Found: 27
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Genotype-First Approach Identifies an Association between rs28374544/FOG2 S657G and Liver Disease through Alterations in mTORC1 Signaling.
- Published in:
- Genes, 2024, v. 15, n. 8, p. 1098, doi. 10.3390/genes15081098
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- Publication type:
- Article
Using knowledge-driven genomic interactions for multi-omics data analysis: metadimensional models for predicting clinical outcomes in ovarian carcinoma.
- Published in:
- 2017
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- Publication type:
- journal article
Collective feature selection to identify crucial epistatic variants.
- Published in:
- BioData Mining, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13040-018-0168-6
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- Publication type:
- Article
Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals.
- Published in:
- BioData Mining, 2017, v. 10, p. 1, doi. 10.1186/s13040-017-0145-5
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- Publication type:
- Article
Identifying gene-gene interactions that are highly associated with Body Mass Index using Quantitative Multifactor Dimensionality Reduction (QMDR).
- Published in:
- BioData Mining, 2015, v. 8, p. 1, doi. 10.1186/s13040-015-0074-0
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- Publication type:
- Article
eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants.
- Published in:
- BMC Medical Genomics, 2016, v. 9, p. 19, doi. 10.1186/s12920-016-0191-8
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- Publication type:
- Article
16 Cross-ancestry analysis of preeclampsia identifies novel maternal susceptibility loci.
- Published in:
- 2023
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- Publication type:
- Abstract
PLATO software provides analytic framework for investigating complexity beyond genome-wide association studies.
- Published in:
- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-00802-2
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- Publication type:
- Article
The joint effect of air pollution exposure and copy number variation on risk for autism.
- Published in:
- Autism Research: Official Journal of the International Society for Autism Research, 2017, v. 10, n. 9, p. 1470, doi. 10.1002/aur.1799
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- Publication type:
- Article
Phenome-wide Association Study Relating Pretreatment Laboratory Parameters With Human Genetic Variants in AIDS Clinical Trials Group Protocols.
- Published in:
- Open Forum Infectious Diseases, 2015, v. 2, n. 1, p. 1, doi. 10.1093/ofid/ofu113
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- Publication type:
- Article
Imputation and quality control steps for combining multiple genome-wide datasets.
- Published in:
- Frontiers in Genetics, 2014, v. 5, p. 1, doi. 10.3389/fgene.2014.00370
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- Publication type:
- Article
Phenome-wide association study (PheWAS) in EMR-linked pediatric cohorts, genetically links PLCL1 to speech language development and IL5-IL13 to Eosinophilic Esophagitis.
- Published in:
- Frontiers in Genetics, 2014, v. 5, p. 1, doi. 10.3389/fgene.2014.00401
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- Publication type:
- Article
Controlling for population structure and genotyping platform bias in the eMERGE multi-institutional biobank linked to electronic health records.
- Published in:
- Frontiers in Genetics, 2014, v. 5, p. 1, doi. 10.3389/fgene.2014.00352
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- Publication type:
- Article
Effect of CYP3A4*22 and PPAR-α Genetic Variants on Platelet Reactivity in Patients Treated with Clopidogrel and Lipid-Lowering Drugs Undergoing Elective Percutaneous Coronary Intervention.
- Published in:
- Genes, 2020, v. 11, n. 9, p. 1068, doi. 10.3390/genes11091068
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- Publication type:
- Article
Association of the V122I Hereditary Transthyretin Amyloidosis Genetic Variant With Heart Failure Among Individuals of African or Hispanic/Latino Ancestry.
- Published in:
- 2019
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- Publication type:
- journal article
Quality Control Procedures for Genome‐Wide Association Studies.
- Published in:
- Current Protocols, 2022, v. 2, n. 11, p. 1, doi. 10.1002/cpz1.603
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- Publication type:
- Article
Genetic liability for substance use associated with medical comorbidities in electronic health records of African‐ and European‐ancestry individuals.
- Published in:
- Addiction Biology, 2022, v. 27, n. 1, p. 1, doi. 10.1111/adb.13099
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- Publication type:
- Article
A simulation study investigating power estimates in phenome-wide association studies.
- Published in:
- BMC Bioinformatics, 2018, v. 19, n. 1, p. 1, doi. 10.1186/s12859-018-2135-0
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- Publication type:
- Article
Concept and design of a genome-wide association genotyping array tailored for transplantation-specific studies.
- Published in:
- Genome Medicine, 2015, v. 7, n. 1, p. 1, doi. 10.1186/s13073-015-0211-x
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- Publication type:
- Article
Novel EDGE encoding method enhances ability to identify genetic interactions.
- Published in:
- PLoS Genetics, 2021, v. 17, n. 6, p. 1, doi. 10.1371/journal.pgen.1009534
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- Publication type:
- Article
Genetics of height and risk of atrial fibrillation: A Mendelian randomization study.
- Published in:
- 2020
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- Publication type:
- journal article
Genetic risk models: Influence of model size on risk estimates and precision.
- Published in:
- Genetic Epidemiology, 2017, v. 41, n. 4, p. 282, doi. 10.1002/gepi.22035
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- Publication type:
- Article
Biology-Driven Gene-Gene Interaction Analysis of Age-Related Cataract in the eMERGE Network.
- Published in:
- Genetic Epidemiology, 2015, v. 39, n. 5, p. 376, doi. 10.1002/gepi.21902
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- Publication type:
- Article
The Penn Medicine BioBank: Towards a Genomics-Enabled Learning Healthcare System to Accelerate Precision Medicine in a Diverse Population.
- Published in:
- Journal of Personalized Medicine, 2022, v. 12, n. 12, p. 1974, doi. 10.3390/jpm12121974
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- Publication type:
- Article
Evaluating the frequency and the impact of pharmacogenetic alleles in an ancestrally diverse Biobank population.
- Published in:
- 2022
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- Publication type:
- journal article
Uncovering myocardial infarction genetic signatures using GWAS exploration in Saudi and European cohorts.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-49105-1
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- Publication type:
- Article
A GWAS Study on Liver Function Test Using eMERGE Network Participants.
- Published in:
- PLoS ONE, 2015, v. 10, n. 9, p. 1, doi. 10.1371/journal.pone.0138677
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- Publication type:
- Article