(Q34170453)

31 July 2017

title

Genome-wide association study identifies susceptibility loci for IgA nephropathy (English)

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genome-wide association study

31 July 2017

main subject

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Francesca Lugani

28

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Yifu Li

Yifu Li

4

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Riccardo Magistroni

Riccardo Magistroni

25

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Robert Wyatt

Robert J Wyatt

10

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Antonio Amoroso

Antonio Amoroso

45

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Gian Marco Ghiggeri

Gian Marco Ghiggeri

26

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Krzysztof Kiryluk

2

Krzysztof Kiryluk

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31 July 2017

16

Weiming Wang

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31 July 2017

Ali G Gharavi

1

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Murim Choi

3

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31 July 2017

Ping Hou

5

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Jingyuan Xie

6

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Simone Sanna-Cherchi

7

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Clara J Men

8

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Bruce A Julian

9

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Jan Novak

11

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John C He

12

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Haiyan Wang

13

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31 July 2017

Jicheng Lv

14

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Li Zhu

15

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31 July 2017

Zhaohui Wang

17

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Kasuhito Yasuno

18

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Murat Gunel

19

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Shrikant Mane

20

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Sheila Umlauf

21

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Irina Tikhonova

22

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31 July 2017

Isabel Beerman

23

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Silvana Savoldi

24

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Monica Bodria

27

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Pietro Ravani

29

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Claudio Ponticelli

30

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Landino Allegri

31

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Giuliano Boscutti

32

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Giovanni Frasca

33

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Alessandro Amore

34

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Licia Peruzzi

35

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Rosanna Coppo

36

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Claudia Izzi

37

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Battista Fabio Viola

38

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31 July 2017

Elisabetta Prati

39

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Maurizio Salvadori

40

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31 July 2017

Renzo Mignani

41

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31 July 2017

Loreto Gesualdo

42

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Francesca Bertinetto

43

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Paola Mesiano

44

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Francesco Scolari

46

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Nan Chen

47

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Hong Zhang

48

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Richard P Lifton

49

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31 July 2017

language of work or name

English

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publication date

13 March 2011

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31 July 2017

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31 July 2017

volume

43

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31 July 2017

issue

4

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31 July 2017

page(s)

321-327

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describes a project that uses

31 July 2017

genome-wide association study

1 reference

Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency

inferred from title

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

HLA has strongest association with IgA nephropathy in genome-wide analysis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

Associations of CFHR1-CFHR3 deletion and a CFH SNP to age-related macular degeneration are not independent

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

Genetic studies of IgA nephropathy: past, present, and future.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

A composite of multiple signals distinguishes causal variants in regions of positive selection

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

HLA-DPB1 and DPB2 are genetic loci for systemic sclerosis: a genome-wide association study in Koreans with replication in North Americans

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

Common variants at five new loci associated with early-onset inflammatory bowel disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

Mouse HORMAD1 and HORMAD2, two conserved meiotic chromosomal proteins, are depleted from synapsed chromosome axes with the help of TRIP13 AAA-ATPase

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regions

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

Report of the Asian Forum of Chronic Kidney Disease Initiative (AFCKDI) 2007. "Current status and perspective of CKD in Asia": diversity and specificity among Asian countries

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

Whole population, genome-wide mapping of hidden relatedness

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

Aberrant IgA1 glycosylation is inherited in familial and sporadic IgA nephropathy

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

HLA DR-DQ haplotypes and genotypes and type 1 diabetes risk: analysis of the type 1 diabetes genetics consortium families

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

Prevalence of chronic kidney disease in the United States

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

Complement factor H and the hemolytic uremic syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

Genetic heterogeneity in Italian families with IgA nephropathy: suggestive linkage for two novel IgA nephropathy loci

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

A common CFH haplotype, with deletion of CFHR1 and CFHR3, is associated with lower risk of age-related macular degeneration

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

Common variation in three genes, including a noncoding variant in CFH, strongly influences risk of age-related macular degeneration

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

The Italian experience of the national registry of renal biopsies

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

Statistical significance for genomewide studies

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

Incidence of latent mesangial IgA deposition in renal allograft donors in Japan

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

Complex HLA-DR and -DQ interactions confer risk of narcolepsy-cataplexy in three ethnic groups

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

Circulating immune complexes in IgA nephropathy consist of IgA1 with galactose-deficient hinge region and antiglycan antibodies

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

Immunoglobulin and complement deposition in glomeruli of 756 subjects who had committed suicide or met with a violent death

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

The commonest glomerulonephritis in the world: IgA nephropathy.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412515

Galactose-deficient IgA1 in African Americans with IgA nephropathy: serum levels and heritability

28 July 2018

1 reference

Aberrant galactosylation of IgA1 is involved in the genetic susceptibility of Chinese patients with IgA nephropathy.

21 January 2018

1 reference

IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22-23.

21 January 2018

1 reference

Genome-Wide Linkage Scan of a Large Family with IgA Nephropathy Localizes a Novel Susceptibility Locus to Chromosome 2q36

21 January 2018

1 reference

Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease

21 January 2018

1 reference

A genome-wide association study identifies variants in the HLA-DP locus associated with chronic hepatitis B in Asians.

21 January 2018

1 reference

A genome-wide study identifies HLA alleles associated with lumiracoxib-related liver injury

21 January 2018

1 reference

Cytoplasmic domains of the transporter associated with antigen processing and P-glycoprotein interact with subunits of the proteasome

21 January 2018

1 reference

A selective inhibitor of the immunoproteasome subunit LMP7 blocks cytokine production and attenuates progression of experimental arthritis.

21 January 2018

1 reference

Oncostatin M deficiency leads to thymic hypoplasia, accumulation of apoptotic thymocytes and glomerulonephritis

21 January 2018

1 reference

An R package for analysis of whole-genome association studies

21 January 2018

1 reference

Origins and functional impact of copy number variation in the human genome

21 January 2018

1 reference

Upregulation of the immunoproteasome in peripheral blood mononuclear cells of patients with IgA nephropathy

21 January 2018

1 reference

21 January 2018

1 reference

12 December 2020

Defective galactosylation and clearance of IgA1 molecules as a possible etiopathogenic factor in IgA nephropathy

1 reference

12 December 2020

1 reference

12 December 2020

Is IgA nephropathy the commonest primary glomerulopathy among young adults in the USA?

1 reference

12 December 2020

Patients with IgA nephropathy have increased serum galactose-deficient IgA1 levels

1 reference

12 December 2020

Identifiers

DOI

10.1038/NG.787

1 reference

31 July 2017

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31 July 2017

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