PredictSNP: robust and accurate consensus classifier for prediction of disease-related mutations von Bendl, Jaroslav, Stourac, Jan, Salanda, Ondrej, Pavelka, Antonin, Wieben, Eric D, Zendulka, Jaroslav, Brezovsky, Jan, Damborsky, Jiri

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A common trinucleotide repeat expansion within the transcription factor 4 (TCF4, E2-2) gene predicts Fuchs corneal dystrophy von Wieben, Eric D, Aleff, Ross A, Tosakulwong, Nirubol, Butz, Malinda L, Highsmith, W Edward, Edwards, Albert O, Baratz, Keith H

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3' tag digital gene expression profiling of human brain and universal reference RNA using Illumina Genome Analyzer von Asmann, Yan W, Klee, Eric W, Thompson, E Aubrey, Perez, Edith A, Middha, Sumit, Oberg, Ann L, Therneau, Terry M, Smith, David I, Poland, Gregory A, Wieben, Eric D, Kocher, Jean-Pierre A

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Comparison of TCF4 repeat expansion length in corneal endothelium and leukocytes of patients with Fuchs endothelial corneal dystrophy von Wieben, Eric D, Aleff, Ross A, Rinkoski, Tommy A, Baratz, Keith H, Basu, Shubham, Patel, Sanjay V, Maguire, Leo J, Fautsch, Michael P

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Sentieon DNASeq Variant Calling Workflow Demonstrates Strong Computational Performance and Accuracy von Kendig, Katherine I, Baheti, Saurabh, Bockol, Matthew A, Drucker, Travis M, Hart, Steven N, Heldenbrand, Jacob R, Hernaez, Mikel, Hudson, Matthew E, Kalmbach, Michael T, Klee, Eric W, Mattson, Nathan R, Ross, Christian A, Taschuk, Morgan, Wieben, Eric D, Wiepert, Mathieu, Wildman, Derek E, Mainzer, Liudmila S

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The genomic landscape of small intestine neuroendocrine tumors von Banck, Michaela S, Kanwar, Rahul, Kulkarni, Amit A, Boora, Ganesh K, Metge, Franziska, Kipp, Benjamin R, Zhang, Lizhi, Thorland, Erik C, Minn, Kay T, Tentu, Ramesh, Eckloff, Bruce W, Wieben, Eric D, Wu, Yanhong, Cunningham, Julie M, Nagorney, David M, Gilbert, Judith A, Ames, Matthew M, Beutler, Andreas S

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Gene expression in the corneal endothelium of Fuchs endothelial corneal dystrophy patients with and without expansion of a trinucleotide repeat in TCF4 von Wieben, Eric D, Aleff, Ross A, Tang, Xiaojia, Kalari, Krishna R, Maguire, Leo J, Patel, Sanjay V, Baratz, Keith H, Fautsch, Michael P

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RNA Toxicity and Missplicing in the Common Eye Disease Fuchs Endothelial Corneal Dystrophy von Du, Jintang, Aleff, Ross A., Soragni, Elisabetta, Kalari, Krishna, Nie, Jinfu, Tang, Xiaojia, Davila, Jaime, Kocher, Jean-Pierre, Patel, Sanjay V., Gottesfeld, Joel M., Baratz, Keith H., Wieben, Eric D.

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Repeat-Associated Non-ATG (RAN) Translation in Fuchs' Endothelial Corneal Dystrophy von Soragni, Elisabetta, Petrosyan, Lina, Rinkoski, Tommy A, Wieben, Eric D, Baratz, Keith H, Fautsch, Michael P, Gottesfeld, Joel M

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Amplification-free long-read sequencing of TCF4 expanded trinucleotide repeats in Fuchs Endothelial Corneal Dystrophy von Wieben, Eric D, Aleff, Ross A, Basu, Shubham, Sarangi, Vivekananda, Bowman, Brett, McLaughlin, Ian J, Mills, John R, Butz, Malinda L, Highsmith, Edward W, Ida, Cristiane M, Ekholm, Jenny M, Baratz, Keith H, Fautsch, Michael P

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Multi-platform analysis of microRNA expression measurements in RNA from fresh frozen and FFPE tissues von Kolbert, Christopher P, Feddersen, Rod M, Rakhshan, Fariborz, Grill, Diane E, Simon, Gyorgy, Middha, Sumit, Jang, Jin Sung, Simon, Vernadette, Schultz, Debra A, Zschunke, Michael, Lingle, Wilma, Carr, Jennifer M, Thompson, E Aubrey, Oberg, Ann L, Eckloff, Bruce W, Wieben, Eric D, Li, Peter, Yang, Ping, Jen, Jin

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TCF4-mediated Fuchs endothelial corneal dystrophy: Insights into a common trinucleotide repeat-associated disease von Fautsch, Michael P., Wieben, Eric D., Baratz, Keith H., Bhattacharyya, Nihar, Sadan, Amanda N., Hafford-Tear, Nathaniel J., Tuft, Stephen J., Davidson, Alice E.

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Recommendations for performance optimizations when using GATK3.8 and GATK4 von Heldenbrand, Jacob R, Baheti, Saurabh, Bockol, Matthew A, Drucker, Travis M, Hart, Steven N, Hudson, Matthew E, Iyer, Ravishankar K, Kalmbach, Michael T, Kendig, Katherine I, Klee, Eric W, Mattson, Nathan R, Wieben, Eric D, Wiepert, Mathieu, Wildman, Derek E, Mainzer, Liudmila S

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Trinucleotide Repeat Expansion in the Transcription Factor 4 (TCF4) Gene Leads to Widespread mRNA Splicing Changes in Fuchs' Endothelial Corneal Dystrophy von Wieben, Eric D, Aleff, Ross A, Tang, Xiaojia, Butz, Malinda L, Kalari, Krishna R, Highsmith, Edward W, Jen, Jin, Vasmatzis, George, Patel, Sanjay V, Maguire, Leo J, Baratz, Keith H, Fautsch, Michael P

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Discovery of recurrent t(6;7)(p25.3;q32.3) translocations in ALK-negative anaplastic large cell lymphomas by massively parallel genomic sequencing von Feldman, Andrew L., Dogan, Ahmet, Smith, David I., Law, Mark E., Ansell, Stephen M., Johnson, Sarah H., Porcher, Julie C., Özsan, Nazan, Wieben, Eric D., Eckloff, Bruce W., Vasmatzis, George

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Autosomal dominant calpainopathy due to heterozygous CAPN3 C.643_663del21 von Martinez‐Thompson, Jennifer M., Niu, Zhiyv, Tracy, Jennifer A., Moore, Steven A., Swenson, Andrea, Wieben, Eric D., Milone, Margherita

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Androgen Receptor Variant AR-V9 Is Coexpressed with AR-V7 in Prostate Cancer Metastases and Predicts Abiraterone Resistance von Kohli, Manish, Ho, Yeung, Hillman, David W, Van Etten, Jamie L, Henzler, Christine, Yang, Rendong, Sperger, Jamie M, Li, Yingming, Tseng, Elizabeth, Hon, Ting, Clark, Tyson, Tan, Winston, Carlson, Rachel E, Wang, Liguo, Sicotte, Hugues, Thai, Ho, Jimenez, Rafael, Huang, Haojie, Vedell, Peter T, Eckloff, Bruce W, Quevedo, Jorge F, Pitot, Henry C, Costello, Brian A, Jen, Jin, Wieben, Eric D, Silverstein, Kevin A T, Lang, Joshua M, Wang, Liewei, Dehm, Scott M

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Characterization of a dual media system for culturing primary normal and Fuchs endothelial corneal dystrophy (FECD) endothelial cells von Rinkoski, Tommy A, Bahler, Cindy K, Pacheco, Johann M, Khanna, Maya L, Holmes, David M, Roy Chowdhury, Uttio, Baratz, Keith H, Patel, Sanjay V, Maguire, Leo J, Wieben, Eric D, Fautsch, Michael P

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εγ-Thalassemia, a New Hemoglobinopathy Category von Oliveira, Jennifer L, Thompson, Christineil H, Saravanaperumal, Siva Arumugam, Koganti, Tejaswi, Jenkinson, Garrett, Hein, Molly S, Kohorst, Mira A, Hasadsri, Linda, Nguyen, Phuong L, Matern, Dietrich, Kipp, Benjamin R, Klee, Eric W, Wieben, Eric D, Hoyer, James D, Rangan, Aruna

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Prevalence of CDKN2A mutations in pancreatic cancer patients: implications for genetic counseling von McWilliams, Robert R, Wieben, Eric D, Rabe, Kari G, Pedersen, Katrina S, Wu, Yanhong, Sicotte, Hugues, Petersen, Gloria M

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