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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2001 1
2002 8
2003 7
2004 6
2005 5
2006 4
2007 8
2008 9
2009 6
2010 7
2011 5
2012 7
2013 8
2014 9
2015 6
2016 7
2017 6
2018 4
2019 6
2020 7
2021 6
2022 1
2023 6
2024 0

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127 results

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Page 1
A Primer on Gene Editing: What Does It Mean for Pathologists?
Cushman-Vokoun A, Schmidt RJ, Hiemenz MC, Fung M, Zhang BM, Bradshaw G, Gandhi M, Yao J, Yohe S, Beckman A, Grody WW, Giannikopoulos P. Cushman-Vokoun A, et al. Among authors: grody ww. Arch Pathol Lab Med. 2023 Aug 23. doi: 10.5858/arpa.2022-0410-CP. Online ahead of print. Arch Pathol Lab Med. 2023. PMID: 37610100 Free article.
A Primer on Gene Editing.
Cushman-Vokoun A, Schmidt RJ, Hiemenz MC, Fung M, Zhang BM, Bradshaw G, Gandhi M, Yao J, Yohe S, Beckman A, Grody WW, Giannikopoulos P. Cushman-Vokoun A, et al. Among authors: grody ww. Arch Pathol Lab Med. 2023 Aug 22. doi: 10.5858/arpa.2022-0410-CP. Online ahead of print. Arch Pathol Lab Med. 2023. PMID: 37603682 Free article.
Synonymous Variants of Uncertain Silence.
Giacoletto CJ, Rotter JI, Grody WW, Schiller MR. Giacoletto CJ, et al. Among authors: grody ww. Int J Mol Sci. 2023 Jun 23;24(13):10556. doi: 10.3390/ijms241310556. Int J Mol Sci. 2023. PMID: 37445732 Free PMC article.
Updated recommendations for CFTR carrier screening: A position statement of the American College of Medical Genetics and Genomics (ACMG).
Deignan JL, Gregg AR, Grody WW, Guo MH, Kearney H, Monaghan KG, Raraigh KS, Taylor J, Zepeda-Mendoza CJ, Ziats C; ACMG Board of Directors. Electronic address: documents@acmg.net. Deignan JL, et al. Among authors: grody ww. Genet Med. 2023 Aug;25(8):100867. doi: 10.1016/j.gim.2023.100867. Epub 2023 Jun 13. Genet Med. 2023. PMID: 37310422 No abstract available.
Stewardship of patient genomic data: A policy statement of the American College of Medical Genetics and Genomics (ACMG).
Best RG, Khushf G, Rabin-Havt SS, Clayton EW, Grebe TA, Hagenkord J, Topper S, Fivecoat J, Chen M, Grody WW; ACMG Social, Ethical and Legal Issues Committee. Electronic address: documents@acmg.net. Best RG, et al. Among authors: grody ww. Genet Med. 2022 Mar;24(3):509-511. doi: 10.1016/j.gim.2021.11.001. Epub 2021 Dec 16. Genet Med. 2022. PMID: 35253644 Free article. No abstract available.
Response to Biesecker et al.
Hamosh A, Amberger JS, Bocchini CA, Bodurtha J, Bult CJ, Chute CG, Cutting GR, Dietz HC, Firth HV, Gibbs RA, Grody WW, Haendel MA, Lupski JR, Posey JE, Robinson PN, Schriml LM, Scott AF, Sobreira NL, Valle D, Wu N, Rasmussen SA. Hamosh A, et al. Among authors: grody ww. Am J Hum Genet. 2021 Sep 2;108(9):1807-1808. doi: 10.1016/j.ajhg.2021.07.004. Am J Hum Genet. 2021. PMID: 34478655 Free PMC article. No abstract available.
Recessive ciliopathy mutations in primary endocardial fibroelastosis: a rare neonatal cardiomyopathy in a case of Alstrom syndrome.
Zhao Y, Wang LK, Eskin A, Kang X, Fajardo VM, Mehta Z, Pineles S, Schmidt RJ, Nagiel A, Satou G, Garg M, Federman M, Reardon LC, Lee SL, Biniwale R, Grody WW, Halnon N, Khanlou N, Quintero-Rivera F, Alejos JC, Nakano A, Fishbein GA, Van Arsdell GS, Nelson SF, Touma M. Zhao Y, et al. Among authors: grody ww. J Mol Med (Berl). 2021 Nov;99(11):1623-1638. doi: 10.1007/s00109-021-02112-z. Epub 2021 Aug 13. J Mol Med (Berl). 2021. PMID: 34387706 Free PMC article.
Central 22q11.2 deletion (LCR22 B-D) in a fetus with severe fetal growth restriction and a mother with severe systemic lupus erythematosus: Further evidence of CRKL haploinsufficiency in the pathogenesis of 22q11.2 deletion syndrome.
Lin I, Afshar Y, Goldstein J, Grossman J, Grody WW, Quintero-Rivera F. Lin I, et al. Among authors: grody ww. Am J Med Genet A. 2021 Oct;185(10):3042-3047. doi: 10.1002/ajmg.a.62346. Epub 2021 Jul 1. Am J Med Genet A. 2021. PMID: 34196458
127 results