Found: 43
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Evaluating construct validity of computable acute respiratory distress syndrome definitions in adults hospitalized with COVID-19: an electronic health records based approach.
- Published in:
- BMC Pulmonary Medicine, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12890-023-02560-y
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- Article
Quantifying the phenome‐wide disease burden of obesity using electronic health records and genomics.
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- Obesity (19307381), 2022, v. 30, n. 12, p. 2477, doi. 10.1002/oby.23561
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- Article
Uterine fibroid polygenic risk score (PRS) associates and predicts risk for uterine fibroid.
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- Human Genetics, 2022, v. 141, n. 11, p. 1739, doi. 10.1007/s00439-022-02442-z
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- Article
Penetrance of Breast Cancer Susceptibility Genes From the eMERGE III Network.
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- JNCI Cancer Spectrum, 2021, v. 5, n. 4, p. 1, doi. 10.1093/jncics/pkab044
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- Article
The FamilyTalk randomized controlled trial: patient-reported outcomes in clinical genetic sequencing for colorectal cancer.
- Published in:
- 2021
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- Publication type:
- journal article
Loci identified by a genome‐wide association study of carotid artery stenosis in the eMERGE network.
- Published in:
- Genetic Epidemiology, 2021, v. 45, n. 1, p. 4, doi. 10.1002/gepi.22360
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- Article
Association between triglycerides, known risk SNVs and conserved rare variation in SLC25A40 in a multi-ancestry cohort.
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- BMC Medical Genomics, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s12920-020-00854-2
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- Article
The polygenic architecture of left ventricular mass mirrors the clinical epidemiology.
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- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-64525-z
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- Article
A Polygenic and Phenotypic Risk Prediction for Polycystic Ovary Syndrome Evaluated by Phenome-Wide Association Studies.
- Published in:
- 2020
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- Publication type:
- journal article
Association of Genetic Risk of Obesity with Postoperative Complications Using Mendelian Randomization.
- Published in:
- World Journal of Surgery, 2020, v. 44, n. 1, p. 84, doi. 10.1007/s00268-019-05202-9
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- Article
A phenome-wide association study to discover pleiotropic effects of PCSK9, APOB, and LDLR.
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- NPJ Genomic Medicine, 2019, v. 4, n. 1, p. N.PAG, doi. 10.1038/s41525-019-0078-7
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- Article
A phenome-wide association study to discover pleiotropic effects of PCSK9, APOB, and LDLR.
- Published in:
- NPJ Genomic Medicine, 2019, v. 4, n. 1, p. N.PAG, doi. 10.1038/s41525-019-0078-7
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- Publication type:
- Article
A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-05624-4
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- Article
A vascular endothelial growth factor A genetic variant is associated with improved ventricular function and transplant-free survival after surgery for non-syndromic CHD.
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- 2018
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- Publication type:
- journal article
Building a family network from genetic testing.
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- Molecular Genetics & Genomic Medicine, 2017, v. 5, n. 2, p. 122, doi. 10.1002/mgg3.259
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- Article
Association Between Absolute Neutrophil Count and Variation at TCIRG1: The NHLBI Exome Sequencing Project.
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- Genetic Epidemiology, 2016, v. 40, n. 6, p. 470, doi. 10.1002/gepi.21976
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- Article
eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants.
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- BMC Medical Genomics, 2016, v. 9, p. 19, doi. 10.1186/s12920-016-0191-8
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- Publication type:
- Article
Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms.
- Published in:
- 2016
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- Publication type:
- journal article
Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records.
- Published in:
- 2016
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- Publication type:
- journal 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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- Article
Biology-Driven Gene-Gene Interaction Analysis of Age-Related Cataract in the eMERGE Network.
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- Genetic Epidemiology, 2015, v. 39, n. 5, p. 376, doi. 10.1002/gepi.21902
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- Article
Prospective participant selection and ranking to maximize actionable pharmacogenetic variants and discovery in the eMERGE Network.
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- Genome Medicine, 2015, v. 7, n. 1, p. 1, doi. 10.1186/s13073-015-0181-z
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- Article
Genetic Variants Associated with Serum Thyroid Stimulating Hormone (TSH) Levels in European Americans and African Americans from the eMERGE Network.
- Published in:
- PLoS ONE, 2014, v. 9, n. 12, p. 1, doi. 10.1371/journal.pone.0111301
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- 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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- Article
Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index.
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- Frontiers in Genetics, 2014, v. 5, p. 1, doi. 10.3389/fgene.2014.00250
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- Article
eMERGEing progress in genomics--the first seven years.
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- Frontiers in Genetics, 2014, v. 5, p. 1, doi. 10.3389/fgene.2014.00184
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- Article
eMERGEing progress in genomics---the first seven years.
- Published in:
- Frontiers in Genetics, 2014, v. 5, p. 1, doi. 10.3389/fgene.2014.00184
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- Publication type:
- Article
Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data.
- Published in:
- Nature Biotechnology, 2013, v. 31, n. 12, p. 1102, doi. 10.1038/nbt.2749
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- Article
Mechanistic Phenotypes: An Aggregative Phenotyping Strategy to Identify Disease Mechanisms Using GWAS Data.
- Published in:
- PLoS ONE, 2013, v. 8, n. 12, p. 1, doi. 10.1371/journal.pone.0081503
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- Article
Enhancing the Power of Genetic Association Studies through the Use of Silver Standard Cases Derived from Electronic Medical Records.
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- PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0063481
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- Article
Genetic variation associated with circulating monocyte count in the eMERGE Network.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 10, p. 2119, doi. 10.1093/hmg/ddt010
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- Article
Confirmation of the Reported Association of Clonal Chromosomal Mosaicism with an Increased Risk of Incident Hematologic Cancer.
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- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0059823
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- Article
GWASTools: an R/Bioconductor package for quality control and analysis of genome-wide association studies.
- Published in:
- Bioinformatics, 2012, v. 28, n. 24, p. 3329, doi. 10.1093/bioinformatics/bts610
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- Article
Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study.
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- Journal of the American Medical Informatics Association, 2012, v. 19, n. 2, p. 212, doi. 10.1136/amiajnl-2011-000439
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- Article
Genome-wide association Scan of dental caries in the permanent dentition.
- Published in:
- BMC Oral Health, 2012, v. 12, n. 1, p. 1, doi. 10.1186/1472-6831-12-57
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- Article
Genome-wide association Scan of dental caries in the permanent dentition.
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- BMC Oral Health, 2012, v. 12, n. 1, p. 57, doi. 10.1186/1472-6831-12-57
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- Article
Aging-related atherosclerosis is exacerbated by arterial expression of tumor necrosis factor receptor-1: evidence from mouse models and human association studies.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 14, p. 2754, doi. 10.1093/hmg/ddq172
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- Article
Assessment of LD Matrix Measures for the Analysis of Biological Pathway Association.
- Published in:
- Statistical Applications in Genetics & Molecular Biology, 2010, v. 9, n. 1, p. 1, doi. 10.2202/1544-6115.1561
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- Article
Genetic effects in the leukotriene biosynthesis pathway and association with atherosclerosis.
- Published in:
- Human Genetics, 2009, v. 125, n. 2, p. 217, doi. 10.1007/s00439-008-0619-0
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- Article
Neuropeptide Y Gene Polymorphisms Confer Risk of Early-Onset Atherosclerosis.
- Published in:
- PLoS Genetics, 2009, v. 5, n. 1, p. 1, doi. 10.1371/journal.pgen.1000318
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- Article
Comprehensive genetic analysis of the platelet activating factor acetylhydrolase (PLA2G7) gene and cardiovascular disease in case–control and family datasets.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 9, p. 1318, doi. 10.1093/hmg/ddn020
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- Article
Genetic and functional association of FAM5C with myocardial infarction.
- Published in:
- BMC Medical Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2350-9-33
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- Publication type:
- Article
GATA2 Is Associated with Familial Early-Onset Coronary Artery Disease.
- Published in:
- PLoS Genetics, 2006, v. 3, n. 2, p. e139, doi. 10.1371/journal.pgen.0020139
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- Article