Vincent D

No ORCID on file · 4 papers in corpus
2024
Hereditary angioedema with normal C1 inhibitor associated with carboxypeptidase N deficiency.
The journal of allergy and clinical immunology. Global ·doi:10.1016/j.jacig.2024.100223

BackgroundHereditary angioedema (HAE) is a potentially life-threatening disorder characterized by recurrent episodes of subcutaneous or submucosal swelling. HAE with normal C1 inhibitor (HAE-nC1-INH) is an underdiagnosed condition. Although…

2020
Development of an improved murine model of necrotizing enterocolitis shows the importance of neutrophils in NEC pathogenesis.
Scientific reports ·doi:10.1038/s41598-020-65120-y

Various research models to induce necrotizing enterocolitis (NEC) in animals exist, yet significant differences in NEC severity between murine animal models and human patients persist. One possible explanation for the difference in severity…

2017
The OncoArray Consortium: A Network for Understanding the Genetic Architecture of Common Cancers.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology ·doi:10.1158/1055-9965.epi-16-0106

BackgroundCommon cancers develop through a multistep process often including inherited susceptibility. Collaboration among multiple institutions, and funding from multiple sources, has allowed the development of an inexpensive genotyping mi…

2013
Epigenetic analysis leads to identification of HNF1B as a subtype-specific susceptibility gene for ovarian cancer.
Nature communications ·doi:10.1038/ncomms2629

HNF1B is overexpressed in clear cell epithelial ovarian cancer, and we observed epigenetic silencing in serous epithelial ovarian cancer, leading us to hypothesize that variation in this gene differentially associates with epithelial ovaria…