Search Page
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
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2003 | 1 |
2006 | 1 |
2007 | 1 |
2011 | 1 |
2013 | 1 |
2014 | 1 |
2015 | 2 |
2024 | 0 |
Search Results
7 results
Results by year
Filters applied: . Clear all
Page 1
Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome.
J Med Genet. 2007 Mar;44(3):193-9. doi: 10.1136/jmg.2006.045328. Epub 2006 Oct 3.
J Med Genet. 2007.
PMID: 17018561
Free PMC article.
Phenotypic Characterization of Complement Factor H R1210C Rare Genetic Variant in Age-Related Macular Degeneration.
Ferrara D, Seddon JM.
Ferrara D, et al.
JAMA Ophthalmol. 2015 Jul;133(7):785-91. doi: 10.1001/jamaophthalmol.2015.0814.
JAMA Ophthalmol. 2015.
PMID: 25880396
Free PMC article.
Item in Clipboard
A rare penetrant mutation in CFH confers high risk of age-related macular degeneration.
Raychaudhuri S, Iartchouk O, Chin K, Tan PL, Tai AK, Ripke S, Gowrisankar S, Vemuri S, Montgomery K, Yu Y, Reynolds R, Zack DJ, Campochiaro B, Campochiaro P, Katsanis N, Daly MJ, Seddon JM.
Raychaudhuri S, et al.
Nat Genet. 2011 Oct 23;43(12):1232-6. doi: 10.1038/ng.976.
Nat Genet. 2011.
PMID: 22019782
Free PMC article.
Item in Clipboard
Three new genetic loci (R1210C in CFH, variants in COL8A1 and RAD51B) are independently related to progression to advanced macular degeneration.
Seddon JM, Reynolds R, Yu Y, Rosner B.
Seddon JM, et al.
PLoS One. 2014 Jan 31;9(1):e87047. doi: 10.1371/journal.pone.0087047. eCollection 2014.
PLoS One. 2014.
PMID: 24498017
Free PMC article.
Item in Clipboard
Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome.
Manuelian T, Hellwage J, Meri S, Caprioli J, Noris M, Heinen S, Jozsi M, Neumann HP, Remuzzi G, Zipfel PF.
Manuelian T, et al.
J Clin Invest. 2003 Apr;111(8):1181-90. doi: 10.1172/JCI16651.
J Clin Invest. 2003.
PMID: 12697737
Free PMC article.
Item in Clipboard
Analysis of rare variants in the CFH gene in patients with the cuticular drusen subtype of age-related macular degeneration.
Duvvari MR, Saksens NT, van de Ven JP, de Jong-Hesse Y, Schick T, Nillesen WM, Fauser S, Hoefsloot LH, Hoyng CB, de Jong EK, den Hollander AI.
Duvvari MR, et al.
Mol Vis. 2015 Mar 15;21:285-92. eCollection 2015.
Mol Vis. 2015.
PMID: 25814826
Free PMC article.
Item in Clipboard
Identification of a rare coding variant in complement 3 associated with age-related macular degeneration.
Zhan X, Larson DE, Wang C, Koboldt DC, Sergeev YV, Fulton RS, Fulton LL, Fronick CC, Branham KE, Bragg-Gresham J, Jun G, Hu Y, Kang HM, Liu D, Othman M, Brooks M, Ratnapriya R, Boleda A, Grassmann F, von Strachwitz C, Olson LM, Buitendijk GH, Hofman A, van Duijn CM, Cipriani V, Moore AT, Shahid H, Jiang Y, Conley YP, Morgan DJ, Kim IK, Johnson MP, Cantsilieris S, Richardson AJ, Guymer RH, Luo H, Ouyang H, Licht C, Pluthero FG, Zhang MM, Zhang K, Baird PN, Blangero J, Klein ML, Farrer LA, DeAngelis MM, Weeks DE, Gorin MB, Yates JR, Klaver CC, Pericak-Vance MA, Haines JL, Weber BH, Wilson RK, Heckenlively JR, Chew EY, Stambolian D, Mardis ER, Swaroop A, Abecasis GR.
Zhan X, et al.
Nat Genet. 2013 Nov;45(11):1375-9. doi: 10.1038/ng.2758. Epub 2013 Sep 15.
Nat Genet. 2013.
PMID: 24036949
Free PMC article.
Item in Clipboard
Cite
Cite