Researcher profile · Semantic Scholar

Brittany C. Thomas

h-index: 16
Works: 35
Citations: 939

Most-cited papers

A clinical scoring system to identify patients with sebaceous neoplasms at risk for the Muir–Torre variant of Lynch syndrome
Maegan E. Roberts, D. Riegert-Johnson, Brittany C. Thomas, Kandelaria M. Rumilla +7 more
2014Genetics in Medicine120 citations Open access
Semantic Scholar
The landscape of reported VUS in multi-gene panel and genomic testing: Time for a change
H. Rehm, J. Alaimo, S. Aradhya, P. Bayrak-Toydemir +58 more
2023Genetics in Medicine118 citations Open access
Semantic Scholar
Frequency of deletions of EPCAM (TACSTD1) in MSH2-associated Lynch syndrome cases.
Kandelaria M. Rumilla, Karen V. Schowalter, N. Lindor, Brittany C. Thomas +14 more
2011Journal of Molecular Diagnostics115 citations Open access
Semantic Scholar
Spindle cell rhabdomyosarcoma of bone with FUS–TFCP2 fusion: confirmation of a very recently described rhabdomyosarcoma subtype
Nooshin K. Dashti, Rebecca N. Wehrs, Brittany C. Thomas, Asha A. Nair +7 more
2018Histopathology86 citations
Semantic Scholar
Screening for Muir-Torre Syndrome Using Mismatch Repair Protein Immunohistochemistry of Sebaceous Neoplasms
Maegan E. Roberts, D. Riegert-Johnson, Brittany C. Thomas, Colleen S. Thomas +7 more
2013Journal of Genetic Counseling76 citations
Semantic Scholar
PMS2 monoallelic mutation carriers: the known unknown
M. Goodenberger, Brittany C. Thomas, D. Riegert-Johnson, C. Boland +26 more
2015Genetics in Medicine61 citations Open access
Semantic Scholar
Homozygosity for the V122I mutation in transthyretin is associated with earlier onset of cardiac amyloidosis in the African American population in the seventh decade of life.
Honey V. Reddi, Sarah M. Jenkins, J. Theis, Brittany C. Thomas +3 more
2014Journal of Molecular Diagnostics47 citations Open access
Semantic Scholar
Development and Verification of an RNA Sequencing (RNA-Seq) Assay for the Detection of Gene Fusions in Tumors.
Jennifer L. Winters, Jaime I. Dávila, A. McDonald, Asha A. Nair +17 more
2018Journal of Molecular Diagnostics46 citations Open access
Semantic Scholar
Origins and prevalence of the American Founder Mutation of MSH2.
M. Clendenning, M. E. Baze, Shu-Ying Sun, K. Walsh +12 more
2008Cancer Research39 citations
Semantic Scholar
The Value of MUTYH Testing in Patients with Early Onset Microsatellite Stable Colorectal Cancer Referred for Hereditary Nonpolyposis Colon Cancer Syndrome Testing
D. Riegert-Johnson, Ruth A. Johnson, K. Rabe, Liang Wang +4 more
2007Genetic Testing33 citations
Semantic Scholar
Increasing genetic counseling referral rates through bundled interventions after ovarian cancer diagnosis.
C. Swanson, Amanika Kumar, Joy Maharaj, J. Kemppainen +6 more
2018Gynecologic Oncology24 citations
Semantic Scholar
Is Self-Disclosure Part of the Genetic Counselor's Clinical Role?
Brittany C. Thomas, P. M. Veach, B. LeRoy
2006Journal of Genetic Counseling21 citations Open access
Semantic Scholar
Self Diagnosis of Lynch Syndrome Using Direct to Consumer Genetic Testing: A Case Study
Maegan E. Roberts, D. Riegert-Johnson, Brittany C. Thomas
2011Journal of Genetic Counseling20 citations Open access
Semantic Scholar
An American Founder Mutation in MLH1
Jerneja Tomsic, S. Liyanarachchi, H. Hampel, M. Morak +10 more
2011International Journal of Cancer19 citations Open access
Semantic Scholar
The Utilization of Counseling Skills by the Laboratory Genetic Counselor
M. Goodenberger, Brittany C. Thomas, K. Wain
2015Journal of Genetic Counseling18 citations Open access
Semantic Scholar
Multiple Endocrine Neoplasia Type 2A Due to an Exon 8 (G533C) Mutation in a Large North American Kindred
M. Castro, Brittany C. Thomas, M. Richards, Jun Zhang +1 more
2013Thyroid18 citations
Semantic Scholar
The Genetic Counselor’s Role in Managing Ethical Dilemmas Arising in the Laboratory Setting
Jessica R Balcom, Katrina E. Kotzer, L. Waltman, J. Kemppainen +1 more
2016Journal of Genetic Counseling14 citations Open access
Semantic Scholar
“What Would You Do if You Were Me?” Effects of Counselor Self-Disclosure Versus Non-disclosure in a Hypothetical Genetic Counseling Session
Amy L. Paine, Patricia McCarthy Veach, Ian M. MacFarlane, Brittany C. Thomas +2 more
2010Journal of Genetic Counseling14 citations Open access
Semantic Scholar
Implementation of genomic medicine for rare disease in a tertiary healthcare system: Mayo Clinic Program for Rare and Undiagnosed Diseases (PRaUD)
F. Vairo, J. Kemppainen, Carolyn R. Rohrer Vitek, Denise A. Whalen +59 more
2023Journal of Translational Medicine13 citations Open access
Semantic Scholar
DNA Mismatch Repair and Lynch Syndrome
Brittany C. Thomas, M. Ferber, N. Lindor
20099 citations
Semantic Scholar
Multiple jejunal cancers resulting from combination of germline APC and MLH1 mutations
N. Lindor, T. Smyrk, Sheila Buehler, Shanaka R. Gunawardena +4 more
2012Familial Cancer8 citations
Semantic Scholar
Reactive gene curation to support interpretation and reporting of a clinical genome test for rare disease: Experience from over 1,000 cases
A. Clause, Julie P. Taylor, Revathi Rajkumar, Krista K. Bluske +22 more
2023Cell Genomics5 citations Open access
Semantic Scholar
Rare TBX4 Variant Causing Pulmonary Arterial Hypertension With Small Patella Syndrome in an Adult Man
S. Shrivastava, Teresa M. Kruisselbrink, A. Mohananey, Brittany C. Thomas +2 more
2021JACC Case Reports4 citations Open access
Semantic Scholar
Genetic Counseling for Cancer: Technology Promises Better Screening for Hereditary Cancer Patients
K. Niendorf, Brittany C. Thomas
2013Current Genetic Medicine Reports3 citations Open access
Semantic Scholar
Development of a flipped learning course to deliver and scale molecular variant evaluation education: A quality improvement initiative
Jessica R Balcom, Marissa S. Ellingson, Carrie Bowler, Darcy M. Richardson +2 more
2024Journal of Genetic Counseling2 citations
Semantic Scholar
Clinical Validation of a Next Generation Sequencing Panel Test for Hereditary Colorectal Cancer
M. Ferber, Lisa M. Peterson, Joseph H. Blommel, Numrah Fadra +1 more
20162 citations Open access
Semantic Scholar
Clinical significance of tumor microsatellite instability and immunohistochemistry for mismatch repair deficiency in colorectal cancers
Brittany C. Thomas, S. Thibodeau, N. Lindor
20052 citations
Semantic Scholar
Comment on: Anti-tumour necrosis factor treatment for the prevention of ischaemic events in patients with deficiency of adenosine deaminase 2 (DADA2).
F. Vairo, M. Koster, J. Kemppainen, Brittany C. Thomas +1 more
2021Rheumatology1 citations
Semantic Scholar
Response to Commercial Genetic Testing and the Future of the Genetic Counseling Profession
M. Goodenberger, Brittany C. Thomas, Teresa M. Kruisselbrink
2018Journal of Genetic Counseling1 citations
Semantic Scholar
Discordant results between biochemical and molecular transthyretin assays: lessons learned from a unique testing algorithm at the Mayo Clinic
Honey V. Reddi, Brittany C. Thomas, Kurt S. Willkomm, M. Ferber +4 more
2013Journal Genetika1 citations
Semantic Scholar
Evaluating the association between family cancer history and variants of uncertain significance
Rebecca Shin, Natalie L. Ayoub, Hai-Bo Lu, Bowen Li +2 more
2025Gynecologic Oncology Reports0 citations Open access
Semantic Scholar
P471: Quad whole genome sequencing detects reciprocal copy number variants in affected siblings, consistent with familial translocation
Katie Golden-Grant, Amanda Buchanan, A. Coffey, Y. Brew +4 more
2023Genetics in Medicine Open0 citations Open access
Semantic Scholar
P572: Detecting short tandem repeat expansions: Three-year experience with clinical whole genome sequencing (cWGS) for a rare and undiagnosed population
Brittany C. Thomas, A. Kesari, Aimé Lumaka, M. Cornejo-Olivas +7 more
2023Genetics in Medicine Open0 citations Open access
Semantic Scholar
Discordant results between biochemical and molecular transthyretin assays: lessons learned from a unique testing algorithm at the Mayo Clinic
Honey V. Reddi, Brittany C. Thomas, Kurt S. Willkomm, M. Ferber +4 more
2013Journal Genetika0 citations
Semantic Scholar
Multiple jejunal cancers resulting from combination of germline APC and MLH1 mutations
N. Lindor, T. Smyrk, Sheila Buehler, Shanaka R. Gunawardena +4 more
2012Familial Cancer0 citations
Semantic Scholar

D. Perry

×4

R. Taft×4

J. Kemppainen×4

Teresa M. Kruisselbrink×4

M. Ferber×4

Maegan E. Roberts×3

Erin Thorpe×3

M. Goodenberger×3