Christopher Arnell

Biochemistry, Genetics and Molecular Biology · Life Sciences

7h-index2.0kcitations25works0.02yr avg
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Research Topics

BRCA gene mutations in cancer(14), Genetic factors in colorectal cancer(12), Nutrition, Genetics, and Disease(6), Cancer Genomics and Diagnostics(5), Genomics and Rare Diseases(4)

Publications25 total

CGE25-106: MHC II More Effectively Predicts Response to Pembrolizumab Than PD-L1 in HER2 Negative Patients
Journal of the National Comprehensive Cancer Network·2025
Guided therapy selection in rheumatoid arthritis using a molecular signature response classifier: an assessment of budget impact and clinical utility
Journal of Managed Care & Specialty Pharmacy·2021· 5 citedOpen Access
Optimization of Quality Assurance to Increase Clinical Utility and Cost Effectiveness of Hereditary Cancer Testing
Personalized Medicine·2017· 3 cited
Impact of Payer Constraints on Access to Genetic Testing
Journal of Oncology Practice·2017· 47 cited
Erratum to: Incidence of BRCA1 and BRCA2 non-founder mutations in patients of Ashkenazi Jewish ancestry
Breast Cancer Research and Treatment·2015· 1 citedOpen Access
A state by state analysis of BRCA1 and BRCA2 testing in patients with ovarian cancer
Gynecologic Oncology·2015
Patients Tested at a Laboratory for Hereditary Cancer Syndromes Show an Overlap for Multiple Syndromes in Their Personal and Familial Cancer Histories
Oncology·2015· 1.5k citedOpen Access
Supplementary Material for: Patients Tested at a Laboratory for Hereditary Cancer Syndromes Show an Overlap for Multiple Syndromes in Their Personal and Familial Cancer Histories
Figshare·2015Open Access
Hereditary Cancer-Associated Mutations in Women Diagnosed with Two Primary Cancers: An Opportunity to Identify Hereditary Cancer Syndromes after the First Cancer Diagnosis
Oncology·2014· 12 citedOpen Access
Incidence of BRCA1 and BRCA2 non-founder mutations in patients of Ashkenazi Jewish ancestry
Breast Cancer Research and Treatment·2014· 52 cited
Design and validation of an oligonucleotide microarray for the detection of genomic rearrangements associated with common hereditary cancer syndromes
Journal of Experimental & Clinical Cancer Research·2014· 5 citedOpen Access
Women with dual gynecologic primary cancers can have mutations in Lynch syndrome genes or BRCA1/BRCA2, reflecting the overlap in clinical histories between these syndromes
Gynecologic Oncology·2014
Analysis of patients with two hereditary cancers (breast/ovarian or colon/endometrial) who met NCCN genetic testing criteria after their first cancer.
Journal of Clinical Oncology·2014
Evaluation of breast cancer incidence in Lynch syndrome patients by MMR gene.
Journal of Clinical Oncology·2014
Proffered papers and posters submitted to the Fifth International Symposium on Hereditary Breast and Ovarian Cancer, BRCA: Twenty Years of Advances
Current Oncology·2014Open Access
Proffered Papers and Posters Submitted to the Fifth International Symposium on Hereditary Breast and Ovarian Cancer, BRCA: Twenty Years of Advances
Current Oncology·2014· 1 citedOpen Access
Analysis of current testing practices for biallelic <i><scp>MUTYH</scp></i> mutations in <i><scp>MUTYH</scp></i>‐associated polyposis
Clinical Genetics·2014· 14 citedOpen Access
Overlapping phenotypes with AFAP and FAP in patients with Lynch syndrome gene mutations.
Journal of Clinical Oncology·2014
Design and validation of an oligonucleotide microarray for the detection of genomic rearrangements associated with common hereditary cancer syndromes
Journal of Experimental & Clinical Cancer Research·2014· 1 citedOpen Access
A comprehensive laboratory‐based program for classification of variants of uncertain significance in hereditary cancer genes
Clinical Genetics·2013· 186 citedOpen Access
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Frequent Co-authors

Kelsey Moyes(12), Richard Wenstrup(11), Jennifer Saam(10), Michelle Landon(7), Aaron Theisen(6), Brian L. Abbott(6), Rajesh Kaldate(6), K. Moyes(5), Eric T. Rosenthal(5), Lynn Anne Burbidge(5), Benjamin B. Roa(4), Thaddeus Judkins(3), Jeremy Schoenberger(3), Brent Evans(3), Brian Strike(3), Ingrid Marino(2), Kirstin M. Roundy(2), Susan Manley(2), B. Roa(2), Jeffrey T. Trost(2)