Author

Michelle Landon

Observed name: M. Landon

Institution: Agendia (United States)

Observed institutions: Myriad Genetics, Agendia (United States)

OpenAlex ID: A5038046017

Lynch Syndrome Patients with Limited Family History Identified in a Laboratory Setting: A Descriptive Study

2015 · Michelle Landon, Jennifer Saam, et al. · Oncology · 1,943

Analysis of current testing practices for biallelic MUTYH mutations in MUTYH ‐associated polyposis

2014 · M. Landon, S. Ceulemans, et al. · Clinical Genetics · 15

Hereditary Cancer-Associated Mutations in Women Diagnosed with Two Primary Cancers: An Opportunity to Identify Hereditary Cancer Syndromes after the First Cancer Diagnosis

2014 · Jennifer Saam, Kelsey Moyes, et al. · Oncology · 13

Discordance between germline genetic findings and abnormal tumor immunohistochemistry staining of mismatch repair proteins in individuals with suspected Lynch syndrome

2023 · Shujuan Pan, Hannah Cox, et al. · Frontiers in Oncology · 12

Abstract PS3-08-17: HR+ HER2- Early Breast Cancer (EBC) Patients ≥70 with High Risk 70-gene signature benefit from (Neo)adjuvant chemotherapy (CT): Real World FLEX Study

2026 · R. Mahtani, H. Wildiers, et al. · Clinical Cancer Research

Utility of genomic assays to guide treatment planning in patients aged 70 and older with early-stage breast cancer enrolled in FLEX

2025 · R. Mahtani, H. Wildiers, et al. · Journal of Geriatric Oncology

Real-world evidence from FLEX: Utility of MammaPrint in guiding treatment planning for patients aged 70 and older with early-stage breast cancer.

2025 · Reshma L. Mahtani, Ana Cristina Sandoval-Leon, et al. · Journal of Clinical Oncology

Proffered papers and posters presented at the Sixth International Symposium on Hereditary Breast and Ovarian Cancer—BRCA: Challenges and Opportunities : Presented by the Hereditary Breast and Ovarian Cancer Foundation in collaboration with the Program in Cancer Genetics, McGill University; Centre Mont-Royal, Montreal, QC; 10–13 May 2016

2016 · Lea M. Starita, Md. Jahirul Islam, et al. · Current Oncology

Abstract P4-12-02: Spectrum of mutations identified in a 25-gene hereditary cancer panel for patients with breast cancer

2015 · Lavania Sharma, Kelsey Moyes, et al. · Cancer Research

Evaluation of breast cancer incidence in Lynch syndrome patients by MMR gene.

2014 · Jamie Willmott, Adam Johnson, et al. · Journal of Clinical Oncology

Analysis of patients with two hereditary cancers (breast/ovarian or colon/endometrial) who met NCCN genetic testing criteria after their first cancer.

2014 · Jennifer Saam, Kelsey Moyes, et al. · Journal of Clinical Oncology

Overlapping phenotypes with AFAP and FAP in patients with Lynch syndrome gene mutations.

2014 · Erin Heckaman, Kelsey Moyes, et al. · Journal of Clinical Oncology

Su1077 Early Onset Colorectal and Endometrial Cancer Correlates With High Lynch Syndrome Mutation Rate but Mutation Rate Remains High Even in Patients Diagnosed in Their 50s and 60s

2013 · Brian Strike, Michelle Landon, et al. · Gastroenterology

Founder mutation versus full sequencing of MYH for increasing clinical sensitivity.

2013 · Sophia Ceulemans, Christopher Arnell, et al. · Journal of Clinical Oncology

Works count: 14

Citation count: 1,983

H-index: 4

I10-index: 4