Generalized Structured Component Analysis in candidate gene association studies: applications and limitations by Thompson, PA, Bishop, DVM, Eising, E, Fisher, SE, Newbury, DF

Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment by Chen, XS, Reader, RH, Hoischen, A, Veltman, JA, Simpson, NH, Francks, C, Newbury, DF, Fisher, SE

No effect of schizophrenia risk genes MIR137, TCF4, and ZNF804A on macroscopic brain structure by Cousijn, H, Eissing, M, Fernández, G, Fisher, SE, Franke, B, Zwiers, M, Harrison, P, Arias-Vásquez, A

The forkhead transcription factor FOXP2 is required for regulation of p21WAF1/CIP1 in 143B osteosarcoma cell growth arrest by Gascoyne, DM, Spearman, H, Lyne, L, Puliyadi, R, Perez-Alcantara, M, Coulton, L, Fisher, SE, Croucher, PI, Banham, AH

Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder. by Newbury, D, Mari, F, Sadighi Akha, E, Macdermot, K, Canitano, R, Monaco, A, Taylor, J, Renieri, A, Fisher, SE, Knight, S

Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder by Newbury, D, Mari, F, Sadighi Akha, E, MacDermot, K, Canitano, R, Monaco, A, Taylor, J, Renieri, A, Fisher, SE, Knight, S

Associations of HLA alleles with specific language impairment. by Nudel, R, Simpson, N, Baird, G, O'Hare, A, Conti-Ramsden, G, Bolton, P, Hennessy, E, Monaco, A, Knight, J, Winney, B, Fisher, SE, Newbury, D

Common variants in left/right asymmetry genes and pathways are associated with relative hand skill by Brandler, WM, Morris, A, Evans, D, Scerri, T, Kemp, J, Timpson, N, St Pourcain, B, Smith, G, Ring, S, Stein, J, Monaco, A, Talcott, J, Fisher, SE, Webber, C, Paracchini, S

Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment by Nudel, R, Simpson, N, Baird, G, O'Hare, A, Conti-Ramsden, G, Bolton, P, Hennessy, E, Ring, S, Davey Smith, G, Francks, C, Paracchini, S, Monaco, A, Fisher, SE, Newbury, D

Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment. by Nudel, R, Simpson, N, Baird, G, O'Hare, A, Conti-Ramsden, G, Bolton, P, Hennessy, E, Ring, S, Davey Smith, G, Francks, C, Paracchini, S, Monaco, A, Fisher, SE, Newbury, D

Genome-wide screening for DNA variants associated with reading and language traits. by Gialluisi, A, Newbury, D, Wilcutt, E, Olson, R, DeFries, J, Brandler, WM, Pennington, B, Smith, S, Scerri, T, Simpson, N, Luciano, M, Evans, D, Bates, T, Stein, J, Talcott, J, Monaco, A, Paracchini, S, Francks, C, Fisher, SE

Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment. by Ceroni, F, Simpson, N, Francks, C, Baird, G, Conti-Ramsden, G, Clark, A, Bolton, P, Hennessy, E, Donnelly, P, Bentley, DR, Martin, H, Parr, J, Pagnamenta, A, Maestrini, E, Bacchelli, E, Fisher, SE, Newbury, D

Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis' by Ceroni, F, Simpson, N, Francks, C, Baird, G, Conti-Ramsden, G, Clark, A, Bolton, P, Hennessy, E, Donnelly, P, Bentley, DR, Martin, H, Parr, J, Pagnamenta, A, Maestrini, E, Bacchelli, E, Fisher, SE, Newbury, D

Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia. by Simpson, N, Addis, L, Brandler, WM, Slonims, V, Clark, A, Watson, J, Scerri, T, Hennessy, E, Bolton, P, Conti-Ramsden, G, Fairfax, B, Knight, J, Stein, J, Talcott, J, O'Hare, A, Baird, G, Paracchini, S, Fisher, SE, Newbury, D

Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia by Simpson, N, Addis, L, Brandler, WM, Slonims, V, Clark, A, Watson, J, Scerri, T, Hennessy, E, Bolton, P, Conti-Ramsden, G, Fairfax, B, Knight, J, Stein, J, Talcott, J, O'Hare, A, Baird, G, Paracchini, S, Fisher, SE, Newbury, D, Nudel, R, Monaco, A, Simonoff, E, Pickles, A, Everitt, A, Seckl, J

Discovery of 42 genome-wide significant loci associated with dyslexia by Doust, C, Fontanillas, P, Eising, E, Gordon, SD, Wang, Z, Alagöz, G, Molz, B, Pourcain, BS, Francks, C, Marioni, RE, Zhao, J, Paracchini, S, Talcott, JB, Monaco, AP, Stein, JF, Gruen, JR, Olson, RK, Willcutt, EG, DeFries, JC, Pennington, BF, Smith, SD, Wright, MJ, Martin, NG, Auton, A, Bates, TC, Fisher, SE, Luciano, M

Low-frequency variation in TP53 has large effects on head circumference and intracranial volume by Haworth, S, Shapland, CY, Hayward, C, Prins, BP, Felix, JF, Medina-Gomez, C, Rivadeneira, F, Wang, C, Ahluwalia, TS, Vrijheid, M, Guxens, M, Sunyer, J, Tachmazidou, I, Walter, K, Iotchkova, V, Jackson, A, Cleal, L, Huffmann, J, Min, JL, Sass, L, Timmers, PRHJ, Smith, G, Fisher, SE, Wilson, JF, Cole, TJ, Fernandez-Orth, D, Bønnelykke, K, Bisgaard, H, Pennell, CE, Jaddoe, VWV, Dedoussis, G, Timpson, N, Zeggini, E, Vitart, V, St Pourcain, B, UK10K consortium, Bhattacharya, S

Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia by Gialluisi, A, Andlauer, TFM, Mirza-Schreiber, N, Moll, K, Becker, J, Hoffmann, P, Ludwig, KU, Czamara, D, St Pourcain, B, Brandler, W, Honbolygó, F, Tóth, D, Csépe, V, Huguet, G, Morris, AP, Hulslander, J, Willcutt, EG, Defries, JC, Olson, RK, Smith, SD, Pennington, BF, Vaessen, A, Maurer, U, Lyytinen, H, Peyrard-Janvid, M, Leppänen, PHT, Brandeis, D, Bonte, M, Stein, JF, Talcott, JB, Fauchereau, F, Wilcke, A, Francks, C, Bourgeron, T, Monaco, AP, Ramus, F, Landerl, K, Kere, J, Scerri, TS, Paracchini, S, Fisher, SE, Schumacher, J, Nöthen, MM, Müller-Myhsok, B, Schulte-Körne, G