Works matching IS 20402392 AND DT 2012 AND VI 3 AND IP 1

Results: 18

Common genetic variants, acting additively, are a major source of risk for autism.

Published in:

Molecular Autism, 2012, v. 3, n. 1, p. 1, doi. 10.1186/2040-2392-3-9

By:

Klei, Lambertus;
Sanders, Stephan J.;
Murtha, Michael T.;
Hus, Vanessa;
Lowe, Jennifer K.;
Jeremy Willsey, A.;
Moreno-De-Luca, Daniel;
Yu, Timothy W.;
Fombonne, Eric;
Geschwind, Daniel;
Grice, Dorothy E.;
Ledbetter, David H.;
Lord, Catherine;
Mane, Shrikant M.;
Martin, Christa Lese;
Martin, Donna M.;
Morrow, Eric M.;
Walsh, Christopher A.;
Melhem, Nadine M.;
Chaste, Pauline

Publication type:

Article

Support for calcium channel gene defects in autism spectrum disorders.

Published in:

Molecular Autism, 2012, v. 3, n. 1, p. 18, doi. 10.1186/2040-2392-3-18

By:

Ake Tzu-Hui Lu;
Xiaoxian Dai;
Martinez-Agosto, Julian A.;
Cantor, Rita M.

Publication type:

Article

Prenatal versus postnatal sex steroid hormone effects on autistic traits in children at 18 to 24 months of age.

Published in:

Molecular Autism, 2012, v. 3, n. 1, p. 17, doi. 10.1186/2040-2392-3-17

By:

Auyeung, Bonnie;
Ahluwalia, Jag;
Thomson, Lynn;
Taylor, Kevin;
Hackett, Gerald;
O¿Donnell, Kieran J.;
Baron-Cohen, Simon

Publication type:

Article

Intranasal oxytocin versus placebo in the treatment of adults with autism spectrum disorders: a randomized controlled trial.

Published in:

Molecular Autism, 2012, v. 3, n. 1, p. 16, doi. 10.1186/2040-2392-3-16

By:

Anagnostou, Evdokia;
Soorya, Latha;
Chaplin, William;
Bartz, Jennifer;
Halpern, Danielle;
Wasserman, Stacey;
Ting Wang, A.;
Pepa, Lauren;
Tanel, Nadia;
Kushki, Azadeh;
Hollander, Eric

Publication type:

Article

Failure to deactivate the default mode network indicates a possible endophenotype of autism.

Published in:

Molecular Autism, 2012, v. 3, n. 1, p. 15, doi. 10.1186/2040-2392-3-15

By:

Spencer, Michael D.;
Chura, Lindsay R.;
Holt, Rosemary J.;
Suckling, John;
Calder, Andrew J.;
Bullmore, Edward T.;
Baron-Cohen, Simon

Publication type:

Article

Self-referential and social cognition in a case of autism and agenesis of the corpus callosum.

Published in:

Molecular Autism, 2012, v. 3, n. 1, p. 14, doi. 10.1186/2040-2392-3-14

By:

Lombardo, Michael V.;
Chakrabarti, Bhismadev;
Meng-Chuan Lai;
Baron-Cohen, Simon

Publication type:

Article

Comparing biobehavioral profiles across two social stress paradigms in children with and without autism spectrum disorders.

Published in:

Molecular Autism, 2012, v. 3, n. 1, p. 13, doi. 10.1186/2040-2392-3-13

By:

Corbett, Blythe A.;
Schupp, Clayton W.;
Lanni, Kimberly E.

Publication type:

Article

Brain region-specific altered expression and association of mitochondria-related genes in autism.

Published in:

Molecular Autism, 2012, v. 3, n. 1, p. 12, doi. 10.1186/2040-2392-3-12

By:

Anitha, Ayyappan;
Kazuhiko Nakamura;
Thanseem, Ismail;
Kazuo Yamada;
Yoshimi Iwayama;
Tomoko Toyota;
Hideo Matsuzaki;
Taishi Miyachi;
Satoru Yamada;
Masatsugu Tsujii;
Tsuchiya, Kenji J.;
Kaori Matsumoto;
Yasuhide Iwata;
Katsuaki Suzuki;
Hironobu Ichikawa;
Toshiro Sugiyama;
Takeo Yoshikawa;
Norio Mori

Publication type:

Article

Vldlr overexpression causes hyperactivity in rats.

Published in:

Molecular Autism, 2012, v. 3, n. 1, p. 11, doi. 10.1186/2040-2392-3-11

By:

Keiko Iwata;
Nobuo Izumo;
Hideo Matsuzaki;
Takayuki Manabe;
Yukiko Ishibashi;
Yukio Ichitani;
Kazuo Yamada;
Thanseem, Ismail;
Anitha, Ayyappan;
Mundalil Vasu, Mahesh;
Chie Shimmura;
Tomoyasu Wakuda;
Yosuke Kameno;
Taro Takahashi;
Yasuhide Iwata;
Katsuaki Suzuki;
Kazuhiko Nakamura;
Norio Mori

Publication type:

Article

A review of the evidence for the canonical Wnt pathway in autism spectrum disorders.

Published in:

Molecular Autism, 2012, v. 3, n. 1, p. 10, doi. 10.1186/2040-2392-3-10

By:

Otto Kalkman, Hans

Publication type:

Article

Identification of rare X-linked neuroligin variants by massively parallel sequencing in males with autism spectrum disorder.

Published in:

Molecular Autism, 2012, v. 3, n. 1, p. 8, doi. 10.1186/2040-2392-3-8

By:

Meltz Steinberg, Karyn;
Ramachandran, Dhanya;
Patel, Viren C.;
Shetty, Amol C.;
Cutler, David J.;
Zwick, Michael E.

Publication type:

Article

Social and monetary reward processing in autism spectrum disorders.

Published in:

Molecular Autism, 2012, v. 3, n. 1, p. 7, doi. 10.1186/2040-2392-3-7

By:

Delmonte, Sonja;
Balsters, Joshua H.;
McGrath, Jane;
Fitzgerald, Jacqueline;
Brennan, Sean;
Fagan, Andrew J.;
Gallagher, Louise

Publication type:

Article

Loci nominally associated with autism from genome-wide analysis show enrichment of brain expression quantitative trait loci but not lymphoblastoid cell line expression quantitativet trait loci.

Published in:

Molecular Autism, 2012, v. 3, n. 1, p. 3, doi. 10.1186/2040-2392-3-3

By:

Davis, Lea K.;
Gamazon, Eric R.;
Kistner-Griffin, Emily;
Badner, Judith A.;
Chunyu Liu;
Cook, Edwin H.;
Sutcliffe, James S.;
Cox, Nancy J.

Publication type:

Article

High-functioning autism spectrum disorder and fragile X syndrome: report of two affected sisters.

Published in:

Molecular Autism, 2012, v. 3, n. 1, p. 5, doi. 10.1186/2040-2392-3-5

By:

Chaste, Pauline;
Betancur, Catalina;
G‚rard-Blanluet, Marion;
Bargiacchi, Bargiacchi;
Kuzbari, Suzanne;
Drunat, S‚verine;
Leboyer, Marion;
Bourgeron, Thomas;
Delorme, Delorme

Publication type:

Article

Immune function genes CD99L2, JARID2 and TPO show association with autism spectrum disorder.

Published in:

Molecular Autism, 2012, v. 3, n. 1, p. 4, doi. 10.1186/2040-2392-3-4

By:

Ramos, Paula S.;
Sajuthi, Satria;
Langefeld, Carl D.;
Walker, Stephen J.

Publication type:

Article

Variation in the autism candidate gene GABRB3 modulates tactile sensitivity in typically developing children.

Published in:

Molecular Autism, 2012, v. 3, n. 1, p. 6, doi. 10.1186/2040-2392-3-6

By:

Tavassoli, Teresa;
Auyeung, Bonnie;
Murphy, Laura C;
Baron-Cohen, Simon;
Chakrabarti, Bhismadev

Publication type:

Article

Evidence of novel fine-scale structural variation at autism spectrum disorder candidate loci.

Published in:: Molecular Autism, 2012, v. 3, n. 1, p. 2, doi. 10.1186/2040-2392-3-2
Publication type:: Article

Optimizing the phenotyping of rodent ASD models: enrichment analysis of mouse and human neurobiological phenotypes associated with high-risk autism genes identifies morphological, electrophysiological, neurological, and behavioral features.

Published in:

Molecular Autism, 2012, v. 3, n. 1, p. 1, doi. 10.1186/2040-2392-3-1

By:

Buxbaum, Joseph D.;
Betancur, Catalina;
Bozdagi, Ozlem;
Dorr, Nate P.;
Elder, Gregory A.;
Hof, Patrick R.

Publication type:

Article