Silhueta de pessoa indiferenciada
Professor auxiliar
Faculdade de Medicina e Ciências Biomédicas
Subsistema
Docentes Universitário
Regime
Exclusividade
Vínculo
CT em Funções Públicas por tempo indeterminado
I completed my PhD in 2003 at The Institute of Cancer Research of the University of London and recently graduated with an Executive MBA from Quantic School of Business and Technology. Previously, I graduated with an MSc in Human Molecular Genetics in 1999 from Imperial College Faculty of Medicine and a 5-year BSc in Applied Chemistry - Biotechnology in 1997 from Universidade Nova de Lisboa Faculdade de Ciências e Tecnologia. I hold an Assistant Professor with Tenure position at the Universidade do Algarve (UAlg) and am a Principal Investigator and the Coordinator of the UAlg's node of the research unit CINTESIS and Laboratório Associado RISE - Rede de Investigação em Saúde: do Laboratório à Saúde Comunitária. I am also an Invited Principal Investigator in Centro de Ciências do Mar since 2023. In 2022, I co-founded expressTEC, a spin-off of UAlg dedicated to developing innovative diagnostic solutions for cancer care. I am interested in studying allelic imbalance in gene expression, a common feature of our genome. Due to regulatory polymorphisms, which can occur both in cis- and trans-, many of our genes are preferentially expressed from one allele. This unequal expression can contribute to susceptibility to common diseases. My main aim is to use this concept to develop a new method to study predisposition to breast cancer. My goal is to identify new breast cancer predisposition loci and understand the mechanisms by which they increase the risk of disease. I hypothesize that the most efficient search for further breast cancer risk loci is to focus susceptibility studies on variants that show regulatory potential. I propose a change in the current approach to identifying genetic cancer risk by introducing the use of a quantifiable read-out of the effect of cis-regulatory variants in case-control studies. Additionally, I am investigating this imbalance's role in tumour biology, namely in the effect of mutations and treatment response.

Atividades

Atividades
2024 - Presente. Orientação. Unveilling the Clinical Significance of Allelic Expression Imbalance of PIK3CA mutations in Treatment Response in Colorectal Cancer.Ciências Biomédicas (Doutoramento). Orientador.
2022 - Presente. Orientação. Analysis of mutational allelic imbalances’ influence on drug treatment response .MSc in Oncobiology (Mestrado). Orientador.
2022/11 - 2023/02. Participação em evento. Participation in Born from Knowledge (Bfk)-RISE (Science and Technology Acceleration Program to enhance the results of Research & Development (R&D) and existing technologies in the National Scientific and Technological System with commercialization potential, through monitoring and intensive training of teams). Oficina (workshop). Agência Nacional de Inovação SA; UPTEC Associação de Transferência de Tecnologia da Asprela.
2015/12/21 - 2021/12/09. Orientação. UNVEILING THE ROLE OF CIS-REGULATORY VARIATION IN BREAST CANCER AETIOLOGY.Outras Ciências Médicas (Doutoramento). Orientador.
2019/01/09 - 2021/04/21. Orientação. Alternative splicing-mediated cis-regulation in breast cancer risk.Oncobiologia - Mecanismos Moleculares do Cancro (Mestrado) (Mestrado). Orientador.
2021 - 2021. Orientação. Alternative splicing-mediated cis-regulation in Breast Cancer Risk.Oncobiologia - Mecanismos Moleculares do Cancro (Mestrado). Orientador.
2021 - 2021. Orientação. Molecular switch behind adult stem cell quiescence in mouse stomach epithelium.Oncobiologia - Mecanismos Moleculares do Cancro (Mestrado). Coorientador.
2019 - 2019. Orientação. INFLUENCE OF SOMATIC MUTANT ALLELIC IMBALANCE IN BREAST CANCER CLINICAL CHARACTERISTICS.Oncobiologia - Mecanismos Moleculares do Cancro (Mestrado). Orientador.
2019 - 2019. Orientação. IDENTIFYING NOVEL GENES ASSOCIATED WITH BREAST CANCER SUSCEPTIBILITY USING DIFFERENTIAL ALLELIC EXPRESSION RATIOS.Oncobiologia - Mecanismos Moleculares do Cancro (Mestrado). Coorientador.
2018 - 2018. Orientação. The role of miRNA-mediated cis-regulation in breast cancer susceptibility.Oncobiologia - Mecanismos Moleculares do Cancro (Mestrado). Orientador.
2018 - 2018. Orientação. Study of the impact of IL7R gain-of-function mutation on in vivo leukemogenesis.Oncobiologia - Mecanismos Moleculares do Cancro (Mestrado). Coorientador.
2012/01/12 - 2017/05/19. Orientação. MOLECULAR AND FUNCTIONAL ANALYSIS OF DAND5 IN HUMAN CONGENITAL HEART DISEASE (CHD).Ciências da Saúde (Doutoramento). Coorientador.
2017 - 2017. Orientação. Functional analysis of genetic variants associated with risk for breast cancer: 12q24, a candidate risk locus.Oncobiologia - Mecanismos Moleculares do Cancro (Mestrado). Orientador.
2017 - 2017. Orientação. Discovery of novel mechanisms of centrosome amplification and their therapeutic value in cancer.Oncobiologia - Mecanismos Moleculares do Cancro (Mestrado). Coorientador.
2016 - 2016. Orientação. Epigenetics and alternative splicing.Oncobiologia - Mecanismos Moleculares do Cancro (Mestrado). Coorientador.
2016 - 2016. Orientação. Role of chemerin and its receptors in mouse models of tumorigenesis.Oncobiologia - Mecanismos Moleculares do Cancro (Mestrado). Coorientador.
2015 - 2015. Orientação. Constitutive OGG1 variant together with BRCA mutations display accelerated telomere shortening.Oncobiologia - Mecanismos Moleculares do Cancro (Mestrado). Coorientador.
2015 - 2015. Orientação. Functional characterisation of putative Cis-Regulatory Risk Loci for breast cancer.Qualidade em Análises (Mestrado). Orientador.
2014 - 2014. Orientação. STUDY OF INFLUENCE OF REGULATORY POLYMORPHISMS OF EXPRESSION IN DEVELOPMENT OF BREAST CANCER.Ciências Biomédicas (Mestrado). Orientador.
2014 - 2014. Orientação. Identification of regulatory polymorphisms associated with breast cancer risk.Ciências Biomédicas (Mestrado). Orientador.

Projetos

Projetos
2025/01/01 - 2027/12. expressCDx – Identifying of RNA Biomarkers for the Development of New Personalised Cancer Diagnostic Methodologies., Portugal2030 - IDT. Investigador responsável. expressTEC.
2025/03/01 - 2027/02/28. expressPIK: Pioneiro em Diagnóstico Complementar baseado em RNA para Oncologia de Precisão, FEDER. Investigador responsável. expressTEC.
2024/07/01 - 2025/06/30. expressPIK, Vouchers para startups - novos produtos verdes e digitais. Investigador responsável. expressTEC.
2022/01 - 2024/10. Lobular Breast Cancer: Discovery Science, Translational Goals, Clinical Impact (LOBSTERPOT).
2023/02/20 - 2024/08/19. Exploring the shared regulatory genetic basis in cancer risk. Investigador. Centro de Investigação em Tecnologias e Serviços de Saúde; Universidade do Algarve.
2021/12 - 2023/12. Unraveling the contribution of mitotic failure in rare syndromes with microcephaly susceptibility. Investigador. Universidade do Algarve.
2019/03/28 - 2023/03/27. INnovating breast cancer GWAS through inTEgRation of functional GENomics, Concurso para Financiamento de Projetos de Investigação Científica e Desenvolvimento Tecnológico em Todos os Domínios Científicos - 2017. Investigador. Universidade do Algarve; Universidade de Lisboa Instituto de Medicina Molecular João Lobo Antunes.
2021/02/01 - 2021/10/07. GenomePT - Laboratório Nacional de Sequenciação e análise de genomas, Programa CRESC ALGARVE 2020. Universidade do Algarve.
2018/07/01 - 2021/06/30. DEvoCancer: Decoding breast cancer evolution through mutant allele differential expression signatures, 9471 - RIDTI. Investigador responsável. Universidade do Algarve.
2019/01/01 - 2020/03/31. Centre for Biomedical Research, 6817 - DCRRNI ID. Universidade do Algarve; Universidade do Algarve Centro de Investigação em Biomedicina.
2015/05 - 2017/12. Unveiling the Cis-Regulation at the Centre of Breast Cancer Susceptibility. Investigador responsável. Universidade do Algarve.
2012/06 - 2017/03. Genetic Control of Gene Expression in Cancer Risk, SEVENTH FRAMEWORK PROGRAMME (FP7). Investigador responsável. Universidade do Algarve Centro de Investigação em Biomedicina.
2013/07 - 2015/12. Cis-regulation of somatic mutations in breast and ovarian cancers. Investigador responsável.
2009 - 2010. Differential Allelic Expression Analysis of Susceptibility Loci in Breast Cancer. Bolseiro de Investigação.
1999/10/01 - 2003/09/30. MOLECULAR GENETICS, NATURAL HISTORY AND AETIOLOGY OF CHILDHOOD LEUKAEMIA.
1998/10/01 - 1999/09/30. MESTRADO EM GENÉTICA MOLECULAR HUMANA.
1997/07/01 - 1998/09/30. CONTRIBUIÇÃO PARA O ESTUDO DA REGIÃO Q24-Q26 DO CROMOSSOMA 10 NO HOMEM. Universidade NOVA de Lisboa NOVA Medical School.

Produções

2025. "expressPIK". Pendente.
Duarte, Isabel; Magno, Ramiro; Maia, Ana-Teresa. 2024. Silent but Significant: Uncovering the Passenger Role of Transcriptionally Silenced Mutations in Breast Cancer Drivers. Em 6th ASPIC International Conference.
Xavier, Joana M.; Magno, Ramiro; Russell, Roslin; de Almeida, Bernardo P.; Jacinta-Fernandes, Ana; Besouro-Duarte, André; Dunning, Mark; et al. 2024. "Identification of candidate causal variants and target genes at 41 breast cancer risk loci through differential allelic expression analysis". Scientific Reports, 14 (1). https://doi.org/10.1038/s41598-024-72163-y
Besouro-Duarte, André; Carrasqueiro, Beatriz; Sousa, Sofia; Xavier, Joana M.; Maia, Ana-Teresa. Autor correspondente: Maia, Ana-Teresa. 2024. "Colocalised Genetic Associations Reveal Alternative Splicing Variants as Candidate Causal Links for Breast Cancer Risk in 10 Loci". Cancers, 16 (17). https://doi.org/10.3390/cancers16173020
2024. "expressPIK". Registada.
2023. "Methods of analysis of allelic expression of PIK3CA in cancer and uses thereof". Protegido.
Correia, Lizelle; Magno, Ramiro; Xavier, Joana; Maia, Ana-Teresa. Autor correspondente: Maia, Ana-Teresa. 2022. "Allelic expression imbalance of PIK3CA mutations is frequent in breast cancer and prognostically significant". npj Breast Cancer, 8 (1). https://doi.org/10.1101/2021.03.05.434137
Joana M. Xavier; Magno, Ramiro; Maia, Ana-Teresa. Autor correspondente: Maia, Ana-Teresa. 2022. "Mapping of cis-regulatory variants by differential allelic expression analysis identifies candidate risk variants and target genes of 27 breast cancer risk loci". medRxiv. MEDRXIV/2022/271889
Filipa Esteves; Joana M. Xavier; Anthony M. Ford; Cátia Rocha; Paul D.P. Pharoah; Carlos Caldas; Suet-Feung Chin; Ana-Teresa Maia. 2022. "Germline allelic expression of genes at 17q22 locus associates with risk of breast cancer". European Journal of Cancer. https://doi.org/10.1016/j.ejca.2022.05.034
Apolónio JD; Dias JS; Fernandes MT; Komosa M; Lipman T; Zhang CH; Leão R; et al. 2022. "THOR is a targetable epigenetic biomarker with clinical implications in breast cancer.". Clinical epigenetics. https://doi.org/10.1186/s13148-022-01396-3
Magno, Ramiro; Duarte, Isabel; Maia, Ana-Teresa. 2022. protean: Sequence Profiles of OncoKB Genes. 0.1.2. Pattern Institute. R.
Ghezzo, Marinella N; Magno, Ramiro; Xavier, Joana M; Maia, Ana-Teresa. 2022. Redesigned case-control study using allelic expression as a quantitative phenotype identifies new risk loci for breast cancer. Em 5th ASPIC International Congress.
2021. "Methods of analysis of polymorphisms associated with allelic expression of PIK3CA in cancer and uses thereof". Protegido.
2021. "Methods of Analysis of polymorphisms associated with cancer and uses thereof". Protegido.
Marta Liber; Guilhermina Isabel dos Santos Duarte; Maia, Ana-Teresa; Hugo Rafael Cardoso Oliveira. 2021. "The history of lentil (Lens culinaris subsp. culinaris) domestication and spread as revealed by Genotyping-by-Sequencing of wild and landrace accessions". Frontiers in Plant Science, 12. https://doi.org/10.3389/fpls.2021.628439
Filipa Esteves; Joana M. Xavier; Ana-Teresa Maia. Autor correspondente: Ana-Teresa Maia. 2021. "Germline Allelic Expression of Genes at 17q22 Locus Associates with Risk of Breast Cancer". deposited at MEDRXIV/2021/267625, Minor Revisions at European Journal of Cancer. https://doi.org/10.1101/2021.12.10.21267625
Xavier, Joana M; Magno, Ramiro; Russel, R; de Almeida, BP; Jacinta-Fernandes, Ana; Duarte, ARB; BARBOSA-MORAIS, NUNO; Maia, Ana-Teresa. 2021. "Mapping of cis-regulatory variants by differential allelic expression analysis identifies regulatory variants and target genes of 31 breast cancer risk loci". Trabalho apresentado em Bioinformatics in Cancer - Virtual Event: 18 - 19 May 2021.
Duarte, Isabel; Magno, Ramiro; Maia, Ana-Teresa. 2021. Monoallelic Expression of Breast Cancer Mutations Reveals Functionally Relevant Cis-Regulation. Em EACR Bioinformatics in Cancer.
Duarte, Isabel; Magno, Ramiro; Maia, Ana-Teresa. 2021. Transcriptionally Silenced Mutations in Breast Cancer Driver Genes act as Functional Passengers. Em EMBL Cancer Genomics.
Duarte, Isabel; Magno, Ramiro; Maia, Ana-Teresa. 2021. Monoallelic Expression of Breast Cancer Driver Genes Reveals Functional Passenger Mutations. Em 25th Annual Meeting SPGH.
Duarte, André; Magno, Ramiro; Paulo José Martel (AD16-8C2A-26CE); Maia, Ana-Teresa. Autor correspondente: Maia, Ana-Teresa. 2020. Alternative splicing in breast cancer risk. https://doi.org/10.5281/ZENODO.3776118
Duarte, ARB; Magno, Ramiro; Martel, Paulo; Ghezzo, Marinella; Xavier, Joana M; Maia, Ana-Teresa. 2020. Exploring the role of alternative splicing in breast cancer risk. Em CANCER BIOLOGY: FROM BASIC TO TRANSLATIONAL RESEARCH.
Juliana Machado; Ramiro Magno; Joana M Xavier; Ana-Teresa Maia. 2019. Alternative splicing regulation by GWAS risk loci for breast cancer. https://doi.org/10.1101/766394
Magno, Ramiro; Maia, Ana-Teresa. 2019. "gwasrapidd: an R package to query, download and wrangle GWAS catalog data". Bioinformatics. https://doi.org/10.1093/bioinformatics/btz605
Esteves, Filipa; Xavier, Joana M; Maia, Ana-Teresa. 2019. DAE identifies COX11 and TOM1L1 as target genes in breast cancer risk locus 17q22. Em EMBL Conference: Cancer Genomics.
Magno, Ramiro; Duarte, Isabel; Maia, Ana-Teresa. 2019. ensemblr: R Client for the Ensembl REST API. 0.1.0. Pattern Institute. R.
Xavier, Joana M; Magno, Ramiro; Rocha, Cátia L; Dunning, M; Russell, Roslin; Maia, Ana-Teresa. 2019. Mapping cis-regulatory variants pinpoints target genes of breast cancer risk loci. Em EMBO | EMBL Symposium: Systems Genetics: From Genomes to Complex Traits..
Matias, A.T.; Jacinta-Fernandes, A.; Magno, R.; Xavier, J.; Cabral, M.G.; Jacinto, A.; Maia, A.T.; Braga, S.. 2018. "Differential molecular signature in patients from African origin with triple-negative breast cancer". Annals of Oncology, 29. https://doi.org/10.1093/annonc/mdy272.290
Xavier, Joana M; Magno, Ramiro; Almeida, Bernardo P.; Maia, Ana-Teresa. 2018. Integrative genomic approach elucidates the risk mechanism for breast cancer associated 5q14.1 locus. Em 3rd ASPIC International Congress.
Martins, Catarina; Xavier, Joana; Magno, Ramiro; Maia, Ana-Teresa. 2018. Identifying novel genes associated with Breast Cancer susceptibility using Allelic Expression Ratios. Em 3rd ASPIC International Congress.
Esteves, Filipa; Magno, Ramiro; Xavier, Joana M; Maia, Ana-Teresa. 2018. A comprehensive analysis of RNA-Seq data to identify risk variants for breast cancer using allelic expression. Em EMBL Conference: From Functional Genomics to Systems Biology.
Esteves, Filipa; Magno, Ramiro; Xavier, Joana M; Maia, Ana-Teresa. 2018. Identification of risk variants for breast cancer: a comprehensive analysis of RNA-Seq data. Em 3rd ASPIC International Congress.
Jacinta-Fernandes, A; Xavier, Joana M; Magno, Ramiro; Jerónimo, Carmen; Maia, Ana-Teresa. 2018. Revealing the role of allele- specific miRNA regulation in prostate cancer susceptibility. Em 3rd ASPIC International Congress..
Maia, A.-T.; Sammut, S.-J.; Jacinta-Fernandes, A.; Chin, S.-F.. 2017. "Big data in cancer genomics". Current Opinion in Systems Biology, 4: 78-84. https://doi.org/10.1016/j.coisb.2017.07.007
Faleiro, I.; Leão, R.; Binnie, A.; de Mello, R.A.; Maia, A.-T.; Castelo-Branco, P.. 2017. "Epigenetic therapy in urologic cancers: An update on clinical trials". Oncotarget, 8 (7): 12484-12500. https://doi.org/10.18632/oncotarget.14226
Xavier, Joana; Russell, Roslin; Almeida, Bernardo P.; Rosli, Nordiana; Rocha, Catia; Samarajiwa, Shamith; Chin, Suet-Feung; et al. 2016. "Abstract A31: Integrative differential allelic expression analysis efficiently reveals the biology underlying risk to breast cancer". Molecular Cancer Research, 14 (2 Suppleme): A31-A31. https://doi.org/10.1158/1557-3125.advbc15-a31
Xavier, J.; Almeida, B.; Sun, C.; Silva, J.; Marreiros, A.; Eldridge, M.; Bernards, R.; et al. 2016. "PIK3CA mutant allele differential expression (MADE) associates with breast cancer clinical features". European Journal of Cancer, 61. https://doi.org/10.1016/s0959-8049(16)61723-9
Peterlongo, P.; Chang-Claude, J.; Moysich, K.B.; Rudolph, A.; Schmutzler, R.K.; Simard, J.; Soucy, P.; et al. 2015. "Candidate genetic modifiers for breast and ovarian cancer risk inBRCA1andBRCA2 mutation carriers". Cancer Epidemiology Biomarkers and Prevention, 24 (1): 308-316. https://doi.org/10.1158/1055-9965.EPI-14-0532
Vollan, H.K.M.; Rueda, O.M.; Chin, S.-F.; Curtis, C.; Turashvili, G.; Shah, S.; Lingjærde, O.C.; et al. 2015. "A tumor DNA complex aberration index is an independent predictor of survival in breast and ovarian cancer". Molecular Oncology, 9 (1): 115-127. https://doi.org/10.1016/j.molonc.2014.07.019
Jones, J.O.; Chin, S.-F.; Wong-Taylor, L.-A.; Leaford, D.; Ponder, B.A.J.; Caldas, C.; Maia, A.-T.. 2013. "TOX3 Mutations in Breast Cancer". PLoS ONE, 8 (9). https://doi.org/10.1371/journal.pone.0074102
French, J.D.; Ghoussaini, M.; Edwards, S.L.; Meyer, K.B.; Michailidou, K.; Ahmed, S.; Khan, S.; et al. 2013. "Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers". American Journal of Human Genetics, 92 (4): 489-503. https://doi.org/10.1016/j.ajhg.2013.01.002
Curtis, C.; Shah, S.P.; Chin, S.-F.; Turashvili, G.; Rueda, O.M.; Dunning, M.J.; Speed, D.; et al. 2012. "The genomic and transcriptomic architecture of 2,000 breast tumours reveals novel subgroups". Nature, 486 (7403): 346-352. https://doi.org/10.1038/nature10983
Maia, A.-T.; Antoniou, A.C.; O'Reilly, M.; Samarajiwa, S.; Dunning, M.; Kartsonaki, C.; Chin, S.-F.; et al. 2012. "Effects of BRCA2 cis-regulation in normal breast and cancer risk amongst BRCA2 mutation carriers". Breast Cancer Research, 14 (2). https://doi.org/10.1186/bcr3169
Liu, R.; Maia, A.; Russell, R.; Caldas, C.; Ponder, B.A.; Ritchie, M.E.. 2012. "Allele-specific expression analysis methods for high-density SNP microarray data". Bioinformatics, 28 (8): 1102-1108. https://doi.org/10.1093/bioinformatics/bts089
Meyer, K.B.; Maia, A.-T.; O'Reilly, M.; Ghoussaini, M.; Prathalingam, R.; Porter-Gill, P.; Ambs, S.; et al. 2011. "A functional variant at a prostate cancer predisposition locus at 8q24 is associated with PVT1 expression". PLoS Genetics, 7 (7). https://doi.org/10.1371/journal.pgen.1002165
Udler, M.S.; Ahmed, S.; Healey, C.S.; Meyer, K.; Struewing, J.; Maranian, M.; Kwon, E.M.; et al. 2010. "Fine scale mapping of the breast cancer 16q12 locus". Human Molecular Genetics, 19 (12): 2507-2515. https://doi.org/10.1093/hmg/ddq122
Azzato, E.M.; Lee, A.J.X.; Teschendorff, A.; Ponder, B.A.J.; Pharoah, P.; Caldas, C.; Maia, A.T.. 2010. "Common germ-line polymorphism of C1QA and breast cancer survival". British Journal of Cancer, 102 (8): 1294-1299. https://doi.org/10.1038/sj.bjc.6605625
Alves, M.; Carreira, I.; Liberato, P.; Ramos, S.; Mafra, M.; Inverno, A.S.; Maia, A.T.; et al. 2010. "Identification of a 0.4 Kb deletion region in 10q26 associated with endometrial carcinoma". Oncology Reports, 23 (2): 519-522. https://doi.org/10.3892/or-00000664
Maia, A.; Spiteri, I.; Lee, A.J.X.; O'Reilly, M.; Jones, L.; Caldas, C.; Ponder, B.A.J.. 2009. "Extent of differential allelic expression of candidate breast cancer genes is similar in blood and breast". Breast Cancer Research, 11 (6). https://doi.org/10.1186/bcr2458
Dunning, A.M.; Healey, C.S.; Baynes, C.; Maia, A.-T.; Scollen, S.; Vega, A.; Rodríguez, R.; et al. 2009. "Association of ESR1 gene tagging SNPs with breast cancer risk". Human Molecular Genetics, 18 (6): 1131-1139. https://doi.org/10.1093/hmg/ddn429
Barber, M.; Murrell, A.; Ito, Y.; Maia, A.-T.; Hyland, S.; Oliveira, C.; Save, V.; et al. 2008. "Mechanisms and sequelae of E-cadherin silencing in hereditary diffuse gastric cancer". Journal of Pathology, 216 (3): 295-306. https://doi.org/10.1002/path.2426
Ito, Y.; Koessler, T.; Ibrahim, A.E.K.; Rai, S.; Vowler, S.L.; Abu-amero, S.; Silva, A.-L.; et al. 2008. "Somatically acquired hypomethylation of IGF2 in breast and colorectal cancer". Human Molecular Genetics, 17 (17): 2633-2643. https://doi.org/10.1093/hmg/ddn163
Meyer, K.B.; Maia, A.-T.; O'Reilly, M.; Teschendorff, A.E.; Chin, S.-F.; Caldas, C.; Ponder, B.A.J.. 2008. "Allele-specific up-regulation of FGFR2 increases susceptibility to breast cancer". PLoS Biology, 6 (5): 1098-1103. https://doi.org/10.1371/journal.pbio.0060108
Udler, M.; Maia, A.-T.; Cebrian, A.; Brown, C.; Greenberg, D.; Shah, M.; Caldas, C.; et al. 2007. "Common germline genetic variation in antioxidant defense genes and survival after diagnosis of breast cancer". Journal of Clinical Oncology, 25 (21): 3015-3023. https://doi.org/10.1200/JCO.2006.10.0099
Bundy, J.G.; Iyer, N.G.; Gentile, M.S.; Hu, D.-E.; Kettunen, M.; Maia, A.-T.; Thorne, N.P.; et al. 2006. "Metabolic consequences of p300 gene deletion in human colon cancer cells". Cancer Research, 66 (15): 7606-7614. https://doi.org/10.1158/0008-5472.CAN-05-2999
Maia, A.T.; Tussiwand, R.; Cazzaniga, G.; Rebulla, P.; Colman, S.; Biondi, A.; Greaves, M.. 2004. "Identification of Preleukemic Precursors of Hyperdiploid Acute Lymphoblastic Leukemia in Cord Blood". Genes Chromosomes and Cancer, 40 (1): 38-43. https://doi.org/10.1002/gcc.20010
Maia, A.T.; Koechling, J.; Corbett, R.; Metzler, M.; Wiemels, J.L.; Greaves, M.. 2004. "Protracted Postnatal Natural Histories in Childhood Leukemia". Genes Chromosomes and Cancer, 39 (4): 335-340. https://doi.org/10.1002/gcc.20003
Zuna, J.; Muzikova, K.; Ford, A.M.; Maia, A.T.; Krejci, O.; Tousovska, K.; Oravkinova, I.; Greaves, M.; Trka, J.. 2003. "Pre-natal, clonal origin of acute lymphoblastic leukaemia in triplets". Leukemia and Lymphoma, 44 (12): 2099-2102. https://doi.org/10.1080/1042819031000123393
Maia, A.T.; van der Velden, V.H.J.; Harrison, C.J.; Szczepanski, T.; Williams, M.D.; Griffiths, M.J.; van Dongen, J.J.M.; Greaves, M.F.. 2003. "Prenatal origin of hyperdiploid acute lymphoblastic leukemia in identical twins". Leukemia, 17 (11): 2202-2206. https://doi.org/10.1038/sj.leu.2403101
Greaves, M.F.; Maia, A.T.; Wiemels, J.L.; Ford, A.M.. 2003. "Leukemia in twins: Lessons in natural history". Blood, 102 (7): 2321-2333. https://doi.org/10.1182/blood-2002-12-3817
Maia, Ana-Teresa. 2003. "Molecular genetics and natural history of childhood leukaemia". Doutoramento.
Wiemels, J.L.; Xiao, Z.; Buffler, P.A.; Maia, A.T.; Ma, X.; Dicks, B.M.; Smith, M.T.; et al. 2002. "In utero origin of t(8;21) AML1-ETO translocations in childhood acute myeloid leukemia". Blood, 99 (10): 3801-3805. https://doi.org/10.1182/blood.V99.10.3801
Maia, A.T.; Ford, A.M.; Reza Jalali, G.; Harrison, C.J.; Malcolm Taylor, G.; Eden, O.B.; Greaves, M.F.. 2001. "Molecular tracking of leukemogenesis in a triplet pregnancy". Blood, 98 (2): 478-482. https://doi.org/10.1182/blood.V98.2.478
 

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