(Q34008876)

30 July 2017

Coding variants in nephrin (NPHS1) and susceptibility to nephropathy in African Americans (English)

1 reference

30 July 2017

8

Carl D Langefeld

1 reference

30 July 2017

9

Barry I Freedman

1 reference

30 July 2017

10

Donald W Bowden

1 reference

30 July 2017

3

Nicholette D Palmer

1 reference

30 July 2017

6

Pamela J Hicks

1 reference

30 July 2017

4

Jacob M Keaton

1 reference

30 July 2017

1

Jason A Bonomo

1 reference

30 July 2017

Maggie C Y Ng

2

1 reference

PubMed ID

24948143

30 July 2017

Chris P Larsen

series ordinal

5

1 reference

PubMed ID

24948143

30 July 2017

T2D-GENES Consortium

series ordinal

7

1 reference

30 July 2017

19 June 2014

1 reference

Clinical Journal of the American Society of Nephrology

30 July 2017

1 reference

30 July 2017

9

1 reference

30 July 2017

8

1 reference

30 July 2017

1434-1440

1 reference

APOL1 risk variants, race, and progression of chronic kidney disease

30 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4123388

Gene-gene interactions in APOL1-associated nephropathy

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4123388

Insights into the genetic architecture of diabetic nephropathy

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4123388

APOL1 genetic variants in focal segmental glomerulosclerosis and HIV-associated nephropathy

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4123388

Polymorphisms in MYH9 are associated with diabetic nephropathy in European Americans

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4123388

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4123388

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4123388

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4123388

Association of trypanolytic ApoL1 variants with kidney disease in African Americans

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4123388

Nephrin-signature molecule of the glomerular podocyte?

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4123388

Nephrin is expressed on the surface of insulin vesicles and facilitates glucose-stimulated insulin release

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4123388

Ethnic differences in the relationship between albuminuria and calcified atherosclerotic plaque: the African American-diabetes heart study

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4123388

Exploration of the utility of ancestry informative markers for genetic association studies of African Americans with type 2 diabetes and end stage renal disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4123388

Nephrin mutations can cause childhood-onset steroid-resistant nephrotic syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4123388

Mutation spectrum in the nephrin gene (NPHS1) in congenital nephrotic syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4123388

Structure of the gene for congenital nephrotic syndrome of the finnish type (NPHS1) and characterization of mutations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4123388

Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4123388

Familial predisposition to nephropathy in African-Americans with non-insulin-dependent diabetes mellitus

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4123388

Nephrin gene (NPHS1) in patients with minimal change nephrotic syndrome (MCNS).

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4123388

Familial risk, age at onset, and cause of end-stage renal disease in white Americans.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4123388

Beyond odds ratios — communicating disease risk based on genetic profiles

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4123388

Nephrin mutations cause childhood- and adult-onset focal segmental glomerulosclerosis

29 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24948143

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.2215/CJN.00290114

1 reference

30 July 2017

1 reference

30 July 2017

1 reference

PubMed ID

24948143