OpenURL Connection Search

Select item for more details and to access through your institution.

A comparison of centric relation with maximum intercuspation based on quantitative electromyography.
Published in:
Journal of Oral Rehabilitation, 1982, v. 9, n. 1, p. 45, doi. 10.1111/j.1365-2842.1982.tb00533.x
By:
- Buxbaum, J. D.;
- Parente, F. J.;
- Ramsey, W. O.;
- Staling, L. M.
Publication type:
Article
Correlation between elevated levels of amyloid beta-peptide in the brain and cognitive decline.
Published in:
2000
By:
- Näslund J;
- Haroutunian V;
- Mohs R;
- Davis KL;
- Davies P;
- Greengard P;
- Buxbaum JD;
- Näslund, J;
- Haroutunian, V;
- Mohs, R;
- Davis, K L;
- Davies, P;
- Greengard, P;
- Buxbaum, J D
Publication type:
journal article
De novo mutation in the dopamine transporter gene associates dopamine dysfunction with autism spectrum disorder.
Published in:
Molecular Psychiatry, 2013, v. 18, n. 12, p. 1315, doi. 10.1038/mp.2013.102
By:
- Hamilton, P J;
- Campbell, N G;
- Sharma, S;
- Erreger, K;
- Herborg Hansen, F;
- Saunders, C;
- Belovich, A N;
- Daly, M J;
- Gibbs, R A;
- Boerwinkle, E;
- Buxbaum, J D;
- Cook, E H;
- Devlin, B;
- Lim, E T;
- Neale, B M;
- Roeder, K;
- Sabo, A;
- Schellenberg, G D;
- Stevens, C;
- Sutcliffe, J S
Publication type:
Article
Advanced paternal age is associated with altered DNA methylation at brain-expressed imprinted loci in inbred mice: implications for neuropsychiatric disease.
Published in:
Molecular Psychiatry, 2013, v. 18, n. 6, p. 635, doi. 10.1038/mp.2012.88
By:
- Smith, R G;
- Reichenberg, A;
- Kember, R L;
- Buxbaum, J D;
- Schalkwyk, L C;
- Fernandes, C;
- Mill, J
Publication type:
Article
Rare structural variation of synapse and neurotransmission genes in autism.
Published in:
Molecular Psychiatry, 2012, v. 17, n. 4, p. 402, doi. 10.1038/mp.2011.10
By:
- 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
Publication type:
Article
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.
Published in:
Molecular Psychiatry, 2010, v. 15, n. 9, p. 954, doi. 10.1038/mp.2009.34
By:
- 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.
Publication type:
Article
SLC25A12 expression is associated with neurite outgrowth and is upregulated in the prefrontal cortex of autistic subjects.
Published in:
Molecular Psychiatry, 2008, v. 13, n. 4, p. 385, doi. 10.1038/sj.mp.4002120
By:
- 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.
Publication type:
Article
Molecular dissection of NRG1-ERBB4 signaling implicates PTPRZ1 as a potential schizophrenia susceptibility gene.
Published in:
Molecular Psychiatry, 2008, v. 13, n. 2, p. 162, doi. 10.1038/sj.mp.4001991
By:
- 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.
Publication type:
Article
Clinical trial of insulin-like growth factor-1 in Phelan-McDermid syndrome.
Published in:
Molecular Autism, 2022, v. 13, n. 1, p. 1, doi. 10.1186/s13229-022-00493-7
By:
- 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.
Publication type:
Article
A proof-of-concept study of growth hormone in children with Phelan–McDermid syndrome.
Published in:
Molecular Autism, 2022, v. 13, n. 1, p. 1, doi. 10.1186/s13229-022-00485-7
By:
- Sethuram, S.;
- Levy, T.;
- Foss-Feig, J.;
- Halpern, D.;
- Sandin, S.;
- Siper, P. M.;
- Walker, H.;
- Buxbaum, J. D.;
- Rapaport, R.;
- Kolevzon, A.
Publication type:
Article
A randomized controlled trial of intranasal oxytocin in Phelan-McDermid syndrome.
Published in:
Molecular Autism, 2021, v. 12, n. 1, p. 1, doi. 10.1186/s13229-021-00459-1
By:
- 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.
Publication type:
Article
Sodium channels SCN1A, SCN2A and SCN3A in familial autism.
Published in:
Molecular Psychiatry, 2003, v. 8, n. 2, p. 186, doi. 10.1038/sj.mp.4001241
By:
- Weiss, L A;
- Escayg, A;
- Kearney, J A;
- Trudeau, M;
- MacDonald, B T;
- Mori, M;
- Reichert, J;
- Buxbaum, J D;
- Meisler, M H
Publication type:
Article
Increased Secretion of the Amino-Terminal Fragment of Amyloid Precursor Protein in Brains of Rats with a Constitutive Up-Regulation of Protein Kinase C.
Published in:
Journal of Neurochemistry, 1997, v. 68, n. 6, p. 2523, doi. 10.1046/j.1471-4159.1997.68062523.x
By:
- Caputi, A.;
- Barindelli, S.;
- Pastorino, L.;
- Cimino, M.;
- Buxbaum, J. D.;
- Cattabeni, F.;
- Di Luca, M.
Publication type:
Article

Found: 13