Schizophrenia is associated with an increase in cortical microRNA biogenesis

- Beveridge, N. J., Gardiner, E., Carroll, A. P., Tooney, P. A., Cairns, M. J.

CCDC22: a novel candidate gene for syndromic X-linked intellectual disability

- Voineagu, I., Huang, L., Field, M., Gecz, J., Geschwind, D., Winden, K., Lazaro, M., Haan, E., Nelson, J., McGaughran, J., Nguyen, L. S., Friend, K., Hackett, A.

Imprinted DLK1-DIO3 region of 14q32 defines a schizophrenia-associated miRNA signature in peripheral blood mononuclear cells

- Gardiner, E., Beveridge, N. J., Wu, J. Q., Carr, V., Scott, R. J., Tooney, P. A., Cairns, M. J.

Genome-wide supported variant MIR137 and severe negative symptoms predict membership of an impaired cognitive subtype of schizophrenia

- Green, M. J., Cairns, M. J., Wu, J., Dragovic, M., Jablensky, A., Tooney, P. A., Scott, R. J., Carr, V. J.

Increased inflammatory markers identified in the dorsolateral prefrontal cortex of individuals with schizophrenia

- Fillman, S.G., Cloonan, N., Catts, V.S., Miller, L.C., Wong, J., McCrossin, T., Cairns, M., Weickert, C.S.

The long non-coding RNA Gomafu is acutely regulated in response to neuronal activation and involved in schizophrenia-associated alternative splicing

- Barry, G., Briggs, J. A., Nakagawa, S., Rigo, F., Taft, R. J., Cairns, M. J., Blackshaw, S., Wolvetang, E. J., Mattick, J. S., Vanichkina, D. P., Poth, E. M., Beveridge, N. J., Ratnu, V. S., Nayler, S. P., Nones, K., Hu, J., Bredy, T. W.

Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53 949)

- Davies, G., Armstrong, N., van der Lee, S. J., Le Hellard, S., Liu, T., Marioni, R. E., Oldmeadow, C., Postmus, I., Smith, A. V., Smith, J. A., Thalamuthu, A., Thomson, R., Bis, J. C., Holliday, E. G., Scott, R. J., Attia, J. R., Schofield, P. W., Bressler, J., Chouraki, V., Giddaluru, S., Hofer, E., Ibrahim-Verbaas, C. A., Kirin, M., Lahti, J.

Brain iron accumulation affects myelin-related molecular systems implicated in a rare neurogenetic disease family with neuropsychiatric features

- Heidari, M., Johnstone, D. M., Olynyk, J. K., Trinder, D., Milward, E. A., Bassett, B., Graham, R. M., Chua, A. C. G., House, M. J., Collingwood, J. F., Bettencourt, C., Houlden, H., Ryten, M.

GWAS for executive function and processing speed suggests involvement of the CADM2 gene

- Ibrahim-Verbaas, C. A., Bressler, J., Chibnik, L. B., Liu, Y., Vitart, V., Kirin, M., Petrovic, K., Polasek, O., Zgaga, L., Fawns-Ritchie, C., Hoffmann, P., Karjalainen, J., Debette, S., Oldmeadow, C., Holliday, E. G., Scott, R. J., Attia, J. R., Schofield, P. W., Schuur, M., Smith, A. V., Bis, J. C., Davies, G., Trompet, S., Smith, J. A., Wolf, C.

MiR-137: an important player in neural development and neoplastic transformation

- Mahmoudi, E., Cairns, M. J.

A missense mutation in Katnal1 underlies behavioural, neurological and ciliary anomalies

- Banks, G., Lassi, G., Sweeting, M., Chesham, J. E., Barnard, A. R., Horner, N., Westerberg, H., Smith, L. B., Molnár, Z., Hastings, M. H., Hirst, R. A., Tucci, V., Hoerder-Suabedissen, A., Nolan, P. M., Tinarelli, F., Simon, M. M., Wilcox, A., Lau, P., Lawson, T. N., Johnson, S., Rutman, A.

Elevated plasma ferritin in elderly individuals with high neocortical amyloid-β load

- Goozee, K., Chatterjee, P., Garg, M. L., Kwok, J. B., Bush, A. I., Chung, R., Magnussen, J. S., Martins, R. N., James, I., Shen, K., Sohrabi, H. R., Asih, P. R., Dave, P., ManYan, C., Taddei, K., Ayton, S. J.

Widespread white matter microstructural differences in schizophrenia across 4322 individuals: results from the ENIGMA Schizophrenia DTI Working Group

- Kelly, S., Jahanshad, N., Bousman, C. A., Brouwer, R. M., Bruggemann, J., Bustillo, J., Cahn, W., Calhoun, V., Cannon, D., Carr, V., Catts, S., Chen, J., Zalesky, A., Henskens, F. A., Michie, P. T., Piras, F., Scott, R. J., Kochunov, P., Agartz, I., Alloza, C., Andreassen, O. A., Arango, C., Banaj, N., Bouix, S.

Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium

- Merino, Jordi, Dashti, Hassan S., Wojczynski, Mary K., Männistö, Satu, Ngwa, Julius S., Kho, Minjung, Ahluwalia, Tarunveer, Pervjakova, Natalia, Houston, Denise K., Bouchard, Claude, Huang, Tao, Orho-Melander, Marju, Li, Sherly X., Pennell, Craig E., Wang, Carol A., Pérusse, L, Pennell, CE, de Vries, PS, Voortman, T, Li, O, Kanoni, S, Rose, LM, Lehtimäki, T, Sarnowski, Chloé, Zhao, JH, Feitosa, MF, Luan, J, McKeown, NM, Smith, JA, Hansen, T, Eklund, N, Nalls, MA, Rankinen, T, Huang, J, Justice, Anne E., Hernandez, DG, Schulz, CA, Manichaikul, A, Li-Gao, R, Vohl, MC, Wang, CA, van Rooij, FJA, Shin, J, Kalafati, IP, Day, F, Graff, Misa, Ridker, PM, Kähönen, M, Siscovick, DS, Langenberg, C, Zhao, W, Astrup, A, Knekt, P, Garcia, M, Rao, DC, Qi, Q, Papoutsakis, Constantina, Ferrucci, L, Ericson, U, Blangero, J, Hofman, A, Pausova, Z, Mikkilä, V, Wareham, NJ, Kardia, SLR, Pedersen, O, Jula, A, Smith, Caren E., Curran, JE, Zillikens, MC, Viikari, JS, Forouhi, NG, Ordovás, JM, Lieske, JC, Rissanen, H, Uitterlinden, AG, Raitakari, OT, Kiefte-de Jong, JC, Dedoussis, George V., Dupuis, J, Rotter, JI, North, KE, Scott, RA, Province, MA, Perola, M, Cupples, LA, Turner, ST, Sørensen, TIA, Salomaa, V, Lemaitre, Rozenn N., Liu, Y, Sung, YJ, Qi, L, Bandinelli, S, Rich, SS, de Mutsert, R, Tremblay, A, Oddy, WH, Franco, OH, Paus, T

Altered white matter microstructure in 22q11.2 deletion syndrome: a multisite diffusion tensor imaging study

- Villalón-Reina, Julio E., Martínez, Kenia, Qu, Xiaoping, Ching, Christopher R. K., Nir, Talia M., Kothapalli, Deydeep, Corbin, Conor, Sun, Daqiang, Lin, Amy, Forsyth, Jennifer K., Kushan, Leila, Vajdi, Ariana, Jalbrzikowski, Maria, Hansen, Laura, Jonas, Rachel K., van Amelsvoort, Therese, Bakker, Geor, Kates, Wendy R., Antshel, Kevin M., Fremont, Wanda, Campbell, Linda E., McCabe, Kathryn L.

Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion

- Cleynen, Isabelle, Engchuan, Worrawat, Hestand, Matthew S., Heung, Tracy, Holleman, Aaron M., Johnston, H. Richard, Monfeuga, Thomas, McDonald-McGinn, Donna M., Gur, Raquel E., Morrow, Bernice E., Swillen, Ann, Vorstman, Jacob A. S., Bearden, Carrie E., Chow, Eva W. C., van den Bree, Marianne, Emanuel, Beverly S., Vermeesch, Joris R., Warren, Stephen T., Owen, Michael J., Chopra, Pankaj, Campbell, Linda E., McCabe, Kathryn L.

Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size

- Sun, Daqiang, Ching, Christopher R. K., Jonas, Rachel K., van Amelsvoort, Therese, Bakker, Geor, Kates, Wendy R., Antshel, Kevin M., Fremont, Wanda, Campbell, Linda E., McCabe, Kathryn L., Daly, Eileen, Gudbrandsen, Maria, Lin, Amy, Murphy, Clodagh M., Murphy, D, Craig, M, Vorstman, J, Fiksinski, A, Koops, S, Ruparel, K, Roalf, DR, Gur, RE, Schmitt, JE, Forsyth, Jennifer K., Simon, TJ, Goodrich-Hunsaker, NJ, Durdle, CA, Bassett, AS, Chow, EWC, Butcher, NJ, Vila-Rodriguez, F, Doherty, J, Cunningham, A, van den Bree, MBM, Kushan, Leila, Linden, DEJ, Moss, H, Owen, MJ, Murphy, KC, McDonald-McGinn, DM, Emanuel, B, van Erp, TGM, Turner, JA, Thompson, PM, Bearden, CE, Vajdi, Ariana, Jalbrzikowski, Maria, Hansen, Laura, Villalon-Reina, Julio E., Qu, Xiaoping

Polygenic disruption of retinoid signalling in schizophrenia and a severe cognitive deficit subtype

- Reay, William R., Atkins, Joshua R., Quidé, Yann, Carr, Vaughan J., Green, Melissa J., Cairns, Murray J.

The role of the retinoids in schizophrenia: genomic and clinical perspectives

- Reay, William R., Cairns, Murray J.

A polygenic resilience score moderates the genetic risk for schizophrenia

- Hess, Jonathan L., Tylee, Daniel S., Mattheisen, Manuel, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Lundbeck Foundation Initiative for Integrative Psychiatric Research (iPSYCH), Børglum, Anders D., Als, Thomas D., Grove, Jakob, Werge, Thomas, Mortensen, Preben Bo, Mors, Ole, Nordentoft, Merete, Hougaard, David M., Byberg-Grauholm, Jonas, Bækvad-Hansen, Maree, Greenwood, Tiffany A., Tsuang, Ming T., Curtis, David, Steinberg, Stacy, Sigurdsson, Engilbert, Stefánsson, Hreinn, Stefánsson, Kári, Edenberg, Howard J., Holmans, Peter, Faraone, Stephen V., Glatt, Steven J., Cairns, Murray J., Carr, Vaughan J., Henskens, Frans A., Kelly, Brian J., Loughland, Carmel M., Michie, Patricia T., Schall, Ulrich A,, Scott, Rodney, Tooney, Paul