Lista de obras -

A Multi-Institutional Cohort of Therapy-Associated Polyposis in Childhood and Young Adulthood Cancer Survivors

artículo científico publicado en 2020

A region-based gene association study combined with a leave-one-out sensitivity analysis identifies SMG1 as a pancreatic cancer susceptibility gene

scientific article published on 30 August 2019

ATM mutations in patients with hereditary pancreatic cancer

artículo científico publicado en 2011

Comparison of Colorectal and Endometrial Microsatellite Instability Tumor Analysis and Premm5 Risk Assessment for Predicting Pathogenic Germline Variants on Multigene Panel Testing

scientific article published on 30 September 2020

Frequent detection of pancreatic lesions in asymptomatic high-risk individuals.

artículo científico publicado en 2012

Incremental value of secretin-enhanced magnetic resonance cholangiopancreatography in detecting ductal communication in a population with high prevalence of small pancreatic cysts

artículo científico publicado en 2015

KRAS and guanine nucleotide-binding protein mutations in pancreatic juice collected from the duodenum of patients at high risk for neoplasia undergoing endoscopic ultrasound

artículo científico publicado en 2014

Linear-array EUS improves detection of pancreatic lesions in high-risk individuals: a randomized tandem study.

artículo científico publicado en 2015

Mutant GNAS detected in duodenal collections of secretin-stimulated pancreatic juice indicates the presence or emergence of pancreatic cysts

artículo científico publicado en 2012

Mutant TP53 in duodenal samples of pancreatic juice from patients with pancreatic cancer or high-grade dysplasia

artículo científico publicado en 2012

Mutations in the pancreatic secretory enzymes CPA1 and CPB1 are associated with pancreatic cancer.

artículo científico publicado en 2018

Pancreatic cancer genetic epidemiology consortium

artículo científico

Phenotypic differences in Juvenile Polyposis Syndrome with or without a disease-causing SMAD4/BMPR1A variant

artículo científico publicado en 2020

Racial variation in frequency and phenotypes of APC and MUTYH mutations in 6,169 individuals undergoing genetic testing

artículo científico publicado en 2015

Recent advances in Lynch syndrome: response to Møller et al

artículo científico publicado en 2020

Relationship between individual and family characteristics and psychosocial factors in persons with familial pancreatic cancer

artículo científico publicado en 2018

Whole Genome Sequencing Defines the Genetic Heterogeneity of Familial Pancreatic Cancer

artículo científico publicado en 2015

Lista de obras de

A Multi-Institutional Cohort of Therapy-Associated Polyposis in Childhood and Young Adulthood Cancer Survivors

A region-based gene association study combined with a leave-one-out sensitivity analysis identifies SMG1 as a pancreatic cancer susceptibility gene

ATM mutations in patients with hereditary pancreatic cancer

Comparison of Colorectal and Endometrial Microsatellite Instability Tumor Analysis and Premm5 Risk Assessment for Predicting Pathogenic Germline Variants on Multigene Panel Testing

Frequent detection of pancreatic lesions in asymptomatic high-risk individuals.

Incremental value of secretin-enhanced magnetic resonance cholangiopancreatography in detecting ductal communication in a population with high prevalence of small pancreatic cysts

KRAS and guanine nucleotide-binding protein mutations in pancreatic juice collected from the duodenum of patients at high risk for neoplasia undergoing endoscopic ultrasound

Linear-array EUS improves detection of pancreatic lesions in high-risk individuals: a randomized tandem study.

Mutant GNAS detected in duodenal collections of secretin-stimulated pancreatic juice indicates the presence or emergence of pancreatic cysts

Mutant TP53 in duodenal samples of pancreatic juice from patients with pancreatic cancer or high-grade dysplasia

Mutations in the pancreatic secretory enzymes CPA1 and CPB1 are associated with pancreatic cancer.

Pancreatic cancer genetic epidemiology consortium

Phenotypic differences in Juvenile Polyposis Syndrome with or without a disease-causing SMAD4/BMPR1A variant

Racial variation in frequency and phenotypes of APC and MUTYH mutations in 6,169 individuals undergoing genetic testing

Recent advances in Lynch syndrome: response to Møller et al

Relationship between individual and family characteristics and psychosocial factors in persons with familial pancreatic cancer

Whole Genome Sequencing Defines the Genetic Heterogeneity of Familial Pancreatic Cancer