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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

54 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Fourteen monogenic genes account for 15% of nephrolithiasis/nephrocalcinosis.
Halbritter J, Baum M, Hynes AM, Rice SJ, Thwaites DT, Gucev ZS, Fisher B, Spaneas L, Porath JD, Braun DA, Wassner AJ, Nelson CP, Tasic V, Sayer JA, Hildebrandt F. Halbritter J, et al. Among authors: hynes am. J Am Soc Nephrol. 2015 Mar;26(3):543-51. doi: 10.1681/ASN.2014040388. Epub 2014 Oct 8. J Am Soc Nephrol. 2015. PMID: 25296721 Free PMC article.
CYP24A1 mutation leading to nephrocalcinosis.
Dowen FE, Sayers JA, Hynes AM, Sayer JA. Dowen FE, et al. Among authors: hynes am. Kidney Int. 2014 Jun;85(6):1475. doi: 10.1038/ki.2013.416. Kidney Int. 2014. PMID: 24875559 Free article. No abstract available.
Nephronophthisis: a genetically diverse ciliopathy.
Simms RJ, Hynes AM, Eley L, Sayer JA. Simms RJ, et al. Among authors: hynes am. Int J Nephrol. 2011;2011:527137. doi: 10.4061/2011/527137. Epub 2011 May 15. Int J Nephrol. 2011. PMID: 21660307 Free PMC article.
Clinical and functional characterization of URAT1 variants.
Tasic V, Hynes AM, Kitamura K, Cheong HI, Lozanovski VJ, Gucev Z, Jutabha P, Anzai N, Sayer JA. Tasic V, et al. Among authors: hynes am. PLoS One. 2011;6(12):e28641. doi: 10.1371/journal.pone.0028641. Epub 2011 Dec 16. PLoS One. 2011. PMID: 22194875 Free PMC article.
A novel LMX1B mutation in a family with end-stage renal disease of 'unknown cause'.
Edwards N, Rice SJ, Raman S, Hynes AM, Srivastava S, Moore I, Al-Hamed M, Xu Y, Santibanez-Koref M, Thwaites DT, Gale DP, Sayer JA. Edwards N, et al. Among authors: hynes am. Clin Kidney J. 2015 Feb;8(1):113-9. doi: 10.1093/ckj/sfu129. Epub 2014 Dec 5. Clin Kidney J. 2015. PMID: 25713721 Free PMC article.
Functional modelling of a novel mutation in BBS5.
Al-Hamed MH, van Lennep C, Hynes AM, Chrystal P, Eley L, Al-Fadhly F, El Sayed R, Simms RJ, Meyer B, Sayer JA. Al-Hamed MH, et al. Among authors: hynes am. Cilia. 2014 Feb 21;3(1):3. doi: 10.1186/2046-2530-3-3. Cilia. 2014. PMID: 24559376 Free PMC article.
54 results