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.

Personal identification

Full name
Manuel António Rodrigues Teixeira

Citation names

  • Teixeira, Manuel R.

Author identifiers

Ciência ID
Researcher Id
Scopus Author Id

Email addresses

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


  • 225084000 Ext.: 7916 (Professional)


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


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

Knowledge fields

  • Medical and Health Sciences - Basic Medicine - Human Genetics


Language Speaking Reading Writing Listening Peer-review
Portuguese (Mother tongue)
English Proficiency (C2) Proficiency (C2) Proficiency (C2) Proficiency (C2) Proficiency (C2)
Norwegian Upper intermediate (B2) Upper intermediate (B2) Upper intermediate (B2) Upper intermediate (B2)
Degree Classification
Habilitado para funções de coordenação científica (Título de Habilitação de Coordenação Científica)
Major in Oncobiology (Cancer Genetics)
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
1994 - 1997
Doctor Medicinae (Doctor of Philosophy)
Major in Medicine (Medical Genetics)
Universitetet i Oslo Det medisinske fakultet, Norway
1986 - 1992
Medicina (Licenciatura)
Universidade do Porto Instituto de Ciências Biomédicas Abel Salazar, Portugal


2008/11/26 - Current Coordinating Researcher (Research)
Instituto Português de Oncologia do Porto Francisco Gentil EPE, Portugal
2001 - 2008 Auxiliary Researcher (Research)
Instituto Português de Oncologia do Porto Francisco Gentil EPE, Portugal
1998 - 2000 Postdoc (Research)
Oslo Universitetssykehus Institutt for kreftforskning, Norway

Teaching in Higher Education

2009 - Current Invited Full Professor (University Teacher)
Universidade do Porto Instituto de Ciências Biomédicas Abel Salazar, Portugal
2007 - 2009 Invited Associate Professor (University Teacher)
Universidade do Porto Instituto de Ciências Biomédicas Abel Salazar, Portugal
2002 - 2007 Invited Assistant Professor (University Teacher)
Universidade do Porto Instituto de Ciências Biomédicas Abel Salazar, Portugal

Other Careers

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


Designation Funders
2017 - Current Exome sequencing of families with strong cancer incidence of unknown genetic cause
CI-IPOP 57-2017
Principal investigator
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
2017 - Current Identification of germline mutations by gene-panel next generation sequencing in familial tubular and mixed tubular-diffuse gastric cancer
CI-IPOP 56-2017
Principal investigator
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
2017 - Current Validation of liquid biopsies for predictive biomarker testing, therapy response monitoring, and resistance mechanism identification in cancer patients
CI-IPOP 54-2017
Principal investigator
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
2016 - Current 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
Principal investigator
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
2016 - Current 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
Principal investigator
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
2015 - Current Inherited predisposition to prostate cancer
CI-IPOP 24-2015
Principal investigator
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
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
Principal investigator
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
Principal investigator
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)
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
Principal investigator
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
Principal investigator
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
Principal investigator
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
Principal investigator
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
Principal investigator
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
Principal investigator
Instituto Português de Oncologia do Porto Francisco Gentil Centro de Investigação, Portugal
Ministério da Saúde


  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.
  4. Teixeira, M.R.; Pandis, N.; Heim, S.. Tumors of the Breast. 2010.
  5. Teixeira, M.R.; Heim, S.. Tumors of the Male Genital Organs. 2010.
Journal article
  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.
  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.
  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.
  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.
  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.
  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.
  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.
  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.
  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. 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.
  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.
  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.
  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.
  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.
  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.
  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.
  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.
  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.
  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.
  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.
  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. 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.
  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.
  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.
  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.
  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.
  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.
  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.
  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.
  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.
  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.
  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.
  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.
  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.
  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.
  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.
  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.
  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.
  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.
  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.
  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.
  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.
  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.
  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.
  49. Teixeira, Manuel R.. "Discontinuation of tyrosine kinase inhibitors in CML patients in real-world clinical practice at a single institution 11 Medical and Health Sciences 1112 Oncology and Carcinogenesis". BMC Cancer 18 1 (2018): http://www.scopus.com/inward/record.url?eid=2-s2.0-85058592413&partnerID=MN8TOARS.
  50. Matejcic, M.; Saunders, E.J.; Dadaev, T.; Brook, M.N.; Wang, K.; Sheng, X.; Olama, A.A.A.; et al. "Germline variation at 8q24 and prostate cancer risk in men of European ancestry". Nature Communications 9 1 (2018): http://www.scopus.com/inward/record.url?eid=2-s2.0-85056250910&partnerID=MN8TOARS.
  51. Lu, Y.; Beeghly-Fadiel, A.; Wu, L.; Guo, X.; Li, B.; Schildkraut, J.M.; Im, H.K.; et al. "A transcriptome-wide association study among 97,898 women to identify candidate susceptibility genes for epithelial ovarian cancer risk". Cancer Research 78 18 (2018): 5419-5430. http://www.scopus.com/inward/record.url?eid=2-s2.0-85053297183&partnerID=MN8TOARS.
  52. Felicio, P.S.; Alemar, B.; Coelho, A.S.; Berardinelli, G.N.; Melendez, M.E.; Lengert, A.V.H.; Miche lli, R.D.; et al. "Screening and characterization of BRCA2 c.156_157insAlu in Brazil: Results from 1380 individuals from the South and Southeast". Cancer Genetics 228-229 (2018): 93-97. http://www.scopus.com/inward/record.url?eid=2-s2.0-85056169948&partnerID=MN8TOARS.
  53. Mancuso, N.; Gayther, S.; Gusev, A.; Zheng, W.; Penney, K.L.; Kote-Jarai, Z.; Eeles, R.; et al. "Large-scale transcriptome-wide association study identifies new prostate cancer risk regions". Nature Communications 9 1 (2018): http://www.scopus.com/inward/record.url?eid=2-s2.0-85054455296&partnerID=MN8TOARS.
  54. Nielsen, S.M.; Eccles, D.M.; Romero, I.L.; Al-Mulla, F.; Balmaña, J.; Biancolella, M.; Blok, R.; et al. "Genetic testing and clinical management practices for variants in non-BRCA1/2 breast (and breast/ovarian) cancer susceptibility genes: An international survey by the Evidence-based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) clinical working group". JCO Precision Oncology 2 (2018): http://www.scopus.com/inward/record.url?eid=2-s2.0-85073273493&partnerID=MN8TOARS.
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  241. Cerveira, N.; Correia, C.; Bizarro, S.; Pinto, C.; Lisboa, S.; Mariz, J.M.; Marques, M.; Teixeira, M.R.. "SEPT2 is a new fusion partner of MLL in acute myeloid leukemia with t(2;11)(q37;q23)". Oncogene 25 45 (2006): 6147-6152. http://www.scopus.com/inward/record.url?eid=2-s2.0-33749836689&partnerID=MN8TOARS.
  242. Ribeiro, F.R.; Diep, C.B.; Jerónimo, C.; Henrique, R.; Lopes, C.; Eknæs, M.; Lingjærde, O.C.; Lothe, R.A.; Teixeira, M.R.. "Statistical dissection of genetic pathways involved in prostate carcinogenesis". Genes Chromosomes and Cancer 45 2 (2006): 154-163. http://www.scopus.com/inward/record.url?eid=2-s2.0-31944449020&partnerID=MN8TOARS.
  243. Diep, C.B.; Kleivi, K.; Ribeiro, F.R.; Teixeira, M.R.; Lindgjærde, O.C.; Lothe, R.A.. "The order of genetic events associated with colorectal cancer progression inferred from meta-analysis of copy number changes". Genes Chromosomes and Cancer 45 1 (2006): 31-41. http://www.scopus.com/inward/record.url?eid=2-s2.0-33644885017&partnerID=MN8TOARS.
  244. Cerveira, N.; Ribeiro, F.R.; Peixoto, A.; Costa, V.; Henrique, R.; Jerónimo, C.; Teixeira, M.R.. "TMPRSS2-ERG gene fusion causing ERG overexpression precedes chromosome copy number changes in prostate carcinomas and paired HGPIN lesions". Neoplasia 8 10 (2006): 826-832. http://www.scopus.com/inward/record.url?eid=2-s2.0-33749870551&partnerID=MN8TOARS.
  245. Henrique, R.; Jerónimo, C.; Hoque, M.O.; Carvalho, A.L.; Oliveira, J.; Teixeira, M.R.; Lopes, C.; Sidransky, D.. "Frequent 14-3-3s promoter methylation in benign and malignant prostate lesions". DNA and Cell Biology 24 4 (2005): 264-269. http://www.scopus.com/inward/record.url?eid=2-s2.0-16844374138&partnerID=MN8TOARS.
  246. Henrique, R.; Jerónimo, C.; Hoque, M.O.; Nomoto, S.; Carvalho, A.L.; Costa, V.L.; Oliveira, J.; et al. "MT1G hypermethylation is associated with higher tumor stage in prostate cancer". Cancer Epidemiology Biomarkers and Prevention 14 5 (2005): 1274-1278. http://www.scopus.com/inward/record.url?eid=2-s2.0-20844459807&partnerID=MN8TOARS.
  247. 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.
  248. 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.
  249. 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.
  250. Modena, P.; Lualdi, E.; Facchinetti, F.; Galli, L.; Teixeira, M.R.; Pilotti, S.; Sozzi, G.. "SMARCB1/INI1 tumor suppressor gene is frequently inactivated in epithelioid sarcomas". Cancer Research 65 10 (2005): 4012-4019. http://www.scopus.com/inward/record.url?eid=2-s2.0-20144386270&partnerID=MN8TOARS.
  251. 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.
  252. Kleivi, K.; Diep, C.B.; Pandis, N.; Heim, S.; Teixeira, M.R.; Lothe, R.A.. "TP53 mutations are associated with a particular pattern of genomic imbalances in breast carcinomas". Journal of Pathology 207 1 (2005): 14-19. http://www.scopus.com/inward/record.url?eid=2-s2.0-23944504305&partnerID=MN8TOARS.
  253. 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.
  254. Jerónimo, C.; Henrique, R.; Hoque, M.O.; Mambo, E.; Ribeiro, F.R.; Varzim, G.; Oliveira, J.; et al. "A quantitative promoter methylation profile of prostate cancer". Clinical Cancer Research 10 24 (2004): 8472-8478. http://www.scopus.com/inward/record.url?eid=2-s2.0-19944429845&partnerID=MN8TOARS.
  255. Jerónimo, C.; Henrique, R.; Oliveira, J.; Lobo, F.; Pais, I.; Teixeira, M.R.; Lopes, C.. "Aberrant cellular retinol binding protein 1 (CRBP1) gene expression and promoter methylation in prostate cancer". Journal of Clinical Pathology 57 8 (2004): 872-876. http://www.scopus.com/inward/record.url?eid=2-s2.0-4043078431&partnerID=MN8TOARS.
  256. Teixeira, M.R.; Ribeiro, F.R.; Torres, L.; Pandis, N.; Andersen, J.A.; Lothe, R.A.; Heim, S.. "Assessment of clonal relationships in ipsilateral and bilateral multiple breast carcinomas by comparative genomic hybridisation and hierarchical clustering analysis". British Journal of Cancer 91 4 (2004): 775-782. http://www.scopus.com/inward/record.url?eid=2-s2.0-4344713690&partnerID=MN8TOARS.
  257. Monteiro, E.; Varzim, G.; Pires, A.M.; Teixeira, M.; Lopes, C.. "Cyclin D1 A870G polymorphism and amplification in laryngeal squamous cell carcinoma: Implications of tumor localization and tobacco exposure". Cancer Detection and Prevention 28 4 (2004): 237-243. http://www.scopus.com/inward/record.url?eid=2-s2.0-12344308940&partnerID=MN8TOARS.
  258. Oliveira, C.; Westra, J.L.; Arango, D.; Ollikainen, M.; Domingo, E.; Ferreira, A.; Velho, S.; et al. "Distinct patterns of KRAS mutations in colorectal carcinomas according to germline mismatch repair defects and hMLH1 methylation status". Human Molecular Genetics 13 19 (2004): 2303-2311. http://www.scopus.com/inward/record.url?eid=2-s2.0-5444224121&partnerID=MN8TOARS.
  259. Diep, C.B.; Teixeira, M.R.; Thorstensen, L.; Wiig, J.N.; Eknæs, M.; Nesland, J.M.; Giercksky, K.-E.; Johansson, B.; Lothe, R.A.. "Genome characteristics of primary carcinomas, local recurrences, carcinomatoses, and liver metastases from colorectal cancer patients". Molecular Cancer 3 (2004): http://www.scopus.com/inward/record.url?eid=2-s2.0-2942616982&partnerID=MN8TOARS.
  260. Kleivi, K.; Teixeira, M.R.; Eknæs, M.; Diep, C.B.; Jakobsen, K.S.; Hamelin, R.; Lothe, R.A.. "Genome signatures of colon carcinoma cell lines". Cancer Genetics and Cytogenetics 155 2 (2004): 119-131. http://www.scopus.com/inward/record.url?eid=2-s2.0-9644295665&partnerID=MN8TOARS.
  261. Micci, F.; Teixeira, M.R.; Haugom, L.; Kristensen, G.; Abeler, V.H.; Heim, S.. "Genomic aberrations in carcinomas of the uterine corpus". Genes Chromosomes and Cancer 40 3 (2004): 229-246. http://www.scopus.com/inward/record.url?eid=2-s2.0-2542619821&partnerID=MN8TOARS.
  262. Teixeira, M.R.; Ribeiro, F.R.; Eknæs, M.; Wæhre, H.; Stenwig, A.E.; Giercksky, K.E.; Heim, S.; Lothe, R.A.. "Genomic analysis of prostate carcinoma specimens obtained via ultrasound-guided needle biopsy may be of use in preoperative decision-making". Cancer 101 8 (2004): 1786-1793. http://www.scopus.com/inward/record.url?eid=2-s2.0-4744361816&partnerID=MN8TOARS.
  263. Cerveira, N.; Torres, L.; Rocha, P.; Bizarro, S.; Pereira, D.; Abreu, J.; Henrique, R.; Teixeira, M.R.; Castedo, S.. "Highly sensitive detection of the MGB1 transcript (mammaglobin) in the peripheral blood of breast cancer patients". International Journal of Cancer 108 4 (2004): 592-595. http://www.scopus.com/inward/record.url?eid=2-s2.0-0348048477&partnerID=MN8TOARS.
  264. Lualdi, E.; Modena, P.; Debiec-Rychter, M.; Pedeutour, F.; Teixeira, M.R.; Facchinetti, F.; Dagrada, G.P.; Pilotti, S.; Sozzi, G.. "Molecular cytogenetic characterization of proximal-type epithelioid sarcoma". Genes Chromosomes and Cancer 41 3 (2004): 283-290. http://www.scopus.com/inward/record.url?eid=2-s2.0-4644309912&partnerID=MN8TOARS.
  265. Salgueiro, N.; Veiga, I.; Fragoso, M.; Sousa, O.; Costa, N.; Pellon, M.L.; Sanches, E.; et al. "Mutations in exon 14 of dihydropyrimidine dehydrogenase and S-Fluorouracil toxicity in Portuguese collorectal cancer patients". Genetics in Medicine 6 2 (2004): 102-107. http://www.scopus.com/inward/record.url?eid=2-s2.0-11144355814&partnerID=MN8TOARS.
  266. Jerónimo, C.; Henrique, R.; Hoque, M.O.; Ribeiro, F.R.; Oliveira, J.; Fonseca, D.; Teixeira, M.R.; Lopes, C.; Sidransky, D.. "Quantitative RARbeta2 hypermethylation: a promising prostate cancer marker.". Clinical cancer research : an official journal of the American Association for Cancer Research 10 12 Pt 1 (2004): 4010-4014. http://www.scopus.com/inward/record.url?eid=2-s2.0-16544372387&partnerID=MN8TOARS.
  267. Papadopoulou, A.; Trangas, T.; Teixeira, M.R.; Heim, S.; Dimitriadis, E.; Tsarouha, H.; Andersen, J.A.; et al. "Telomerase activity and genetic alterations in primary breast carcinomas". Neoplasia 5 2 (2003): 170-178. http://www.scopus.com/inward/record.url?eid=2-s2.0-0037352353&partnerID=MN8TOARS.
  268. Ioannidis, P.; Mahaira, L.; Papadopoulou, A.; Teixeira, M.R.; Heim, S.; Andersen, J.A.; Evangelou, E.; et al. "8q24 copy number gains and expression of the c-myc mRNA stabilizing protein CRD-BP in primary breast carcinomas". International Journal of Cancer 104 1 (2003): 54-59. http://www.scopus.com/inward/record.url?eid=2-s2.0-0037430255&partnerID=MN8TOARS.
  269. Ioannidis, P.; Mahaira, L.; Papadopoulou, A.; Teixeira, M.R.; Heim, S.; Andersen, J.A.; Evangelou, E.; et al. "CRD-BP: A c-myc mRNA stabilizing protein with an oncofetal pattern of expression". Anticancer Research 23 3 A (2003): 2179-2183. http://www.scopus.com/inward/record.url?eid=2-s2.0-0042807286&partnerID=MN8TOARS.
  270. Micci, F.; Walter, C.U.; Teixeira, M.R.; Panagopoulos, I.; Bjerkehagen, B.; Sæter, G.; Heim, S.. "Cytogenetic and molecular genetic analyses of endometrial stromal sarcoma: Nonrandom involvement of chromosome arms 6p and 7p and confirmation of JAZF1/JJAZ1 gene fusion in t(7;17)". Cancer Genetics and Cytogenetics 144 2 (2003): 119-124. http://www.scopus.com/inward/record.url?eid=2-s2.0-0038016605&partnerID=MN8TOARS.
  271. Micci, F.; Teixeira, M.R.; Scheistrøen, M.; Abeler, V.M.; Heim, S.. "Cytogenetic characterization of tumors of the vulva and vagina". Genes Chromosomes and Cancer 38 2 (2003): 137-148. http://www.scopus.com/inward/record.url?eid=2-s2.0-0041332883&partnerID=MN8TOARS.
  272. Jerónimo, C.; Costa, I.; Conceição Martins, M.; Monteiro, P.; Lisboa, S.; Palmeira, C.; Henrique, R.; Teixeira, M.R.; Lopes, C.. "Detection of gene promoter hypermethylation in fine needle washings from breast lesions". Clinical Cancer Research 9 9 (2003): 3413-3417. http://www.scopus.com/inward/record.url?eid=2-s2.0-0042334827&partnerID=MN8TOARS.
  273. Cerveira, N.; Correia, C.; Dória, S.; Bizarro, S.; Rocha, P.; Gomes, P.; Torres, L.; et al. "Frequency of NUP98-NSD1 fusion transcript in childhood acute myeloid leukaemia [7]". Leukemia 17 11 (2003): 2244-2247. http://www.scopus.com/inward/record.url?eid=2-s2.0-10744231835&partnerID=MN8TOARS.
  274. Diep, C.B.; Parada, L.A.; Teixeira, M.R.; Eknæs, M.; Nesland, J.M.; Johansson, B.; Lothe, R.A.. "Genetic profiling of colorectal cancer liver metastases by combined comparative genomic hybridization and G-banding analysis". Genes Chromosomes and Cancer 36 2 (2003): 189-197. http://www.scopus.com/inward/record.url?eid=2-s2.0-0037299471&partnerID=MN8TOARS.
  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.
  276. Teixeira, M.R.; Pandis, N.; Heim, S.; Middleton, L.P.; Eva Singletary, S.; Sahin, A.A.. "Multicentric mammary carcinoma: Evidence of monoclonal proliferation [2] (multiple letters)". Cancer 97 3 (2003): 715-717. http://www.scopus.com/inward/record.url?eid=2-s2.0-0037303495&partnerID=MN8TOARS.
  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.
  278. 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.
  279. 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.
  280. 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.
  281. 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.
  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.
  283. 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.
  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.
  285. 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.
  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.
  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.
  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.
  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.
  291. 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.
  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.
  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.
  294. 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.
  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.
  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.
  297. 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.
  298. 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.
  299. 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.
  300. 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.
  301. 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.
  302. 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.
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Association member

Society Organization name Role
2017 - Current Correspondent member of the National Medical Academy of Portugal
2013 - Current European Association for Cancer Research
2011 - 2013 Direction of Portuguese Society of Human Genetics (SPGH) - President 2012; Elected 2011; Outgoing 2013

Committee member

Activity description
Institution / Organization
2013 - 2017 Coordinator of the Scientific Committee of the Portuguese Society of Human Genetics (SPGH)


Activity description Institution / Organization
2008 - 2017 Visiting Professor, Center for Cancer Biomedicine, University of Oslo, Norway

Evaluation committee

Activity description
Institution / Organization Funding entity
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


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