NCCN guidelines insights: genetic/familial high-risk assessment: colorectal, version 2.2019: featured updates to the NCCN guidelines

…, S Haraldsdottir, AJ Markowitz, TP Slavin Jr… - Journal of the National …, 2019 - jnccn.org
Identifying individuals with hereditary syndromes allows for improved cancer surveillance,
risk reduction, and optimized management. Establishing criteria for assessment allows for the …

Personalized circulating tumor DNA analysis to detect residual disease after neoadjuvant therapy in breast cancer

…, BK Patel, JN Weitzel, TP Slavin… - Science translational …, 2019 - science.org
Longitudinal analysis of circulating tumor DNA (ctDNA) has shown promise for monitoring
treatment response. However, most current methods lack adequate sensitivity for residual …

Baseline surveillance in Li-Fraumeni syndrome using whole-body magnetic resonance imaging: a meta-analysis

…, M Walsh, L Manelli, A Villani, DM Thomas… - JAMA …, 2017 - jamanetwork.com
Importance Guidelines for clinical management in Li-Fraumeni syndrome, a multiple-organ
cancer predisposition condition, are limited. Whole-body magnetic resonance imaging (…

[HTML][HTML] The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer risk

…, SN Hart, V Ravichandran, T Thomas… - NPJ breast …, 2017 - nature.com
Understanding the gene-specific risks for development of breast cancer will lead to improved
clinical care for those carrying germline mutations in cancer predisposition genes. We …

Circulating tumor DNA as an early cancer detection tool

…, SW Gray, L Goetz, A Goel, N Schork, TP Slavin - Pharmacology & …, 2020 - Elsevier
Circulating tumor DNA holds substantial promise as an early detection biomarker, particularly
for cancers that do not have currently accepted screening methodologies, such as ovarian, …

Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline CDH1 sequence variants

…, C Pardo, T Pesaran, M Richardson, TP Slavin… - Human …, 2018 - Wiley Online Library
The variant curation guidelines published in 2015 by the American College of Medical Genetics
and Genomics and the Association for Molecular Pathology (ACMG/AMP) provided the …

Specifications of the ACMG/AMP variant interpretation guidelines for germline TP53 variants

…, K McGoldrick, J Mester, BA Seifert, TP Slavin… - Human …, 2021 - Wiley Online Library
Germline pathogenic variants in TP53 are associated with Li‐Fraumeni syndrome, a cancer
predisposition disorder inherited in an autosomal dominant pattern associated with a high …

NCCN guidelines insights: colorectal cancer screening, version 1.2018

…, PM Lynch, J Mikkelson, RM Ness, TP Slavin… - Journal of the National …, 2018 - jnccn.org
The NCCN Guidelines for Colorectal Cancer (CRC) Screening outline various screening
modalities as well as recommended screening strategies for individuals at average or increased…

NCCN guidelines insights: genetic/familial high-risk assessment: colorectal, version 3.2017

…, SE Regenbogen, H Hampel, TP Slavin… - Journal of the National …, 2017 - jnccn.org
The NCCN Guidelines for Genetic/Familial High-Risk Assessment: Colorectal provide
recommendations for the management of patients with high-risk syndromes associated with an …

[PDF][PDF] Evaluation of ACMG-guideline-based variant classification of cancer susceptibility and non-cancer-associated genes in families affected by breast cancer

…, J Vijai, KA Schrader, TP Slavin, T Thomas… - The American Journal of …, 2016 - cell.com
Sequencing tests assaying panels of genes or whole exomes are widely available for cancer
risk evaluation. However, methods for classification of variants resulting from this testing …