Mutations in zebrafish lrp2 result in adult-onset ocular pathogenesis that models myopia and other risk factors for glaucoma von Veth, Kerry N, Willer, Jason R, Collery, Ross F, Gray, Matthew P, Willer, Gregory B, Wagner, Daniel S, Mullins, Mary C, Udvadia, Ava J, Smith, Richard S, John, Simon W M, Gregg, Ronald G, Link, Brian A

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Neural and synaptic defects in slytherin, a zebrafish model for human congenital disorders of glycosylation von Song, Yuanquan, Willer, Jason R, Scherer, Paul C, Panzer, Jessica A, Kugath, Amy, Skordalakes, Emmanuel, Gregg, Ronald G, Willer, Gregory B, Balice-Gordon, Rita J

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Zebrafish blowout provides genetic evidence for Patched1-mediated negative regulation of Hedgehog signaling within the proximal optic vesicle of the vertebrate eye von Lee, Jiwoon, Willer, Jason R., Willer, Gregory B., Smith, Kierann, Gregg, Ronald G., Gross, Jeffrey M.

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Muscle Contractions Guide Rohon-Beard Peripheral Sensory Axons von Paulus, Jeremiah D, Willer, Gregory B, Willer, Jason R, Gregg, Ronald G, Halloran, Mary C

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Mutations in laminin alpha 1 result in complex, lens-independent ocular phenotypes in zebrafish von Semina, Elena V., Bosenko, Dmitry V., Zinkevich, Natalya C., Soules, Kelly A., Hyde, David R., Vihtelic, Thomas S., Willer, Gregory B., Gregg, Ronald G., Link, Brian A.

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Positional Cloning of the young Mutation Identifies an Essential Role for the Brahma Chromatin Remodeling Complex in Mediating Retinal Cell Differentiation von Gregg, Ronald G., Willer, Gregory B., Fadool, James M., Dowling, John E., Link, Brian A.

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Mechanisms underlying metabolic and neural defects in zebrafish and human multiple acyl-CoA dehydrogenase deficiency (MADD) von Song, Yuanquan, Selak, Mary A, Watson, Corey T, Coutts, Christopher, Scherer, Paul C, Panzer, Jessica A, Gibbs, Sarah, Scott, Marion O, Willer, Gregory, Gregg, Ronald G, Ali, Declan W, Bennett, Michael J, Balice-Gordon, Rita J

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Phosphatidylinositol synthase is required for lens structural integrity and photoreceptor cell survival in the zebrafish eye von Murphy, Taylor R., Vihtelic, Thomas S., Ile, Kristina E., Watson, Corey T., Willer, Gregory B., Gregg, Ronald G., Bankaitis, Vytas A., Hyde, David R.

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The loss of vacuolar protein sorting 11 (vps11) causes retinal pathogenesis in a vertebrate model of syndromic albinism von Thomas, Jennifer L, Vihtelic, Thomas S, denDekker, Aaron D, Willer, Gregory, Luo, Xixia, Murphy, Taylor R, Gregg, Ronald G, Hyde, David R, Thummel, Ryan

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Mutations in Zebrafish lrp2 Result in Adult-Onset Ocular Pathogenesis That Models Myopia and Other Risk Factors for Glaucoma: e1001310 von Veth, Kerry N, Willer, Jason R, Collery, Ross F, Gray, Matthew P, Willer, Gregory B, Wagner, Daniel S, Mullins, Mary C, Udvadia, Ava J, Smith, Richard S, John, Simon WM, Gregg, Ronald G, Link, Brian A

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Mutations in zebrafish Irp2 result in adult-onset ocular pathogenesis that models myopia and other risk factors for glaucoma von Veth, Kerry N, Wilier, Jason R, Collery, Ross F, Gray, Matthew P, Willer, Gregory B, Wagner, Daniel S, Mullins, Mary C, Udvadia, Ava J, Smith, Richard S, John, Simon W.M, Gregg, Ronald G, Link, Brian A

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Structural element having thin-film solar cell and thin-film antenna element von WILLER GREGORY TARN

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Space debris capturing device and implementation method thereof von WILLER GREGORY TARN

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Receptor-Mediated ER Export of Lipoproteins Controls Lipid Homeostasis in Mice and Humans von Wang, Xiao, Wang, Huimin, Xu, Bolin, Huang, Dong, Nie, Chao, Pu, Longjun, Zajac, Gregory J.M., Yan, Han, Zhao, Jingru, Shi, Fangyuan, Emmer, Brian T., Lu, Jia, Wang, Rui, Dong, Xiaohui, Dai, Jianye, Zhou, Wenjing, Wang, Chu, Gao, Ge, Wang, Yan, Willer, Cristen, Lu, Xiangfeng, Zhu, Yuangang, Chen, Xiao-Wei

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Sex-Based Differences in Affective and Cognitive Empathy Following Severe Traumatic Brain Injury von Zupan, Barbra, Neumann, Dawn, Babbage, Duncan, Willer, Barry

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The Lin28/let-7 Axis Regulates Glucose Metabolism von Zhu, Hao, Shyh-Chang, Ng, Segrè, Ayellet V., Shinoda, Gen, Shah, Samar P., Einhorn, William S., Takeuchi, Ayumu, Engreitz, Jesse M., Hagan, John P., Kharas, Michael G., Urbach, Achia, Thornton, James E., Triboulet, Robinson, Gregory, Richard I., Altshuler, David, Daley, George Q.

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A fast linkage method for population GWAS cohorts with related individuals von Zajac, Gregory J. M., Gagliano Taliun, Sarah A., Sidore, Carlo, Graham, Sarah E., Åsvold, Bjørn O., Brumpton, Ben, Nielsen, Jonas B., Zhou, Wei, Gabrielsen, Maiken, Skogholt, Anne H., Fritsche, Lars G., Schlessinger, David, Cucca, Francesco, Hveem, Kristian, Willer, Cristen J., Abecasis, Gonçalo R.

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Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors von Bakker, Mark K., van der Spek, Rick A. A., van Rheenen, Wouter, Morel, Sandrine, Bourcier, Romain, Hostettler, Isabel C., Alg, Varinder S., van Eijk, Kristel R., Koido, Masaru, Akiyama, Masato, Terao, Chikashi, Matsuda, Koichi, Walters, Robin G., Lin, Kuang, Li, Liming, Millwood, Iona Y., Chen, Zhengming, Rouleau, Guy A., Zhou, Sirui, Rannikmäe, Kristiina, Sudlow, Cathie L. M., Houlden, Henry, van den Berg, Leonard H., Dina, Christian, Naggara, Olivier, Gentric, Jean-Christophe, Shotar, Eimad, Eugène, François, Desal, Hubert, Winsvold, Bendik S., Børte, Sigrid, Johnsen, Marianne Bakke, Brumpton, Ben M., Sandvei, Marie Søfteland, Willer, Cristen J., Hveem, Kristian, Zwart, John-Anker, Verschuren, W. M. Monique, Friedrich, Christoph M., Hirsch, Sven, Schilling, Sabine, Dauvillier, Jérôme, Martin, Olivier, Jones, Gregory T., Bown, Matthew J., Ko, Nerissa U., Kim, Helen, Coleman, Jonathan R. I., Breen, Gerome, Zaroff, Jonathan G., Klijn, Catharina J. M., Malik, Rainer, Dichgans, Martin, Sargurupremraj, Muralidharan, Tatlisumak, Turgut, Amouyel, Philippe, Debette, Stéphanie, Rinkel, Gabriel J. E., Worrall, Bradford B., Pera, Joanna, Slowik, Agnieszka, Gaál-Paavola, Emília I., Niemelä, Mika, Jääskeläinen, Juha E., von Und Zu Fraunberg, Mikael, Lindgren, Antti, Broderick, Joseph P., Werring, David J., Woo, Daniel, Redon, Richard, Bijlenga, Philippe, Kamatani, Yoichiro, Veldink, Jan H., Ruigrok, Ynte M.

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Mutations in B3GALNT2 Cause Congenital Muscular Dystrophy and Hypoglycosylation of α-Dystroglycan von Stevens, Elizabeth, Carss, Keren J., Cirak, Sebahattin, Foley, A. Reghan, Torelli, Silvia, Willer, Tobias, Tambunan, Dimira E., Yau, Shu, Brodd, Lina, Sewry, Caroline A., Feng, Lucy, Haliloglu, Goknur, Orhan, Diclehan, Dobyns, William B., Enns, Gregory M., Manning, Melanie, Krause, Amanda, Salih, Mustafa A., Walsh, Christopher A., Hurles, Matthew, Campbell, Kevin P., Manzini, M. Chiara, Stemple, Derek, Lin, Yung-Yao, Muntoni, Francesco

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Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol von Lange, Leslie A., Schmidt, Ellen M., Bizon, Chris, Jun, Goo, Auer, Paul, Li, Kuo-ping, Locke, Adam, Rivas, Manuel A., Feitosa, Mary F., Zhang, Qunyuan, Huffman, Jennifer E., Crosby, Jacy, Robinson, Jennifer G., Crosslin, David R., Rosenthal, Elisabeth A., Tsai, Michael, Rieder, Mark J., Fox, Ervin R., van Duijn, Cornelia M., Taylor, Herman A., Loos, Ruth J.F., Ballantyne, Christie M., Reiner, Alexander P., Cupples, L. Adrienne, Kang, Hyun Min, Lettre, Guillaume, Rader, Daniel J., Reilly, Muredach P., Stoletzki, Nina, Barr, R. Graham, Benjamin, Emelia J., Carr, Jeff, Dupuis, Josée, Ellis, Jaclyn, Fornage, Myriam, Goff, David, Grody, Wayne, Heard-Costa, Nancy L., Levy, Daniel, Li, Dalin, Loria, Cay, Mackey, Rachel, Quinlan, Aaron R., Rice, Kenneth, Sanders, Jill P., Tracy, Russell P., Tsai, Michael Y., Wassel, Chrstina L., Watson, Karol, Wilson, Gregory, Wilson, James G., Zakai, Neil A., Nalls, Michael, Bamshad, Michael J., Accurso, Frank, Beaty, Terri, Caplan, Daniel, Chidekel, Aaron, Christiani, David C., De Paula, Alicia, Gutierrez, Hector, Hassoun, Paul M., Hiatt, Peter, Hummer, Laura K., Kim, Yoonhee, Lin, Xihong, Louie, Tin L., Mathias, Rasika A., McNamara, John, McNamara, Sharon, Nielson, Dennis, Orenstein, David, O’Sullivan, Brian, Passero, Mary Ann, Perkett, Elizabeth, Spencer, Terry, Tabor, Holly K., Weiss, Robert, Wigley, Fred, Wise, Robert A., Wurfel, Mark M., Eichler, Evan E., Fu, Wenqing, Smith, Joshua D., Tennessen, Jacob A., Peters, Ulrike, Brzyski, Robert, Curb, J. David, Eaton, Charles B., Heiss, Gerardo, Johnson, Karen C., Lasser, Norman, Lin, Dan-Yu, Logsdon, Benjamin A., Manson, JoAnn E., Martin, Lisa, Stein, Evan, Applebaum-Bowden, Deborah, Paltoo, Dina N., Sturcke, Anne

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