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Carcinogenesis|September 20, 2014
Transcriptome analysis of pancreatic cancer reveals a tumor suppressor function for HNF1AJason W Hoskins, Jinping Jia, Marta Flandez, et al.
Nature Communications|April 30, 2025
Allelic effects on KLHL17 expression underlie a pancreatic cancer genome-wide association signal at chr1p36.33Katelyn E Connelly, Katherine Hullin, Ehssan Abdolalizadeh, et al.
Medrxiv : the Preprint Server for Health Sciences|October 7, 2024
Allelic effects on KLHL17 expression likely mediated by JunB/D underlie a PDAC GWAS signal at chr1p36.33Katelyn E Connelly, Katherine Hullin, Ehssan Abdolalizadeh, et al.
Biorxiv : the Preprint Server for Biology|August 30, 2024
A common CTRB misfolding variant associated with pancreatic cancer risk causes ER stress and inflammation in miceCristina Bodas, Irene Felipe, Brice Chanez, et al.
Cancer Research|March 21, 2014
CLPTM1L promotes growth and enhances aneuploidy in pancreatic cancer cellsJinping Jia, Allen D Bosley, Abbey Thompson, et al.
Gut|October 8, 2025
Large-scale multiomic analysis identifies non-coding somatic driver mutations and nominates ZFP36L2 as a driver gene for pancreatic ductal adenocarcinomaJun Zhong, Aidan O'Brien, Minal B Patel, et al.
Medrxiv : the Preprint Server for Health Sciences|October 7, 2024
Large-scale multi-omic analysis identifies noncoding somatic driver mutations and nominates ZFP36L2 as a driver gene for pancreatic ductal adenocarcinomaJun Zhong, Aidan O'Brien, Minal Patel, et al.
American Journal of Human Genetics|September 24, 2021
A 584 bp deletion in CTRB2 inhibits chymotrypsin B2 activity and secretion and confers risk of pancreatic cancerAshley Jermusyk, Jun Zhong, Katelyn E Connelly, et al.
Human Molecular Genetics|February 8, 2017
Functional characterization of a chr13q22.1 pancreatic cancer risk locus reveals long-range interaction and allele-specific effects on DIS3 expressionJason W Hoskins, Abdisamad Ibrahim, Mickey A Emmanuel, et al.
Medrxiv : the Preprint Server for Health Sciences|August 26, 2024
3D chromatin-based variant-to-gene maps across 57 human cell types reveal the cellular and genetic architecture of autoimmune disease susceptibilityKhanh B Trang, Prabhat Sharma, Laura Cook, et al.
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