Examining the Efficacy of a Family Peer Advocate Model for Black and Hispanic Caregivers of Children with Autism Spectrum Disorder von Jamison, J. M., Fourie, E., Siper, P. M., Trelles, M. P., George-Jones, Julia, Buxbaum Grice, A., Krata, J., Holl, E., Shaoul, J., Hernandez, B., Mitchell, L., McKay, M. M., Buxbaum, J. D., Kolevzon, Alexander

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Rare structural variation of synapse and neurotransmission genes in autism von Gai, X, Xie, H M, Perin, J C, Takahashi, N, Murphy, K, Wenocur, A S, D'arcy, M, O'Hara, R J, Goldmuntz, E, Grice, D E, Shaikh, T H, Hakonarson, H, Buxbaum, J D, Elia, J, White, P S

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A randomized controlled trial of intranasal oxytocin in Phelan-McDermid syndrome von Fastman, J., Foss-Feig, J., Frank, Y., Halpern, D., Harony-Nicolas, H., Layton, C., Sandin, S., Siper, P., Tang, L., Trelles, P., Zweifach, J., Buxbaum, J. D., Kolevzon, A.

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A proof-of-concept study of growth hormone in children with Phelan-McDermid syndrome von Sethuram, S, Levy, T, Foss-Feig, J, Halpern, D, Sandin, S, Siper, P M, Walker, H, Buxbaum, J D, Rapaport, R, Kolevzon, A

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Clinical trial of insulin-like growth factor-1 in Phelan-McDermid syndrome von Kolevzon, A, Breen, M S, Siper, P M, Halpern, D, Frank, Y, Rieger, H, Weismann, J, Trelles, M P, Lerman, B, Rapaport, R, Buxbaum, J D

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Latrepirdine improves cognition and arrests progression of neuropathology in an Alzheimer's mouse model von Steele, J W, Lachenmayer, M L, Ju, S, Stock, A, Liken, J, Kim, S H, Delgado, L M, Alfaro, I E, Bernales, S, Verdile, G, Bharadwaj, P, Gupta, V, Barr, R, Friss, A, Dolios, G, Wang, R, Ringe, D, Fraser, P, Westaway, D, St George-Hyslop, P H, Szabo, P, Relkin, N R, Buxbaum, J D, Glabe, C G, Protter, A A, Martins, R N, Ehrlich, M E, Petsko, G A, Yue, Z, Gandy, S

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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 von 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 de, Minderaa, R B, Mulder, E J, Morris, A P, Bailey, A J, Monaco, A P

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Association between a GABRB3 polymorphism and autism von BUXBAUM, J. D, SILVERMAN, J. M, SMITH, C. J, GREENBERG, D. A, KILIFARSKI, M, REICHERT, J, COOK, E. H, FANG, Y, SONG, C-Y, VITALE, R

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Correlation Between Elevated Levels of Amyloid β-Peptide in the Brain and Cognitive Decline von Näslund, Jan, Haroutunian, Vahram, Mohs, Richard, Davis, Kenneth L, Davies, Peter, Greengard, Paul, Buxbaum, Joseph D

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Sodium channels SCN1A, SCN2A and SCN3A in familial autism von WEISS, L. A, ESCAYG, A, KEARNEY, J. A, TRUDEAU, M, MACDONALD, B. T, MORI, M, REICHERT, J, BUXBAUM, J. D, MEISLER, M. H

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Molecular dissection of NRG1-ERBB4 signaling implicates PTPRZ1 as a potential schizophrenia susceptibility gene von Buxbaum, J D, Georgieva, L, Young, J J, Plescia, C, Kajiwara, Y, Jiang, Y, Moskvina, V, Norton, N, Peirce, T, Williams, H, Craddock, N J, Carroll, L, Corfas, G, Davis, K L, Owen, M J, Harroch, S, Sakurai, T, O'Donovan, M C

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Copy number variants analysis in a cohort of isolated and syndromic developmental delay/intellectual disability reveals novel genomic disorders, position effects and candidate dise... von Di Gregorio, E., Riberi, E., Belligni, E.F., Biamino, E., Spielmann, M., Ala, U., Calcia, A., Bagnasco, I., Carli, D., Gai, G., Giordano, M., Guala, A., Keller, R., Mandrile, G., Arduino, C., Maffè, A., Naretto, V.G., Sirchia, F., Sorasio, L., Ungari, S., Zonta, A., Zacchetti, G., Talarico, F., Pappi, P., Cavalieri, S., Giorgio, E., Mancini, C., Ferrero, M., Brussino, A., Savin, E., Gandione, M., Pelle, A., Giachino, D.F., De Marchi, M., Restagno, G., Provero, P., Cirillo Silengo, M., Grosso, E., Buxbaum, J.D., Pasini, B., De Rubeis, S., Brusco, A., Ferrero, G.B.

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Linkage analysis for autism in a subset families with obsessive-compulsive behaviors: Evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibil... von BUXBAUM, J. D, SILVERMAN, J, KEDDACHE, M, SMITH, C. J, HOLLANDER, E, RAMOZ, N, REICHERT, J. G

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Tau protein abnormalities associated with the progression of alzheimer disease type dementia von Haroutunian, V, Davies, P, Vianna, C, Buxbaum, J.D, Purohit, D.P

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SLC25A12 expression is associated with neurite outgrowth and is upregulated in the prefrontal cortex of autistic subjects von Lepagnol-Bestel, A-M, Maussion, G, Boda, B, Cardona, A, Iwayama, Y, Delezoide, A-L, Moalic, J-M, Muller, D, Dean, B, Yoshikawa, T, Gorwood, P, Buxbaum, J D, Ramoz, N, Simonneau, M

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De novo mutation in the dopamine transporter gene associates dopamine dysfunction with autism spectrum disorder von Hamilton, P J, Campbell, N G, Sharma, S, Erreger, K, Herborg Hansen, F, Saunders, C, Belovich, A N, Sahai, M A, Cook, E H, Gether, U, Mchaourab, H S, Matthies, H J G, Sutcliffe, J S, Galli, A

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No Obvious Abnormality in Mice Deficient in Receptor Protein Tyrosine Phosphatase β von Harroch, S., Palmeri, M., Rosenbluth, J., Custer, A., Okigaki, M., Shrager, P., Blum, M., Buxbaum, J. D., Schlessinger, J.

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BACE (β-secretase) modulates the processing of APLP2 in vivo von Pastorino, L, Ikin, A.F, Lamprianou, S, Vacaresse, N, Revelli, J.P, Platt, K, Paganetti, P, Mathews, P.M, Harroch, S, Buxbaum, J.D

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Calsenilin: A calcium-binding protein that interacts with the presenilins and regulates the levels of a presenilin fragment von Buxbaum, Joseph D, Choi, Eun-Kyoung, Luo, Yuxia, Lilliehook, Christina, Crowley, Annette C, Merriam, David E, Wasco, Wilma

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Protein Phosphorylation Inhibits Production of Alzheimer Amyloid β/ A4 Peptide von BUXBAUM, J. D, KOO, E. H, GREENGARD, P

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