Replication of association between schizophrenia and ZNF804A in the Irish Case–Control Study of Schizophrenia sample von Riley, B, Thiselton, D, Maher, B S, Bigdeli, T, Wormley, B, McMichael, G O, Fanous, A H, Vladimirov, V, O'Neill, F A, Walsh, D, Kendler, K S

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Sequence variations in CREB1 cosegregate with depressive disorders in women von ZUBENKO, G. S, HUGHES, H. B, STIFFLER, J. S, BRECHBIEL, A, ZUBENKO, W. N, MAHER, B. S, MARAZITA, M. L

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Association study of SNAP25 and schizophrenia in Irish family and case-control samples von Fanous, A.H., Zhao, Z., van den Oord, E.J.C.G., Maher, B.S., Thiselton, D.L., Bergen, S.E., Wormley, B., Bigdeli, T., Amdur, R.L., O'Neill, F.A., Walsh, D., Kendler, K.S., Riley, B.P.

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Genetic Association of MMP10, MMP14, and MMP16 with Dental Caries von Reis, Steven E., Crout, Richard, Weyant, R. J., Levy, Steven M., Vieira, Alexandre Rezende, Marazita, Mary L., Willing, M. C., Slayton, R. L., Maher, B. S., Vanyukov, M. M., Cooper, Margaret E., Feingold, Eleanor, Shaffer, John R., Lewis, D. D., McNeil, Daniel W.

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Association analysis of the PIP4K2A gene on chromosome 10p12 and schizophrenia in the Irish study of high density schizophrenia families (ISHDSF) and the Irish case-control study o... von Thiselton, D.L., Maher, B.S., Webb, B.T., Bigdeli, T.B., O'Neill, F.A., Walsh, D., Kendler, K.S., Riley, B.P.

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Segregation Analysis of Mandibular Prognathism in Libya von El-Gheriani, A.A., Maher, B.S., El-Gheriani, A.S., Sciote, J.J., Abu-shahba, F.A., Al-Azemi, R., Marazita, M.L.

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A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication von Arcos-Burgos, M, Jain, M, Acosta, M T, Shively, S, Stanescu, H, Wallis, D, Domené, S, Vélez, J I, Karkera, J D, Balog, J, Berg, K, Kleta, R, Gahl, W A, Roessler, E, Long, R, Lie, J, Pineda, D, Londoño, A C, Palacio, J D, Arbelaez, A, Lopera, F, Elia, J, Hakonarson, H, Johansson, S, Knappskog, P M, Haavik, J, Ribases, M, Cormand, B, Bayes, M, Casas, M, Ramos-Quiroga, J A, Hervas, A, Maher, B S, Faraone, S V, Seitz, C, Freitag, C M, Palmason, H, Meyer, J, Romanos, M, Walitza, S, Hemminger, U, Warnke, A, Romanos, J, Renner, T, Jacob, C, Lesch, K-P, Swanson, J, Vortmeyer, A, Bailey-Wilson, J E, Castellanos, F X, Muenke, M

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Meta-analysis of genome-wide association studies of anxiety disorders von Otowa, T, Hek, K, Lee, M, Byrne, E M, Mirza, S S, Nivard, M G, Bigdeli, T, Aggen, S H, Adkins, D, Wolen, A, Fanous, A, Keller, M C, Castelao, E, Kutalik, Z, der Auwera, S V, Homuth, G, Nauck, M, Teumer, A, Milaneschi, Y, Hottenga, J-J, Direk, N, Hofman, A, Uitterlinden, A, Mulder, C L, Henders, A K, Medland, S E, Gordon, S, Heath, A C, Madden, P A F, Pergadia, M L, van der Most, P J, Nolte, I M, van Oort, F V A, Hartman, C A, Oldehinkel, A J, Preisig, M, Grabe, H J, Middeldorp, C M, Penninx, B W J H, Boomsma, D, Martin, N G, Montgomery, G, Maher, B S, van den Oord, E J, Wray, N R, Tiemeier, H, Hettema, J M

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Genetic Association of MPPED2 and ACTN2 with Dental Caries von Stanley, B.O.C., Feingold, E., Cooper, M., Vanyukov, M.M., Maher, B.S., Slayton, R.L., Willing, M.C., Reis, S.E., McNeil, D.W., Crout, R.J., Weyant, R.J., Levy, S.M., Vieira, A.R., Marazita, M.L., Shaffer, J.R.

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Idiopathic congenital central hypoventilation syndrome: Analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHO... von Weese-Mayer, Debra E., Berry-Kravis, Elizabeth M., Zhou, Lili, Maher, Brion S., Silvestri, Jean M., Curran, Mark E., Marazita, Mary L.

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GWA study data mining and independent replication identify cardiomyopathy-associated 5 ( ) as a risk gene for schizophrenia von Chen, X, Lee, G, Maher, B S, Fanous, A H, Chen, J, Zhao, Z, Guo, A, van den Oord, E, Sullivan, P F, Shi, J, Levinson, D F, Gejman, P V, Sanders, A, Duan, J, Owen, M J, Craddock, N J, O'Donovan, M C, Blackman, J, Lewis, D, Kirov, G K, Qin, W, Schwab, S, Wildenauer, D, Chowdari, K, Nimgaonkar, V, Straub, R E, Weinberger, D R, O'Neill, F A, Walsh, D, Bronstein, M, Darvasi, A, Lencz, T, Malhotra, A K, Rujescu, D, Giegling, I, Werge, T, Hansen, T, Ingason, A, Nöethen, M M, Rietschel, M, Cichon, S, Djurovic, S, Andreassen, O A, Cantor, R M, Ophoff, R, Corvin, A, Morris, D W, Gill, M, Pato, C N, Pato, M T, Macedo, A, Gurling, H M D, McQuillin, A, Pimm, J, Hultman, C, Lichtenstein, P, Sklar, P, Purcell, S M, Scolnick, E, St Clair, D, Blackwood, D H R, Kendler, K S

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Meta-Analysis of 13 Genome Scans Reveals Multiple Cleft Lip/Palate Genes with Novel Loci on 9q21 and 2q32-35 von Marazita, Mary L., Murray, Jeffrey C., Lidral, Andrew C., Arcos-Burgos, Mauricio, Cooper, Margaret E., Goldstein, Toby, Maher, Brion S., Daack-Hirsch, Sandra, Schultz, Rebecca, Mansilla, M. Adela, Field, L. Leigh, Liu, You-e, Prescott, Natalie, Malcolm, Sue, Winter, Robin, Ray, Ajit, Moreno, Lina, Valencia, Consuelo, Neiswanger, Katherine, Wyszynski, Diego F., Bailey-Wilson, Joan E., Albacha-Hejazi, Hasan, Beaty, Terri H., McIntosh, Iain, Hetmanski, Jacqueline B., Tunçbilek, Gökhan, Edwards, Matthew, Harkin, Louise, Scott, Rodney, Roddick, Laurence G.

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Liability to substance use disorders: 1. Common mechanisms and manifestations von Vanyukov, Michael M, Tarter, Ralph E, Kirisci, Levent, Kirillova, Galina P, Maher, Brion S, Clark, Duncan B

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Segregation analysis of attention deficit hyperactivity disorder von Maher, Brion S., Marazita, Mary L., Moss, Howard B., Vanyukov, Michael M.

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Genome Scan for Loci Involved in Cleft Lip With or Without Cleft Palate, in Chinese Multiplex Families von Marazita, Mary L., Field, L. Leigh, Cooper, Margaret E., Tobias, Rose, Maher, Brion S., Peanchitlertkajorn, Supakit, Liu, You-e

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Association of the serotonin transporter gene with sudden infant death syndrome: A haplotype analysis von Weese-Mayer, Debra E., Zhou, Lili, Berry-Kravis, Elizabeth M., Maher, Brion S., Silvestri, Jean M., Marazita, Mary L.

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0988 Interaction Of Race/Ethnicity And Adverse Childhood Experiences: Links To Subsequent Childhood Sleep Duration von Rojo-Wissar, D M, Sosnowski, D W, Jackson, C L, Maher, B S, Spira, A P

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Parental craniofacial morphology in cleft lip with or without cleft palate as determined by cephalometry: a meta-analysis von Weinberg, SM, Maher, BS, Marazita, ML

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Quantitative Trait Linkage Analysis of the Liability Underlying a Common Oligogenic Disease von Maher, Brion S., Vanyukov, Michael M., Cooper, Margaret E., Neiwswanger, Katherine, Marazita, Mary L.

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Liability to substance use disorders: 2. A measurement approach von Vanyukov, Michael M., Kirisci, Levent, Tarter, Ralph E., Simkevitz, Howard F., Kirillova, Galina P., Maher, Brion S., Clark, Duncan B.

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