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
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
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
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
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
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
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
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
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
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