Works matching IS 20402392 AND DT 2010 AND VI 1 AND IP 1

Results: 15

Candidate gene study of HOXB1 in autism spectrum disorder.

Published in:

Molecular Autism, 2010, v. 1, n. 1, p. 1, doi. 10.1186/2040-2392-1-9

By:

Muscarella, Lucia A.;
Guarnieri, Vito;
Sacco, Roberto;
Curatolo, Paolo;
Manzi, Barbara;
Alessandrelli, Riccardo;
Giana, Grazia;
Militerni, Roberto;
Bravaccio, Carmela;
Lenti, Carlo;
Saccani, Monica;
Schneider, Cindy;
Melmed, Raun;
D'Agruma, Leonardo;
Persico, Antonio M.

Publication type:

Article

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

Published in:

Molecular Autism, 2010, v. 1, n. 1, p. 1, doi. 10.1186/2040-2392-1-8

By:

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

Publication type:

Article

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

Published in:

Molecular Autism, 2010, v. 1, n. 1, p. 1, doi. 10.1186/2040-2392-1-7

By:

Sousa, Inês;
Clark, Taane G.;
Holt, Richard;
Pagnamenta, Alistair T.;
Mulder, Erik J.;
Minderaa, Ruud B.;
Bailey, Anthony J.;
Battaglia, Agatino;
Klauck, Sabine M.;
Poustka, Fritz;
Monaco, Anthony P.

Publication type:

Article

Genetics in psychiatry: common variant association studies.

Published in:

Molecular Autism, 2010, v. 1, n. 1, p. 1, doi. 10.1186/2040-2392-1-6

By:

Buxbaum, Joseph D.;
Baron-Cohen, Simon;
Devlin, Bernie

Publication type:

Article

A large-scale survey of the novel 15q24 microdeletion syndrome in autism spectrum disorders identifies an atypical deletion that narrows the critical region.

Published in:

Molecular Autism, 2010, v. 1, n. 1, p. 1, doi. 10.1186/2040-2392-1-5

By:

McInnes, L. Alison;
Nakamine, Alisa;
Pilorge, Marion;
Brandt, Tracy;
González, Patricia Jiménez;
Fallas, Marietha;
Manghi, Elina R.;
Edelmann, Lisa;
Glessner, Joseph;
Hakonarson, Hakon;
Betancur, Catalina;
Buxbaum, Joseph D.

Publication type:

Article

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

Published in:

Molecular Autism, 2010, v. 1, n. 1, p. 1, doi. 10.1186/2040-2392-1-4

By:

Carayol, Jerome;
Schellenberg, Gerard D.;
Tores, Frederic;
Hager, Jörg;
Ziegler, Andreas;
Dawson, Geraldine

Publication type:

Article

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

Published in:

Molecular Autism, 2010, v. 1, n. 1, p. 1, doi. 10.1186/2040-2392-1-3

By:

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

Publication type:

Article

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

Published in:

Molecular Autism, 2010, v. 1, n. 1, p. 1, doi. 10.1186/2040-2392-1-2

By:

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

Publication type:

Article

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

Published in:

Molecular Autism, 2010, v. 1, n. 1, p. 1, doi. 10.1186/2040-2392-1-15

By:

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

Publication type:

Article

PCR and serology find no association between xenotropic murine leukemia virus-related virus (XMRV) and autism.

Published in:

Molecular Autism, 2010, v. 1, n. 1, p. 1, doi. 10.1186/2040-2392-1-14

By:

Satterfield, Brent C.;
Garcia, Rebecca A.;
Gurrieri, Fiorella;
Schwartz, Charles E.

Publication type:

Article

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

Published in:

Molecular Autism, 2010, v. 1, n. 1, p. 1, doi. 10.1186/2040-2392-1-13

By:

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

Publication type:

Article

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

Published in:

Molecular Autism, 2010, v. 1, n. 1, p. 1, doi. 10.1186/2040-2392-1-12

By:

Hagerman, Randi;
Hoem, Gry;
Hagerman, Paul

Publication type:

Article

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

Published in:

Molecular Autism, 2010, v. 1, n. 1, p. 1, doi. 10.1186/2040-2392-1-11

By:

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

Publication type:

Article

Defining the broader, medium and narrow autism phenotype among parents using the Autism Spectrum Quotient (AQ).

Published in:

Molecular Autism, 2010, v. 1, n. 1, p. 1, doi. 10.1186/2040-2392-1-10

By:

Wheelwright, Sally;
Auyeung, Bonnie;
Allison, Carrie;
Baron-Cohen, Simon

Publication type:

Article

Molecular Autism: accelerating and integrating research into neurodevelopmental conditions.

Published in:

2010

By:

Buxbaum, Joseph D.;
Baron-Cohen, Simon

Publication type:

Editorial