a Ciência e a Tecnologia
2006 - 2010 Identification and characterization of novel MLL partner fusion genes in acute leukemia patients
Investigador responsável
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
2005/07/01 - 2008/06/30 In mismatch repair deficiency colorectal cancer are BRAF and KRAS new prognostic and therapeutic tools?
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
2005/04 - 2008/03 Identification of target genes of genomic deletions and amplifications common to breast and prostate cancer
Investigador responsável
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Fundação para a Ciência e a Tecnologia
2002 - 2006 Diagnostic and prognostic value of cytogenetic and molecular genetic analyses of sextant biopsies from prostate cancer suspects
Investigador responsável
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Fundação para a Ciência e a Tecnologia
2002 - 2004 Comparative genomic hybridization analysis of sextant biopsies from prostate cancer suspects
Investigador responsável
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Ministério da Saúde
1995/01/01 - 1997/12/31 Cytogenetic Heterogeneity in Breast Cancer
Bolseiro de Doutoramento
Fundação para a Ciência e a Tecnologia


Artigo em revista
  1. 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
  2. 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.
  3. Dareng, Eileen O.; Tyrer, Jonathan P.; Barnes, Daniel R.; Jones, Michelle R.; Yang, Xin; Aben, Katja K. H.; Adank, Muriel A.; et al. "Polygenic risk modeling for prediction of epithelial ovarian cancer risk". European Journal of Human Genetics (2022): https://publons.com/publon/50982916/.
  4. Barnes, D.R.; Silvestri, V.; Leslie, G.; McGuffog, L.; Dennis, J.; Yang, X.; Adlard, J.; et al. "Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores". Journal of the National Cancer Institute 114 1 (2022): 109-122. http://www.scopus.com/inward/record.url?eid=2-s2.0-85122613384&partnerID=MN8TOARS.
  5. Custódio, N.; Savisaar, R.; Carvalho, C.; Bak-Gordon, P.; Ribeiro, M.I.; Tavares, J.; Nunes, P.B.; et al. "Expression Profiling in Ovarian Cancer Reveals Coordinated Regulation of BRCA1/2 and Homologous Recombination Genes". Biomedicines 10 2 (2022): http://www.scopus.com/inward/record.url?eid=2-s2.0-85123732202&partnerID=MN8TOARS.
  6. Lakeman, I.M.M.; van den Broek, A.J.; Vos, J.A.M.; Barnes, D.R.; Adlard, J.; Andrulis, I.L.; Arason, A.; et al. "The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant". Genetics in Medicine 23 9 (2021): 1726-1737. http://www.scopus.com/inward/record.url?eid=2-s2.0-85115935642&partnerID=MN8TOARS.
  7. Escudeiro, C.; Pinto, C.; Vieira, J.; Peixoto, A.; Pinto, P.; Pinheiro, M.; Santos, C.; et al. "The role of TP53 pathogenic variants in early-onset HER2-positive breast cancer". Familial Cancer 20 3 (2021): 173-180. http://www.scopus.com/inward/record.url?eid=2-s2.0-85092355459&partnerID=MN8TOARS.
  8. Marques, I.J.; Gomes, I.; Pojo, M.; Pires, C.; Moura, M.M.; Cabrera, R.; Santos, C.; et al. "Identification of SPRY4 as a novel candidate susceptibility gene for familial nonmedullary thyroid cancer". Thyroid 31 9 (2021): 1366-1375. http://www.scopus.com/inward/record.url?eid=2-s2.0-85115047606&partnerID=MN8TOARS.
  9. Lin, H.-Y.; Huang, P.-Y.; Cheng, C.-H.; Tung, H.-Y.; Fang, Z.; Berglund, A.E.; Chen, A.; et al. "KLK3 SNP–SNP interactions for prediction of prostate cancer aggressiveness". Scientific Reports 11 1 (2021): http://www.scopus.com/inward/record.url?eid=2-s2.0-85105127432&partnerID=MN8TOARS.
  10. Bancroft, E.K.; Page, E.C.; Brook, M.N.; Thomas, S.; Taylor, N.; Pope, J.; McHugh, J.; et al. "A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study". The Lancet. Oncology 22 11 (2021): 1618-1631. http://www.scopus.com/inward/record.url?eid=2-s2.0-85118246064&partnerID=MN8TOARS.
  11. Huynh-Le, M.-P.; Fan, C.C.; Karunamuni, R.; Thompson, W.K.; Martinez, M.E.; Eeles, R.A.; Kote-Jarai, Z.; et al. "Polygenic hazard score is associated with prostate cancer in multi-ethnic populations". Nature Communications 12 1 (2021): http://www.scopus.com/inward/record.url?eid=2-s2.0-85101701053&partnerID=MN8TOARS.
  12. Duarte, D.B.; Ferreira, L.; Santos, A.P.; Costa, C.; Lima, J.; Santos, C.; Afonso, M.; et al. "Case Report: Pheochromocytoma and Synchronous Neuroblastoma in a Family With Hereditary Pheochromocytoma Associated With a MAX Deleterious Variant". Frontiers in Endocrinology 12 (2021): http://www.scopus.com/inward/record.url?eid=2-s2.0-85103508527&partnerID=MN8TOARS.
  13. Petronilho, S.; Sequeira, J.P.; Paulino, S.; Lopes, P.; Lisboa, S.; Chacim, S.; Lobo, J.; et al. "Prognostic value of histone modifying enzyme EZH2 in RCHOP-treated diffuse large B-cell lymphoma and high grade B-cell lymphoma". Journal of Personalized Medicine 11 12 (2021): http://www.scopus.com/inward/record.url?eid=2-s2.0-85121615245&partnerID=MN8TOARS.
  14. Karlsson, Q.; Brook, M.N.; Dadaev, T.; Wakerell, S.; Saunders, E.J.; Muir, K.; Neal, D.E.; et al. "Rare Germline Variants in ATM Predispose to Prostate Cancer: A PRACTICAL Consortium Study". European urology oncology 4 4 (2021): 570-579. http://www.scopus.com/inward/record.url?eid=2-s2.0-85100645237&partnerID=MN8TOARS.
  15. Karunamuni, R.A.; Huynh-Le, M.-P.; Fan, C.C.; Thompson, W.; Eeles, R.A.; Kote-Jarai, Z.; Muir, K.; et al. "Additional SNPs improve risk stratification of a polygenic hazard score for prostate cancer". Prostate Cancer and Prostatic Diseases 24 2 (2021): 532-541. http://www.scopus.com/inward/record.url?eid=2-s2.0-85102762943&partnerID=MN8TOARS.
  16. Pereira, F.; Teixeira, M.R.; Dinis Ribeiro, M.; Brandão, C.. "Multi-Gene Panel Testing in Gastroenterology: Are We Ready for the Results?". GE Portuguese Journal of Gastroenterology 28 6 (2021): 403-409. http://www.scopus.com/inward/record.url?eid=2-s2.0-85100744969&partnerID=MN8TOARS.
  17. Conti, D.V.; Darst, B.F.; Moss, L.C.; Saunders, E.J.; Sheng, X.; Chou, A.; Schumacher, F.R.; et al. "Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction". Nature Genetics 53 1 (2021): 65-75. http://www.scopus.com/inward/record.url?eid=2-s2.0-85098923871&partnerID=MN8TOARS.
  18. Cerveira, N.; Bizarro, S.; Teixeira, M.R.; Mariz, J.M.. "When to Stop TKIs in Patients with Chronic Myeloid Leukemia and How to Follow Them Subsequently". Current Treatment Options in Oncology 22 6 (2021): http://www.scopus.com/inward/record.url?eid=2-s2.0-85104519120&partnerID=MN8TOARS.
  19. Barbosa, A.; Pinto, P.; Peixoto, A.; Guerra, J.; Pinheiro, M.; Santos, C.; Pinto, C.; et al. "Next Generation Sequencing of Tumor and Matched Plasma Samples: Identification of Somatic Variants in ctDNA From Ovarian Cancer Patients". Frontiers in Oncology 11 (2021): http://www.scopus.com/inward/record.url?eid=2-s2.0-85117094719&partnerID=MN8TOARS.
  20. Couto, M.E.; Bizarro, S.; Sousa, D.; Domingues, N.; Oliveira, I.; Martins, G.; Teixeira, M.R.; Mariz, M.. "Myeloid Disease with the CSF3R T618I Mutation after CLL". Case Reports in Hematology 2020 (2020): 1-4. http://dx.doi.org/10.1155/2020/6670965.
  21. Fachal, L.; Aschard, H.; Beesley, J.; Barnes, D.R.; Allen, J.; Kar, S.; Pooley, K.A.; et al. "Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes". Nature Genetics 52 1 (2020): 56-73. http://www.scopus.com/inward/record.url?eid=2-s2.0-85077675544&partnerID=MN8TOARS.
  22. Escala-Garcia, M.; Abraham, J.; Andrulis, I.L.; Anton-Culver, H.; Arndt, V.; Ashworth, A.; Auer, P.L.; et al. "A network analysis to identify mediators of germline-driven differences in breast cancer prognosis". Nature Communications 11 1 (2020): http://www.scopus.com/inward/record.url?eid=2-s2.0-85077940819&partnerID=MN8TOARS.
  23. Figlioli, G.; Kvist, A.; Tham, E.; Soukupova, J.; Kleiblova, P.; Muranen, T.A.; Andrieu, N.; et al. "The spectrum of fancm protein truncating variants in European breast cancer cases". Cancers 12 2 (2020): http://www.scopus.com/inward/record.url?eid=2-s2.0-85078848552&partnerID=MN8TOARS.
  24. Feng, H.; Gusev, A.; Pasaniuc, B.; Wu, L.; Long, J.; Abu-full, Z.; Aittomäki, K.; et al. "Transcriptome-wide association study of breast cancer risk by estrogen-receptor status". Genetic Epidemiology (2020): http://www.scopus.com/inward/record.url?eid=2-s2.0-85081379482&partnerID=MN8TOARS.
  25. Patel, V.L.; Busch, E.L.; Friebel, T.M.; Cronin, A.; Leslie, G.; McGuffog, L.; Adlard, J.; et al. "Association of genomic domains in BRCA1 and BRCA2 with prostate cancer risk and aggressiveness". Cancer Research 80 3 (2020): 624-638. http://www.scopus.com/inward/record.url?eid=2-s2.0-85079022145&partnerID=MN8TOARS.
  26. Barnes, D.R.; Rookus, M.A.; McGuffog, L.; Leslie, G.; Mooij, T.M.; Dennis, J.; Mavaddat, N.; et al. "Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants". Genetics in Medicine 22 10 (2020): 1653-1666. http://www.scopus.com/inward/record.url?eid=2-s2.0-85091841899&partnerID=MN8TOARS.
  27. Karunamuni, R.A.; Huynh-Le, M.-P.; Fan, C.C.; Eeles, R.A.; Easton, D.F.; Kote-Jarai, Z.S.; Amin Al Olama, A.; et al. "The effect of sample size on polygenic hazard models for prostate cancer". European Journal of Human Genetics 28 10 (2020): 1467-1475. http://www.scopus.com/inward/record.url?eid=2-s2.0-85086170171&partnerID=MN8TOARS.
  28. Brandão, A.; Paulo, P.; Teixeira, M.R.. "Hereditary predisposition to prostate cancer: From genetics to clinical implications". International Journal of Molecular Sciences 21 14 (2020): 1-23. http://www.scopus.com/inward/record.url?eid=2-s2.0-85088485750&partnerID=MN8TOARS.
  29. Pinheiro, M.; Peixoto, A.; Santos, C.; Escudeiro, C.; Bizarro, S.; Pinto, P.; Santos, R.; et al. "Pathogenicity reclassification of two BRCA1/BRCA2 exonic duplications after identification of genomic breakpoints and tandem orientation". Cancer Genetics 248-249 (2020): 18-24. http://www.scopus.com/inward/record.url?eid=2-s2.0-85091235182&partnerID=MN8TOARS.
  30. Huynh-Le, M.-P.; Fan, C.C.; Karunamuni, R.; Walsh, E.I.; Turner, E.L.; Athene Lane, J.; Martin, R.M.; et al. "A genetic risk score to personalize prostate cancer screening, applied to population data". Cancer Epidemiology Biomarkers and Prevention 29 9 (2020): 1731-1738. http://www.scopus.com/inward/record.url?eid=2-s2.0-85096010016&partnerID=MN8TOARS.
  31. Lobo, J.; Pinto, C.; Pinheiro, M.; Lobo, F.; Sousa, N.; Lopes, P.; Looijenga, L.H.J.; et al. "Widening the spectrum of Lynch syndrome: first report of testicular seminoma attributable to MSH2 loss". Histopathology 76 3 (2020): 486-489. http://www.scopus.com/inward/record.url?eid=2-s2.0-85073749849&partnerID=MN8TOARS.
  32. Muranen, T.A.; Khan, S.; Fagerholm, R.; Aittomäki, K.; Cunningham, J.M.; Dennis, J.; Leslie, G.; et al. "Association of germline variation with the survival of women with BRCA1/2 pathogenic variants and breast cancer". npj Breast Cancer 6 1 (2020): http://www.scopus.com/inward/record.url?eid=2-s2.0-85090501112&partnerID=MN8TOARS.
  33. Barbosa, A.; Pinto, P.; Peixoto, A.; Guerra, J.; Pinto, C.; Santos, C.; Pinheiro, M.; et al. "Gene panel tumor testing in ovarian cancer patients significantly increases the yield of clinically actionable germline variants beyond BRCA1/BRCA2". Cancers 12 10 (2020): 1-16. http://www.scopus.com/inward/record.url?eid=2-s2.0-85091853327&partnerID=MN8TOARS.
  34. Martins, R.G.; Cunha, N.; Simões, H.; Matos, M.J.; Silva, J.; Torres, I.; Rodrigues, F.; et al. "Surveillance of succinate dehydrogenase gene mutation carriers: Insights from a nationwide cohort". Clinical Endocrinology 92 6 (2020): 545-553. http://www.scopus.com/inward/record.url?eid=2-s2.0-85083494328&partnerID=MN8TOARS.
  35. Peixoto, A.; Pinto, P.; Guerra, J.; Pinheiro, M.; Santos, C.; Pinto, C.; Santos, R.; et al. "Tumor Testing for Somatic and Germline BRCA1/BRCA2 Variants in Ovarian Cancer Patients in the Context of Strong Founder Effects". Frontiers in Oncology 10 (2020): http://www.scopus.com/inward/record.url?eid=2-s2.0-85089524652&partnerID=MN8TOARS.
  36. Tuazon, A.M.A.; Lott, P.; Bohórquez, M.; Benavides, J.; Ramirez, C.; Criollo, A.; Estrada-Florez, A.; et al. "Haplotype analysis of the internationally distributed BRCA1 c.3331_3334delCAAG founder mutation reveals a common ancestral origin in Iberia". Breast cancer research : BCR 22 1 (2020): 108-108. http://www.scopus.com/inward/record.url?eid=2-s2.0-85094153616&partnerID=MN8TOARS.
  37. Brandão, A.; Paulo, P.; Maia, S.; Pinheiro, M.; Peixoto, A.; Cardoso, M.; Silva, M.P.; et al. "The CHEK2 variant C.349A>G is associated with prostate cancer risk and carriers share a common ancestor". Cancers 12 11 (2020): 1-17. http://www.scopus.com/inward/record.url?eid=2-s2.0-85096384312&partnerID=MN8TOARS.
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  240. Tsarouha, H.; Kyriazoglou, A.I.; Ribeiro, F.R.; Teixeira, M.R.; Agnantis, N.; Pandis, N.. "Chromosome analysis and molecular cytogenetic investigations of an epithelioid hemangioendothelioma". Cancer Genetics and Cytogenetics 169 2 (2006): 164-168. http://www.scopus.com/inward/record.url?eid=2-s2.0-33747870517&partnerID=MN8TOARS.
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  252. Cerveira, N.; Torres, L.; Ribeiro, F.R.; Henrique, R.; Pinto, A.; Bizarro, S.; Ferreira, A.M.; Lopes, C.; Teixeira, M.R.. "Multimodal genetic diagnosis of solid variant alveolar rhabdomyosarcoma". Cancer Genetics and Cytogenetics 163 2 (2005): 138-143. http://www.scopus.com/inward/record.url?eid=2-s2.0-28744456471&partnerID=MN8TOARS.
  253. Teixeira, M.R.; Heim, S.. "Multiple numerical chromosome aberrations in cancer: What are their causes and what are their consequences?". Seminars in Cancer Biology 15 1 (2005): 3-12. http://www.scopus.com/inward/record.url?eid=2-s2.0-10944219726&partnerID=MN8TOARS.
  254. Mesquita, B.; Veiga, I.; Pereira, D.; Tavares, A.; Pinto, I.M.; Pinto, C.; Teixeira, M.R.; Castedo, S.. "No significant role for beta tubulin mutations and mismatch repair defects in ovarian cancer resistance to paclitaxel/cisplatin". BMC Cancer 5 (2005): http://www.scopus.com/inward/record.url?eid=2-s2.0-26844480242&partnerID=MN8TOARS.
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  256. Lind, G.E.; Skotheim, R.I.; Fraga, M.F.; Abeler, V.M.; Henrique, R.; Saatcioglu, F.; Esteller, M.; Teixeira, M.R.; Lothe, R.A.. "The loss of NKX3.1 expression in testicular - And prostate - Cancers is not caused by promoter hypermethylation". Molecular Cancer 4 (2005): http://www.scopus.com/inward/record.url?eid=2-s2.0-13644259352&partnerID=MN8TOARS.
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  258. Castro, P.; Eknæs, M.; Teixeira, M.R.; Danielsen, H.E.; Soares, P.; Lothe, R.A.; Sobrinho-Simoões, M.. "Adenomas and follicular carcinomas of the thyroid display two major patterns of chromosomal changes". Journal of Pathology 206 3 (2005): 305-311. http://www.scopus.com/inward/record.url?eid=2-s2.0-21344452129&partnerID=MN8TOARS.
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  286. 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.
  287. 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.
  288. 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.
  289. 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.
  290. 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.
  291. 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.
  292. 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.
  293. 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.
  294. 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.
  295. 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.
  296. 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.
  297. 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.
  298. 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.
  299. 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.
  300. 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.
  301. 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.
  302. 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.
  303. 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.
  304. 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.
  305. 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.
  306. 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.
  307. 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.
  308. 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.
  309. 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.
  310. 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.
  311. 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.
  312. 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.
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.
  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.
  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.
  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.
  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.
  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.
  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.
  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

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

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
2017 - Atual Correspondent member of the National Medical Academy of Portugal
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)


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