Maegan E. Roberts

1.4k citations

33 papers · 723 indexed · h-index 14

Impact in

Pathology and Forensic Medicine top 5%
- Genetic factors in colorectal cancer
Cancer Research top 10%
- Cancer Genomics and Diagnostics

Papers in

Pathology and Forensic Medicine 17
- Genetic factors in colorectal cancer 16
Cancer Research 11
- Cancer Genomics and Diagnostics 10

Co-authors: Douglas L. Riegert‐Johnson Lisa A. Boardman Lisa R. Susswein Megan L. Marshall Kathleen S. Hruska Rachel T. Klein Brittany C. Thomas Ferga C. Gleeson
Journals: Genetics in Medicine (4 papers)Familial Cancer (3 papers)Annals of Surgical Oncology (2 papers)Journal of Clinical Oncology (2 papers)Clinical Cancer Research (1 paper)
Partner nations: United States Australia Belgium

In The Last Decade

Maegan E. Roberts

30 papers receiving 712 citations

Peers

Countries citing papers authored by Maegan E. Roberts

Since Specialization

Citations

This map shows the geographic impact of Maegan E. Roberts's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Maegan E. Roberts with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Maegan E. Roberts more than expected).

Fields of papers citing papers by Maegan E. Roberts

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Maegan E. Roberts. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Maegan E. Roberts. The network helps show where Maegan E. Roberts may publish in the future.

Co-authors

The 25 scholars most cited alongside Maegan E. Roberts, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Maegan E. Roberts Line = papers co-authored together Maegan E. Roberts links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Prevalence of CFTR Pathogenic Variants in Pancreatitis: A Systematic Review and Meta-Analysis Clinical and Translational Gastroenterology ·G. A. GAUGER, Margil Vanderhoff, Chao Ge, Spencer Harris, Maegan E. Roberts, Yevgeniya Gokun, A. Jay Freeman, Samuel Han, Phil A. Hart, Luis F. Lara, Peter J. Lee, Somashekar G. Krishna, 正思江澤, Peter P. Stanich, Mitchell L. Ramsey	2025	1
2	Prevalence of Pathogenic Germline Variants in Patients With Gastric Cancer Ascertained Through Multigene Panel Testing JCO Precision Oncology ·Sierd Hadley, Diah Lestari Ayudiarti, Emily M. Russell, Sarah M. Nielsen, Brandie Heald, Edward D. Esplin, W. Michael Korn, Maegan E. Roberts, Carol A. Burke, Sonia S. Kupfer	2025	1
3	Germline multigene panel testing in acute and chronic pancreatitis PLoS ONE ·Mitchell L. Ramsey, Brandie Heald, Yevgeniya Gokun, Kaori Katagiri, Cecilia Dente, Samuel Han, Phil A. Hart, Somashekar G. Krishna, Luis F. Lara, Peter J. Lee, Georgios I. Papachristou, Rachel Pearlman, DiQiong HU, Maegan E. Roberts, Peter P. Stanich	2024	3
4	Classification of BRCA2 Variants of Uncertain Significance (VUS) Using an ACMG/AMP Model Incorporating a Homology-Directed Repair (HDR) Functional Assay Clinical Cancer Research ·Chunling Hu, Lisa R. Susswein, Maegan E. Roberts, Hana Yang, Megan L. Marshall, Susan Hiraki, Windy Berkofsky‐Fessler, Sounak Gupta, Wei Shen, Carolyn Dunn, Woon Yong Park, Jie Na, Susan M. Domchek, Siddhartha Yadav, Álvaro N.A. Monteiro, Eric C. Polley, Steven N. Hart, Kathleen S. Hruska, Fergus J. Couch	2022	6
5	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 Journal of Genetic Counseling ·Rachel Hodan, Linda Rodgers, Sanjeevani Arora, Mev Dominguez–Valentin, Priyanka Kanth, Bryson W. Katona, Xiaoyu Ye, Maegan E. Roberts, Eduardo Vilar, Nikolina Grbavac, Randall E. Brand, Edward D. Esplin, Kimberly Perez	2022	3
6	Fibroblast testing can inform medical management in individuals with mosaic variants detected on hereditary cancer panels Cancer Genetics ·Deji Kaveri, Jessica L. Mester, Lisa R. Susswein, Maegan E. Roberts, Megan L. Marshall, Kathleen S. Hruska	2022	0
7	Monoallelic MUTYH pathogenic variants ascertained via multi-gene hereditary cancer panels are not associated with colorectal, endometrial, or breast cancer Familial Cancer ·Amanda Thompson, Deji Kaveri, Kevin J. Arvai, Maegan E. Roberts, Lisa R. Susswein, Megan L. Marshall, Rebecca I. Torene, Kristen J. Vogel Postula, Kathleen S. Hruska, Shaochun Bai	2022	14
8	Differences in cancer prevalence among CHEK2 carriers identified via multi-gene panel testing Cancer Genetics ·Deji Kaveri, María Martínez‐Ceres, Karen Mauney, Elvis Berguer Mariz Moreira, Megan L. Marshall, Maegan E. Roberts, Lisa R. Susswein, Kevin J. Arvai, Rachel T. Klein, Patricia D. Murphy, Kathleen S. Hruska	2020	25
9	Multi-gene panel testing confirms phenotypic variability in MUTYH-Associated Polyposis Familial Cancer ·Deji Kaveri, Amanda Thompson, María Martínez‐Ceres, Megan L. Marshall, Maegan E. Roberts, Lisa R. Susswein, Ying Wang, Rachel T. Klein, Kathleen S. Hruska, Benjamin D. Solomon	2019	29
10	Utility of Expedited Hereditary Cancer Testing in the Surgical Management of Patients with a New Breast Cancer Diagnosis Annals of Surgical Oncology ·G. Quintaliani, Lisa R. Susswein, Megan L. Marshall, Maegan E. Roberts, Jessica L. Mester, Niels Cein, Field Jb, Gavin Young, Elvis Berguer Mariz Moreira, Patricia D. Murphy, Rachel T. Klein, Kathleen S. Hruska, Benjamin D. Solomon	2018	6
11	MSH6 and PMS2 germ-line pathogenic variants implicated in Lynch syndrome are associated with breast cancer Genetics in Medicine ·Maegan E. Roberts, Sarah A. Jackson, Lisa R. Susswein, Nur Zeinomar, Wei-Jeng Suen, Megan L. Marshall, María Martínez‐Ceres, Arshad Norrasyidah, Zhixiong Xu, Benjamin D. Solomon, Mary Beth Terry, Kathleen S. Hruska, Rachel T. Klein, Wendy K. Chung	2018	105
12	Determining the clinical validity of hereditary colorectal cancer and polyposis susceptibility genes using the Clinical Genome Resource Clinical Validity Framework Genetics in Medicine ·Bryce A. Seifert, Jennifer McGlaughon, Sarah A. Jackson, Deborah Ritter, Maegan E. Roberts, Ryan J. Schmidt, Bryony A. Thompson, Angela Marseglia, 宋豪飞, Kristy Lee, Sharon E. Plon, Kenneth Offit, Zsofia K. Stadler, Liying Zhang, Marc S. Greenblatt, Matthew J. Ferber	2018	17
13	High prevalence of pathogenic variants in individuals with colorectal cancer ≤ age 35. Journal of Clinical Oncology ·Megan L. Marshall, Maegan E. Roberts, Lisa R. Susswein, Аліна Юріївна Ковтун, Zhixiong Xu, Rachel T. Klein, Kathleen S. Hruska	2018	2
14	Assessing, Counseling, and Treating Patients at High Risk for Breast Cancer Annals of Surgical Oncology ·Edward Clifford, Kevin S. Hughes, Maegan E. Roberts, Sara Pirzadeh‐Miller, Sarah A. McLaughlin	2016	1
15	High-grade endometrial stromal sarcoma as the initial presentation of an adult patient with Peutz-Jeghers Syndrome: a case report Hereditary Cancer in Clinical Practice ·Patachia Silvia, Gerardo Colón‐Otero, Benjamin R. Kipp, John A. Copland, Matthew J. Ferber, Laura A. Marlow, Maegan E. Roberts, Matthew Robertson, Tri A. Dinh, Steven Attia, Xochiquetzal J. Geiger, Douglas L. Riegert‐Johnson	2015	1
16	A clinical scoring system to identify patients with sebaceous neoplasms at risk for the Muir–Torre variant of Lynch syndrome Genetics in Medicine ·Maegan E. Roberts, Douglas L. Riegert‐Johnson, Brittany C. Thomas, Kandelaria M. Rumilla, Colleen S. Thomas, Michael G. Heckman, Maria Luana Gonçalves Bezerra, Nancy Hanson, Kathleen A. Leppig, Justin Lim, Mark A. Cappel	2014	81
17	Appreciating the broad clinical features of SMAD4 mutation carriers: a multicenter chart review Genetics in Medicine ·Karen E. Wain, Marissa S. Ellingson, Jamie McDonald, Amanda Gammon, Maegan E. Roberts, Pavel N. Pichurin, Ingrid Winship, Douglas L. Riegert‐Johnson, Jeffrey N. Weitzel, Noralane M. Lindor	2014	54
18	Case studies in the diagnosis and management of Peutz-Jeghers syndrome Familial Cancer ·Douglas L. Riegert‐Johnson, Maegan E. Roberts, Ferga C. Gleeson, Murli Krishna, Lisa A. Boardman	2011	9
19	Cancer and Lhermitte-Duclos disease are common in Cowden syndrome patients Hereditary Cancer in Clinical Practice ·Douglas L. Riegert‐Johnson, Ferga C. Gleeson, Maegan E. Roberts, Camila Araujo Dias, W Zamanek, D. Hoak, Lisa A. Boardman	2010	108
20	RECURRENT VOLVULUS OF THE SIGMOID COLON DURING PREGNANCY COMPLICATED BY TOXEMIA OF PREGNANCY. PubMed ·Huques Chap, Maria Ramos-e- Silva, Maegan E. Roberts	1964	4

About Maegan E. Roberts

Maegan E. Roberts is a scholar working on Pathology and Forensic Medicine, Cancer Research, Genetics, Oncology and Pulmonary and Respiratory Medicine, having authored 33 papers that have together received 723 indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (16 papers), BRCA gene mutations in cancer (10 papers), Cancer Genomics and Diagnostics (10 papers), Genomics and Rare Diseases (8 papers), Multiple and Secondary Primary Cancers (4 papers), Genomic variations and chromosomal abnormalities (3 papers), Colorectal Cancer Screening and Detection (2 papers) and Colorectal Cancer Treatments and Studies (2 papers). The work is most often cited by research in Pathology and Forensic Medicine (411 citations), Cancer Research (212 citations), Genetics (237 citations), Oncology (175 citations) and Dermatology (42 citations). Maegan E. Roberts has collaborated with scholars based in United States, Australia and Belgium. Frequent co-authors include Douglas L. Riegert‐Johnson, Lisa A. Boardman, Lisa R. Susswein, Megan L. Marshall, Kathleen S. Hruska, Rachel T. Klein, Brittany C. Thomas, Ferga C. Gleeson, Colleen S. Thomas and Mark A. Cappel. Their work appears in journals such as Genetics in Medicine, Familial Cancer, Annals of Surgical Oncology, Journal of Clinical Oncology and Clinical Cancer Research.

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