PubMed for id: 3756

Year	Number of Results
1994	1
1998	2
1999	1
2000	1
2002	4
2004	2
2005	2
2006	3
2007	5
2008	4
2009	2
2010	11
2011	9
2012	14
2013	7
2014	7
2015	9
2016	10
2017	8
2018	2
2019	2
2020	5
2021	10
2022	5
2023	2
2024	0

1

Phenotypic expansion of KCNH1-associated disorders to include isolated epilepsy and its associations with genotypes and molecular sub-regional locations.

Tian MQ, Li RK, Yang F, Shu XM, Li J, Chen J, Peng LY, Yu XH, Yang CJ. Tian MQ, et al. CNS Neurosci Ther. 2023 Jan;29(1):270-281. doi: 10.1111/cns.14001. Epub 2022 Oct 25. CNS Neurosci Ther. 2023. PMID: 36285361 Free PMC article.

2

Potassium Channel KCNH1 Activating Variants Cause Altered Functional and Morphological Ciliogenesis.

Napoli G, Panzironi N, Traversa A, Catalanotto C, Pace V, Petrizzelli F, Giovannetti A, Lazzari S, Cogoni C, Tartaglia M, Carella M, Mazza T, Pizzuti A, Parisi C, Caputo V. Napoli G, et al. Mol Neurobiol. 2022 Aug;59(8):4825-4838. doi: 10.1007/s12035-022-02886-4. Epub 2022 May 31. Mol Neurobiol. 2022. PMID: 35639255 Free PMC article.

3

Hysteretic hERG channel gating current recorded at physiological temperature.

Jones DK. Jones DK. Sci Rep. 2022 Apr 8;12(1):5950. doi: 10.1038/s41598-022-10003-7. Sci Rep. 2022. PMID: 35396394 Free PMC article.

4

Molecular Dynamics-Derived Pharmacophore Model Explaining the Nonselective Aspect of K_V10.1 Pore Blockers.

Toplak Ž, Merzel F, Pardo LA, Peterlin Mašič L, Tomašič T. Toplak Ž, et al. Int J Mol Sci. 2021 Aug 20;22(16):8999. doi: 10.3390/ijms22168999. Int J Mol Sci. 2021. PMID: 34445705 Free PMC article.

5

Insights into the Molecular Inhibition of the Oncogenic Channel K_V10.1 by Globular Toxins.

Hernández-Meza JM, Mares-Sámano S, Garduño-Juárez R. Hernández-Meza JM, et al. J Chem Inf Model. 2021 May 24;61(5):2328-2340. doi: 10.1021/acs.jcim.0c01353. Epub 2021 Apr 26. J Chem Inf Model. 2021. PMID: 33900765

6

Patients with KCNH1-related intellectual disability without distinctive features of Zimmermann-Laband/Temple-Baraitser syndrome.

Aubert Mucca M, Patat O, Whalen S, Arnaud L, Barcia G, Buratti J, Cogné B, Doummar D, Karsenty C, Kenis S, Leguern E, Lesca G, Nava C, Nizon M, Piton A, Valence S, Villard L, Weckhuysen S, Keren B, Mignot C. Aubert Mucca M, et al. J Med Genet. 2022 May;59(5):505-510. doi: 10.1136/jmedgenet-2020-107511. Epub 2021 Apr 2. J Med Genet. 2022. PMID: 33811134

7

Novel KCNH1 Mutations Associated with Epilepsy: Broadening the Phenotypic Spectrum of KCNH1-Associated Diseases.

von Wrede R, Jeub M, Ariöz I, Elger CE, von Voss H, Klein HG, Becker AJ, Schoch S, Surges R, Kunz WS. von Wrede R, et al. Genes (Basel). 2021 Jan 21;12(2):132. doi: 10.3390/genes12020132. Genes (Basel). 2021. PMID: 33494179 Free PMC article.

8

Neurological disorder-associated genetic variants in individuals with psychogenic nonepileptic seizures.

Leu C, Bautista JF, Sudarsanam M, Niestroj LM, Stefanski A, Ferguson L, Daly MJ, Jehi L, Najm IM, Busch RM, Lal D. Leu C, et al. Sci Rep. 2020 Sep 16;10(1):15205. doi: 10.1038/s41598-020-72101-8. Sci Rep. 2020. PMID: 32938993 Free PMC article.

9

Eag1 Gene and Protein Expression in Human Retinoblastoma Tumors and its Regulation by pRb in HeLa Cells.

Chávez-López MG, Zúñiga-García V, Castro-Magdonel BE, Vera E, Garrido E, Sánchez-Ramos J, Ponce-Castañeda MV, Cabrera-Muñoz ML, Escobar Y, Ortiz CS, Hernández-Gallegos E, Avalos-Fuentes A, Camacho J. Chávez-López MG, et al. Genes (Basel). 2020 Jan 21;11(2):119. doi: 10.3390/genes11020119. Genes (Basel). 2020. PMID: 31973216 Free PMC article.

10

High-throughput phenotyping of heteromeric human ether-à-go-go-related gene potassium channel variants can discriminate pathogenic from rare benign variants.

Ng CA, Perry MD, Liang W, Smith NJ, Foo B, Shrier A, Lukacs GL, Hill AP, Vandenberg JI. Ng CA, et al. Heart Rhythm. 2020 Mar;17(3):492-500. doi: 10.1016/j.hrthm.2019.09.020. Epub 2019 Sep 23. Heart Rhythm. 2020. PMID: 31557540

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