Works matching IS 13594184 AND DT 2012 AND VI 17 AND IP 4

Results: 20

Hierarchical temporal processing deficit model of reality distortion and psychoses.

Published in:

2012

By:

Krishnan, R R;
Fivaz, M;
Kraus, M S;
Keefe, R S E

Publication type:

Correction Notice

Chromaffin cells: the peripheral brain.

Published in:

Molecular Psychiatry, 2012, v. 17, n. 4, p. 354, doi. 10.1038/mp.2011.176

By:

Bornstein, S R;
Ehrhart-Bornstein, M;
Androutsellis-Theotokis, A;
Eisenhofer, G;
Vukicevic, V;
Licinio, J;
Wong, M L;
Calissano, P;
Nisticò, G;
Preziosi, P;
Levi-Montalcini, R

Publication type:

Article

New structural brain imaging endophenotype in bipolar disorder.

Published in:

Molecular Psychiatry, 2012, v. 17, n. 4, p. 412, doi. 10.1038/mp.2011.3

By:

Matsuo, K;
Kopecek, M;
Nicoletti, M A;
Hatch, J P;
Watanabe, Y;
Nery, F G;
Zunta-Soares, G;
Soares, J C

Publication type:

Article

Little things on which happiness depends: microRNAs as novel therapeutic targets for the treatment of anxiety and depression.

Published in:

Molecular Psychiatry, 2012, v. 17, n. 4, p. 359, doi. 10.1038/mp.2011.162

By:

O'Connor, R M;
Dinan, T G;
Cryan, J F

Publication type:

Article

ADH1B is associated with alcohol dependence and alcohol consumption in populations of European and African ancestry.

Published in:

Molecular Psychiatry, 2012, v. 17, n. 4, p. 445, doi. 10.1038/mp.2011.124

By:

Bierut, L J;
Goate, A M;
Breslau, N;
Johnson, E O;
Bertelsen, S;
Fox, L;
Agrawal, A;
Bucholz, K K;
Grucza, R;
Hesselbrock, V;
Kramer, J;
Kuperman, S;
Nurnberger, J;
Porjesz, B;
Saccone, N L;
Schuckit, M;
Tischfield, J;
Wang, J C;
Foroud, T;
Rice, J P

Publication type:

Article

The dappled nature of causes of psychiatric illness: replacing the organic-functional/hardware-software dichotomy with empirically based pluralism.

Published in:

Molecular Psychiatry, 2012, v. 17, n. 4, p. 377, doi. 10.1038/mp.2011.182

By:

Kendler, K S

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

Converging evidence for central 5-HT effects in acute tryptophan depletion.

Published in:

2012

By:

Crockett, M J;
Clark, L;
Roiser, J P;
Robinson, O J;
Cools, R;
Chase, H W;
den Ouden, H;
Apergis-Schoute, A;
Campbell-Meiklejohn, D;
Seymour, B;
Sahakian, B J;
Rogers, R D;
Robbins, T W

Publication type:

Correction Notice

A review of research trends in physiological abnormalities in autism spectrum disorders: immune dysregulation, inflammation, oxidative stress, mitochondrial dysfunction and environmental toxicant exposures.

Published in:

Molecular Psychiatry, 2012, v. 17, n. 4, p. 389, doi. 10.1038/mp.2011.165

By:

Rossignol, D A;
Frye, R E

Publication type:

Article

A genome-wide association study of attempted suicide.

Published in:

Molecular Psychiatry, 2012, v. 17, n. 4, p. 433, doi. 10.1038/mp.2011.4

By:

Willour, V L;
Seifuddin, F;
Mahon, P B;
Jancic, D;
Pirooznia, M;
Steele, J;
Schweizer, B;
Goes, F S;
Mondimore, F M;
MacKinnon, D F;
Perlis, R H;
Lee, P H;
Huang, J;
Kelsoe, J R;
Shilling, P D;
Rietschel, M;
Nöthen, M;
Cichon, S;
Gurling, H;
Purcell, S

Publication type:

Article

Touch gives new life: mechanosensation modulates spinal cord adult neurogenesis.

Published in:

2012

By:

Shechter, R;
Baruch, K;
Schwartz, M;
Rolls, A

Publication type:

Correction Notice

Gestational immune activation and Tsc2 haploinsufficiency cooperate to disrupt fetal survival and may perturb social behavior in adult mice.

Published in:

2012

By:

Ehninger, D;
Sano, Y;
de Vries, P J;
Dies, K;
Franz, D;
Geschwind, D H;
Kaur, M;
Lee, Y-S;
Li, W;
Lowe, J K;
Nakagawa, J A;
Sahin, M;
Smith, K;
Whittemore, V;
Silva, A J

Publication type:

Correction Notice

Synaptic modulators Nrxn1 and Nrxn3 are disregulated in a Disc1 mouse model of schizophrenia.

Published in:

2012

By:

Brown, S M;
Clapcote, S J;
Millar, J K;
Torrance, H S;
Anderson, S M;
Walker, R;
Rampino, A;
Roder, J C;
Thomson, P A;
Porteous, D J;
Evans, K L

Publication type:

Correction Notice

No association between serotonin 5-HT1A receptors and spirituality among patients with major depressive disorders or healthy volunteers.

Published in:

2012

By:

Karlsson, H;
Hirvonen, J;
Salminen, J K;
Hietala, J

Publication type:

Correction Notice

A neuropeptide S receptor variant associated with overinterpretation of fear reactions: a potential neurogenetic basis for catastrophizing.

Published in:

2012

By:

Raczka, K A;
Gartmann, N;
Mechias, M-L;
Reif, A;
Büchel, C;
Deckert, J;
Kalisch, R

Publication type:

Correction Notice

Neurodevelopmental and neuropsychiatric behaviour defects arise from 14-3-3ζ deficiency.

Published in:

Molecular Psychiatry, 2012, v. 17, n. 4, p. 451, doi. 10.1038/mp.2011.158

By:

Cheah, P-S;
Ramshaw, H S;
Thomas, P Q;
Toyo-oka, K;
Xu, X;
Martin, S;
Coyle, P;
Guthridge, M A;
Stomski, F;
van den Buuse, M;
Wynshaw-Boris, A;
Lopez, A F;
Schwarz, Q P

Publication type:

Article

Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder.

Published in:

Molecular Psychiatry, 2012, v. 17, n. 4, p. 421, doi. 10.1038/mp.2011.8

By:

Priebe, L;
Degenhardt, F A;
Herms, S;
Haenisch, B;
Mattheisen, M;
Nieratschker, V;
Weingarten, M;
Witt, S;
Breuer, R;
Paul, T;
Alblas, M;
Moebus, S;
Lathrop, M;
Leboyer, M;
Schreiber, S;
Grigoroiu-Serbanescu, M;
Maier, W;
Propping, P;
Rietschel, M;
Nöthen, M M

Publication type:

Article

Common features between chromaffin and neural progenitor cells.

Published in:

Molecular Psychiatry, 2012, v. 17, n. 4, p. 351, doi. 10.1038/mp.2012.18

By:

Androutsellis-Theotokis, A;
Rubin de Celis, M F;
Ehrhart-Bornstein, M;
Bornstein, S R

Publication type:

Article

Dopamine D2/D3 receptor availability in genetically leptin-deficient patients after long-term leptin replacement.

Published in:

Molecular Psychiatry, 2012, v. 17, n. 4, p. 352, doi. 10.1038/mp.2011.156

By:

Ishibashi, K;
Berman, S M;
Paz-Filho, G;
Lee, B;
Robertson, C;
Mandelkern, M A;
Wong, M-L;
Licinio, J;
London, E D

Publication type:

Article

A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders.

Published in:

2012

By:

Addington, A M;
Gauthier, J;
Piton, A;
Hamdan, F F;
Raymond, A;
Gogtay, N;
Miller, R;
Tossell, J;
Bakalar, J;
Germain, G;
Gochman, P;
Long, R;
Rapoport, J L;
Rouleau, G A

Publication type:

Correction Notice

Works matching IS 13594184 AND DT 2012 AND VI 17 AND IP 4

Hierarchical temporal processing deficit model of reality distortion and psychoses.

Chromaffin cells: the peripheral brain.

New structural brain imaging endophenotype in bipolar disorder.

Little things on which happiness depends: microRNAs as novel therapeutic targets for the treatment of anxiety and depression.

ADH1B is associated with alcohol dependence and alcohol consumption in populations of European and African ancestry.

The dappled nature of causes of psychiatric illness: replacing the organic-functional/hardware-software dichotomy with empirically based pluralism.

Rare structural variation of synapse and neurotransmission genes in autism.

Converging evidence for central 5-HT effects in acute tryptophan depletion.

A review of research trends in physiological abnormalities in autism spectrum disorders: immune dysregulation, inflammation, oxidative stress, mitochondrial dysfunction and environmental toxicant exposures.

A genome-wide association study of attempted suicide.

Touch gives new life: mechanosensation modulates spinal cord adult neurogenesis.

Gestational immune activation and Tsc2 haploinsufficiency cooperate to disrupt fetal survival and may perturb social behavior in adult mice.

Synaptic modulators Nrxn1 and Nrxn3 are disregulated in a Disc1 mouse model of schizophrenia.

No association between serotonin 5-HT<sub>1A</sub> receptors and spirituality among patients with major depressive disorders or healthy volunteers.

A neuropeptide S receptor variant associated with overinterpretation of fear reactions: a potential neurogenetic basis for catastrophizing.

Neurodevelopmental and neuropsychiatric behaviour defects arise from 14-3-3ζ deficiency.

Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder.

Common features between chromaffin and neural progenitor cells.

Dopamine D<sub>2</sub>/D<sub>3</sub> receptor availability in genetically leptin-deficient patients after long-term leptin replacement.

A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders.