User profiles for "author:Rita T Lawlor"
Rita T. LawlorARC-Net, University of Verona Verified email at univr.it Cited by 20467 |
[HTML][HTML] Molecular tumor boards in clinical practice
Next-generation sequencing (NGS) application in clinical practice requires the
implementation of molecular tumor boards (MTBs). Starting from a systematic review of …
implementation of molecular tumor boards (MTBs). Starting from a systematic review of …
[HTML][HTML] Tumor mutational burden as a potential biomarker for immunotherapy in pancreatic cancer: systematic review and still-open questions
Simple Summary Tumor mutational burden (TMB) represents the number of mutations per
megabase (muts/Mb) harbored by tumor cells in a given neoplasm, and can be determined …
megabase (muts/Mb) harbored by tumor cells in a given neoplasm, and can be determined …
Genomic analyses identify molecular subtypes of pancreatic cancer
Integrated genomic analysis of 456 pancreatic ductal adenocarcinomas identified 32
recurrently mutated genes that aggregate into 10 pathways: KRAS, TGF-β, WNT, NOTCH …
recurrently mutated genes that aggregate into 10 pathways: KRAS, TGF-β, WNT, NOTCH …
Whole genomes redefine the mutational landscape of pancreatic cancer
Pancreatic cancer remains one of the most lethal of malignancies and a major health
burden. We performed whole-genome sequencing and copy number variation (CNV) …
burden. We performed whole-genome sequencing and copy number variation (CNV) …
Whole-genome landscape of pancreatic neuroendocrine tumours
The diagnosis of pancreatic neuroendocrine tumours (PanNETs) is increasing owing to
more sensitive detection methods, and this increase is creating challenges for clinical …
more sensitive detection methods, and this increase is creating challenges for clinical …
Exome sequencing identifies frequent inactivating mutations in BAP1, ARID1A and PBRM1 in intrahepatic cholangiocarcinomas
Through exomic sequencing of 32 intrahepatic cholangiocarcinomas, we discovered
frequent inactivating mutations in multiple chromatin-remodeling genes (including BAP1 …
frequent inactivating mutations in multiple chromatin-remodeling genes (including BAP1 …
[HTML][HTML] KRAS wild-type pancreatic ductal adenocarcinoma: molecular pathology and therapeutic opportunities
C Luchini, G Paolino, P Mattiolo, ML Piredda… - Journal of Experimental …, 2020 - Springer
Pancreatic ductal adenocarcinoma (PDAC) is a deadly disease, whose main molecular trait
is the MAPK pathway activation due to KRAS mutation, which is present in 90% of cases …
is the MAPK pathway activation due to KRAS mutation, which is present in 90% of cases …
[HTML][HTML] Genomic characterization of biliary tract cancers identifies driver genes and predisposing mutations
Background & Aims Biliary tract cancers (BTCs) are clinically and pathologically
heterogeneous and respond poorly to treatment. Genomic profiling can offer a clearer …
heterogeneous and respond poorly to treatment. Genomic profiling can offer a clearer …
Targeted next‐generation sequencing of cancer genes dissects the molecular profiles of intraductal papillary neoplasms of the pancreas
Intraductal neoplasms are important precursors to invasive pancreatic cancer and provide
an opportunity to detect and treat pancreatic neoplasia before an invasive carcinoma …
an opportunity to detect and treat pancreatic neoplasia before an invasive carcinoma …
[HTML][HTML] DNA qualification workflow for next generation sequencing of histopathological samples
Histopathological samples are a treasure-trove of DNA for clinical research. However, the
quality of DNA can vary depending on the source or extraction method applied. Thus a …
quality of DNA can vary depending on the source or extraction method applied. Thus a …