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

501 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Targeted long-read sequencing identifies missing pathogenic variants in unsolved Werner syndrome cases.
Miller DE, Lee L, Galey M, Kandhaya-Pillai R, Tischkowitz M, Amalnath D, Vithlani A, Yokote K, Kato H, Maezawa Y, Takada-Watanabe A, Takemoto M, Martin GM, Eichler EE, Hisama FM, Oshima J. Miller DE, et al. Among authors: martin gm. J Med Genet. 2022 May 9;59(11):1087-94. doi: 10.1136/jmedgenet-2022-108485. Online ahead of print. J Med Genet. 2022. PMID: 35534204 Free PMC article.
Clinical utility gene card for: Werner syndrome.
Hisama FM, Kubisch C, Martin GM, Oshima J. Hisama FM, et al. Among authors: martin gm. Eur J Hum Genet. 2012 May;20(5). doi: 10.1038/ejhg.2011.265. Epub 2012 Jan 18. Eur J Hum Genet. 2012. PMID: 22258520 Free PMC article. No abstract available.
Clinical utility gene card for: Werner Syndrome--Update 2014.
Hisama FM, Kubisch C, Martin GM, Oshima J. Hisama FM, et al. Among authors: martin gm. Eur J Hum Genet. 2015 Jun;23(6):891-. doi: 10.1038/ejhg.2014.171. Epub 2014 Sep 3. Eur J Hum Genet. 2015. PMID: 25182132 Free PMC article. No abstract available.
Ageing: Dietary protection for genes.
Oshima J, Martin GM. Oshima J, et al. Among authors: martin gm. Nature. 2016 Sep 15;537(7620):316-317. doi: 10.1038/nature19427. Epub 2016 Aug 24. Nature. 2016. PMID: 27556941 Free PMC article.
ERCC4 variants identified in a cohort of patients with segmental progeroid syndromes.
Mori T, Yousefzadeh MJ, Faridounnia M, Chong JX, Hisama FM, Hudgins L, Mercado G, Wade EA, Barghouthy AS, Lee L, Martin GM, Nickerson DA, Bamshad MJ; University of Washington Center for Mendelian Genomics; Niedernhofer LJ, Oshima J. Mori T, et al. Among authors: martin gm. Hum Mutat. 2018 Feb;39(2):255-265. doi: 10.1002/humu.23367. Epub 2017 Nov 17. Hum Mutat. 2018. PMID: 29105242 Free PMC article.
501 results