PubMed (RefSeq) for id: 2462575921

Year	Number of Results
1993	3
1995	1
1996	1
1997	1
1999	1
2001	1
2004	4
2005	6
2006	7
2007	14
2008	14
2009	9
2010	16
2011	13
2012	16
2013	18
2014	7
2015	8
2016	14
2017	7
2018	13
2019	10
2020	16
2021	10
2022	6
2023	12
2024	4

1

Identification and In-Silico study of non-synonymous functional SNPs in the human SCN9A gene.

Waheed S, Ramzan K, Ahmad S, Khan MS, Wajid M, Ullah H, Umar A, Iqbal R, Ullah R, Bari A. Waheed S, et al. PLoS One. 2024 Feb 23;19(2):e0297367. doi: 10.1371/journal.pone.0297367. eCollection 2024. PLoS One. 2024. PMID: 38394191 Free PMC article.

2

COMT and SCN9A gene variants do not contribute to chronic low back pain in Mexican-Mestizo patients.

Nava-Bringas TI, Manrique CMJ, González-Huerta NC, Morales-Hernández E, Miranda-Duarte A. Nava-Bringas TI, et al. Acta Neurochir (Wien). 2024 Feb 8;166(1):73. doi: 10.1007/s00701-024-05937-y. Acta Neurochir (Wien). 2024. PMID: 38329587

3

Structural basis for severe pain caused by mutations in the voltage sensors of sodium channel NaV1.7.

Wisedchaisri G, Gamal El-Din TM, Powell NM, Zheng N, Catterall WA. Wisedchaisri G, et al. J Gen Physiol. 2023 Dec 4;155(12):e202313450. doi: 10.1085/jgp.202313450. Epub 2023 Oct 30. J Gen Physiol. 2023. PMID: 37903281 Free PMC article.

4

Erythromelalgia caused by the missense mutation p.Arg220Pro in an alternatively spliced exon of SCN9A (NaV1.7).

Deuis JR, Kumble S, Keramidas A, Ragnarsson L, Simons C, Pais L, White SM, Vetter I. Deuis JR, et al. Hum Mol Genet. 2024 Jan 7;33(2):103-109. doi: 10.1093/hmg/ddad152. Hum Mol Genet. 2024. PMID: 37721535

5

Identification of motif-based interactions between SARS-CoV-2 protein domains and human peptide ligands pinpoint antiviral targets.

Mihalič F, Benz C, Kassa E, Lindqvist R, Simonetti L, Inturi R, Aronsson H, Andersson E, Chi CN, Davey NE, Överby AK, Jemth P, Ivarsson Y. Mihalič F, et al. Nat Commun. 2023 Sep 13;14(1):5636. doi: 10.1038/s41467-023-41312-8. Nat Commun. 2023. PMID: 37704626 Free PMC article.

6

Genetic, electrophysiological, and pathological studies on patients with SCN9A-related pain disorders.

Yuan JH, Cheng X, Matsuura E, Higuchi Y, Ando M, Hashiguchi A, Yoshimura A, Nakachi R, Mine J, Taketani T, Maeda K, Kawakami S, Kira R, Tanaka S, Kanai K, Dib-Hajj F, Dib-Hajj SD, Waxman SG, Takashima H. Yuan JH, et al. J Peripher Nerv Syst. 2023 Dec;28(4):597-607. doi: 10.1111/jns.12590. Epub 2023 Aug 18. J Peripher Nerv Syst. 2023. PMID: 37555797

7

A novel mutation in the SCN9A gene associated with congenital insensitivity to pain, anhidrosis, and mild cognitive impairment.

Romagnuolo M, Moltrasio C, Cavalli R, Brena M, Tadini G. Romagnuolo M, et al. Pediatr Dermatol. 2024 Jan-Feb;41(1):80-83. doi: 10.1111/pde.15366. Epub 2023 Jun 22. Pediatr Dermatol. 2024. PMID: 37345838

8

Novel SCN9A variant associated with congenital insensitivity to pain.

Yammine T, Aprahamian R, Souaid M, Salem N, Awwad J, Farra C. Yammine T, et al. Mol Biol Rep. 2023 Jul;50(7):6293-6298. doi: 10.1007/s11033-023-08507-0. Epub 2023 May 25. Mol Biol Rep. 2023. PMID: 37231219

9

Pain-causing stinging nettle toxins target TMEM233 to modulate Na_V1.7 function.

Jami S, Deuis JR, Klasfauseweh T, Cheng X, Kurdyukov S, Chung F, Okorokov AL, Li S, Zhang J, Cristofori-Armstrong B, Israel MR, Ju RJ, Robinson SD, Zhao P, Ragnarsson L, Andersson Å, Tran P, Schendel V, McMahon KL, Tran HNT, Chin YK, Zhu Y, Liu J, Crawford T, Purushothamvasan S, Habib AM, Andersson DA, Rash LD, Wood JN, Zhao J, Stehbens SJ, Mobli M, Leffler A, Jiang D, Cox JJ, Waxman SG, Dib-Hajj SD, Neely GG, Durek T, Vetter I. Jami S, et al. Nat Commun. 2023 Apr 28;14(1):2442. doi: 10.1038/s41467-023-37963-2. Nat Commun. 2023. PMID: 37117223 Free PMC article.

10

SCN9A rs6746030 Polymorphism and Pain Perception in Combat Athletes and Non-Athletes.

Leźnicka K, Pawlak M, Sawczuk M, Gasiorowska A, Leońska-Duniec A. Leźnicka K, et al. Genes (Basel). 2023 Mar 16;14(3):733. doi: 10.3390/genes14030733. Genes (Basel). 2023. PMID: 36981004 Free PMC article.

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