(Q30384517)

5 November 2017

Complement factor H gene associations with end-stage kidney disease in African Americans. (English)

1 reference

5 November 2017

5

Mark D Okusa

1 reference

5 November 2017

6

Carl D Langefeld

1 reference

5 November 2017

8

Barry I Freedman

1 reference

5 November 2017

7

Donald W Bowden

1 reference

5 November 2017

2

Nicholette D Palmer

1 reference

5 November 2017

3

Pamela J Hicks

1 reference

5 November 2017

4

Janice P Lea

1 reference

5 November 2017

1

Jason A Bonomo

1 reference

PMCID

4081633

5 November 2017

language of work or name

English

0 references

publication date

28 February 2014

1 reference

Nephrology Dialysis Transplantation

5 November 2017

1 reference

5 November 2017

29

1 reference

5 November 2017

1409-1414

1 reference

5 November 2017

7

1 reference

Socioeconomic factors and racial disparities in kidney disease outcomes

5 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4081633

Determining the population frequency of the CFHR3/CFHR1 deletion at 1q32.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4081633

Pathogenesis of immunoglobulin A nephropathy: recent insight from genetic studies

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4081633

Geographic differences in genetic susceptibility to IgA nephropathy: GWAS replication study and geospatial risk analysis

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4081633

Genetic association and gene-gene interaction analyses in African American dialysis patients with nondiabetic nephropathy

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4081633

Rare-variant association testing for sequencing data with the sequence kernel association test

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4081633

Differential effects of MYH9 and APOL1 risk variants on FRMD3 Association with Diabetic ESRD in African Americans

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4081633

Association of genetic variants in complement factor H and factor H-related genes with systemic lupus erythematosus susceptibility

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4081633

Genome-wide association study identifies susceptibility loci for IgA nephropathy

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4081633

A genome-wide association study for diabetic nephropathy genes in African Americans

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4081633

Coincident idiopathic focal segmental glomerulosclerosis collapsing variant and diabetic nephropathy in an African American homozygous for MYH9 risk variants

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4081633

Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4081633

Association of trypanolytic ApoL1 variants with kidney disease in African Americans

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4081633

Association of factor H autoantibodies with deletions of CFHR1, CFHR3, CFHR4, and with mutations in CFH, CFI, CD46, and C3 in patients with atypical hemolytic uremic syndrome

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4081633

Genetic variation in an individual human exome

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4081633

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)

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4081633

Complement factor H polymorphism in age-related macular degeneration

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4081633

Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4081633

The link between hypertension and nephrosclerosis

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4081633

Functions and mechanism of action of complement

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4081633

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4081633

Complement Factor H Limits Immune Complex Deposition and Prevents Inflammation and Scarring in Glomeruli of Mice with Chronic Serum Sickness

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24586071

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

1 reference

https://pubmed.ncbi.nlm.nih.gov/24586071

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Inaccuracy of clinical phenotyping parameters for hypertensive nephrosclerosis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24586071

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/NDT/GFU036

1 reference

5 November 2017

1 reference

5 November 2017

1 reference

PMCID

4081633