Similar articles for PMID: 19793310

Year	Number of Results
2000	1
2002	3
2004	3
2005	2
2006	4
2007	9
2008	14
2009	22
2010	37
2011	41
2012	31
2013	39
2014	34
2015	13
2016	7
2017	6
2019	3
2020	2
2021	1
2022	2
2024	0

1

Copy number changes of the microcephalin 1 gene (MCPH1) in patients with autism spectrum disorders.

Ozgen HM, van Daalen E, Bolton PF, Maloney VK, Huang S, Cresswell L, van den Boogaard MJ, Eleveld MJ, van 't Slot R, Hochstenbach R, Beemer FA, Barrow M, Barber JC, Poot M. Ozgen HM, et al. Clin Genet. 2009 Oct;76(4):348-56. doi: 10.1111/j.1399-0004.2009.01254.x. Clin Genet. 2009. PMID: 19793310

2

Copy number and sequence variants implicate APBA2 as an autism candidate gene.

Babatz TD, Kumar RA, Sudi J, Dobyns WB, Christian SL. Babatz TD, et al. Autism Res. 2009 Dec;2(6):359-64. doi: 10.1002/aur.107. Autism Res. 2009. PMID: 20029827

3

Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder.

Fernandez BA, Roberts W, Chung B, Weksberg R, Meyn S, Szatmari P, Joseph-George AM, Mackay S, Whitten K, Noble B, Vardy C, Crosbie V, Luscombe S, Tucker E, Turner L, Marshall CR, Scherer SW. Fernandez BA, et al. J Med Genet. 2010 Mar;47(3):195-203. doi: 10.1136/jmg.2009.069369. Epub 2009 Sep 15. J Med Genet. 2010. PMID: 19755429

4

Copy number variations associated with idiopathic autism identified by whole-genome microarray-based comparative genomic hybridization.

Cho SC, Yim SH, Yoo HK, Kim MY, Jung GY, Shin GW, Kim BN, Hwang JW, Kang JJ, Kim TM, Chung YJ. Cho SC, et al. Psychiatr Genet. 2009 Aug;19(4):177-85. doi: 10.1097/YPG.0b013e32832bdafa. Psychiatr Genet. 2009. PMID: 19407672

5

[Copy number variation analysis of a Chinese Han family with autism spectrum disorder].

Yan G, Liang Y, Wang Y, Huang W, Zou X, Zhong N. Yan G, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Dec;27(6):654-8. doi: 10.3760/cma.j.issn.1003-9406.2010.06.011. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010. PMID: 21154326 Chinese.

6

Autism spectrum disorders: molecular genetic advances.

Bacchelli E, Maestrini E. Bacchelli E, et al. Am J Med Genet C Semin Med Genet. 2006 Feb 15;142C(1):13-23. doi: 10.1002/ajmg.c.30078. Am J Med Genet C Semin Med Genet. 2006. PMID: 16419096 Review.

7

Identification and molecular characterization of two novel chromosomal deletions associated with autism.

Chien WH, Gau SS, Wu YY, Huang YS, Fang JS, Chen YJ, Soong WT, Chiu YN, Chen CH. Chien WH, et al. Clin Genet. 2010 Nov;78(5):449-56. doi: 10.1111/j.1399-0004.2010.01395.x. Clin Genet. 2010. PMID: 20236125

8

Phenotypic spectrum associated with duplication of Xp11.22-p11.23 includes Autism Spectrum Disorder.

Chung BH, Drmic I, Marshall CR, Grafodatskaya D, Carter M, Fernandez BA, Weksberg R, Roberts W, Scherer SW. Chung BH, et al. Eur J Med Genet. 2011 Sep-Oct;54(5):e516-20. doi: 10.1016/j.ejmg.2011.05.008. Epub 2011 Jun 29. Eur J Med Genet. 2011. PMID: 21689796

9

A case with a ring chromosome 13 in a cohort of 203 children with non-syndromic autism and review of the cytogenetic literature.

Charalsawadi C, Maisrikhaw W, Praphanphoj V, Wirojanan J, Hansakunachai T, Roongpraiwan R, Sombuntham T, Ruangdaraganon N, Limprasert P. Charalsawadi C, et al. Cytogenet Genome Res. 2014;144(1):1-8. doi: 10.1159/000365909. Epub 2014 Aug 23. Cytogenet Genome Res. 2014. PMID: 25171325 Review.

10

A translocation t(6;7)(p11-p12;q22) associated with autism and mental retardation: localization and identification of candidate genes at the breakpoints.

Vincent JB, Choufani S, Horike S, Stachowiak B, Li M, Dill FJ, Marshall C, Hrynchak M, Pewsey E, Ukadike KC, Friedman JM, Srivastava AK, Scherer SW. Vincent JB, et al. Psychiatr Genet. 2008 Jun;18(3):101-9. doi: 10.1097/YPG.0b013e3282f97df7. Psychiatr Genet. 2008. PMID: 18496206

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