Publications by authors named "Maegan Roberts"

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First Report of BAP1-Associated Polyposis.
Angela L Jacobson, Maegan E Roberts, Lindsey Byrne, Jenna Wolfe, Peter P Stanich

Am J Med Genet A· December 2025

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Updated genetic testing in individuals with unexplained adenomatous polyposis and the diagnostic yield.
Blake Rowell, Maegan E Roberts, Pamela L Brock, Julia Cooper, Rachel Pearlman

Fam Cancer· November 2025

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Sirolimus for Colon Polyposis in PTEN Hamartoma Tumor Syndrome.
Peter P Stanich, Kebire Gofar, Maegan E Roberts, Hisham Hussan

Clin Transl Gastroenterol· August 2025

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Prevalence of CFTR Pathogenic Variants in Pancreatitis: A Systematic Review and Meta-Analysis.
Joanna Jiang, Gavisha Waidyaratne, Shiab Mussad, Spencer Harris, Maegan E Roberts

Clin Transl Gastroenterol· July 2025

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Prevalence of Pathogenic Germline Variants in Patients With Gastric Cancer Ascertained Through Multigene Panel Testing.
Ophir Gilad, Emma Keel, Emily M Russell, Sarah M Nielsen, Brandie Heald, Maegan E Roberts

JCO Precis Oncol· June 2025

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Germline multigene panel testing in acute and chronic pancreatitis.
Mitchell L Ramsey, Brandie Heald, Yevgeniya Gokun, Josie Baker, J Royce Groce, Maegan E Roberts

PLoS One· August 2024

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Functional and Clinical Characterization of Variants of Uncertain Significance Identifies a Hotspot for Inactivating Missense Variants in RAD51C.
Chunling Hu, Anil Belur Nagaraj, Hermela Shimelis, Gemma Montalban, Kun Y Lee, Maegan E Roberts

Cancer Res· August 2023

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Optimising clinical care through -specific germline variant curation: improvement of clinical assertions and updated curation guidelines.
Xi Luo, Jamie L Maciaszek, Bryony A Thompson, Huei San Leong, Katherine Dixon, Maegan E Roberts

J Med Genet· June 2023

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Monoallelic MUTYH pathogenic variants ascertained via multi-gene hereditary cancer panels are not associated with colorectal, endometrial, or breast cancer.
Amanda Bartenbaker Thompson, Erin G Sutcliffe, Kevin Arvai, Maegan E Roberts, Lisa R Susswein

Fam Cancer· October 2022

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Phenotypic continuum between POLE-related recessive disorders: A case report and literature review.
Maegan E Roberts, Sarah Nimrichter, Megan L Marshall, Elizabeth K Flynn, Rick Person

Am J Med Genet A· October 2022

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Classification of BRCA2 Variants of Uncertain Significance (VUS) Using an ACMG/AMP Model Incorporating a Homology-Directed Repair (HDR) Functional Assay.
Chunling Hu, Lisa R Susswein, Maegan E Roberts, Hana Yang, Megan L Marshall

Clin Cancer Res· September 2022

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Patterns of germline and somatic testing after universal tumor screening for Lynch syndrome: A clinical practice survey of active members of the Collaborative Group of the Americas on Inherited Gastrointestinal Cancer.
Rachel Hodan, Linda Rodgers-Fouche, Sanjeevani Arora, Mev Dominguez-Valentin, Priyanka Kanth, Maegan E Roberts

J Genet Couns· August 2022

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Fibroblast testing can inform medical management in individuals with mosaic variants detected on hereditary cancer panels.
Erin G Sutcliffe, Jessica L Mester, Lisa R Susswein, Maegan E Roberts, Megan L Marshall

Cancer Genet· August 2022

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Ancestry-specific hereditary cancer panel yields: Moving toward more personalized risk assessment.
Maegan E Roberts, Lisa R Susswein, Wanchun Janice Cheng, Natalie J Carter, Amber C Carter

J Genet Couns· August 2020

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Differences in cancer prevalence among CHEK2 carriers identified via multi-gene panel testing.
Erin G Sutcliffe, Amy R Stettner, Stacey A Miller, Sheila R Solomon, Megan L Marshall, Maegan E Roberts

Cancer Genet· August 2020

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Response to Wang et al.
Maegan E Roberts, Nur Zeinomar, Benjamin D Solomon, Mary Beth Terry, Wendy K Chung

Genet Med· September 2019

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Comparison of CDH1 Penetrance Estimates in Clinically Ascertained Families vs Families Ascertained for Multiple Gastric Cancers.
Maegan E Roberts, John Michael O Ranola, Megan L Marshall, Lisa R Susswein, Sara Graceffo

JAMA Oncol· September 2019

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Response to Evans et al.
Maegan E Roberts, Nur Zeinomar, Benjamin D Solomon, Mary Beth Terry, Wendy K Chung

Genet Med· August 2019

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Determining the clinical validity of hereditary colorectal cancer and polyposis susceptibility genes using the Clinical Genome Resource Clinical Validity Framework.
Bryce A Seifert, Jennifer L McGlaughon, Sarah A Jackson, Deborah I Ritter, Maegan E Roberts

Genet Med· July 2019

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Age-adjusted association of homologous recombination genes with ovarian cancer using clinical exomes as controls.
Kevin J Arvai, Maegan E Roberts, Rebecca I Torene, Lisa R Susswein, Megan L Marshall

Hered Cancer Clin Pract· July 2019

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Multi-gene panel testing confirms phenotypic variability in MUTYH-Associated Polyposis.
Erin G Sutcliffe, Amanda Bartenbaker Thompson, Amy R Stettner, Megan L Marshall, Maegan E Roberts

Fam Cancer· April 2019

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Response to ten Broeke et al.
Maegan E Roberts, Nur Zeinomar, Benjamin D Solomon, Mary Beth Terry, Wendy K Chung

Genet Med· January 2019

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Utility of Expedited Hereditary Cancer Testing in the Surgical Management of Patients with a New Breast Cancer Diagnosis.
Kristin A Theobald, Lisa R Susswein, Megan L Marshall, Maegan E Roberts, Jessica L Mester

Ann Surg Oncol· November 2018

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Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline CDH1 sequence variants.
Kristy Lee, Kate Krempely, Maegan E Roberts, Michael J Anderson, Fatima Carneiro

Hum Mutat· November 2018

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MSH6 and PMS2 germ-line pathogenic variants implicated in Lynch syndrome are associated with breast cancer.
Maegan E Roberts, Sarah A Jackson, Lisa R Susswein, Nur Zeinomar, Xinran Ma

Genet Med· October 2018

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