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CFHR1 gene

Known as: COMPLEMENT FACTOR H-RELATED 1, FHR1, HFL1 
This gene plays a role in complement regulation.
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Abstract Age related macular degeneration (AMD) is a common form of blindness in the western world and genetic variations of… 
2017
2017
  • 2017
  • Corpus ID: 49234956
Blueprint Genetics Hemolytic Uremic Syndrome Panel (version 1, March 9, 2016) consists of sequence analysis of genes associated… 
2017
2017
Complement‐mediated atypical haemolytic uraemic syndrome (aHUS) is a rare disease with high mortality and morbidity if left… 
2016
2016
4. Caprioli J,NorisM,BrioschiSetal (2006)Geneticsof HUS: the impact ofMCP, CFH, and IFmutations on clinical presentation… 
2012
2012
In a recent GWAS, we localized five IgAN susceptibility loci on Chr.6p21 (HLADQB1/DRB1, PSMB9/TAP1, and DPA1/DPB2 loci), Chr.1q32… 
2011
2011
Copy number variations can be identified using newer genotyping arrays with higher single nucleotide polymorphisms (SNPs) density… 
2010
2010
nature genetics | volume 42 | number 7 | july 2010 553 To the Editor: Hughes et al.1 suggested that a common deletion of the… 
2007
2007
Purpose: Studies have shown geographic atrophy to be more common in Iceland than elsewhere. Several possible causes for this are…