The SickKids Genome Clinic: developing and evaluating a pediatric model for individualized genomic medicine. - Wikidata - wikimedia - TriplyDB

The SickKids Genome Clinic: developing and evaluating a pediatric model for individualized genomic medicine.

The SickKids Genome Clinic: developing and evaluating a pediatric model for individualized genomic medicine.

http://www.wikidata.org/entity/Q38392363

about

Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies.Clinical care models in the era of next-generation sequencing.My46: a Web-based tool for self-guided management of genomic test results in research and clinical settings Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test.A microcosting and cost-consequence analysis of clinical genomic testing strategies in autism spectrum disorder.Expect the unexpected: screening for secondary findings in clinical genomics research.Genetic Testing among Children in a Complex Care Program.The clinical utility of next-generation sequencing in the neonatal intensive care unit Care and cost consequences of pediatric whole genome sequencing compared to chromosome microarray.Views of rare disease participants in a UK whole-genome sequencing study towards secondary findings: a qualitative study.

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P2860

The SickKids Genome Clinic: developing and evaluating a pediatric model for individualized genomic medicine.

http://www.wikidata.org/entity/Q38392363

description

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N Monfared

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R D Cohn

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R Z Hayeems

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S C Bowdin

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P2860

Comparison of family history and SNPs for predicting risk of complex disease

A guide for functional analysis of BRCA1 variants of uncertain significance

Recommendations for returning genomic incidental findings? We need to talk!

Beyond diagnostic accuracy: the clinical utility of diagnostic tests

Return of individual research results and incidental findings: facing the challenges of translational science

Presymptomatic and predictive genetic testing in minors: a systematic review of guidelines and position papers

Reflections on the cost of "low-cost" whole genome sequencing: framing the health policy debate

The implications of familial incidental findings from exome sequencing: the NIH Undiagnosed Diseases Program experience

Integrating multiple genomic data to predict disease-causing nonsynonymous single nucleotide variants in exome sequencing studies.

High burden of private mutations due to explosive human population growth and purifying selection

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10.1111/CGE.12579

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