Ultrasonic vocalizations of adult male Foxp2‐mutant mice: behavioral contexts of arousal and emotion von Gaub, S., Fisher, S. E., Ehret, G.

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An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning von French, C A, Jin, X, Campbell, T G, Gerfen, E, Groszer, M, Fisher, S E, Costa, R M

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CNTNAP2 variants affect early language development in the general population von Whitehouse, A. J. O., Bishop, D. V. M., Ang, Q. W., Pennell, C. E., Fisher, S. E.

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Excess mortality following hip fracture : the role of underlying health status von TOSTESON, A. N. A, GOTTLIEB, D. J, RADLEY, D. C, FISHER, E. S, MELTON, L. J

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LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia von Francks, C, Maegawa, S, Laurén, J, Abrahams, B S, Velayos-Baeza, A, Medland, S E, Colella, S, Groszer, M, McAuley, E Z, Caffrey, T M, Timmusk, T, Pruunsild, P, Koppel, I, Lind, P A, Matsumoto-Itaba, N, Nicod, J, Xiong, L, Joober, R, Enard, W, Krinsky, B, Nanba, E, Richardson, A J, Riley, B P, Martin, N G, Strittmatter, S M, Möller, H-J, Rujescu, D, St Clair, D, Muglia, P, Roos, J L, Fisher, S E, Wade-Martins, R, Rouleau, G A, Stein, J F, Karayiorgou, M, Geschwind, D H, Ragoussis, J, Kendler, K S, Airaksinen, M S, Oshimura, M, DeLisi, L E, Monaco, A P

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The structure of innate vocalizations in Foxp2‐deficient mouse pups von Gaub, S., Groszer, M., Fisher, S. E., Ehret, G.

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Neighborhood‐contingent indirect interactions between native and exotic plants: multiple shared pollinators mediate reproductive success during invasions von Waters, S. M, Fisher, S. E, Hille Ris Lambers, J

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Genome‐wide screening for DNA variants associated with reading and language traits von Gialluisi, A., Newbury, D. F., Wilcutt, E. G., Olson, R. K., DeFries, J. C., Brandler, W. M., Pennington, B. F., Smith, S. D., Scerri, T. S., Simpson, N. H., Luciano, M., Evans, D. M., Bates, T. C., Stein, J. F., Talcott, J. B., Monaco, A. P., Paracchini, S., Francks, C., Fisher, S. E.

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

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A genome‐wide search for quantitative trait loci affecting the cortical surface area and thickness of Heschl's gyrus von Cai, D.‐C., Fonteijn, H., Guadalupe, T., Zwiers, M., Wittfeld, K., Teumer, A., Hoogman, M., Arias‐Vásquez, A., Yang, Y., Buitelaar, J., Fernández, G., Brunner, H. G., van Bokhoven, H., Franke, B., Hegenscheid, K., Homuth, G., Fisher, S. E., Grabe, H. J., Francks, C., Hagoort, P.

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Genetic and phenotypic effects of phonological short‐term memory and grammatical morphology in specific language impairment von Falcaro, M., Pickles, A., Newbury, D. F., Addis, L., Banfield, E., Fisher, S. E., Monaco, A. P., Simkin, Z., Conti‐Ramsden, G.

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FOXP2 Is Not a Major Susceptibility Gene for Autism or Specific Language Impairment von Newbury, D.F., Bonora, E., Lamb, J.A., Fisher, S.E., Lai, C.S.L., Baird, G., Jannoun, L., Slonims, V., Stott, C.M., Merricks, M.J., Bolton, P.F., Bailey, A.J., Monaco, A.P.

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Evaluation of results from genome‐wide studies of language and reading in a novel independent dataset von Carrion‐Castillo, A., van Bergen, E., Vino, A., van Zuijen, T., de Jong, P. F., Francks, C., Fisher, S. E.

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Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder localizes pleiotropic loci von Gayán, J., Willcutt, E.G., Fisher, S.E., Francks, C., Cardon, L.R., Olson, R.K., Pennington, B.F., Smith, S.D., Monaco, A.P., DeFries, J.C.

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A Quantitative-Trait Locus on Chromosome 6p Influences Different Aspects of Developmental Dyslexia von Fisher, Simon E., Marlow, Angela J., Lamb, Janine, Maestrini, Elena, Williams, Dianne F., Richardson, Alex J., Weeks, Daniel E., Stein, John F., Monaco, Anthony P.

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Variation in Carotid Endarterectomy Mortality in the Medicare Population: Trial Hospitals, Volume, and Patient Characteristics von Wennberg, David E, Lucas, F. L, Birkmeyer, John D, Bredenberg, Carl E, Fisher, Elliott S

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Localisation of a gene implicated in a severe speech and language disorder von Fisher, Simon E., Vargha-Khadem, Faraneh, Watkins, Kate E., Monaco, Anthony P., Pembrey, Marcus E.

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ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties von St Pourcain, B, Robinson, E B, Anttila, V, Sullivan, B B, Maller, J, Golding, J, Skuse, D, Ring, S, Evans, D M, Zammit, S, Fisher, S E, Neale, B M, Anney, R J L, Ripke, S, Hollegaard, M V, Werge, T, Ronald, A, Grove, J, Hougaard, D M, Børglum, A D, Mortensen, P B, Daly, M J, Davey Smith, G

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Health-related quality of life and clinical function after primary surgery for oral cancer von Rogers, S.N., Lowe, D., Fisher, S.E., Brown, J.S., Vaughan, E.D.

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Lack of replication for the myosin‐18B association with mathematical ability in independent cohorts von Pettigrew, K. A., Fajutrao Valles, S. F., Moll, K., Northstone, K., Ring, S., Pennell, C., Wang, C., Leavett, R., Hayiou‐Thomas, M. E., Thompson, P., Simpson, N. H., Fisher, S. E., Whitehouse, A. J. O., Snowling, M. J., Newbury, D. F., Paracchini, S.

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