Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk (Q34114297)

31 July 2017

Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk (English)

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31 July 2017

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lymphoblastic leukemia

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7

Elli Papaemmanuil

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31 July 2017

37

Mel Greaves

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14

Eamonn Sheridan

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Rashmi B Prasad

3

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Agnes F. Semsei

Agnes F Semsei

27

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Fay J Hosking

Fay J Hosking

2

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Anthony V. Moorman

Anthony V Moorman

21

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Daniel Sinnett

Daniel Sinnett

30

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Rajiv Kumar

Rajiv Kumar

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Christine J Harrison

Christine J Harrison

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Richard Houlston

Richard S Houlston

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Kari Hemminki

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Kari Hemminki

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Martin Schrappe

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Martin Stanulla

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Anna Gonzalez Neira

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Ian P Tomlinson

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Jayaram Vijayakrishnan

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Jayaram Vijayakrishnan

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Julie A E Irving

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Eve Roman

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Amy L Sherborne

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Rolf Koehler

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Claus R Bartram

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Andreas Gast

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Sara E Dobbins

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Yussanne Ma

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Malcolm Taylor

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Sally E Kinsey

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Tracey Lightfoot

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James M Allan

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Sue Richards

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Martin Zimmermann

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Csaba Szalai

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Daniel J Erdelyi

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Maja Krajinovic

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Jasmine Healy

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Norihiko Kawamata

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Seishi Ogawa

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H Phillip Koeffler

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language of work or name

English

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publication date

9 May 2010

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492-494

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https://scigraph.springernature.com/pub.10.1038/ng.585

31 July 2017

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cites work

Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3434228

Germline genomic variants associated with childhood acute lymphoblastic leukemia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3434228

Genome-wide association study identifies five susceptibility loci for glioma

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3434228

Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3434228

Genome-wide association study identifies three loci associated with melanoma risk

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3434228

New common variants affecting susceptibility to basal cell carcinoma

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3434228

Genome-wide profiling of genetic alterations in acute lymphoblastic leukemia: recent insights and future directions.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3434228

A comprehensive analysis of the CDKN2A gene in childhood acute lymphoblastic leukemia reveals genomic deletion, copy number neutral loss of heterozygosity, and association with specific cytogenetic subgroups.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3434228

A common allele on chromosome 9 associated with coronary heart disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3434228

A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3434228

Genome-wide associations of gene expression variation in humans

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3434228

Different isoforms of the B-cell mutator activation-induced cytidine deaminase are aberrantly expressed in BCR-ABL1-positive acute lymphoblastic leukemia patients.

5 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.585

The prognostic significance of CDKN2A, CDKN2B and MTAP inactivation in B-lineage acute lymphoblastic leukemia of childhood. Results of the EORTC studies 58881 and 58951.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3434228

Prevalent involvement of illegitimate V(D)J recombination in chromosome 9p21 deletions in lymphoid leukemia

28 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20453839

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NG.585

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31 July 2017

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31 July 2017

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