REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants von Ioannidis, Nilah M., Rothstein, Joseph H., Pejaver, Vikas, Middha, Sumit, McDonnell, Shannon K., Baheti, Saurabh, Musolf, Anthony, Li, Qing, Holzinger, Emily, Karyadi, Danielle, Cannon-Albright, Lisa A., Teerlink, Craig C., Stanford, Janet L., Isaacs, William B., Xu, Jianfeng, Cooney, Kathleen A., Lange, Ethan M., Schleutker, Johanna, Carpten, John D., Powell, Isaac J., Cussenot, Olivier, Cancel-Tassin, Geraldine, Giles, Graham G., MacInnis, Robert J., Maier, Christiane, Hsieh, Chih-Lin, Wiklund, Fredrik, Catalona, William J., Foulkes, William D., Mandal, Diptasri, Eeles, Rosalind A., Kote-Jarai, Zsofia, Bustamante, Carlos D., Schaid, Daniel J., Hastie, Trevor, Ostrander, Elaine A., Bailey-Wilson, Joan E., Radivojac, Predrag, Thibodeau, Stephen N., Whittemore, Alice S., Sieh, Weiva

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Isozymes of mammalian hexokinase: structure, subcellular localization and metabolic function von Wilson, John E

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Synthesis of Functionalized Cyclopentenes through Catalytic Asymmetric [3+2] Cycloadditions of Allenes with Enones von Wilson, Jonathan E., Fu, Gregory C.

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NLRP12 Suppresses Colon Inflammation and Tumorigenesis through the Negative Regulation of Noncanonical NF-κB Signaling von Allen, Irving C., Wilson, Justin E., Schneider, Monika, Lich, John D., Roberts, Reid A., Arthur, Janelle C., Woodford, Rita-Marie T., Davis, Beckley K., Uronis, Joshua M., Herfarth, Hans H., Jobin, Christian, Rogers, Arlin B., Ting, Jenny P.-Y.

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Two-stage Study of Familial Prostate Cancer by Whole-exome Sequencing and Custom Capture Identifies 10 Novel Genes Associated with the Risk of Prostate Cancer von Schaid, Daniel J., McDonnell, Shannon K., FitzGerald, Liesel M., DeRycke, Lissa, Fogarty, Zachary, Giles, Graham G., MacInnis, Robert J., Southey, Melissa C., Nguyen-Dumont, Tu, Cancel-Tassin, Geraldine, Cussenot, Oliver, Whittemore, Alice S., Sieh, Weiva, Ioannidis, Nilah Monnier, Hsieh, Chih-Lin, Stanford, Janet L., Schleutker, Johanna, Cropp, Cheryl D., Carpten, John, Hoegel, Josef, Eeles, Rosalind, Kote-Jarai, Zsofia, Ackerman, Michael J., Klein, Christopher J., Mandal, Diptasri, Cooney, Kathleen A., Bailey-Wilson, Joan E., Helfand, Brian, Catalona, William J., Wiklund, Fredrick, Riska, Shaun, Bahetti, Saurabh, Larson, Melissa C., Cannon Albright, Lisa, Teerlink, Craig, Xu, Jianfeng, Isaacs, William, Ostrander, Elaine A., Thibodeau, Stephen N.

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HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG) von Xu, Jianfeng, Lange, Ethan M., Lu, Lingyi, Zheng, Siqun L., Wang, Zhong, Thibodeau, Stephen N., Cannon-Albright, Lisa A., Teerlink, Craig C., Camp, Nicola J., Johnson, Anna M., Zuhlke, Kimberly A., Stanford, Janet L., Ostrander, Elaine A., Wiley, Kathleen E., Isaacs, Sarah D., Walsh, Patrick C., Maier, Christiane, Luedeke, Manuel, Vogel, Walther, Schleutker, Johanna, Wahlfors, Tiina, Tammela, Teuvo, Schaid, Daniel, McDonnell, Shannon K., DeRycke, Melissa S., Cancel-Tassin, Geraldine, Cussenot, Olivier, Wiklund, Fredrik, Grönberg, Henrik, Eeles, Ros, Easton, Doug, Kote-Jarai, Zsofia, Whittemore, Alice S., Hsieh, Chih-Lin, Giles, Graham G., Hopper, John L., Severi, Gianluca, Catalona, William J., Mandal, Diptasri, Ledet, Elisa, Foulkes, William D., Hamel, Nancy, Mahle, Lovise, Moller, Pal, Powell, Isaac, Bailey-Wilson, Joan E., Carpten, John D., Seminara, Daniela, Cooney, Kathleen A., Isaacs, William B.

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Youth diet quality and hazard of mood disorder in adolescence and adulthood among an Australian cohort von Wilson, JE, Blizzard, L, Gall, SL, Magnussen, CG, Oddy, WH, Dwyer, T, Venn, AJ, Smith, KJ

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A genetic model for determining MSH2 and MLH1 carrier probabilities based on family history and tumor microsatellite instability von Marroni, F, Pastrello, C, Benatti, P, Torrini, M, Barana, D, Cordisco, EL, Viel, A, Mareni, C, Oliani, C, Genuardi, M, Bailey-Wilson, JE, Ponz de Leon, M, Presciuttini, S

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Asymmetric Synthesis of Highly Substituted β-Lactones by Nucleophile-Catalyzed [2+2] Cycloadditions of Disubstituted Ketenes with Aldehydes von Wilson, Jonathan E., Fu, Gregory C.

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Determination of the allelic frequency in Smith-Lemli-Opitz syndrome by analysis of massively parallel sequencing data sets von Cross, J.L., Iben, J., Simpson, C.L., Thurm, A., Swedo, S., Tierney, E., Bailey-Wilson, J.E., Biesecker, L.G., Porter, F.D., Wassif, C.A.

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Attention-deficit/hyperactivity disorder (ADHD): feasibility of linkage analysis in a genetic isolate using extended and multigenerational pedigrees von Arcos-Burgos, M, Castellanos, FX, Lopera, F, Pineda, D, Palacio, JD, Garcia, M, Henao, GC, Palacio, LG, Berg, K, Bailey-Wilson, JE, Muenke, M

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Gene-Gene Interaction Among WNT Genes for Oral Cleft in Trios von Li, Qing, Kim, Yoonhee, Suktitipat, Bhoom, Hetmanski, Jacqueline B., Marazita, Mary L., Duggal, Priya, Beaty, Terri H., Bailey-Wilson, Joan E.

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A Major Lung Cancer Susceptibility Locus Maps to Chromosome 6q23–25 von Bailey-Wilson, J.E., Amos, C.I., Pinney, S.M., Petersen, G.M., de Andrade, M., Wiest, J.S., Fain, P., Schwartz, A.G., You, M., Franklin, W., Klein, C., Gazdar, A., Rothschild, H., Mandal, D., Coons, T., Slusser, J., Lee, J., Gaba, C., Kupert, E., Perez, A., Zhou, X., Zeng, D., Liu, Q., Zhang, Q., Seminara, D., Minna, J., Anderson, M.W.

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Initiation of Protein Synthesis from the A Site of the Ribosome von Wilson, Joan E, Pestova, Tatyana V, Hellen, Christopher U.T, Sarnow, Peter

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Microfracture analysis of fault growth and wear processes, Punchbowl Fault, San Andreas system, California von Wilson, J.E, Chester, J.S, Chester, F.M

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Attention-Deficit/Hyperactivity Disorder in a Population Isolate: Linkage to Loci at 4q13.2, 5q33.3, 11q22, and 17p11 von Arcos-Burgos, Mauricio, Castellanos, F. Xavier, Pineda, David, Lopera, Francisco, David Palacio, Juan, Guillermo Palacio, Luis, Rapoport, Judith L., Berg, Kate, Bailey-Wilson, Joan E., Muenke, Maximilian

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Functional annotation of a novel NFKB1 promoter polymorphism that increases risk for ulcerative colitis von Karban, Amir S., Okazaki, Toshihiko, Panhuysen, Carolien I.M., Gallegos, Thomas, Potter, James J., Bailey-Wilson, Joan E., Silverberg, Mark S., Duerr, Richard H., Cho, Judy H., Gregersen, Peter K., Wu, Yuqiong, Achkar, Jean-Paul, Dassopoulos, Themistocles, Mezey, Esteban, Bayless, Theodore M., Nouvet, Franklin J., Brant, Steven R.

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Genomewide Linkage Scan for Myopia Susceptibility Loci among Ashkenazi Jewish Families Shows Evidence of Linkage on Chromosome 22q12 von Stambolian, Dwight, Ibay, Grace, Reider, Lauren, Dana, Debra, Moy, Chris, Schlifka, Melissa, Holmes, Taura, Ciner, Elise, Bailey-Wilson, Joan E.

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Naturally Occurring Dicistronic Cricket Paralysis Virus RNA Is Regulated by Two Internal Ribosome Entry Sites von Wilson, Joan E., Powell, Marguerite J., Hoover, Susan E., Sarnow, Peter

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Clustering of Non-Major Histocompatibility Complex Susceptibility Candidate Loci in Human Autoimmune Diseases von Becker, Kevin G., Simon, Richard M., Bailey-Wilson, Joan E., Freidlin, Boris, Biddison, William E., McFarland, Henry F., Trent, Jeffrey M.

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