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Aberrant landscapes of maternal meiotic crossovers contribute to aneuploidies in human embryos.
Genome Res. 2024 Feb 7;34(1):70-84. doi: 10.1101/gr.278168.123.
Genome Res. 2024.
PMID: 38071472
Identifying risk variants for embryo aneuploidy using ultra-low coverage whole-genome sequencing from preimplantation genetic testing.
Sun S, Aboelenain M, Ariad D, Haywood ME, Wageman CR, Duke M, Bag A, Viotti M, Katz-Jaffe M, McCoy RC, Schindler K, Xing J.
Sun S, et al. Among authors: ariad d.
Am J Hum Genet. 2023 Dec 7;110(12):2092-2102. doi: 10.1016/j.ajhg.2023.11.002. Epub 2023 Nov 28.
Am J Hum Genet. 2023.
PMID: 38029743
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Identifying risk genes for embryo aneuploidy using ultra-low coverage whole-genome sequencing.
Sun S, Aboelenain M, Ariad D, Haywood ME, Wageman CR, Duke M, Bag A, Viotti M, Katz-Jaffe M, McCoy RC, Schindler K, Xing J.
Sun S, et al. Among authors: ariad d.
medRxiv [Preprint]. 2023 Jul 24:2023.07.22.23292618. doi: 10.1101/2023.07.22.23292618.
medRxiv. 2023.
PMID: 37546814
Free PMC article.
Updated.
Preprint.
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Aberrant landscapes of maternal meiotic crossovers contribute to aneuploidies in human embryos.
Ariad D, Madjunkova S, Madjunkov M, Chen S, Abramov R, Librach C, McCoy RC.
Ariad D, et al.
bioRxiv [Preprint]. 2023 Nov 17:2023.06.07.543910. doi: 10.1101/2023.06.07.543910.
bioRxiv. 2023.
PMID: 37333422
Free PMC article.
Updated.
Preprint.
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A method for low-coverage single-gamete sequence analysis demonstrates adherence to Mendel's first law across a large sample of human sperm.
Carioscia SA, Weaver KJ, Bortvin AN, Pan H, Ariad D, Bell AD, McCoy RC.
Carioscia SA, et al. Among authors: ariad d.
Elife. 2022 Dec 7;11:e76383. doi: 10.7554/eLife.76383.
Elife. 2022.
PMID: 36475543
Free PMC article.
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Haplotype-aware inference of human chromosome abnormalities.
Ariad D, Yan SM, Victor AR, Barnes FL, Zouves CG, Viotti M, McCoy RC.
Ariad D, et al.
Proc Natl Acad Sci U S A. 2021 Nov 16;118(46):e2109307118. doi: 10.1073/pnas.2109307118.
Proc Natl Acad Sci U S A. 2021.
PMID: 34772814
Free PMC article.
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