Found: 25
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Identification of Functional Variants in the FAM13A Chronic Obstructive Pulmonary Disease Genome-Wide Association Study Locus by Massively Parallel Reporter Assays.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Exome Array Analysis Identifies a Common Variant in IL27 Associated with Chronic Obstructive Pulmonary Disease.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Exome Sequencing Analysis in Severe, Early-Onset Chronic Obstructive Pulmonary Disease.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Interaction of Cigarette Smoking and Polygenic Risk Score on Reduced Lung Function.
- Published in:
- JAMA Network Open, 2021, v. 4, n. 12, p. e2139525, doi. 10.1001/jamanetworkopen.2021.39525
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- Publication type:
- Article
Connecting COPD GWAS Genes: FAM13A Controls TGFβ2 Secretion by Modulating AP-3 Transport.
- Published in:
- American Journal of Respiratory Cell & Molecular Biology, 2021, v. 65, n. 5, p. 532, doi. 10.1165/rcmb.2021-0016OC
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- Publication type:
- Article
Whole-Genome Sequencing in Severe Chronic Obstructive Pulmonary Disease.
- Published in:
- American Journal of Respiratory Cell & Molecular Biology, 2018, v. 59, n. 5, p. 614, doi. 10.1165/rcmb.2018-0088OC
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- Publication type:
- Article
Handling the data management needs of high-throughput sequencing data: SpeedGene, a compression algorithm for the efficient storage of genetic data.
- Published in:
- BMC Bioinformatics, 2012, v. 13, n. 1, p. 100, doi. 10.1186/1471-2105-13-100
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- Publication type:
- Article
metaFARVAT: An Efficient Tool for Meta-Analysis of Family-Based, Case-Control, and Population-Based Rare Variant Association Studies.
- Published in:
- Frontiers in Genetics, 2019, p. N.PAG, doi. 10.3389/fgene.2019.00572
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- Publication type:
- Article
WISARD: workbench for integrated superfast association studies for related datasets.
- Published in:
- BMC Medical Genomics, 2018, v. 11, p. N.PAG
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- Publication type:
- Article
A Genome-Wide Linkage Study for Chronic Obstructive Pulmonary Disease in a Dutch Genetic Isolate Identifies Novel Rare Candidate Variants.
- Published in:
- Frontiers in Genetics, 2018, p. 1, doi. 10.3389/fgene.2018.00133
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- Publication type:
- Article
Whole exome sequencing analysis in severe chronic obstructive pulmonary disease.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 21, p. 3801, doi. 10.1093/hmg/ddy269
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- Publication type:
- Article
PLD3 gene variants and Alzheimer's disease.
- Published in:
- Nature, 2015, v. 520, n. 7545, p. E7, doi. 10.1038/nature14040
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- Publication type:
- Article
Boosting Gene Mapping Power and Efficiency with Efficient Exact Variance Component Tests of Single Nucleotide Polymorphism Sets.
- Published in:
- Genetics, 2016, v. 204, n. 3, p. 921, doi. 10.1534/genetics.116.190454
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- Publication type:
- Article
A comparative analysis of family-based and population-based association tests using whole genome sequence data.
- Published in:
- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S33
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- Publication type:
- Article
Partial correlation network analysis identifies coordinated gene expression within a regional cluster of COPD genome-wide association signals.
- Published in:
- PLoS Computational Biology, 2024, v. 20, n. 10, p. 1, doi. 10.1371/journal.pcbi.1011079
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- Publication type:
- Article
Selecting cases and controls for DNA sequencing studies using family histories of disease.
- Published in:
- 2017
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- Publication type:
- journal article
A robust and adaptive framework for interaction testing in quantitative traits between multiple genetic loci and exposure variables.
- Published in:
- PLoS Genetics, 2022, v. 18, n. 11, p. 1, doi. 10.1371/journal.pgen.1010464
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- Publication type:
- Article
Genome‐wide association analysis of COVID‐19 mortality risk in SARS‐CoV‐2 genomes identifies mutation in the SARS‐CoV‐2 spike protein that colocalizes with P.1 of the Brazilian strain.
- Published in:
- Genetic Epidemiology, 2021, v. 45, n. 7, p. 685, doi. 10.1002/gepi.22421
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- Publication type:
- Article
Statistical considerations for the analysis of massively parallel reporter assays data.
- Published in:
- Genetic Epidemiology, 2020, v. 44, n. 7, p. 785, doi. 10.1002/gepi.22337
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- Publication type:
- Article
Gene-based segregation method for identifying rare variants in family-based sequencing studies.
- Published in:
- Genetic Epidemiology, 2017, v. 41, n. 4, p. 309, doi. 10.1002/gepi.22037
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- Publication type:
- Article
FARVATX: Family-Based Rare Variant Association Test for X-Linked Genes.
- Published in:
- Genetic Epidemiology, 2016, v. 40, n. 6, p. 475, doi. 10.1002/gepi.21979
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- Publication type:
- Article
Family-Based Rare Variant Association Analysis: A Fast and Efficient Method of Multivariate Phenotype Association Analysis.
- Published in:
- Genetic Epidemiology, 2016, v. 40, n. 6, p. 502, doi. 10.1002/gepi.21985
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- Publication type:
- Article
On Association Analysis of Rare Variants Under Population Substructure: An Approach for the Detection of Subjects That Can Cause Bias in the Analysis-T<sub>opt</sub>: An Outlier Detection Method.
- Published in:
- Genetic Epidemiology, 2013, v. 37, n. 5, p. 431, doi. 10.1002/gepi.21734
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- Publication type:
- Article
On the simultaneous association analysis of large genomic regions: a massive multi-locus association test.
- Published in:
- Bioinformatics, 2014, v. 30, n. 2, p. 157, doi. 10.1093/bioinformatics/btt654
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- Publication type:
- Article
Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-18334-7
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- Publication type:
- Article