Ausgabe 1/2012
Inhalt (18 Artikel)
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
Joseph D Buxbaum, Catalina Betancur, Ozlem Bozdagi, Nate P Dorr, Gregory A Elder, Patrick R Hof
Evidence of novel fine-scale structural variation at autism spectrum disorder candidate loci
Dale J Hedges, Kara L Hamilton-Nelson, Stephanie J Sacharow, Laura Nations, Gary W Beecham, Zhanna M Kozhekbaeva, Brittany L Butler, Holly N Cukier, Patrice L Whitehead, Deqiong Ma, James M Jaworski, Lubov Nathanson, Joycelyn M Lee, Stephen L Hauser, Jorge R Oksenberg, Michael L Cuccaro, Jonathan L Haines, John R Gilbert, Margaret A Pericak-Vance
Variation in the autism candidate gene GABRB3 modulates tactile sensitivity in typically developing children
Teresa Tavassoli, Bonnie Auyeung, Laura C Murphy, Simon Baron-Cohen, Bhismadev Chakrabarti
Immune function genes CD99L2, JARID2 and TPO show association with autism spectrum disorder
Paula S Ramos, Satria Sajuthi, Carl D Langefeld, Stephen J Walker
High-functioning autism spectrum disorder and fragile X syndrome: report of two affected sisters
Pauline Chaste, Catalina Betancur, Marion Gérard-Blanluet, Anne Bargiacchi, Suzanne Kuzbari, Séverine Drunat, Marion Leboyer, Thomas Bourgeron, Richard Delorme
Loci nominally associated with autism from genome-wide analysis show enrichment of brain expression quantitative trait loci but not lymphoblastoid cell line expression quantitative trait loci
Lea K Davis, Eric R Gamazon, Emily Kistner-Griffin, Judith A Badner, Chunyu Liu, Edwin H Cook, James S Sutcliffe, Nancy J Cox
Identification of rare X-linked neuroligin variants by massively parallel sequencing in males with autism spectrum disorder
Karyn Meltz Steinberg, Dhanya Ramachandran, Viren C Patel, Amol C Shetty, David J Cutler, Michael E Zwick
A review of the evidence for the canonical Wnt pathway in autism spectrum disorders
Hans Otto Kalkman
Social and monetary reward processing in autism spectrum disorders
Sonja Delmonte, Joshua H Balsters, Jane McGrath, Jacqueline Fitzgerald, Sean Brennan, Andrew J Fagan, Louise Gallagher
Self-referential and social cognition in a case of autism and agenesis of the corpus callosum
Michael V Lombardo, Bhismadev Chakrabarti, Meng-Chuan Lai, Simon Baron-Cohen
Brain region-specific altered expression and association of mitochondria-related genes in autism
Ayyappan Anitha, Kazuhiko Nakamura, Ismail Thanseem, Kazuo Yamada, Yoshimi Iwayama, Tomoko Toyota, Hideo Matsuzaki, Taishi Miyachi, Satoru Yamada, Masatsugu Tsujii, Kenji J Tsuchiya, Kaori Matsumoto, Yasuhide Iwata, Katsuaki Suzuki, Hironobu Ichikawa, Toshiro Sugiyama, Takeo Yoshikawa, Norio Mori
Vldlr overexpression causes hyperactivity in rats
Keiko Iwata, Nobuo Izumo, Hideo Matsuzaki, Takayuki Manabe, Yukiko Ishibashi, Yukio Ichitani, Kazuo Yamada, Ismail Thanseem, Ayyappan Anitha, Mahesh Mundalil Vasu, Chie Shimmura, Tomoyasu Wakuda, Yosuke Kameno, Taro Takahashi, Yasuhide Iwata, Katsuaki Suzuki, Kazuhiko Nakamura, Norio Mori
Comparing biobehavioral profiles across two social stress paradigms in children with and without autism spectrum disorders
Blythe A Corbett, Clayton W Schupp, Kimberly E Lanni
Failure to deactivate the default mode network indicates a possible endophenotype of autism
Michael D Spencer, Lindsay R Chura, Rosemary J Holt, John Suckling, Andrew J Calder, Edward T Bullmore, Simon Baron-Cohen
Intranasal oxytocin versus placebo in the treatment of adults with autism spectrum disorders: a randomized controlled trial
Evdokia Anagnostou, Latha Soorya, William Chaplin, Jennifer Bartz, Danielle Halpern, Stacey Wasserman, A Ting Wang, Lauren Pepa, Nadia Tanel, Azadeh Kushki, Eric Hollander
Prenatal versus postnatal sex steroid hormone effects on autistic traits in children at 18 to 24 months of age
Bonnie Auyeung, Jag Ahluwalia, Lynn Thomson, Kevin Taylor, Gerald Hackett, Kieran J O’Donnell, Simon Baron-Cohen
Support for calcium channel gene defects in autism spectrum disorders
Ake Tzu-Hui Lu, Xiaoxian Dai, Julian A Martinez-Agosto, Rita M Cantor
Common genetic variants, acting additively, are a major source of risk for autism
Lambertus Klei, Stephan J Sanders, Michael T Murtha, Vanessa Hus, Jennifer K Lowe, A Jeremy Willsey, Daniel Moreno-De-Luca, Timothy W Yu, Eric Fombonne, Daniel Geschwind, Dorothy E Grice, David H Ledbetter, Catherine Lord, Shrikant M Mane, Christa Lese Martin, Donna M Martin, Eric M Morrow, Christopher A Walsh, Nadine M Melhem, Pauline Chaste, James S Sutcliffe, Matthew W State, Edwin H Cook Jr, Kathryn Roeder, Bernie Devlin