Confidentiality & the Risk of Genetic Discrimination: What Surgeons Need to Know

Por Gammon, Amanda, Neklason, Deborah W.
Publicado no Surg Oncol Clin N Am (2015)

Hereditary and Familial Colon Cancer

Por Jasperson, Kory W., Tuohy, Thérèse M., Neklason, Deborah W., Burt, Randall W.
Publicado em 2010

Evidence for a heritable contribution to neuroendocrine tumors of the small intestine

Por Neklason, Deborah W., VanDerslice, James, Curtin, Karen, Cannon-Albright, Lisa A.
Publicado no Endocr Relat Cancer (2015)

Mutation-negative FAP patients with mRNA defects of APC

Por Condie, Michelle W, Tuohy, Therese MF, Shires, Patricia, Burt, Randall W, Neklason, Deborah W
Publicado em 2010

Differential gene expression in primary colonic tissue from control, FAP and AFAP patients reveals unique signatures with diagnostic potential

Por Neklason, Deborah W, Milash, Brett A, Tuohy, Therese M, Lilley, Jennifer, Burt, Randall W
Publicado em 2010

Descriptive review and comparison of clinical outcomes of AFAP patients

Por McCoy, Heidi, Kohlmann, Wendy, Neklason, Deborah W, Burt, Randall W, Boucher, Ken M
Publicado em 2011

Germ Cell Mosaicism: A Rare Cause of Li-Fraumeni Recurrence Among Siblings

Por Donovan, Lauren N., Kohlmann, Wendy, Snow, Angela K., Neklason, Deborah W., Schiffman, Joshua D., Maese, Luke
Publicado no JCO Precis Oncol (2020)

Outcomes and complications of radiation therapy in patients with familial adenomatous polyposis

Por Gan, Meng, Boothe, Dustin, Neklason, Deborah W., Samadder, N. Jewel, Frandsen, Jonathan, Keener, Megan B., Lloyd, Shane
Publicado no J Gastrointest Oncol (2017)

POLR2C Mutations Are Associated With Primary Ovarian Insufficiency in Women

Por Moriwaki, Mika, Moore, Barry, Mosbruger, Timothy, Neklason, Deborah W., Yandell, Mark, Jorde, Lynn B., Welt, Corrine K.
Publicado no J Endocr Soc (2017)

Evolution of a High-Risk Cancer Registry: past, present and future

Por Lewandowski, Michelle S, Day, Thomas M, Christensen, Joslin, Tuohy, Therese MF, Kohlmann, Wendy, Neklason, Deborah W, Burt, Randall W
Publicado em 2010

Deciphering the molecular pathways disrupted in normal and neoplastic colonic tissue in inherited colorectal cancer syndromes

Por Neklason, Deborah W, Done, Michelle W, Milash, Brett, Frey, Lewis, Sargent, Nykole, Tuohy, Thérèse M, Burt, Randall W
Publicado em 2011

Effect of smoking on urothelial cancer risk in individuals with Lynch syndrome

Por Kohlmann Wendy, Pappas Lisa M, Jasperson Kory, Neklason Deborah W, Burt Randall W, Weitzel Jeffrey N, Stoffel Elena M
Publicado em 2010-05-01

Effect of smoking on urothelial cancer risk in individuals with Lynch syndrome

Por Kohlmann, Wendy, Pappas, Lisa M, Jasperson, Kory, Neklason, Deborah W, Burt, Randall W, Weitzel, Jeffrey N, Stoffel, Elena M
Publicado em 2010

APC promoter 1B deletion in seven American families with familial adenomatous polyposis

Por Snow, Angela K., Tuohy, Thérèse M.F., Sargent, Nykole R., Smith, Laurel J., Burt, Randall W., Neklason, Deborah W.
Publicado no Clin Genet (2014)

Associations of tobacco and alcohol use with risk of neuroendocrine tumors of the small intestine in Utah

Por Curtin, Karen, Cannon-Albright, Lisa A., VanDerslice, James, Yu, Zhe, Herget, Kimberly A., Thota, Ramya, Neklason, Deborah W.
Publicado no Cancer Epidemiol Biomarkers Prev (2019)

Gene Signature in Sessile Serrated Polyps Identifies Colon Cancer Subtype

Por Kanth, Priyanka, Bronner, Mary P., Boucher, Kenneth M., Burt, Randall W., Neklason, Deborah W., Hagedorn, Curt H., Delker, Don A.
Publicado no Cancer Prev Res (Phila) (2016)

Defining the overlap between sporadic and attenuated familial adenoma risk

Por Tuohy, Thérèse M, Neklason, Deborah W, Boucher, Kenneth M, Pimentel, Richard G, Rowe, Kerry G, Mineau, Geraldine P, Burt, Randall W
Publicado em 2011

Early life exposures associated with risk of small intestinal neuroendocrine tumors

Por VanDerslice, James, Taddie, Marissa C., Curtin, Karen, Miller, Caroline, Yu, Zhe, Hemmert, Rachael, Cannon-Albright, Lisa A., Neklason, Deborah W.
Publicado no PLoS One (2020)

Evaluating Lynch syndrome in very early onset colorectal cancer probands without apparent polyposis

Por Jasperson, Kory W., Vu, Thuy M., Schwab, Angela L., Neklason, Deborah W., Rodriguez-Bigas, Miguel A., Burt, Randall W., Weitzel, Jeffrey N.
Publicado em 2010

Shared Genomic Segment Analysis: The Power to Find Rare Disease Variants

Por Knight, Stacey, Abo, Ryan P, Abel, Haley J, Neklason, Deborah W, Tuohy, Therese M, Burt, Randall W, Thomas, Alun, Camp, Nicola J
Publicado em 2012