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Publications - Anthony Bailey

2006/07 to 2010/11

Braeutigam, S., Swithenby, S., & Bailey, A.J., (2011). Magnetoencephalography (MEG) as a tool to investigate the neurophysiology of autism.In: Researching the Autism Spectrum. (Eds) Roth, S and Rezaie P. CUP.

Parr, J.R., Le Couteur, A., Baird, G., Rutter, M., Pickles, A., Fombonne, E., Bailey, A.J. & The International Molecular Genetic Study of Autism Consortium (IMGSAC) (2011). Early Developmental Regression in Autism Spectrum Disorder: Evidence from an International Multiplex Sample. J Autism Dev Disord., 41(3), 332-340.

Wallace, S., Sebastian, C., Pellicano, E., Parr, J., & Bailey, A.J. (2010). Face processing abilities in relatives of individuals with ASD. Autism Research, 3(6): 345-349.

Lai, M.C., Lombardo, M.V., Chakrabarti, B., Sadek, S.A., Pasco, G., Wheelwright, S.J., Bullmore, E.T., Baron-Cohen, S. & MRC AIMS Consortium, Suckling, J. (2010). A Shift to Randomness of Brain Oscillations in People with Autism. Biol Psychiatry., 68(12), 1092-9.

Parr, J.R., Le Couteur, A., Baird, G., Rutter, M., Pickles, A., Fombonne, E., & Bailey, A.J.; The International Molecular Genetic Study of Autism Consortium (IMGSAC) (2011). Early Developmental Regression in Autism Spectrum Disorder: Evidence from an International Multiplex Sample. J Autism Dev Disord., 41(3), 332-340.

Anney, R., Klei, L., Pinto, D., Regan, R., Conroy, J., Magalhaes, T.R., Correia, C., Abrahams, B.S., Sykes, N., Pagnamenta, A.T., Almeida, J., Bacchelli, E., Bailey, A.J., Baird, G., Battaglia, A., Berney, T., Bolshakova, N., Bölte, S., Bolton, P.F., Bourgeron, T., Brennan, S., Brian, J., Carson, A.R., Casallo, G., Casey, J., Chu, S., Cochrane, L., Corsello, C., Crawford, E.L., Crossett, A., Dawson, G., de Jonge, M., Delorme, R., Drmic, I., Duketis, E., Duque, F., Estes, A., Farrar, P., Fernandez, B.A., Folstein, S.E., Fombonne, E., Freitag, C.M., Gilbert, J., Gillberg, C., Glessner, J.T., Goldberg, J., Green, A., Green, J., Guter, S.J., Hakonarson, H. Heron, E.A., Hill, M., Holt, R., Howe. J.L., Hughes, G., Hus, V., Igliozzi, R., Kim, C., Klauck, S.M., Kolevzon, A., Korvatska, O., Kustanovich, V., Lajonchere, C.M., Lamb, J.A., Laskawiec, M., Leboyer, M., Le Couteur, A., Leventhal, B.L., Lionel, A.C., Liu, X.Q., Lord, C., Lotspeich, L., Lund, S.C., Maestrini, E., Mahoney, W., Mantoulan, C., Marshall, C.R., McConachie, H., McDougle, C.J., McGrath, J., McMahon, W.M., Melhem, N.M., Merikangas, A., Migita, O., Minshew, N.J., Mirza, G.K., Munson, J., Nelson, S.F., Noakes, C., Noor, A., Nygren, G., Oliveira, G., Papanikolaou, K., Parr, J.R., Parrini, B., Paton, T., Pickles, A., Piven, J., Posey, D.J., Poustka, A., Poustka, F., Prasad, A., Ragoussis, J., Renshaw, K., Rickaby, J., Roberts, W., Roeder, K., Roge, B., Rutter, M.L., Bierut, L.J., Rice, J.P., Salt, J., Sansom, K., Sato, D., Segurado, R., Senman, L., Shah, N., Sheffield, V.C., Soorya, L., Sousa, I., Stoppioni, V., Strawbridge, C., Tancredi, R., Tansey, K., Thiruvahindrapduram, B., Thompson, A.P., Thomson, S., Tryfon, A., Tsiantis, J., Van Engeland, H., Vincent, J.B., Volkmar, F., Wallace, S., Wang, K., Wang, Z., Wassink, T.H., Wing, K., Wittemeyer, K., Wood, S., Yaspan, B.L., Zurawiecki, D., Zwaigenbaum, L., Betancur, C., Buxbaum, J.D., Cantor, R.M., Cook, E.H., Coon, H., Cuccaro, M.L., Gallagher, L., Geschwind, D.H., Gill, M., Haines, J.L., Miller, J., Monaco, A.P., Nurnberger, J.I. Jr., Paterson, A.D., Pericak-Vance, M.A., Schellenberg, G.D., Scherer, S.W., Sutcliffe, J.S., Szatmari, P., Vicente, A.M., Vieland, V.J., Wijsman, E.M., Devlin, B., Ennis, S., & Hallmayer (2010). A genomewide scan for common alleles affecting risk for autism. J. Hum Mol Genet, 19 (20), 4072-4082.

Pagnamenta, A.T., Bacchelli, E., de Jonge, M.V., Mirza, G., Scerri, T.S., Minopoli, F., Chiocchetti, A., Ludwig, K.U., Hoffmann, P., Paracchini, S., Lowy, E., Harold, D.H., Chapman, J.A., Klauck, S.M., Poustka, F., Houben, R.H., Staal, W.G., Ophoff, R.A., O'Donovan, M.C., Williams, J., Nöthen, M.M., Schulte-Körne, G., Deloukas, P., Ragoussis, J., Bailey, A.J., Maestrini, E., Monaco, A.P. & International Molecular Genetic Study Of Autism Consortium. (2010) Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia. Biol Psychiatry, 68(4), 320-8.

Pinto, D., Pagnamenta, A.T., Klei, L., Anney, R., Merico, D., Regan, R., Conroy, J., Magalhaes, T.R., Correia, C., Abrahams, B.S., Almeida, J., Bacchelli, E., Bader, G.D., Bailey, A.J., Baird, G., Battaglia, A., Berney, T., Bolshakova, N., Bölte, S., Bolton, P.F., Bourgeron, T., Brennan, S., Brian, J., Bryson, S.E., Carson, A.R., Casallo, G., Casey, J., Chung, B.H., Cochrane, L., Corsello, C., Crawford, E.L., Crossett, A., Cytrynbaum, C., Dawson, G., de Jonge, M., Delorme, R., Drmic, I., Duketis, E., Duque, F., Estes, A., Farrar, P., Fernandez, B.A., Folstein, S.E., Fombonne, E., Freitag, C.M., Gilbert, J., Gillberg, C., Glessner, J.T., Goldberg, J., Green, A., Green, J., Guter, S.J., Hakonarson, H., Heron, E.A., Hill, M., Holt, R., Howe, J.L., Hughes, G., Hus, V., Igliozzi, R., Kim, C., Klauck, S.M., Kolevzon, A., Korvatska, O., Kustanovich, V., Lajonchere, C.M., Lamb, J.A., Laskawiec, M., Leboyer, M., Le Couteur, A., Leventhal, B.L., Lionel, A.C., Liu, X.Q., Lord, C., Lotspeich, L., Lund, S.C., Maestrini, E., Mahoney, W., Mantoulan, C., Marshall, C.R., McConachie, H., McDougle, C.J., McGrath, J., McMahon, W.M., Merikangas, A., Migita, O., Minshew, N.J., Mirza, G.K., Munson, J., Nelson, S.F., Noakes, C., Noor, A., Nygren, G., Oliveira, G., Papanikolaou, K., Parr, J.R., Parrini, B., Paton, T., Pickles, A., Pilorge, M., Piven, J., Ponting, C.P., Posey, D.J., Poustka, A., Poustka, F., Prasad, A., Ragoussis, J., Renshaw, K., Rickaby, J., Roberts, W., Roeder, K., Roge, B., Rutter, M.L., Bierut, L.J., Rice, J.P., Salt, J., Sansom, K., Sato, D., Segurado, R., Sequeira, A.F., Senman, L., Shah, N., Sheffield, V.C., Soorya, L., Sousa, I., Stein, O., Sykes, N., Stoppioni, V., Strawbridge, C., Tancredi, R., Tansey, K., Thiruvahindrapduram, B., Thompson, A.P., Thomson, S., Tryfon, A., Tsiantis, J., Van Engeland, H., Vincent, J.B., Volkmar, F., Wallace, S., Wang, K., Wang, Z., Wassink, T.H., Webber, C., Weksberg, R., Wing, K., Wittemeyer, K., Wood, S., Wu, J., Yaspan, B.L., Zurawiecki, D., Zwaigenbaum, L., Buxbaum, J.D., Cantor, R.M., Cook, E.H., Coon, H., Cuccaro, M.L., Devlin, B., Ennis, S., Gallagher, L., Geschwind, D.H., Gill, M., Haines, J.L., Hallmayer, J., Miller, J., Monaco, A.P., Nurnberger, J.I. Jr., Paterson ,A.D., Pericak-Vance, M.A., Schellenberg, G.D., Szatmari, P., Vicente, A.M., Vieland, V.J., Wijsman, E.M., Scherer, S.W., Sutcliffe, J.S., & Betancur, C. (2010). Functional impact of global rare copy number variation in autism spectrum disorders. Nature, 15, 466(7304), 368-72.

Holt, R., Barnby, G., Maestrini, E., Bacchelli, E., Brocklebank, D., Sousa, I., Mulder, E.J., Kantojärvi, K., Järvelä, I., Klauck, S.M., Poustka, F., Bailey, A.J., & Monaco, A.P. (2010). Linkage and candidate gene studies of autism spectrum disorders in European populations. Eur J Hum Genet. 18, 1013-9

Ecker, C., Rocha-Rego, V., Johnston, P., Mourao-Miranda, J., Marquand, A., Daly, E.M., Brammer, M.J., Murphy, C., Murphy, D.G. & MRC AIMS Consortium (2010). Investigating the predictive value of whole-brain structural MR scans in autism: A pattern classification approach. Neuroimage, 49, 44-56.

Wallace, S., Parsons, S., Westbury, A., White, K., & Bailey, A.J. (2010). Sense of presence and atypical social judgments in immersive virtual environments: Responses of adolescents with Autism Spectrum Disorders. Autism, 14, 199-213.

Sousa, I., Clark, T.G., Holt, R., Pagnamenta, A.T., Mulder, E.J., Minderaa, R.B., Bailey, A.J., Battaglia, A., Klauck, S.M., Poustka, F., Monaco, A.P. & The International Molecular Genetic Study of Autism Consortium (IMGSAC) (2010). Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry. Mol Autism., 1(1), 7.

Lombardo, M.V., Chakrabarti, B., Bullmore, E.T., Sadek, S.A., Pasco, G., Wheelwright, S.J., & Suckling, J.; MRC AIMS Consortium, Baron-Cohen, S. (2010). Atypical neural self-representation in autism. Brain, 133, 611-24.

Sykes, N.H., Toma, C., Wilson, N., Volpi, E.V., Sousa, I., Pagnamenta, A.T., Tancredi, R., Battaglia, A., Maestrini, E., Bailey, A.J., & Monaco, A.P.; International Molecular Genetic Study of Autism Consortium (IMGSAC) (2009). Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection. European Journal of Human Genetics, 17,1347-53.

Maestrini, E., Pagnamenta, A.T., Lamb, J.A., Bacchelli, E., Sykes, N.H., Sousa, I., Toma, C., Barnby, G., Butler, H., Winchester, L., Scerri, T.S., Minopoli, F., Reichert, J., Cai, G., Buxbaum, J.D., Korvatska, O., Schellenberg, G.D., Dawson, G., Bildt, A.D., Minderaa, R.B., Mulder, E.J., Morris, A.P., Bailey, A.J.,& Monaco, A.P. (2010). High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility. Molecular Psychiatry, 15, 954–968.

Carrington, S.J., & Bailey, A.J. (2009). Are there Theory of Mind regions in the brain? A review of the neuroimaging literature. Hum Brain Mapp, 30, 2313-2335

Pagnamenta, A.T., Wing, K., Akha, E.S., Knight, S.J., Bölte, S., Schmötzer, G., Duketis, E., Poustka, F., Klauck, S.M., Poustka, A., Ragoussis, J., Bailey, A.J., Monaco, A.P., & The International Molecular Genetic Study of Autism Consortium (2009). A 15q13.3 microdeletion segregating with autism. Eur J Hum Genet, 17, 687-92.

Sousa, I., Clark, T.G., Toma, C., Kobayashi, K., Choma, M., Holt, R., Sykes, N.H., Lamb, J.A., Bailey, A.J., Battaglia, A., Maestrini, E., & Monaco, A.P. (2009). MET and autism susceptibility: family and case-control studies. Eur J Hum Genet, 17, 749-58.

Liu, X.Q., Paterson, A.D., Szatmari, P., & The Autism Genome Project Consortium (2008). Genome-wide linkage analyses of quantitative and categorical autism subphenotypes. Biol Psychiatry, 64, 561-70.

Gong, X., Bacchelli, E., Blasi, F., Toma, C., Betancur, C., Chaste, P., Delorme, R., Durand, C.M., Fauchereau, F., Botros, H.G., Leboyer, M., Mouren-Simeoni, M.C., Nygren, G., Anckarsäter, H., Rastam, M., Gillberg, I.C., Gillberg, C., Moreno-De-Luca, D., Carone, S., Nummela, I., Rossi, M., Battaglia, A. International Molecular Genetic Study of Autism Consortium (IMGSAC), Jarvela, I., Maestrini, E., & Bourgeron, T. (2008). Analysis of X chromosome inactivation in autism spectrum disorders. American Journal of Medical Genetics B; Neuropsychiatric Genetics, 147(6), 830-835.

Wallace, S., Coleman, M., & Bailey, A.J. (2008). An investigation of basic facial expression recognition in autism spectrum disorders. Cognition and Emotion, 22, 1353-1380.

Wallace, S., Coleman, M., & Bailey, A.J. (2008). Face and object processing in autism spectrum disorders. Autism Res, 1, 43-51.

Braeutigam, S., Swithenby, S.J., & Bailey, A.J. (2008). Contextual integration the unusual way: a magnetoencephalographic study of responses to semantic violation in individuals with autism spectrum disorders. Eur J Neurosci, 27(4), 1026-36.

The Autism Genome Project Consortium (2007). Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nature Genetics, 39, 319-328.

Bonora, E., Lamb, J.A., Barnby, G. Bailey, A.J., & Monaco, A.P. (2006) Genetic Basis of Autism. In S.O. Moldin, and J.L.R Rubenstein, (Eds.), Understanding Autism: From Basic Neuroscience to Treatment. Boca Raton, FL: CRC Press.

Wallace, S., Coleman, M., Pascalis, O., & Bailey, A.J. (2006). A study of impaired judgement of eye-gaze direction and related face-processing deficits in autism spectrum disorders. Perception, 35(12), 1651-64.

Kylliäinen, A., Bräutigam, S., Hietanen, J.K., Swithenby, S.J., & Bailey, A.J. (2006). Face- and gaze-sensitive neural responses in children with autism: a magnetoencephalographic study. Eur J Neurosci, 24(9), 2679-90.

Blasi, F., Bacchelli, E., Pesaresi, G., Carone, S., Bailey, A.J., Maestrini, E. & The International Molecular Genetic Study of Autism Consortium (IMGSAC) (2006). Absence of coding mutations in the X-linked genes neuroligin 3 and neuroligin 4 in individuals with autism from the IMGSAC collection. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 141(3), 220-221.