Common variation at 2q22.3 (ZEB2) influences the risk of renal cancer (Q28943459)

12

0 references

Nathaniel Rothman

14

0 references

Demetrius Albanes

20

0 references

Marc Henrion

Marc Henrion

1

0 references

Peter Broderick

Peter Broderick

6

0 references

Mattias Johansson

Mattias Johansson

11

0 references

Stephen Chanock

24

Stephen Chanock

1 reference

14 March 2017

18

W. Ryan Diver

1 reference

14 March 2017

21

Jarmo Virtamo

1 reference

14 March 2017

15

Zhaoming Wang

1 reference

14 March 2017

19

Susan M. Gapstur

1 reference

14 March 2017

17

Victoria L. Stevens

1 reference

14 March 2017

4

Mark Purdue

1 reference

14 March 2017

3

Ghislaine Scelo

1 reference

14 March 2017

Matthew Frampton

2

1 reference

14 March 2017

Yuanqing Ye

5

1 reference

14 March 2017

Alastair Ritchie

7

1 reference

14 March 2017

Richard Kaplan

8

1 reference

14 March 2017

Angela Meade

9

1 reference

14 March 2017

James McKay

10

1 reference

14 March 2017

James Larkin

13

1 reference

14 March 2017

Wong-Ho Chow

16

1 reference

14 March 2017

Xifeng Wu

22

1 reference

14 March 2017

Timothy Eisen

25

1 reference

14 March 2017

Richard S. Houlston

Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk

26

1 reference

14 March 2017

15 February 2013

1 reference

14 March 2017

Human Molecular Genetics

1 reference

14 March 2017

22

1 reference

14 March 2017

4

1 reference

14 March 2017

825–831

1 reference

14 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3554205

Common variation at 10p12.31 near MLLT10 influences meningioma risk

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3554205

Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3554205

Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3554205

A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3)

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3554205

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3554205

Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3554205

A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3554205

The structure of haplotype blocks in the human genome

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3554205

Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3554205

Snail, Zeb and bHLH factors in tumour progression: an alliance against the epithelial phenotype?

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3554205

Common regulatory variation impacts gene expression in a cell type-dependent manner

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3554205

Genome-wide association study of prostate cancer identifies a second risk locus at 8q24

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3554205

Patterns of cis regulatory variation in diverse human populations

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3554205

The chromosome 2p21 region harbors a complex genetic architecture for association with risk for renal cell carcinoma

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3554205

Genome-wide high-density SNP linkage search for glioma susceptibility loci: results from the Gliogene Consortium

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3554205

A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3554205

The architecture of gene regulatory variation across multiple human tissues: the MuTHER study

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3554205

Epidemiology and risk factors for kidney cancer

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3554205

Hereditary kidney cancer: unique opportunity for disease-based therapy.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3554205

Atypical Mowat-Wilson patient confirms the importance of the novel association between ZFHX1B/SIP1 and NuRD corepressor complex

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3554205

Genetics of coeliac disease

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3554205

Hypoxia-inducible factor-1-dependent repression of E-cadherin in von Hippel-Lindau tumor suppressor-null renal cell carcinoma mediated by TCF3, ZFHX1A, and ZFHX1B.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3554205

Systematic Population-Based Assessment of Cancer Risk in First-Degree Relatives of Cancer Probands

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23184150