Predisposition to cancer in children and adolescents
CP Kratz, MC Jongmans, H Cavé… - The lancet child & …, 2021 - thelancet.com
Childhood malignancies are rarely related to known environmental exposures, and it has
become increasingly evident that inherited genetic factors play a substantial causal role …
become increasingly evident that inherited genetic factors play a substantial causal role …
[HTML][HTML] Li-fraumeni syndrome
K Schneider, K Zelley, KE Nichols… - GeneReviews® …, 2024 - ncbi.nlm.nih.gov
Li-Fraumeni syndrome (LFS) is a cancer predisposition syndrome associated with high risks
for a broad spectrum of cancers including early-onset cancers. Five cancer types account for …
for a broad spectrum of cancers including early-onset cancers. Five cancer types account for …
The mutational constraint spectrum quantified from variation in 141,456 humans
Genetic variants that inactivate protein-coding genes are a powerful source of information
about the phenotypic consequences of gene disruption: genes that are crucial for the …
about the phenotypic consequences of gene disruption: genes that are crucial for the …
Variation across 141,456 human exomes and genomes reveals the spectrum of loss-of-function intolerance across human protein-coding genes
Genetic variants that inactivate protein-coding genes are a powerful source of information
about the phenotypic consequences of gene disruption: genes critical for an organism's …
about the phenotypic consequences of gene disruption: genes critical for an organism's …
The global prevalence and ethnic heterogeneity of primary ciliary dyskinesia gene variants: a genetic database analysis
WB Hannah, BA Seifert, R Truty… - The Lancet …, 2022 - thelancet.com
Background Primary ciliary dyskinesia (PCD) is a motile ciliopathy characterised by
otosinopulmonary infections. Inheritance is commonly autosomal recessive, with extensive …
otosinopulmonary infections. Inheritance is commonly autosomal recessive, with extensive …
Guidelines for the Li–Fraumeni and heritable TP53-related cancer syndromes
T Frebourg, S Bajalica Lagercrantz, C Oliveira… - European Journal of …, 2020 - nature.com
Fifty years after the recognition of the Li–Fraumeni syndrome (LFS), our perception of
cancers related to germline alterations of TP53 has drastically changed:(i) germline TP53 …
cancers related to germline alterations of TP53 has drastically changed:(i) germline TP53 …
Specifications of the ACMG/AMP variant interpretation guidelines for germline TP53 variants
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 …
Detection of germline variants in Brazilian breast cancer patients using multigene panel testing
RSC Guindalini, DV Viana, JPFW Kitajima… - Scientific reports, 2022 - nature.com
Genetic diversity of germline variants in breast cancer (BC) predisposition genes is
unexplored in miscegenated populations, such those living in Latin America. We evaluated …
unexplored in miscegenated populations, such those living in Latin America. We evaluated …
[HTML][HTML] Hereditary pancreatic cancer
DCF Klatte, MB Wallace, M Löhr, MJ Bruno… - Best Practice & …, 2022 - Elsevier
Pancreatic cancer is one of the deadliest malignancies. Therefore, there is an urgent need to
detect pancreatic cancer in an earlier stage to improve outcomes. A variety of hereditary …
detect pancreatic cancer in an earlier stage to improve outcomes. A variety of hereditary …
Spontaneous and inherited TP53 genetic alterations
AJ Levine - Oncogene, 2021 - nature.com
The p53 protein is a transcription factor that prevents tumors from developing. In
spontaneous and inherited cancers there are many different missense mutations in the DNA …
spontaneous and inherited cancers there are many different missense mutations in the DNA …