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Genome-wide identification of transcriptional targets of RORA reveals direct regulation of multiple genes associated with autism spectrum disorder
Tewarit Sarachana, Valerie W Hu Molecular Autism 2013, 4:14 (22 May 2013)
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Autism in DSM-5: progress and challenges
Fred R Volkmar, Brian Reichow Molecular Autism 2013, 4:13 (15 May 2013)
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DSM-5 and autism spectrum disorders (ASDs): an opportunity for identifying ASD subtypes
Rebecca Grzadzinski, Marisela Huerta, Catherine Lord Molecular Autism 2013, 4:12 (15 May 2013)
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DSM-5: the debate continues
Joseph D Buxbaum, Simon Baron-Cohen Molecular Autism 2013, 4:11 (15 May 2013)
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Editor’s summary
Joseph Buxbaum and Simon Baron-Cohen comment on the debate surrounding the forthcoming edition of the Diagnostic and Statistical Manual of Mental Disorders (DSM-5) and the potential implications of the new diagnostic criteria for the autism spectrum.
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Sex-biased gene expression in the developing brain: implications for autism spectrum disorders
Mark N Ziats, Owen M Rennert Molecular Autism 2013, 4:10 (7 May 2013)
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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 Molecular Autism 2013, 4:9 (27 April 2013)
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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 Molecular Autism 2013, 4:8 (18 April 2013)
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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 Molecular Autism 2013, 4:7 (9 April 2013)
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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 Molecular Autism 2013, 4:6 (26 March 2013)
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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 Molecular Autism 2013, 4:5 (20 March 2013)
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Spatial localisation in autism: evidence for differences in early cortical visual processing
Keziah Latham, Susana TL Chung, Peter M Allen, Teresa Tavassoli, Simon Baron-Cohen Molecular Autism 2013, 4:4 (19 February 2013)
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MeCP2 modulates gene expression pathways in astrocytes
Dag H Yasui, Huichun Xu, Keith W Dunaway, Janine M LaSalle, Lee-Way Jin, Izumi Maezawa Molecular Autism 2013, 4:3 (25 January 2013)
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Evidence of reactive oxygen species-mediated damage to mitochondrial DNA in children with typical autism
Eleonora Napoli, Sarah Wong, Cecilia Giulivi Molecular Autism 2013, 4:2 (25 January 2013)
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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 Molecular Autism 2013, 4:1 (12 January 2013)
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Support for calcium channel gene defects in autism spectrum disorders
Ake Tzu-Hui Lu, Xiaoxian Dai, Julian A Martinez-Agosto, Rita M Cantor Molecular Autism 2012, 3:18 (15 December 2012)
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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 Molecular Autism 2012, 3:17 (11 December 2012)
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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 Molecular Autism 2012, 3:16 (5 December 2012)
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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 Molecular Autism 2012, 3:15 (3 December 2012)
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Self-referential and social cognition in a case of autism and agenesis of the corpus callosum
Michael V Lombardo, Bhismadev Chakrabarti, Meng-Chuan Lai, MRC AIMS Consortium, Simon Baron-Cohen Molecular Autism 2012, 3:14 (21 November 2012)
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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 Molecular Autism 2012, 3:13 (17 November 2012)
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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 Molecular Autism 2012, 3:12 (1 November 2012)
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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 Vasu, Chie Shimmura, Tomoyasu Wakuda, Yosuke Kameno, Taro Takahashi, Yasuhide Iwata, Katsuaki Suzuki, Kazuhiko Nakamura, Norio Mori Molecular Autism 2012, 3:11 (30 October 2012)
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A review of the evidence for the canonical Wnt pathway in autism spectrum disorders
Hans Kalkman Molecular Autism 2012, 3:10 (19 October 2012)
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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 Willsey, Daniel Moreno-De-Luca, Timothy W Yu, Eric Fombonne, Daniel Geschwind, Dorothy E Grice, David H Ledbetter, Catherine Lord, Shrikant M Mane, Christa Martin, Donna M Martin, Eric M Morrow, Christopher A Walsh, Nadine M Melhem, Pauline Chaste, James S Sutcliffe, Matthew W State, Edwin H Cook, Kathryn Roeder, Bernie Devlin Molecular Autism 2012, 3:9 (15 October 2012)
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Editor’s summary
Common genetic variants have a substantial additive genetic effect on autism spectrum disorder liability and this effect differs between simplex and multiplex families.
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Identification of rare X-linked neuroligin variants by massively parallel sequencing in males with autism spectrum disorder
Karyn Steinberg, Dhanya Ramachandran, Viren C Patel, Amol C Shetty, David J Cutler, Michael E Zwick Molecular Autism 2012, 3:8 (28 September 2012)
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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 Molecular Autism 2012, 3:7 (26 September 2012)
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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 Molecular Autism 2012, 3:6 (6 July 2012)
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Editor’s summary
Novel human study shows an association between GABRB3 variation and tactile sensitivity, supporting previous evidence from animal models implicating the role of GABRB3 variation in the atypical sensory sensitivity in autism spectrum conditions.
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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 Molecular Autism 2012, 3:5 (27 June 2012)
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Immune function genes CD99L2, JARID2 and TPO show association with autism spectrum disorder
Paula S Ramos, Satria Sajuthi, Carl D Langefeld, Stephen J Walker Molecular Autism 2012, 3:4 (9 June 2012)
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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 Molecular Autism 2012, 3:3 (16 May 2012)
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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 Molecular Autism 2012, 3:2 (2 April 2012)
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Editor’s summary
Support for the role of rare structural variants at multiple genomic loci in autism spectrum disorders, and in particular the significant enrichment of rare exonic deletions in NRXN1 in autistic vs. non-autistic individuals.
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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 Molecular Autism 2012, 3:1 (20 February 2012)
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Increased copy number for methylated maternal 15q duplications leads to changes in gene and protein expression in human cortical samples
Haley A Scoles, Nora Urraca, Samuel W Chadwick, Lawrence T Reiter, Janine M LaSalle Molecular Autism 2011, 2:19 (12 December 2011)
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An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in males
Ren-Hua Chung, Deqiong Ma, Kai Wang, Dale J Hedges, James M Jaworski, John R Gilbert, Michael L Cuccaro, Harry H Wright, Ruth K Abramson, Ioanna Konidari, Patrice L Whitehead, Gerard D Schellenberg, Hakon Hakonarson, Jonathan L Haines, Margaret A Pericak-Vance, Eden R Martin Molecular Autism 2011, 2:18 (4 November 2011)
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Editor’s summary
TBL1X, which is part of the Wnt signaling pathway, is identified as a candidate gene for autism spectrum disorder (ASD), in the largest chromosome-wide study of the X chromosome in association with ASD.
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Autism risk assessment in siblings of affected children using sex-specific genetic scores
Jerome Carayol, Gerard D Schellenberg, Beth Dombroski, Emmanuelle Genin, Francis Rousseau, Geraldine Dawson Molecular Autism 2011, 2:17 (21 October 2011)
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Investigation of the serum levels of anterior pituitary hormones in male children with autism
Keiko Iwata, Hideo Matsuzaki, Taishi Miyachi, Chie Shimmura, Shiro Suda, Kenji J Tsuchiya, Kaori Matsumoto, Katsuaki Suzuki, Yasuhide Iwata, Kazuhiko Nakamura, Masatsugu Tsujii, Toshirou Sugiyama, Kohji Sato, Norio Mori Molecular Autism 2011, 2:16 (19 October 2011)
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Facial phenotypes in subgroups of prepubertal boys with autism spectrum disorders are correlated with clinical phenotypes
Kristina Aldridge, Ian D George, Kimberly K Cole, Jordan R Austin, T Nicole Takahashi, Ye Duan, Judith H Miles Molecular Autism 2011, 2:15 (14 October 2011)
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Editor’s summary
A distinctive facial phenotype in boys with autism, which differs from that of typically developing boys, may reflect alterations in embryologic brain development in children with autism spectrum disorders.
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Decreased expression of axon-guidance receptors in the anterior cingulate cortex in autism
Shiro Suda, Keiko Iwata, Chie Shimmura, Yosuke Kameno, Ayyappan Anitha, Ismail Thanseem, Kazuhiko Nakamura, Hideo Matsuzaki, Kenji J Tsuchiya, Genichi Sugihara, Yasuhide Iwata, Katsuaki Suzuki, Keita Koizumi, Haruhiro Higashida, Nori Takei, Norio Mori Molecular Autism 2011, 2:14 (22 August 2011)
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Increased midgestational IFN-γ, IL-4 and IL-5 in women bearing a child with autism: A case-control study
Paula E Goines, Lisa A Croen, Daniel Braunschweig, Cathleen K Yoshida, Judith Grether, Robin Hansen, Martin Kharrazi, Paul Ashwood, Judy Van de Water Molecular Autism 2011, 2:13 (2 August 2011)
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The ongoing dissection of the genetic architecture of autistic spectrum disorder
Rob F Gillis, Guy A Rouleau Molecular Autism 2011, 2:12 (8 July 2011)
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Transient and steady-state auditory gamma-band responses in first-degree relatives of people with autism spectrum disorder
Donald C Rojas, Peter D Teale, Keeran Maharajh, Eugene Kronberg, Katie Youngpeter, Lisa B Wilson, Alissa Wallace, Susan Hepburn Molecular Autism 2011, 2:11 (5 July 2011)
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Variation in the human cannabinoid receptor CNR1 gene modulates gaze duration for happy faces
Bhismadev Chakrabarti, Simon Baron-Cohen Molecular Autism 2011, 2:10 (29 June 2011)
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Editor’s summary
Variations in the CNR1 gene are associated with how long people look at facial expression of emotion, particularly happy faces; these findings could lead to further understanding of clinical conditions marked by atypical eye contact and facial emotion processing such as autism.
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Gene expression analysis in lymphoblasts derived from patients with autism spectrum disorder
Yuka Yasuda, Ryota Hashimoto, Hidenaga Yamamori, Kazutaka Ohi, Motoyuki Fukumoto, Satomi Umeda-Yano, Ikuko Mohri, Akira Ito, Masako Taniike, Masatoshi Takeda Molecular Autism 2011, 2:9 (26 May 2011)
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A quantitative association study of SLC25A12 and restricted repetitive behavior traits in autism spectrum disorders
Soo-Jeong Kim, Raquel M Silva, Cindi G Flores, Suma Jacob, Stephen Guter, Gregory Valcante, Annette M Zaytoun, Edwin H Cook, Judith A Badner Molecular Autism 2011, 2:8 (24 May 2011)
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Histopathologic characterization of the BTBR mouse model of autistic-like behavior reveals selective changes in neurodevelopmental proteins and adult hippocampal neurogenesis
Diane T Stephenson, Sharon M O'Neill, Sapna Narayan, Aadhya Tiwari, Elizabeth Arnold, Harry D Samaroo, Fu Du, Robert H Ring, Brian Campbell, Mathew Pletcher, Vidita A Vaidya, Daniel Morton Molecular Autism 2011, 2:7 (16 May 2011)
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Dysregulation of fragile X mental retardation protein and metabotropic glutamate receptor 5 in superior frontal cortex of individuals with autism: a postmortem brain study
S Hossein Fatemi, Timothy D Folsom Molecular Autism 2011, 2:6 (6 May 2011)
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Further characterization of autoantibodies to GABAergic neurons in the central nervous system produced by a subset of children with autism
Sharifia Wills, Christy C Rossi, Jeffrey Bennett, Veronica Martinez-Cerdeño, Paul Ashwood, David G Amaral, Judy Van de Water Molecular Autism 2011, 2:5 (26 April 2011)
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Review of neuroimaging in autism spectrum disorders: what have we learned and where we go from here
Evdokia Anagnostou, Margot J Taylor Molecular Autism 2011, 2:4 (18 April 2011)
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Functionality of promoter microsatellites of arginine vasopressin receptor 1A (AVPR1A): implications for autism
Katherine E Tansey, Matthew J Hill, Lynne E Cochrane, Michael Gill, Richard JL Anney, Louise Gallagher Molecular Autism 2011, 2:3 (31 March 2011)
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Neuropathologic features in the hippocampus and cerebellum of three older men with fragile X syndrome
Claudia M Greco, Celestine S Navarro, Michael R Hunsaker, Izumi Maezawa, John F Shuler, Flora Tassone, Mary Delany, Jacky W Au, Robert F Berman, Lee-Way Jin, Cynthia Schumann, Paul J Hagerman, Randi J Hagerman Molecular Autism 2011, 2:2 (8 February 2011)
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