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2019 | 1 |
2021 | 1 |
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Shared and distinct ultra-rare genetic risk for diverse epilepsies: A whole-exome sequencing study of 54,423 individuals across multiple genetic ancestries.
medRxiv [Preprint]. 2023 Feb 24:2023.02.22.23286310. doi: 10.1101/2023.02.22.23286310.
medRxiv. 2023.
PMID: 36865150
Free PMC article.
Preprint.
Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals.
Epi25 Collaborative. Electronic address: jm4279@cumc.columbia.edu; Epi25 Collaborative.
Epi25 Collaborative. Electronic address: jm4279@cumc.columbia.edu, et al.
Am J Hum Genet. 2021 Jun 3;108(6):965-982. doi: 10.1016/j.ajhg.2021.04.009. Epub 2021 Apr 30.
Am J Hum Genet. 2021.
PMID: 33932343
Free PMC article.
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Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals.
Epi25 Collaborative. Electronic address: s.berkovic@unimelb.edu.au; Epi25 Collaborative.
Epi25 Collaborative. Electronic address: s.berkovic@unimelb.edu.au, et al.
Am J Hum Genet. 2019 Aug 1;105(2):267-282. doi: 10.1016/j.ajhg.2019.05.020. Epub 2019 Jul 18.
Am J Hum Genet. 2019.
PMID: 31327507
Free PMC article.
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