(Q35675247)

9 August 2017

title

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

1 reference

9 August 2017

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Rebekah S Rasooly

10

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Man Li

Man Li

3

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Sudha Iyengar

Sudha K Iyengar

6

0 references

Erwin Böttinger

16

Erwin P Bottinger

1 reference

9 August 2017

Josef Coresh

12

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9 August 2017

22

Carl D Langefeld

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9 August 2017

25

Barry I Freedman

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9 August 2017

24

Donald W Bowden

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9 August 2017

21

Pamela J Hicks

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9 August 2017

2

W H Linda Kao

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9 August 2017

23

Rulan S Parekh

1 reference

9 August 2017

8

Robert L Hanson

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9 August 2017

1

Meredith A Bostrom

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9 August 2017

17

Michael S Lipkowitz

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9 August 2017

11

John R Sedor

1 reference

9 August 2017

9

Susanne B Nicholas

1 reference

9 August 2017

18

Lucy A Meoni

1 reference

9 August 2017

13

Orly F Kohn

1 reference

9 August 2017

14

David J Leehey

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9 August 2017

Denyse P Thornley-Brown

15

Denyse Thornley-Brown

1 reference

9 August 2017

20

Lingyi Lu

1 reference

9 August 2017

Hanna E Abboud

4

1 reference

9 August 2017

Sharon G Adler

5

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9 August 2017

Paul L Kimmel

7

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9 August 2017

Michael J Klag

19

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9 August 2017

Family Investigation of Nephropathy and Diabetes (FIND) Research Group

26

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9 August 2017

language of work or name

1 reference

25 November 2011

1 reference

American Journal of Kidney Diseases

9 August 2017

published in

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9 August 2017

volume

59

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9 August 2017

issue

2

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9 August 2017

page(s)

210-221

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Identification of the nephropathy-susceptibility locus HIVAN4

9 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

Genome-wide association study identifies susceptibility loci for IgA nephropathy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

The apolipoprotein L1 (APOL1) gene and nondiabetic nephropathy in African Americans

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

Association of trypanolytic ApoL1 variants with kidney disease in African Americans

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

Candidate genes for non-diabetic ESRD in African Americans: a genome-wide association study using pooled DNA.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

Genetic loci influencing kidney function and chronic kidney disease

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

Podocin inactivation in mature kidneys causes focal segmental glomerulosclerosis and nephrotic syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

Susceptibility loci for murine HIV-associated nephropathy encode trans-regulators of podocyte gene expression

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

INSIG2 SNPs associated with obesity and glucose homeostasis traits in Hispanics: the IRAS Family Study

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

Polymorphisms in the non-muscle myosin heavy chain 9 gene (MYH9) are strongly associated with end-stage renal disease historically attributed to hypertension in African Americans

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

MYH9 is associated with nondiabetic end-stage renal disease in African Americans

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

Polymorphisms in the 3' UTR in the neurocalcin delta gene affect mRNA stability, and confer susceptibility to diabetic nephropathy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

Admixture mapping of an allele affecting interleukin 6 soluble receptor and interleukin 6 levels

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

NPHS2 R229Q functional variant is associated with microalbuminuria in the general population

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

Patient's view of dialysis care: development of a taxonomy and rating of importance of different aspects of care. CHOICE study. Choices for Healthy Outcomes in Caring for ESRD.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

The familial risk of end-stage renal disease in African Americans

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

A multiple testing correction method for genetic association studies using correlated single nucleotide polymorphisms

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2).

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259209

A genome scan for ESRD in black families enriched for nondiabetic nephropathy

25 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22119407

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1053/J.AJKD.2011.09.020

1 reference

9 August 2017

1 reference

9 August 2017

1 reference