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A genotype-directed phase I-IV dose-finding study of irinotecan in combination with fluorouracil leucovorin as first-line treatment in advanced colorectal cancer

British journal of cancer, 2011-06, Vol.105 (1), p.53-57

2011

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Pharmacogenetic prediction of clinical outcome in advanced colorectal cancer patients receiving oxaliplatin 5-fluorouracil as first-line chemotherapy

British journal of cancer, 2008-10, Vol.99 (7), p.1050-1055

2008

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UGT1A1 gene variations and irinotecan treatment in patients with metastatic colorectal cancer

British journal of cancer, 2004-08, Vol.91 (4), p.678-682

2004

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Impact of CYP2D6 polymorphisms in tamoxifen adjuvant breast cancer treatment

Breast cancer research and treatment, 2010-01, Vol.119 (1), p.33-38

2010

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The c.859G>C variant in the SMN2 gene is associated with types II and III SMA and originates from a common ancestor

Journal of medical genetics, 2010-09, Vol.47 (9), p.640-642

2010

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Methylenetetrahydrofolate reductase gene polymorphisms : genomic predictors of clinical response to fluoropyrimidine-based chemotherapy?

Cancer chemotherapy and pharmacology, 2006-06, Vol.57 (6), p.835-840

2006

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Improving detection and genetic counseling in carriers of spinal muscular atrophy with two copies of the SMN1 gene

Clinical genetics, 2014-05, Vol.85 (5), p.470-475

2014

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Overview of Bardet-Biedl syndrome in Spain: identification of novel mutations in BBS1, BBS10 and BBS12 genes

Clinical genetics, 2014-12, Vol.86 (6), p.601-602

2014

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Methotrexate consolidation treatment according to pharmacogenetics of MTHFR ameliorates event-free survival in childhood acute lymphoblastic leukaemia

The pharmacogenomics journal, 2012-10, Vol.12 (5), p.379-385

2012

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Genetic variations in the VEGF pathway as prognostic factors in metastatic colorectal cancer patients treated with oxaliplatin-based chemotherapy

The pharmacogenomics journal, 2015-10, Vol.15 (5), p.397-404

2015

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KRAS genetic variant as a prognostic factor for recurrence in resectable non-small cell lung cancer

Clinical & translational oncology, 2017-07, Vol.19 (7), p.884-890

2017

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Pharmacogenomics in colorectal cancer: a genome-wide association study to predict toxicity after 5-fluorouracil or FOLFOX administration

The pharmacogenomics journal, 2013-06, Vol.13 (3), p.209-217

2013

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205 SPARC gene variants predict survival of locally advanced and metastatic pancreatic cancer patients treated with chemotherapy

European journal of cancer (1990), 2015-09, Vol.51, p.S28-S28

2015

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EGFR ligands and DNA repair genes: genomic predictors of complete response after capecitabine-based chemoradiotherapy in locally advanced rectal cancer

The pharmacogenomics journal, 2015-02, Vol.15 (1), p.77-83

2015

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A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility variant for colorectal cancer

Human genetics, 2014-05, Vol.133 (5), p.525-534

2014

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Intergenic polymorphisms in the amphiregulin gene region as biomarkers in metastatic colorectal cancer patients treated with anti-EGFR plus irinotecan

The pharmacogenomics journal, 2014-06, Vol.14 (3), p.256-262

2014

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Analysis of the involvement of the NR2E3 gene in autosomal recessive retinal dystrophies

Clinical genetics, 2008-04, Vol.73 (4), p.360-366

2008

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Identification of 14 novel mutations in the long isoform of USH2A in Spanish patients with Usher syndrome type II

Journal of medical genetics, 2006-11, Vol.43 (11), p.e55-e55

2006

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Dystrophinopathies: A NGS approach for the molecular analysis of DMD gene

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S300-S300

2015

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MYO7A mutation screening in Usher syndrome type I patients from diverse origins

Journal of medical genetics, 2007-03, Vol.44 (3), p.e71-e71

2007

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SMN2 copy number predicts acute or chronic spinal muscular atrophy but does not account for intrafamilial variability in siblings

Journal of neurology, 2006, Vol.253 (1), p.21-25

2006

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AB0189 Polymorphisms in genes involved in the metotrexate action mechanism. are they associated with response/toxicity of the drug?

Annals of the rheumatic diseases, 2013-06, Vol.72 (Suppl 3), p.A843-A844

2013

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Study of the involvement of the RGR, CRPB1, and CRB1 genes in the pathogenesis of autosomal recessive retinitis pigmentosa

Journal of medical genetics, 2003-07, Vol.40 (7), p.e89-89

2003

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Isolated cardiomyopathy caused by a DMD nonsense mutation in somatic mosaicism: genetic normalization in skeletal muscle

Clinical genetics, 2012-12, Vol.82 (6), p.574-578

2012

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SIMULTANEOUS GENOTYPING OF CYP2D63, 4, 5 AND 6 POLYMORPHISMS IN A SPANISH POPULATION THROUGH MULTIPLEX LONG POLYMERASE CHAIN REACTION AND MINISEQUENCING MULTIPLEX SINGLE BASE EXTENSION ANALYSIS

Clinical and experimental pharmacology & physiology, 2007-10, Vol.34 (10), p.992-997

2007

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A genotype-directed phase I-IV dose-finding study of irinotecan in combination with fluorouracil leucovorin as first-line treatment in advanced colorectal cancer

Pharmacogenetic prediction of clinical outcome in advanced colorectal cancer patients receiving oxaliplatin 5-fluorouracil as first-line chemotherapy

UGT1A1 gene variations and irinotecan treatment in patients with metastatic colorectal cancer

Impact of CYP2D6 polymorphisms in tamoxifen adjuvant breast cancer treatment

The c.859G>C variant in the SMN2 gene is associated with types II and III SMA and originates from a common ancestor

Methylenetetrahydrofolate reductase gene polymorphisms : genomic predictors of clinical response to fluoropyrimidine-based chemotherapy?

Improving detection and genetic counseling in carriers of spinal muscular atrophy with two copies of the SMN1 gene

Overview of Bardet-Biedl syndrome in Spain: identification of novel mutations in BBS1, BBS10 and BBS12 genes

Methotrexate consolidation treatment according to pharmacogenetics of MTHFR ameliorates event-free survival in childhood acute lymphoblastic leukaemia

Genetic variations in the VEGF pathway as prognostic factors in metastatic colorectal cancer patients treated with oxaliplatin-based chemotherapy

KRAS genetic variant as a prognostic factor for recurrence in resectable non-small cell lung cancer

Pharmacogenomics in colorectal cancer: a genome-wide association study to predict toxicity after 5-fluorouracil or FOLFOX administration

205 SPARC gene variants predict survival of locally advanced and metastatic pancreatic cancer patients treated with chemotherapy

EGFR ligands and DNA repair genes: genomic predictors of complete response after capecitabine-based chemoradiotherapy in locally advanced rectal cancer

A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility variant for colorectal cancer

Intergenic polymorphisms in the amphiregulin gene region as biomarkers in metastatic colorectal cancer patients treated with anti-EGFR plus irinotecan

Analysis of the involvement of the NR2E3 gene in autosomal recessive retinal dystrophies

Identification of 14 novel mutations in the long isoform of USH2A in Spanish patients with Usher syndrome type II

Dystrophinopathies: A NGS approach for the molecular analysis of DMD gene

MYO7A mutation screening in Usher syndrome type I patients from diverse origins

SMN2 copy number predicts acute or chronic spinal muscular atrophy but does not account for intrafamilial variability in siblings

AB0189 Polymorphisms in genes involved in the metotrexate action mechanism. are they associated with response/toxicity of the drug?

Study of the involvement of the RGR, CRPB1, and CRB1 genes in the pathogenesis of autosomal recessive retinitis pigmentosa

Isolated cardiomyopathy caused by a DMD nonsense mutation in somatic mosaicism: genetic normalization in skeletal muscle

SIMULTANEOUS GENOTYPING OF CYP2D63, 4, 5 AND 6 POLYMORPHISMS IN A SPANISH POPULATION THROUGH MULTIPLEX LONG POLYMERASE CHAIN REACTION AND MINISEQUENCING MULTIPLEX SINGLE BASE EXTENSION ANALYSIS

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