Interaction between Chromatin Proteins MECP2 and ATRX Is Disrupted by Mutations That Cause Inherited Mental Retardation von Nan, Xinsheng, Hou, Jianghui, Maclean, Alan, Nasir, Jamal, Lafuente, Maria Jose, Shu, Xinhua, Kriaucionis, Skirmantas, Bird, Adrian

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A Cytogenetic Abnormality and Rare Coding Variants Identify ABCA13 as a Candidate Gene in Schizophrenia, Bipolar Disorder, and Depression von Knight, Helen M., Pickard, Benjamin S., Maclean, Alan, Malloy, Mary P., Soares, Dinesh C., McRae, Allan F., Condie, Alison, White, Angela, Hawkins, William, McGhee, Kevin, van Beck, Margaret, MacIntyre, Donald J., Starr, John M., Deary, Ian J., Visscher, Peter M., Porteous, David J., Cannon, Ronald E., St Clair, David, Muir, Walter J., Blackwood, Douglas H.R.

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Association of GPR50, an X-linked orphan G protein-coupled receptor, and affective disorder in an independent sample of the Scottish population von MacIntyre, Donald J., McGhee, Kevin A., MacLean, Alan W., Afzal, Maryam, Briffa, Katy, Henry, Brian, Thomson, Pippa A., Muir, Walter J., Blackwood, Douglas H.R.

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Genetic mechanisms of critical illness in COVID-19 von Pairo-Castineira, Erola, Clohisey, Sara, Klaric, Lucija, Bretherick, Andrew D., Rawlik, Konrad, Pasko, Dorota, Walker, Susan, Parkinson, Nick, Fourman, Max Head, Russell, Clark D., Furniss, James, Richmond, Anne, Gountouna, Elvina, Wrobel, Nicola, Harrison, David, Wang, Bo, Wu, Yang, Meynert, Alison, Griffiths, Fiona, Oosthuyzen, Wilna, Kousathanas, Athanasios, Moutsianas, Loukas, Yang, Zhijian, Zhai, Ranran, Zheng, Chenqing, Grimes, Graeme, Beale, Rupert, Millar, Jonathan, Shih, Barbara, Keating, Sean, Zechner, Marie, Haley, Chris, Porteous, David J., Hayward, Caroline, Yang, Jian, Knight, Julian, Summers, Charlotte, Shankar-Hari, Manu, Klenerman, Paul, Turtle, Lance, Ho, Antonia, Moore, Shona C., Hinds, Charles, Horby, Peter, Nichol, Alistair, Maslove, David, Ling, Lowell, McAuley, Danny, Montgomery, Hugh, Walsh, Timothy, Pereira, Alexandre C., Renieri, Alessandra, Shen, Xia, Ponting, Chris P., Fawkes, Angie, Tenesa, Albert, Caulfield, Mark, Scott, Richard, Rowan, Kathy, Murphy, Lee, Openshaw, Peter J. M., Semple, Malcolm G., Law, Andrew, Vitart, Veronique, Wilson, James F., Baillie, J. Kenneth

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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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Repeated nebulisation of non-viral CFTR gene therapy in patients with cystic fibrosis: a randomised, double-blind, placebo-controlled, phase 2b trial von Alton, Eric W F W, Prof, Armstrong, David K, MB ChB, Ashby, Deborah, Prof, Bayfield, Katie J, BSc, Bilton, Diana, Prof, Bloomfield, Emily V, BSc, Boyd, A Christopher, PhD, Brand, June, BSc, Buchan, Ruaridh, MPharm, Calcedo, Roberto, PhD, Carvelli, Paula, BN, Chan, Mario, MSc, Cheng, Seng H, PhD, Collie, D David S, MRCVS, Cunningham, Steve, MB ChB, Davidson, Heather E, Davies, Gwyneth, MBChB, Davies, Jane C, Prof, Davies, Lee A, DPhil, Dewar, Maria H, BSc, Doherty, Ann, BSc, Donovan, Jackie, PhD, Dwyer, Natalie S, RN, Elgmati, Hala I, MRCP, Featherstone, Rosanna F, BSc, Gavino, Jemyr, RN, Gea-Sorli, Sabrina, PhD, Geddes, Duncan M, Prof, Gibson, James S R, BSc, Gill, Deborah R, PhD, Greening, Andrew P, Prof, Griesenbach, Uta, Prof, Hansell, David M, Prof, Harman, Katharine, MRCPH, Higgins, Tracy E, BSc, Hodges, Samantha L, BSc, Hyde, Stephen C, DPhil, Hyndman, Laura, MSc, Innes, J Alastair, FRCPE, Jacob, Joseph, FRCR, Jones, Nancy, BPharm, Keogh, Brian F, FRCA, Limberis, Maria P, PhD, Lloyd-Evans, Paul, PhD, Maclean, Alan W, BSc, Manvell, Michelle C, BSc, McCormick, Dominique, PhD, McGovern, Michael, MRCP, McLachlan, Gerry, PhD, Meng, Cuixiang, BSc, Montero, M Angeles, MD, Milligan, Hazel, BSc, Moyce, Laura J, BSc, Murray, Gordon D, Prof, Nicholson, Andrew G, Prof, Osadolor, Tina, MSc, Parra-Leiton, Javier, Porteous, David J, Prof, Pringle, Ian A, DPhil, Punch, Emma K, BSc, Pytel, Kamila M, PhD, Quittner, Alexandra L, Prof, Rivellini, Gina, Saunders, Clare J, BSc, Scheule, Ronald K, PhD, Sheard, Sarah, FRCR, Simmonds, Nicholas J, FRCP, Smith, Keith, BSc, Smith, Stephen N, PhD, Soussi, Najwa, BSc, Soussi, Samia, BSc, Spearing, Emma J, MSc, Stevenson, Barbara J, BSc, Sumner-Jones, Stephanie G, PhD, Turkkila, Minna, BSc, Ureta, Rosa P, BN, Waller, Michael D, MRCP, Wasowicz, Marguerite Y, PhD, Wilson, James M, Prof, Wolstenholme-Hogg, Paul, PhD

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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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Quantitative T1 brain mapping in early relapsing-remitting multiple sclerosis: longitudinal changes, lesion heterogeneity and disability von Harper, James G., York, Elizabeth N., Meijboom, Rozanna, Kampaite, Agniete, Thrippleton, Michael J., Kearns, Patrick K. A., Valdés Hernández, Maria del C., Chandran, Siddharthan, Waldman, Adam D.

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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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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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Runs of homozygosity implicate autozygosity as a schizophrenia risk factor von Keller, Matthew C, Simonson, Matthew A, Ripke, Stephan, Neale, Ben M, Gejman, Pablo V, Howrigan, Daniel P, Lee, Sang Hong, Lencz, Todd, Levinson, Douglas F, Sullivan, Patrick F

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Reverse transcriptase inhibitors in Aicardi-Goutières syndrome: A crossover clinical trial von Crow, Yanick J, Briggs, Tracy A, Eleftheriou, Despina, Parida, Amitav, Battison, Claire, Giddings, Annabel, Kennel, Titouan, Parker, Richard 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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Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function von Raychaudhuri, Soumya, Korn, Joshua M, McCarroll, Steven A, Altshuler, David, Sklar, Pamela, Purcell, Shaun, Daly, Mark J

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Homozygosity mapping of depressive disorder in a large family from Pakistan: Significant linkage on chromosome 6 and 9 von Ayub, Muhammad, Irfan, Muhammad, Maclean, Alan, Naeem, Farooq, Blackwood, Douglas

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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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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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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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