Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

225 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
ECFS standards of care on CFTR-related disorders: Towards a comprehensive program for affected individuals.
De Wachter E, De Boeck K, Sermet-Gaudelus I, Simmonds NJ, Munck A, Naehrlich L, Barben J, Boyd C, Veen SJ, Carr SB, Fajac I, Farrell PM, Girodon E, Gonska T, Grody WW, Jain M, Jung A, Kerem E, Raraigh KS, van Koningsbruggen-Rietschel S, Waller MD, Southern KW, Castellani C; ECFS Diagnostic Network Working Group. De Wachter E, et al. Among authors: grody ww. J Cyst Fibros. 2024 Feb 21:S1569-1993(24)00011-0. doi: 10.1016/j.jcf.2024.01.012. Online ahead of print. J Cyst Fibros. 2024. PMID: 38388234
Genetics of Disorders of Sex Development: The DSD-TRN Experience.
Délot EC, Papp JC; DSD-TRN Genetics Workgroup; Sandberg DE, Vilain E. Délot EC, et al. Endocrinol Metab Clin North Am. 2017 Jun;46(2):519-537. doi: 10.1016/j.ecl.2017.01.015. Epub 2017 Mar 28. Endocrinol Metab Clin North Am. 2017. PMID: 28476235 Free PMC article. Review.
High-Throughput Genomics Identify Novel FBN1/2 Variants in Severe Neonatal Marfan Syndrome and Congenital Heart Defects.
Zodanu GKE, Hwang JH, Mehta Z, Sisniega C, Barsegian A, Kang X, Biniwale R, Si MS, Satou GM, Halnon N, Ucla Congenital Heart Defect BioCore Faculty, Grody WW, Van Arsdell GS, Nelson SF, Touma M. Zodanu GKE, et al. Among authors: grody ww. Int J Mol Sci. 2024 May 17;25(10):5469. doi: 10.3390/ijms25105469. Int J Mol Sci. 2024. PMID: 38791509 Free PMC article.
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.
225 results