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 …
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 …
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
Importance Guidelines for clinical management in Li-Fraumeni syndrome, a multiple-organ
cancer predisposition condition, are limited. Whole-body magnetic resonance imaging (…
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 …
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, …
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 …
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 …
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…
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 …
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 …
risk evaluation. However, methods for classification of variants resulting from this testing …