Affective symptoms in the chronic stage of traumatic brain injury: A study of married couples von Linn, Richard T., Allen, Karen, Willer, Barry S.

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Prevalence of speaking and hearing disabilities among adults with traumatic brain injury from a national household survey von LUBINSKI, R., STEGER MOSCATO, B., WILLER, B. S.

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The effects of parental traumatic brain injury on the behaviour of parents and children von Pessar, Linda F., Coad, Mary Lou, Linn, Richard T., Willer, Barry S.

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The prevalence of traumatic brain injury and co-occurring disabilities in a national household survey of adults von Moscato, B S, Trevisan, M, Willer, B S

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Problems and coping strategies of individuals with traumatic brain injury and their spouses von Willer, B S, Allen, K M, Liss, M, Zicht, M S

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Family Burden Following Traumatic Brain Injury von Allen, Karen, Linn, Richard T, Gutierrez, Horacio, Willer, Barry S

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Problems and coping stategies of individuals with traumatic brain injury and their spouses von WILLER, B. S, ALLEN, K. M, ZICHT, M. S

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Individualized Patient Programming: An Experiment in the Use of Evaluation and Feedback for Hospital Psychiatry von Willer, Barry S.

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Copy-Number Variation Contributes to the Mutational Load of Bardet-Biedl Syndrome von Lindstrand, Anna, Frangakis, Stephan, Carvalho, Claudia M.B., Richardson, Ellen B., McFadden, Kelsey A., Willer, Jason R., Pehlivan, Davut, Liu, Pengfei, Pediaditakis, Igor L., Sabo, Aniko, Lewis, Richard Alan, Banin, Eyal, Lupski, James R., Davis, Erica E., Katsanis, Nicholas

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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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Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses von Brumpton, Ben, Sanderson, Eleanor, Heilbron, Karl, Hartwig, Fernando Pires, Harrison, Sean, Vie, Gunnhild Åberge, Cho, Yoonsu, Howe, Laura D., Hughes, Amanda, Boomsma, Dorret I., Havdahl, Alexandra, Hopper, John, Neale, Michael, Nivard, Michel G., Pedersen, Nancy L., Reynolds, Chandra A., Tucker-Drob, Elliot M., Grotzinger, Andrew, Howe, Laurence, Morris, Tim, Li, Shuai, Auton, Adam, Windmeijer, Frank, Chen, Wei-Min, Bjørngaard, Johan Håkon, Hveem, Kristian, Willer, Cristen, Evans, David M., Kaprio, Jaakko, Davey Smith, George, Åsvold, Bjørn Olav, Hemani, Gibran, Davies, Neil M.

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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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Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies von Zhou, Wei, Nielsen, Jonas B., Fritsche, Lars G., Dey, Rounak, Gabrielsen, Maiken E., Wolford, Brooke N., LeFaive, Jonathon, VandeHaar, Peter, Gagliano, Sarah A., Gifford, Aliya, Bastarache, Lisa A., Wei, Wei-Qi, Denny, Joshua C., Lin, Maoxuan, Hveem, Kristian, Kang, Hyun Min, Abecasis, Goncalo R., Willer, Cristen J., Lee, Seunggeun

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Exploring and visualizing large-scale genetic associations by using PheWeb von Gagliano Taliun, Sarah A., VandeHaar, Peter, Boughton, Andrew P., Welch, Ryan P., Taliun, Daniel, Schmidt, Ellen M., Zhou, Wei, Nielsen, Jonas B., Willer, Cristen J., Lee, Seunggeun, Fritsche, Lars G., Boehnke, Michael, Abecasis, Gonçalo R.

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Genetic variation across the human olfactory receptor repertoire alters odor perception von Trimmer, C., Keller, A., Murphy, N. R., Snyder, L. L., Willer, J. R., Nagai, M. H., Katsanis, N., Vosshall, L. B., Matsunami, H., Mainland, J. D.

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A flexible multicriteria decision-making methodology to support the strategic management of Science, Technology and Innovation research funding programs von Parreiras, R.O., Kokshenev, I., Carvalho, M.O.M., Willer, A.C.M., Dellezzopolles, C.F., Nacif, D.B., Santana, J.A.

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Biological and clinical insights from genetics of insomnia symptoms von Lane, Jacqueline M., Jones, Samuel E., Dashti, Hassan S., Wood, Andrew R., Aragam, Krishna G., van Hees, Vincent T., Strand, Linn B., Winsvold, Bendik S., Wang, Heming, Bowden, Jack, Song, Yanwei, Patel, Krunal, Anderson, Simon G., Beaumont, Robin N., Bechtold, David A., Cade, Brian E., Haas, Mary, Kathiresan, Sekar, Little, Max A., Luik, Annemarie I., Loudon, Andrew S., Purcell, Shaun, Richmond, Rebecca C., Scheer, Frank A. J. L., Schormair, Barbara, Tyrrell, Jessica, Winkelman, John W., Winkelmann, Juliane, Hveem, Kristian, Zhao, Chen, Nielsen, Jonas B., Willer, Cristen J., Redline, Susan, Spiegelhalder, Kai, Kyle, Simon D., Ray, David W., Zwart, John-Anker, Brumpton, Ben, Frayling, Timothy M., Lawlor, Deborah A., Rutter, Martin K., Weedon, Michael N., Saxena, Richa

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Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis von Graham, Sarah E., Nielsen, Jonas B., Zawistowski, Matthew, Zhou, Wei, Fritsche, Lars G., Gabrielsen, Maiken E., Skogholt, Anne Heidi, Surakka, Ida, Hornsby, Whitney E., Fermin, Damian, Larach, Daniel B., Kheterpal, Sachin, Brummett, Chad M., Lee, Seunggeun, Kang, Hyun Min, Abecasis, Goncalo R., Romundstad, Solfrid, Hallan, Stein, Sampson, Matthew G., Hveem, Kristian, Willer, Cristen J.

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Electromyography guides toward subgroups of mutations in muscle channelopathies von Fournier, Emmanuel, Arzel, Marianne, Sternberg, Damien, Vicart, Savine, Laforet, Pascal, Eymard, Bruno, Willer, Jean-Claude, Tabti, Nacira, Fontaine, Bertrand

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Scalable generalized linear mixed model for region-based association tests in large biobanks and cohorts von Zhou, Wei, Zhao, Zhangchen, Nielsen, Jonas B., Fritsche, Lars G., LeFaive, Jonathon, Gagliano Taliun, Sarah A., Bi, Wenjian, Gabrielsen, Maiken E., Daly, Mark J., Neale, Benjamin M., Hveem, Kristian, Abecasis, Goncalo R., Willer, Cristen J., Lee, Seunggeun

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