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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1995 | 1 |
2012 | 1 |
2013 | 1 |
2021 | 1 |
2022 | 3 |
2023 | 1 |
2024 | 0 |
PubMed for id: 1829778929
6 results
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Page 1
A deleterious frameshift insertion mutation in the ZNF142 gene leads to intellectual developmental disorder with impaired speech in three affected siblings: Clinical features and literature review.
Mol Genet Genomic Med. 2023 Dec;11(12):e2261. doi: 10.1002/mgg3.2261. Epub 2023 Jul 26.
Mol Genet Genomic Med. 2023.
PMID: 37496384
Free PMC article.
Review.
ZNF142 mutation causes neurodevelopmental disorder with speech impairment and seizures: Novel variants and literature review.
Kamal N, Khamirani HJ, Mohammadi S, Dastgheib SA, Dianatpour M, Tabei SMB.
Kamal N, et al.
Eur J Med Genet. 2022 Jul;65(7):104522. doi: 10.1016/j.ejmg.2022.104522. Epub 2022 May 23.
Eur J Med Genet. 2022.
PMID: 35618198
Review.
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Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder.
Christensen MB, Levy AM, Mohammadi NA, Niceta M, Kaiyrzhanov R, Dentici ML, Al Alam C, Alesi V, Benoit V, Bhatia KP, Bierhals T, Boßelmann CM, Buratti J, Callewaert B, Ceulemans B, Charles P, De Wachter M, Dehghani M, D'haenens E, Doco-Fenzy M, Geßner M, Gobert C, Guliyeva U, Haack TB, Hammer TB, Heinrich T, Hempel M, Herget T, Hoffmann U, Horvath J, Houlden H, Keren B, Kresge C, Kumps C, Lederer D, Lermine A, Magrinelli F, Maroofian R, Vahidi Mehrjardi MY, Moudi M, Müller AJ, Oostra AJ, Pletcher BA, Ros-Pardo D, Samarasekera S, Tartaglia M, Van Schil K, Vogt J, Wassmer E, Winkelmann J, Zaki MS, Zech M, Lerche H, Radio FC, Gomez-Puertas P, Møller RS, Tümer Z.
Christensen MB, et al.
Clin Genet. 2022 Aug;102(2):98-109. doi: 10.1111/cge.14165. Epub 2022 Jun 8.
Clin Genet. 2022.
PMID: 35616059
Free PMC article.
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Biallelic null variants in ZNF142 cause global developmental delay with familial epilepsy and dysmorphic features.
Kameyama S, Mizuguchi T, Fukuda H, Moey LH, Keng WT, Okamoto N, Tsuchida N, Uchiyama Y, Koshimizu E, Hamanaka K, Fujita A, Miyatake S, Matsumoto N.
Kameyama S, et al.
J Hum Genet. 2022 Mar;67(3):169-173. doi: 10.1038/s10038-021-00978-y. Epub 2021 Sep 17.
J Hum Genet. 2022.
PMID: 34531528
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Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.
Ahmeti KB, Ajroud-Driss S, Al-Chalabi A, Andersen PM, Armstrong J, Birve A, Blauw HM, Brown RH, Bruijn L, Chen W, Chio A, Comeau MC, Cronin S, Diekstra FP, Soraya Gkazi A, Glass JD, Grab JD, Groen EJ, Haines JL, Hardiman O, Heller S, Huang J, Hung WY; ITALSGEN consortium; Jaworski JM, Jones A, Khan H, Landers JE, Langefeld CD, Leigh PN, Marion MC, McLaughlin RL, Meininger V, Melki J, Miller JW, Mora G, Pericak-Vance MA, Rampersaud E, Robberecht W, Russell LP, Salachas F, Saris CG, Shatunov A, Shaw CE, Siddique N, Siddique T, Smith BN, Sufit R, Topp S, Traynor BJ, Vance C, van Damme P, van den Berg LH, van Es MA, van Vught PW, Veldink JH, Yang Y, Zheng JG; ALSGEN Consortium.
Ahmeti KB, et al.
Neurobiol Aging. 2013 Jan;34(1):357.e7-19. doi: 10.1016/j.neurobiolaging.2012.07.017. Epub 2012 Sep 5.
Neurobiol Aging. 2013.
PMID: 22959728
Free PMC article.
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Isolation and fine mapping of 16 novel human zinc finger-encoding cDNAs identify putative candidate genes for developmental and malignant disorders.
Tommerup N, Vissing H.
Tommerup N, et al.
Genomics. 1995 May 20;27(2):259-64. doi: 10.1006/geno.1995.1040.
Genomics. 1995.
PMID: 7557990
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