Ausgabe 1/2013
Inhalt (51 Artikel)
Task-related functional connectivity in autism spectrum conditions: an EEG study using wavelet transform coherence
Ana Catarino, Alexandre Andrade, Owen Churches, Adam P Wagner, Simon Baron-Cohen, Howard Ring
MeCP2 modulates gene expression pathways in astrocytes
Dag H Yasui, Huichun Xu, Keith W Dunaway, Janine M LaSalle, Lee-Way Jin, Izumi Maezawa
Evidence of reactive oxygen species-mediated damage to mitochondrial DNA in children with typical autism
Eleonora Napoli, Sarah Wong, Cecilia Giulivi
Spatial localisation in autism: evidence for differences in early cortical visual processing
Keziah Latham, Susana L Chung, Peter M Allen, Teresa Tavassoli, Simon Baron-Cohen
Lack of association of rare functional variants in TSC1/TSC2 genes with autism spectrum disorder
Samira Bahl, Colby Chiang, Roberta L Beauchamp, Benjamin M Neale, Mark J Daly, James F Gusella, Michael E Talkowski, Vijaya Ramesh
Enzymes in the glutamate-glutamine cycle in the anterior cingulate cortex in postmortem brain of subjects with autism
Chie Shimmura, Katsuaki Suzuki, Yasuhide Iwata, Kenji J Tsuchiya, Koji Ohno, Hideo Matsuzaki, Keiko Iwata, Yosuke Kameno, Taro Takahashi, Tomoyasu Wakuda, Kazuhiko Nakamura, Kenji Hashimoto, Norio Mori
Whole-genome sequencing in an autism multiplex family
Lingling Shi, Xu Zhang, Ryan Golhar, Frederick G Otieno, Mingze He, Cuiping Hou, Cecilia Kim, Brendan Keating, Gholson J Lyon, Kai Wang, Hakon Hakonarson
Prevalence of autism in mainland China, Hong Kong and Taiwan: a systematic review and meta-analysis
Xiang Sun, Carrie Allison, Fiona E Matthews, Stephen J Sharp, Bonnie Auyeung, Simon Baron-Cohen, Carol Brayne
Insulin-like growth factor-1 rescues synaptic and motor deficits in a mouse model of autism and developmental delay
Ozlem Bozdagi, Teresa Tavassoli, Joseph D Buxbaum
Sex-biased gene expression in the developing brain: implications for autism spectrum disorders
Mark N Ziats, Owen M Rennert
Genome-wide identification of transcriptional targets of RORA reveals direct regulation of multiple genes associated with autism spectrum disorder
Tewarit Sarachana, Valerie W Hu
DSM-5 and autism spectrum disorders (ASDs): an opportunity for identifying ASD subtypes
Rebecca Grzadzinski, Marisela Huerta, Catherine Lord
Is metabotropic glutamate receptor 5 upregulated in prefrontal cortex in fragile X syndrome?
Talakad G Lohith, Emily K Osterweil, Masahiro Fujita, Kimberly J Jenko, Mark F Bear, Robert B Innis
Decreased tryptophan metabolism in patients with autism spectrum disorders
Luigi Boccuto, Chin-Fu Chen, Ayla R Pittman, Cindy D Skinner, Heather J McCartney, Kelly Jones, Barry R Bochner, Roger E Stevenson, Charles E Schwartz
SHANK3 haploinsufficiency: a “common” but underdiagnosed highly penetrant monogenic cause of autism spectrum disorders
Catalina Betancur, Joseph D Buxbaum
Serum levels of soluble platelet endothelial cell adhesion molecule-1 and vascular cell adhesion molecule-1 are decreased in subjects with autism spectrum disorder
Yosuke Kameno, Keiko Iwata, Hideo Matsuzaki, Taishi Miyachi, Kenji J Tsuchiya, Kaori Matsumoto, Yasuhide Iwata, Katsuaki Suzuki, Kazuhiko Nakamura, Masato Maekawa, Masatsugu Tsujii, Toshirou Sugiyama, Norio Mori
Episodic memory retrieval for story characters in high-functioning autism
Hidetsugu Komeda, Hirotaka Kosaka, Daisuke N Saito, Keisuke Inohara, Toshio Munesue, Makoto Ishitobi, Makoto Sato, Hidehiko Okazawa
Impairment of fragile X mental retardation protein-metabotropic glutamate receptor 5 signaling and its downstream cognates ras-related C3 botulinum toxin substrate 1, amyloid beta A4 precursor protein, striatal-enriched protein tyrosine phosphatase, and homer 1, in autism: a postmortem study in cerebellar vermis and superior frontal cortex
SHossein Fatemi, Timothy D Folsom, Rachel E Kneeland, Mahtab K Yousefi, Stephanie B Liesch, Paul D Thuras
Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency
Latha Soorya, Alexander Kolevzon, Jessica Zweifach, Teresa Lim, Yuriy Dobry, Lily Schwartz, Yitzchak Frank, A Ting Wang, Guiqing Cai, Elena Parkhomenko, Danielle Halpern, David Grodberg, Benjamin Angarita, Judith P Willner, Amy Yang, Roberto Canitano, William Chaplin, Catalina Betancur, Joseph D Buxbaum
Non-synonymous single-nucleotide variations of the human oxytocin receptor gene and autism spectrum disorders: a case–control study in a Japanese population and functional analysis
Wen-Jie Ma, Minako Hashii, Toshio Munesue, Kenshi Hayashi, Kunimasa Yagi, Masakazu Yamagishi, Haruhiro Higashida, Shigeru Yokoyama
Increased gene expression of FOXP1 in patients with autism spectrum disorders
Wei-Hsien Chien, SusanShur-Fen Gau, Chun-Houh Chen, Wen-Che Tsai, Yu-Yu Wu, Po-Hsu Chen, Chi-Yung Shang, Chia-Hsiang Chen
Comparison of white matter integrity between autism spectrum disorder subjects and typically developing individuals: a meta-analysis of diffusion tensor imaging tractography studies
Yuta Aoki, Osamu Abe, Yasumasa Nippashi, Hidenori Yamasue
Do girls with anorexia nervosa have elevated autistic traits?
Simon Baron-Cohen, Tony Jaffa, Sarah Davies, Bonnie Auyeung, Carrie Allison, Sally Wheelwright
Identification of an age-dependent biomarker signature in children and adolescents with autism spectrum disorders
Jordan M Ramsey, Paul C Guest, Jantine AC Broek, Jeffrey C Glennon, Nanda Rommelse, Barbara Franke, Hassan Rahmoune, Jan K Buitelaar, Sabine Bahn
A potentiated startle study of uncertainty and contextual anxiety in adolescents diagnosed with autism spectrum disorder
Paul D Chamberlain, Jacqui Rodgers, Michael J Crowley, Sarah E White, Mark H Freeston, Mikle South
Presence of autism, hyperserotonemia, and severe expressive language impairment in Williams-Beuren syndrome
Sylvie Tordjman, George M Anderson, David Cohen, Solenn Kermarrec, Michèle Carlier, Yvan Touitou, Pascale Saugier-Veber, Céline Lagneaux, Claire Chevreuil, Alain Verloes
Test-retest reliability of the ‘Reading the Mind in the Eyes’ test: a one-year follow-up study
Enrique G Fernández-Abascal, Rosario Cabello, Pablo Fernández-Berrocal, Simon Baron-Cohen
Evidence for differential alternative splicing in blood of young boys with autism spectrum disorders
Boryana S Stamova, Yingfang Tian, Christine W Nordahl, Mark D Shen, Sally Rogers, David G Amaral, Frank R Sharp
Genetic background modulates phenotypes of serotonin transporter Ala56 knock-in mice
Travis M Kerr, Christopher L Muller, Mahfuzur Miah, Christopher S Jetter, Rita Pfeiffer, Charisma Shah, Nicole Baganz, George M Anderson, Jacqueline N Crawley, James S Sutcliffe, Randy D Blakely, Jeremy Veenstra-VanderWeele
SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs)
Brett S Abrahams, Dan E Arking, Daniel B Campbell, Heather C Mefford, Eric M Morrow, Lauren A Weiss, Idan Menashe, Tim Wadkins, Sharmila Banerjee-Basu, Alan Packer
Expression of non-protein-coding antisense RNAs in genomic regions related to autism spectrum disorders
Dmitry Velmeshev, Marco Magistri, Mohammad Ali Faghihi
A review of the serotonin transporter and prenatal cortisol in the development of autism spectrum disorders
Roselyn Rose’Meyer
Common variation contributes to the genetic architecture of social communication traits
Beate St Pourcain, AndrewJ O Whitehouse, Wei Q Ang, Nicole M Warrington, Joseph T Glessner, Kai Wang, Nicholas J Timpson, David M Evans, John P Kemp, Susan M Ring, Wendy L McArdle, Jean Golding, Hakon Hakonarson, Craig E Pennell, George Davey Smith
Atypical brain lateralisation in the auditory cortex and language performance in 3- to 7-year-old children with high-functioning autism spectrum disorder: a child-customised magnetoencephalography (MEG) study
Yuko Yoshimura, Mitsuru Kikuchi, Kiyomi Shitamichi, Sanae Ueno, Toshio Munesue, Yasuki Ono, Tsunehisa Tsubokawa, Yasuhiro Haruta, Manabu Oi, Yo Niida, Gerard B Remijn, Tsutomu Takahashi, Michio Suzuki, Haruhiro Higashida, Yoshio Minabe
Differential recruitment of coregulators to the RORA promoter adds another layer of complexity to gene (dys) regulation by sex hormones in autism
Tewarit Sarachana, Valerie W Hu
Rare coding variants of the adenosine A3 receptor are increased in autism: on the trail of the serotonin transporter regulome
Nicholas G Campbell, Chong-Bin Zhu, Kathryn M Lindler, Brian L Yaspan, Emily Kistner-Griffin, William A Hewlett, Christopher G Tate, Randy D Blakely, James S Sutcliffe
Deep exon resequencing of DLGAP2 as a candidate gene of autism spectrum disorders
Wei-Hsien Chien, SusanShur-Fen Gau, Hsiao-Mei Liao, Yen-Nan Chiu, Yu-Yu Wu, Yu-Shu Huang, Wen-Che Tsai, Ho-Min Tsai, Chia-Hsiang Chen
Increased abundance of Sutterella spp. and Ruminococcus torques in feces of children with autism spectrum disorder
Lv Wang, Claus T Christophersen, Michael J Sorich, Jacobus P Gerber, Manya T Angley, Michael A Conlon
Platelets of mice heterozygous for neurobeachin, a candidate gene for autism spectrum disorder, display protein changes related to aberrant protein kinase A activity
Kim Nuytens, Krizia Tuand, Michela Di Michele, Kurt Boonen, Etienne Waelkens, Kathleen Freson, John WM Creemers
Is synaesthesia more common in autism?
Simon Baron-Cohen, Donielle Johnson, Julian Asher, Sally Wheelwright, Simon E Fisher, Peter K Gregersen, Carrie Allison
Transcriptomic analysis of genetically defined autism candidate genes reveals common mechanisms of action
Thomas A Lanz, Edward Guilmette, Mark M Gosink, James E Fischer, Lawrence W Fitzgerald, Diane T Stephenson, Mathew T Pletcher
Exploring autistic traits in anorexia: a clinical study
Kate Tchanturia, Emma Smith, Felicitas Weineck, Eliz Fidanboylu, Nikola Kern, Janet Treasure, Simon Baron Cohen
Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk?
Claire Amiet, Isabelle Gourfinkel-An, Claudine Laurent, Nicolas Bodeau, Bérengère Génin, Eric Leguern, Sylvie Tordjman, David Cohen
Transcriptome profiling in engrailed-2 mutant mice reveals common molecular pathways associated with autism spectrum disorders
Paola Sgadò, Giovanni Provenzano, Erik Dassi, Valentina Adami, Giulia Zunino, Sacha Genovesi, Simona Casarosa, Yuri Bozzi
Capping four years of growth of Molecular Autism: impact factor coming in 2014
Joseph D Buxbaum, Simon Baron-Cohen
RAADS-14 Screen: validity of a screening tool for autism spectrum disorder in an adult psychiatric population
Jonna M Eriksson, Lisa MJ Andersen, Susanne Bejerot
Genetic variation in GABRB3 is associated with Asperger syndrome and multiple endophenotypes relevant to autism
Varun Warrier, Simon Baron-Cohen, Bhismadev Chakrabarti
Decitabine alters the expression of Mecp2 isoforms via dynamic DNA methylation at the Mecp2 regulatory elements in neural stem cells
Vichithra RB Liyanage, Robby M Zachariah, Mojgan Rastegar
Phosphorylated fragile X mental retardation protein at serine 499, is reduced in cerebellar vermis and superior frontal cortex of subjects with autism: implications for fragile X mental retardation protein-metabotropic glutamate receptor 5 signaling
Øyvind G Rustan, Timothy D Folsom, Mahtab K Yousefi, S Hossein Fatemi