S. Scollon

发表

Why Patients Decline Genomic Sequencing Studies: Experiences from the CSER Consortium

B. Bernhardt, J. Wynn, C. Blout, 2018, Journal of Genetic Counseling.

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.

Nikhil Wagle, Peter Tarczy-Hornoch, Richard M Myers, 2016, American journal of human genetics.

Diagnostic Yield of Clinical Tumor and Germline Whole-Exome Sequencing for Children With Solid Tumors.

Tao Wang, Katie Bergstrom, Amy L McGuire, 2016, JAMA oncology.

Germline POLE mutation in a child with hypermutated medulloblastoma and features of constitutional mismatch repair deficiency

D. Parsons, S. Plon, Angshumoy Roy, 2019, Cold Spring Harbor molecular case studies.

Consent for clinical genome sequencing: considerations from the Clinical Sequencing Exploratory Research Consortium.

B. Wilfond, P. Appelbaum, B. Bernhardt, 2019, Personalized medicine.

Recommendations for Surveillance for Children with Leukemia-Predisposing Conditions

T. Druley, L. Strong, J. Schiffman, 2017, Clinical Cancer Research.

A review and definition of ‘usual care’ in genetic counseling trials to standardize use in research

Sarah E Lillie, Marian J. Gilmore, Julianne M. O’Daniel, 2020, Journal of genetic counseling.

Scaling Genetic Counseling in the Genomics Era.

K. Golden-Grant, L. Amendola, S. Scollon, 2021, Annual review of genomics and human genetics.

FOCAD Indel in a Family With Juvenile Polyposis Syndrome

S. Plon, G. Brodeur, S. Scollon, 2022, Journal of pediatric gastroenterology and nutrition.

Parent decision‐making around the genetic testing of children for germline TP53 mutations

A. Patenaude, J. Garber, S. Plon, 2015, Cancer.

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

D. Wheeler, D. Parsons, R. Person, 2016, Cold Spring Harbor molecular case studies.

Clinical and molecular features of pediatric cancer patients with Lynch syndrome

R. Gibbs, D. Muzny, D. Parsons, 2021, Pediatric blood & cancer.

Erratum: Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine (American Journal of Human Genetics (2016) 98(6) (1067–1076) (S0002929716301069) (10.1016/j.ajhg.2016.04.011))

Sara Chandros Hull, Robert C. Green, Sean D. Mooney, 2016 .

Pediatric Oncologists’ Experiences Returning and Incorporating Genomic Sequencing Results into Cancer Care

D. Parsons, A. McGuire, R. Street, 2021, Journal of personalized medicine.

Return of non-ACMG recommended incidental genetic findings to pediatric patients: considerations and opportunities from experiences in genomic sequencing

G. Cooper, B. Korf, K. Bowling, 2022, Genome Medicine.

A Comprehensive Review of Pediatric Tumors and Associated Cancer Predisposition Syndromes

S. Scollon, Joyce T. Turner, K. Wolfe Schneider, 2017, Journal of Genetic Counseling.

Haploinsufficiency of the Chromatin Remodeler BPTF Causes Syndromic Developmental and Speech Delay, Postnatal Microcephaly, and Dysmorphic Features.

Juliane Hoyer, Bernt Popp, André Reis, 2017, American journal of human genetics.

Retinoblastoma and Neuroblastoma Predisposition and Surveillance

W. Foulkes, A. Nakagawara, L. Diller, 2017, Clinical Cancer Research.

Phenotypic Differences in Juvenile Polyposis Syndrome With or Without a Disease-causing SMAD4/BMPR1A Variant

S. Plon, Z. Stadler, R. Brand, 2020, Cancer Prevention Research.

Cancer Screening Recommendations and Clinical Management of Inherited Gastrointestinal Cancer Syndromes in Childhood

W. Foulkes, D. Evans, K. Nathanson, 2017, Clinical Cancer Research.

The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations.

N. Risch, P. Kwok, S. Fullerton, 2018, American journal of human genetics.

Genetic Counselor Recommendations for Cancer Predisposition Evaluation and Surveillance in the Pediatric Oncology Patient

K. Schneider, W. Kohlmann, S. Scollon, 2017, Clinical Cancer Research.

Pediatric Cancer Genetics Research and an Evolving Preventive Ethics Approach for Return of Results after Death of the Subject

A. McGuire, S. Plon, L. Mccullough, 2015, Journal of Law, Medicine & Ethics.

Illustrative case studies in the return of exome and genome sequencing results

B. Bernhardt, G. Jarvik, J. Wynn, 2015, Personalized medicine.

Obtaining informed consent for clinical tumor and germline exome sequencing of newly diagnosed childhood cancer patients

R. Gibbs, S. Hilsenbeck, A. McGuire, 2014, Genome Medicine.

“Not Tied Up Neatly with a Bow”: Professionals’ Challenging Cases in Informed Consent for Genomic Sequencing

Debra Skinner, Denise L. Perry, Barbara A. Bernhardt, 2016, Journal of Genetic Counseling.

Experiences with obtaining informed consent for genomic sequencing

Denise L. Perry, D. Skinner, B. Bernhardt, 2015, American journal of medical genetics. Part A.

Views of Adolescents and Young Adults with Cancer and Their Oncologists Toward Patients' Participation in Genomic Research.

A. McGuire, S. Plon, J. Robinson, 2023, Journal of adolescent and young adult oncology.

Clinical providers’ experiences with returning results from genomic sequencing: an interview study

B. Bernhardt, J. Wynn, C. McMullen, 2018, BMC Medical Genomics.

Genomic Sequencing Results Disclosure in Diverse and Medically Underserved Populations: Themes, Challenges, and Strategies from the CSER Consortium

Julianne M. O’Daniel, Shannon Rego, Marian Gilmore, 2021, Journal of personalized medicine.

Exome sequencing disclosures in pediatric cancer care: Patterns of communication among oncologists, genetic counselors, and parents.

S. Hilsenbeck, A. McGuire, R. Street, 2018, Patient education and counseling.

Implementation and evaluation of clinical exome sequencing in childhood cancer care: The BASIC3 study.

R. Gibbs, S. Hilsenbeck, D. Wheeler, 2013 .

Distinct somatic DICER1 hotspot mutations in three metachronous ovarian Sertoli-Leydig cell tumors in a patient with DICER1 syndrome

R. Gibbs, D. Muzny, S. Plon, 2022, Cancer Genetics.

Agents of empathy: How medical interpreters bridge sociocultural gaps in genomic sequencing disclosures with Spanish-speaking families.

A. McGuire, R. Street, S. Plon, 2019, Patient education and counseling.

Clinical providers’ experiences with returning results from genomic sequencing: an interview study

B. Bernhardt, J. Wynn, C. McMullen, 2018, BMC Medical Genomics.

Haploinsufficiency of STK11 and neighboring genes cause a contiguous gene syndrome including Peutz–Jeghers phenotype

T. Slavin, S. Scollon, K. Abe, 2012, American journal of medical genetics. Part A.

Portero versus portador: Spanish interpretation of genomic terminology during whole exome sequencing results disclosure.

A. McGuire, R. Street, S. Plon, 2017, Personalized medicine.

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.

Matthew S. Lebo, Victoria A. Miller, Jeffrey W. Pennington, 2016, American journal of human genetics.

Evolution of germline TP53 variant classification in children with cancer.

D. Ritter, S. Scollon, S. Plon, 2022, Cancer genetics.

Obtaining informed consent for clinical tumor and germline exome sequencing of newly diagnosed childhood cancer patients

R. Gibbs, S. Hilsenbeck, A. McGuire, 2014, Genome Medicine.

Genetic Counselor Recommendations for Cancer Predisposition Evaluation and Surveillance in the Pediatric Oncology Patient

K. Schneider, W. Kohlmann, S. Scollon, 2017, Clinical Cancer Research.

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.

Joseph S. Salama, W. Chung, I. Krantz, 2016, American journal of human genetics.

Diagnostic Yield of Clinical Tumor and Germline Whole-Exome Sequencing for Children With Solid Tumors.

R. Gibbs, S. Hilsenbeck, D. Wheeler, 2016, JAMA oncology.

Clinical and molecular features of pediatric cancer patients with Lynch syndrome

Jianhong Hu, V. Korchina, S. Plon, 2022, Pediatric blood & cancer.

Genomic analysis and preclinical xenograft model development identify potential therapeutic targets for MYOD1‐mutant soft‐tissue sarcoma of childhood

S. Plon, Angshumoy Roy, Raghu Chandramohan, 2021, The Journal of pathology.

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

S. Plon, Angshumoy Roy, M. Chintagumpala, 2016, Cold Spring Harbor molecular case studies.

Families' experiences accessing care after genomic sequencing in the pediatric cancer context: "It's just been a big juggle".

J. Robinson, S. Scollon, Blake Vuocolo, 2024, Journal of genetic counseling.