The genetics of common kidney disease: a pathway toward clinical relevance. (Q37895457)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21712849 AND SRC:MED&resulttype=core&format=json

6 February 2020

review article

1 reference

title

The genetics of common kidney disease: a pathway toward clinical relevance (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21712849 AND SRC:MED&resulttype=core&format=json

6 February 2020

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21712849 AND SRC:MED&resulttype=core&format=json

6 February 2020

author name string

John R Sedor

series ordinal

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21712849 AND SRC:MED&resulttype=core&format=json

6 February 2020

language of work or name

English

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publication date

28 June 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21712849 AND SRC:MED&resulttype=core&format=json

Nature Reviews Nephrology

6 February 2020

published in

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21712849 AND SRC:MED&resulttype=core&format=json

6 February 2020

volume

7

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21712849 AND SRC:MED&resulttype=core&format=json

6 February 2020

issue

8

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21712849 AND SRC:MED&resulttype=core&format=json

6 February 2020

page(s)

458-468

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21712849 AND SRC:MED&resulttype=core&format=json

‘Mendelian randomization’: can genetic epidemiology contribute to understanding environmental determinants of disease?*

6 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Genome-wide linkage analysis of serum creatinine in three isolated European populations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

A genome-wide search for linkage to renal function phenotypes in West Africans with type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Mining the genome for susceptibility to diabetic nephropathy: the role of large-scale studies and consortia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Genetics of diabetes and its complications

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Genetic mapping in human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

New loci associated with kidney function and chronic kidney disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Genetic factors in common complex renal and cardiovascular diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Molecular genetic approaches for studying the etiology of diabetic nephropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Discovery and validation of new molecular targets in treating dyslipidemia: the role of human genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Complement factor H polymorphism and age-related macular degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Complement factor H polymorphism in age-related macular degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Genome-Wide Association Studies in Nephrology Research

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Common genetic variation and human traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Genetic heterogeneity in human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Genome-wide association study of blood pressure and hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Genome-wide association study identifies eight loci associated with blood pressure

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Rare independent mutations in renal salt handling genes contribute to blood pressure variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Multiple loci associated with indices of renal function and chronic kidney disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Genetic loci influencing kidney function and chronic kidney disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Identification of PVT1 as a candidate gene for end-stage renal disease in type 2 diabetes using a pooling-based genome-wide single nucleotide polymorphism association study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Variants in the plasmacytoma variant translocation gene (PVT1) are associated with end-stage renal disease attributed to type 1 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Genetic variations in the gene encoding ELMO1 are associated with susceptibility to diabetic nephropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Confirmation of genetic associations at ELMO1 in the GoKinD collection supports its role as a susceptibility gene in diabetic nephropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Variants in intron 13 of the ELMO1 gene are associated with diabetic nephropathy in African Americans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Evidence for a gene influencing blood pressure on chromosome 17. Genome scan linkage results for longitudinal blood pressure phenotypes in subjects from the framingham heart study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

A genome-wide association study of hypertension and blood pressure in African Americans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Blood pressure and hypertension are associated with 7 loci in the Japanese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Molecular mechanisms of human hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

The spectrum of MYH9-associated nephropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Hypertension-associated kidney disease: perhaps no more

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Association of trypanolytic ApoL1 variants with kidney disease in African Americans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

A risk allele for focal segmental glomerulosclerosis in African Americans is located within a region containing APOL1 and MYH9

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

The APOL1 Gene and Allograft Survival after Kidney Transplantation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Finding the missing heritability of complex diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Hints of hidden heritability in GWAS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Common SNPs explain a large proportion of the heritability for human height

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Personal genomes: The case of the missing heritability

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Transgenerational genetic effects on phenotypic variation and disease risk

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Missing heritability and strategies for finding the underlying causes of complex disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Genomewide association studies and assessment of the risk of disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Polymorphisms associated with cholesterol and risk of cardiovascular events

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Comparative effects of lovastatin and niacin in primary hypercholesterolemia. A prospective trial.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Rare variants create synthetic genome-wide associations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Predicting type 2 diabetes based on polymorphisms from genome-wide association studies: a population-based study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Assessing the combined impact of 18 common genetic variants of modest effect sizes on type 2 diabetes risk

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Clinical risk factors, DNA variants, and the development of type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Utility of genetic and non-genetic risk factors in prediction of type 2 diabetes: Whitehall II prospective cohort study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Advances in measuring the effect of individual predictors of cardiovascular risk: the role of reclassification measures

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Evaluating the added predictive ability of a new marker: from area under the ROC curve to reclassification and beyond

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

SCreening for Occult REnal Disease (SCORED): a simple prediction model for chronic kidney disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

A simple algorithm to predict incident kidney disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Predicting the Risk of Dialysis and Transplant Among Patients With CKD: A Retrospective Cohort Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Risk scores for predicting outcomes in patients with type 2 diabetes and nephropathy: the RENAAL study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

A prediction model for the risk of incident chronic kidney disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Predicting the risk of chronic Kidney Disease in men and women in England and Wales: prospective derivation and external validation of the QKidney Scores

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

A predictive model for progression of chronic kidney disease to kidney failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

TCF7L2 polymorphisms and progression to diabetes in the Diabetes Prevention Program

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Variation in TCF7L2 influences therapeutic response to sulfonylureas: a GoDARTs study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Outcomes in hypertensive black and nonblack patients treated with chlorthalidone, amlodipine, and lisinopril.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Renin angiotensin system gene polymorphisms modify angiotensin-converting enzyme inhibitors' effect on cognitive function: the health, aging and body composition study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Pharmacogenetic association of the angiotensin-converting enzyme insertion/deletion polymorphism on blood pressure and cardiovascular risk in relation to antihypertensive treatment: the Genetics of Hypertension-Associated Treatment (GenHAT) study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Pharmacogenetic association of the NPPA T2238C genetic variant with cardiovascular disease outcomes in patients with hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Targeted capture and massively parallel sequencing of 12 human exomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Functional characterization of genetic variants in NPC1L1 supports the sequencing extremes strategy to identify complex trait genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Clinical assessment incorporating a personal genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

A systematic review of perceived risks, psychological and behavioral impacts of genetic testing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

An agenda for personalized medicine

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Genetic variation at the SLC12A3 locus is unlikely to explain risk for advanced diabetic nephropathy in Caucasians with type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

A multi-marker approach to predict incident CKD and microalbuminuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

ELMO1 variants and susceptibility to diabetic nephropathy in American Indians

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Genetics of Chronic Kidney Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Individual genomes on the horizon

31 March 2020

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Genomewide association studies--illuminating biologic pathways

31 March 2020

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Uromodulin and translational medicine: will the SNPs bring zip to clinical practice?

31 March 2020

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

31 March 2020

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Genetic risk prediction--are we there yet?

31 March 2020

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

The limitations of risk factors as prognostic tools

31 March 2020

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Risks of presymptomatic direct-to-consumer genetic testing

31 March 2020

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Preparing for a Consumer-Driven Genomic Age

31 March 2020

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Sequence variants in the PLEKHH2 region are associated with diabetic nephropathy in the GoKinD study population

31 March 2020

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Genome-wide SNP genotyping study using pooled DNA to identify candidate markers mediating susceptibility to end-stage renal disease attributed to Type 1 diabetes

31 March 2020

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Association of solute carrier family 12 (sodium/chloride) member 3 with diabetic nephropathy, identified by genome-wide analyses of single nucleotide polymorphisms

31 March 2020

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Genome-wide association study for renal traits in the Framingham Heart and Atherosclerosis Risk in Communities Studies

31 March 2020

1 reference

https://api.crossref.org/works/10.1038/NRNEPH.2011.85

Renin-angiotensin system gene polymorphisms influence blood pressure and the response to angiotensin converting enzyme inhibition.

31 March 2020

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21712849

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Expression of the nonmuscle myosin heavy chain IIA in the human kidney and screening for MYH9 mutations in Epstein and Fechtner syndromes

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21712849

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NRNEPH.2011.85

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21712849 AND SRC:MED&resulttype=core&format=json

release_hncyvhvysbampcr36af5ajsuva

6 February 2020

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/hncyvhvysbampcr36af5ajsuva

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference