Found: 116
Select item for more details and to access through your institution.
Genomics of the NF-κB signaling pathway: hypothesized role in ovarian cancer.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Germline mutations in the p73 gene do not predispose to familial prostate-brain cancer.
- Published in:
- Prostate, 2001, v. 48, n. 4, p. 292, doi. 10.1002/pros.1109
- By:
- Publication type:
- Article
Understanding the Return of Genomic Sequencing Results Process: Content Review of Participant Summary Letters in the eMERGE Research Network.
- Published in:
- Journal of Personalized Medicine, 2020, v. 10, n. 2, p. 38, doi. 10.3390/jpm10020038
- By:
- Publication type:
- Article
Returning Results in the Genomic Era: Initial Experiences of the eMERGE Network.
- Published in:
- Journal of Personalized Medicine, 2020, v. 10, n. 2, p. 30, doi. 10.3390/jpm10020030
- By:
- Publication type:
- Article
Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-30678-w
- By:
- Publication type:
- Article
Evidence for genetic influences on smoking in adult women twins.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 5, p. 236, doi. 10.1111/j.1399-0004.1995.tb04303.x
- 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
A Polygenic and Phenotypic Risk Prediction for Polycystic Ovary Syndrome Evaluated by Phenome-Wide Association Studies.
- Published in:
- 2020
- By:
- Publication type:
- journal 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
Uterine fibroid polygenic risk score (PRS) associates and predicts risk for uterine fibroid.
- Published in:
- Human Genetics, 2022, v. 141, n. 11, p. 1739, doi. 10.1007/s00439-022-02442-z
- By:
- Publication type:
- Article
Heritability of longitudinal measures of body mass index and lipid and lipoprotein levels in aging twins.
- Published in:
- 2007
- By:
- Publication type:
- journal 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
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
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
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
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
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
Returning negative results from large‐scale genomic screening: Experiences from the eMERGE III network.
- Published in:
- American Journal of Medical Genetics. Part A, 2021, v. 185, n. 2, p. 508, doi. 10.1002/ajmg.a.62002
- By:
- Publication type:
- Article
Patients' ratings of genetic conditions validate a taxonomy to simplify decisions about preconception carrier screening via genome sequencing.
- Published in:
- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 3, p. 574, doi. 10.1002/ajmg.a.37477
- By:
- Publication type:
- Article
Generating a taxonomy for genetic conditions relevant to reproductive planning.
- Published in:
- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 3, p. 565, doi. 10.1002/ajmg.a.37513
- 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
"Getting off the Bus Closer to Your Destination": Patients' Views about Pharmacogenetic Testing.
- Published in:
- Permanente Journal, 2015, v. 19, n. 3, p. 21, doi. 10.7812/TPP/15-046
- 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
Clinical associations with a polygenic predisposition to benign lower white blood cell counts.
- Published in:
- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-47804-5
- By:
- Publication type:
- 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
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
- By:
- Publication type:
- 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
- By:
- Publication type:
- 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
- By:
- Publication type:
- Article
Confirmation of the Reported Association of Clonal Chromosomal Mosaicism with an Increased Risk of Incident Hematologic Cancer.
- Published in:
- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0059823
- By:
- Publication type:
- Article
Results of Genome-Wide Analyses on Neurodevelopmental Phenotypes at Four-Year Follow- Up following Cardiac Surgery in Infancy.
- Published in:
- PLoS ONE, 2012, v. 7, n. 9, p. 1, doi. 10.1371/journal.pone.0045936
- By:
- Publication type:
- Article
Identification of Four Novel Loci in Asthma in European American and African American Populations.
- Published in:
- 2017
- By:
- Publication type:
- journal article
The FamilyTalk randomized controlled trial: patient-reported outcomes in clinical genetic sequencing for colorectal cancer.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Penetrance of Breast Cancer Susceptibility Genes From the eMERGE III Network.
- Published in:
- JNCI Cancer Spectrum, 2021, v. 5, n. 4, p. 1, doi. 10.1093/jncics/pkab044
- By:
- Publication type:
- Article
Rare loss of function variants in candidate genes and risk of colorectal cancer.
- Published in:
- Human Genetics, 2018, v. 137, n. 10, p. 795, doi. 10.1007/s00439-018-1938-4
- By:
- Publication type:
- Article
Identifying gene-gene interactions that are highly associated with four quantitative lipid traits across multiple cohorts.
- Published in:
- Human Genetics, 2017, v. 136, n. 2, p. 165, doi. 10.1007/s00439-016-1738-7
- By:
- Publication type:
- Article
A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects.
- Published in:
- Human Genetics, 2014, v. 133, n. 1, p. 95, doi. 10.1007/s00439-013-1355-7
- By:
- Publication type:
- 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
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
- By:
- Publication type:
- 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
- By:
- Publication type:
- Article
47 Cross-ancestry GWAS meta-analysis of keloids discovers novel susceptibility loci in diverse populations.
- Published in:
- 2024
- By:
- Publication type:
- Abstract
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
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
- By:
- 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