Publications by authors named "Kelly Fulk"

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Functional analysis and clinical classification of 462 germline BRCA2 missense variants affecting the DNA binding domain.
Chunling Hu, Huaizhi Huang, Jie Na, Carolyn Lumby, Mohamed Abozaid, Kelly Fulk

Am J Hum Genet· March 2024

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Characterization of POT1 tumor predisposition syndrome: Tumor prevalence in a clinically diverse hereditary cancer cohort.
Jennifer Herrera-Mullar, Kelly Fulk, Terra Brannan, Amal Yussuf, Linda Polfus

Genet Med· November 2023

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RNA sequencing uncovers clinically actionable germline intronic variants in previously unresolved Lynch syndrome families.
Kelly Fulk, Morgan Turner, Amanda Eppolito, Rebekah Krukenberg

BMJ Case Rep· April 2022

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Strong functional data for pathogenicity or neutrality classify BRCA2 DNA-binding-domain variants of uncertain significance.
Marcy E Richardson, Chunling Hu, Kun Y Lee, Holly LaDuca, Kelly Fulk

Am J Hum Genet· March 2021

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A clinical guide to hereditary cancer panel testing: evaluation of gene-specific cancer associations and sensitivity of genetic testing criteria in a cohort of 165,000 high-risk patients.
Holly LaDuca, Eric C Polley, Amal Yussuf, Lily Hoang, Stephanie Gutierrez, Kelly Fulk

Genet Med· February 2020

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Monoallelic MUTYH carrier status is not associated with increased breast cancer risk in a multigene panel cohort.
Kelly Fulk, Holly LaDuca, Mary Helen Black, Dajun Qian, Yuan Tian

Fam Cancer· April 2019

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Women with breast and uterine cancer are more likely to harbor germline mutations than women with breast or uterine cancer alone: A case for expanded gene testing.
Kelly Fulk, Michael R Milam, Shuwei Li, Amal Yussuf, Mary Helen Black

Gynecol Oncol· March 2019

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Comprehensive Paired Tumor/Germline Testing for Lynch Syndrome: Bringing Resolution to the Diagnostic Process.
Monalyn U Salvador, Melissa R F Truelson, Carla Mason, Beth Souders, Holly LaDuca, Kelly Fulk

J Clin Oncol· March 2019

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