Fan Y - Search Results

1

Genetic testing of the FBN1 gene in Chinese patients with Marfan/Marfan-like syndrome.

Yang H, Luo M, Chen Q, Fu Y, Zhang J, Qian X, Sun X, Fan Y, Zhou Z, Chang Q. Yang H, et al. Among authors: fan y. Clin Chim Acta. 2016 Aug 1;459:30-35. doi: 10.1016/j.cca.2016.05.021. Epub 2016 May 24. Clin Chim Acta. 2016. PMID: 27234404

2

Paucity of skeletal manifestations in Hispanic families with FBN1 mutations.

Villamizar C, Regalado ES, Fadulu VT, Hasham SN, Gupta P, Willing MC, Kuang SQ, Guo D, Muilenburg A, Yee RW, Fan Y, Towbin J, Coselli JS, LeMaire SA, Milewicz DM. Villamizar C, et al. Among authors: fan y. Eur J Med Genet. 2010 Mar-Apr;53(2):80-4. doi: 10.1016/j.ejmg.2009.11.001. Epub 2009 Nov 23. Eur J Med Genet. 2010. PMID: 19941982 Free PMC article.

3

Missense mutations in FBN1 exons 41 and 42 cause Weill-Marchesani syndrome with thoracic aortic disease and Marfan syndrome.

Cecchi A, Ogawa N, Martinez HR, Carlson A, Fan Y, Penny DJ, Guo DC, Eisenberg S, Safi H, Estrera A, Lewis RA, Meyers D, Milewicz DM. Cecchi A, et al. Among authors: fan y. Am J Med Genet A. 2013 Sep;161A(9):2305-10. doi: 10.1002/ajmg.a.36044. Epub 2013 Jul 29. Am J Med Genet A. 2013. PMID: 23897642 Free PMC article.

4

Genetic testing of 10 patients with features of Loeys-Dietz syndrome.

Luo M, Yang H, Yin K, Chen Q, Zhang J, Fan Y, Zhou Z, Chang Q. Luo M, et al. Among authors: fan y. Clin Chim Acta. 2016 May 1;456:144-148. doi: 10.1016/j.cca.2016.02.005. Epub 2016 Feb 11. Clin Chim Acta. 2016. PMID: 26877057

5

Genetic testing of 248 Chinese aortopathy patients using a panel assay.

Yang H, Luo M, Fu Y, Cao Y, Yin K, Li W, Meng C, Ma Y, Zhang J, Fan Y, Shu C, Chang Q, Zhou Z. Yang H, et al. Among authors: fan y. Sci Rep. 2016 Sep 9;6:33002. doi: 10.1038/srep33002. Sci Rep. 2016. PMID: 27611364 Free PMC article.

6

A Novel Exonic Splicing Mutation in the TAZ (G4.5) Gene in a Case with Atypical Barth Syndrome.

Fan Y, Steller J, Gonzalez IL, Kulik W, Fox M, Chang R, Westerfield BA, Batra AS, Wang RY, Gallant NM, Pena LS, Wang H, Huang T, Bhuta S, Penny DJ, McCabe ER, Kimonis VE. Fan Y, et al. JIMD Rep. 2013;11:99-106. doi: 10.1007/8904_2013_228. Epub 2013 Apr 19. JIMD Rep. 2013. PMID: 23606313 Free PMC article.

7

Genetic screening for monogenic hypertension in hypertensive individuals in a clinical setting.

Bao M, Li P, Li Q, Chen H, Zhong Y, Li S, Jin L, Wang W, Chen Z, Zhong J, Geng B, Fan Y, Yang X, Cai J. Bao M, et al. Among authors: fan y. J Med Genet. 2020 Aug;57(8):571-580. doi: 10.1136/jmedgenet-2019-106145. Epub 2020 Jun 19. J Med Genet. 2020. PMID: 32561571 Free PMC article.

8

Mutations in NEXN, a Z-disc gene, are associated with hypertrophic cardiomyopathy.

Wang H, Li Z, Wang J, Sun K, Cui Q, Song L, Zou Y, Wang X, Liu X, Hui R, Fan Y. Wang H, et al. Among authors: fan y. Am J Hum Genet. 2010 Nov 12;87(5):687-93. doi: 10.1016/j.ajhg.2010.10.002. Epub 2010 Oct 21. Am J Hum Genet. 2010. PMID: 20970104 Free PMC article.

9

Loss-of-Function SCN5A Mutations Associated With Sinus Node Dysfunction, Atrial Arrhythmias, and Poor Pacemaker Capture.

Chiang DY, Kim JJ, Valdes SO, de la Uz C, Fan Y, Orcutt J, Domino M, Smith M, Wehrens XH, Miyake CY. Chiang DY, et al. Among authors: fan y. Circ Arrhythm Electrophysiol. 2015 Oct;8(5):1105-12. doi: 10.1161/CIRCEP.115.003098. Epub 2015 Jun 25. Circ Arrhythm Electrophysiol. 2015. PMID: 26111534 Free PMC article.

10

LAMP2 microdeletions in patients with Danon disease.

Yang Z, Funke BH, Cripe LH, Vick GW 3rd, Mancini-Dinardo D, Peña LS, Kanter RJ, Wong B, Westerfield BH, Varela JJ, Fan Y, Towbin JA, Vatta M. Yang Z, et al. Among authors: fan y. Circ Cardiovasc Genet. 2010 Apr;3(2):129-37. doi: 10.1161/CIRCGENETICS.109.901785. Epub 2010 Feb 20. Circ Cardiovasc Genet. 2010. PMID: 20173215 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

18,479 results

Search Page