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1.
1167 Accesses
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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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2.
1020 Accesses
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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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3.
932 Accesses
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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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4.
854 Accesses
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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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5.
837 Accesses
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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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6.
737 Accesses
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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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7.
618 Accesses
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PCR and serology find no association between xenotropic murine leukemia virus-related virus (XMRV) and autism
Brent C Satterfield, Rebecca A Garcia, Fiorella Gurrieri, Charles E Schwartz Molecular Autism 2010, 1:14 (14 October 2010)
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8.
571 Accesses
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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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9.
483 Accesses
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A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism
John P Hussman, Ren-Hua Chung, Anthony J Griswold, James M Jaworski, Daria Salyakina, Deqiong Ma, Ioanna Konidari, Patrice L Whitehead, Jeffery M Vance, Eden R Martin, Michael L Cuccaro, John R Gilbert, Jonathan L Haines, Margaret A Pericak-Vance Molecular Autism 2011, 2:1 (19 January 2011)
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10.
472 Accesses
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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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11.
465 Accesses
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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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12.
417 Accesses
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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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13.
415 Accesses
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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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14.
349 Accesses
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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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15.
327 Accesses
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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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16.
326 Accesses
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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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17.
324 Accesses
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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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18.
311 Accesses
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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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19.
297 Accesses
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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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20.
290 Accesses
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Fragile X and autism: Intertwined at the molecular level leading to targeted treatments
Randi Hagerman, Gry Hoem, Paul Hagerman Molecular Autism 2010, 1:12 (21 September 2010)
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21.
280 Accesses
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Foetal testosterone and autistic traits in 18 to 24-month-old children
Bonnie Auyeung, Kevin Taylor, Gerald Hackett, Simon Baron-Cohen Molecular Autism 2010, 1:11 (12 July 2010)
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Editor’s summary
Increased prenatal exposure to testosterone is associated with autistic traits in children aged 18 to 24 months and is consistent with positive correlations previously identified in older children and adults.
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22.
276 Accesses
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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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23.
268 Accesses
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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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24.
266 Accesses
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Defining the broader, medium and narrow autism phenotype among parents using the Autism Spectrum Quotient (AQ)
Sally Wheelwright, Bonnie Auyeung, Carrie Allison, Simon Baron-Cohen Molecular Autism 2010, 1:10 (17 June 2010)
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Editor’s summary
The Autism Spectrum Quotient self-report questionnaire can be used to assess the broader, medium and narrow autism phenotypes in non-clinical samples, including first-degree relatives of individuals with autism spectrum conditions.
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25.
269 Accesses
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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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