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Author Details
Full Name
Sarah Scollon
Affiliation
Texas Children's Cancer Center, Texas Children's Hospital
ORCID
Career Start Year
2012
Papers
37
H Index
19
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36595372
Views of Adolescents and Young Adults with Cancer and Their Oncologists Toward Patients' Participation in Genomic Research.
J Adolesc Young Adult Oncol
2023
37212252
Information-seeking preferences in diverse patients receiving a genetic testing result in the Clinical Sequencing Evidence-Generating Research (CSER) study.
Genet Med
2023
35026696
Distinct somatic DICER1 hotspot mutations in three metachronous ovarian Sertoli-Leydig cell tumors in a patient with DICER1 syndrome.
Cancer Genet
2022
35622075
FOCAD Indel in a Family With Juvenile Polyposis Syndrome.
J Pediatr Gastroenterol Nutr
2022
35713195
Clinical and molecular features of pediatric cancer patients with Lynch syndrome.
Pediatr Blood Cancer
2022
36414972
Return of non-ACMG recommended incidental genetic findings to pediatric patients: considerations and opportunities from experiences in genomic sequencing.
Genome Med
2022
35306447
Evolution of germline TP53 variant classification in children with cancer.
Cancer Genet
2022
33097490
Phenotypic Differences in Juvenile Polyposis Syndrome With or Without a Disease-causing <i>SMAD4</i>/<i>BMPR1A</i> Variant.
Cancer Prev Res (Phila)
2021
33805616
Genomic Sequencing Results Disclosure in Diverse and Medically Underserved Populations: Themes, Challenges, and Strategies from the CSER Consortium.
J Pers Med
2021
33722076
Scaling Genetic Counseling in the Genomics Era.
Annu Rev Genomics Hum Genet
2021
34207141
Pediatric Oncologists' Experiences Returning and Incorporating Genomic Sequencing Results into Cancer Care.
J Pers Med
2021
34086347
Genomic analysis and preclinical xenograft model development identify potential therapeutic targets for MYOD1-mutant soft-tissue sarcoma of childhood.
J Pathol
2021
33278053
A review and definition of 'usual care' in genetic counseling trials to standardize use in research.
J Genet Couns
2021
30581014
Agents of empathy: How medical interpreters bridge sociocultural gaps in genomic sequencing disclosures with Spanish-speaking families.
Patient Educ Couns
2019
31313633
Consent for clinical genome sequencing: considerations from the Clinical Sequencing Exploratory Research Consortium.
Per Med
2019
30482469
Exome sequencing disclosures in pediatric cancer care: Patterns of communication among oncologists, genetic counselors, and parents.
Patient Educ Couns
2019
29739461
Clinical providers' experiences with returning results from genomic sequencing: an interview study.
BMC Med Genomics
2018
30193136
The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations.
Am J Hum Genet
2018
29497922
Why Patients Decline Genomic Sequencing Studies: Experiences from the CSER Consortium.
J Genet Couns
2018
28674117
Genetic Counselor Recommendations for Cancer Predisposition Evaluation and Surveillance in the Pediatric Oncology Patient.
Clin Cancer Res
2017
28357779
A Comprehensive Review of Pediatric Tumors and Associated Cancer Predisposition Syndromes.
J Genet Couns
2017
29749861
Portero versus portador: Spanish interpretation of genomic terminology during whole exome sequencing results disclosure.
Per Med
2017
28942966
Haploinsufficiency of the Chromatin Remodeler BPTF Causes Syndromic Developmental and Speech Delay, Postnatal Microcephaly, and Dysmorphic Features.
Am J Hum Genet
2017
28572263
Recommendations for Surveillance for Children with Leukemia-Predisposing Conditions.
Clin Cancer Res
2017
28674119
Cancer Screening Recommendations and Clinical Management of Inherited Gastrointestinal Cancer Syndromes in Childhood.
Clin Cancer Res
2017
28674118
Retinoblastoma and Neuroblastoma Predisposition and Surveillance.
Clin Cancer Res
2017
25911622
"Not Tied Up Neatly with a Bow": Professionals' Challenging Cases in Informed Consent for Genomic Sequencing.
J Genet Couns
2016
27626068
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.
Cold Spring Harb Mol Case Stud
2016
27392080
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.
Am J Hum Genet
2016
27181682
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.
Am J Hum Genet
2016
26822237
Diagnostic Yield of Clinical Tumor and Germline Whole-Exome Sequencing for Children With Solid Tumors.
JAMA Oncol
2016
25223899
Parent decision-making around the genetic testing of children for germline TP53 mutations.
Cancer
2015
26479562
Pediatric Cancer Genetics Research and an Evolving Preventive Ethics Approach for Return of Results after Death of the Subject.
J Law Med Ethics
2015
26478737
Illustrative case studies in the return of exome and genome sequencing results.
Per Med
2015
26198374
Experiences with obtaining informed consent for genomic sequencing.
Am J Med Genet A
2015
25317207
Obtaining informed consent for clinical tumor and germline exome sequencing of newly diagnosed childhood cancer patients.
Genome Med
2014
22987620
Haploinsufficiency of STK11 and neighboring genes cause a contiguous gene syndrome including Peutz-Jeghers phenotype.
Am J Med Genet A
2012
1 - 37 of 37
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