about
Genetics and outcomes after traumatic brain injury (TBI): what do we know about pediatric TBI?Common variants at 5q22 associate with pediatric eosinophilic esophagitisRank-based genome-wide analysis reveals the association of ryanodine receptor-2 gene variants with childhood asthma among human populationsRhinovirus infection results in stronger and more persistent genomic dysregulation: Evidence for altered innate immune response in asthmatics at baseline, early in infection, and during convalescenceCommon variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel diseaseMeta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhageDifferences in candidate gene association between European ancestry and African American asthmatic children.High prevalence of eosinophilic esophagitis in patients with inherited connective tissue disorders.Quality assessment of buccal versus blood genomic DNA using the Affymetrix 500 K GeneChip.Genetic variants in SCN5A promoter are associated with arrhythmia phenotype severity in patients with heterozygous loss-of-function mutationQuantitative trait locus-specific genotype x alcoholism interaction on linkage for evoked electroencephalogram oscillationsAccuracy of haplotype estimation in a region of low linkage disequilibriumDNA methylation at the mu-1 opioid receptor gene (OPRM1) promoter predicts preoperative, acute, and chronic postsurgical pain after spine fusion.INSIG1 influences obesity-related hypertriglyceridemia in humans.Genetic architecture of lipid traits changes over time and differs by race: Princeton Lipid Follow-up Study.Variants of thymic stromal lymphopoietin and its receptor associate with eosinophilic esophagitis.Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease.Identification of KIF3A as a novel candidate gene for childhood asthma using RNA expression and population allelic frequencies differences.Increased prevalence of eosinophilic gastrointestinal disorders in pediatric PTEN hamartoma tumor syndromesComparison of measures of marker informativeness for ancestry and admixture mapping.Application of genetic/genomic approaches to allergic disorders.Genetics of pain perception, COMT and postoperative pain management in children.MiR-375 is downregulated in epithelial cells after IL-13 stimulation and regulates an IL-13-induced epithelial transcriptome.Effect of population stratification analysis on false-positive rates for common and rare variants.Population structure analysis using rare and common functional variants.Detection of associations with rare and common SNPs for quantitative traits: a nonparametric Bayes-based approachAccounting for a quantitative trait locus for plasma triglyceride levels: utilization of variants in multiple genes.Searching for genes underlying normal variation in human adiposity.Functional variant in the autophagy-related 5 gene promotor is associated with childhood asthma.MicroRNA signature in patients with eosinophilic esophagitis, reversibility with glucocorticoids, and assessment as disease biomarkers.Epistasis between serine protease inhibitor Kazal-type 5 (SPINK5) and thymic stromal lymphopoietin (TSLP) genes contributes to childhood asthmaThe role of mitochondrial genome in essential hypertension in a Chinese Han population.Bicuspid aortic valve is heritable.Quantitative criteria for improving performance of buccal DNA for high-throughput genetic analysis.Twin and family studies reveal strong environmental and weaker genetic cues explaining heritability of eosinophilic esophagitisPolymorphisms in adiponectin receptor genes ADIPOR1 and ADIPOR2 and insulin resistance.Hypoplastic left heart syndrome is heritable.Genetic risk signatures of opioid-induced respiratory depression following pediatric tonsillectomyHypoplastic left heart syndrome links to chromosomes 10q and 6q and is genetically related to bicuspid aortic valveAssociation of INSIG2 polymorphism with overweight and LDL in children.
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description
hulumtuese
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researcher
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wetenschapper
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հետազոտող
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name
Lisa J. Martin
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Lisa J. Martin
@en
Lisa J. Martin
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Lisa J. Martin
@nl
Lisa J. Martin
@sl
type
label
Lisa J. Martin
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Lisa J. Martin
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Lisa J. Martin
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Lisa J. Martin
@nl
Lisa J. Martin
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Lisa J. Martin
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prefLabel
Lisa J. Martin
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Lisa J. Martin
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Lisa J. Martin
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Lisa J. Martin
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Lisa J. Martin
@sl
P1053
E-2425-2016
P106
P1153
55382763200
P21
P2798
P31
P3829
P496
0000-0001-8702-9946