(Q34114297)

31 July 2017

title

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

1 reference

31 July 2017

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lymphoblastic leukemia

1 reference

7

Elli Papaemmanuil

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31 July 2017

37

Mel Greaves

1 reference

31 July 2017

14

Eamonn Sheridan

1 reference

31 July 2017

Rashmi B Prasad

3

0 references

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

4

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Christine J Harrison

Christine J Harrison

22

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Richard Houlston

Richard S Houlston

38

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Kari Hemminki

36

Kari Hemminki

1 reference

31 July 2017

10

Martin Schrappe

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31 July 2017

9

Martin Stanulla

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31 July 2017

32

Anna Gonzalez Neira

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23

Ian P Tomlinson

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31 July 2017

Jayaram Vijayakrishnan

6

Jayaram Vijayakrishnan

1 reference

31 July 2017

19

Julie A E Irving

1 reference

31 July 2017

18

Eve Roman

1 reference

31 July 2017

Amy L Sherborne

1

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31 July 2017

Rolf Koehler

5

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31 July 2017

Claus R Bartram

8

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31 July 2017

Andreas Gast

11

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31 July 2017

Sara E Dobbins

12

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31 July 2017

Yussanne Ma

13

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31 July 2017

Malcolm Taylor

15

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31 July 2017

Sally E Kinsey

16

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31 July 2017

Tracey Lightfoot

17

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31 July 2017

James M Allan

20

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31 July 2017

Sue Richards

24

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31 July 2017

Martin Zimmermann

25

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31 July 2017

Csaba Szalai

26

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31 July 2017

Daniel J Erdelyi

28

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31 July 2017

Maja Krajinovic

29

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31 July 2017

Jasmine Healy

31

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31 July 2017

Norihiko Kawamata

33

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31 July 2017

Seishi Ogawa

34

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31 July 2017

H Phillip Koeffler

35

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31 July 2017

language of work or name

English

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publication date

9 May 2010

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31 July 2017

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31 July 2017

volume

42

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31 July 2017

issue

6

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31 July 2017

page(s)

492-494

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

31 July 2017

cites work

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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