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Author Details

Sharon E Plon
Baylor College of Medicine
1982
217
64
PMIDPaper TitleJournal TitlePublished Year
37788149Pediatric cancer incidence among individuals with overgrowth syndromes and overgrowth features: A population-based assessment in seven million children.Cancer2024
37800450Gene-specific ACMG/AMP classification criteria for germline APC variants: Recommendations from the ClinGen InSiGHT Hereditary Colorectal Cancer/Polyposis Variant Curation Expert Panel.Genet Med2024
38007624Should secondary pharmacogenomic variants be actively screened and reported when diagnostic genome-wide sequencing is performed in a child?Genet Med2024
36595372Views of Adolescents and Young Adults with Cancer and Their Oncologists Toward Patients' Participation in Genomic Research.J Adolesc Young Adult Oncol2023
37289514Identification of USP9X as a leukemia susceptibility gene.Blood Adv2023
37115922The genomic landscape of familial glioma.Sci Adv2023
37366624Associations between birth defects and childhood and adolescent germ cell tumors according to sex, histologic subtype, and site.Cancer2023
37366551Circulating tumor DNA sequencing of pediatric solid and brain tumor patients: An institutional feasibility study.Pediatr Hematol Oncol2023
37194615TP53 germline pathogenic variant frequency in anaplastic rhabdomyosarcoma: A Children's Oncology Group report.Pediatr Blood Cancer2023
36813544Germline pathogenic <i>SMARCA4</i> variants in neuroblastoma.J Med Genet2023
36600593Optimising clinical care through <i>CDH1</i>-specific germline variant curation: improvement of clinical assertions and updated curation guidelines.J Med Genet2023
34793247Importance of Population-Based Cancer Risk Information in the Care of Patients With Rare Genetic Disorders.J Clin Oncol2022
35487348A Validation Framework for Somatic Copy Number Detection in Targeted Sequencing Panels.J Mol Diagn2022
35622075FOCAD Indel in a Family With Juvenile Polyposis Syndrome.J Pediatr Gastroenterol Nutr2022
35713195Clinical and molecular features of pediatric cancer patients with Lynch syndrome.Pediatr Blood Cancer2022
36001348Collaboration to Promote Research and Improve Clinical Care in the Evolving Field of Childhood Cancer Predisposition.Cancer Prev Res (Phila)2022
36063163Standards 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).Genet Med2022
35101336Standards 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).Genet Med2022
35245469The annual ASHG dinner.Am J Hum Genet2022
35306447Evolution of germline TP53 variant classification in children with cancer.Cancer Genet2022
35026696Distinct somatic DICER1 hotspot mutations in three metachronous ovarian Sertoli-Leydig cell tumors in a patient with DICER1 syndrome.Cancer Genet2022
32313107Clinical and functional characterization of telomerase variants in patients with pediatric acute myeloid leukemia/myelodysplastic syndrome.Leukemia2021
34651095Durable Response to Larotrectinib in a Child With Histologic Diagnosis of Recurrent Disseminated Ependymoma Discovered to Harbor an <i>NTRK2</i> Fusion: The Impact of Integrated Genomic Profiling.JCO Precis Oncol2021
34065162Pediatric Rhabdomyosarcoma: Epidemiology and Genetic Susceptibility.J Clin Med2021
34207141Pediatric Oncologists' Experiences Returning and Incorporating Genomic Sequencing Results into Cancer Care.J Pers Med2021
34086347Genomic analysis and preclinical xenograft model development identify potential therapeutic targets for MYOD1-mutant soft-tissue sarcoma of childhood.J Pathol2021
33372952Germline Cancer Predisposition Variants inâ¿¿Pediatric Rhabdomyosarcoma: A Report From the Children's Oncology Group.J Natl Cancer Inst2021
33300245Specifications of the ACMG/AMP variant interpretation guidelines for germline TP53 variants.Hum Mutat2021
33097490Phenotypic Differences in Juvenile Polyposis Syndrome With or Without a Disease-causing <i>SMAD4</i>/<i>BMPR1A</i> Variant.Cancer Prev Res (Phila)2021
32469081Cancer diagnostic profile in children with structural birth defects: An assessment in 15,000 childhood cancer cases.Cancer2020
31915397A brief history of human disease genetics.Nature2020
33134832Male Sex and the Risk of Childhood Cancer: The Mediating Effect of Birth Defects.JNCI Cancer Spectr2020
30581014Agents of empathy: How medical interpreters bridge sociocultural gaps in genomic sequencing disclosures with Spanish-speaking families.Patient Educ Couns2019
31645350A case for expert curation: an overview of cancer curation in the Clinical Genome Resource (ClinGen).Cold Spring Harb Mol Case Stud2019
31648317ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variants.Blood Adv2019
30181607Development of Clinical Domain Working Groups for the Clinical Genome Resource (ClinGen): lessons learned and plans for the future.Genet Med2019
29895853Genome-wide sequencing in acutely ill infants: genomic medicine's critical application?Genet Med2019
31303264Mutations in ANAPC1, Encoding a Scaffold Subunit of the Anaphase-Promoting Complex, Cause Rothmund-Thomson Syndrome Type 1.Am J Hum Genet2019
31186522Responsibility, culpability, and parental views on genomic testing for seriously ill children.Genet Med2019
31219523Association Between Birth Defects and Cancer Risk Among Children and Adolescents in a Population-Based Assessment of 10 Million Live Births.JAMA Oncol2019
30977242Characterization of pediatric hepatocellular carcinoma reveals genomic heterogeneity and diverse signaling pathway activation.Pediatr Blood Cancer2019
31082280Genetic Predisposition to Childhood Cancer in the Genomic Era.Annu Rev Genomics Hum Genet2019
31050187Severe therapy-related toxicities after treatment for Hodgkin lymphoma due to a pathogenic TERT variant and shortened telomeres.Pediatr Blood Cancer2019
30523343Determining the clinical validity of hereditary colorectal cancer and polyposis susceptibility genes using the Clinical Genome Resource Clinical Validity Framework.Genet Med2019
30398677Current Controversies in Prenatal Diagnosis 2: NIPT results suggesting maternal cancer should always be disclosed.Prenat Diagn2019
30482469Exome sequencing disclosures in pediatric cancer care: Patterns of communication among oncologists, genetic counselors, and parents.Patient Educ Couns2019
30287922Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.Genet Med2019
30670880Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.Genet Med2019
30504931Clinical validity assessment of genes frequently tested on hereditary breast and ovarian cancer susceptibility sequencing panels.Genet Med2019
30302893Framework for microRNA variant annotation and prioritization using human population and disease datasets.Hum Mutat2019
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Collaborators

Texas Children's Hospital
Co-authored papers 31
Baylor College of Medicine
Co-authored papers 27
Baylor College of Medicine
Co-authored papers 25
Texas Children's Cancer Center, Texas Children's Hospital
Co-authored papers 21
The Broad Institute of MIT and Harvard
Co-authored papers 19
Baylor College of Medicine.
Co-authored papers 18
Baylor College of Medicine
Co-authored papers 17
University of North Carolina
Co-authored papers 16
Baylor College of Medicine
Co-authored papers 16
Baylor College of Medicine
Co-authored papers 15
Texas Children's Cancer Center, Baylor College of Medicine
Co-authored papers 15
University of Washington Medical Center
Co-authored papers 14
Texas Children's Hospital and Baylor College of Medicine
Co-authored papers 14
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 11
Baylor College of Medicine
Co-authored papers 11
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 10
Oregon Health & Science University (OHSU)
Co-authored papers 10
Illumina Inc.
Co-authored papers 10
Baylor College of Medicine, Texas Children's Hospital
Co-authored papers 9
Baylor College of Medicine.
Co-authored papers 8
The University of North Carolina at Chapel Hill
Co-authored papers 8
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Co-authored papers 8
Brigham and Women's Hospital, Broad Institute Ariadne Labs and Harvard Medical School
Co-authored papers 8
Baylor College of Medicine
Co-authored papers 8
Washington University School of Medicine
Co-authored papers 7
The Perelman School of Medicine at the University of Pennsylvania
Co-authored papers 7
HudsonAlpha Institute for Biotechnology
Co-authored papers 7
St. Jude Children's Research Hospital
Co-authored papers 7
University of Washington Medical Center
Co-authored papers 7
QIMR Berghofer Medical Research Institute
Co-authored papers 7