PubMed (GeneRIF) for id: 775

Year	Number of Results
2002	1
2003	3
2004	6
2005	12
2006	5
2007	6
2008	13
2009	21
2010	29
2011	26
2012	14
2013	32
2014	25
2015	25
2016	21
2017	20
2018	21
2019	23
2020	15
2021	13
2022	17
2023	10
2024	0

1

Structural basis for human Ca_v1.2 inhibition by multiple drugs and the neurotoxin calciseptine.

Gao S, Yao X, Chen J, Huang G, Fan X, Xue L, Li Z, Wu T, Zheng Y, Huang J, Jin X, Wang Y, Wang Z, Yu Y, Liu L, Pan X, Song C, Yan N. Gao S, et al. Cell. 2023 Nov 22;186(24):5363-5374.e16. doi: 10.1016/j.cell.2023.10.007. Epub 2023 Nov 15. Cell. 2023. PMID: 37972591

2

A novel risk variant block across introns 36-45 of CACNA1C for schizophrenia: a cohort-wise replication and cerebral region-wide validation study.

Guo X, Wang S, Lin X, Wang Z, Dou Y, Cao Y, Zhang Y, Luo X, Kang L, Yu T, Wang Z, Tan Y, Gao S, Zheng H, Zhao F, Wang H, Wang K, Xie F, Chen W, Luo X. Guo X, et al. Psychiatr Genet. 2023 Oct 1;33(5):182-190. doi: 10.1097/YPG.0000000000000344. Epub 2023 Jun 16. Psychiatr Genet. 2023. PMID: 37706495

3

Effect of rs1108580 of DBH and rs1006737 of CACNA1C on Cognition and Tardive Dyskinesia in a North Indian Schizophrenia Cohort.

Punchaichira TJ, Kukshal P, Bhatia T, Deshpande SN, Thelma BK. Punchaichira TJ, et al. Mol Neurobiol. 2023 Dec;60(12):6826-6839. doi: 10.1007/s12035-023-03496-4. Epub 2023 Jul 26. Mol Neurobiol. 2023. PMID: 37493923

4

The rs216009 single-nucleotide polymorphism of the CACNA1C gene is associated with phantom tooth pain.

Morii M, Ohka S, Nishizawa D, Hasegawa J, Nakayama K, Ebata Y, Soeda M, Fukuda KI, Yoshida K, Koshika K, Ichinohe T, Ikeda K. Morii M, et al. Mol Pain. 2023 Jan-Dec;19:17448069231193383. doi: 10.1177/17448069231193383. Mol Pain. 2023. PMID: 37489644 Free PMC article.

5

EMC chaperone-Ca_V structure reveals an ion channel assembly intermediate.

Chen Z, Mondal A, Abderemane-Ali F, Jang S, Niranjan S, Montaño JL, Zaro BW, Minor DL Jr. Chen Z, et al. Nature. 2023 Jul;619(7969):410-419. doi: 10.1038/s41586-023-06175-5. Epub 2023 May 17. Nature. 2023. PMID: 37196677 Free PMC article.

6

Phenotypic Characterization of Timothy Syndrome Caused by the CACNA1C p.Gly402Ser Variant.

Delinière A, Haddad C, Herrera-Siklódy C, Hermida A, Pruvot E, Bressieux-Degueldre S, Millat G, Janin A, Hermida JS, Asatryan B, Chevalier P. Delinière A, et al. Circ Genom Precis Med. 2023 Jun;16(3):280-282. doi: 10.1161/CIRCGEN.122.004010. Epub 2023 Apr 3. Circ Genom Precis Med. 2023. PMID: 37009738 No abstract available.

7

CACNA1C-Related Channelopathies.

Herold KG, Hussey JW, Dick IE. Herold KG, et al. Handb Exp Pharmacol. 2023;279:159-181. doi: 10.1007/164_2022_624. Handb Exp Pharmacol. 2023. PMID: 36598608 Free PMC article. Review.

8

A Cross-Sectional Study of the Neuropsychiatric Phenotype of CACNA1C-Related Disorder.

Levy RJ, Timothy KW, Underwood JFG, Hall J, Bernstein JA, Pașca SP. Levy RJ, et al. Pediatr Neurol. 2023 Jan;138:101-106. doi: 10.1016/j.pediatrneurol.2022.10.013. Epub 2022 Nov 2. Pediatr Neurol. 2023. PMID: 36436328

9

Analysis of CACNA1C and KCNH2 Risk Variants on Cardiac Autonomic Function in Patients with Schizophrenia.

Refisch A, Komatsuzaki S, Ungelenk M, Schumann A, Chung HY, Schilling SS, Jantzen W, Schröder S, Nöthen MM, Mühleisen TW, Hübner CA, Bär KJ. Refisch A, et al. Genes (Basel). 2022 Nov 16;13(11):2132. doi: 10.3390/genes13112132. Genes (Basel). 2022. PMID: 36421807 Free PMC article.

10

A CACNA1C variant associated with cardiac arrhythmias provides mechanistic insights in the calmodulation of L-type Ca²⁺ channels.

Zhao J, Segura E, Marsolais M, Parent L. Zhao J, et al. J Biol Chem. 2022 Dec;298(12):102632. doi: 10.1016/j.jbc.2022.102632. Epub 2022 Oct 21. J Biol Chem. 2022. PMID: 36273583 Free PMC article.

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