(Q46040078)

18 December 2017

title

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

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18 December 2017

author

Yurii S. Aulchenko

2

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18 December 2017

Caroline Hayward

5

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18 December 2017

Ozren Polašek

7

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18 December 2017

Thomas Meitinger

13

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18 December 2017

James F. Wilson

16

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18 December 2017

Irene Pichler

17

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18 December 2017

Andrew A Hicks

18

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18 December 2017

Fabio Marroni

24

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18 December 2017

Ivana Kolcic

Ivana Kolcic

8

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Gordan Lauc

Gordan Lauc

12

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Igor Rudan

21

Igor Rudan

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PubMed ID

19387472

18 December 2017

Cornelia M. van Duijn

22

Cornelia M van Duijn

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18 December 2017

15

Ulf Gyllensten

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18 December 2017

Harry Campbell

19

Harry Campbell

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18 December 2017

Ben A Oostra

14

Ben A Oostra

1 reference

18 December 2017

Peter P. Pramstaller

25

Peter P Pramstaller

1 reference

18 December 2017

Aaron Isaacs

3

Aaron Isaacs

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18 December 2017

Cristian Pattaro

1

Cristian Pattaro

1 reference

18 December 2017

Zrinka Biloglav

9

Zrinka Biloglav

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18 December 2017

Christopher Franklin

6

Christopher S Franklin

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18 December 2017

Nicholas D Hastie

11

Nick Hastie

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18 December 2017

Peter Riegler

23

Peter Riegler

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18 December 2017

EUROSPAN Consortium

26

EUROSPAN Consortium

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18 December 2017

author name string

Veronique Vitart

4

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18 December 2017

Susan Campbell

10

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18 December 2017

Alan F Wright

20

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18 December 2017

language of work or name

English

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publication date

22 April 2009

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18 December 2017

published in

Kidney International

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18 December 2017

volume

76

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18 December 2017

page(s)

297-306

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18 December 2017

issue

3

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18 December 2017

https://scigraph.springernature.com/pub.10.1038/ki.2009.135

exact match

0 references

cites work

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Genotype by diabetes interaction effects on the detection of linkage of glomerular filtration rate to a region on chromosome 2q in Mexican Americans

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Linkage of serum creatinine and glomerular filtration rate to chromosome 2 in Utah pedigrees

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A genome-wide linkage scan for genes controlling variation in renal function estimated by serum cystatin C levels in extended families with type 2 diabetes

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

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7 January 2021

Linkage of creatinine clearance to chromosome 10 in Utah pedigrees replicates a locus for end-stage renal disease in humans and renal failure in the fawn-hooded rat.

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Linkage analysis of glomerular filtration rate in American Indians.

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Refined mapping of suggestive linkage to renal function in African Americans: the HyperGEN study.

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

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Assessing kidney function--measured and estimated glomerular filtration rate

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7 January 2021

Use of population isolates for mapping complex traits

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7 January 2021

The value of isolated populations

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7 January 2021

Estimates of genetic and environmental contribution to 43 quantitative traits support sharing of a homogeneous environment in an isolated population from South Tyrol, Italy.

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https://api.crossref.org/works/10.1038%2FKI.2009.135

7 January 2021

Use of isolated inbred human populations for identification of disease genes

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7 January 2021

Population isolates: their special value for locating genes for bipolar disorder

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7 January 2021

Use of isolated populations in the study of a human obesity syndrome, the Bardet-Biedl syndrome

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7 January 2021

Using standardized serum creatinine values in the modification of diet in renal disease study equation for estimating glomerular filtration rate

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7 January 2021

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

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7 January 2021

Genetic and physical mapping of the locus for autosomal dominant renal Fanconi syndrome, on chromosome 15q15.3.

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7 January 2021

A genome-wide linkage scan for genes controlling variation in urinary albumin excretion in type II diabetes

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7 January 2021

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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https://api.crossref.org/works/10.1038%2FKI.2009.135

7 January 2021

Measuring inconsistency in meta-analyses

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https://api.crossref.org/works/10.1038%2FKI.2009.135

7 January 2021

The effects of inheritance on constituents of plasma: a twin study on some biochemical variables

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7 January 2021

Polymorphisms in IGF-binding protein 1 are associated with impaired renal function in type 2 diabetes.

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7 January 2021

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

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7 January 2021

Gene expression profiling in glomeruli from human kidneys with diabetic nephropathy.

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7 January 2021

Creatine and creatinine metabolism

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7 January 2021

Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis

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7 January 2021

The genetic study of three population microisolates in South Tyrol (MICROS): study design and epidemiological perspectives

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https://api.crossref.org/works/10.1038%2FKI.2009.135

7 January 2021

The Effect of Genetic Drift in a Young Genetically Isolated Population

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https://api.crossref.org/works/10.1038%2FKI.2009.135

7 January 2021

3000 years of solitude: extreme differentiation in the island isolates of Dalmatia, Croatia.

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https://api.crossref.org/works/10.1038%2FKI.2009.135

7 January 2021

A high-resolution recombination map of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.135

7 January 2021

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

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https://api.crossref.org/works/10.1038%2FKI.2009.135

7 January 2021

PEDSTATS: descriptive statistics, graphics and quality assessment for gene mapping data

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https://api.crossref.org/works/10.1038%2FKI.2009.135

7 January 2021

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

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https://api.crossref.org/works/10.1038%2FKI.2009.135

7 January 2021

Multipoint quantitative-trait linkage analysis in general pedigrees

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https://api.crossref.org/works/10.1038%2FKI.2009.135

7 January 2021

Testing the robustness of the likelihood-ratio test in a variance-component quantitative-trait loci-mapping procedure

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https://api.crossref.org/works/10.1038%2FKI.2009.135

7 January 2021

Robust LOD scores for variance component-based linkage analysis

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https://api.crossref.org/works/10.1038%2FKI.2009.135

7 January 2021

GenABEL: an R library for genome-wide association analysis

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https://api.crossref.org/works/10.1038%2FKI.2009.135

7 January 2021

Identifiers

DOI

10.1038/KI.2009.135

1 reference

18 December 2017

PubMed ID

19387472

1 reference

18 December 2017