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Genomics of the NF-κB signaling pathway: hypothesized role in ovarian cancer.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Linkage and association analyses identify a candidate region for apoB level on chromosome 4q32.3 in FCHL families.
- Published in:
- Human Genetics, 2010, v. 127, n. 6, p. 705, doi. 10.1007/s00439-010-0819-2
- By:
- 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
- By:
- Publication type:
- Article
Genome scan for quantitative trait loci influencing HDL levels: evidence for multilocus inheritance in familial combined hyperlipidemia.
- Published in:
- Human Genetics, 2005, v. 117, n. 5, p. 494, doi. 10.1007/s00439-005-1338-4
- By:
- Publication type:
- Article
Evidence of linkage of HDL level variation to APOC3 in two samples with different ascertainment.
- Published in:
- Human Genetics, 2003, v. 113, n. 6, p. 522, doi. 10.1007/s00439-003-1006-5
- By:
- Publication type:
- Article
Harmonizing Outcomes for Genomic Medicine: Comparison of eMERGE Outcomes to ClinGen Outcome/Intervention Pairs.
- Published in:
- Healthcare (2227-9032), 2018, v. 6, n. 3, p. 83, doi. 10.3390/healthcare6030083
- By:
- Publication type:
- Article
A research agenda to support the development and implementation of genomics-based clinical informatics tools and resources.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Enrichment sampling for a multi-site patient survey using electronic health records and census data.
- Published in:
- 2019
- By:
- Publication type:
- journal article
CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record.
- Published in:
- 2015
- By:
- Publication type:
- journal 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.
- Published in:
- 2018
- By:
- 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
- By:
- Publication type:
- Article
The eMERGE Network: A consortium of biorepositories linked to electronic medical records data for conducting genomic studies.
- Published in:
- BMC Medical Genomics, 2011, v. 4, n. 1, p. 13, doi. 10.1186/1755-8794-4-13
- By:
- Publication type:
- Article
Barriers to family history knowledge and family communication among LGBTQ+ individuals in the context of hereditary cancer risk assessment.
- Published in:
- Journal of Genetic Counseling, 2022, v. 31, n. 1, p. 230, doi. 10.1002/jgc4.1476
- By:
- Publication type:
- Article
Insurance coverage does not predict outcomes of genetic testing: The search for meaning in payer decisions for germline cancer tests.
- Published in:
- Journal of Genetic Counseling, 2019, v. 28, n. 6, p. 1208, doi. 10.1002/jgc4.1155
- By:
- Publication type:
- Article
The Feelings About genomiC Testing Results (FACToR) Questionnaire: Development and Preliminary Validation.
- Published in:
- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 477, doi. 10.1007/s10897-018-0286-9
- By:
- Publication type:
- Article
Next Generation Sequencing in the Clinic: a Patterns of Care Study in a Retrospective Cohort of Subjects Referred to a Genetic Medicine Clinic for Suspected Lynch Syndrome.
- Published in:
- Journal of Genetic Counseling, 2016, v. 25, n. 3, p. 515, doi. 10.1007/s10897-015-9902-0
- By:
- Publication type:
- Article
Assessment and implications of linkage disequilibrium in genome-wide single-nucleotide polymorphism and microsatellite panels.
- Published in:
- Genetic Epidemiology, 2005, v. 29, n. S1, p. S72, doi. 10.1002/gepi.20112
- By:
- Publication type:
- Article
Linkage analysis of 150 high-risk prostate cancer families at 1q24-25.
- Published in:
- Genetic Epidemiology, 2000, v. 18, n. 3, p. 251, doi. 10.1002/(SICI)1098-2272(200003)18:3<251::AID-GEPI5>3.0.CO;2-X
- By:
- Publication type:
- Article
Preface.
- Published in:
- Genetic Epidemiology, 1999, v. 17, p. Sxxxi, doi. 10.1002/gepi.1370170702
- By:
- Publication type:
- Article
Impact of family structure on the power of linkage tests using sib-pair methods.
- Published in:
- Genetic Epidemiology, 1999, v. 17, p. S575, doi. 10.1002/gepi.1370170793
- By:
- Publication type:
- Article
Segregation and linkage analysis of a quantitative versus a qualitative trait in large pedigrees.
- Published in:
- Genetic Epidemiology, 1997, v. 14, n. 6, p. 999, doi. 10.1002/(SICI)1098-2272(1997)14:6<999::AID-GEPI73>3.0.CO;2-F
- By:
- Publication type:
- Article
Genetic influences on age-related change in total cholesterol, low density lipoprotein-cholesterol and triglyceride levels: Longitudinal apolipoprotein E genotype effects.
- Published in:
- Genetic Epidemiology, 1994, v. 11, n. 4, p. 375, doi. 10.1002/gepi.1370110407
- By:
- Publication type:
- Article
Genotype at a major locus with large effects on apolipoprotein B levels predicts familial combined hyperlipidemia.
- Published in:
- Genetic Epidemiology, 1993, v. 10, n. 4, p. 257, doi. 10.1002/gepi.1370100406
- By:
- Publication type:
- Article
Genetic Linkage Analysis of Prostate Cancer Families to Xq27-28.
- Published in:
- Human Heredity, 2001, v. 51, n. 1/2, p. 107, doi. 10.1159/000022965
- By:
- Publication type:
- Article
The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities.
- Published in:
- Communications Biology, 2024, v. 7, n. 1, p. 1, doi. 10.1038/s42003-023-05708-y
- By:
- Publication type:
- Article
Author Correction: The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities.
- Published in:
- 2024
- By:
- Publication type:
- Correction Notice
47 Cross-ancestry GWAS meta-analysis of keloids discovers novel susceptibility loci in diverse populations.
- Published in:
- 2024
- By:
- Publication type:
- Abstract
Heritability and genome-wide association study of benign prostatic hyperplasia (BPH) in the eMERGE network.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-42427-z
- By:
- Publication type:
- Article
Genetic sex validation for sample tracking in next-generation sequencing clinical testing.
- Published in:
- BMC Research Notes, 2024, v. 17, n. 1, p. 1, doi. 10.1186/s13104-024-06723-w
- By:
- Publication type:
- Article
Mendelian randomization analysis of plasma levels of CD209 and MICB proteins and the risk of varicose veins of lower extremities.
- Published in:
- PLoS ONE, 2022, v. 17, n. 5, p. 1, doi. 10.1371/journal.pone.0268725
- By:
- Publication type:
- Article
Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study.
- Published in:
- Journal of the American Medical Informatics Association, 2012, v. 19, n. 2, p. 212, doi. 10.1136/amiajnl-2011-000439
- By:
- Publication type:
- Article
Development of FamilyTalk: an Intervention to Support Communication and Educate Families About Colorectal Cancer Risk.
- Published in:
- 2020
- By:
- Publication type:
- journal 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
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
- By:
- Publication type:
- 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
- By:
- Publication type:
- 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
- By:
- Publication type:
- Article
Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations.
- Published in:
- Genome Medicine, 2022, v. 14, p. 1, doi. 10.1186/s13073-022-01074-2
- By:
- Publication type:
- Article
Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations.
- Published in:
- Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01074-2
- By:
- Publication type:
- Article
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.
- Published in:
- Nature Genetics, 2011, v. 43, n. 5, p. 436, doi. 10.1038/ng.801
- By:
- Publication type:
- Article
Longitudinal adherence to breast cancer surveillance following cancer genetic testing in an integrated health care system.
- Published in:
- Breast Cancer Research & Treatment, 2023, v. 201, n. 3, p. 461, doi. 10.1007/s10549-023-07007-w
- By:
- Publication type:
- Article
Pleiotropy in the Genetic Predisposition to Rheumatoid Arthritis: A Phenome‐Wide Association Study and Inverse Variance–Weighted Meta‐Analysis.
- Published in:
- Arthritis & Rheumatology, 2020, v. 72, n. 9, p. 1483, doi. 10.1002/art.41291
- By:
- 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
- By:
- Publication type:
- Article
Additional Common Polymorphisms in the PON Gene Cluster Predict PON1 Activity but Not Vascular Disease.
- Published in:
- Journal of Lipids, 2012, p. 1, doi. 10.1155/2012/476316
- By:
- Publication type:
- Article
Refining the structure and content of clinical genomic reports.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2014, v. 166C, n. 1, p. 85, doi. 10.1002/ajmg.c.31395
- By:
- Publication type:
- Article
Return of results: Ethical and legal distinctions between research and clinical care.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2014, v. 166C, n. 1, p. 105, doi. 10.1002/ajmg.c.31393
- By:
- Publication type:
- Article
Characterizing genetic variants for clinical action.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2014, v. 166C, n. 1, p. 93, doi. 10.1002/ajmg.c.31386
- By:
- Publication type:
- Article
Sequencing of sporadic Attention-Deficit Hyperactivity Disorder (ADHD) identifies novel and potentially pathogenic de novo variants and excludes overlap with genes associated with autism spectrum disorder.
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2017, v. 174, n. 4, p. 381, doi. 10.1002/ajmg.b.32527
- By:
- Publication type:
- Article
National Institutes of Health State-of-the-Science Conference Statement: Family History and Improving Health.
- Published in:
- 2009
- By:
- Publication type:
- Proceeding
Interaction between Fibrinogen and IL-6 Genetic Variants and Associations with Cardiovascular Disease Risk in the Cardiovascular Health Study.
- Published in:
- Annals of Human Genetics, 2010, v. 74, n. 1, p. 1, doi. 10.1111/j.1469-1809.2009.00551.x
- By:
- Publication type:
- Article