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Research   Open Access

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)

Abstract | Provisional PDF

Commentary   Open Access

Autism in DSM-5: progress and challenges

Fred R Volkmar, Brian Reichow Molecular Autism 2013, 4:13 (15 May 2013)

Abstract | Provisional PDF | PubMed

Review   Open Access

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)

Abstract | Provisional PDF | PubMed

Editorial   Open Access

DSM-5: the debate continues

Joseph D Buxbaum, Simon Baron-Cohen Molecular Autism 2013, 4:11 (15 May 2013)

Abstract | Provisional PDF | PubMed |  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.

Letter to the Editor   Open Access

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)

Abstract | Full text | PDF | ePUB | PubMed

Short report   Open Access

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)

Abstract | Full text | PDF | ePUB | PubMed

Research   Open Access Highly Accessed

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)

Abstract | Full text | PDF | ePUB | PubMed

Review   Open Access

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)

Abstract | Full text | PDF | ePUB | PubMed

Research   Open Access

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)

Abstract | Full text | PDF | PubMed

Research   Open Access

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)

Abstract | Full text | PDF | ePUB | PubMed

Short report   Open Access

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)

Abstract | Full text | PDF | PubMed

Research   Open Access

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)

Abstract | Full text | PDF | PubMed

Short report   Open Access

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)

Abstract | Full text | PDF | PubMed

Research   Open Access

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)

Abstract | Full text | PDF | PubMed

Research   Open Access

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)

Abstract | Full text | PDF | PubMed

Short report   Open Access

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)

Abstract | Full text | PDF | PubMed

Research   Open Access Highly Accessed

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)

Abstract | Full text | PDF | PubMed | Cited on BioMed Central

Short report   Open Access

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)

Abstract | Full text | PDF | PubMed

Research   Open Access

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)

Abstract | Full text | PDF | PubMed

Research   Open Access

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)

Abstract | Full text | PDF | PubMed | F1000 Biology

Research   Open Access

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)

Abstract | Full text | PDF | PubMed

Research   Open Access

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)

Abstract | Full text | PDF | PubMed

Review   Open Access

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

Hans Kalkman Molecular Autism 2012, 3:10 (19 October 2012)

Abstract | Full text | PDF | PubMed

Research   Open Access Highly Accessed

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)

Abstract | Full text | PDF | PubMed |  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.

Research   Open Access

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)

Abstract | Full text | PDF | PubMed

Research   Open Access

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)

Abstract | Full text | PDF | PubMed

Short report   Open Access

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)

Abstract | Full text | PDF | PubMed |  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.

Research   Open Access

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)

Abstract | Full text | PDF | PubMed

Short report   Open Access

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)

Abstract | Full text | PDF | PubMed | Cited on BioMed Central

Research   Open Access

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)

Abstract | Full text | PDF | PubMed | Cited on BioMed Central

Research   Open Access Highly Accessed

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)

Abstract | Full text | PDF | PubMed |  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.

Short report   Open Access

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)

Abstract | Full text | PDF | PubMed

Research   Open Access

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)

Abstract | Full text | PDF | PubMed

Research   Open Access Highly Accessed

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)

Abstract | Full text | PDF | PubMed | Cited on BioMed Central |  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.

Research   Open Access

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)

Abstract | Full text | PDF | PubMed

Short report   Open Access

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)

Abstract | Full text | PDF | PubMed

Research   Open Access Highly Accessed

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)

Abstract | Full text | PDF | PubMed |  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.

Short report   Open Access

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)

Abstract | Full text | PDF | PubMed

Research   Open Access

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)

Abstract | Full text | PDF | PubMed | Cited on BioMed Central

Review   Open Access

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)

Abstract | Full text | PDF | PubMed | Cited on BioMed Central

Research   Open Access

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)

Abstract | Full text | PDF | PubMed | Cited on BioMed Central

Research   Open Access

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)

Abstract | Full text | PDF | PubMed |  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.

Research   Open Access

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)

Abstract | Full text | PDF | PubMed

Research   Open Access

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)

Abstract | Full text | PDF | PubMed | Cited on BioMed Central

Research   Open Access Highly Accessed

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)

Abstract | Full text | PDF | PubMed | Cited on BioMed Central

Research   Open Access

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)

Abstract | Full text | PDF | PubMed

Research   Open Access

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)

Abstract | Full text | PDF | PubMed

Review   Open Access Highly Accessed

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)

Abstract | Full text | PDF | PubMed | Cited on BioMed Central

Research   Open Access

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)

Abstract | Full text | PDF | PubMed

Research   Open Access

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)

Abstract | Full text | PDF | PubMed

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