CGA-IGC 2019

Collaborative Group of the Americas on Inherited Colorectal Cancer annual meeting


Research

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Scientific Posters

Poster # tbd

Saturday, December 14, 2019 7:00 - 9:00am Abstract

Holly LaDuca, Lily Hoang, Jill Dolinsky, Jessica Profato, Amal Yussuf, Carolyn Horton, Ann Bunnell, C. Dresbold, Cassie Garcia, Catherine Koptiuch, Chantalle Raimondi, Cristina Ruiz, Daniella Menashe, Danielle Dondanville, Danielle McKenna, Deborah Oleskowicz, Deborah Wham, Deepika Nathan, Diane Samad, Eden Faye, Elizabeth Hoodfar, Gayle Patel, Jen Moore, Jennifer Geurts, John Lee, Kara Milliron, Kate Principe, Khateriaa Pyrtel, Meagan Farmer, Meredith Seidel, Morgan Depas, Nichole Morman, Olivia Tan, Rebekah Krukenberg, Rikki Gaber, Rob Pilarski, Samantha Stachowiak, Sandra Jenkinson, Sara Pirzadeh-Miller, Seth Marcus, Shraddha Gaonkar, Trisha Nichols, Brigette Tippin Davis, Elizabeth Chao, Rachid Karam. Concurrent DNA and RNA genetic testing identifies more patients with Lynch Syndrome than DNA testing alone.

Poster # tbd

Sunday, November 3, 2019 8:00 - 12:00pm Abstract

Carolyn Horton, Kirsten Blanco, Holly LaDuca, Mary Helen Black, Kyle Allen, Jill Dolinsky. Impact of multigene panel testing on medical management: Preliminary results of a pre- and post-genetic testing clinician survey.

Poster # tbd

Sunday, November 3, 2019 8:00 - 12:00pm Abstract

Kathryn A. Mraz, Marcy Richardson. Possible founder mutation in CDKN2A in the Latino population.

Poster # tbd

Sunday, November 3, 2019 8:00 - 12:00pm

Carla Mason, Kelly Fulk, Beth Souders, Holly LaDuca, Rachid Karam, Felicia Hernandez, Noriko Yokoyama, Blair R. Conner, Ritter Hagadorn, Kyle Allen, Tyler Landrith, Bhuvan Molparia, Ashley Cass, Virginia Speare, Rebekah Krukenberg, Elizabeth Chao. RNA testing increases the diagnostic yield in an unresolved cohort of patients with paired Lynch Syndrome DNA testing.

Oral Presentations

Session # tbd

Sunday, November 3, 2019 8:00 - 12:00pm Abstract

Heather Hampel, Rachel Pearlman, Sarah Campian, Polly Newcomb, Mercy Laurino, Bryony Thompson. The R659Q and K618A MLH1 variants (of uncertain significance and benign independently) are pathogenic when inherited in cis

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