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Year Number of Results
2013 4
2014 5
2015 2
2016 3
2019 1
2020 2
2021 2
2022 2
2023 1
2024 0

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20 results

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Page 1
Whole-genome sequencing across 449 samples spanning 47 ethnolinguistic groups provides insights into genetic diversity in Nigeria.
Joshi E, Biddanda A, Popoola J, Yakubu A, Osakwe O, Attipoe D; 54gene Team; NCD-GHS Consortium; Dogbo E, Salako B, Nash O, Salako O, Oyedele O, Eze-Echesi G, Fatumo S, Ene-Obong A, O'Dushlaine C. Joshi E, et al. Cell Genom. 2023 Aug 8;3(9):100378. doi: 10.1016/j.xgen.2023.100378. eCollection 2023 Sep 13. Cell Genom. 2023. PMID: 37719143 Free PMC article.
Genetic testing in severe aplastic anemia is required for optimal hematopoietic cell transplant outcomes.
McReynolds LJ, Rafati M, Wang Y, Ballew BJ, Kim J, Williams VV, Zhou W, Hendricks RM, Dagnall C, Freedman ND, Carter B, Strollo S, Hicks B, Zhu B, Jones K, Paczesny S, Marsh SGE, Spellman SR, He M, Wang T, Lee SJ, Savage SA, Gadalla SM. McReynolds LJ, et al. Among authors: ballew bj. Blood. 2022 Aug 25;140(8):909-921. doi: 10.1182/blood.2022016508. Blood. 2022. PMID: 35776903 Free PMC article.
Promoting the genomic revolution in Africa through the Nigerian 100K Genome Project.
Fatumo S, Yakubu A, Oyedele O, Popoola J, Attipoe DA, Eze-Echesi G, Modibbo FZ, Ado-Wanka N; 54gene Team; NCD-GHS Consortium; Salako O, Nashiru O, Salako BL, O'Dushlaine C, Ene-Obong A. Fatumo S, et al. Nat Genet. 2022 May;54(5):531-536. doi: 10.1038/s41588-022-01071-6. Nat Genet. 2022. PMID: 35534563 No abstract available.
Lack of transgenerational effects of ionizing radiation exposure from the Chernobyl accident.
Yeager M, Machiela MJ, Kothiyal P, Dean M, Bodelon C, Suman S, Wang M, Mirabello L, Nelson CW, Zhou W, Palmer C, Ballew B, Colli LM, Freedman ND, Dagnall C, Hutchinson A, Vij V, Maruvka Y, Hatch M, Illienko I, Belayev Y, Nakamura N, Chumak V, Bakhanova E, Belyi D, Kryuchkov V, Golovanov I, Gudzenko N, Cahoon EK, Albert P, Drozdovitch V, Little MP, Mabuchi K, Stewart C, Getz G, Bazyka D, Berrington de Gonzalez A, Chanock SJ. Yeager M, et al. Among authors: ballew b. Science. 2021 May 14;372(6543):725-729. doi: 10.1126/science.abg2365. Epub 2021 Apr 22. Science. 2021. PMID: 33888597 Free PMC article.
Whole genome sequencing of skull-base chordoma reveals genomic alterations associated with recurrence and chordoma-specific survival.
Bai J, Shi J, Li C, Wang S, Zhang T, Hua X, Zhu B, Koka H, Wu HH, Song L, Wang D, Wang M, Zhou W, Ballew BJ, Zhu B, Hicks B, Mirabello L, Parry DM, Zhai Y, Li M, Du J, Wang J, Zhang S, Liu Q, Zhao P, Gui S, Goldstein AM, Zhang Y, Yang XR. Bai J, et al. Among authors: ballew bj. Nat Commun. 2021 Feb 3;12(1):757. doi: 10.1038/s41467-021-21026-5. Nat Commun. 2021. PMID: 33536423 Free PMC article.
Corrigendum: 1q21.1 deletion and a rare functional polymorphism in siblings with thrombocytopenia-absent radius-like phenotypes.
Brodie SA, Rodriguez-Aulet JP, Giri N, Dai J, Steinberg M, J Waterfall J, Roberson D, Ballew BJ, Zhou W, Anzick SL, Jiang Y, Wang Y, Zhu YJ, Meltzer PS, Boland J, Alter BP, Savage SA. Brodie SA, et al. Among authors: ballew bj. Cold Spring Harb Mol Case Stud. 2020 Feb 3;6(1):a005116. doi: 10.1101/mcs.a005116. Print 2020 Feb. Cold Spring Harb Mol Case Stud. 2020. PMID: 32014861 Free PMC article. No abstract available.
Population Frequency of Fanconi Pathway Gene Variants and Their Association with Survival After Hematopoietic Cell Transplantation for Severe Aplastic Anemia.
McReynolds LJ, Wang Y, Thompson AS, Ballew BJ, Kim J, Alter BP, Hicks B, Zhu B, Jones K, Spellman SR, Wang T, Lee SJ, Savage SA, Gadalla SM. McReynolds LJ, et al. Among authors: ballew bj. Biol Blood Marrow Transplant. 2020 May;26(5):817-822. doi: 10.1016/j.bbmt.2020.01.011. Epub 2020 Jan 23. Biol Blood Marrow Transplant. 2020. PMID: 31982544 Free PMC article.
1q21.1 deletion and a rare functional polymorphism in siblings with thrombocytopenia-absent radius-like phenotypes.
Brodie SA, Rodriguez-Aulet JP, Giri N, Dai J, Steinberg M, Waterfall JJ, Roberson D, Ballew BJ, Zhou W, Anzick SL, Jiang Y, Wang Y, Zhu YJ, Meltzer PS, Boland J, Alter BP, Savage SA. Brodie SA, et al. Among authors: ballew bj. Cold Spring Harb Mol Case Stud. 2019 Dec 13;5(6):a004564. doi: 10.1101/mcs.a004564. Print 2019 Dec. Cold Spring Harb Mol Case Stud. 2019. PMID: 31836590 Free PMC article.
Hoyeraal-Hreidarsson Syndrome due to PARN Mutations: Fourteen Years of Follow-Up.
Burris AM, Ballew BJ, Kentosh JB, Turner CE, Norton SA; NCI DCEG Cancer Genomics Research Laboratory; NCI DCEG Cancer Sequencing Working Group; Giri N, Alter BP, Nellan A, Gamper C, Hartman KR, Savage SA. Burris AM, et al. Among authors: ballew bj. Pediatr Neurol. 2016 Mar;56:62-68.e1. doi: 10.1016/j.pediatrneurol.2015.12.005. Epub 2015 Dec 19. Pediatr Neurol. 2016. PMID: 26810774 Free PMC article.
20 results