PubMed for id: 8604

Year	Number of Results
1998	1
1999	2
2000	1
2001	1
2002	1
2003	1
2004	3
2005	2
2006	3
2007	6
2008	8
2009	7
2010	8
2011	4
2012	6
2013	2
2014	4
2015	9
2016	6
2017	3
2018	15
2019	12
2020	10
2021	10
2022	9
2023	8
2024	0

1

[Prognostic Value of SLC25A12 Expression in Patients with Acute Myeloid Leukemia Based on Integrated Analysis of Multi-dimensional Clinical Data].

Liu YC, Yin CL, Chen Q, Chen J, Ma YQ, Wang LL, Liu DH, Shi JL, Dou LP. Liu YC, et al. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2020 Apr;28(2):377-384. doi: 10.19746/j.cnki.issn.1009-2137.2020.02.004. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2020. PMID: 32319366 Chinese.

2

Association between genetic variants in SLC25A12 and risk of autism spectrum disorders: An integrated meta-analysis.

Liu J, Yang A, Zhang Q, Yang G, Yang W, Lei H, Quan J, Qu F, Wang M, Zhang Z, Yu K. Liu J, et al. Am J Med Genet B Neuropsychiatr Genet. 2015 Jun;168B(4):236-46. doi: 10.1002/ajmg.b.32304. Epub 2015 Apr 29. Am J Med Genet B Neuropsychiatr Genet. 2015. PMID: 25921325

3

Mitochondrial Aspartate/Glutamate Carrier SLC25A12 and Autism Spectrum Disorder: a Meta-Analysis.

Aoki Y, Cortese S. Aoki Y, et al. Mol Neurobiol. 2016 Apr;53(3):1579-1588. doi: 10.1007/s12035-015-9116-3. Epub 2015 Feb 10. Mol Neurobiol. 2016. PMID: 25663199 Review.

4

AGC1 Deficiency Causes Infantile Epilepsy, Abnormal Myelination, and Reduced N-Acetylaspartate.

Falk MJ, Li D, Gai X, McCormick E, Place E, Lasorsa FM, Otieno FG, Hou C, Kim CE, Abdel-Magid N, Vazquez L, Mentch FD, Chiavacci R, Liang J, Liu X, Jiang H, Giannuzzi G, Marsh ED, Yiran G, Tian L, Palmieri F, Hakonarson H. Falk MJ, et al. JIMD Rep. 2014;14:77-85. doi: 10.1007/8904_2013_287. Epub 2014 Feb 11. JIMD Rep. 2014. PMID: 24515575 Free PMC article.

5

The mitochondrial aspartate/glutamate carrier AGC1 and calcium homeostasis: physiological links and abnormalities in autism.

Napolioni V, Persico AM, Porcelli V, Palmieri L. Napolioni V, et al. Mol Neurobiol. 2011 Aug;44(1):83-92. doi: 10.1007/s12035-011-8192-2. Epub 2011 Jun 21. Mol Neurobiol. 2011. PMID: 21691713 Review.

6

A quantitative association study of SLC25A12 and restricted repetitive behavior traits in autism spectrum disorders.

Kim SJ, Silva RM, Flores CG, Jacob S, Guter S, Valcante G, Zaytoun AM, Cook EH, Badner JA. Kim SJ, et al. Mol Autism. 2011 May 24;2(1):8. doi: 10.1186/2040-2392-2-8. Mol Autism. 2011. PMID: 21609426 Free PMC article.

7

Association study of the SLC25A12 gene and autism in Han Chinese in Taiwan.

Chien WH, Wu YY, Gau SS, Huang YS, Soong WT, Chiu YN, Chen CH. Chien WH, et al. Prog Neuropsychopharmacol Biol Psychiatry. 2010 Feb 1;34(1):189-92. doi: 10.1016/j.pnpbp.2009.11.004. Epub 2009 Nov 10. Prog Neuropsychopharmacol Biol Psychiatry. 2010. PMID: 19913066

8

AGC1 deficiency associated with global cerebral hypomyelination.

Wibom R, Lasorsa FM, Töhönen V, Barbaro M, Sterky FH, Kucinski T, Naess K, Jonsson M, Pierri CL, Palmieri F, Wedell A. Wibom R, et al. N Engl J Med. 2009 Jul 30;361(5):489-95. doi: 10.1056/NEJMoa0900591. N Engl J Med. 2009. PMID: 19641205 Free article.

9

Mitochondrial aspartate/glutamate carrier SLC25A12 gene is associated with autism.

Turunen JA, Rehnström K, Kilpinen H, Kuokkanen M, Kempas E, Ylisaukko-Oja T. Turunen JA, et al. Autism Res. 2008 Jun;1(3):189-92. doi: 10.1002/aur.25. Autism Res. 2008. PMID: 19360665

10

Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1.

Palmieri L, Papaleo V, Porcelli V, Scarcia P, Gaita L, Sacco R, Hager J, Rousseau F, Curatolo P, Manzi B, Militerni R, Bravaccio C, Trillo S, Schneider C, Melmed R, Elia M, Lenti C, Saccani M, Pascucci T, Puglisi-Allegra S, Reichelt KL, Persico AM. Palmieri L, et al. Mol Psychiatry. 2010 Jan;15(1):38-52. doi: 10.1038/mp.2008.63. Epub 2008 Jul 8. Mol Psychiatry. 2010. PMID: 18607376

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