Publicacións nas que colabora con María Torres Español (25)
2023
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DNA polymorphisms associated with lactase persistence, self-perceived symptoms of lactose intolerance, milk and dairy consumption, and ancestry, in the Uruguayan population
American Journal of Human Biology, Vol. 35, Núm. 6
2017
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A new panel of SNPs to assess thyroid carcinoma risk: A pilot study in a Brazilian admixture population
BMC Medical Genetics, Vol. 18, Núm. 1
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Correction: A european spectrum of pharmacogenomic biomarkers: Implications for clinical pharmacogenomics (PLoS ONE (2016) 11:9 (e0162866) DOI: 10.1371/journal.pone.0162866)
PLoS ONE
2016
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A European spectrum of pharmacogenomic biomarkers: Implications for clinical pharmacogenomics
PLoS ONE, Vol. 11, Núm. 9
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Development of a methylation marker set for forensic age estimation using analysis of public methylation data and the Agena Bioscience EpiTYPER system
Forensic Science International: Genetics, Vol. 24, pp. 65-74
2015
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Investigation of gene-environment interactions between 47 newly identified breast cancer susceptibility loci and environmental risk factors
International Journal of Cancer, Vol. 136, Núm. 6, pp. E685-E696
2014
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Building a forensic ancestry panel from the ground up: The EUROFORGEN Global AIM-SNP set
Forensic Science International: Genetics, Vol. 11, Núm. 1, pp. 13-25
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Cuba: Exploring the History of Admixture and the Genetic Basis of Pigmentation Using Autosomal and Uniparental Markers
PLoS Genetics, Vol. 10, Núm. 7
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Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
Nature Genetics, Vol. 46, Núm. 8, pp. 826-836
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High-throughput genotyping assay for the large-scale genetic characterization of Cryptosporidium parasites from human and bovine samples
Parasitology, Vol. 141, Núm. 4, pp. 491-500
2013
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Association of thromboxane A1 synthase (TBXAS1) gene polymorphism with acute urticaria induced by nonsteroidal anti-inflammatory drugs
Journal of Allergy and Clinical Immunology, Vol. 132, Núm. 4, pp. 989-991
2012
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Development of a panel of genome-wide ancestry informative markers to study admixture throughout the americas
PLoS Genetics, Vol. 8, Núm. 3
2010
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A new approach to long QT syndrome mutation detection by Sequenom MassARRAY® system
Electrophoresis, Vol. 31, Núm. 10, pp. 1648-1655
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Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk
Nature Genetics, Vol. 42, Núm. 2, pp. 132-136
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Identification of a novel mutation in the human PDE6A gene in autosomal recessive retinitis pigmentosa: Homology with the nmf28/nmf28 mice model
Clinical Genetics
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LARGE-SCALE MUTATION SCREENING IN SUDDEN CARDIAC DEATH (SCD)
ACTA MEDICINAE LEGALIS ET SOCIALIS (UNIV COIMBRA), pp. 211-217
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New technologies in the genetic approach to sudden cardiac death in the young
Forensic Science International, Vol. 203, Núm. 1-3, pp. 15-24
2008
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Analyses of variants located in estrogen metabolism genes (ESR1, ESR2, COMT and APOE) and schizophrenia
Schizophrenia Research, Vol. 100, Núm. 1-3, pp. 308-315
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Association of schizophrenia with DTNBP1 but not with DAO, DAOA, NRG1 and RGS4 nor their genetic interaction
Journal of Psychiatric Research, Vol. 42, Núm. 4, pp. 278-288
2006
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SUMO4 and MAP3K7IP2 single nucleotide polymorphisms and susceptibility to rheumatoid arthritis
Journal of Rheumatology, Vol. 33, Núm. 6, pp. 1048-1051