Pages that link to "Q37148894"
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The following pages link to Exploring concordance and discordance for return of incidental findings from clinical sequencing (Q37148894):
Displaying 50 items.
- Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech. (Q21198726) (← links)
- Incidental Findings with Genomic Testing: Implications for Genetic Counseling Practice (Q26777211) (← links)
- Do researchers have an obligation to actively look for genetic incidental findings? (Q28654427) (← links)
- Characterizing genetic variants for clinical action (Q28655937) (← links)
- Attitudes of Canadian researchers toward the return to participants of incidental and targeted genomic findings obtained in a pediatric research setting (Q28659644) (← links)
- Ethical and legal implications of whole genome and whole exome sequencing in African populations. (Q28684652) (← links)
- ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing (Q29616235) (← links)
- Public preferences for communicating personal genomic risk information: a focus group study (Q30830961) (← links)
- Genomic sequencing: assessing the health care system, policy, and big-data implications (Q30835712) (← links)
- Self-guided management of exome and whole-genome sequencing results: changing the results return model (Q33566296) (← links)
- Genetic epidemiology: the potential benefits and challenges of using genetic information to improve human health (Q33698750) (← links)
- Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies (Q33737044) (← links)
- Genetics patients' perspectives on clinical genomic testing (Q33771605) (← links)
- Clinical genome sequencing and population preferences for information about 'incidental' findings-From medically actionable genes (MAGs) to patient actionable genes (PAGs) (Q33865515) (← links)
- Returning findings within longitudinal cohort studies: the 1958 birth cohort as an exemplar (Q34040535) (← links)
- Growing up in the genomic era: implications of whole-genome sequencing for children, families, and pediatric practice (Q34157264) (← links)
- Translating personalized medicine using new genetic technologies in clinical practice: the ethical issues (Q34159801) (← links)
- Genomic sequencing for psychiatric disorders: promise and challenge (Q34338419) (← links)
- The Human Gene Mutation Database: building a comprehensive mutation repository for clinical and molecular genetics, diagnostic testing and personalized genomic medicine (Q34374148) (← links)
- Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine (Q34526631) (← links)
- Informed consent for whole-genome sequencing studies in the clinical setting. Proposed recommendations on essential content and process (Q34549035) (← links)
- Promises, pitfalls and practicalities of prenatal whole exome sequencing (Q34558273) (← links)
- An update to returning genetic research results to individuals: perspectives of the industry pharmacogenomics working group (Q35008569) (← links)
- Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium (Q35033000) (← links)
- Lynch syndrome patients' views of and preferences for return of results following whole exome sequencing (Q35671138) (← links)
- Association of Researcher Characteristics with Views on Return of Incidental Findings from Genomic Research (Q35862795) (← links)
- Preferences for the provision of whole genome sequencing services among young adults (Q36320065) (← links)
- The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies (Q36324942) (← links)
- Physicians' perspectives on the uncertainties and implications of chromosomal microarray testing of children and families (Q36481170) (← links)
- High-throughput sequencing and rare genetic diseases. (Q36493309) (← links)
- An informatics approach to analyzing the incidentalome (Q36514318) (← links)
- Compare and contrast: a cross-national study across UK, USA and Greek experts regarding return of incidental findings from clinical sequencing (Q36585040) (← links)
- Ethical Considerations for the Return of Incidental Findings in Ophthalmic Genomic Research (Q36590467) (← links)
- Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records (Q36592201) (← links)
- Disclosure of incidental findings from next-generation sequencing in pediatric genomic research (Q36637088) (← links)
- Incidentalome from Genomic Sequencing: A Barrier to Personalized Medicine? (Q36754075) (← links)
- Dealing with the unexpected: consumer responses to direct-access BRCA mutation testing (Q36773744) (← links)
- Incidental variants are critical for genomics (Q36817320) (← links)
- Preferences for return of incidental findings from genome sequencing among women diagnosed with breast cancer at a young age. (Q36868046) (← links)
- Clinical genomic database (Q36932299) (← links)
- A closer look at the recommended criteria for disclosing genetic results: perspectives of medical genetic specialists, genomic researchers, and institutional review board chairs (Q36983135) (← links)
- Return of results in translational iPS cell research: considerations for donor informed consent (Q36998497) (← links)
- The attitudes of people with sarcoma and their family towards genomics and incidental information arising from genetic research (Q37116458) (← links)
- Management of incidental findings in clinical genomic sequencing (Q37148891) (← links)
- Returning genetic research results: study type matters (Q37198193) (← links)
- Disease-targeted sequencing: a cornerstone in the clinic (Q37205397) (← links)
- Managing incidental genomic findings: legal obligations of clinicians (Q37248265) (← links)
- Views of genetics health professionals on the return of genomic results. (Q37257165) (← links)
- Genomic sequencing in clinical practice: applications, challenges, and opportunities (Q37344774) (← links)
- Stakeholders' opinions on the implementation of pediatric whole exome sequencing: implications for informed consent (Q37360685) (← links)