Genome-wide analyses of vocabulary size in infancy and toddlerhood: Associations with Attention-Deficit/Hyperactivity Disorder, literacy, and cognition-related traits

- Verhoef, Ellen, Allegrini, Andrea G., Franken, Marie-Christine, Hypponen, Elina, Mansell, Toby, Olislagers, Mitchell, Omerovic, Emina, Rimfeld, Kaili, Schlag, Fenja, Selzam, Saskia, Shapland, Chin Yang, Tiemeier, Henning, Jansen, Philip R., Whitehouse, Andrew J.O., Saffery, Richard, Bønnelykke, Klaus, Reilly, Sheena, Pennell, Craig E., Wake, Melissa, Cecil, Charlotte A.M., Plomin, Robert, Fisher, Simon E., St. Pourcain, Beate, Lange, Katherine, Wang, Carol A. Wang, Morgan, Angela T., Ahluwalia, Tarunveer S., Symeonides, Christos, EAGLE Working Group,, Eising, Else

Genetic and molecular differences of multiple sclerosis subgroups. Is there a failure in viral and aberrant immune cell clearance driving disease course?

- Burnard, Sean Michael

Genetic association and causal inference converge on hyperglycaemia as a modifiable factor to improve lung function

- Reay, William R, El Shair, Sahar I El, Cairns, Murray J., Geaghan, Michael P, Riveros, Carlos, Holliday, Elizabeth G, McEvoy, Mark A., Hancock, Stephen, Peel, Roseanne, Scott, Rodney J, Attia, John R.

Transcriptome-wide association study of breast cancer risk by estrogen-receptor status

- Feng, Helian, Gusev, Alexander, Arason, Adalgeir, Scott, Rodney J., Arndt, Volker, Aronson, Kristan J., Arun, Banu K., Asseryanis, Ella, Auer, Paul L., Azzollini, Jacopo, Balmaña, Judith, Barkardottir, Rosa B., Barnes, Daniel R., Pasaniuc, Bogdan, Barrowdale, Daniel, Beckmann, MW, Behrens, S, Benitez, J, Bermisheva, M, Bialkowska, K, Blanco, A, Blomqvist, C, Boeckx, B, Bogdanova, NV, Wu, Lang, Bojesen, SE, Bolla, MK, Bonanni, B, Borg, A, Brauch, H, Brenner, H, Briceno, I, Broeks, A, Brüning, T, Burwinkel, B, Long, Jirong, Cai, Q, Caldés, T, Caligo, MA, Campbell, I, Canisius, S, Campa, D, Carter, BD, Carter, J, Castelao, JE, Chang-Claude, J, Abu-full, Zomoroda, Chanock, SJ, Christiansen, H, Chung, WK, Claes, KBM, Clarke, CL, Couch, FJ, Cox, A, Cross, SS, Cybulski, C, Czene, K, Aittomäki, Kristiina, Daly, MB, de la Hoya, M, De Leeneer, K, Dennis, J, Devilee, P, Diez, O, Domchek, SM, Dörk, T, dos-Santos-Silva, I, Dunning, AM, Andrulis, Irene L., Dwek, M, Eccles, DM, Ejlertsen, B, Ellberg, C, Engel, C, Eriksson, M, Fasching, PA, Fletcher, O, Flyger, H, Fostira, F, Anton-Culver, Hoda, Friedman, E, Fritschi, L, Frost, D, Gabrielson, M, Ganz, PA, Gapstur, SM, Garber, J, García-Closas, M, García-Sáenz, JA, Gaudet, MM, Antoniou, Antonis C., Giles, GG, Glendon, G, Godwin, AK, Goldberg, MS, Goldgar, DE, González-Neira, A, Greene, MH, Gronwald, J, Guénel, P, Haiman, CA

A missense variant in PTPN22 is a risk factor for drug-induced liver injury

- Cirulli, Elizabeth T., Nicoletti, Paola, Abramson, Karen, Andrade, Raul J., Bjornsson, Einar S., Chalasani, Naga, Fontana, Robert J., Hallberg, Par, Li, Yi Ju, Lucena, M. Isabel, Long, Nanye, Molokhia, Mariam, Nelson, Matthew R., Odin, Joseph A., Pirmohamed, Munir, Rafnar, Thorunn, Serrano, Jose, Stefánsson, Kari, Stolz, Andrew, Martin, Jennifer H.

Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders

- Lee, Phil H., Anttila, Verneri, Wang, Meg M.-J., Cairns, Murray, Henskens, Frans A., Kelly, Brian J., Loughland, Carmel M., Schall, Ulrich A., Scott, Rodney, Tooney, Paul A., Yu, Dongmei, Stahl, Eli A., Walters, Raymond K., Anney, Richard J. L., Duncan, Laramie E., Ge, Tian, Adolfsson, Rolf, Banaschewski, Tobias, Belangero, Sintia, Won, Hyejung, Cook, Edwin H., Coppola, G, Derks, EM, Hoekstra, PJ, Kaprio, J, Keski-Rahkonen, A, Kirov, G, Kranzler, HR, Luykx, JJ, Rohde, LA, Feng, Yen-Chen A., Zai, CC, Agerbo, E, Arranz, MJ, Asherson, P, Bækvad-Hansen, M, Baldursson, G, Bellgrove, M, Belliveau, RA, Buitelaar, J, Burton, CL, Rosenthal, Jacob, Bybjerg-Grauholm, J, Casas, M, Cerrato, F, Chambert, K, Churchhouse, C, Cormand, B, Crosbie, J, Dalsgaard, S, Demontis, D, Doyle, AE, Zhu, Zhaozhong, Dumont, A, Elia, J, Grove, J, Gudmundsson, OO, Haavik, J, Hakonarson, H, Hansen, CS, Hartman, CA, Hawi, Z, Hervás, A, Tucker-Drob, Elliot M., Hougaard, DM, Howrigan, DP, Huang, H, Kuntsi, J, Langley, K, Lesch, KP, Leung, PWL, Loo, SK, Martin, J, Martin, AR, Nivard, Michel G., McGough, JJ, Medland, SE, Moran, JL, Mors, O, Mortensen, PB, Oades, RD, Palmer, DS, Pedersen, CB, Pedersen, MG, Peters, T, Grotzinger, Andrew D., Poterba, T, Poulsen, JB, Ramos-Quiroga, JA, Reif, A, Ribasés, M, Rothenberger, A, Rovira, P, Sánchez-Mora, C, Satterstrom, FK, Schachar, R, Posthuma, Danielle, Artigas, MS, Steinberg, S, Stefansson, H, Turley, P, Walters, GB, Werge, T, Zayats, T, Arking, DE, Bettella, F, Buxbaum, JD

Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia

- Harold, Denise, Connolly, Siobhan, Riley, Brien P., Kendler, Kenneth S., McCarthy, Shane E., McCombie, William R., Richards, Alex, Owen, Michael J., O'Donovan, Michael C., Walters, James, Donnelly, Peter, Bates, Lesley, Barroso, Ines, Blackwell, Jenefer M., Bramon, Elvira, Brown, Matthew A., Casas, Juan P., Corvin, Aiden, Deloukas, Panos, Duncanson, Audrey, Henskens, Frans A., Loughland, Carmel M., Michie, Patricia T., Schall, Ulrich, Scott, Rodney J.

Identification of gene loci that overlap between schizophrenia and educational attainment

- Le Hellard, Stephanie, Wang, Yunpeng, Schork, Andrew J., Thompson, Wesley K., Dale, Anders M., Djurovic, Srdjan, Andreassen, Ole A., Cairns, Murray J., Henskens, Frans, Kelly, Brian J., Loughland, Carmel, Michie, Patricia T., Witoelar, Aree, Schall, Ulrich, Scott, Rodney J., Tooney, Paul A., Wu, Jing Qin, Zuber, Verena, Bettella, Francesco, Hugdahl, Kenneth, Espeseth, Thomas, Steen, Vidar M., Melle, Ingrid, Desikan, Rahul

Novel blood pressure locus and gene discovery using genome-wide association study and expression data sets from blood and the kidney

- Wain, Louise V., Vaez, Ahmad, Verwoert, Germaine C., Hottenga, Jouke-Jan, Strawbridge, Rona J., Esko, Tonu, Arking, Dan E., Hwang, Shih-Jen, Guo, Xiuqing, Kutalik, Zoltan, Trompet, Stella, Shrine, Nick, Jansen, Rick, Oldmeadow, Christopher, Scott, Rodney, Joehanes, Roby, van Der Most, Peter J., Erzurumluoglu, A. Mesut, O'Reilly, Paul F., Cabrera, Claudia P., Warren, Helen R., Rose, Lynda M.

Genetic markers of human evolution are enriched in schizophrenia

- Srinivasan, Saurabh, Bettella, Francesco, Mattingsdal, Morten, Wang, Yunpeng, Witoelar, Aree, Schork, Andrew J., Thompson, Wesley K., Zuber, Verena, Schizophrenia Working Group of the Psychiatric Genomics Consortium,, International Headache Genetics Consortium, Winsvold, Bendik S., Zwart, John-Anker, Collier, David A., Desikan, Rahul S., Melle, Ingrid, Werge, Thomas, Dale, Anders M., Djurovic, Srdjan, Andreassen, Ole A., Henskens, Frans A., Cairns, Murray J., Kelly, Brian J., Loughland, Carmel M., Schall, Ulrich, Tooney, Paul A., Mitchie, Patricia T., Scott, Rodney J.

Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness

- Bigdeli, Tim B., Ripke, Stephan, Kirov, George, McQuillin, Andrew, Gurling, Hugh, Rujescu, Dan, Andreassen, Ole A., Werge, Thomas, Blackwood, Douglas H. R., Pato, Carlos N., Pato, Michele T., Malhotra, Anil K., Bacanu, Silviu-Alin, O'Donovan, Michael C., Kendler, Kenneth S., Fanous, Ayman H., Schizophrenia Working Group of the Psychiatric Genomics Consortium,, Henskens, Frans A., Lee, Sang Hong, Wray, Naomi R., Gejman, Pablo V., Rietschel, Marcella, Cichon, Sven, St Clair, David, Corvin, Aiden

GPU acceleration of an entroy-based model to quantify epistatic interactions between SNPs

- Riveros, Carlos, Ujaldón, Manuel, Moscato, Pablo

Genetics of hand grip strength in mid to late life

- Chan, Jessica P. L., Thalamuthu, Anbupalam, Reppermund, Simone, Menant, Jasmine, Trollor, Julian N., Brodaty, Henry, Schofield, Peter R., Attia, John R., Sachdev, Perminder S., Scott, Rodney J., Mather, Karen A., Oldmeadow, Christopher, Armstrong, Nicola J., Holliday, Elizabeth G., McEvoy, Mark, Kwok, John B., Assareh, Amelia A., Peel, Rosanne, Hancock, Stephen J.

Combined analysis of exon splicing and genome wide polymorphism data predict schizophrenia risk loci.

- Oldmeadow, Christopher, Mossman, David, Evans, Tiffany-Jane, Holliday, Elizabeth G., Tooney, Paul A., Cairns, Murray J., Wu, Jingqin, Carr, Vaughan, Attia, John R., Scott, Rodney J.

Genome-wide analysis of blood pressure variability and ischemic stroke

- Yadav, Sunaina, Cotlarciuc, Ioana, Holliday, Elizabeth G., Speed, Douglas, Hasan, Nazeeha, Pucek, Mateusz, Rinne, Paul E., Sever, Peter, Stanton, Alice, Shields, Denis C., Maguire, Jane M., McEvoy, Mark, Munroe, Patricia B., Scott, Rodney J., Ferrucci, Luigi, Macleod, Mary J., Attia, John, Markus, Hugh S., Sale, Michele M., Worrall, Bradford B., Mitchell, Braxton D., Dichgans, Martin, Sudlow, Cathy, Khan, Muhammad S., Meschia, James F., Rothwell, Peter M., Caulfield, Mark, Sharma, Pankaj, International Stroke Genetics Consortium,, Nalls, Michael A., Bevan, Steve, Cheng, Yu-Ching, Chen, Wei-Min, Malik, Rainer, McCarthy, Nina S.

Genetic polymorphisms and childhood acute lymphoblastic leukemia: GWAS of the ESCALE study (SFCE)

- Orsi, L., Rudant, J., Michel, G., Sirvent, N., Chastagner, P., Ducassou, S., Rialland, X., Hémon, D., Milne, E., Scott, R. J., Baruchel, A., Clavel, J., Bonaventure, A., Goujon-Bellec, S., Corda, E., Evans, T. J., Petit, A., Bertrand, Y., Nelken, B., Robert, A.