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PLON, SHARON

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

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overview	Dr. Sharon Plon is a board-certified medical geneticist and a longstanding cancer genetics researcher identifying new cancer susceptibility genes and stuyding the implementation of genomic testing in medicine. Dr. Plon holds the Dan L Duncan Comprehensive Cancer Center Professorship at Baylor College of Medicine. Dr. Plon served as PI with Donald (Will) Parsons and Amy McGuire on the NHGRI/NCI- U01 Texas KidsCanSeq multi-institutional trial that studied the incorporation of CLIA clinical genome-scale exome sequencing into the care of childhood cancer patients in the diverse patient populations in Texas. Since 2013, Dr. Plon has served as one of the Principal Investigators of the Clinical Genome (ClinGen) Resource and co-chairs the ClinGen hereditary cancer effort. She also currently co-chairs the germline reporting effort of the national NCI/COG Pediatric MATCH Precision Oncology trial. She is also working closely with Dr. Philip Lupo on a population-based study to understand the association between birth defects and cancer risk in children. Dr. Plon recently served on the Board of Directors of the American Society of Human Genetics and was a member of the Human Genome Research Advisory Council of the National Human Genome Research Institute from 2017-2020. She is the Assistant Dean of Dual Degree Programs and Pathways in the School of Medicine at Baylor College of Medicine.

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overview

Dr. Sharon Plon is a board-certified medical geneticist and a longstanding cancer genetics researcher identifying new cancer susceptibility genes and stuyding the implementation of genomic testing in medicine. Dr. Plon holds the Dan L Duncan Comprehensive Cancer Center Professorship at Baylor College of Medicine. Dr. Plon served as PI with Donald (Will) Parsons and Amy McGuire on the NHGRI/NCI- U01 Texas KidsCanSeq multi-institutional trial that studied the incorporation of CLIA clinical genome-scale exome sequencing into the care of childhood cancer patients in the diverse patient populations in Texas. Since 2013, Dr. Plon has served as one of the Principal Investigators of the Clinical Genome (ClinGen) Resource and co-chairs the ClinGen hereditary cancer effort. She also currently co-chairs the germline reporting effort of the national NCI/COG Pediatric MATCH Precision Oncology trial. She is also working closely with Dr. Philip Lupo on a population-based study to understand the association between birth defects and cancer risk in children. Dr. Plon recently served on the Board of Directors of the American Society of Human Genetics and was a member of the Human Genome Research Advisory Council of the National Human Genome Research Institute from 2017-2020. She is the Assistant Dean of Dual Degree Programs and Pathways in the School of Medicine at Baylor College of Medicine.

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

Item Type	Name
Academic Article	Identification of TP53 as an acute lymphocytic leukemia susceptibility gene through exome sequencing.
Academic Article	A survey of informatics approaches to whole-exome and whole-genome clinical reporting in the electronic health record.
Academic Article	Clinical whole-exome sequencing for the diagnosis of mendelian disorders.
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	Genetic diagnosis through whole-exome sequencing.
Academic Article	De novo truncating mutations in AHDC1 in individuals with syndromic expressive language delay, hypotonia, and sleep apnea.
Academic Article	Obtaining informed consent for clinical tumor and germline exome sequencing of newly diagnosed childhood cancer patients.
Academic Article	Molecular findings among patients referred for clinical whole-exome sequencing.
Academic Article	Germline mutations in shelterin complex genes are associated with familial glioma.
Academic Article	Diagnostic Yield of Clinical Tumor and Germline Whole-Exome Sequencing for Children With Solid Tumors.
Academic Article	Is Whole-Exome Sequencing an Ethically Disruptive Technology? Perspectives of Pediatric Oncologists and Parents of Pediatric Patients With Solid Tumors.
Academic Article	Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.
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	Molecular diagnostic experience of whole-exome sequencing in adult patients.
Academic Article	ITD assembler: an algorithm for internal tandem duplication discovery from short-read sequencing data.
Academic Article	Integrated tumor and germline whole-exome sequencing identifies mutations in MAPK and PI3K pathway genes in an adolescent with rosette-forming glioneuronal tumor of the fourth ventricle.
Academic Article	Family-based exome-wide assessment of maternal genetic effects on susceptibility to childhood B-cell acute lymphoblastic leukemia in hispanics.
Academic Article	Resolution of Disease Phenotypes Resulting from Multilocus Genomic Variation.
Academic Article	Lessons learned from additional research analyses of unsolved clinical exome cases.
Academic Article	Family-based exome-wide association study of childhood acute lymphoblastic leukemia among Hispanics confirms role of ARID5B in susceptibility.
Academic Article	Use of Exome Sequencing for Infants in Intensive Care Units: Ascertainment of Severe Single-Gene Disorders and Effect on Medical Management.
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	Updated recommendation for the benign stand-alone ACMG/AMP criterion.
Academic Article	Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.
Academic Article	Exome sequencing disclosures in pediatric cancer care: Patterns of communication among oncologists, genetic counselors, and parents.
Academic Article	Framework for microRNA variant annotation and prioritization using human population and disease datasets.
Grant	Genomic Approaches to Defining Inherited Basis of Childhood Cancer
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
Concept	Exome
Academic Article	Genetic Predisposition to Childhood Cancer in the Genomic Era.
Academic Article	Parental Perspectives on Whole Exome Sequencing in Pediatric Cancer: A Typology of Perceived Utility.
Academic Article	Should secondary pharmacogenomic variants be actively screened and reported when diagnostic genome-wide sequencing is performed in a child?

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