(Q37781545)

23 August 2017

title

Genome-wide association studies in nephrology research (English)

1 reference

23 August 2017

Genome-Wide Association Studies in Nephrology Research (English)

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

genome-wide association study

20 June 2024

main subject

0 references

genetic predisposition to disease

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20728256

20 June 2024

1

Anna Köttgen

0 references

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=20728256

20 June 2024

publication date

21 August 2010

1 reference

full work available at URL

23 August 2017

https://api.elsevier.com/content/article/PII:S0272638610010371?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

https://api.elsevier.com/content/article/PII:S0272638610010371?httpAccept=text/plain

20 June 2024

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

American Journal of Kidney Diseases

20 June 2024

published in

1 reference

23 August 2017

volume

56

1 reference

23 August 2017

issue

4

1 reference

23 August 2017

page(s)

743-758

1 reference

A second generation human haplotype map of over 3.1 million SNPs

23 August 2017

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Problems of reporting genetic associations with complex outcomes

20 June 2024

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Genome-wide association studies for complex traits: consensus, uncertainty and challenges

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Genetic mapping in human disease

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Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

20 June 2024

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Unravelling the genetic basis of renal diseases; from single gene to multifactorial disorders

20 June 2024

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Susceptibility genes in common complex kidney disease

20 June 2024

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Complement factor H polymorphism in age-related macular degeneration

20 June 2024

25

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The future of genetic studies of complex human diseases

20 June 2024

26

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The Sequence of the Human Genome

20 June 2024

28

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dbSNP: the NCBI database of genetic variation

20 June 2024

29

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The International HapMap Project

20 June 2024

30

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A haplotype map of the human genome

20 June 2024

31

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Principal components analysis corrects for stratification in genome-wide association studies

20 June 2024

33

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20 June 2024

Genotype imputation

34

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GenABEL: an R library for genome-wide association analysis

20 June 2024

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A new multipoint method for genome-wide association studies by imputation of genotypes

20 June 2024

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PLINK: a tool set for whole-genome association and population-based linkage analyses

20 June 2024

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The positives, protocols, and perils of genome-wide association

20 June 2024

38

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Common statistical issues in genome-wide association studies: a review on power, data quality control, genotype calling and population structure

20 June 2024

39

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https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Estimation of the multiple testing burden for genomewide association studies of nearly all common variants

20 June 2024

41

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https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

20 June 2024

42

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

New loci associated with kidney function and chronic kidney disease

20 June 2024

43

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

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

20 June 2024

44

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

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

20 June 2024

45

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

20 June 2024

46

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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

20 June 2024

47

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

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

20 June 2024

48

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

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

20 June 2024

49

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

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

20 June 2024

50

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

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

20 June 2024

51

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

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

20 June 2024

52

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

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

20 June 2024

53

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Association of single-nucleotide polymorphisms in the polymeric immunoglobulin receptor gene with immunoglobulin A nephropathy (IgAN) in Japanese patients

20 June 2024

54

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Association of a single-nucleotide polymorphism in the immunoglobulin mu-binding protein 2 gene with immunoglobulin A nephropathy

20 June 2024

55

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Variation in IGHMBP2 is not associated with IgA nephropathy in independent studies of UK Caucasian and Chinese Han patients

20 June 2024

56

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study

20 June 2024

57

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

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

20 June 2024

58

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

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

20 June 2024

59

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density

20 June 2024

60

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

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

20 June 2024

61

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

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

20 June 2024

62

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

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

20 June 2024

63

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

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

20 June 2024

64

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Non-muscle myosin heavy chain 9 gene MYH9 associations in African Americans with clinically diagnosed type 2 diabetes mellitus-associated ESRD

20 June 2024

65

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

The association of the MYH9 gene and kidney outcomes in American Indians: the Strong Heart Family Study

20 June 2024

66

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

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

20 June 2024

67

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

African ancestry allelic variation at the MYH9 gene contributes to increased susceptibility to non-diabetic end-stage kidney disease in Hispanic Americans

20 June 2024

68

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level

20 June 2024

69

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Genetic loci influencing kidney function and chronic kidney disease

20 June 2024

70

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Genome-wide association study of hematological and biochemical traits in a Japanese population

20 June 2024

71

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium: Design of prospective meta-analyses of genome-wide association studies from 5 cohorts

20 June 2024

72

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Tamm-Horsfall glycoprotein: biology and clinical relevance

20 June 2024

74

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

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

20 June 2024

75

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Alterations of uromodulin biology: a common denominator of the genetically heterogeneous FJHN/MCKD syndrome.

20 June 2024

76

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics

20 June 2024

77

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29.

20 June 2024

78

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Methods for high-density admixture mapping of disease genes

20 June 2024

79

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Genotype-phenotype correlation in MYH9-related thrombocytopenia

20 June 2024

80

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Common disorders are quantitative traits

20 June 2024

81

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

The shroom family proteins play broad roles in the morphogenesis of thickened epithelial sheets

20 June 2024

82

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

A novel human cDNA highly homologous to the fish hormone stanniocalcin

20 June 2024

83

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Anti-inflammatory and renal protective actions of stanniocalcin-1 in a model of anti-glomerular basement membrane glomerulonephritis

20 June 2024

84

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Megalin and nonmuscle myosin heavy chain IIA interact with the adaptor protein Disabled-2 in proximal tubule cells

20 June 2024

85

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

The role of VEGF-A in glomerular development and function

20 June 2024

86

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Creatine and creatinine metabolism

20 June 2024

87

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Structure and expression of the human cystatin C gene

20 June 2024

88

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Genomewide association studies--illuminating biologic pathways

20 June 2024

89

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium

20 June 2024

90

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Finding the missing heritability of complex diseases

20 June 2024

91

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Genomic control for association studies

20 June 2024

92

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Assessing kidney function--measured and estimated glomerular filtration rate

20 June 2024

93

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

The GLUT9 gene is associated with serum uric acid levels in Sardinia and Chianti cohorts

20 June 2024

94

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

SLC2A9 influences uric acid concentrations with pronounced sex-specific effects

20 June 2024

95

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout

20 June 2024

96

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study

20 June 2024

97

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https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Plasma urate level is directly regulated by a voltage-driven urate efflux transporter URATv1 (SLC2A9) in humans

20 June 2024

98

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

SLC2A9 is a high-capacity urate transporter in humans

20 June 2024

99

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Identification of a urate transporter, ABCG2, with a common functional polymorphism causing gout

20 June 2024

100

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Uromodulin levels associate with a common UMOD variant and risk for incident CKD.

20 June 2024

101

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

Rare variants create synthetic genome-wide associations

20 June 2024

102

1 reference

https://api.crossref.org/works/10.1053/J.AJKD.2010.05.018

20 June 2024

Identifiers

1 reference

23 August 2017

1 reference