Lisa J Martin


Ontology type: schema:Person     


Person Info

NAME

Lisa J

SURNAME

Martin

Publications in SciGraph latest 50 shown

  • 2019-01-07 Reply to ‘Double-outlet right ventricle is not hypoplastic left heart syndrome’ in NATURE GENETICS
  • 2018-08 The Genetic Landscape of Hypoplastic Left Heart Syndrome in PEDIATRIC CARDIOLOGY
  • 2018-06-08 Genetic variants at the 16p13 locus confer risk for eosinophilic esophagitis in GENES & IMMUNITY
  • 2017-03 Complement drives glucosylceramide accumulation and tissue inflammation in Gaucher disease in NATURE
  • 2017-03 ABCC3 genetic variants are associated with postoperative morphine-induced respiratory depression and morphine pharmacokinetics in children in THE PHARMACOGENOMICS JOURNAL
  • 2015-10 Novel associations between FAAH genetic variants and postoperative central opioid-related adverse effects in THE PHARMACOGENOMICS JOURNAL
  • 2015-06 Does Breastfeeding Protect Against Childhood Obesity? Moving Beyond Observational Evidence in CURRENT OBESITY REPORTS
  • 2015-06 Association of OPRM1 A118G variant with risk of morphine-induced respiratory depression following spine fusion in adolescents in THE PHARMACOGENOMICS JOURNAL
  • 2015-04 N-acetyltransferase 1 polymorphism increases cotinine levels in Caucasian children exposed to secondhand smoke: the CCAAPS birth cohort in THE PHARMACOGENOMICS JOURNAL
  • 2015-04 Opioid-induced respiratory depression: ABCB1 transporter pharmacogenetics in THE PHARMACOGENOMICS JOURNAL
  • 2014-12 Erratum to: The Impact of Supervision Training on Genetic Counselor Supervisory Identity Development in JOURNAL OF GENETIC COUNSELING
  • 2014-12 The Impact of Supervision Training on Genetic Counselor Supervisory Identity Development in JOURNAL OF GENETIC COUNSELING
  • 2014-08 Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease in NATURE GENETICS
  • 2014-06 Modeling of multivariate longitudinal phenotypes in family genetic studies with Bayesian multiplicity adjustment in BMC PROCEEDINGS
  • 2014-06 Using Mendelian inheritance errors as quality control criteria in whole genome sequencing data set in BMC PROCEEDINGS
  • 2014-06 On family-based genome-wide association studies with large pedigrees: observations and recommendations in BMC PROCEEDINGS
  • 2014-02 A novel method, the Variant Impact On Linkage Effect Test (VIOLET), leads to improved identification of causal variants in linkage regions in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2013-12 Rank-based genome-wide analysis reveals the association of Ryanodine receptor-2 gene variants with childhood asthma among human populations in HUMAN GENOMICS
  • 2013-01 Regions of homozygosity identified by SNP microarray analysis aid in the diagnosis of autosomal recessive disease and incidentally detect parental blood relationships in GENETICS IN MEDICINE
  • 2012-12 Novel variations in the adiponectin gene (ADIPOQ) may affect distribution of oligomeric complexes in SPRINGERPLUS
  • 2012-12 Quantitative criteria for improving performance of buccal DNA for high-throughput genetic analysis in BMC GENETICS
  • 2012-07 MiR-375 is downregulated in epithelial cells after IL-13 stimulation and regulates an IL-13-induced epithelial transcriptome in MUCOSAL IMMUNOLOGY
  • 2012-04 Barriers to and Motivations for Physician Referral of Patients to Cancer Genetics Clinics in JOURNAL OF GENETIC COUNSELING
  • 2012-03 Insulin resistance and arterial stiffness in healthy adolescents and young adults in DIABETOLOGIA
  • 2011-12 Effect of population stratification analysis on false-positive rates for common and rare variants in BMC PROCEEDINGS
  • 2011-12 Detection of associations with rare and common SNPs for quantitative traits: a nonparametric Bayes-based approach in BMC PROCEEDINGS
  • 2011-12 Population structure analysis using rare and common functional variants in BMC PROCEEDINGS
  • 2011-12 Comparison of measures of marker informativeness for ancestry and admixture mapping in BMC GENOMICS
  • 2011-12 Family- and population-based designs identify different rare causal variants in BMC PROCEEDINGS
  • 2010-06 Retrospective comparison of patient outcomes after in-person and telephone results disclosure counseling for BRCA1/2 genetic testing in FAMILIAL CANCER
  • 2010-04 Common variants at 5q22 associate with pediatric eosinophilic esophagitis in NATURE GENETICS
  • 2009-12 Genetic Analysis Workshop 16: Strategies for genome-wide association study analyses in BMC PROCEEDINGS
  • 2009-12 The effect of minor allele frequency on the likelihood of obtaining false positives in BMC PROCEEDINGS
  • 2009-11 The role of mitochondrial genome in essential hypertension in a Chinese Han population in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2009-10 Gender differences in the relationships among obesity, adiponectin and brachial artery distensibility in adolescents and young adults in INTERNATIONAL JOURNAL OF OBESITY
  • 2007-12 Quality assessment of buccal versus blood genomic DNA using the Affymetrix 500 K GeneChip in BMC GENETICS
  • 2007-12 Comparison of false-discovery rate for genome-wide and fine mapping regions in BMC PROCEEDINGS
  • 2007-08 A locus on chromosome 10 influences C-reactive protein levels in two independent populations in HUMAN GENETICS
  • 2007-04 Evidence in favor of linkage to human chromosomal regions 18q, 5q and 13q for bicuspid aortic valve and associated cardiovascular malformations in HUMAN GENETICS
  • 2006-09-01 Linkage Analysis for Complex Diseases Using Variance Component Analysis: SOLAR in CARDIOVASCULAR DISEASE, VOLUME 1: GENETICS
  • 2006-07 Response by Dr Molloy in MOLECULAR PSYCHIATRY
  • 2006 Linkage Analysis for Complex Diseases Using Variance Component Analysis in CARDIOVASCULAR DISEASE
  • 2005-12 Quantitative trait locus-specific genotype × alcoholism interaction on linkage for evoked electroencephalogram oscillations in BMC GENETICS
  • 2005-12 Accuracy of haplotype estimation in a region of low linkage disequilibrium in BMC GENETICS
  • 2005-08 Evidence for linkage on 21q and 7q in a subset of autism characterized by developmental regression in MOLECULAR PSYCHIATRY
  • 2003-12 Phenotypic, genetic, and genome-wide structure in the metabolic syndrome in BMC GENETICS
  • 2003-12 HDL cholesterol in females in the Framingham Heart Study is linked to a region of chromosome 2q in BMC GENETICS
  • 2003-07 Genetics of leptin expression in baboons in INTERNATIONAL JOURNAL OF OBESITY
  • 2003-03 Genotype-by-smoking interaction for leptin levels in the Metabolic Risk Complications of Obesity Genes project in INTERNATIONAL JOURNAL OF OBESITY
  • 2002-02 A comprehensive linkage analysis for myocardial infarction and its related risk factors in NATURE GENETICS
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