Similar articles for PMID: 22892527

Year	Number of Results
1998	1
2004	2
2005	1
2007	4
2008	2
2009	15
2010	4
2011	20
2012	17
2013	9
2014	13
2015	2
2016	4
2017	1
2018	9
2019	6
2020	3
2021	2
2022	3
2024	0

1

Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders.

Boccuto L, Lauri M, Sarasua SM, Skinner CD, Buccella D, Dwivedi A, Orteschi D, Collins JS, Zollino M, Visconti P, Dupont B, Tiziano D, Schroer RJ, Neri G, Stevenson RE, Gurrieri F, Schwartz CE. Boccuto L, et al. Eur J Hum Genet. 2013 Mar;21(3):310-6. doi: 10.1038/ejhg.2012.175. Epub 2012 Aug 15. Eur J Hum Genet. 2013. PMID: 22892527 Free PMC article.

2

Lack of association between NLGN3, NLGN4, SHANK2 and SHANK3 gene variants and autism spectrum disorder in a Chinese population.

Liu Y, Du Y, Liu W, Yang C, Liu Y, Wang H, Gong X. Liu Y, et al. PLoS One. 2013;8(2):e56639. doi: 10.1371/journal.pone.0056639. Epub 2013 Feb 26. PLoS One. 2013. PMID: 23468870 Free PMC article.

3

A sex-specific association of common variants of neuroligin genes (NLGN3 and NLGN4X) with autism spectrum disorders in a Chinese Han cohort.

Yu J, He X, Yao D, Li Z, Li H, Zhao Z. Yu J, et al. Behav Brain Funct. 2011 May 14;7:13. doi: 10.1186/1744-9081-7-13. Behav Brain Funct. 2011. PMID: 21569590 Free PMC article.

4

A comparative study of the genetic components of three subcategories of autism spectrum disorder.

Li J, Hu S, Zhang K, Shi L, Zhang Y, Zhao T, Wang L, He X, Xia K, Liu C, Sun Z. Li J, et al. Mol Psychiatry. 2019 Nov;24(11):1720-1731. doi: 10.1038/s41380-018-0081-x. Epub 2018 Jun 6. Mol Psychiatry. 2019. PMID: 29875476

5

SHANK3 as an autism spectrum disorder-associated gene.

Uchino S, Waga C. Uchino S, et al. Brain Dev. 2013 Feb;35(2):106-10. doi: 10.1016/j.braindev.2012.05.013. Epub 2012 Jun 29. Brain Dev. 2013. PMID: 22749736 Review.

6

Further evidence that the rs1858830 C variant in the promoter region of the MET gene is associated with autistic disorder.

Jackson PB, Boccuto L, Skinner C, Collins JS, Neri G, Gurrieri F, Schwartz CE. Jackson PB, et al. Autism Res. 2009 Aug;2(4):232-6. doi: 10.1002/aur.87. Autism Res. 2009. PMID: 19681062

7

SHANK3 variant as a cause of nonsyndromal autism in an 11-year-old boy and a review of published literature.

Kanani F, Study D, Balasubramanian M. Kanani F, et al. Clin Dysmorphol. 2018 Oct;27(4):113-115. doi: 10.1097/MCD.0000000000000232. Clin Dysmorphol. 2018. PMID: 29939863 Free article. Review.

8

Association study of the CNS patterning genes and autism in Han Chinese in Taiwan.

Chien YL, Wu YY, Chiu YN, Liu SK, Tsai WC, Lin PI, Chen CH, Gau SS, Chien WH. Chien YL, et al. Prog Neuropsychopharmacol Biol Psychiatry. 2011 Aug 1;35(6):1512-7. doi: 10.1016/j.pnpbp.2011.04.010. Epub 2011 May 5. Prog Neuropsychopharmacol Biol Psychiatry. 2011. PMID: 21575668

9

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I. Muhle R, et al. Pediatrics. 2004 May;113(5):e472-86. doi: 10.1542/peds.113.5.e472. Pediatrics. 2004. PMID: 15121991 Review.

10

Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1.

Gregor A, Albrecht B, Bader I, Bijlsma EK, Ekici AB, Engels H, Hackmann K, Horn D, Hoyer J, Klapecki J, Kohlhase J, Maystadt I, Nagl S, Prott E, Tinschert S, Ullmann R, Wohlleber E, Woods G, Reis A, Rauch A, Zweier C. Gregor A, et al. BMC Med Genet. 2011 Aug 9;12:106. doi: 10.1186/1471-2350-12-106. BMC Med Genet. 2011. PMID: 21827697 Free PMC article.

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