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Published in Brain (London, England : 1878) (01.11.2014)
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Usher Syndrome in the Inner Ear: Etiologies and Advances in Gene Therapy
de Joya, Evan M, Colbert, Brett M, Tang, Pei-Ciao, Lam, Byron L, Yang, Jun, Blanton, Susan H, Dykxhoorn, Derek M, Liu, Xuezhong
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Published in Ear and hearing (01.01.2022)
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Traditional Cardiovascular Risk Factors Explain the Minority of the Variability in Carotid Plaque
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Published in Stroke (1970) (01.07.2012)
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The genetic basis of deafness in populations of African descent
Rudman, Jason R., Kabahuma, Rosemary I., Bressler, Sara E., Feng, Yong, Blanton, Susan H., Yan, Denise, Liu, Xue-Zhong
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Molecular and Epidemiologic Trends of Caliciviruses Associated with Outbreaks of Acute Gastroenteritis in the United States, 2000–2004
Blanton, Lenee H., Adams, Susan M., Beard, R. Suzanne, Wei, Gang, Bulens, Sandra N., Widdowson, Marc-Alain, Glass, Roger I., Monroe, Stephan S.
Published in The Journal of infectious diseases (01.02.2006)
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Genetics and the Individualized Therapy of Vestibular Disorders
Mei, Christine, Dong, Hongsong, Nisenbaum, Eric, Thielhelm, Torin, Nourbakhsh, Aida, Yan, Denise, Smeal, Molly, Lundberg, Yesha, Hoffer, Michael E, Angeli, Simon, Telischi, Fred, Nie, Guohui, Blanton, Susan H, Liu, Xuezhong
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Exome-Based Mapping and Variant Prioritization for Inherited Mendelian Disorders
Koboldt, Daniel C., Larson, David E., Sullivan, Lori S., Bowne, Sara J., Steinberg, Karyn M., Churchill, Jennifer D., Buhr, Aimee C., Nutter, Nathan, Pierce, Eric A., Blanton, Susan H., Weinstock, George M., Wilson, Richard K., Daiger, Stephen P.
Published in American journal of human genetics (06.03.2014)
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Screening of deafness-causing DNA variants that are common in patients of European ancestry using a microarray-based approach
Yan, Denise, Xiang, Guangxin, Chai, Xingping, Qing, Jie, Shang, Haiqiong, Zou, Bing, Mittal, Rahul, Shen, Jun, Smith, Richard J H, Fan, Yao-Shan, Blanton, Susan H, Tekin, Mustafa, Morton, Cynthia, Xing, Wanli, Cheng, Jing, Liu, Xue Zhong
Published in PloS one (08.03.2017)
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A dominant mutation in hexokinase 1 (HK1) causes retinitis pigmentosa
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Association of the sirtuin and mitochondrial uncoupling protein genes with carotid plaque
Dong, Chuanhui, Della-Morte, David, Wang, Liyong, Cabral, Digna, Beecham, Ashley, McClendon, Mark S, Luca, Corneliu C, Blanton, Susan H, Sacco, Ralph L, Rundek, Tatjana
Published in PloS one (07.11.2011)
Published in PloS one (07.11.2011)
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Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing Loss
Bademci, G., Cengiz, F. B., Foster II, J., Duman, D., Sennaroglu, L., Diaz-Horta, O., Atik, T., Kirazli, T., Olgun, L., Alper, H., Menendez, I., Loclar, I., Sennaroglu, G., Tokgoz-Yilmaz, S., Guo, S., Olgun, Y., Mahdieh, N., Bonyadi, M., Bozan, N., Ayral, A., Ozkinay, F., Yildirim-Baylan, M., Blanton, S. H., Tekin, M.
Published in Scientific reports (26.08.2016)
Published in Scientific reports (26.08.2016)
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COVID19: A Systematic Approach to Early Identification and Healthcare Worker Protection
Zhao, Yu, Cui, Chong, Zhang, Kun, Liu, Jialin, Xu, Jinfu, Nisenbaum, Eric, Huang, Yixiang, Qin, Guoyou, Chen, Bing, Hoffer, Michael, Blanton, Susan H, Telischi, Fred, Hare, Joshua M, Daunert, Sylvia, Shukla, Bhavarth, Pahwa, Savita G, Jayaweera, Dushyantha T, Farmer, Paul E, Del Rio, Carlos, Liu, Xuezhong, Shu, Yilai
Published in Frontiers in public health (19.05.2020)
Published in Frontiers in public health (19.05.2020)
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homozygous mutation in LTBP2 causes isolated microspherophakia
Kumar, Arun, Duvvari, Maheswara R, Prabhakaran, Venkatesh C, Shetty, Jyoti S, Murthy, Gowri J, Blanton, Susan H
Published in Human genetics (01.10.2010)
Published in Human genetics (01.10.2010)
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