Similar articles for PMID: 12676915

Year	Number of Results
1996	1
1997	1
1999	2
2000	3
2001	8
2002	3
2003	2
2004	7
2005	6
2006	6
2007	3
2008	5
2009	4
2010	1
2011	2
2012	2
2014	2
2016	1
2018	1
2024	0

1

The metabotropic glutamate receptor 8 gene at 7q31: partial duplication and possible association with autism.

Serajee FJ, Zhong H, Nabi R, Huq AH. Serajee FJ, et al. J Med Genet. 2003 Apr;40(4):e42. doi: 10.1136/jmg.40.4.e42. J Med Genet. 2003. PMID: 12676915 Free PMC article. No abstract available.

2

A genetic variant that disrupts MET transcription is associated with autism.

Campbell DB, Sutcliffe JS, Ebert PJ, Militerni R, Bravaccio C, Trillo S, Elia M, Schneider C, Melmed R, Sacco R, Persico AM, Levitt P. Campbell DB, et al. Proc Natl Acad Sci U S A. 2006 Nov 7;103(45):16834-9. doi: 10.1073/pnas.0605296103. Epub 2006 Oct 19. Proc Natl Acad Sci U S A. 2006. PMID: 17053076 Free PMC article.

3

Localization of two metabotropic glutamate receptor genes, GRM3 and GRM8, to human chromosome 7q.

Scherer SW, Duvoisin RM, Kuhn R, Heng HH, Belloni E, Tsui LC. Scherer SW, et al. Genomics. 1996 Jan 15;31(2):230-3. doi: 10.1006/geno.1996.0036. Genomics. 1996. PMID: 8824806 Free article.

4

Autism and mental retardation: the genetic relationship and contribution.

el-Hazmi MA. el-Hazmi MA. East Mediterr Health J. 2001 May;7(3):536-43. East Mediterr Health J. 2001. PMID: 12690777 Free article. Review.

5

Association between the FOXP2 gene and autistic disorder in Chinese population.

Gong X, Jia M, Ruan Y, Shuang M, Liu J, Wu S, Guo Y, Yang J, Ling Y, Yang X, Zhang D. Gong X, et al. Am J Med Genet B Neuropsychiatr Genet. 2004 May 15;127B(1):113-6. doi: 10.1002/ajmg.b.20162. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15108192

6

An autosomal genomic screen for autism.

Collaborative Linkage Study of Autism. Collaborative Linkage Study of Autism. Am J Med Genet. 2001 Dec 8;105(8):609-15. Am J Med Genet. 2001. PMID: 11811142

7

No association of FOXP2 and PTPRZ1 on 7q31 with autism from the Japanese population.

Marui T, Koishi S, Funatogawa I, Yamamoto K, Matsumoto H, Hashimoto O, Nanba E, Kato C, Ishijima M, Watanabe K, Kasai K, Kato N, Sasaki T. Marui T, et al. Neurosci Res. 2005 Sep;53(1):91-4. doi: 10.1016/j.neures.2005.05.003. Neurosci Res. 2005. PMID: 15998549

8

The human metabotropic glutamate receptor 8 (GRM8) gene: a disproportionately large gene located at 7q31.3-q32.1.

Scherer SW, Soder S, Duvoisin RM, Huizenga JJ, Tsui LC. Scherer SW, et al. Genomics. 1997 Sep 1;44(2):232-6. doi: 10.1006/geno.1997.4842. Genomics. 1997. PMID: 9299241 Free article.

9

De novo partial duplication of chromosome 7p in a male with autistic disorder.

Wolpert CM, Donnelly SL, Cuccaro ML, Hedges DJ, Poole CP, Wright HH, Gilbert JR, Pericak-Vance MA. Wolpert CM, et al. Am J Med Genet. 2001 Apr 8;105(3):222-5. doi: 10.1002/ajmg.1258. Am J Med Genet. 2001. PMID: 11353439

10

Identification of the human cortactin-binding protein-2 gene from the autism candidate region at 7q31.

Cheung J, Petek E, Nakabayashi K, Tsui LC, Vincent JB, Scherer SW. Cheung J, et al. Genomics. 2001 Nov;78(1-2):7-11. doi: 10.1006/geno.2001.6651. Genomics. 2001. PMID: 11707066

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