Genotyping of 73 UM-SCC head and neck squamous cell carcinoma cell lines von Brenner, J. Chad, Graham, Martin P., Kumar, Bhavna, Saunders, Lindsay M., Kupfer, Robbi, Lyons, Robert H., Bradford, Carol R., Carey, Thomas E.

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Evaluation of portability and cost of a fluorescent PCR ribotyping protocol for Clostridium difficile epidemiology von Martinson, Jonathan N V, Broadaway, Susan, Lohman, Egan, Johnson, Christina, Alam, M Jahangir, Khaleduzzaman, Mohammed, Garey, Kevin W, Schlackman, Jessica, Young, Vincent B, Santhosh, Kavitha, Rao, Krishna, Lyons, Jr, Robert H, Walk, Seth T

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Next-generation sequencing identifies the Danforth's short tail mouse mutation as a retrotransposon insertion affecting Ptf1a expression von Vlangos, Christopher N, Siuniak, Amanda N, Robinson, Dan, Chinnaiyan, Arul M, Lyons, Jr, Robert H, Cavalcoli, James D, Keegan, Catherine E

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Discovery of mutations in Saccharomyces cerevisiae by pooled linkage analysis and whole-genome sequencing von Birkeland, Shanda R, Jin, Natsuko, Ozdemir, Alev Cagla, Lyons, Jr, Robert H, Weisman, Lois S, Wilson, Thomas E

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Identification of the Genomic Insertion Site of the Thyroid Peroxidase Promoter–Cre Recombinase Transgene Using a Novel, Efficient, Next-Generation DNA Sequencing Method von Raman, Priyadarshini, Grachtchouk, Vladimir, Lyons, Robert H., Koenig, Ronald J.

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Comparison of constitutional and replication stress-induced genome structural variation by SNP array and mate-pair sequencing von Arlt, Martin F, Ozdemir, Alev Cagla, Birkeland, Shanda R, Lyons, Jr, Robert H, Glover, Thomas W, Wilson, Thomas E

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Discovery of transcriptional regulators and signaling pathways in the developing pituitary gland by bioinformatic and genomic approaches von BRINKMEIER, Michelle L, DAVIS, Shannon W, CAMINCI, Piero, MACDONALD, James W, KAWAI, Jun, GHOSH, Debashis, HAYASHIZAKI, Yoshihide, LYONS, Robert H, CAMPER, Sally A

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Signal Transduction by DR3, a Death Domain-Containing Receptor Related to TNFR-1 and CD95 von Chinnaiyan, Arul M., O'Rourke, Karen, Yu, Guo-Liang, Lyons, Robert H., Garg, Manish, Duan, D. Roxanne, Xing, Lily, Gentz, Reiner, Ni, Jian, Dixit, Vishva M.

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Exome Sequencing Reveals Cubilin Mutation as a Single-Gene Cause of Proteinuria von OVUNC, Bugsu, OTTO, Edgar A, YILMAZ, Engin, HILDEBRANDT, Friedhelm, VEGA-WARNER, Virginia, SAISAWAT, Pawaree, ASHRAF, Shazia, RAMASWAMI, Gokul, FATHY, Hanan M, SCHOEB, Dominik, CHERNIN, Gil, LYONS, Robert H

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High-throughput mutation analysis in patients with a nephronophthisis-associated ciliopathy applying multiplexed barcoded array-based PCR amplification and next-generation sequenci... von Halbritter, Jan, Diaz, Katrina, Chaki, Moumita, Porath, Jonathan D, Tarrier, Brendan, Fu, Clementine, Innis, Jamie L, Allen, Susan J, Lyons, Robert H, Stefanidis, Constantinos J, Omran, Heymut, Soliman, Neveen A, Otto, Edgar A

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Rare variant genotype imputation with thousands of study-specific whole-genome sequences: implications for cost-effective study designs von Pistis, Giorgio, Porcu, Eleonora, Vrieze, Scott I, Sidore, Carlo, Steri, Maristella, Danjou, Fabrice, Busonero, Fabio, Mulas, Antonella, Zoledziewska, Magdalena, Maschio, Andrea, Brennan, Christine, Lai, Sandra, Miller, Michael B, Marcelli, Marco, Urru, Maria Francesca, Pitzalis, Maristella, Lyons, Robert H, Kang, Hyun M, Jones, Chris M, Angius, Andrea, Iacono, William G, Schlessinger, David, McGue, Matt, Cucca, Francesco, Abecasis, Gonçalo R, Sanna, Serena

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Estimation of DNA contamination and its sources in genotyped samples von Zajac, Gregory J. M., Fritsche, Lars G., Weinstock, Joshua S., Dagenais, Susan L., Lyons, Robert H., Brummett, Chad M., Abecasis, Gonçalo R.

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Evaluation of commercially available RNA amplification kits for RNA sequencing using very low input amounts of total RNA von Shanker, Savita, Paulson, Ariel, Edenberg, Howard J, Peak, Allison, Perera, Anoja, Alekseyev, Yuriy O, Beckloff, Nicholas, Bivens, Nathan J, Donnelly, Robert, Gillaspy, Allison F, Grove, Deborah, Gu, Weikuan, Jafari, Nadereh, Kerley-Hamilton, Joanna S, Lyons, Robert H, Tepper, Clifford, Nicolet, Charles M

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Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy von Otto, Edgar A, Hurd, Toby W, Airik, Rannar, Chaki, Moumita, Zhou, Weibin, Stoetzel, Corinne, Patil, Suresh B, Levy, Shawn, Ghosh, Amiya K, Murga-Zamalloa, Carlos A, van Reeuwijk, Jeroen, Letteboer, Stef J F, Sang, Liyun, Giles, Rachel H, Liu, Qin, Coene, Karlien L M, Estrada-Cuzcano, Alejandro, Collin, Rob W J, McLaughlin, Heather M, Held, Susanne, Kasanuki, Jennifer M, Ramaswami, Gokul, Conte, Jinny, Lopez, Irma, Washburn, Joseph, MacDonald, James, Hu, Jinghua, Yamashita, Yukiko, Maher, Eamonn R, Guay-Woodford, Lisa M, Neumann, Hartmut P H, Obermüller, Nicholas, Koenekoop, Robert K, Bergmann, Carsten, Bei, Xiaoshu, Lewis, Richard A, Katsanis, Nicholas, Lopes, Vanda, Williams, David S, Lyons, Robert H, Dang, Chi V, Brito, Daniela A, Dias, Mónica Bettencourt, Zhang, Xinmin, Cavalcoli, James D, Nürnberg, Gudrun, Nürnberg, Peter, Pierce, Eric A, Jackson, Peter K, Antignac, Corinne, Saunier, Sophie, Roepman, Ronald, Dollfus, Helene, Khanna, Hemant, Hildebrandt, Friedhelm

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Comparative genomics reveals functional transcriptional control sequences in the Prop1 gene von Ward, Robert D, Davis, Shannon W, Cho, MinChul, Esposito, Constance, Lyons, Robert H, Cheng, Jan-Fang, Rubin, Edward M, Rhodes, Simon J, Raetzman, Lori T, Smith, Timothy P. L, Camper, Sally A

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A Comprehensive Mutation Analysis of RP2 and RPGR in a North American Cohort of Families with X-Linked Retinitis Pigmentosa von Breuer, Debra K., Yashar, Beverly M., Filippova, Elena, Hiriyanna, Suja, Lyons, Robert H., Mears, Alan J., Asaye, Bersabell, Acar, Ceren, Vervoort, Raf, Wright, Alan F., Musarella, Maria A., Wheeler, Patricia, MacDonald, Ian, Iannaccone, Alessandro, Birch, David, Hoffman, Dennis R., Fishman, Gerald A., Heckenlively, John R., Jacobson, Samuel G., Sieving, Paul A., Swaroop, Anand

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Correction of Deafness in shaker-2 Mice by an Unconventional Myosin in a BAC Transgene von Probst, Frank J., Fridell, Robert A., Raphael, Yehoash, Saunders, Thomas L., Wang, Aihui, Liang, Yong, Morell, Robert J., Touchman, Jeffrey W., Lyons, Robert H., Noben-Trauth, Konrad, Friedman, Thomas B., Camper, Sally A.

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Genomic characterization of human SEC14L1 splice variants within a 17q25 candidate tumor suppressor gene region and identification of an unrelated embedded expressed sequence tag von Kalikin, Linda M, Bugeaud, Emily M, Palmbos, Philip L, Lyons, Jr., Robert H, Petty, Elizabeth M

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Identification of members of the Wnt signaling pathway in the embryonic pituitary gland von Douglas, Kristin R, Brinkmeier, Michelle L, Kennell, Jennifer A, Eswara, Pallavi, Harrison, Tabitha A, Patrianakos, Athena I, Sprecher, Bradley S, Potok, Mary Anne, Lyons, Jr., Robert H, MacDougald, Ormond A, Camper, Sally A

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Genetic variation in C57BL/6 ES cell lines and genetic instability in the Bruce4 C57BL/6 ES cell line von Hughes, Elizabeth D, Qu, Yun Yan, Genik, Suzanne J, Lyons, Robert H, Pacheco, Christopher D, Lieberman, Andrew P, Samuelson, Linda C, Nasonkin, Igor O, Camper, Sally A, Van Keuren, Margaret L, Saunders, Thomas L

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