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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2019 | 1 |
2020 | 1 |
2021 | 2 |
2024 | 0 |
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4 results
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Page 1
Comprehensive analysis of coding variants highlights genetic complexity in developmental and epileptic encephalopathy.
Nat Commun. 2019 Jun 7;10(1):2506. doi: 10.1038/s41467-019-10482-9.
Nat Commun. 2019.
PMID: 31175295
Free PMC article.
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.
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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.
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Recent ultra-rare inherited variants implicate new autism candidate risk genes.
Wilfert AB, Turner TN, Murali SC, Hsieh P, Sulovari A, Wang T, Coe BP, Guo H, Hoekzema K, Bakken TE, Winterkorn LH, Evani US, Byrska-Bishop M, Earl RK, Bernier RA; SPARK Consortium; Zody MC, Eichler EE.
Wilfert AB, et al.
Nat Genet. 2021 Aug;53(8):1125-1134. doi: 10.1038/s41588-021-00899-8. Epub 2021 Jul 26.
Nat Genet. 2021.
PMID: 34312540
Free PMC article.
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