PubMed for id: 2895

Year	Number of Results
1993	3
1998	3
1999	1
2000	2
2002	4
2003	3
2006	1
2008	1
2010	2
2011	3
2012	1
2013	4
2014	3
2015	3
2016	3
2017	1
2020	2
2021	5
2022	3
2024	1
2025	1

1

Neurodevelopmental Syndrome with Intellectual Disability, Speech Impairment, and Quadrupedia Is Associated with Glutamate Receptor Delta 2 Gene Defect.

Grigorenko AP, Protasova MS, Lisenkova AA, Reshetov DA, Andreeva TV, Garcias GL, Martino Roth MDG, Papassotiropoulos A, Rogaev EI. Grigorenko AP, et al. Cells. 2022 Jan 25;11(3):400. doi: 10.3390/cells11030400. Cells. 2022. PMID: 35159210 Free PMC article.

2

Autosomal recessive spinocerebellar ataxia 18 caused by homozygous exon 14 duplication in GRID2 and review of the literature.

Ceylan AC, Acar Arslan E, Erdem HB, Kavus H, Arslan M, Topaloğlu H. Ceylan AC, et al. Acta Neurol Belg. 2021 Dec;121(6):1457-1462. doi: 10.1007/s13760-020-01328-z. Epub 2020 Mar 13. Acta Neurol Belg. 2021. PMID: 32170608 Review.

3

Association of Gene Variations in Ionotropic Glutamate Receptor and Attention-Deficit/Hyperactivity Disorder in the Chinese Population: A Two-Stage Case-Control Study.

Zhang Q, Huang X, Chen XZ, Li SY, Yao T, Wu J. Zhang Q, et al. J Atten Disord. 2021 Aug;25(10):1362-1373. doi: 10.1177/1087054720905089. Epub 2020 Feb 17. J Atten Disord. 2021. PMID: 32065002

4

Homozygous GRID2 missense mutation predicts a shift in the D-serine binding domain of GluD2 in a case with generalized brain atrophy and unusual clinical features.

Ali Z, Zulfiqar S, Klar J, Wikström J, Ullah F, Khan A, Abdullah U, Baig S, Dahl N. Ali Z, et al. BMC Med Genet. 2017 Dec 6;18(1):144. doi: 10.1186/s12881-017-0504-6. BMC Med Genet. 2017. PMID: 29207948 Free PMC article.

5

GRID2 mutations span from congenital to mild adult-onset cerebellar ataxia.

Coutelier M, Burglen L, Mundwiller E, Abada-Bendib M, Rodriguez D, Chantot-Bastaraud S, Rougeot C, Cournelle MA, Milh M, Toutain A, Bacq D, Meyer V, Afenjar A, Deleuze JF, Brice A, Héron D, Stevanin G, Durr A. Coutelier M, et al. Neurology. 2015 Apr 28;84(17):1751-9. doi: 10.1212/WNL.0000000000001524. Epub 2015 Apr 3. Neurology. 2015. PMID: 25841024

6

GRID2 a novel gene possibly associated with mevalonate kinase deficiency.

Moura R, Tricarico PM, Campos Coelho AV, Crovella S. Moura R, et al. Rheumatol Int. 2015 Apr;35(4):657-9. doi: 10.1007/s00296-014-3115-y. Epub 2014 Aug 22. Rheumatol Int. 2015. PMID: 25146332

7

Early-onset autosomal recessive cerebellar ataxia associated with retinal dystrophy: new human hotfoot phenotype caused by homozygous GRID2 deletion.

Van Schil K, Meire F, Karlstetter M, Bauwens M, Verdin H, Coppieters F, Scheiffert E, Van Nechel C, Langmann T, Deconinck N, De Baere E. Van Schil K, et al. Genet Med. 2015 Apr;17(4):291-9. doi: 10.1038/gim.2014.95. Epub 2014 Aug 14. Genet Med. 2015. PMID: 25122145 Free article.

8

A homozygous deletion in GRID2 causes a human phenotype with cerebellar ataxia and atrophy.

Utine GE, Haliloğlu G, Salanci B, Çetinkaya A, Kiper PÖ, Alanay Y, Aktas D, Boduroğlu K, Alikaşifoğlu M. Utine GE, et al. J Child Neurol. 2013 Jul;28(7):926-32. doi: 10.1177/0883073813484967. Epub 2013 Apr 22. J Child Neurol. 2013. PMID: 23611888

9

Clinical features, functional consequences, and rescue pharmacology of missense GRID1 and GRID2 human variants.

Allen JP, Garber KB, Perszyk R, Khayat CT, Kell SA, Kaneko M, Quindipan C, Saitta S, Ladda RL, Hewson S, Inbar-Feigenberg M, Prasad C, Prasad AN, Olewiler L, Mu W, Rosenthal LS, Scala M, Striano P, Zara F, McCullock TW, Jauss RT, Lemke JR, MacLean DM, Zhu C, Yuan H, Myers SJ, Traynelis SF. Allen JP, et al. Hum Mol Genet. 2024 Feb 1;33(4):355-373. doi: 10.1093/hmg/ddad188. Hum Mol Genet. 2024. PMID: 37944084 Free PMC article.

10

Potential of GRID2 receptor gene for preventing TNF-induced neurodegeneration in autism.

Kalkan Z, Durasi İM, Sezerman U, Atasever-Arslan B. Kalkan Z, et al. Neurosci Lett. 2016 May 4;620:62-9. doi: 10.1016/j.neulet.2016.03.043. Epub 2016 Mar 25. Neurosci Lett. 2016. PMID: 27019035

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PubMed for id: 2895

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