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Rare Variant Association Testing Under Low-Coverage Sequencing.
- Published in:
- Genetics, 2013, v. 194, n. 3, p. 769, doi. 10.1534/genetics.113.150169
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- Article
An Optimal Weighted Aggregated Association Test for Identification of Rare Variants Involved in Common Diseases.
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- Genetics, 2011, v. 188, n. 1, p. 181, doi. 10.1534/genetics.110.125070
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- Article
Mixed models can correct for population structure for genomic regions under selection.
- Published in:
- Nature Reviews Genetics, 2013, v. 14, n. 4, p. 300, doi. 10.1038/nrg2813-c1
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- Article
Synaptic processes and immune-related pathways implicated in Tourette syndrome.
- Published in:
- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-020-01082-z
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- Article
Publisher Correction: Accurate estimation of cell composition in bulk expression through robust integration of single-cell information.
- Published in:
- 2020
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- Correction Notice
Accurate estimation of cell composition in bulk expression through robust integration of single-cell information.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-15816-6
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- Article
Engineered exosomes with a photoinducible protein delivery system enable CRISPR-Cas–based epigenome editing in Alzheimer's disease.
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- Science Translational Medicine, 2024, v. 16, n. 759, p. 1, doi. 10.1126/scitranslmed.adi4830
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- Article
Engineered small extracellular vesicles displaying ACE2 variants on the surface protect against SARS‐CoV‐2 infection.
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- Journal of Extracellular Vesicles, 2022, v. 11, n. 1, p. 1, doi. 10.1002/jev2.12179
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- Article
Extracellular vesicles from adipose tissue‐derived stem cells alleviate osteoporosis through osteoprotegerin and miR‐21‐5p.
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- Journal of Extracellular Vesicles, 2021, v. 10, n. 12, p. 1, doi. 10.1002/jev2.12152
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- Article
Effectively identifying regulatory hotspots while capturing expression heterogeneity in gene expression studies.
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- Genome Biology, 2014, v. 15, n. 4, p. 1, doi. 10.1186/gb-2014-15-4-r61
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- Article
xGAP: a python based efficient, modular, extensible and fault tolerant genomic analysis pipeline for variant discovery.
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- Bioinformatics, 2021, v. 37, n. 1, p. 9, doi. 10.1093/bioinformatics/btaa1097
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- Article
Applying meta-analysis to genotype-tissue expression data from multiple tissues to identify eQTLs and increase the number of eGenes.
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- Bioinformatics, 2017, v. 33, n. 14, p. i67, doi. 10.1093/bioinformatics/btx227
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- Article
Using genomic annotations increases statistical power to detect eGenes.
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- Bioinformatics, 2016, v. 32, n. 12, p. i156, doi. 10.1093/bioinformatics/btw272
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- Article
The Minnesota Center for Twin and Family Research Genome-Wide Association Study.
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- Twin Research & Human Genetics, 2012, v. 15, n. 6, p. 767, doi. 10.1017/thg.2012.62
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- Article
Accounting for Population Structure in Gene-by-Environment Interactions in Genome-Wide Association Studies Using Mixed Models.
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- PLoS Genetics, 2016, v. 12, n. 3, p. 1, doi. 10.1371/journal.pgen.1005849
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- Article
Effectively Identifying eQTLs from Multiple Tissues by Combining Mixed Model and Meta-analytic Approaches.
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- PLoS Genetics, 2013, v. 9, n. 6, p. 1, doi. 10.1371/journal.pgen.1003491
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- Article
Alzheimer's disease-causing presenilin-1 mutations have deleterious effects on mitochondrial function.
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- Theranostics, 2021, v. 11, n. 18, p. 8855, doi. 10.7150/thno.59776
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- Article
A general framework for meta-analyzing dependent studies with overlapping subjects in association mapping.
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- Human Molecular Genetics, 2016, v. 25, n. 9, p. 1857, doi. 10.1093/hmg/ddw049
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- Article
A Genome-Wide Association Study Identifies Potential Susceptibility Loci for Hirschsprung Disease.
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- PLoS ONE, 2014, v. 9, n. 10, p. 1, doi. 10.1371/journal.pone.0110292
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- Article
Characterization of Genome-Methylome Interactions in 22 Nuclear Pedigrees.
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- PLoS ONE, 2014, v. 9, n. 7, p. 1, doi. 10.1371/journal.pone.0099313
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- Article
Variance component model to account for sample structure in genome-wide association studies.
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- Nature Genetics, 2010, v. 42, n. 4, p. 348, doi. 10.1038/ng.548
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- Article
Contribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolates.
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- Translational Psychiatry, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41398-020-0758-1
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- Article
Accurate diagnosis of atopic dermatitis by combining transcriptome and microbiota data with supervised machine learning.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-021-04373-7
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- Article
Leveraging allelic imbalance to refine fine-mapping for eQTL studies.
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- PLoS Genetics, 2019, v. 15, n. 12, p. 1, doi. 10.1371/journal.pgen.1008481
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- Article
Population structure in genetic studies: Confounding factors and mixed models.
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- PLoS Genetics, 2018, v. 14, n. 12, p. 1, doi. 10.1371/journal.pgen.1007309
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- Article
CoPheScan: phenome-wide association studies accounting for linkage disequilibrium.
- Published in:
- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-49990-8
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- Article
Rare variants in the endocytic pathway are associated with Alzheimer's disease, its related phenotypes, and functional consequences.
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- PLoS Genetics, 2021, v. 17, n. 9, p. 1, doi. 10.1371/journal.pgen.1009772
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- Article
Rare variants regulate expression of nearby individual genes in multiple tissues.
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- PLoS Genetics, 2021, v. 17, n. 6, p. 1, doi. 10.1371/journal.pgen.1009596
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- Article
ForestQC: Quality control on genetic variants from next-generation sequencing data using random forest.
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- PLoS Computational Biology, 2019, v. 15, n. 12, p. 1, doi. 10.1371/journal.pcbi.1007556
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- Article
Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative.
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- Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01106-x
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- Article
Author Correction: Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative.
- Published in:
- 2022
- By:
- Publication type:
- Correction Notice
Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative.
- Published in:
- Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01106-x
- By:
- Publication type:
- Article