C3P publications
https://pubmed.ncbi.nlm.nih.gov/36001348/
Selected publications by C3P members:
Pediatric Cancer Predisposition and Surveillance: An Overview, and a Tribute to Alfred G. Knudson Jr
https://pubmed.ncbi.nlm.nih.gov/28572261/
The Future of Surveillance in the Context of Cancer Predisposition: Through the Murky Looking Glass
https://pubmed.ncbi.nlm.nih.gov/29093018/
Pathogenic Variants in Adult-Onset Cancer Predisposition Genes in Pediatric Cancer: Prevalence and Impact on Tumor Molecular Features and Clinical Management
https://pubmed.ncbi.nlm.nih.gov/36693186/
Adolescent and Young Adult Understanding of Their Childhood Cancer Predisposition Diagnosis: A Qualitative Study
https://pubmed.ncbi.nlm.nih.gov/37279817/
Multiple Germline Events Contribute to Cancer Development in Patients with Li-Fraumeni Syndrome
https://pubmed.ncbi.nlm.nih.gov/37377903/
Heterozygous BRCA1 and BRCA2 and Mismatch Repair Gene Pathogenic Variants in Children and Adolescents With Cancer
https://pubmed.ncbi.nlm.nih.gov/35980168/
Clinical and molecular features of pediatric cancer patients with Lynch syndrome
https://pubmed.ncbi.nlm.nih.gov/35713195/
Association Between Birth Defects and Cancer Risk Among Children and Adolescents in a Population-Based Assessment of 10 Million Live Births
https://pubmed.ncbi.nlm.nih.gov/31219523/
Pediatric Somatic Tumor Sequencing Identifies Underlying Cancer Predisposition
https://pubmed.ncbi.nlm.nih.gov/32783018/
Germline genomic findings in children and young adults with melanocytic tumors
https://pubmed.ncbi.nlm.nih.gov/37073685/
A novel mobile health application to support cancer surveillance needs of patients and families with cancer predisposition syndromes
https://pubmed.ncbi.nlm.nih.gov/37415085/
Stopping Leukemia in Its Tracks: Should Preemptive Hematopoietic Stem-Cell Transplantation be Offered to Patients at Increased Genetic Risk for Acute Myeloid Leukemia?
https://pubmed.ncbi.nlm.nih.gov/31170028/
The clinical utility of integrative genomics in childhood cancer extends beyond targetable mutations
https://pubmed.ncbi.nlm.nih.gov/36585449/
Tumor surveillance for children and adolescents with cancer predisposition syndromes: The psychosocial impact reported by adolescents and caregivers
https://pubmed.ncbi.nlm.nih.gov/33788392/
Germline pathogenic variants in cancer risk genes among patients with thyroid cancer and suspected predisposition
https://pubmed.ncbi.nlm.nih.gov/35174967/
Different Fumarate Hydratase Gene Variants Are Associated With Distinct Cancer Phenotypes
https://pubmed.ncbi.nlm.nih.gov/34994643/
Germline Sequencing Improves Tumor-Only Sequencing Interpretation in a Precision Genomic Study of Patients With Pediatric Solid Tumor
https://pubmed.ncbi.nlm.nih.gov/34964003/
Linking population-based registries to identify familial cancer risk in childhood cancer
https://pubmed.ncbi.nlm.nih.gov/32315449/
FOCAD Indel in a Family With Juvenile Polyposis Syndrome
https://pubmed.ncbi.nlm.nih.gov/35622075/
Phenotypic Differences in Juvenile Polyposis Syndrome With or Without a Disease-causing SMAD4/ BMPR1A Variant
https://pubmed.ncbi.nlm.nih.gov/33097490/
Severe congenital neutropenia, SRP54 pathogenicity, and a framework for surveillance
https://pubmed.ncbi.nlm.nih.gov/36815775/
Germ Cell Mosaicism: A Rare Cause of Li-Fraumeni Recurrence Among Siblings
https://pubmed.ncbi.nlm.nih.gov/32923893/
Interest in Cancer Predisposition Testing and Carrier Screening Offered as Part of Routine Healthcare Among an Ethnically Diverse Sample of Young Women
https://pubmed.ncbi.nlm.nih.gov/35495140/
Considerations for total thyroidectomy in an adolescent with PTEN mutation
https://pubmed.ncbi.nlm.nih.gov/30181857/