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Author Details

Clesson Turner
National Human Genome Research Institute, National Institutes of Health
2001
42
15
PMIDPaper TitleJournal TitlePublished Year
37436924Assessing Clinical Utility of Pharmacogenetic Testing in the Military Health System.Mil Med2024
36608682Genotype first: Clinical genomics research through a reverse phenotyping approach.Am J Hum Genet2023
37481019Prevalence of Heart Failure Stages in a Universal Health Care System: The Military Health System Experience.Am J Med2023
37607111Computational in silico genetic variant prediction tools in cardiovascular disease.Ann Noninvasive Electrocardiol2023
37090550<i>ATP1A1</i> -linked diseases require a malfunctioning protein product from one allele.bioRxiv2023
35292633Germline mutation landscape of DNA damage repair genes in African Americans with prostate cancer highlights potentially targetable RAD genes.Nat Commun2022
35868102Influence of germline test results on surgical decision making in women with invasive breast cancer.Cancer Genet2022
36384096Proteogenomic analysis of lung adenocarcinoma reveals tumor heterogeneity, survival determinants, and therapeutically relevant pathways.Cell Rep Med2022
36091166Eligibility, uptake and response to germline genetic testing in women with DCIS.Front Oncol2022
35950707Are genetic counselors prepared to counsel active-duty service members? A survey of genetic counselors' self-efficacy, counseling techniques, and knowledge of military policy.J Genet Couns2022
34906450Genetic testing in Non-Hispanic Black women with breast cancer treated within an equal-access healthcare system.Genet Med2022
33206196Cancer Previvors in an Active Duty Service Women Population: An Opportunity for Prevention and Increased Force Readiness.Mil Med2021
33504652Whole-exome sequencing reveals germline-mutated small cell lung cancer subtype with favorable response to DNA repair-targeted therapies.Sci Transl Med2021
34967403Genetic Counseling Considerations for Military Beneficiaries.Mil Med2021
34967401Applying Pharmacogenomic Guidelines to Combat Medical Care.Mil Med2021
34129457Philadelphia Prostate Cancer Genetic Consensus Conference 2019 and implications for military medicine.Can J Urol2021
33083949Frequency and spectrum of mutations across 94 cancer predisposition genes in African American women with invasive breast cancer.Fam Cancer2021
32666089Exercise Dose Associated With Military Service: Implications for the Clinical Management of Inherited Risk for Arrhythmogenic Right Ventricular Cardiomyopathy.Mil Med2020
31786583Toward Personalized Medicine Implementation: Survey of Military Medicine Providers in the Area of Pharmacogenomics.Mil Med2020
31963545Should Genetic Testing for Cancer Predisposition Be Standard-of-Care for Women with Invasive Breast Cancer? The Murtha Cancer Center Experience.Cancers (Basel)2020
33302456Heritability of Low ER Staining/HER2-Breast Tumors: Are We Missing an Opportunity for Germline Testing?Genes (Basel)2020
30415494Return of secondary findings in genomic sequencing: Military implications.Mol Genet Genomic Med2019
31240828Patient-centered care and genomic medicine: A qualitative provider study in the military health system.J Genet Couns2019
31353023De Novo Heterozygous POLR2A Variants Cause a Neurodevelopmental Syndrome with Profound Infantile-Onset Hypotonia.Am J Hum Genet2019
31379942A 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 Genetic Elements.J Oncol2019
30838639From Discovery to Practice and Survivorship: Building a National Real-World Data Learning Healthcare Framework for Military and Veteran Cancer Patients.Clin Pharmacol Ther2019
28055140EIF2S3 Mutations Associated with Severe X-Linked Intellectual Disability Syndrome MEHMO.Hum Mutat2017
28125078Frequent inactivating germline mutations in DNA repair genes in patients with Ewing sarcoma.Genet Med2017
29178650Military genomics: a perspective on the successes and challenges of genomic medicine in the Armed Services.Mol Genet Genomic Med2017
26810774Hoyeraal-Hreidarsson Syndrome due to PARN Mutations: Fourteen Years of Follow-Up.Pediatr Neurol2016
29263806Genomic medicine in the military.NPJ Genom Med2016
27681385De novo missense variants in PPP1CB are associated with intellectual disability and congenital heart disease.Hum Genet2016
27545680De Novo Mutations in SON Disrupt RNA Splicing of Genes Essential for Brain Development and Metabolism, Causing an Intellectual-Disability Syndrome.Am J Hum Genet2016
26069456Management of Incidental Findings in the Era of Next-generation Sequencing.Curr Genomics2015
26100565Hypogammaglobulinemia and impaired antibody response in a child with chromosome 2p15-16.1 microdeletion syndrome.Ann Allergy Asthma Immunol2015
23533844Diagnosis of bardet-biedl syndrome in consecutive pregnancies affected with echogenic kidneys and polydactyly in a consanguineous couple.Case Rep Genet2013
22182842Correlation of rare coding variants in the gene encoding human glucokinase regulatory protein with phenotypic, cellular, and kinetic outcomes.J Clin Invest2012
208325091.3 Mb de novo deletion in chromosome band 3q29 associated with normal intelligence in a child.Eur J Med Genet2010
19602640The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicine.Genome Res2009
17935231Trisomy 9 mosaicism and XX sex reversal.Am J Med Genet A2007
12545275Human genetic disease caused by de novo mitochondrial-nuclear DNA transfer.Hum Genet2003
11746013Molecularly defined interstitial tandem duplication 6p case with mild manifestations.Am J Med Genet2001
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Collaborators

Walter Reed National Military Medical Center
Co-authored papers 11
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 5
Uniformed Services University of the Health Sciences
Co-authored papers 3
Walter Reed National Military Medical Center
Co-authored papers 2
National Human Genome Research Institute
Co-authored papers 2
Women's Health Integrated Research Center, Inova Health System
Co-authored papers 2
Center for Cancer Research, National Cancer Institute
Co-authored papers 2
Center for Cancer Research, National Cancer Institute
Co-authored papers 2
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 2
Sun Yat-sen Memorial Hospital, Sun Yat-sen University
Co-authored papers 2
Co-authored papers 2
National Institutes of Health, National Cancer Institute, Center for Cancer Research
Co-authored papers 2
Duke University School of Medicine
Co-authored papers 2
Chan Soon-Shiong Institute of Molecular Medicine at Windber
Co-authored papers 1
Co-authored papers 1
Co-authored papers 1
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 1
Vanderbilt Genetics Institute, Vanderbilt University Medical Center
Co-authored papers 1
Johns Hopkins McKusick-Nathans Department of Genetic Medicine
Co-authored papers 1
University of Michigan ann arbor
Co-authored papers 1
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Co-authored papers 1
Drew University, National Institutes of Health, Rutgers University New Brunswick, University of North Carolina at Chapel Hill
Co-authored papers 1
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Center for Precision Health Research, National Human Genome Research Institute
Co-authored papers 1
Motol University Hospital and Second Faculty of Medicine, Charles University
Co-authored papers 1
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Moores Cancer Center, University of California San Diego
Co-authored papers 1
Duke University School of Medicine
Co-authored papers 1
Peking University Third Hospital
Co-authored papers 1