about
Moors and Saracens in Europe: estimating the medieval North African male legacy in southern EuropeGenetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degenerationThe genetic legacy of religious diversity and intolerance: paternal lineages of Christians, Jews, and Muslims in the Iberian PeninsulaGenetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarizationHierarchical analysis of 30 Y-chromosome SNPs in European populationsGenetic data on eight STRs (D5S818, D7S820, F13B, LPL, TH01, TPOX, VWA31, CSF1PO) from a Colombian population.Population data of Galicia (NW Spain) on the new Y-STRs DYS437, DYS438, DYS439, GATA A10, GATA A7.1, GATA A7.2, GATA C4 and GATA H4.Nineteen autosomal microsatellite data from Antioquia (Colombia).Autosomal microsatellite data from Northwestern Colombia.A new approach to long QT syndrome mutation detection by Sequenom MassARRAY system.Prevalence of HCM and long QT syndrome mutations in young sudden cardiac death-related cases.RAS gene polymorphisms, classical risk factors and the advent of coronary artery disease in the Portuguese populationAncestry analysis in the 11-M Madrid bomb attack investigation.New technologies in the genetic approach to sudden cardiac death in the young.Sarcomeric gene mutations in sudden infant death syndrome (SIDS).Association between SNPs of Metalloproteinases and Prostaglandin F2α Receptor Genes and Latanoprost Response in Open-Angle Glaucoma.The relationship between surname frequency and Y chromosome variation in Spain.Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome.SNPs in forensic genetics: a review on SNP typing methodologies.Molecular genetics of sudden cardiac death.Massive parallel sequencing applied to the molecular autopsy in sudden cardiac death in the young.Broad-based molecular autopsy: a potential tool to investigate the involvement of subtle cardiac conditions in sudden unexpected death in infancy and early childhood.Medico-legal perspectives on sudden cardiac death in young athletes.The genetic component of bicuspid aortic valve and aortic dilation. An exome-wide association study.Resequencing and association analysis of coding regions at twenty candidate genes suggest a role for rare risk variation at AKAP9 and protective variation at NRXN1 in schizophrenia susceptibility.Y-chromosome haplotype analysis in Antioquia (Colombia).A strong genetic association between the tumor necrosis factor locus and proliferative vitreoretinopathy: the retina 4 project.Development of predictive models of proliferative vitreoretinopathy based on genetic variables: the Retina 4 project.Pharmacogenomics of anti-platelet therapy focused on peripheral blood cells of coronary arterial disease patients.Phylogenetic evidence for multiple independent duplication events at the DYS19 locus.Novel splice donor site mutation in MERTK gene associated with retinitis pigmentosa.Methylenetetrahydrofolate reductase gene, homocysteine and coronary artery disease: the A1298C polymorphism does matter. Inferences from a case study (Madeira, Portugal).Genetic association study of age-related macular degeneration in the Spanish population.Insights into Iberian population origins through the construction of highly informative Y-chromosome haplotypes using biallelic markers, STRs, and the MSY1 minisatellite.PRKG1 and genetic diagnosis of early-onset thoracic aortic disease.Relationship between fibrillin-1 genotype and severity of cardiovascular involvement in Marfan syndrome.Predicting proliferative vitreoretinopathy: temporal and external validation of models based on genetic and clinical variables.A genetic case-control study confirms the implication of SMAD7 and TNF locus in the development of proliferative vitreoretinopathy.Prospective and Retrospective Diagnosis of Barth Syndrome Aided by Next-Generation Sequencing.The genetic male component of two South-Western Colombian populations.
P50
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P50
description
hulumtuese
@sq
researcher
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wetenschapper
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հետազոտող
@hy
name
Maria Brion
@ast
Maria Brion
@en
Maria Brion
@es
Maria Brion
@nl
Maria Brion
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type
label
Maria Brion
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Maria Brion
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Maria Brion
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Maria Brion
@nl
Maria Brion
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prefLabel
Maria Brion
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Maria Brion
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Maria Brion
@es
Maria Brion
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Maria Brion
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P1053
J-8059-2014
P106
P1153
7006040163
P2038
Maria_Brion
P21
P31
P3829
P496
0000-0001-7463-2148