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2016
S. Shanmugan, Wolf, D. H., Calkins, M. E., Moore, T. M., Ruparel, K., Hopson, R. D., Vandekar, S. N., Roalf, D. R., Elliott, M. A., Jackson, C., Gennatas, E. D., Leibenluft, E., Pine, D. S., Shinohara, R. T., Hakonarson, H., Gur, R. C., Gur, R. E., and Satterthwaite, T. D., Common and Dissociable Mechanisms of Executive System Dysfunction Across Psychiatric Disorders in Youth., Am J Psychiatry, vol. 173, no. 5, pp. 517-26, 2016.
D. R. Roalf, Quarmley, M., Elliott, M. A., Satterthwaite, T. D., Vandekar, S. N., Ruparel, K., Gennatas, E. D., Calkins, M. E., Moore, T. M., Hopson, R., Prabhakaran, K., Jackson, C. T., Verma, R., Hakonarson, H., Gur, R. C., and Gur, R. E., The impact of quality assurance assessment on diffusion tensor imaging outcomes in a large-scale population-based cohort., Neuroimage, vol. 125, pp. 903-919, 2016.
T. D. Satterthwaite, Connolly, J. J., Ruparel, K., Calkins, M. E., Jackson, C., Elliott, M. A., Roalf, D. R., Hopson, R., Prabhakaran, K., Behr, M., Qiu, H., Mentch, F. D., Chiavacci, R., Sleiman, P. M. A., Gur, R. C., Hakonarson, H., and Gur, R. E., The Philadelphia Neurodevelopmental Cohort: A publicly available resource for the study of normal and abnormal brain development in youth., Neuroimage, vol. 124, no. Pt B, pp. 1115-1119, 2016.
T. L. Wenger, Kao, C., McDonald-McGinn, D. M., Zackai, E. H., Bailey, A., Schultz, R. T., Morrow, B. E., Emanuel, B. S., and Hakonarson, H., The Role of mGluR Copy Number Variation in Genetic and Environmental Forms of Syndromic Autism Spectrum Disorder., Sci Rep, vol. 6, p. 19372, 2016.
T. D. Satterthwaite, Wolf, D. H., Calkins, M. E., Vandekar, S. N., Erus, G., Ruparel, K., Roalf, D. R., Linn, K. A., Elliott, M. A., Moore, T. M., Hakonarson, H., Shinohara, R. T., Davatzikos, C., Gur, R. C., and Gur, R. E., Structural Brain Abnormalities in Youth With Psychosis Spectrum Symptoms., JAMA Psychiatry, vol. 73, no. 5, pp. 515-24, 2016.
2015
D. H. Wolf, Satterthwaite, T. D., Calkins, M. E., Ruparel, K., Elliott, M. A., Hopson, R. D., Jackson, C. T., Prabhakaran, K., Bilker, W. B., Hakonarson, H., Gur, R. C., and Gur, R. E., Functional neuroimaging abnormalities in youth with psychosis spectrum symptoms., JAMA Psychiatry, vol. 72, no. 5, pp. 456-65, 2015.
F. Sun, Oristaglio, J., Levy, S. E., Hakonarson, H., Sullivan, N., Fontanarosa, J., and Schoelles, K. M., Genetic Testing for Developmental Disabilities, Intellectual Disability, and Autism Spectrum Disorder, 2015.
B. St Pourcain, Haworth, C. M. A., Davis, O. S. P., Wang, K., Timpson, N. J., Evans, D. M., Kemp, J. P., Ronald, A., Price, T., Meaburn, E., Ring, S. M., Golding, J., Hakonarson, H., Plomin, R., and Smith, G. Davey, Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence., Hum Genet, vol. 134, no. 6, pp. 539-51, 2015.
G. Erus, Battapady, H., Satterthwaite, T. D., Hakonarson, H., Gur, R. E., Davatzikos, C., and Gur, R. C., Imaging patterns of brain development and their relationship to cognition., Cereb Cortex, vol. 25, no. 6, pp. 1676-84, 2015.
T. D. Satterthwaite, Wolf, D. H., Roalf, D. R., Ruparel, K., Erus, G., Vandekar, S., Gennatas, E. D., Elliott, M. A., Smith, A., Hakonarson, H., Verma, R., Davatzikos, C., Gur, R. E., and Gur, R. C., Linked Sex Differences in Cognition and Functional Connectivity in Youth., Cereb Cortex, vol. 25, no. 9, pp. 2383-94, 2015.
M. E. Calkins, Merikangas, K. R., Moore, T. M., Burstein, M., Behr, M. A., Satterthwaite, T. D., Ruparel, K., Wolf, D. H., Roalf, D. R., Mentch, F. D., Qiu, H., Chiavacci, R., Connolly, J. J., Sleiman, P. M. A., Gur, R. C., Hakonarson, H., and Gur, R. E., The Philadelphia Neurodevelopmental Cohort: constructing a deep phenotyping collaborative., J Child Psychol Psychiatry, vol. 56, no. 12, pp. 1356-1369, 2015.
T. M. Moore, Reise, S. P., Gur, R. E., Hakonarson, H., and Gur, R. C., Psychometric properties of the Penn Computerized Neurocognitive Battery., Neuropsychology, vol. 29, no. 2, pp. 235-46, 2015.
2014
D. Pinto, Delaby, E., Merico, D., Barbosa, M., Merikangas, A., Klei, L., Thiruvahindrapuram, B., Xu, X., Ziman, R., Wang, Z., Vorstman, J. A. S., Thompson, A., Regan, R., Pilorge, M., Pellecchia, G., Pagnamenta, A. T., Oliveira, B., Marshall, C. R., Magalhaes, T. R., Lowe, J. K., Howe, J. L., Griswold, A. J., Gilbert, J., Duketis, E., Dombroski, B. A., De Jonge, M. V., Cuccaro, M., Crawford, E. L., Correia, C. T., Conroy, J., Conceição, I. C., Chiocchetti, A. G., Casey, J. P., Cai, G., Cabrol, C., Bolshakova, N., Bacchelli, E., Anney, R., Gallinger, S., Cotterchio, M., Casey, G., Zwaigenbaum, L., Wittemeyer, K., Wing, K., Wallace, S., van Engeland, H., Tryfon, A., Thomson, S., Soorya, L., Rogé, B., Roberts, W., Poustka, F., Mouga, S., Minshew, N., L McInnes, A., McGrew, S. G., Lord, C., Leboyer, M., Le Couteur, A. S., Kolevzon, A., González, P. Jiménez, Jacob, S., Holt, R., Guter, S., Green, J., Green, A., Gillberg, C., Fernandez, B. A., Duque, F., Delorme, R., Dawson, G., Chaste, P., Café, C., Brennan, S., Bourgeron, T., Bolton, P. F., Bölte, S., Bernier, R., Baird, G., Bailey, A. J., Anagnostou, E., Almeida, J., Wijsman, E. M., Vieland, V. J., Vicente, A. M., Schellenberg, G. D., Pericak-Vance, M., Paterson, A. D., Parr, J. R., Oliveira, G., Nurnberger, J. I., Monaco, A. P., Maestrini, E., Klauck, S. M., Hakonarson, H., Haines, J. L., Geschwind, D. H., Freitag, C. M., Folstein, S. E., Ennis, S., Coon, H., Battaglia, A., Szatmari, P., Sutcliffe, J. S., Hallmayer, J., Gill, M., Cook, E. H., Buxbaum, J. D., Devlin, B., Gallagher, L., Betancur, C., and Scherer, S. W., Convergence of genes and cellular pathways dysregulated in autism spectrum disorders., Am J Hum Genet, vol. 94, no. 5, pp. 677-94, 2014.
J. J. Connolly and Hakonarson, H., Etiology of autism spectrum disorder: a genomics perspective., Curr Psychiatry Rep, vol. 16, no. 11, p. 501, 2014.
N. Matsunami, Hensel, C. H., Baird, L., Stevens, J., Otterud, B., Leppert, T., Varvil, T., Hadley, D., Glessner, J. T., Pellegrino, R., Kim, C., Thomas, K., Wang, F., Otieno, F. G., Ho, K., Christensen, G. B., Li, D., Prekeris, R., Lambert, C. G., Hakonarson, H., and Leppert, M. F., Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population., Mol Autism, vol. 5, no. 1, p. 5, 2014.
D. Hadley, Wu, Z. - L., Kao, C., Kini, A., Mohamed-Hadley, A., Thomas, K., Vazquez, L., Qiu, H., Mentch, F., Pellegrino, R., Kim, C., Connolly, J., Glessner, J., and Hakonarson, H., The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism., Nat Commun, vol. 5, p. 4074, 2014.
T. D. Satterthwaite, Elliott, M. A., Ruparel, K., Loughead, J., Prabhakaran, K., Calkins, M. E., Hopson, R., Jackson, C., Keefe, J., Riley, M., Mentch, F. D., Sleiman, P., Verma, R., Davatzikos, C., Hakonarson, H., Gur, R. C., and Gur, R. E., Neuroimaging of the Philadelphia neurodevelopmental cohort., Neuroimage, vol. 86, pp. 544-53, 2014.
M. Ingalhalikar, Smith, A., Parker, D., Satterthwaite, T. D., Elliott, M. A., Ruparel, K., Hakonarson, H., Gur, R. E., Gur, R. C., and Verma, R., Sex differences in the structural connectome of the human brain., Proc Natl Acad Sci U S A, vol. 111, no. 2, pp. 823-8, 2014.
B. St Pourcain, Skuse, D. H., Mandy, W. P., Wang, K., Hakonarson, H., Timpson, N. J., Evans, D. M., Kemp, J. P., Ring, S. M., McArdle, W. L., Golding, J., and Smith, G. Davey, Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence., Mol Autism, vol. 5, no. 1, p. 18, 2014.
D. R. Roalf, Gur, R. E., Ruparel, K., Calkins, M. E., Satterthwaite, T. D., Bilker, W. B., Hakonarson, H., Harris, L. Julius, and Gur, R. C., Within-individual variability in neurocognitive performance: age- and sex-related differences in children and youths from ages 8 to 21., Neuropsychology, vol. 28, no. 4, pp. 506-18, 2014.
2013
B. St Pourcain, Whitehouse, A. J. O., Ang, W. Q., Warrington, N. M., Glessner, J. T., Wang, K., Timpson, N. J., Evans, D. M., Kemp, J. P., Ring, S. M., McArdle, W. L., Golding, J., Hakonarson, H., Pennell, C. E., and Smith, G. Davey, Common variation contributes to the genetic architecture of social communication traits., Mol Autism, vol. 4, no. 1, p. 34, 2013.
O. Gottesman, Kuivaniemi, H., Tromp, G., W Faucett, A., Li, R., Manolio, T. A., Sanderson, S. C., Kannry, J., Zinberg, R., Basford, M. A., Brilliant, M., Carey, D. J., Chisholm, R. L., Chute, C. G., Connolly, J. J., Crosslin, D., Denny, J. C., Gallego, C. J., Haines, J. L., Hakonarson, H., Harley, J., Jarvik, G. P., Kohane, I., Kullo, I. J., Larson, E. B., McCarty, C., Ritchie, M. D., Roden, D. M., Smith, M. E., Böttinger, E. P., and Williams, M. S., The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future., Genet Med, vol. 15, no. 10, pp. 761-71, 2013.
T. D. Satterthwaite, Wolf, D. H., Erus, G., Ruparel, K., Elliott, M. A., Gennatas, E. D., Hopson, R., Jackson, C., Prabhakaran, K., Bilker, W. B., Calkins, M. E., Loughead, J., Smith, A., Roalf, D. R., Hakonarson, H., Verma, R., Davatzikos, C., Gur, R. C., and Gur, R. E., Functional maturation of the executive system during adolescence., J Neurosci, vol. 33, no. 41, pp. 16249-61, 2013.
H. S Lee, Ripke, S., Neale, B. M., Faraone, S. V., Purcell, S. M., Perlis, R. H., Mowry, B. J., Thapar, A., Goddard, M. E., Witte, J. S., Absher, D., Agartz, I., Akil, H., Amin, F., Andreassen, O. A., Anjorin, A., Anney, R., Anttila, V., Arking, D. E., Asherson, P., Azevedo, M. H., Backlund, L., Badner, J. A., Bailey, A. J., Banaschewski, T., Barchas, J. D., Barnes, M. R., Barrett, T. B., Bass, N., Battaglia, A., Bauer, M., Bayés, M., Bellivier, F., Bergen, S. E., Berrettini, W., Betancur, C., Bettecken, T., Biederman, J., Binder, E. B., Black, D. W., Blackwood, D. H. R., Bloss, C. S., Boehnke, M., Boomsma, D. I., Breen, G., Breuer, R., Bruggeman, R., Cormican, P., Buccola, N. G., Buitelaar, J. K., Bunney, W. E., Buxbaum, J. D., Byerley, W. F., Byrne, E. M., Caesar, S., Cahn, W., Cantor, R. M., Casas, M., Chakravarti, A., Chambert, K., Choudhury, K., Cichon, S., C Cloninger, R., Collier, D. A., Cook, E. H., Coon, H., Cormand, B., Corvin, A., Coryell, W. H., Craig, D. W., Craig, I. W., Crosbie, J., Cuccaro, M. L., Curtis, D., Czamara, D., Datta, S., Dawson, G., Day, R., De Geus, E. J., Degenhardt, F., Djurovic, S., Donohoe, G. J., Doyle, A. E., Duan, J., Dudbridge, F., Duketis, E., Ebstein, R. P., Edenberg, H. J., Elia, J., Ennis, S., Etain, B., Fanous, A., Farmer, A. E., I Ferrier, N., Flickinger, M., Fombonne, E., Foroud, T., Frank, J., Franke, B., Fraser, C., Freedman, R., Freimer, N. B., Freitag, C. M., Friedl, M., Frisén, L., Gallagher, L., Gejman, P. V., Georgieva, L., Gershon, E. S., Geschwind, D. H., Giegling, I., Gill, M., Gordon, S. D., Gordon-Smith, K., Green, E. K., Greenwood, T. A., Grice, D. E., Gross, M., Grozeva, D., Guan, W., Gurling, H., De Haan, L., Haines, J. L., Hakonarson, H., Hallmayer, J., Hamilton, S. P., Hamshere, M. L., Hansen, T. F., Hartmann, A. M., Hautzinger, M., Heath, A. C., Henders, A. K., Herms, S., Hickie, I. B., Hipolito, M., Hoefels, S., Holmans, P. A., Holsboer, F., Hoogendijk, W. J., Hottenga, J. - J., Hultman, C. M., Hus, V., Ingason, A., Ising, M., Jamain, S., Jones, E. G., Jones, I., Jones, L., Tzeng, J. - Y., Kähler, A. K., Kahn, R. S., Kandaswamy, R., Keller, M. C., Kennedy, J. L., Kenny, E., Kent, L., Kim, Y., Kirov, G. K., Klauck, S. M., Klei, L., Knowles, J. A., Kohli, M. A., Koller, D. L., Konte, B., Korszun, A., Krabbendam, L., Krasucki, R., Kuntsi, J., Kwan, P., Landén, M., Långström, N., Lathrop, M., Lawrence, J., Lawson, W. B., Leboyer, M., Ledbetter, D. H., Lee, P. H., Lencz, T., Lesch, K. - P., Levinson, D. F., Lewis, C. M., Li, J., Lichtenstein, P., Lieberman, J. A., Lin, D. - Y., Linszen, D. H., Liu, C., Lohoff, F. W., Loo, S. K., Lord, C., Lowe, J. K., Lucae, S., MacIntyre, D. J., Madden, P. A. F., Maestrini, E., Magnusson, P. K. E., Mahon, P. B., Maier, W., Malhotra, A. K., Mane, S. M., Martin, C. L., Martin, N. G., Mattheisen, M., Matthews, K., Mattingsdal, M., McCarroll, S. A., McGhee, K. A., McGough, J. J., McGrath, P. J., McGuffin, P., McInnis, M. G., McIntosh, A., McKinney, R., McLean, A. W., McMahon, F. J., McMahon, W. M., McQuillin, A., Medeiros, H., Medland, S. E., Meier, S., Melle, I., Meng, F., Meyer, J., Middeldorp, C. M., Middleton, L., Milanova, V., Miranda, A., Monaco, A. P., Montgomery, G. W., Moran, J. L., Moreno-De-Luca, D., Morken, G., Morris, D. W., Morrow, E. M., Moskvina, V., Muglia, P., Mühleisen, T. W., Muir, W. J., Müller-Myhsok, B., Murtha, M., Myers, R. M., Myin-Germeys, I., Neale, M. C., Nelson, S. F., Nievergelt, C. M., Nikolov, I., Nimgaonkar, V., Nolen, W. A., Nöthen, M. M., Nurnberger, J. I., Nwulia, E. A., Nyholt, D. R., O'Dushlaine, C., Oades, R. D., Olincy, A., Oliveira, G., Olsen, L., Ophoff, R. A., Osby, U., Owen, M. J., Palotie, A., Parr, J. R., Paterson, A. D., Pato, C. N., Pato, M. T., Penninx, B. W., Pergadia, M. L., Pericak-Vance, M. A., Pickard, B. S., Pimm, J., Piven, J., Posthuma, D., Potash, J. B., Poustka, F., Propping, P., Puri, V., Quested, D. J., Quinn, E. M., Ramos-Quiroga, J. Antoni, Rasmussen, H. B., Raychaudhuri, S., Rehnström, K., Reif, A., Ribasés, M., Rice, J. P., Rietschel, M., Roeder, K., Roeyers, H., Rossin, L., Rothenberger, A., Rouleau, G., Ruderfer, D., Rujescu, D., Sanders, A. R., Sanders, S. J., Santangelo, S. L., Sergeant, J. A., Schachar, R., Schalling, M., Schatzberg, A. F., Scheftner, W. A., Schellenberg, G. D., Scherer, S. W., Schork, N. J., Schulze, T. G., Schumacher, J., Schwarz, M., Scolnick, E., Scott, L. J., Shi, J., Shilling, P. D., Shyn, S. I., Silverman, J. M., Slager, S. L., Smalley, S. L., Smit, J. H., Smith, E. N., Sonuga-Barke, E. J. S., St Clair, D., State, M., Steffens, M., Steinhausen, H. - C., Strauss, J. S., Strohmaier, J., T Stroup, S., Sutcliffe, J. S., Szatmari, P., Szelinger, S., Thirumalai, S., Thompson, R. C., Todorov, A. A., Tozzi, F., Treutlein, J., Uhr, M., van den Oord, E. J. C. G., Van Grootheest, G., Van Os, J., Vicente, A. M., Vieland, V. J., Vincent, J. B., Visscher, P. M., Walsh, C. A., Wassink, T. H., Watson, S. J., Weissman, M. M., Werge, T., Wienker, T. F., Wijsman, E. M., Willemsen, G., Williams, N., A Willsey, J., Witt, S. H., Xu, W., Young, A. H., Yu, T. W., Zammit, S., Zandi, P. P., Zhang, P., Zitman, F. G., Zöllner, S., Devlin, B., Kelsoe, J. R., Sklar, P., Daly, M. J., O'Donovan, M. C., Craddock, N., Sullivan, P. F., Smoller, J. W., Kendler, K. S., and Wray, N. R., Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs., Nat Genet, vol. 45, no. 9, pp. 984-94, 2013.
T. D. Satterthwaite, Wolf, D. H., Ruparel, K., Erus, G., Elliott, M. A., Eickhoff, S. B., Gennatas, E. D., Jackson, C., Prabhakaran, K., Smith, A., Hakonarson, H., Verma, R., Davatzikos, C., Gur, R. E., and Gur, R. C., Heterogeneous impact of motion on fundamental patterns of developmental changes in functional connectivity during youth., Neuroimage, vol. 83, pp. 45-57, 2013.
A. N. Kho, Rasmussen, L. V., Connolly, J. J., Peissig, P. L., Starren, J., Hakonarson, H., and M Hayes, G., Practical challenges in integrating genomic data into the electronic health record., Genet Med, vol. 15, no. 10, pp. 772-8, 2013.
2012
T. D. Satterthwaite, Wolf, D. H., Loughead, J., Ruparel, K., Elliott, M. A., Hakonarson, H., Gur, R. C., and Gur, R. E., Impact of in-scanner head motion on multiple measures of functional connectivity: relevance for studies of neurodevelopment in youth., Neuroimage, vol. 60, no. 1, pp. 623-32, 2012.
R. Anney, Klei, L., Pinto, D., Almeida, J., Bacchelli, E., Baird, G., Bolshakova, N., Bölte, S., Bolton, P. F., Bourgeron, T., Brennan, S., Brian, J., Casey, J., Conroy, J., Correia, C., Corsello, C., Crawford, E. L., de Jonge, M., Delorme, R., Duketis, E., Duque, F., Estes, A., Farrar, P., Fernandez, B. A., Folstein, S. E., Fombonne, E., Gilbert, J., Gillberg, C., Glessner, J. T., Green, A., Green, J., Guter, S. J., Heron, E. A., Holt, R., Howe, J. L., Hughes, G., Hus, V., Igliozzi, R., Jacob, S., Kenny, G. P., Kim, C., Kolevzon, A., Kustanovich, V., Lajonchere, C. M., Lamb, J. A., Law-Smith, M., Leboyer, M., Le Couteur, A., Leventhal, B. L., Liu, X. - Q., Lombard, F., Lord, C., Lotspeich, L., Lund, S. C., Magalhaes, T. R., Mantoulan, C., McDougle, C. J., Melhem, N. M., Merikangas, A., Minshew, N. J., Mirza, G. K., Munson, J., Noakes, C., Nygren, G., Papanikolaou, K., Pagnamenta, A. T., Parrini, B., Paton, T., Pickles, A., Posey, D. J., Poustka, F., Ragoussis, J., Regan, R., Roberts, W., Roeder, K., Rogé, B., Rutter, M. L., Schlitt, S., Shah, N., Sheffield, V. C., Soorya, L., Sousa, I., Stoppioni, V., Sykes, N., Tancredi, R., Thompson, A. P., Thomson, S., Tryfon, A., Tsiantis, J., van Engeland, H., Vincent, J. B., Volkmar, F., Vorstman, J. A. S., Wallace, S., Wing, K., Wittemeyer, K., Wood, S., Zurawiecki, D., Zwaigenbaum, L., Bailey, A. J., Battaglia, A., Cantor, R. M., Coon, H., Cuccaro, M. L., Dawson, G., Ennis, S., Freitag, C. M., Geschwind, D. H., Haines, J. L., Klauck, S. M., McMahon, W. M., Maestrini, E., Miller, J., Monaco, A. P., Nelson, S. F., Nurnberger, J. I., Oliveira, G., Parr, J. R., Pericak-Vance, M. A., Piven, J., Schellenberg, G. D., Scherer, S. W., Vicente, A. M., Wassink, T. H., Wijsman, E. M., Betancur, C., Buxbaum, J. D., Cook, E. H., Gallagher, L., Gill, M., Hallmayer, J., Paterson, A. D., Sutcliffe, J. S., Szatmari, P., Vieland, V. J., Hakonarson, H., and Devlin, B., Individual common variants exert weak effects on the risk for autism spectrum disorders., Hum Mol Genet, vol. 21, no. 21, pp. 4781-92, 2012.
J. P. Casey, Magalhaes, T., Conroy, J. M., Regan, R., Shah, N., Anney, R., Shields, D. C., Abrahams, B. S., Almeida, J., Bacchelli, E., Bailey, A. J., Baird, G., Battaglia, A., Berney, T., Bolshakova, N., Bolton, P. F., Bourgeron, T., Brennan, S., Cali, P., Correia, C., Corsello, C., Coutanche, M., Dawson, G., de Jonge, M., Delorme, R., Duketis, E., Duque, F., Estes, A., Farrar, P., Fernandez, B. A., Folstein, S. E., Foley, S., Fombonne, E., Freitag, C. M., Gilbert, J., Gillberg, C., Glessner, J. T., Green, J., Guter, S. J., Hakonarson, H., Holt, R., Hughes, G., Hus, V., Igliozzi, R., Kim, C., Klauck, S. M., Kolevzon, A., Lamb, J. A., Leboyer, M., Le Couteur, A., Leventhal, B. L., Lord, C., Lund, S. C., Maestrini, E., Mantoulan, C., Marshall, C. R., McConachie, H., McDougle, C. J., McGrath, J., McMahon, W. M., Merikangas, A., Miller, J., Minopoli, F., Mirza, G. K., Munson, J., Nelson, S. F., Nygren, G., Oliveira, G., Pagnamenta, A. T., Papanikolaou, K., Parr, J. R., Parrini, B., Pickles, A., Pinto, D., Piven, J., Posey, D. J., Poustka, A., Poustka, F., Ragoussis, J., Rogé, B., Rutter, M. L., Sequeira, A. F., Soorya, L., Sousa, I., Sykes, N., Stoppioni, V., Tancredi, R., Tauber, M., Thompson, A. P., Thomson, S., Tsiantis, J., van Engeland, H., Vincent, J. B., Volkmar, F., Vorstman, J. A. S., Wallace, S., Wang, K., Wassink, T. H., White, K., Wing, K., Wittemeyer, K., Yaspan, B. L., Zwaigenbaum, L., Betancur, C., Buxbaum, J. D., Cantor, R. M., Cook, E. H., Coon, H., Cuccaro, M. L., Geschwind, D. H., Haines, J. L., Hallmayer, J., Monaco, A. P., Nurnberger, J. I., Pericak-Vance, M. A., Schellenberg, G. D., Scherer, S. W., Sutcliffe, J. S., Szatmari, P., Vieland, V. J., Wijsman, E. M., Green, A., Gill, M., Gallagher, L., Vicente, A., and Ennis, S., A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder., Hum Genet, vol. 131, no. 4, pp. 565-79, 2012.
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2010
B. St Pourcain, Wang, K., Glessner, J. T., Golding, J., Steer, C., Ring, S. M., Skuse, D. H., Grant, S. F. A., Hakonarson, H., Smith, G. D., and Smith, G. Davey, Association between a high-risk autism locus on 5p14 and social communication spectrum phenotypes in the general population., Am J Psychiatry, vol. 167, no. 11, pp. 1364-72, 2010.
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A. L McInnes, Nakamine, A., Pilorge, M., Brandt, T., González, P. Jiménez, Fallas, M., Manghi, E. R., Edelmann, L., Glessner, J., Hakonarson, H., Betancur, C., and Buxbaum, J. D., A large-scale survey of the novel 15q24 microdeletion syndrome in autism spectrum disorders identifies an atypical deletion that narrows the critical region., Mol Autism, vol. 1, no. 1, p. 5, 2010.
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2009
J. T. Glessner, Wang, K., Cai, G., Korvatska, O., Kim, C. E., Wood, S., Zhang, H., Estes, A., Brune, C. W., Bradfield, J. P., Imielinski, M., Frackelton, E. C., Reichert, J., Crawford, E. L., Munson, J., Sleiman, P. M. A., Chiavacci, R., Annaiah, K., Thomas, K., Hou, C., Glaberson, W., Flory, J., Otieno, F., Garris, M., Soorya, L., Klei, L., Piven, J., Meyer, K. J., Anagnostou, E., Sakurai, T., Game, R. M., Rudd, D. S., Zurawiecki, D., McDougle, C. J., Davis, L. K., Miller, J., Posey, D. J., Michaels, S., Kolevzon, A., Silverman, J. M., Bernier, R., Levy, S. E., Schultz, R. T., Dawson, G., Owley, T., McMahon, W. M., Wassink, T. H., Sweeney, J. A., Nurnberger, J. I., Coon, H., Sutcliffe, J. S., Minshew, N. J., Grant, S. F. A., Bućan, M., Cook, E. H., Buxbaum, J. D., Devlin, B., Schellenberg, G. D., and Hakonarson, H., Autism genome-wide copy number variation reveals ubiquitin and neuronal genes., Nature, vol. 459, no. 7246, pp. 569-73, 2009.
K. Wang, Zhang, H., Ma, D., Bućan, M., Glessner, J. T., Abrahams, B. S., Salyakina, D., Imielinski, M., Bradfield, J. P., Sleiman, P. M. A., Kim, C. E., Hou, C., Frackelton, E., Chiavacci, R., Takahashi, N., Sakurai, T., Rappaport, E., Lajonchere, C. M., Munson, J., Estes, A., Korvatska, O., Piven, J., Sonnenblick, L. I., Retuerto, A. I. Alvarez, Herman, E. I., Dong, H., Hutman, T., Sigman, M., Ozonoff, S., Klin, A., Owley, T., Sweeney, J. A., Brune, C. W., Cantor, R. M., Bernier, R., Gilbert, J. R., Cuccaro, M. L., McMahon, W. M., Miller, J., State, M. W., Wassink, T. H., Coon, H., Levy, S. E., Schultz, R. T., Nurnberger, J. I., Haines, J. L., Sutcliffe, J. S., Cook, E. H., Minshew, N. J., Buxbaum, J. D., Dawson, G., Grant, S. F. A., Geschwind, D. H., Pericak-Vance, M. A., Schellenberg, G. D., and Hakonarson, H., Common genetic variants on 5p14.1 associate with autism spectrum disorders., Nature, vol. 459, no. 7246, pp. 528-33, 2009.
M. Bućan, Abrahams, B. S., Wang, K., Glessner, J. T., Herman, E. I., Sonnenblick, L. I., Retuerto, A. I. Alvarez, Imielinski, M., Hadley, D., Bradfield, J. P., Kim, C., Gidaya, N. B., Lindquist, I., Hutman, T., Sigman, M., Kustanovich, V., Lajonchere, C. M., Singleton, A., Kim, J., Wassink, T. H., McMahon, W. M., Owley, T., Sweeney, J. A., Coon, H., Nurnberger, J. I., Li, M., Cantor, R. M., Minshew, N. J., Sutcliffe, J. S., Cook, E. H., Dawson, G., Buxbaum, J. D., Grant, S. F. A., Schellenberg, G. D., Geschwind, D. H., and Hakonarson, H., Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes., PLoS Genet, vol. 5, no. 6, p. e1000536, 2009.