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Author Details

Daryl Waggott
Ontario Institute for Cancer Research
2009
42
27
PMIDPaper TitleJournal TitlePublished Year
30665349BPG: Seamless, automated and interactive visualization of scientific data.BMC Bioinformatics2019
33323209The effect of digital physical activity interventions on daily step count: a randomised controlled crossover substudy of the MyHeart Counts Cardiovascular Health Study.Lancet Digit Health2019
31235787Pathologic gene network rewiring implicates PPP1R3A as a central regulator in pressure overload heart failure.Nat Commun2019
30920161Extracutaneous manifestations in phacomatosis cesioflammea and cesiomarmorata: Case series and literature review.Am J Med Genet A2019
30975992Physical activity, sleep and cardiovascular health data for 50,000 individuals from the MyHeart Counts Study.Sci Data2019
28640241Long-read genome sequencing identifies causal structural variation in a Mendelian disease.Genet Med2018
29691431Biological Insights Into Muscular Strength: Genetic Findings in the UK Biobank.Sci Rep2018
29478781Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder.Am J Hum Genet2018
28068672Genomic hallmarks of localized, non-indolent prostate cancer.Nature2017
28077964Erratum to: A bedr way of genomic interval processing.Source Code Biol Med2017
28538708Accuracy in Wrist-Worn, Sensor-Based Measurements of Heart Rate and Energy Expenditure in a Diverse Cohort.J Pers Med2017
28050602Exome sequencing identifies de novo pathogenic variants in <i>FBN1</i> and <i>TRPS1</i> in a patient with a complex connective tissue phenotype.Cold Spring Harb Mol Case Stud2017
26757801Sports genetics moving forward: lessons learned from medical research.Physiol Genomics2016
27999613A bedr way of genomic interval processing.Source Code Biol Med2016
27173062A genome-wide association study of non-HPV-related head and neck squamous cell carcinoma identifies prognostic genetic sequence variants in the MAP-kinase and hormone pathways.Cancer Epidemiol2016
26932475Medical implications of technical accuracy in genome sequencing.Genome Med2016
27058611De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects.PLoS Genet2016
25738365Identification of a microRNA signature associated with risk of distant metastasis in nasopharyngeal carcinoma.Oncotarget2015
26448358Sequence to Medical Phenotypes: A Framework for Interpretation of Human Whole Genome DNA Sequence Data.PLoS Genet2015
25880806Developing a prognostic micro-RNA signature for human cervical carcinoma.PLoS One2015
25984700Combining tumor genome simulation with crowdsourcing to benchmark somatic single-nucleotide-variant detection.Nat Methods2015
26005866Spatial genomic heterogeneity within localized, multifocal prostate cancer.Nat Genet2015
24942367Novel PRKD gene rearrangements and variant fusions in cribriform adenocarcinoma of salivary gland origin.Genes Chromosomes Cancer2014
25271301Integrated omic analysis of oropharyngeal carcinomas reveals human papillomavirus (HPV)-dependent regulation of the activator protein 1 (AP-1) pathway.Mol Cell Proteomics2014
25240283Hotspot activating PRKD1 somatic mutations in polymorphous low-grade adenocarcinomas of the salivary glands.Nat Genet2014
24952745Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.Nat Genet2014
23169800Systematic evaluation of medium-throughput mRNA abundance platforms.RNA2013
23653877A case report and genetic characterization of a massive acinic cell carcinoma of the parotid with delayed distant metastases.Case Rep Oncol Med2013
22513995NanoStringNorm: an extensible R package for the pre-processing of NanoString mRNA and miRNA data.Bioinformatics2012
23028342New susceptibility loci associated with kidney disease in type 1 diabetes.PLoS Genet2012
22704111Pilot genome-wide association search identifies potential loci for risk of erectile dysfunction in type 1 diabetes using the DCCT/EDIC study cohort.J Urol2012
21246217BR-squared: a practical solution to the winner's curse in genome-wide scans.Hum Genet2011
21278746Common variants in ZNF365 are associated with both mammographic density and breast cancer risk.Nat Genet2011
19626703Were genome-wide linkage studies a waste of time? Exploiting candidate regions within genome-wide association studies.Genet Epidemiol2010
19875614A genome-wide association study identifies a novel major locus for glycemic control in type 1 diabetes, as measured by both A1C and glucose.Diabetes2010
18840781Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes.Diabetes2009
19252134Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes.Diabetes2009
19729612Genome-wide association identifies the ABO blood group as a major locus associated with serum levels of soluble E-selectin.Arterioscler Thromb Vasc Biol2009
19587794Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies.PLoS One2009
20017967Genome-wide association analyses of North American Rheumatoid Arthritis Consortium and Framingham Heart Study data utilizing genome-wide linkage results.BMC Proc2009
20017993Region-based analysis in genome-wide association study of Framingham Heart Study blood lipid phenotypes.BMC Proc2009
20018044Transmission-ratio distortion in the Framingham Heart Study.BMC Proc2009
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Collaborators

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University of California los angeles
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Co-authored papers 13
Andrew D Paterson
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Co-authored papers 12
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Nicholas Buchner
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Jennefer N Kohler
Stanford Center for Undiagnosed Diseases
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Kathleen E Houlahan
University of California los angeles
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Maud H W Starmans
Ontario Institute for Cancer Research
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Christine How
Ontario Cancer Institute, University Health Network (UHN)
Co-authored papers 3
Natalie S Fox
University of California los angeles
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Brian O'Sullivan
Princess Margaret Cancer Centre/University Health Network, University of Toronto
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Wei Xu
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Jianxin Wang
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Co-authored papers 3
Bayardo Perez-Ordonez
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Release 1.2