I. Veiga

发表

Target gene mutational pattern in Lynch syndrome colorectal carcinomas according to tumour location and germline mutation

Raquel Seruca, Rui Henrique, Isabel Veiga, 2015, British Journal of Cancer.

p53 alterations in gastric carcinoma: a study of 56 primary tumors and 204 nodal metastases.

R. Seruca, A. Børresen, M. Sobrinho-Simões, 1994, Cancer genetics and cytogenetics.

The nonsense mutation MSH2 c.2152C>T shows a founder effect in Portuguese Lynch syndrome families

R. Henrique, M. Teixeira, S. Maia, 2019, Genes, chromosomes & cancer.

Carcinogenic ability of Schistosoma haematobium possibly through oncogenic mutation of KRAS gene.

C. Lopes, M. Teixeira, P. Oliveira, 2013, Advances in cancer: research & treatment.

E-Cadherin (CDH1) and p53 rather than SMAD4 and Caspase-10 germline mutations contribute to genetic predisposition in Portuguese gastric cancer patients.

R. Seruca, C. Lopes, S. Castedo, 2004, European journal of cancer.

E-Cadherin ( CDH 1 ) and p 53 rather than SMAD 4 and Caspase-10 germline mutations contribute to genetic predisposition in Portuguese gastric cancer patients

R. Seruca, C. Lopes, Carla Oliveira, 2004 .

Validation of a Next-Generation Sequencing Pipeline for the Molecular Diagnosis of Multiple Inherited Cancer Predisposing Syndromes.

G. Soares, M. Teixeira, P. Paulo, 2017, The Journal of molecular diagnostics : JMD.

Analysis of Estrogen Receptor Polymorphism in Codon 325 by PCR‐SSCP in Breast Cancer: Association With Lymph Node Metastasis

C. Lopes, R. Medeiros, D. Pereira, 2002 .

Pathological exon skipping in an HNPCC proband with MLH1 splice acceptor site mutation

P. Jordan, S. Castedo, L. Clarke, 2000, Genes, chromosomes & cancer.

Co-occurrence of nonsense mutations in MSH6 and MSH2 in Lynch syndrome families evidencing that not all truncating mutations are equal

R. Henrique, M. Teixeira, A. Peixoto, 2015, Journal of Human Genetics.

Hereditary gastrointestinal stromal tumors sharing the KIT Exon 17 germline mutation p.Asp820Tyr develop through different cytogenetic progression pathways

C. Lopes, M. Soares, M. Teixeira, 2010, Genes, chromosomes & cancer.

Increasing levels of MYC and MET co-amplification during tumor progression of a case of gastric cancer.

R. Seruca, M. Sobrinho-Simões, S. Castedo, 1995, Cancer genetics and cytogenetics.

The role of targeted BRCA1/BRCA2 mutation analysis in hereditary breast/ovarian cancer families of Portuguese ancestry

M. Teixeira, S. Maia, S. Bizarro, 2015, Clinical genetics.

High resolution melting analysis of KRAS, BRAF and PIK3CA in KRAS exon 2 wild-type metastatic colorectal cancer

R. Henrique, M. Teixeira, A. Peixoto, 2013, BMC Cancer.

POLE somatic mutations in advanced colorectal cancer

R. Henrique, M. Teixeira, A. Peixoto, 2017, Cancer medicine.

Comparison of methodologies for KRAS mutation detection in metastatic colorectal cancer.

R. Henrique, M. Teixeira, A. Peixoto, 2011, Cancer genetics.

Implementation of next-generation sequencing for molecular diagnosis of hereditary breast and ovarian cancer highlights its genetic heterogeneity

M. Teixeira, P. Paulo, A. Peixoto, 2016, Breast Cancer Research and Treatment.

Distinct patterns of KRAS mutations in colorectal carcinomas according to germline mismatch repair defects and hMLH1 methylation status.

L. Aaltonen, D. Arango, P. Laiho, 2004, Human molecular genetics.

Promoter methylation and large intragenic rearrangements of DPYD are not implicated in severe toxicity to 5-fluorouracil-based chemotherapy in gastrointestinal cancer patients

J. Ramalho-Carvalho, R. Henrique, C. Jerónimo, 2010, BMC Cancer.

articleChromosome copy number changes carry prognostic information independent of KIT / PDGFRA point mutations in gastrointestinal stromal tumors

C. Lopes, M. Soares, M. Teixeira, 2015 .

Open Access Research Article Chromosome Copy Number Changes Carry Prognostic Information Independent of Kit/pdgfra Point Mutations in Gastrointestinal Stromal Tumors

C. Lopes, M. Soares, M. Teixeira, 2022 .

TP53 germline mutations in Portugal and genetic modifiers of age at cancer onset

R. Hofstra, R. Reis, R. Seruca, 2009, Familial Cancer.

A novel exonic rearrangement affecting MLH1 and the contiguous LRRFIP2 is a founder mutation in Portuguese Lynch syndrome families

R. Henrique, M. Teixeira, A. Peixoto, 2011, Genetics in Medicine.

No significant role for beta tubulin mutations and mismatch repair defects in ovarian cancer resistance to paclitaxel/cisplatin

D. Pereira, M. Teixeira, S. Castedo, 2005, BMC Cancer.

A new insight into fragile X syndrome among Basque population

O. Peñagarikano, B. Criado, I. Veiga, 2004, American journal of medical genetics. Part A.

A New Insight Into Fragile X Syndrome Among

O. Peñagarikano, I. Veiga, I. Arrieta, 2004 .

The FMR1 CGG repeat and linked microsatellite markers in two Basque valleys

O. Peñagarikano, B. Criado, C. Lostao, 2003, Heredity.

The MSH2 c.388_389del mutation shows a founder effect in Portuguese Lynch syndrome families

S. Farrington, R. Henrique, D. Evans, 2013, Clinical genetics.

Performance of Lynch syndrome predictive models in quantifying the likelihood of germline mutations in patients with abnormal MLH1 immunoexpression

R. Henrique, M. Teixeira, A. Peixoto, 2016, Familial Cancer.

MSH6 germline mutations in early-onset colorectal cancer patients without family history of the disease

C. Lopes, C. Jerónimo, M. Teixeira, 2006, British Journal of Cancer.

Identification of previously unrecognized FAP in children with Gardner fibroma

R. Henrique, M. Teixeira, P. Lopes, 2014, European Journal of Human Genetics.

KRAS and NRAS mutational analysis in plasma ctDNA from patients with metastatic colorectal cancer by real-time PCR and digital PCR

M. Teixeira, A. Peixoto, M. Pinheiro, 2022, International Journal of Colorectal Disease.

Detection of prognostic significant translocations in childhood acute lymphoblastic leukaemia by one‐step multiplex reverse transcription polymerase chain reaction

S. Castedo, N. Cerveira, I. Veiga, 2000, British journal of haematology.

Colorectal carcinomas with microsatellite instability display a different pattern of target gene mutations according to large bowel site of origin

R. Lothe, T. Ahlquist, S. Danielsen, 2010, BMC Cancer.

Colorectal cancers show distinct mutation spectra in members of the canonical WNT signaling pathway according to their anatomical location and type of genetic instability

R. Fodde, R. Smits, I. Fonseca, 2010, Genes, chromosomes & cancer.

Mutations in exon 14 of dihydropyrimidine dehydrogenase and 5-Fluorouracil toxicity in Portuguese colorectal cancer patients

M. Teixeira, S. Castedo, I. Veiga, 2004, Genetics in Medicine.

Analysis of estrogen receptor polymorphism in codon 325 by PCR-SSCP in breast cancer: association with lymph node metastasis.

C. Lopes, R. Medeiros, D. Pereira, 2002, The Breast Journal.

Microsatellite instability in hyperplastic and adenomatous polyps of the stomach

R. Seruca, M. Sobrinho-Simões, J. Machado, 1999, Cancer.

High resolution melting analysis of KRAS, BRAF and PIK3CA in KRAS exon 2 wild-type metastatic colorectal cancer

R. Henrique, M. Teixeira, A. Peixoto, 2013, BMC Cancer.

Four novel MSH2 / MLH1 gene mutations in Portuguese HNPCC families

Julio Cesar Sampaio P. Leite, S. Castedo, S. Bizarro, 2000, Human mutation.

Implementation of upfront DPYD genotyping with a low-cost and high-throughput assay to guide fluoropyrimidine treatment in cancer patients

M. Teixeira, Miguel Porto, A. Peixoto, 2023, Pharmacogenetics and genomics.