Explaining Disability: Parents’ Stories of Raising Children with Visual Impairments in a Sighted World von Jenks, Elaine Bass

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Explaining disability: Parents' stories of raising children with visual impairments in a sighted world: Ethnography and disability studies von JENKS, Elaine Bass

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Ethnography and disability studies von CASPER, Monica J, TALLEY, Heather Laine

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Oxygen Dependency of in vivoPhotophosphorylation von KRALL, A. R., BASS, ELAINE R.

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Oxygen dependency of in vivo photophosphorylation von KRALL, A R, BASS, E R

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The Arts Tool Kit. Priority Academic Student Skills: Visual Art and General Music, Grades 1-12. Revised von Foster, Gayla, Alexander, JoAnne C, Bass, Elaine, Black, Paulette, Cesario, Robert, Clow, Jo Ellen, Dalton, Doug, Dedmon, Charla, Gabbard, Susan, Gabel, Barbara, Goree, Gary, Kyle, Nicholas, Martin, Rita, Merklin, Roxy, Riley, Patrick, Reed, John

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Genome-wide association study identifies five new schizophrenia loci von Ripke, Stephan, Sanders, Alan R, Kendler, Kenneth S, Levinson, Douglas F, Sklar, Pamela, Holmans, Peter A, Lin, Dan-Yu, Duan, Jubao, Ophoff, Roel A, Andreassen, Ole A, Scolnick, Edward, Cichon, Sven, St Clair, David, Corvin, Aiden, Gurling, Hugh, Werge, Thomas, Rujescu, Dan, Blackwood, Douglas H R, Pato, Carlos N, Malhotra, Anil K, Purcell, Shaun, Dudbridge, Frank, Neale, Benjamin M, Rossin, Lizzy, Visscher, Peter M, Posthuma, Danielle, Ruderfer, Douglas M, Fanous, Ayman, Stefansson, Hreinn, Steinberg, Stacy, Mowry, Bryan J, Golimbet, Vera, De Hert, Marc, Jonsson, Erik G, Bitter, Istvan, Pietilaeinen, Olli P H, Collier, David A, Tosato, Sarah, Agartz, Ingrid, Albus, Margot, Alexander, Madeline, Amdur, Richard L, Amin, Farooq, Bass, Nicholas, Bergen, Sarah E, Black, Donald W, Boerglum, Anders D, Brown, Matthew A, Bruggeman, Richard, Buccola, Nancy G

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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder von Purcell, Shaun M, Wray, Naomi R, Stone, Jennifer L, Visscher, Peter M, O'Donovan, Michael C, Sullivan, Patrick F, Sklar, Pamela

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The Role of Inherited TPMT and COMT Genetic Variation in Cisplatin-Induced Ototoxicity in Children With Cancer von Yang, J J, Lim, J Y S, Huang, J, Bass, J, Wu, J, Wang, C, Fang, J, Stewart, E, Harstead, E H, E, S, Robinson, G W, Evans, W E, Pappo, A, Zuo, J, Relling, M V, Onar-Thomas, A, Gajjar, A, Stewart, C F

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Rare chromosomal deletions and duplications increase risk of schizophrenia von Stone, Jennifer L., O'Donovan, Michael C., Gurling, Hugh, Kirov, George K., Blackwood, Douglas H. R., Corvin, Aiden, Craddock, Nick J., Gill, Michael, Hultman, Christina M., Lichtenstein, Paul, McQuillin, Andrew, Pato, Carlos N., Ruderfer, Douglas M., Owen, Michael J., St Clair, David, Sullivan, Patrick F., Sklar, Pamela, Purcell, Shaun M.

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Phase 2 study of azacitidine (AZA) plus pembrolizumab (pembro) as second-line treatment in patients with advanced pancreatic ductal adenocarcinoma von Safyan, Rachael A, Manji, Gulam Abbas, Lee, Shing Mirn, Silva, Rebecca, Bates, Susan Elaine, White, Ruth Aroon, Jamison, Jacob K.R., Bass, Adam Joel, Schwartz, Gary K., Oberstein, Paul Eliezer, Gonda, Tamas

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Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders von Andlauer, Till F. M., Guzman-Parra, Jose, Streit, Fabian, Strohmaier, Jana, González, Maria José, Gil Flores, Susana, Cabaleiro Fabeiro, Francisco J., del Río Noriega, Francisco, Perez, Fermin Perez, Haro González, Jesus, Orozco Diaz, Guillermo, de Diego-Otero, Yolanda, Moreno-Küstner, Berta, Auburger, Georg, Degenhardt, Franziska, Heilmann-Heimbach, Stefanie, Herms, Stefan, Hoffmann, Per, Frank, Josef, Foo, Jerome C., Treutlein, Jens, Witt, Stephanie H., Cichon, Sven, Kogevinas, Manolis, Rivas, Fabio, Mayoral, Fermín, Müller-Myhsok, Bertram, Forstner, Andreas J., Nöthen, Markus M., Rietschel, Marcella

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Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions von Raychaudhuri, Soumya, Plenge, Robert M, Rossin, Elizabeth J, Ng, Aylwin C Y, Purcell, Shaun M, Sklar, Pamela, Scolnick, Edward M, Xavier, Ramnik J, Altshuler, David, Daly, Mark J

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Seeking Excellence in End of Life Care (SEE Care): A Multi-Centered Acute Hospitals Service Evaluation von Tavabie, Simon, Berglund, Anja, Barclay, David, Bass, Steve, Collins, Naomi, Edwards, Elaine, Malik, Farida, Minton, Ollie, Peters, Deborah, Stewart, Eleanor, Winter, Jayne, Ford-Dunn, Suzanne

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Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility von O'Dushlaine, C, Kenny, E, Heron, E, Donohoe, G, Gill, M, Morris, D, Corvin, A

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Genetic Schizophrenia Risk Variants Jointly Modulate Total Brain and White Matter Volume von Terwisscha van Scheltinga, Afke F, Bakker, Steven C, van Haren, Neeltje E.M, Derks, Eske M, Buizer-Voskamp, Jacobine E, Boos, Heleen B.M, Cahn, Wiepke, Hulshoff Pol, Hilleke E, Ripke, Stephan, Ophoff, Roel A, Kahn, René S

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Additive Genetic Variation in Schizophrenia Risk Is Shared by Populations of African and European Descent von de Candia, Teresa R., Lee, S. Hong, Yang, Jian, Browning, Brian L., Gejman, Pablo V., Levinson, Douglas F., Mowry, Bryan J., Hewitt, John K., Goddard, Michael E., O’Donovan, Michael C., Purcell, Shaun M., Posthuma, Danielle, Visscher, Peter M., Wray, Naomi R., Keller, Matthew C.

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New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis von Lee, S Hong, Byrne, Enda M, Hultman, Christina M, Kähler, Anna, Vinkhuyzen, Anna A E, Ripke, Stephan, Andreassen, Ole A, Frisell, Thomas, Gusev, Alexander, Hu, Xinli, Karlsson, Robert, Mantzioris, Vasilis X, McGrath, John J, Mehta, Divya, Stahl, Eli A, Zhao, Qiongyi, Kendler, Kenneth S, Sullivan, Patrick F, Price, Alkes L, O'Donovan, Michael, Okada, Yukinori, Mowry, Bryan J, Raychaudhuri, Soumya, Wray, Naomi R, Byerley, William, Cahn, Wiepke, Cantor, Rita M, Cichon, Sven, Cormican, Paul, Curtis, David, Djurovic, Srdjan, Escott-Price, Valentina, Gejman, Pablo V, Georgieva, Lyudmila, Giegling, Ina, Hansen, Thomas F, Ingason, Andrés, Kim, Yunjung, Konte, Bettina, Lee, Phil H, McIntosh, Andrew, McQuillin, Andrew, Morris, Derek W, Nöthen, Markus M, O'Dushlaine, Colm, Olincy, Ann, Olsen, Line, Pato, Carlos N, Pato, Michele T, Pickard, Benjamin S, Posthuma, Danielle, Rasmussen, Henrik B, Rietschel, Marcella, Rujescu, Dan, Schulze, Thomas G, Silverman, Jeremy M, Thirumalai, Srinivasa, Werge, Thomas, Agartz, Ingrid, Amin, Farooq, Azevedo, Maria H, Bass, Nicholas, Black, Donald W, Blackwood, Douglas H R, Bruggeman, Richard, Buccola, Nancy G, Choudhury, Khalid, Cloninger, Robert C, Corvin, Aiden, Craddock, Nicholas, Daly, Mark J, Datta, Susmita, Donohoe, Gary J, Duan, Jubao, Dudbridge, Frank, Fanous, Ayman, Freedman, Robert, Freimer, Nelson B, Friedl, Marion, Gill, Michael, Gurling, Hugh, De Haan, Lieuwe, Hamshere, Marian L, Hartmann, Annette M, Holmans, Peter A, Kahn, René S, Keller, Matthew C, Kenny, Elaine, Kirov, George K, Krabbendam, Lydia, Krasucki, Robert, Lawrence, Jacob, Lencz, Todd, Levinson, Douglas F, Lieberman, Jeffrey A, Lin, Dan-Yu, Linszen, Don H, Magnusson, Patrik K E, Maier, Wolfgang, Malhotra, Anil K

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Genetic Overlap Between Alzheimer's Disease and Bipolar Disorder Implicates the MARK2 and VAC14 Genes von Drange, Ole Kristian, Smeland, Olav Bjerkehagen, Shadrin, Alexey A, Finseth, Per Ivar, Witoelar, Aree, Frei, Oleksandr, Wang, Yunpeng, Hassani, Sahar, Djurovic, Srdjan, Dale, Anders M, Andreassen, Ole A

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Network-assisted investigation of combined causal signals from genome-wide association studies in schizophrenia von Jia, Peilin, Wang, Lily, Fanous, Ayman H, Pato, Carlos N, Edwards, Todd L, Zhao, Zhongming

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