Histological, histochemical and fine structure studies of the lacrimal gland and superficial gland of the third eyelid and their significance on the proper function of the eyeball... von Klećkowska-Nawrot, J, Nowaczyk, R, Goździewska-Harłajczuk, K, Krasucki, K, Janeczek, M

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Morphology and a proposed model of innervation of the human deltoid muscle: a pilot study von Wysiadecki, G, Polguj, M, Krasucki, K, Zytkowski, A, Smigielski, J, Topol, M, Orkisz, S

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Improved Detection of Common Variants Associated with Schizophrenia by Leveraging Pleiotropy with Cardiovascular-Disease Risk Factors von Andreassen, Ole A., Djurovic, Srdjan, Thompson, Wesley K., Schork, Andrew J., Kendler, Kenneth S., O’Donovan, Michael C., Rujescu, Dan, Werge, Thomas, van de Bunt, Martijn, Morris, Andrew P., McCarthy, Mark I., Roddey, J. Cooper, McEvoy, Linda K., Desikan, Rahul S., Dale, Anders M.

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Optical response of WSe2-based vertical tunneling junction von Walczyk, K., Krasucki, G., Olkowska-Pucko, K., Chen, Z., Taniguchi, T., Watanabe, K., Babiński, A., Koperski, M., Molas, M.R., Zawadzka, N.

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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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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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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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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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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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Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain von Richards, A L, Jones, L, Moskvina, V, Kirov, G, Gejman, P V, Levinson, D F, Sanders, A R, Purcell, S, Visscher, P M, Craddock, N, Owen, M J, Holmans, P, O'Donovan, M C

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Investigation of the genetic association between quantitative measures of psychosis and schizophrenia: a polygenic risk score analysis von Derks, Eske M, Vorstman, Jacob A S, Ripke, Stephan, Kahn, Rene S, Ophoff, Roel A

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GWA study data mining and independent replication identify cardiomyopathy-associated 5 ( ) as a risk gene for schizophrenia von Chen, X, Lee, G, Maher, B S, Fanous, A H, Chen, J, Zhao, Z, Guo, A, van den Oord, E, Sullivan, P F, Shi, J, Levinson, D F, Gejman, P V, Sanders, A, Duan, J, Owen, M J, Craddock, N J, O'Donovan, M C, Blackman, J, Lewis, D, Kirov, G K, Qin, W, Schwab, S, Wildenauer, D, Chowdari, K, Nimgaonkar, V, Straub, R E, Weinberger, D R, O'Neill, F A, Walsh, D, Bronstein, M, Darvasi, A, Lencz, T, Malhotra, A K, Rujescu, D, Giegling, I, Werge, T, Hansen, T, Ingason, A, Nöethen, M M, Rietschel, M, Cichon, S, Djurovic, S, Andreassen, O A, Cantor, R M, Ophoff, R, Corvin, A, Morris, D W, Gill, M, Pato, C N, Pato, M T, Macedo, A, Gurling, H M D, McQuillin, A, Pimm, J, Hultman, C, Lichtenstein, P, Sklar, P, Purcell, S M, Scolnick, E, St Clair, D, Blackwood, D H R, Kendler, K S

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Variability in Working Memory Performance Explained by Epistasis vs Polygenic Scores in the ZNF804A Pathway von Nicodemus, Kristin K, Hargreaves, April, Morris, Derek, Anney, Richard, Gill, Michael, Corvin, Aiden, Donohoe, Gary

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Schizophrenia genetic variants are not associated with intelligence von van Scheltinga, A. F. Terwisscha, Bakker, S. C., van Haren, N. E. M., Derks, E. M., Buizer-Voskamp, J. E., Cahn, W., Ripke, S., Ophoff, R. A., Kahn, R. S.

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A bias-reducing pathway enrichment analysis of genome-wide association data confirmed association of the MHC region with schizophrenia von Jia, Peilin, Wang, Lily, Fanous, Ayman H, Chen, Xiangning, Kendler, Kenneth S, Zhao, Zhongming

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Fine Mapping by Genetic Association Implicates the Chromosome 1q23.3 Gene UHMK1, Encoding a Serine/Threonine Protein Kinase, as a Novel Schizophrenia Susceptibility Gene von Puri, Vinay, McQuillin, Andrew, Choudhury, Khalid, Datta, Susmita, Pimm, Jonathan, Thirumalai, Srinivasa, Krasucki, Robert, Lawrence, Jacob, Quested, Digby, Bass, Nicholas, Moorey, Helen, Morgan, Jenny, Punukollu, Bhaskar, Kandasami, Gomathinayagam, Curtis, David, Gurling, Hugh

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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 Ae, 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 Ke, Maier, Wolfgang, Malhotra, Anil K

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Failure to Confirm Allelic Association Between Markers at the CAPON Gene Locus and Schizophrenia in a British Sample von Puri, Vinay, McQuillin, Andrew, Thirumalai, Srinivasa, Lawrence, Jacob, Krasucki, Robert, Choudhury, Khalid, Datta, Susmita, Kerwin, Simon, Quested, Digby, Bass, Nicholas, Pimm, Jonathan, Lamb, Graham, Moorey, Helen, Kandasami, Gomathinayagam, Badacsonyi, Allison, Kelly, Katie, Morgan, Jenny, Punukollu, Bhaskar, Nadeem, Haitham, Curtis, David, Gurling, Hugh M.D.

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Two non-synonymous markers in PTPN21 , identified by genome-wide association study data-mining and replication, are associated with schizophrenia von Chen, Jingchun, Lee, Grace, Fanous, Ayman H, Zhao, Zhongming, Jia, Peilin, O'Neill, Anthony, Walsh, Dermot, Kendler, Kenneth S, Chen, Xiangning, The International Schizophrenia Consortium

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