- Alvarez-Paiva, MD, Gustavo A.
- Ayoade, MD , PhD, Katherine O.
- Bierbaum, MD, W. Frederick
- Bridge, MD, Julia A.
- Chang, MD, Dongkun Jack
- Chenault, MD, FCAP, Carrie
- Czapla, MD, Aggie
- Dang, MD, Daniel N.
- Driver, MD, Brandon
- El-Zayaty, MD, Chad
- Eze, MD, MHS, Ogechukwu P.
- Hernandez, MD, Amanda K.
- Hick, MD, Ryan W.
- Hill, MD, Isabel C.
- Hosler, MD, PhD, Gregory A.
- Hu, MD, PhD, Xiaofeng
- Joldoshova, MD, Albina
- Juarez, MD , Valerie M.
- Koo, MD, Jamie
- Law, MD, Robert M.
- Lemeshev, MD, Yan H.
- Lewin, MD, Matthew
- Lewin, MD, Marc R.
- Litz, MD, Craig E.
- Ly, DO, Uyen Debbie
- Ly, MD, Linda
- Malhotra, MD, Reenu
- Miles, MD, Janet M.
- Murphy, PhD, Kathleen M.
- Music, MD, Jodi S.
- O’Leary, MD, Erin
- Oliai, MD, Bahram Robert
- Onyeagocha, MD, Chukwuma O.
- Paluru, MD, Swetha
- Patel, DDS, Paras B.
- Patel, MD, Ravi A.
- Patel, MD, Kirtesh
- Peters, MD, PhD, John M.
- Podberezin, MD, PhD, Mark
- Rainwater, MD, Gina
- Roberts, MD, MBA, Cory A.
- Ruiz, MD, Monica I.
- Sarode, MD, Venetia R.
- Simms, MD, Anthony
- Smith MD, Stacey L.
- Snowden, MD, Cindi
- Susa, DO, Joseph S.
- Tarabishy, MD, Yaman
- Tumminello, MD, Katherine
- Underwood, MD, Caroline I.M.
- Vinovrski, MD, Todd J.
- Wagner, DO, Diana
- Washington, MD, Paula J.
- Wu, MD, Horace C.
Xiaofeng Hu, MD, PhD
Board Certifications
Laboratory Genetics and Genomics
Fellowship
Clinical Cytogenetics, Molecular Genetics
Interests
Cytogenetics
Biography
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Graduate School – The Netherlands National Ophthalmic Research Institute, The Netherlands
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Medical School – Tongji Medical University, China
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Prior to joining ProPath, Dr. Hu was the Clinical Director of Sonora Quest Laboratories and the Assistant Director of Cancer Cytogenetics and Genomics Diagnostics at Baylor College of Medicine.
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Joined ProPath in 2017
Peer-Reviewed Articles
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Li MM, Monzon FA, Biegel JA, Jobanputra V, Laffin JJ, Levy B, Leon A, Miron P, Rossi MR, Alvarez K, Doho K, Dougherty MG, Hu X, Kash S, Streck D, Znoyko L, Hagenford JM, Wolff DJ. A multicenter, cross-platform clinical validation study of cancer cytogenomic arrays. Cancer Genet. 2015;208(11):525-536.
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Ledet EM, Hu X, Sartor O, Rayford W, Li M, Mandal D. Characterization of germline copy number variation in high-risk African American families with prostate cancer. Prostate. 2013;73(6):614-623.
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Song J, Mercer D, Hu X, Liu H, Li MM. Common leukemia- and lymphoma-associated genetic aberrations in healthy individuals. J Mol Diagnostics. 2011;13(2):213-219.
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Xiang B, Zhu H, Shen Y, Miller DT, Lu K, Hu X, Andersson HC, Naramuchi TM, Wang Y, Martinez JE, Wu BL, Li P, Li MM, Chen TJ, Fan YS. Genome-wide oligonucleotide array comparative genomic hybridization for etiological diagnosis of mental retardation. J Mol Diagn. 2010;12(2):204-212.
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Hu X, Dai S, Wu W-J, et al. Stromal cell-derived factor-1α confers protection against myocardial ischemia/reperfusion injury role of the cardiac stromal cell-derived factor-1α CXCR4 axis. Circulation. 2007;116(6):654-663.
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Bergen AAB, Plomp AS, Hu X, De Jong PTVM, Gorgels TGMF. ABCC6 and pseudoxanthoma elasticum. Pflugers Arch Eur J Physiol. 2007;53(5):685-691.
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Wegman JJ, Hu X, Tan H, et al. Patients with premature coronary artery disease who carry the ABCC6 R1141X mutation have no Pseudoxanthoma Elasticum phenotype. Int J Cardiol. 2005;100(3):389-393.
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Gorgels TGMF, Hu X, Scheffer GL, et al. Disruption of Abcc6 in the mouse: novel insight in the pathogenesis of pseudoxanthoma elasticum. Hum Mol Genet. 2005;14(13):1763-1773.
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Fu S, Dong J, Chen G, Hu X. Mitochondrial DNA mutation and aminoglycoside antibiotic induced deafness. Chinese J Birth Heal Hered. 2004;4:6-8.
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Hu X, Plomp A, Grogels T, et al. Efficient molecular diagnostic strategy for ABCC6 in pseudoxanthoma elasticum. Genet Test. 2004;8(3):292-300.
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Fu S, Hu X, Chen G. Mutation of 235delC in connexin26 gene in patients with congenital hearing impairment. Matern Child Heal Care China. 2004;19(2):60-61.
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Plomp AS, Hu X, de Jong PTVM, Bergen AAB. Does autosomal dominant pseudoxanthoma elasticum exist? Am J Med Genet A. 2004;126A(4):403-412.
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Teng Y, Wang W, Tian H, Wang H, Hu X, Chen Y. Autosomal dominant retinitis pigmentosa in a five-generation pedigree in People’s Republic of China. Eye. 2003;17(9):1036-1039.
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Teng Y, Tian H, Wang H, Hu X, Chen Y, Yang Z, Wang W. Screening of candidate genes in a family with autosomal dominant retinitis pigmentosa. Zhonghua Yi Xue Yi Chuan Xue Za Zhi [Chinese J Med Genet.] 2003;20(2):164-166.
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Hu X, Plomp A, Wijnholds J, et al. ABCC6/MRP6 mutations: further insight into the molecular pathology of pseudoxanthoma elasticum. Eur J Hum Genet. 2003;11(3):215-224.
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Teng Y, Tian H, Wang H, Hu X, Wang W, Chen Y, Yang Z. Mutation identification in a 5-generation pedigree with autosomal dominant retinitis pigmentosa. J Huazhong Univ Sci Technol [Med Sci]. 2003;23(3):242-244.
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Hu X, Peek R, Plomp A, et al. Analysis of the frequent R1141X mutation in the ABCC6 gene in pseudoxanthoma elasticum. Investig Ophthalmol Vis Sci. 2003;44(5):1824-1829.
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Hu X, Plomp AS, van Soest S, Wijnholds J, De Jong PTVM, Bergen AAB. Pseudoxanthoma elasticum: A clinical, histopathological, and molecular update. Surv Ophthalmol. 2003;48(4):424-438.
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Trip MD, Smulders YM, Wegman JJ, Hu X, Boer JM, ten Brink JB, Zwinderman AH, Kastelein JJ, Feskens EJ, Bergen AA. Frequent mutation in the ABCC6 gene (R1141X) is associated with a strong increase in the prevalence of coronary artery disease. Circulation. 2002;106(7):773-775.
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Chen G, Guo Z, Fu S, Cui Y, Hu X. An etiological study on hearing loss of 813 deaf students in Hubei province. J Audiol Speech Pathol. 2002;10(4):229-231.
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Scheffer GL, Hu X, Pijnenborg ACLM, Wijnholds J, Bergen AAB, Scheper RJ. MRP6 (ABCC6) Detection in Normal Human Tissues and Tumors. Lab Invest. 2002;82(4):515-518.
Book Chapters
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Li M, Patel A, Hu X. Clinical applications of microarrays in cancer. In: Hu P, Hegde M, Lennon A, eds. Modern Clinical Molecular Techniques. New York: Springer; 2012:307-322.
Books
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Hu X. Analysis of ABCC6: Elucidation of the Molecular Pathology of Pseudoxanthoma Elasticum. Netherlands: University of Erasmus; 2003. ISBN 9057761130.