Prevalence of Heart Failure Stages in a Universal Health Care System: The Military Health System Experience von Roger, Véronique L., Banaag, Amanda, Korona-Bailey, Jessica, Wiley, Tiffany M. Powell, Turner, Clesson E., Haigney, Mark C., Koehlmoos, Tracey Perez

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Frequent inactivating germline mutations in DNA repair genes in patients with Ewing sarcoma von Brohl, Andrew S., Patidar, Rajesh, Turner, Clesson E., Wen, Xinyu, Song, Young K., Wei, Jun S., Calzone, Kathleen A., Khan, Javed

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Germline mutation landscape of DNA damage repair genes in African Americans with prostate cancer highlights potentially targetable RAD genes von Kohaar, Indu, Zhang, Xijun, Tan, Shyh-Han, Nousome, Darryl, Babcock, Kevin, Ravindranath, Lakshmi, Sukumar, Gauthaman, Mcgrath-Martinez, Elisa, Rosenberger, John, Alba, Camille, Ali, Amina, Young, Denise, Chen, Yongmei, Cullen, Jennifer, Rosner, Inger L., Sesterhenn, Isabell A., Dobi, Albert, Chesnut, Gregory, Turner, Clesson, Dalgard, Clifton, Wilkerson, Matthew D., Pollard, Harvey B., Srivastava, Shiv, Petrovics, Gyorgy

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Genetic Counseling Considerations for Military Beneficiaries von Hellwig, Lydia D, Krokosky, Alyson, Vargason, Ashlee, Turner, Clesson

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Computational in silico genetic variant prediction tools in cardiovascular disease von Hellwig, Lydia D., Villar, Joaquin, Turner, Clesson

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Eligibility, uptake and response to germline genetic testing in women with DCIS von Turza, Lauren, Lovejoy, Leann A, Turner, Clesson E, Shriver, Craig D, Ellsworth, Rachel E

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Genetic testing in Non-Hispanic Black women with breast cancer treated within an equal-access healthcare system von Vargason, Ashlee B., Turner, Clesson E., Shriver, Craig D., Ellsworth, Rachel E.

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Cancer Previvors in an Active Duty Service Women Population: An Opportunity for Prevention and Increased Force Readiness von Lovejoy, Leann A, Turner, Clesson E, Shriver, Craig D, Ellsworth, Rachel E

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A Review of the Hereditary Component of Triple Negative Breast Cancer: High- and Moderate-Penetrance Breast Cancer Genes, Low-Penetrance Loci, and the Role of Nontraditional Geneti... von Ellsworth, Darrell L., Ellsworth, Rachel E., Turner, Clesson E.

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EIF2S3 Mutations Associated with Severe X‐Linked Intellectual Disability Syndrome MEHMO von Skopkova, Martina, Hennig, Friederike, Shin, Byung‐Sik, Turner, Clesson E., Stanikova, Daniela, Brennerova, Katarina, Stanik, Juraj, Fischer, Ute, Henden, Lyndal, Müller, Ulrich, Steinberger, Daniela, Leshinsky‐Silver, Esther, Bottani, Armand, Kurdiova, Timea, Ukropec, Jozef, Nyitrayova, Olga, Kolnikova, Miriam, Klimes, Iwar, Borck, Guntram, Bahlo, Melanie, Haas, Stefan A., Kim, Joo‐Ran, Lotspeich‐Cole, Leda E., Gasperikova, Daniela, Dever, Thomas E., Kalscheuer, Vera M.

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The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicine von Biesecker, Leslie G, Mullikin, James C, Facio, Flavia M, Turner, Clesson, Cherukuri, Praveen F, Blakesley, Robert W, Bouffard, Gerard G, Chines, Peter S, Cruz, Pedro, Hansen, Nancy F, Teer, Jamie K, Maskeri, Baishali, Young, Alice C, Manolio, Teri A, Wilson, Alexander F, Finkel, Toren, Hwang, Paul, Arai, Andrew, Remaley, Alan T, Sachdev, Vandana, Shamburek, Robert, Cannon, Richard O, Green, Eric D

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Influence of germline test results on surgical decision making in women with invasive breast cancer von Vargason, Ashlee B., Turner, Clesson E., Shriver, Craig D., Ellsworth, Rachel E.

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Applying Pharmacogenomic Guidelines to Combat Medical Care von DeLuca, Jesse, Oliver, Thomas, Hulsopple, Chad, Selig, Daniel, Por, Elaine, Turner, Clesson, Hellwig, Lydia, Livezey, Jeffrey

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Frequency and spectrum of mutations across 94 cancer predisposition genes in African American women with invasive breast cancer von Lovejoy, Leann A., Rummel, Seth K., Turner, Clesson E., Shriver, Craig D., Ellsworth, Rachel E.

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Toward Personalized Medicine Implementation: Survey of Military Medicine Providers in the Area of Pharmacogenomics von DeLuca, Jesse, Selig, Daniel, Poon, Lucas, Livezey, Jeffrey, Oliver, Thomas, Barrett, John, Turner, Clesson, Hellwig, Lydia

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Hoyeraal-Hreidarsson Syndrome due to PARN Mutations: Fourteen Years of Follow-Up von Burris, Ashley M., DO, Ballew, Bari J., PhD, Kentosh, Joshua B., DO, Turner, Clesson E., MD, Norton, Scott A., MD, MPH, Giri, Neelam, MD, Alter, Blanche P., MD, MPH, Nellan, Anandani, MD, Gamper, Christopher, MD, PhD, Hartman, Kip R., MD, Savage, Sharon A., MD

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Exercise Dose Associated With Military Service: Implications for the Clinical Management of Inherited Risk for Arrhythmogenic Right Ventricular Cardiomyopathy von Segre, Elena M, Hellwig, Lydia D, Turner, Clesson, Dobson, Craig P, Haigney, Mark C

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Hypogammaglobulinemia and impaired antibody response in a child with chromosome 2p15-16.1 microdeletion syndrome von Ottolini, Katherine M., MD, Turner, Clesson E., MD, Gada, Satyen M., MD

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De novo missense variants in PPP1CB are associated with intellectual disability and congenital heart disease von Ma, Lijiang, Bayram, Yavuz, McLaughlin, Heather M., Cho, Megan T., Krokosky, Alyson, Turner, Clesson E., Lindstrom, Kristin, Bupp, Caleb P., Mayberry, Katey, Mu, Weiyi, Bodurtha, Joann, Weinstein, Veronique, Zadeh, Neda, Alcaraz, Wendy, Powis, Zöe, Shao, Yunru, Scott, Daryl A., Lewis, Andrea M., White, Janson J., Jhangiani, Shalani N., Gulec, Elif Yilmaz, Lalani, Seema R., Lupski, James R., Retterer, Kyle, Schnur, Rhonda E., Wentzensen, Ingrid M., Bale, Sherri, Chung, Wendy K.

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Using a pilot-centric, qualitative drug risk assessment model to identify opportunities for implementing pharmacogenetics von Kinard, Jeffrey L., Collie, Jacob, Turner, Clesson, Chapleau, Richard R.

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