A genome-wide assessment of the role of untagged copy number variants in type 1 diabetes (Q30412627)

17 September 2017

A genome-wide assessment of the role of untagged copy number variants in type 1 diabetes (English)

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17 September 2017

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6

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5 June 2020

Suna Onengut

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Neil M Walker

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Deborah Smyth

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5 June 2020

Vincent Plagnol

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Matthew E Hurles

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11

Stephen S Rich

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8

John A Todd

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4

Corina Shtir

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1

Manuela Zanda

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5 June 2020

author name string

Daniel Gallo

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5 June 2020

publication date

29 May 2014

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17 September 2017

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5 June 2020

volume

10

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5 June 2020

issue

5

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5 June 2020

page(s)

e1004367

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Creative Commons Attribution 4.0 International

5 June 2020

copyright license

start time

29 May 2014

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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Validity of the family-based association test for copy number variant data in the case of non-linear intensity-genotype relationship.

20 June 2018

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Mapping copy number variation by population-scale genome sequencing

20 June 2018

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

20 June 2018

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20 June 2018

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

20 June 2018

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Prediction and interaction in complex disease genetics: experience in type 1 diabetes

20 June 2018

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Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes

20 June 2018

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Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes

20 June 2018

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A robust statistical method for case-control association testing with copy number variation

20 June 2018

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Integrated detection and population-genetic analysis of SNPs and copy number variation

20 June 2018

1 reference

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The association between ultraviolet B irradiance, vitamin D status and incidence rates of type 1 diabetes in 51 regions worldwide

20 June 2018

1 reference

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The complete genome of an individual by massively parallel DNA sequencing

20 June 2018

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Structural variation of chromosomes in autism spectrum disorder

20 June 2018

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

20 June 2018

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Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

20 June 2018

1 reference

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FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity

20 June 2018

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Population structure, differential bias and genomic control in a large-scale, case-control association study

20 June 2018

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The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility

20 June 2018

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The effect of infections on susceptibility to autoimmune and allergic diseases

20 June 2018

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A note on power approximations for the transmission/disequilibrium test

20 June 2018

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Trends in the prevalence and incidence of diabetes: insulin-dependent diabetes mellitus in childhood.

20 June 2018

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The changing face of the epidemiology of insulin-dependent diabetes mellitus (IDDM): research designs and models of disease causation

20 June 2018

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Remapping the insulin gene/IDDM2 locus in type 1 diabetes

20 June 2018

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On the analysis of copy-number variations in genome-wide association studies: a translation of the family-based association test

21 January 2018

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Common deletion polymorphisms in the human genome.

21 January 2018

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Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus

26 November 2018

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10.1371/JOURNAL.PGEN.1004367

26 November 2018

Identifiers

DOI

1 reference

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5 June 2020

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5 June 2020

PubMed publication ID

24875393

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24875393 AND SRC:MED&resulttype=core&format=json