Lisa J Strug


Ontology type: schema:Person     


Person Info

NAME

Lisa J

SURNAME

Strug

Publications in SciGraph latest 50 shown

  • 2018-12 Improving imputation in disease-relevant regions: lessons from cystic fibrosis in NPJ GENOMIC MEDICINE
  • 2018-09-11 Visceral fat-related systemic inflammation and the adolescent brain: a mediating role of circulating glycerophosphocholines in INTERNATIONAL JOURNAL OF OBESITY
  • 2017-05-25 Corrigendum: Novel variation at chr11p13 associated with cystic fibrosis lung disease severity in HUMAN GENOME VARIATION
  • 2017-04 Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder in NATURE NEUROSCIENCE
  • 2016-12 Novel variation at chr11p13 associated with cystic fibrosis lung disease severity in HUMAN GENOME VARIATION
  • 2016-12 Parental attitudes to genetic testing differ by ethnicity and immigration in childhood nephrotic syndrome: a cross-sectional study in CANADIAN JOURNAL OF KIDNEY HEALTH AND DISEASE
  • 2016-04 Prevalence of meconium ileus marks the severity of mutations of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene in GENETICS IN MEDICINE
  • 2015-12 Genome-wide association meta-analysis identifies five modifier loci of lung disease severity in cystic fibrosis in NATURE COMMUNICATIONS
  • 2014-02 Unraveling the complex genetic model for cystic fibrosis: pleiotropic effects of modifier genes on early cystic fibrosis-related morbidities in HUMAN GENETICS
  • 2013-09 GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction in NATURE GENETICS
  • 2013-04 Response Inhibition and ADHD Traits: Correlates and Heritability in a Community Sample in JOURNAL OF ABNORMAL CHILD PSYCHOLOGY
  • 2012-05 Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis in NATURE GENETICS
  • 2011-06 Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2 in NATURE GENETICS
  • 2010-08 A pure likelihood approach to the analysis of genetic association data: an alternative to Bayesian and frequentist analysis in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2010-02 Panic disorder is associated with the serotonin transporter gene (SLC6A4) but not the promoter region (5-HTTLPR) in MOLECULAR PSYCHIATRY
  • 2009-12 Modifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping results in HUMAN GENETICS
  • 2009-09 Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4) in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2005-12 Construction of the model for the Genetic Analysis Workshop 14 simulated data: genotype-phenotype relationships, gene interaction, linkage, association, disequilibrium, and ascertainment effects for a complex phenotype in BMC GENETICS
  • 2003-12 The genetics of cross-sectional and longitudinal body mass index in BMC GENETICS
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