(Q43905998)

27 November 2017

Complement factor H polymorphisms, renal phenotypes and age-related macular degeneration: the Blue Mountains Eye Study (English)

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27 November 2017

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1

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27 November 2017

T A Sivakumaran

2

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27 November 2017

J J Wang

3

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27 November 2017

E Rochtchina

4

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27 November 2017

T Joshi

5

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27 November 2017

W Smith

6

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27 November 2017

P Mitchell

7

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27 November 2017

S K Iyengar

8

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27 November 2017

language of work or name

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13 March 2008

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27 November 2017

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27 November 2017

9

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27 November 2017

3

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27 November 2017

231-239

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https://scigraph.springernature.com/pub.10.1038/gene.2008.10

27 November 2017

0 references

cites work

Structure and composition of drusen associated with glomerulonephritis: implications for the role of complement activation in drusen biogenesis.

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

A more accurate method to estimate glomerular filtration rate from serum creatinine: a new prediction equation. Modification of Diet in Renal Disease Study Group

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

Prevalence of age-related maculopathy in Australia. The Blue Mountains Eye Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

The Wisconsin age-related maculopathy grading system

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

The simple design of complement factor H: Looks can be deceiving

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

The human complement factor H: functional roles, genetic variations and disease associations

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Complement and diseases: defective alternative pathway control results in kidney and eye diseases

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Visual impairment caused by retinal abnormalities in mesangiocapillary (membranoproliferative) glomerulonephritis type II ("dense deposit disease")

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Fundus changes in (type II) mesangiocapillary glomerulonephritis simulating drusen: a histopathological report

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Fundus changes in mesangiocapillary glomerulonephritis type II: clinical and fluorescein angiographic findings

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Drusen associated with aging and age-related macular degeneration contain proteins common to extracellular deposits associated with atherosclerosis, elastosis, amyloidosis, and dense deposit disease

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Variations in the complement regulatory genes factor H (CFH) and factor H related 5 (CFHR5) are associated with membranoproliferative glomerulonephritis type II (dense deposit disease)

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Spontaneous hemolytic uremic syndrome triggered by complement factor H lacking surface recognition domains

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

The interactive Factor H-atypical hemolytic uremic syndrome mutation database and website: update and integration of membrane cofactor protein and Factor I mutations with structural models

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

An interactive web database of factor H-associated hemolytic uremic syndrome mutations: insights into the structural consequences of disease-associated mutations

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Critical role of the C-terminal domains of factor H in regulating complement activation at cell surfaces

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

A common site within factor H SCR 7 responsible for binding heparin, C-reactive protein and streptococcal M protein.

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Disease-associated sequence variations congregate in a polyanion recognition patch on human factor H revealed in three-dimensional structure

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Molecular modelling of the C-terminal domains of factor H of human complement: a correlation between haemolytic uraemic syndrome and a predicted heparin binding site

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Complement factor H polymorphism and age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Complement factor H variant increases the risk of age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Complement factor H polymorphism in age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Linkage of a gene causing familial membranoproliferative glomerulonephritis type III to chromosome 1

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Mapping a gene (SRN1) to chromosome 1q25-q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosis.

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

The gene for human fibronectin glomerulopathy maps to 1q32, in the region of the regulation of complement activation gene cluster

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Mouse podocyte complement factor H: the functional analog to human complement receptor 1

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Hereditary porcine membranoproliferative glomerulonephritis type II is caused by factor H deficiency

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Uncontrolled C3 activation causes membranoproliferative glomerulonephritis in mice deficient in complement factor H

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

CKD increases the risk of age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Genomewide linkage analysis to serum creatinine, GFR, and creatinine clearance in a community-based population: the Framingham Heart Study

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Linkage of serum creatinine and glomerular filtration rate to chromosome 2 in Utah pedigrees

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Complement factor H and hemicentin-1 in age-related macular degeneration and renal phenotypes

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

A haplotype map of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Prediction of creatinine clearance from serum creatinine

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

A Comparison of Prediction Equations for Estimating Glomerular Filtration Rate in Adults without Kidney Disease

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Performance of the modification of diet in renal disease and Cockcroft-Gault equations in the estimation of GFR in health and in chronic kidney disease

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Analysis of the Y402H variant of the complement factor H gene in age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Complement factor H polymorphism, complement activators, and risk of age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Assessment of the contribution of CFH and chromosome 10q26 AMD susceptibility loci in a Russian population isolate.

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

CFH Y402H confers similar risk of soft drusen and both forms of advanced AMD

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

CFH, ELOVL4, PLEKHA1 and LOC387715 genes and susceptibility to age-related maculopathy: AREDS and CHS cohorts and meta-analyses

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

A prospective assessment of the Y402H variant in complement factor H, genetic variants in C-reactive protein, and risk of age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Use and misuse of population attributable fractions.

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Unraveling a complex genetic disease: age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

HTRA1 promoter polymorphism in wet age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Variation in factor B (BF) and complement component 2 (C2) genes is associated with age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

A common CFH haplotype, with deletion of CFHR1 and CFHR3, is associated with lower risk of age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Common variation in three genes, including a noncoding variant in CFH, strongly influences risk of age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Variation in complement factor 3 is associated with risk of age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

A variant of the HTRA1 gene increases susceptibility to age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

National Kidney Foundation practice guidelines for chronic kidney disease: evaluation, classification, and stratification

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

An international classification and grading system for age-related maculopathy and age-related macular degeneration. The International ARM Epidemiological Study Group

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Longitudinal data analysis for discrete and continuous outcomes

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Best linear unbiased allele-frequency estimation in complex pedigrees.

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Haploview: analysis and visualization of LD and haplotype maps

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Case-control single-marker and haplotypic association analysis of pedigree data

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Score tests for association between traits and haplotypes when linkage phase is ambiguous

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.10

7 January 2021

Identifiers

DOI

10.1038/GENE.2008.10

1 reference

27 November 2017

1 reference