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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
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- 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
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- 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
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- 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
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- Publication type:
- Article
Enrichment sampling for a multi-site patient survey using electronic health records and census data.
- Published in:
- 2019
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- 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
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- 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
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- Publication type:
- journal 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
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- 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
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- 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
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- 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
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- 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
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- 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
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- Publication type:
- Article
Preface.
- Published in:
- Genetic Epidemiology, 1999, v. 17, p. Sxxxi, doi. 10.1002/gepi.1370170702
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- 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
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- 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
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- 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
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- Publication type:
- Article
47 Cross-ancestry GWAS meta-analysis of keloids discovers novel susceptibility loci in diverse populations.
- Published in:
- 2024
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- 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
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- 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
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- 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
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- 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
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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
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
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
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
Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records.
- Published in:
- 2016
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- 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
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- 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
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- 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
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- 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
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- 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
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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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- 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
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- 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
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- 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
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- 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
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- 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
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- Publication type:
- Article
National Institutes of Health State-of-the-Science Conference Statement: Family History and Improving Health.
- Published in:
- 2009
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- 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
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- Publication type:
- Article
Childhood exposures to environmental chemicals and neurodevelopmental outcomes in congenital heart disease.
- Published in:
- PLoS ONE, 2022, v. 17, n. 11, p. 1, doi. 10.1371/journal.pone.0277611
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- Publication type:
- 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
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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- Publication type:
- Article
A case for expanding carrier testing to include actionable X‐linked disorders.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
The polygenic architecture of left ventricular mass mirrors the clinical epidemiology.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-64525-z
- 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
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- 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
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- 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
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- 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
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- Publication type:
- Article
Risk‐reducing surgery in unaffected individuals receiving cancer genetic testing in an integrated health care system.
- Published in:
- Cancer (0008543X), 2022, v. 128, n. 16, p. 3090, doi. 10.1002/cncr.34349
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- Publication type:
- Article