Manuel R Teixeira


Ontology type: schema:Person     


Person Info

NAME

Manuel R

SURNAME

Teixeira

Publications in SciGraph latest 50 shown

  • 2019-12 Shared heritability and functional enrichment across six solid cancers in NATURE COMMUNICATIONS
  • 2019-02 Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci in NATURE GENETICS
  • 2018-12 Ponatinib induces a sustained deep molecular response in a chronic myeloid leukaemia patient with an early relapse with a T315I mutation following allogeneic hematopoietic stem cell transplantation: a case report in BMC CANCER
  • 2018-12 Discontinuation of tyrosine kinase inhibitors in CML patients in real-world clinical practice at a single institution in BMC CANCER
  • 2018-07 Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci in NATURE GENETICS
  • 2018-01 Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition in BRITISH JOURNAL OF CANCER
  • 2017-12 Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer in NATURE GENETICS
  • 2017-08-22 Height, selected genetic markers and prostate cancer risk: results from the PRACTICAL consortium in BRITISH JOURNAL OF CANCER
  • 2017-05 Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer in NATURE GENETICS
  • 2017-03 Ovarian metastasis from uveal melanoma with MLH1/PMS2 protein loss in a patient with germline MLH1 mutated Lynch syndrome: consequence or coincidence? in VIRCHOWS ARCHIV
  • 2017-01 Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3 in BREAST CANCER RESEARCH AND TREATMENT
  • 2017-01 Performance of Lynch syndrome predictive models in quantifying the likelihood of germline mutations in patients with abnormal MLH1 immunoexpression in FAMILIAL CANCER
  • 2016-12 Lapatinib-capecitabine versus capecitabine alone as radiosensitizers in RAS wild-type resectable rectal cancer, an adaptive randomized phase II trial (LaRRC trial): study protocol for a randomized controlled trial in TRIALS
  • 2016-12 Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women in BREAST CANCER RESEARCH
  • 2016-12 Pubertal development and prostate cancer risk: Mendelian randomization study in a population-based cohort in BMC MEDICINE
  • 2016-12 Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2 in BREAST CANCER RESEARCH
  • 2016-12 Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus in BREAST CANCER RESEARCH
  • 2016-09-07 Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast–ovarian cancer susceptibility locus in NATURE COMMUNICATIONS
  • 2016-09 Implementation of next-generation sequencing for molecular diagnosis of hereditary breast and ovarian cancer highlights its genetic heterogeneity in BREAST CANCER RESEARCH AND TREATMENT
  • 2016-08 Polyunsaturated fatty acids and prostate cancer risk: a Mendelian randomisation analysis from the PRACTICAL consortium in BRITISH JOURNAL OF CANCER
  • 2016-04-27 Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer in NATURE COMMUNICATIONS
  • 2016-04-07 Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation in NATURE COMMUNICATIONS
  • 2016-04 Gene and pathway level analyses of germline DNA-repair gene variants and prostate cancer susceptibility using the iCOGS-genotyping array in BRITISH JOURNAL OF CANCER
  • 2016-04 Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170 in NATURE GENETICS
  • 2016-03-10 Correspondence: SEMA4A variation and risk of colorectal cancer in NATURE COMMUNICATIONS
  • 2016-02 Co-occurrence of nonsense mutations in MSH6 and MSH2 in Lynch syndrome families evidencing that not all truncating mutations are equal in JOURNAL OF HUMAN GENETICS
  • 2016-01 The role of germline mutations in the BRCA1/2 and mismatch repair genes in men ascertained for early-onset and/or familial prostate cancer in FAMILIAL CANCER
  • 2015-12 Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1 in SCIENTIFIC REPORTS
  • 2015-12 An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers in BREAST CANCER RESEARCH
  • 2015-12 Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer in SCIENTIFIC REPORTS
  • 2015-12 Frequent alterations in cytoskeleton remodelling genes in primary and metastatic lung adenocarcinomas in NATURE COMMUNICATIONS
  • 2015-11 The effects of height and BMI on prostate cancer incidence and mortality: a Mendelian randomization study in 20,848 cases and 20,214 controls from the PRACTICAL consortium in CANCER CAUSES & CONTROL
  • 2015-08 Target gene mutational pattern in Lynch syndrome colorectal carcinomas according to tumour location and germline mutation in BRITISH JOURNAL OF CANCER
  • 2015-05 Identification of previously unrecognized FAP in children with Gardner fibroma in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2015-02 Identification of six new susceptibility loci for invasive epithelial ovarian cancer in NATURE GENETICS
  • 2014-12 Immunohistochemical molecular phenotypes of gastric cancer based on SOX2 and CDX2 predict patient outcome in BMC CANCER
  • 2014-12 Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers in BREAST CANCER RESEARCH
  • 2014-12 Transcriptome instability as a molecular pan-cancer characteristic of carcinomas in BMC GENOMICS
  • 2014-10 A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer in NATURE GENETICS
  • 2014-05 Gene amplification of the histone methyltransferase SETDB1 contributes to human lung tumorigenesis in ONCOGENE
  • 2014-04 Constitutional and somatic rearrangement of chromosome 21 in acute lymphoblastic leukaemia in NATURE
  • 2013-12 POU1F1 is a novel fusion partner of NUP98 in acute myeloid leukemia with t(3;11)(p11;p15) in MOLECULAR CANCER
  • 2013-12 High resolution melting analysis of KRAS, BRAF and PIK3CA in KRASexon 2 wild-type metastatic colorectal cancer in BMC CANCER
  • 2013-11 The MLL recombinome of acute leukemias in 2013 in LEUKEMIA
  • 2013-04 Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array in NATURE GENETICS
  • 2013-02 Genomic characterization of two large Alu-mediated rearrangements of the BRCA1 gene in JOURNAL OF HUMAN GENETICS
  • 2013-02 Frequent copy number gains at 1q21 and 1q32 are associated with overexpression of the ETS transcription factors ETV3 and ELF3 in breast cancer irrespective of molecular subtypes in BREAST CANCER RESEARCH AND TREATMENT
  • 2012-12 Portuguese c.156_157insAlu BRCA2 founder mutation: gastrointestinal and tongue neoplasias may be part of the phenotype in FAMILIAL CANCER
  • 2012-12 EGFR exon mutation distribution and outcome in non-small-cell lung cancer: a Portuguese retrospective study in TUMOR BIOLOGY
  • 2012-12 Li-Fraumeni-like syndrome associated with a large BRCA1 intragenic deletion in BMC CANCER
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