Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.
about
Mutations in EBF3 Disturb Transcriptional Profiles and Cause Intellectual Disability, Ataxia, and Facial DysmorphismAssigning clinical meaning to somatic and germ-line whole-exome sequencing data in a prospective cancer precision medicine study.Challenges and strategies for implementing genomic services in diverse settings: experiences from the Implementing GeNomics In pracTicE (IGNITE) networkGenomic diagnosis for children with intellectual disability and/or developmental delayGenome sequencing and carrier testing: decisions on categorization and whether to disclose results of carrier testing.Newborn Sequencing in Genomic Medicine and Public Health.Taming the genome: towards better genetic test interpretation.Genomic sequencing in clinical practice: applications, challenges, and opportunities.Information Topics of Greatest Interest for Return of Genome Sequencing Results among Women Diagnosed with Breast Cancer at a Young Age.Navigating the research-clinical interface in genomic medicine: analysis from the CSER Consortium.Exploring the feasibility of delivering standardized genomic care using ophthalmology as an example.Precision medicine in pediatric oncology: Lessons learned and next steps.Implementing genomics and pharmacogenomics in the clinic: The National Human Genome Research Institute's genomic medicine portfolio.Clinical laboratories collaborate to resolve differences in variant interpretations submitted to ClinVar.The current state of implementation science in genomic medicine: opportunities for improvement.Aggregate penetrance of genomic variants for actionable disorders in European and African Americans.Recent advances in genetic testing for familial hypercholesterolemia.Consideration of Cosegregation in the Pathogenicity Classification of Genomic Variants.Genetic identification of a common collagen disease in puerto ricans via identity-by-descent mapping in a health system.The fuzzy world of precision medicine: deliberations of a precision medicine tumor board.How do providers discuss the results of pediatric exome sequencing with families?The NextGen Study: patient motivation for participation in genome sequencing for carrier status.No Panacea: Next-Gen Sequencing Will Not Mitigate Adoptees' Lack of Genetic Family Health History.Genomic medicine for kidney disease.Characterizing reduced coverage regions through comparison of exome and genome sequencing data across 10 centers.The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients: A Pilot Randomized Trial.Genetic prediction of myopia: prospects and challenges.Utility and limitations of exome sequencing in the molecular diagnosis of pediatric inherited platelet disorders.Anticipated responses of early adopter genetic specialists and nongenetic specialists to unsolicited genomic secondary findings.Communication challenges for nongeneticist physicians relaying clinical genomic results.Research directions in the clinical implementation of pharmacogenomics - An Overview of US programs and projects.Improving -Omics-Based Research and Precision Health in Minority Populations: Recommendations for Nurse Scientists.An Observational Study of Children's Involvement in Informed Consent for Exome Sequencing Research.Analysis of state laws on informed consent for clinical genetic testing in the era of genomic sequencing.Genetic counselling in the era of genomic medicine.Why Patients Decline Genomic Sequencing Studies: Experiences from the CSER Consortium.Clinical providers' experiences with returning results from genomic sequencing: an interview study.Clinotator: analyzing ClinVar variation reports to prioritize reclassification efforts.Integrating next-generation sequencing into pediatric oncology practice: An assessment of physician confidence and understanding of clinical genomics.Assessment of willingness to pay for expanded carrier screening among women and couples undergoing preconception carrier screening
P2860
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P2860
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.
description
2016 nî lūn-bûn
@nan
2016 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2016 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
name
Clinical Sequencing Explorator ...... Practice of Genomic Medicine.
@ast
Clinical Sequencing Explorator ...... Practice of Genomic Medicine.
@en
Clinical Sequencing Explorator ...... Practice of Genomic Medicine.
@nl
type
label
Clinical Sequencing Explorator ...... Practice of Genomic Medicine.
@ast
Clinical Sequencing Explorator ...... Practice of Genomic Medicine.
@en
Clinical Sequencing Explorator ...... Practice of Genomic Medicine.
@nl
prefLabel
Clinical Sequencing Explorator ...... Practice of Genomic Medicine.
@ast
Clinical Sequencing Explorator ...... Practice of Genomic Medicine.
@en
Clinical Sequencing Explorator ...... Practice of Genomic Medicine.
@nl
P2093
P2860
P50
P1476
Clinical Sequencing Explorator ...... Practice of Genomic Medicine.
@en
P2093
Amy McGuire
Arul M Chinnaiyan
Brian Shirts
CSER Consortium
Carolyn M Hutter
Carrie L Blout
Charlisse F Caga-Anan
Dan Robinson
David Kaufman
David L Veenstra
P2860
P304
P356
10.1016/J.AJHG.2016.04.011
P407
P50
P577
2016-05-12T00:00:00Z