PubMed (GeneRIF) for id: 773

Year	Number of Results
2001	5
2002	7
2003	10
2004	17
2005	11
2006	8
2007	10
2008	26
2009	21
2010	17
2011	11
2012	9
2013	11
2014	9
2015	10
2016	10
2017	9
2018	8
2019	9
2020	7
2021	16
2022	3
2023	3
2024	0

1

Adult-onset Migraine and Very Late Onset Ataxia Due to a Novel Pathogenic Variant of the CACNA1A Gene.

Bhattacharjee S, Paramanandam V. Bhattacharjee S, et al. Neurol India. 2023 Nov-Dec;71(6):1307-1308. doi: 10.4103/0028-3886.391362. Neurol India. 2023. PMID: 38174495 Free article. No abstract available.

2

High-Throughput Sequencing Data Reveal an Antiangiogenic Role of HNF4A-Mediated CACNA1A/VEGFA Axis in Proliferative Diabetic Retinopathy.

Yin Y, Wu S, Niu L, Huang S. Yin Y, et al. Invest Ophthalmol Vis Sci. 2023 Jun 1;64(7):32. doi: 10.1167/iovs.64.7.32. Invest Ophthalmol Vis Sci. 2023. PMID: 37342032 Free PMC article.

3

CACNA1A-Related Channelopathies: Clinical Manifestations and Treatment Options.

Indelicato E, Boesch S. Indelicato E, et al. Handb Exp Pharmacol. 2023;279:227-248. doi: 10.1007/164_2022_625. Handb Exp Pharmacol. 2023. PMID: 36592223 Review.

4

Clinical and genetic characterization of CACNA1A-related disease.

Lipman AR, Fan X, Shen Y, Chung WK. Lipman AR, et al. Clin Genet. 2022 Oct;102(4):288-295. doi: 10.1111/cge.14180. Epub 2022 Jun 26. Clin Genet. 2022. PMID: 35722745 Free PMC article.

5

[Diversity of CACNA1A-related disorders].

Rudenskaya GE, Sermyagina IG, Chukhrova AL, Dadali EL, Lozier ER, Shchagina OA. Rudenskaya GE, et al. Zh Nevrol Psikhiatr Im S S Korsakova. 2021;121(12):106-111. doi: 10.17116/jnevro2021121121106. Zh Nevrol Psikhiatr Im S S Korsakova. 2021. PMID: 35041321 Russian.

6

Next-generation sequencing identified a novel CACNA1A I1379F variant in a familial hemiplegic migraine type 1 pedigree: A case report.

Luan H, Zhang L, Zhang S, Zhang M. Luan H, et al. Medicine (Baltimore). 2021 Dec 23;100(51):e28141. doi: 10.1097/MD.0000000000028141. Medicine (Baltimore). 2021. PMID: 34941060 Free PMC article.

7

The complexities of CACNA1A in clinical neurogenetics.

Hommersom MP, van Prooije TH, Pennings M, Schouten MI, van Bokhoven H, Kamsteeg EJ, van de Warrenburg BPC. Hommersom MP, et al. J Neurol. 2022 Jun;269(6):3094-3108. doi: 10.1007/s00415-021-10897-9. Epub 2021 Nov 22. J Neurol. 2022. PMID: 34806130

8

Clinical and molecular spectrum of P/Q type calcium channel Cav2.1 in epileptic patients.

Alehabib E, Esmaeilizadeh Z, Ranji-Burachaloo S, Tafakhori A, Darvish H, Movafagh A. Alehabib E, et al. Orphanet J Rare Dis. 2021 Nov 2;16(1):461. doi: 10.1186/s13023-021-02101-y. Orphanet J Rare Dis. 2021. PMID: 34727962 Free PMC article.

9

CACNA1A-p.Thr501Met mutation associated with familial hemiplegic migraine: a family report.

Romozzi M, Primiano G, Rollo E, Travaglini L, Calabresi P, Servidei S, Vollono C. Romozzi M, et al. J Headache Pain. 2021 Jul 28;22(1):85. doi: 10.1186/s10194-021-01297-5. J Headache Pain. 2021. PMID: 34320921 Free PMC article.

10

Biallelic variants in genes previously associated with dominant inheritance: CACNA1A, RET and SLC20A2.

Arteche-López A, Álvarez-Mora MI, Sánchez Calvin MT, Lezana Rosales JM, Palma Milla C, Gómez Rodríguez MJ, Gomez Manjón I, Blázquez A, Juarez Rufián A, Ramos Gómez P, Sierra Tomillo O, Hidalgo Mayoral I, Pérez de la Fuente R, Posada Rodríguez IJ, González Granado LI, Martin MA, Quesada-Espinosa JF, Moreno-García M. Arteche-López A, et al. Eur J Hum Genet. 2021 Oct;29(10):1520-1526. doi: 10.1038/s41431-021-00919-5. Epub 2021 Jul 15. Eur J Hum Genet. 2021. PMID: 34267336 Free PMC article.

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