Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with albuminuria in hypertensive African Americans: the HyperGEN study (Q37359254)

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scientific article published on 20 January 2009

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English	Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with albuminuria in hypertensive African Americans: the HyperGEN study	scientific article published on 20 January 2009

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with albuminuria in hypertensive African Americans: the HyperGEN study (English)

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Jeffrey B. Kopp

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Jeffrey B Kopp

2

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11

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Steven C Hunt

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Europe PubMed Central

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19 August 2017

Cheryl A Winkler

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Cheryl A Winkler

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19 August 2017

Carl D. Langefeld

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Carl D Langefeld

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Barry I Freedman

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Jasmin Divers

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Europe PubMed Central

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19 August 2017

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Pamela J Hicks

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19 August 2017

author name string

George W Nelson

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19 August 2017

D C Rao

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Europe PubMed Central

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19 August 2017

John H Eckfeldt

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19 August 2017

Mark F Leppert

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19 August 2017

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publication date

20 January 2009

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19 August 2017

American Journal of Nephrology

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19 August 2017

29

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19 August 2017

6

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19 August 2017

626-632

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19 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2749685

6 September 2017

Hypertension-associated kidney disease: perhaps no more

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2749685

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2749685

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2749685

6 September 2017

Long-term effects of renin-angiotensin system-blocking therapy and a low blood pressure goal on progression of hypertensive chronic kidney disease in African Americans

1 reference

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6 September 2017

Actin up: regulation of podocyte structure and function by components of the actin cytoskeleton

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TRPC6 and FSGS: the latest TRP channelopathy

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A New Statistical Method for Haplotype Reconstruction from Population Data

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6 September 2017

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

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6 September 2017

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

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6 September 2017

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

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6 September 2017

Population-based screening for family history of end-stage renal disease among incident dialysis patients

1 reference

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14 September 2017

The link between hypertension and nephrosclerosis

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14 September 2017

NHLBI family blood pressure program: methodology and recruitment in the HyperGEN network. Hypertension genetic epidemiology network

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28 September 2017

Clinical documentation of end-stage renal disease due to hypertension

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2749685

28 September 2017

Accuracy of the diagnosis of hypertensive nephrosclerosis in African Americans: a report from the African American Study of Kidney Disease (AASK) Trial. AASK Pilot Study Investigators

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26 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2749685

26 June 2018

Renal function change in hypertensive members of the Multiple Risk Factor Intervention Trial. Racial and treatment effects. The MRFIT Research Group

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26 June 2018

Hypertensive nephrosclerosis in African Americans versus Caucasians

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2749685

2 September 2018

Effect of ramipril vs amlodipine on renal outcomes in hypertensive nephrosclerosis: a randomized controlled trial

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2 September 2018

Race and end-stage renal disease. Socioeconomic status and access to health care as mediating factors

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2 September 2018

Renal biopsy findings in presumed hypertensive nephrosclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19153477

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Blood pressure and end-stage renal disease in men

1 reference

https://pubmed.ncbi.nlm.nih.gov/19153477

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inaccuracy of clinical phenotyping parameters for hypertensive nephrosclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19153477

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Renal insufficiency in treated essential hypertension

1 reference

https://pubmed.ncbi.nlm.nih.gov/19153477

12 December 2020

based on heuristic

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Prognostic value of serum creatinine and effect of treatment of hypertension on renal function. Results from the hypertension detection and follow-up program. The Hypertension Detection and Follow-up Program Cooperative Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/19153477

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1159/000194791

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

ResearchGate publication ID

0 references

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