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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2021 | 2 |
2023 | 2 |
2024 | 0 |
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Page 1
Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals.
Nat Commun. 2023 Jul 20;14(1):4392. doi: 10.1038/s41467-023-39539-6.
Nat Commun. 2023.
PMID: 37474567
Free PMC article.
Cancer genetic mutation prevalence in sub-Saharan Africa: A review of existing data.
Shain J, Michel A, May MS, Qunaj L, El-Sadr W, Chung WK, Appelbaum PS, Jacobson JS, Justman J, Neugut AI.
Shain J, et al.
Semin Oncol. 2023 Dec;50(6):123-130. doi: 10.1053/j.seminoncol.2023.12.001. Epub 2023 Dec 27.
Semin Oncol. 2023.
PMID: 38171987
Review.
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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 Oct 7;108(10):2024. doi: 10.1016/j.ajhg.2021.08.008.
Am J Hum Genet. 2021.
PMID: 34626584
Free PMC article.
No abstract available.
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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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