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Molecular Autism

ISSN Print: 2040-2392

ISSN Online:

Website: http://www.molecularautism.com

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Evidence of reactive oxygen species-mediated damage to mitochondrial DNA in children with typical autism

Napoli Eleonora,Wong Sarah,Giulivi Cecilia

Task-related functional connectivity in autism spectrum conditions: an EEG study using wavelet transform coherence

Catarino Ana,Andrade Alexandre,Churches Owen,Wagner Adam P

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

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

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

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

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

Kalkman Hans

Failure to deactivate the default mode network indicates a possible endophenotype of autism

Spencer Michael D,Chura Lindsay R,Holt Rosemary J,Suckling John

Vldlr overexpression causes hyperactivity in rats

Iwata Keiko,Izumo Nobuo,Matsuzaki Hideo,Manabe Takayuki

Identification of rare X-linked neuroligin variants by massively parallel sequencing in males with autism spectrum disorder

Steinberg Karyn,Ramachandran Dhanya,Patel Viren C,Shetty Amol C

Comparing biobehavioral profiles across two social stress paradigms in children with and without autism spectrum disorders

Corbett Blythe A,Schupp Clayton W,Lanni Kimberly E

Self-referential and social cognition in a case of autism and agenesis of the corpus callosum

Lombardo Michael V,Chakrabarti Bhismadev,Lai Meng-Chuan

Support for calcium channel gene defects in autism spectrum disorders

Lu Ake Tzu-Hui,Dai Xiaoxian,Martinez-Agosto Julian A,Cantor Rita M

Prenatal versus postnatal sex steroid hormone effects on autistic traits in children at 18 to 24 months of age

Auyeung Bonnie,Ahluwalia Jag,Thomson Lynn,Taylor Kevin

Common genetic variants, acting additively, are a major source of risk for autism

Klei Lambertus,Sanders Stephan J,Murtha Michael T,Hus Vanessa

Intranasal oxytocin versus placebo in the treatment of adults with autism spectrum disorders: a randomized controlled trial

Anagnostou Evdokia,Soorya Latha,Chaplin William,Bartz Jennifer

Social and monetary reward processing in autism spectrum disorders

Delmonte Sonja,Balsters Joshua H,McGrath Jane,Fitzgerald Jacqueline

Brain region-specific altered expression and association of mitochondria-related genes in autism

Anitha Ayyappan,Nakamura Kazuhiko,Thanseem Ismail,Yamada Kazuo

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

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

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

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

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

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

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-Cerde？o, Paul Ashwood, David G Amaral, Judy Van de Water

The ongoing dissection of the genetic architecture of autistic spectrum disorder

Rob F Gillis, Guy A Rouleau

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

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

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

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

Review of neuroimaging in autism spectrum disorders: what have we learned and where we go from here

Evdokia Anagnostou, Margot J Taylor

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

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

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

Variation in the human cannabinoid receptor CNR1 gene modulates gaze duration for happy faces

Bhismadev Chakrabarti, Simon Baron-Cohen

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

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

Paternal age increases the risk for autism in an Iranian population sample

Roksana Sasanfar, Stephen A Haddad, Ala Tolouei, Majid Ghadami, Dongmei Yu, Susan L Santangelo

Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigrees

Hilary Coon, Michele E Villalobos, Reid J Robison, Nicola J Camp, Dale S Cannon, Kristina Allen-Brady, Judith S Miller, William M McMahon

Foetal testosterone and autistic traits in 18 to 24-month-old children

Bonnie Auyeung, Kevin Taylor, Gerald Hackett, Simon Baron-Cohen

Fragile X and autism: Intertwined at the molecular level leading to targeted treatments

Randi Hagerman, Gry Hoem, Paul Hagerman

Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication

Ozlem Bozdagi, Takeshi Sakurai, Danae Papapetrou, Xiaobin Wang, Dara L Dickstein, Nagahide Takahashi, Yuji Kajiwara, Mu Yang, Adam M Katz, Maria Scattoni, Mark J Harris, Roheeni Saxena, Jill L Silverman, Jacqueline N Crawley, Qiang Zhou, Patrick R Hof, Joseph D Buxbaum

Molecular Autism: accelerating and integrating research into neurodevelopmental conditions

Joseph D Buxbaum, Simon Baron-Cohen

Genome-wide linkage analyses of two repetitive behavior phenotypes in Utah pedigrees with autism spectrum disorders

Dale S Cannon, Judith S Miller, Reid J Robison, Michele E Villalobos, Natalie K Wahmhoff, Kristina Allen-Brady, William M McMahon, Hilary Coon

Assessing the impact of a combined analysis of four common low-risk genetic variants on autism risk

Jerome Carayol, Gerard D Schellenberg, Frederic Tores, J？rg Hager, Andreas Ziegler, Geraldine Dawson

Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry

Inês Sousa, Taane G Clark, Richard Holt, Alistair T Pagnamenta, Erik J Mulder, Ruud B Minderaa, Anthony J Bailey, Agatino Battaglia, Sabine M Klauck, Fritz Poustka, Anthony P Monaco, International Molecular Genetic Study of Autism Consortium (IMGSAC)

Elevated cortisol during play is associated with age and social engagement in children with autism

Blythe A Corbett, Clayton W Schupp, David Simon, Niles Ryan, Sally Mendoza

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

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