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Manuel António Rodrigues Teixeira completed the medical degree in Medicine in 1992 by Universidade do Porto, Instituto de Ciências Biomédicas Abel Salazar, and Doctor Medicinae in 1997 by Universitetet i Oslo, Det medisinske fakultet. He is Coordinating Researcher in Instituto Português de Oncologia do Porto Francisco Gentil EPE (IPO Porto), where is is the Director of the Department of Genetics and of the IPO Porto Research Center (CI-IPOP). He is also Invited Full Professor in Universidade do Porto, Instituto de Ciências Biomédicas Abel Salazar. He published 307 articles in journals and has co-authored 5 books. He has received 1 scientific awards, participates and/or participated as Principal investigator in 14 projects, and as researcher in two other projects. He works in the areas of Medical and Health Sciences, with emphasis in Cancer Genetics. In his professional activities he interacted with 4697 co-authors of scientific papers.
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. Genetics, IPO Porto, Rua Dr. António Bernardino Almeida, 4200-072, Porto, Porto, Portugal (Profissional)

Websites

  • http://publicationslist.org/manuel.r.teixeira (Pessoal)

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 independente (B2) Utilizador independente (B2) Utilizador independente (B2)
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
1986 - 1992
Concluído
Medicina (Licenciatura)
Universidade do Porto Instituto de Ciências Biomédicas Abel Salazar, Portugal
17
Percurso profissional

Ciência

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

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

1993 - 1993 Interno (Médica)
Centro Hospitalar Universitário do Porto EPE, Portugal
Projetos

Projeto

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
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
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
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
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
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
2019 - 2021 The role of chromosome segregation machinery defects in genetic predisposition to prostate cancer
POCI-01-0145-FEDER-028245
Investigador
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Fundação para a Ciência e a Tecnologia
2016 - 2018/12 Inherited predisposition to prostate cancer: finding the missing heritability by combining exome sequencing and haplotype analyses in a population with strong founder effects
grant.Provided by PTCRIS: 139933
PTDC/DTPPIC/1308/2014
Investigador responsável
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Stichting Weten
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
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
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 - 2010/08 Characterization of fusion genes involving the ETS family of transcription factors and their role as diagnostic and prognostic markers in prostate cancer
grant.Provided by PTCRIS: 70543
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
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
2005 - 2008/03 Identification of target genes of genomic deletions and amplifications common to breast and prostate cancer
grant.Provided by PTCRIS: 58357
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
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
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
Produções

Publicações

Artigo em revista
  1. Teixeira, Manuel R.. "Polygenic hazard score is associated with prostate cancer in multi-ethnic populations.". Nature communications (2021): https://doi.org/10.1038/s41467-021-21287-0.
    10.1038/s41467-021-21287-0
  2. Teixeira, Manuel R.. "Rare Germline Variants in ATM Predispose to Prostate Cancer: A PRACTICAL Consortium Study.". European urology oncology (2021): https://doi.org/10.1016/j.euo.2020.12.001.
    10.1016/j.euo.2020.12.001
  3. Teixeira, Manuel R.. "Additional SNPs improve risk stratification of a polygenic hazard score for prostate cancer.". Prostate cancer and prostatic diseases (2021): https://doi.org/10.1038/s41391-020-00311-2.
    10.1038/s41391-020-00311-2
  4. Teixeira, Manuel R.. "Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction.". Nature genetics (2021): https://doi.org/10.1038/s41588-020-00748-0.
    10.1038/s41588-020-00748-0
  5. Maria Eduarda Couto; Susana Bizarro; Domingos Sousa; Nelson Domingues; Isabel Oliveira; Gabriela Martins; Manuel R. Teixeira; Mário Mariz; Stephen E. Langabeer. "Myeloid Disease with the CSF3R T618I Mutation after CLL". Case Reports in Hematology (2020): https://doi.org/10.1155/2020/6670965.
    10.1155/2020/6670965
  6. Lobo, João; Pinto, Carla; Pinheiro, Manuela; Lobo, Francisco; Sousa, Nuno; Lopes, Paula; Looijenga, Leendert HJ; et al. "Widening the spectrum of Lynch syndrome: first report of testicular seminoma attributable to MSH2 loss". Histopathology 76 3 (2020): 486-489. http://dx.doi.org/10.1111/his.13979.
    10.1111/his.13979
  7. Teixeira, Manuel R.. "The CHEK2 Variant C.349A>G Is Associated with Prostate Cancer Risk and Carriers Share a Common Ancestor". Cancers (2020): https://www.mdpi.com/2072-6694/12/11/3254.
    10.3390/cancers12113254
  8. Teixeira, Manuel R.. "Haplotype analysis of the internationally distributed BRCA1 c.3331_3334delCAAG founder mutation reveals a common ancestral origin in Iberia.". Breast cancer research : BCR (2020): https://europepmc.org/articles/PMC7579869.
    10.1186/s13058-020-01341-3
  9. 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 (2020): http://europepmc.org/abstract/med/33051812.
    10.1007/s10689-020-00212-2
  10. Teixeira, Manuel R.. "Gene Panel Tumor Testing in Ovarian Cancer Patients Significantly Increases the Yield of Clinically Actionable Germline Variants beyond BRCA1/BRCA2". Cancers (2020): https://www.mdpi.com/2072-6694/12/10/2834.
    10.3390/cancers12102834
  11. 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 (2020): http://europepmc.org/abstract/med/32971473.
    10.1016/j.cancergen.2020.09.001
  12. Muranen TA; Khan S; Fagerholm R; Aittomäki K; Cunningham JM; 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 (2020): http://europepmc.org/abstract/med/32964118.
    10.1038/s41523-020-00185-6
  13. Teixeira, Manuel R.. "Characterization of the Cancer Spectrum in Men With Germline BRCA1 and BRCA2 Pathogenic Variants: Results From the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA).". JAMA oncology (2020): https://doi.org/10.1001/jamaoncol.2020.2134.
    10.1001/jamaoncol.2020.2134
  14. Teixeira, Manuel R.. "Tumor Testing for Somatic and Germline BRCA1/BRCA2 Variants in Ovarian Cancer Patients in the Context of Strong Founder Effects.". Frontiers in oncology (2020): https://europepmc.org/articles/PMC7412538.
    10.3389/fonc.2020.01318
  15. Andreia Brandão; Paula Paulo; Manuel R. Teixeira. "Hereditary Predisposition to Prostate Cancer: From Genetics to Clinical Implications". International Journal of Molecular Sciences 21 14 (2020): 5036-5036. https://doi.org/10.3390/ijms21145036.
    10.3390/ijms21145036
  16. Teixeira, Manuel R.. "Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants.". Genetics in medicine : official journal of the American College of Medical Genetics (2020): https://europepmc.org/articles/PMC7521995.
    10.1038/s41436-020-0862-x
  17. Teixeira, Manuel R.. "A Genetic Risk Score to Personalize Prostate Cancer Screening, Applied to Population Data.". Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology (2020): https://doi.org/10.1158/1055-9965.EPI-19-1527.
    10.1158/1055-9965.epi-19-1527
  18. Teixeira, Manuel R.. "The effect of sample size on polygenic hazard models for prostate cancer.". European journal of human genetics : EJHG (2020): https://doi.org/10.1038/s41431-020-0664-2.
    10.1038/s41431-020-0664-2
  19. Teixeira, Manuel R.. "Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses.". Nature genetics (2020): https://doi.org/10.1038/s41588-020-0609-2.
    10.1038/s41588-020-0609-2
  20. Martins RG; Cunha N; Simões H; Matos MJ; Silva J; Torres I; Rodrigues F; et al. "Surveillance of succinate dehydrogenase gene mutation carriers: Insights from a nationwide cohort.". Clinical endocrinology (2020): http://europepmc.org/abstract/med/32181896.
    10.1111/cen.14184
  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.
    10.1038/s41588-019-0537-1
  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.
    10.1038/s41467-019-14100-6
  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.
    10.3390/cancers12020292
  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.
    10.1002/gepi.22288
  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.
    10.1158/0008-5472.CAN-19-1840
  26. Adams, C.D.; Richmond, R.; Santos Ferreira, D.L.; Spiller, W.; Tan, V.; Zheng, J.; Würtz, P.; et al. "Circulating metabolic biomarkers of screen-detected prostate cancer in the ProtecT study". Cancer Epidemiology Biomarkers and Prevention 28 1 (2019): 208-216. http://www.scopus.com/inward/record.url?eid=2-s2.0-85059928972&partnerID=MN8TOARS.
    10.1158/1055-9965.EPI-18-0079
  27. Jiang, X.; Finucane, H.K.; Schumacher, F.R.; Schmit, S.L.; Tyrer, J.P.; Han, Y.; Michailidou, K.; et al. "Shared heritability and functional enrichment across six solid cancers". Nature Communications 10 1 (2019): http://www.scopus.com/inward/record.url?eid=2-s2.0-85060528251&partnerID=MN8TOARS.
    10.1038/s41467-018-08054-4
  28. Ferreira, M.A.; Gamazon, E.R.; Al-Ejeh, F.; Aittomäki, K.; Andrulis, I.L.; Anton-Culver, H.; Arason, A.; et al. "Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer". Nature Communications 10 1 (2019): http://www.scopus.com/inward/record.url?eid=2-s2.0-85064432929&partnerID=MN8TOARS.
    10.1038/s41467-018-08053-5
  29. Law, P.J.; Timofeeva, M.; Fernandez-Rozadilla, C.; Broderick, P.; Studd, J.; Fernandez-Tajes, J.; Farrington, S.; et al. "Association analyses identify 31 new risk loci for colorectal cancer susceptibility". Nature Communications 10 1 (2019): http://www.scopus.com/inward/record.url?eid=2-s2.0-85065767394&partnerID=MN8TOARS.
    10.1038/s41467-019-09775-w
  30. Singer, C.F.; Balmaña, J.; Bürki, N.; Delaloge, S.; Filieri, M.E.; Gerdes, A.-M.; Grindedal, E.M.; et al. "Genetic counselling and testing of susceptibility genes for therapeutic decision-making in breast cancer—an European consensus statement and expert recommendations". European Journal of Cancer 106 (2019): 54-60. http://www.scopus.com/inward/record.url?eid=2-s2.0-85056856124&partnerID=MN8TOARS.
    10.1016/j.ejca.2018.10.007
  31. Escala-Garcia, M.; Guo, Q.; Dörk, T.; Canisius, S.; Keeman, R.; Dennis, J.; Beesley, J.; et al. "Genome-wide association study of germline variants and breast cancer-specific mortality". British Journal of Cancer 120 6 (2019): 647-657. http://www.scopus.com/inward/record.url?eid=2-s2.0-85061925826&partnerID=MN8TOARS.
    10.1038/s41416-019-0393-x
  32. Page, E.C.; Bancroft, E.K.; Brook, M.N.; Assel, M.; Hassan Al Battat, M.; Thomas, S.; Taylor, N.; et al. "Interim Results from the IMPACT Study: Evidence for Prostate-specific Antigen Screening in BRCA2 Mutation Carriers". European Urology 76 6 (2019): 831-842. http://www.scopus.com/inward/record.url?eid=2-s2.0-85074388214&partnerID=MN8TOARS.
    10.1016/j.eururo.2019.08.019
  33. Cerveira, N.; Diamond, J.; Matos, S.; Amorim, M.L.; Coucelo, M.; Bizarro, S.; Simões, A.T.; et al. "Negative MR4·0 chronic myeloid leukaemia and its possible implications for treatment-free remission". British Journal of Haematology 186 6 (2019): e181-e184. http://www.scopus.com/inward/record.url?eid=2-s2.0-85067473220&partnerID=MN8TOARS.
    10.1111/bjh.16058
  34. Figlioli, G.; Bogliolo, M.; Catucci, I.; Caleca, L.; Lasheras, S.V.; Pujol, R.; Kiiski, J.I.; et al. "The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer". npj Breast Cancer 5 1 (2019): http://www.scopus.com/inward/record.url?eid=2-s2.0-85074364016&partnerID=MN8TOARS.
    10.1038/s41523-019-0127-5
  35. Qian, F.; Wang, S.; Mitchell, J.; McGuffog, L.; Barrowdale, D.; Leslie, G.; Oosterwijk, J.C.; et al. "Height and body mass index as Modifiers of breast cancer risk in BRCA1/2 mutation carriers: A Mendelian randomization study". Journal of the National Cancer Institute 111 4 (2019): 350-364. http://www.scopus.com/inward/record.url?eid=2-s2.0-85064286333&partnerID=MN8TOARS.
    10.1093/jnci/djy132
  36. Pinheiro, M.; Francisco, I.; Pinto, C.; Peixoto, A.; Veiga, I.; Filipe, B.; Santos, C.; et al. "The nonsense mutation MSH2 c.2152C>T shows a founder effect in Portuguese Lynch syndrome families". Genes Chromosomes and Cancer 58 9 (2019): 657-664. http://www.scopus.com/inward/record.url?eid=2-s2.0-85065014893&partnerID=MN8TOARS.
    10.1002/gcc.22759
  37. Vos, J.R.; Giepmans, L.; Röhl, C.; Geverink, N.; Hoogerbrugge, N.; Ligtenberg, M.; Kets, M.; et al. "Boosting care and knowledge about hereditary cancer: European Reference Network on Genetic Tumour Risk Syndromes". Familial Cancer 18 2 (2019): 281-284. http://www.scopus.com/inward/record.url?eid=2-s2.0-85054801434&partnerID=MN8TOARS.
    10.1007/s10689-018-0110-6
  38. Qian, F.; Rookus, M.A.; Leslie, G.; Risch, H.A.; Greene, M.H.; Aalfs, C.M.; Adank, M.A.; et al. "Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers". British Journal of Cancer 121 2 (2019): 180-192. http://www.scopus.com/inward/record.url?eid=2-s2.0-85067846442&partnerID=MN8TOARS.
    10.1038/s41416-019-0492-8
  39. Pinto, D.; Pinto, C.; Guerra, J.; Pinheiro, M.; Santos, R.; Vedeld, H.M.; Yohannes, Z.; et al. "Contribution of MLH1 constitutional methylation for Lynch syndrome diagnosis in patients with tumor MLH1 downregulation". Cancer Medicine 7 2 (2018): 433-444. http://www.scopus.com/inward/record.url?eid=2-s2.0-85040657087&partnerID=MN8TOARS.
    10.1002/cam4.1285
  40. Fewings, E.; Larionov, A.; Redman, J.; Goldgraben, M.A.; Scarth, J.; Richardson, S.; Brewer, C.; et al. "Germline pathogenic variants in PALB2 and other cancer-predisposing genes in families with hereditary diffuse gastric cancer without CDH1 mutation: a whole-exome sequencing study". The Lancet Gastroenterology and Hepatology (2018): http://www.scopus.com/inward/record.url?eid=2-s2.0-85046162774&partnerID=MN8TOARS.
    10.1016/S2468-1253(18)30079-7
  41. Vijayakrishnan, J.; Studd, J.; Broderick, P.; Kinnersley, B.; Holroyd, A.; Law, P.J.; Kumar, R.; et al. "Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia". Nature Communications 9 1 (2018): http://www.scopus.com/inward/record.url?eid=2-s2.0-85045221334&partnerID=MN8TOARS.
    10.1038/s41467-018-03178-z
  42. Mikropoulos, C.; Selkirk, C.G.H.; Saya, S.; Bancroft, E.; Vertosick, E.; Dadaev, T.; Brendler, C.; et al. "Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition". British Journal of Cancer 118 2 (2018): 266-276. http://www.scopus.com/inward/record.url?eid=2-s2.0-85041064923&partnerID=MN8TOARS.
    10.1038/bjc.2017.429
  43. Caputo, S.M.; Léone, M.; Damiola, F.; Ehlen, A.; Carreira, A.; Gaidrat, P.; Martins, A.; et al. "Full in-frame exon 3 skipping of BRCA2 confers high risk of breast and/or ovarian cancer". Oncotarget 9 25 (2018): 17334-17348. http://www.scopus.com/inward/record.url?eid=2-s2.0-85044827158&partnerID=MN8TOARS.
    10.18632/oncotarget.24671
  44. Rebbeck, T.R.; Friebel, T.M.; Friedman, E.; Hamann, U.; Huo, D.; Kwong, A.; Olah, E.; et al. "Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations". Human Mutation 39 5 (2018): 593-620. http://www.scopus.com/inward/record.url?eid=2-s2.0-85043494756&partnerID=MN8TOARS.
    10.1002/humu.23406
  45. Seibert, T.M.; Fan, C.C.; Wang, Y.; Zuber, V.; Karunamuni, R.; Parsons, J.K.; Eeles, R.A.; et al. "Polygenic hazard score to guide screening for aggressive prostate cancer: Development and validation in large scale cohorts". BMJ (Online) 360 (2018): http://www.scopus.com/inward/record.url?eid=2-s2.0-85040518909&partnerID=MN8TOARS.
    10.1136/bmj.j5757
  46. Ana Barbosa; Ana Peixoto; Pedro Pinto; Manuela Pinheiro; Manuel R. Teixeira. "Potential clinical applications of circulating cell-free DNA in ovarian cancer patients". Expert Reviews in Molecular Medicine 20 (2018): https://doi.org/10.1017/erm.2018.5.
    10.1017/erm.2018.5
  47. Went, M.; Sud, A.; Försti, A.; Halvarsson, B.-M.; Weinhold, N.; Kimber, S.; van Duin, M.; et al. "Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma". Nature Communications 9 1 (2018): http://www.scopus.com/inward/record.url?eid=2-s2.0-85053336514&partnerID=MN8TOARS.
    10.1038/s41467-018-04989-w
  48. Paulo, P.; Maia, S.; Pinto, C.; Pinto, P.; Monteiro, A.; Peixoto, A.; Teixeira, M.R.. "Targeted next generation sequencing identifies functionally deleterious germline mutations in novel genes in early-onset/familial prostate cancer". PLoS Genetics 14 4 (2018): http://www.scopus.com/inward/record.url?eid=2-s2.0-85046415026&partnerID=MN8TOARS.
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  275. Teixeira, M.R.; Ribeiro, F.R.; Cerveira, N.; Torres, L.; Amaro, T.; Henrique, R.; Lopes, C.. "Karyotypic divergence and convergence in two synchronous lung metastases of a clear cell sarcoma of tendons and aponeuroses with t(12;22)(q13;q12) and type 1 EWS/ATF1". Cancer Genetics and Cytogenetics 145 2 (2003): 121-125. http://www.scopus.com/inward/record.url?eid=2-s2.0-0043165097&partnerID=MN8TOARS.
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  277. 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.
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  282. 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.
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  284. 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.
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  286. 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.
  287. 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.
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  288. 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.
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  289. 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.
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  290. 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.
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  292. 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.
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  293. 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.
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  295. 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.
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  296. 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.
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Livro
  1. Teixeira, M.R.; Heim, S.. Tumors of the male genital organs. 2015.
  2. Teixeira, M.R.; Pandis, N.; Heim, S.. Tumors of the breast. 2015.
  3. Teixeira, M.R.; Heim, S.. Cytogenetic Analysis of Tumor Clonality. 2011.
    10.1016/B978-0-12-387688-1.00005-3
  4. Teixeira, M.R.; Pandis, N.; Heim, S.. Tumors of the Breast. 2010.
    10.1002/9781118010136.ch15
  5. Teixeira, M.R.; Heim, S.. Tumors of the Male Genital Organs. 2010.
    10.1002/9781118010136.ch17
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
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)
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