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1775. A Community-wide Study to Evaluate the Accuracy of Self-testing for Influenza: Works in Progress.
- Published in:
- Open Forum Infectious Diseases, 2019, v. 6, p. S654, doi. 10.1093/ofid/ofz360.1638
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- Publication type:
- Article
LB21. The Seattle Flu Study: A Community-Based Study of Influenza.
- Published in:
- Open Forum Infectious Diseases, 2019, v. 6, p. S1002, doi. 10.1093/ofid/ofz415.2504
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- Publication type:
- Article
Remote surveillance and detection of SARS-CoV-2 transmission among household members in King County, Washington.
- Published in:
- BMC Infectious Diseases, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12879-024-09160-z
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- Publication type:
- Article
Integrating Host Genomics with Surveillance for Invasive Bacterial Diseases.
- Published in:
- Emerging Infectious Diseases, 2008, v. 14, n. 7, p. 1138, doi. 10.3201/eid1407.071287
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- Publication type:
- Article
'Mandibulofacial dysostosis with microcephaly' caused by EFTUD2 mutations: Expanding the phenotype.
- Published in:
- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 1, p. 108, doi. 10.1002/ajmg.a.35696
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- Publication type:
- Article
High-throughput sequencing of T-cell receptors reveals a homogeneous repertoire of tumour-infiltrating lymphocytes in ovarian cancer.
- Published in:
- Journal of Pathology, 2013, v. 231, n. 4, p. 433, doi. 10.1002/path.4260
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- Publication type:
- Article
Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis.
- Published in:
- Nature Genetics, 2012, v. 44, n. 8, p. 886, doi. 10.1038/ng.2344
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- Publication type:
- Article
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
- Published in:
- 2012
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- Publication type:
- Correction Notice
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
- Published in:
- Nature Genetics, 2011, v. 43, n. 6, p. 585, doi. 10.1038/ng.835
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- Publication type:
- Article
Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome.
- Published in:
- Nature Genetics, 2010, v. 42, n. 9, p. 790, doi. 10.1038/ng.646
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- Publication type:
- Article
Corrigendum: Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.
- Published in:
- 2008
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- Publication type:
- Correction Notice
Estimating coverage and power for genetic association studies using near-complete variation data.
- Published in:
- Nature Genetics, 2008, v. 40, n. 7, p. 841, doi. 10.1038/ng.180
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- Publication type:
- Article
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.
- Published in:
- Nature Genetics, 2008, v. 40, n. 2, p. 189, doi. 10.1038/ng.75
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- Publication type:
- Article
Evidence for substantial fine-scale variation in recombination rates across the human genome.
- Published in:
- Nature Genetics, 2004, v. 36, n. 7, p. 700, doi. 10.1038/ng1376
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- Publication type:
- Article
Additional SNPs and linkage-disequilibrium analyses are necessary for whole-genome association studies in humans.
- Published in:
- Nature Genetics, 2003, v. 33, n. 4, p. 518, doi. 10.1038/ng1128
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- Publication type:
- Article
Sequence variation in the human angiotensin converting enzyme.
- Published in:
- Nature Genetics, 1999, v. 22, n. 1, p. 59, doi. 10.1038/8760
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- Publication type:
- Article
Detection of structural variants and indels within exome data.
- Published in:
- Nature Methods, 2012, v. 9, n. 2, p. 176, doi. 10.1038/nmeth.1810
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- Publication type:
- Article
Variation in LPA Is Associated with Lp(a) Levels in Three Populations from the Third National Health and Nutrition Examination Survey.
- Published in:
- PLoS ONE, 2011, v. 6, n. 1, p. 1, doi. 10.1371/journal.pone.0016604
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- Publication type:
- Article
VKORC1 Common Variation and Bone Mineral Density in the Third National Health and Nutrition Examination Survey.
- Published in:
- PLoS ONE, 2010, v. 5, n. 12, p. 1, doi. 10.1371/journal.pone.0015088
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- Publication type:
- Article
Genome-Wide Association of Lipid-Lowering Response to Statins in Combined Study Populations.
- Published in:
- PLoS ONE, 2010, v. 5, n. 3, p. 1, doi. 10.1371/journal.pone.0009763
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- Publication type:
- Article
CYP2C9 haplotype structure in European American warfarin patients and association with clinical outcomes.
- Published in:
- Clinical Pharmacology & Therapeutics, 2005, v. 77, n. 5, p. 353, doi. 10.1016/j.clpt.2005.01.019
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- Publication type:
- Article
TagSNP evaluation for the association of 42 inflammation loci and vascular disease: evidence of IL6, FGB, ALOX5, NFKBIA, and IL4R loci effects.
- Published in:
- Human Genetics, 2007, v. 121, n. 1, p. 65, doi. 10.1007/s00439-006-0289-8
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- Publication type:
- Article
Efficient selection of tagging single-nucleotide polymorphisms in multiple populations.
- Published in:
- Human Genetics, 2006, v. 120, n. 1, p. 58, doi. 10.1007/s00439-006-0182-5
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- Publication type:
- Article
Allelic spectrum of the natural variation in CRP.
- Published in:
- Human Genetics, 2006, v. 119, n. 5, p. 496, doi. 10.1007/s00439-006-0160-y
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- Publication type:
- Article
New genetic variant that might improve warfarin dose prediction in African Americans.
- Published in:
- British Journal of Clinical Pharmacology, 2010, v. 70, n. 3, p. 393, doi. 10.1111/j.1365-2125.2010.03709.x
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- Publication type:
- Article
Rare Variation Facilitates Inferences of Fine-Scale Population Structure in Humans.
- Published in:
- Molecular Biology & Evolution, 2015, v. 32, n. 3, p. 653, doi. 10.1093/molbev/msu326
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- Publication type:
- Article
Automating the identification of DNA variations using quality‐based fluorescence re‐sequencing: analysis of the human mitochondrial genome.
- Published in:
- Nucleic Acids Research, 1998, v. 26, n. 4, p. 967, doi. 10.1093/nar/26.4.967
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- Publication type:
- Article
Sequence variation in the human transcription factor gene POU5F1.
- Published in:
- BMC Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2156-9-15
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- Publication type:
- Article
Using synthetic templates to design an unbiased multiplex PCR assay.
- Published in:
- Nature Communications, 2013, v. 4, n. 10, p. 2680, doi. 10.1038/ncomms3680
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- Publication type:
- Article
High-throughput pairing of T cell receptor α and β sequences.
- Published in:
- Science Translational Medicine, 2015, v. 7, n. 301, p. 1, doi. 10.1126/scitranslmed.aac5624
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- Publication type:
- Article
Novel Hispanic American CYP2C9 Genetic Variants and Assessment of Their Impact on Gene Expression.
- Published in:
- FASEB Journal, 2007, v. 21, n. 5, p. A415
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- Publication type:
- Article
Comparison of Symptoms and RNA Levels in Children and Adults With SARS-CoV-2 Infection in the Community Setting.
- Published in:
- JAMA Pediatrics, 2021, v. 175, n. 10, p. e212025, doi. 10.1001/jamapediatrics.2021.2025
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- Publication type:
- Article
A case study of acenocoumarol sensitivity and genotype-phenotype discordancy explained by combinations of polymorphisms in VKORC1 and CYP2C9.
- Published in:
- British Journal of Clinical Pharmacology, 2006, v. 62, n. 5, p. 617, doi. 10.1111/j.1365-2125.2006.02688.x
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- Publication type:
- Article
Quantifying rare, deleterious variation in 12 human cytochrome P450 drug-metabolism genes in a large-scale exome dataset.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 8, p. 1957
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- Publication type:
- Article
Hypertension and single nucleotide polymorphisms.
- Published in:
- Current Hypertension Reports, 2000, v. 2, n. 1, p. 44, doi. 10.1007/s11906-000-0057-4
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- Publication type:
- Article
Renin-Angiotensin System Haplotypes and the Risk of Myocardial Infarction and Stroke in Pharmacologically Treated Hypertensive Patients.
- Published in:
- American Journal of Epidemiology, 2007, v. 166, n. 1, p. 19, doi. 10.1093/aje/kwm059
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- Publication type:
- Article
Common Genetic Variation in the Prothrombin Gene, Hormone Therapy, and Incident Nonfatal Myocardial Infarction in Postmenopausal Women.
- Published in:
- American Journal of Epidemiology, 2006, v. 163, n. 7, p. 600, doi. 10.1093/aje/kwj092
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- Publication type:
- Article
Common Missense Variant in the Glucokinase Regulatory Protein Gene Is Associated With Increased Plasma Triglyceride and C-Reactive Protein but Lower Fasting Glucose Concentrations.
- Published in:
- Diabetes, 2008, v. 57, n. 11, p. 3112, doi. 10.2337/db08-0516
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- Publication type:
- Article
Population History and Natural Selection Shape Patterns of Genetic Variation in 132 Genes.
- Published in:
- PLoS Biology, 2004, v. 2, n. 10, p. 1591, doi. 10.1371/journal.pbio.0020286
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- Publication type:
- Article
Population History and Natural Selection Shape Patterns of Genetic Variation in 132 Genes.
- Published in:
- PLoS Biology, 2004, v. 2, n. 9, p. 1, doi. 10.1371/journal.pbio.0020286
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- Publication type:
- Article
A statin-dependent QTL for GATM expression is associated with statin-induced myopathy.
- Published in:
- Nature, 2013, v. 502, n. 7471, p. 377, doi. 10.1038/nature12508
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- Publication type:
- Article
Corrigendum: Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants.
- Published in:
- Nature, 2013, v. 495, n. 7440, p. 270, doi. 10.1038/nature12022
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- Publication type:
- Article
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
- Published in:
- Nature, 2012, v. 485, n. 7397, p. 246, doi. 10.1038/nature10989
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- Publication type:
- Article
IGF1R variants associated with isolated single suture craniosynostosis.
- Published in:
- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 1, p. 91, doi. 10.1002/ajmg.a.33781
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- Publication type:
- Article
Effects of weather-related social distancing on city-scale transmission of respiratory viruses: a retrospective cohort study.
- Published in:
- 2021
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- Publication type:
- journal article
Correction: Exome Sequencing of Phenotypic Extremes Identifies CAV2 and TMC6 as Interacting Modifiers of Chronic Pseudomonas aeruginosa Infection in Cystic Fibrosis.
- Published in:
- 2015
- By:
- Publication type:
- Correction Notice
Exome Sequencing of Phenotypic Extremes Identifies CAV2 and TMC6 as Interacting Modifiers of Chronic Pseudomonas aeruginosa Infection in Cystic Fibrosis.
- Published in:
- PLoS Genetics, 2015, v. 11, n. 6, p. 1, doi. 10.1371/journal.pgen.1005273
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- Publication type:
- Article
Identification, Replication, and Functional Fine-Mapping of Expression Quantitative Trait Loci in Primary Human Liver Tissue.
- Published in:
- PLoS Genetics, 2011, v. 7, n. 5, p. 1, doi. 10.1371/journal.pgen.1002078
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- Publication type:
- Article
Allele Frequency Matching Between SNPs Reveals an Excess of Linkage Disequilibrium in Genic Regions of the Human Genome.
- Published in:
- PLoS Genetics, 2006, v. 3, n. 3, p. e142, doi. 10.1371/journal.pgen.0020142
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- Publication type:
- Article
Direct detection of null alleles in SNP genotyping data.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 12, p. 1931, doi. 10.1093/hmg/ddl115
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- Publication type:
- Article