Cited In for PMID: 23241247

Year	Number of Results
2012	1
2013	3
2014	2
2015	6
2016	4
2017	6
2018	3
2019	5
2020	4
2021	4
2022	13
2023	2
2024	0

1

Support for calcium channel gene defects in autism spectrum disorders.

Lu AT, Dai X, Martinez-Agosto JA, Cantor RM. Lu AT, et al. Mol Autism. 2012 Dec 15;3(1):18. doi: 10.1186/2040-2392-3-18. Mol Autism. 2012. PMID: 23241247 Free PMC article.

2

Maternal adverse childhood experiences (ACEs) and DNA methylation of newborns in cord blood.

Collender P, Bozack AK, Veazie S, Nwanaji-Enwerem JC, Van Der Laan L, Kogut K, Riddell C, Eskenazi B, Holland N, Deardorff J, Cardenas A. Collender P, et al. Clin Epigenetics. 2023 Oct 16;15(1):162. doi: 10.1186/s13148-023-01581-y. Clin Epigenetics. 2023. PMID: 37845746 Free PMC article.

3

Alterations of presynaptic proteins in autism spectrum disorder.

Yeo XY, Lim YT, Chae WR, Park C, Park H, Jung S. Yeo XY, et al. Front Mol Neurosci. 2022 Nov 17;15:1062878. doi: 10.3389/fnmol.2022.1062878. eCollection 2022. Front Mol Neurosci. 2022. PMID: 36466804 Free PMC article. Review.

4

More than a marker: potential pathogenic functions of MAP2.

DeGiosio RA, Grubisha MJ, MacDonald ML, McKinney BC, Camacho CJ, Sweet RA. DeGiosio RA, et al. Front Mol Neurosci. 2022 Sep 16;15:974890. doi: 10.3389/fnmol.2022.974890. eCollection 2022. Front Mol Neurosci. 2022. PMID: 36187353 Free PMC article.

5

CaV1.2 channelopathic mutations evoke diverse pathophysiological mechanisms.

Bamgboye MA, Herold KG, Vieira DCO, Traficante MK, Rogers PJ, Ben-Johny M, Dick IE. Bamgboye MA, et al. J Gen Physiol. 2022 Nov 7;154(11):e202213209. doi: 10.1085/jgp.202213209. Epub 2022 Sep 27. J Gen Physiol. 2022. PMID: 36167061 Free PMC article.

6

The Ca_V1.2 G406R mutation decreases synaptic inhibition and alters L-type Ca²⁺ channel-dependent LTP at hippocampal synapses in a mouse model of Timothy Syndrome.

Sanderson JL, Freund RK, Castano AM, Benke TA, Dell'Acqua ML. Sanderson JL, et al. Neuropharmacology. 2022 Dec 1;220:109271. doi: 10.1016/j.neuropharm.2022.109271. Epub 2022 Sep 24. Neuropharmacology. 2022. PMID: 36162529 Free PMC article.

7

Investigation of CACNA1I Cav3.3 Dysfunction in Hemiplegic Migraine.

Maksemous N, Blayney CD, Sutherland HG, Smith RA, Lea RA, Tran KN, Ibrahim O, McArthur JR, Haupt LM, Cader MZ, Finol-Urdaneta RK, Adams DJ, Griffiths LR. Maksemous N, et al. Front Mol Neurosci. 2022 Jul 19;15:892820. doi: 10.3389/fnmol.2022.892820. eCollection 2022. Front Mol Neurosci. 2022. PMID: 35928792 Free PMC article.

8

The Voltage-Gated Calcium Channel EGL-19 Acts on Glia to Drive Olfactory Adaptation.

Chen D, Cheng H, Liu S, Al-Sheikh U, Fan Y, Duan D, Zou W, Zhu L, Kang L. Chen D, et al. Front Mol Neurosci. 2022 Jun 17;15:907064. doi: 10.3389/fnmol.2022.907064. eCollection 2022. Front Mol Neurosci. 2022. PMID: 35782381 Free PMC article.

9

Whole Genome Analysis of Dizygotic Twins With Autism Reveals Prevalent Transposon Insertion Within Neuronal Regulatory Elements: Potential Implications for Disease Etiology and Clinical Assessment.

Okay K, Varış PÜ, Miral S, Pavlopoulou A, Oktay Y, Karakülah G. Okay K, et al. J Autism Dev Disord. 2023 Mar;53(3):1091-1106. doi: 10.1007/s10803-022-05636-6. Epub 2022 Jun 27. J Autism Dev Disord. 2023. PMID: 35759154

10

Rare CACNA1H and RELN variants interact through mTORC1 pathway in oligogenic autism spectrum disorder.

Teles E Silva AL, Glaser T, Griesi-Oliveira K, Corrêa-Velloso J, Wang JYT, da Silva Campos G, Ulrich H, Balan A, Zarrei M, Higginbotham EJ, Scherer SW, Passos-Bueno MR, Sertié AL. Teles E Silva AL, et al. Transl Psychiatry. 2022 Jun 6;12(1):234. doi: 10.1038/s41398-022-01997-9. Transl Psychiatry. 2022. PMID: 35668055 Free PMC article.

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