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Results: 16

Related Articles by Review for PubMed (Select 21969575)

1.

Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism.

Horev G, Ellegood J, Lerch JP, Son YE, Muthuswamy L, Vogel H, Krieger AM, Buja A, Henkelman RM, Wigler M, Mills AA.

Proc Natl Acad Sci U S A. 2011 Oct 11;108(41):17076-81. doi: 10.1073/pnas.1114042108. Epub 2011 Oct 3.

2.

Animal models of psychiatric disorders that reflect human copy number variation.

Nomura J, Takumi T.

Neural Plast. 2012;2012:589524. doi: 10.1155/2012/589524. Epub 2012 Jul 30. Review.

3.

[Mouse model for human chromosome abnormality].

Takumi T.

Nihon Shinkei Seishin Yakurigaku Zasshi. 2011 Nov;31(5-6):219-22. Review. Japanese.

PMID:
22256610
4.
5.

Copy number variations in neurodevelopmental disorders.

Grayton HM, Fernandes C, Rujescu D, Collier DA.

Prog Neurobiol. 2012 Oct;99(1):81-91. doi: 10.1016/j.pneurobio.2012.07.005. Epub 2012 Jul 17. Review.

PMID:
22813947
6.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

Pediatrics. 2004 May;113(5):e472-86. Review.

PMID:
15121991
7.

[A mouse model with human chromosomal abnormality observed in autism].

Gobayashi Y, Takumi T.

Brain Nerve. 2011 Oct;63(10):1111-6. Review. Japanese.

PMID:
21987567
8.

Autistic-like symptomatology in Prader-Willi syndrome: a review of recent findings.

Dimitropoulos A, Schultz RT.

Curr Psychiatry Rep. 2007 Apr;9(2):159-64. Review.

PMID:
17389128
9.

Genetic architecture of reciprocal CNVs.

Golzio C, Katsanis N.

Curr Opin Genet Dev. 2013 Jun;23(3):240-8. doi: 10.1016/j.gde.2013.04.013. Epub 2013 Jun 5. Review.

10.

Copy number variants at Williams-Beuren syndrome 7q11.23 region.

Merla G, Brunetti-Pierri N, Micale L, Fusco C.

Hum Genet. 2010 Jul;128(1):3-26. doi: 10.1007/s00439-010-0827-2. Epub 2010 May 1. Review.

PMID:
20437059
11.

Detection and characterization of copy number variation in autism spectrum disorder.

Marshall CR, Scherer SW.

Methods Mol Biol. 2012;838:115-35. doi: 10.1007/978-1-61779-507-7_5. Review.

PMID:
22228009
12.

Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation.

Guilmatre A, Dubourg C, Mosca AL, Legallic S, Goldenberg A, Drouin-Garraud V, Layet V, Rosier A, Briault S, Bonnet-Brilhault F, Laumonnier F, Odent S, Le Vacon G, Joly-Helas G, David V, Bendavid C, Pinoit JM, Henry C, Impallomeni C, Germano E, Tortorella G, Di Rosa G, Barthelemy C, Andres C, Faivre L, Fr├ębourg T, Saugier Veber P, Campion D.

Arch Gen Psychiatry. 2009 Sep;66(9):947-56. doi: 10.1001/archgenpsychiatry.2009.80. Review.

13.

Mouse behavioral assays relevant to the symptoms of autism.

Crawley JN.

Brain Pathol. 2007 Oct;17(4):448-59. Review.

PMID:
17919130
14.

Case with autistic syndrome and chromosome 22q13.3 deletion detected by FISH.

Goizet C, Excoffier E, Taine L, Taupiac E, El Moneim AA, Arveiler B, Bouvard M, Lacombe D.

Am J Med Genet. 2000 Dec 4;96(6):839-44. Review.

PMID:
11121193
15.

New techniques to understand chromosome dosage: mouse models of aneuploidy.

Tybulewicz VL, Fisher EM.

Hum Mol Genet. 2006 Oct 15;15 Spec No 2:R103-9. Review.

16.

Diametric gene-dosage effects as windows into neurogenetic architecture.

Crespi B.

Curr Opin Neurobiol. 2013 Feb;23(1):143-51. doi: 10.1016/j.conb.2012.08.005. Epub 2012 Sep 17. Review.

PMID:
22995549
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