Mutations in zebrafish lrp2 result in adult-onset ocular pathogenesis that models myopia and other risk factors for glaucoma by 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 by 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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Muscle Contractions Guide Rohon-Beard Peripheral Sensory Axons by 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 by 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 by Gregg, Ronald G., Willer, Gregory B., Fadool, James M., Dowling, John E., Link, Brian A.

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Phosphatidylinositol synthase is required for lens structural integrity and photoreceptor cell survival in the zebrafish eye by 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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Zebrafish blowout provides genetic evidence for Patched1-mediated negative regulation of Hedgehog signaling within the proximal optic vesicle of the vertebrate eye by Lee, Jiwoon, Willer, Jason R., Willer, Gregory B., Smith, Kierann, Gregg, Ronald G., Gross, Jeffrey M.

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Mutations in Zebrafish lrp2 Result in Adult-Onset Ocular Pathogenesis That Models Myopia and Other Risk Factors for Glaucoma: e1001310 by 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 by 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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A fast linkage method for population GWAS cohorts with related individuals by 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 by Bakker, Mark K, Spek, Rick A.A. var der, Rheenen, Wouter van, Morel, Sandrine, Bourcier, Romain, Hostettler, Isabel C, Varinder, S. Alg, Eijk, Kristel R. van, 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, Rannikmae, Kristiina, Sudlow, Cathie L.M, Houlden, Henry, Berg, Leonard H. van den, Dina, Christian, Naggara, Olivier, Gentric, Jean-Christophe, Shotar, Eimad, Eugène, François, Desal, Hubert, Winsvold, Bendik K S, Børte, Sigrid, Johnsen, Marianne Bakke, Brumpton, Ben Michael, 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

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Mutations in B3GALNT2 Cause Congenital Muscular Dystrophy and Hypoglycosylation of α-Dystroglycan by 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 by 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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Protein-altering and regulatory genetic variants near GATA4 implicated in bicuspid aortic valve by Yang, Bo, Zhou, Wei, Jiao, Jiao, Nielsen, Jonas B., Mathis, Michael R., Heydarpour, Mahyar, Lettre, Guillaume, Folkersen, Lasse, Prakash, Siddharth, Schurmann, Claudia, Fritsche, Lars, Farnum, Gregory A., Lin, Maoxuan, Othman, Mohammad, Hornsby, Whitney, Driscoll, Anisa, Levasseur, Alexandra, Thomas, Marc, Farhat, Linda, Dubé, Marie-Pierre, Isselbacher, Eric M., Franco-Cereceda, Anders, Guo, Dong-chuan, Bottinger, Erwin P., Deeb, G. Michael, Booher, Anna, Kheterpal, Sachin, Chen, Y. Eugene, Kang, Hyun Min, Kitzman, Jacob, Cordell, Heather J., Keavney, Bernard D., Goodship, Judith A., Ganesh, Santhi K., Abecasis, Gonçalo, Eagle, Kim A., Boyle, Alan P., Loos, Ruth J. F., Eriksson, Per, Tardif, Jean-Claude, Brummett, Chad M., Milewicz, Dianna M., Body, Simon C., Willer, Cristen J.

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Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity by Bakker, Mark K., Kanning, Jos P., Abraham, Gad, Martinsen, Amy E., Winsvold, Bendik S., Zwart, John-Anker, Bourcier, Romain, Sawada, Tomonobu, Koido, Masaru, Kamatani, Yoichiro, Morel, Sandrine, Amouyel, Philippe, Debette, Stéphanie, Bijlenga, Philippe, Berrandou, Takiy, Ganesh, Santhi K., Bouatia-Naji, Nabila, Jones, Gregory, Bown, Matthew, Rinkel, Gabriel J.E., Veldink, Jan H., Ruigrok, Ynte M.

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Genus β human papillomaviruses and incidence of basal cell and squamous cell carcinomas of skin: population based case-control study by Karagas, Margaret R, Waterboer, Tim, Li, Zhongze, Nelson, Heather H, Michael, Kristina M, Bavinck, Jan Nico Bouwes, Perry, Ann E, Spencer, Steven K, Daling, Janet, Green, Adele C, Pawlita, Michael

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Rare loss of function variants in candidate genes and risk of colorectal cancer by Rosenthal, Elisabeth A., Shirts, Brian H., Amendola, Laura M., Horike-Pyne, Martha, Robertson, Peggy D., Hisama, Fuki M., Bennett, Robin L., Dorschner, Michael O., Nickerson, Deborah A., Stanaway, Ian B., Nassir, Rami, Vickers, Kathy T., Li, Christopher, Grady, William M., Peters, Ulrike, Jarvik, Gail P.

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Involuntary stepping after chronic spinal cord injury : evidence for a central rhythm generator for locomotion in man by CALANCIE, B, NEEDHAM-SHROPSHIRE, B, JACOBS, P, WILLER, K, ZYCH, G, GREEN, B. A

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Mutations in B3GALNT2 Cause Congenital Muscular Dystrophy and Hypoglycosylation of [alpha]-Dystroglycan by 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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Model-based assessment of replicability for genome-wide association meta-analysis by McGuire, Daniel, Jiang, Yu, Eckert, Scott, Yang, Lina, Chen, Fang, Wedow, Robbee, Li, Yue, Tian, Chao, Zhan, Xiaowei, Docherty, Anna R, Faul, Jessica D, Foerster, Johanna R, Fritsche, Lars, Gabrielsen, Maiken Elvestad, Gordon, Scott D, Haessler, Jeffrey, Hottenga, Jouke-Jan, Jang, Seon-Kyeong, Jansen, Philip R, Ling, Yueh, Ma ̈gi, Reedik, Matoba, Nana, McMahon, George, Mulas, Antonella, Orru, Valeria, Palviainen, Teemu, Pandit, Anita, Skogholt, Anne Heidi, Smith, Jennifer A, Taylor, Amy E, Willemsen, Gonneke, Young, Kendra A, Zajac, Gregory J. M, Zhou, Wei, Bjornsdottir, Gyda, Boehnke, Michael, Chen, Chu, Cucca, Francesco, Eaton, Charles B, Ehringer, Marissa A, Esko, Tõnu, Fiorillo, Edoardo, Gillespie, Nathan A, Gudbjartsson, Daniel F, Haller, Toomas, Heath, Andrew C, Hickie, Ian B, Hokanson, John E, Hopfer, Christian J, Iacono, William G, Johnson, Eric O, Kardia, Sharon L. R, Keller, Matthew C, Kellis, Manolis, Kooperberg, Charles, Krauter, Kenneth S, Lind, Penelope A, Loukola, Anu, Martin, Nicholas G, McGue, Matt, McQueen, Matthew B, Medland, Sarah E, Metspalu, Andres, Okada, Yukinori, Peters, Ulrike, Polderman, Tinca J. C, Posthuma, Danielle, Reiner, Alexander P, Rice, JP, Rimm, Eric, Rose, Richard J, Runarsdottir, Valgerdur, Stallings, Michael C, Stanˇca ́kova, Alena, Stefansson, Hreinn, Thai, Khanh K, Wall, Tamara L, Weir, David R, Weisner, Constance M, Whitfield, John B, Yin, Jie, Zuccolo, Luisa, Bierut, Laura J, Hveem, Kristian, Lee, James J, Saccone, Nancy L, Willer, Cristen J, Cornelis, Marilyn C, David, Sean P, Hinds, David, Jorgenson, Eric, Kaprio, Jaakko, Stitzel, Jerry A, Stefansson, Kari, Thorgeirsson, Thorgeir E, Abecasis, Goncalo, Liu, Dajiang J, Vrieze, Scott, Berg, Arthur, Li, Qunhua

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