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BOERWINKLE, ERIC

One or more keywords matched the following items that are connected to BOERWINKLE, ERIC

Item Type	Name
Academic Article	Gene expression profiling and functional proteomic analysis reveal perturbed kinase-mediated signaling in genetic stroke susceptibility.
Academic Article	A genome-wide linkage scan for ankle-brachial index in African American and non-Hispanic white subjects participating in the GENOA study.
Academic Article	Investigating the complex genetic architecture of ankle-brachial index, a measure of peripheral arterial disease, in non-Hispanic whites.
Academic Article	Interactions between the single nucleotide polymorphisms in the homocysteine pathway (MTHFR 677C>T, MTHFR 1298 A>C, and CBSins) and the efficacy of HMG-CoA reductase inhibitors in preventing cardiovascular disease in high-risk patients of hypertension: the GenHAT study.
Academic Article	Antihypertensive pharmacogenetic effect of fibrinogen-beta variant -455G>A on cardiovascular disease, end-stage renal disease, and mortality: the GenHAT study.
Academic Article	The effect of nine common polymorphisms in coagulation factor genes (F2, F5, F7, F12 and F13 ) on the effectiveness of statins: the GenHAT study.
Academic Article	A multilocus approach to the antihypertensive pharmacogenetics of hydrochlorothiazide.
Academic Article	Lack of association between polymorphisms in STK39, a putative thiazide response gene, and blood pressure response to hydrochlorothiazide.
Academic Article	The landscape of recombination in African Americans.
Academic Article	Clan genomics and the complex architecture of human disease.
Academic Article	The Centers for Mendelian Genomics: a new large-scale initiative to identify the genes underlying rare Mendelian conditions.
Academic Article	NOS3 polymorphisms, cigarette smoking, and cardiovascular disease risk: the Atherosclerosis Risk in Communities study.
Academic Article	Relevance of genetics and genomics for prevention and treatment of cardiovascular disease: a scientific statement from the American Heart Association Council on Epidemiology and Prevention, the Stroke Council, and the Functional Genomics and Translational Biology Interdisciplinary Working Group.
Academic Article	A whole-genome scan for stroke or myocardial infarction in family blood pressure program families.
Academic Article	Polymorphisms in genes coding for GRK2 and GRK5 and response differences in antihypertensive-treated patients.
Academic Article	Gene panels to help identify subgroups at high and low risk of coronary heart disease among those randomized to antihypertensive treatment: the GenHAT study.
Academic Article	Translational genomics is not a spectator sport: a call to action.
Academic Article	Determinants of the success of whole-genome association testing.
Academic Article	Kininogen gene (KNG) variation has a consistent effect on aldosterone response to antihypertensive drug therapy: the GERA study.
Concept	Genomics
Academic Article	Whole-genome sequence-based analysis of high-density lipoprotein cholesterol.
Academic Article	Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium.
Academic Article	Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline.
Academic Article	Following-up genome-wide association study signals: lessons learned from Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study.
Academic Article	Strategies to design and analyze targeted sequencing data: cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study.
Academic Article	Sequence variation in TMEM18 in association with body mass index: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study.
Academic Article	Sequencing of 2 subclinical atherosclerosis candidate regions in 3669 individuals: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study.
Academic Article	Sequencing of SCN5A identifies rare and common variants associated with cardiac conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium.
Academic Article	Association of levels of fasting glucose and insulin with rare variants at the chromosome 11p11.2-MADD locus: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study.
Academic Article	Pharmacogenetic effects of 'candidate gene complexes' on stroke in the GenHAT study.
Academic Article	Molecular findings among patients referred for clinical whole-exome sequencing.
Academic Article	Whole exome sequencing identifies novel genes for fetal hemoglobin response to hydroxyurea in children with sickle cell anemia.
Academic Article	No evidence for genome-wide interactions on plasma fibrinogen by smoking, alcohol consumption and body mass index: results from meta-analyses of 80,607 subjects.
Academic Article	Gene-environment interplay in common complex diseases: forging an integrative model?recommendations from an NIH workshop.
Academic Article	In silico prediction of splice-altering single nucleotide variants in the human genome.
Academic Article	PacBio-LITS: a large-insert targeted sequencing method for characterization of human disease-associated chromosomal structural variations.
Academic Article	Assessing structural variation in a personal genome-towards a human reference diploid genome.
Academic Article	Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair.
Academic Article	Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.
Academic Article	Generating a robust statistical causal structure over 13 cardiovascular disease risk factors using genomics data.
Academic Article	A Genetic Response Score for Hydrochlorothiazide Use: Insights From Genomics and Metabolomics Integration.
Academic Article	Exome sequencing in mostly consanguineous Arab families with neurologic disease provides a high potential molecular diagnosis rate.
Academic Article	A hybrid computational strategy to address WGS variant analysis in >5000 samples.
Academic Article	Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders.
Academic Article	Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease.
Academic Article	Practical Approaches for Whole-Genome Sequence Analysis of Heart- and Blood-Related Traits.
Academic Article	Novel plasma biomarker of atenolol-induced hyperglycemia identified through a metabolomics-genomics integrative approach.
Academic Article	Lessons learned from additional research analyses of unsolved clinical exome cases.
Academic Article	Sphingolipid Metabolic Pathway Impacts Thiazide Diuretics Blood Pressure Response: Insights From Genomics, Metabolomics, and Lipidomics.
Academic Article	Blood pressure signature genes and blood pressure response to thiazide diuretics: results from the PEAR and PEAR-2 studies.
Academic Article	Targeted sequencing identifies a missense variant in the BEST3 gene associated with antihypertensive response to hydrochlorothiazide.
Academic Article	Insights into genetics, human biology and disease gleaned from family based genomic studies.
Academic Article	Genetic architecture of laterality defects revealed by whole exome sequencing.
Grant	FUNCTIONAL GENOMICS OF ARTERIAL THROMBOSIS
Grant	The Baylor-Hopkins Clinical Genomics Center for All of Us
Academic Article	Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project.
Academic Article	Innovation in Genomic Data Sharing at the NIH.
Academic Article	The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance.
Academic Article	Cohort Profile: The Right Drug, Right Dose, Right Time: Using Genomic Data to Individualize Treatment Protocol (RIGHT Protocol).
Academic Article	A Genocentric Approach to Discovery of Mendelian Disorders.
Academic Article	Evaluation of mitochondrial DNA copy number estimation techniques.
Academic Article	Alternative genomic diagnoses for individuals with a clinical diagnosis of Dubowitz syndrome.
Academic Article	Cerebral small vessel disease genomics and its implications across the lifespan.
Academic Article	Parliament2: Accurate structural variant calling at scale.
Academic Article	Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium.
Academic Article	Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program.
Grant	ImplementatioN ScIence for Genomic Health Translation (INSIGHT)
Academic Article	Rare coding variants in RCN3 are associated with blood pressure.
Academic Article	Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension.
Academic Article	Integrated proteomic and metabolomic modules identified as biomarkers of mortality in the Atherosclerosis Risk in Communities study and the African American Study of Kidney Disease?and Hypertension.
Academic Article	The genomic landscape of familial glioma.
Academic Article	Epigenome-wide association study using peripheral blood leukocytes identifies genomic regions associated with periodontal disease and edentulism in the Atherosclerosis Risk in Communities study.

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Genomics