Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 234,380,342 papers from all fields of science
Search
Sign In
Create Free Account
CFHR1 gene
Known as:
COMPLEMENT FACTOR H-RELATED 1
, FHR1
, HFL1
Expand
This gene plays a role in complement regulation.
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
6 relations
CFH gene
CFH wt Allele
CFHR1 protein, human
CFHR3 gene
Expand
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Chapter 2 The Role of Complement in AMD
P. Zipfel
,
N. Lauer
,
C. Skerka
2019
Corpus ID: 102505388
Abstract Age related macular degeneration (AMD) is a common form of blindness in the western world and genetic variations of…
Expand
2017
2017
Hemolytic Uremic Syndrome Panel REFERRING HEALTHCARE PROFESSIONAL
2017
Corpus ID: 49234956
Blueprint Genetics Hemolytic Uremic Syndrome Panel (version 1, March 9, 2016) consists of sequence analysis of genes associated…
Expand
2017
2017
Indications of underdiagnosis of atypical haemolytic uraemic syndrome in a cohort referred to the Coagulation Unit in Malmo, Sweden, for analysis of ADAMTS13 2007–2012
A. Åkesson
,
A. Blom
,
J. Klintman
,
E. Zetterberg
Nephrology
2017
Corpus ID: 10482969
Complement‐mediated atypical haemolytic uraemic syndrome (aHUS) is a rare disease with high mortality and morbidity if left…
Expand
2016
2016
Erratum zu: „Klug entscheiden“ bei Infektionskrankheiten
N. Jung
,
H. Koop
,
R. Riessen
,
J. Galle
,
B. Jany
,
E. Märker-Hermann
Der Internist
2016
Corpus ID: 9313791
4. Caprioli J,NorisM,BrioschiSetal (2006)Geneticsof HUS: the impact ofMCP, CFH, and IFmutations on clinical presentation…
Expand
2013
2013
Glomerular disease: Familial CFHR1 mutation identified in C3 glomerulopathy
Nature Reviews Nephrology
2013
Corpus ID: 43294708
2012
2012
2) INTERFERON REGULATED IMMUNOPROTEASOMES IN CLINICAL AND PATHOLOGY FEATURES OF PATIENTS WITH IGAN. GENETIC AND PHENOTYPIC STUDY
A. Gharavi
,
Krzysztof Kiryluc
,
R. Coppo
,
A. Amore
,
L. Turin
2012
Corpus ID: 813145
In a recent GWAS, we localized five IgAN susceptibility loci on Chr.6p21 (HLADQB1/DRB1, PSMB9/TAP1, and DPA1/DPB2 loci), Chr.1q32…
Expand
2011
2011
Copy number polymorphisms in new HapMap III and Singapore populations
C. Ku
,
S. Teo
,
+6 authors
A. Salim
Journal of Human Genetics
2011
Corpus ID: 9979430
Copy number variations can be identified using newer genotyping arrays with higher single nucleotide polymorphisms (SNPs) density…
Expand
2010
2010
Associations of CFHR 1 – CFHR 3 deletion and a CFH snp to age-related macular degeneration
S. Raychaudhuri
,
S. Ripke
,
+8 authors
M. Daly
2010
Corpus ID: 291704
nature genetics | volume 42 | number 7 | july 2010 553 To the Editor: Hughes et al.1 suggested that a common deletion of the…
Expand
2007
2007
Why is geographic atrophy more common in Iceland than in other white populations.
F. Jónasson
2007
Corpus ID: 71090404
Purpose: Studies have shown geographic atrophy to be more common in Iceland than elsewhere. Several possible causes for this are…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE