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PLON, SHARON

One or more keywords matched the following properties of PLON, SHARON

Property	Value
keywords	cancer genetics, genetic testing, medical genetics, genomic instability, clinical genomics

One or more keywords matched the following items that are connected to PLON, SHARON

Item Type	Name
Academic Article	Susceptibility to insulin-dependent diabetes mellitus maps to a locus (IDDM11) on human chromosome 14q24.3-q31.
Academic Article	The practice of adult genetics: a 7-year experience from a single center.
Concept	Genomics
Academic Article	Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium.
Academic Article	Clinical tumor sequencing: an incidental casualty of the American College of Medical Genetics and Genomics recommendations for reporting of incidental findings.
Academic Article	Molecular findings among patients referred for clinical whole-exome sequencing.
Academic Article	Pharmacogenetic characterization of naturally occurring germline NT5C1A variants to chemotherapeutic nucleoside analogs.
Academic Article	Identifying gene disruptions in novel balanced de novo constitutional translocations in childhood cancer patients by whole-genome sequencing.
Academic Article	CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record.
Academic Article	Pediatric Cancer Genetics Research and an Evolving Preventive Ethics Approach for Return of Results after Death of the Subject.
Academic Article	Germline Findings in Tumor-Only Sequencing: Points to Consider for Clinicians and Laboratories.
Academic Article	Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.
Academic Article	Current state of pediatric sarcoma biology and opportunities for future discovery: A report from the sarcoma translational research workshop.
Academic Article	Recommendations for the integration of genomics into clinical practice.
Academic Article	Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium.
Academic Article	Lessons learned from additional research analyses of unsolved clinical exome cases.
Academic Article	Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource.
Academic Article	Key Implications of Data Sharing in Pediatric Genomics.
Academic Article	Portero versus portador: Spanish interpretation of genomic terminology during whole exome sequencing results disclosure.
Academic Article	The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations.
Academic Article	Development of Clinical Domain Working Groups for the Clinical Genome Resource (ClinGen): lessons learned and plans for the future.
Academic Article	Integrating somatic variant data and biomarkers for germline variant classification in cancer predisposition genes.
Academic Article	The clinical imperative for inclusivity: Race, ethnicity, and ancestry (REA) in genomics.
Academic Article	Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline CDH1 sequence variants.
Academic Article	ClinGen Variant Curation Expert Panel experiences and standardized processes for disease and gene-level specification of the ACMG/AMP guidelines for sequence variant interpretation.
Academic Article	Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.
Academic Article	Agents of empathy: How medical interpreters bridge sociocultural gaps in genomic sequencing disclosures with Spanish-speaking families.
Grant	Clinically Relevant Genome Variation Database
Grant	Evaluating utility and improving implementation of genomic sequencing for pediatric cancer patients in the diverse population and healthcare settings of Texas: The KidsCanSeq Study
Grant	Clinical Genome Resource (ClinGen)
Grant	Do Physicians Understand Uncertain Variants and Other Genetic Test Results?
Academic Article	Genetic Predisposition to Childhood Cancer in the Genomic Era.
Academic Article	Responsibility, culpability, and parental views on genomic testing for seriously ill children.
Academic Article	ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variants.
Academic Article	A case for expert curation: an overview of cancer curation in the Clinical Genome Resource (ClinGen).
Academic Article	A brief history of human disease genetics.
Academic Article	Points to consider for reporting of germline variation in patients undergoing tumor testing: a statement of the American College of Medical Genetics and Genomics (ACMG).
Academic Article	Clinical Genetics Lacks Standard Definitions and Protocols for the Collection and Use of Diversity Measures.
Academic Article	Genomic analysis and preclinical xenograft model development identify potential therapeutic targets for MYOD1-mutant soft-tissue sarcoma of childhood.
Academic Article	ClinGen Variant Curation Interface: a variant classification platform for the application of evidence criteria from ACMG/AMP guidelines.
Academic Article	Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC).
Academic Article	Views of Adolescents and Young Adults with Cancer and Their Oncologists Toward Patients' Participation in Genomic Research.
Academic Article	Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC).
Academic Article	The genomic landscape of familial glioma.
Academic Article	Ten Years of Incidental, Secondary, and Actionable Findings.
Academic Article	Should secondary pharmacogenomic variants be actively screened and reported when diagnostic genome-wide sequencing is performed in a child?

Search Criteria

Genomics