Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia (Q28943339)

14 March 2017

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Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia (English)

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genome-wide association study

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main subject

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chronic lymphocytic leukemia

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129

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Dimitris Trichopoulos

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Edward L. Giovannucci

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Elio Riboli

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Anne Zeleniuch-Jacquotte

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Demetrius Albanes

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María-Dolores Chirlaque

María-Dolores Chirlaque

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Hans-Olov Adami

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Henrik Hjalgrim

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Karin E. Smedby

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Mads Melbye

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Silvia de Sanjosé

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Silvia de Sanjose

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Vijai Joseph

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Maria Grazia Ennas

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Itziar Salaverria

Itziar Salaverria

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Andrew D Zelenetz

Andrew Zelenetz

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Claire Melissa Vajdic

Claire M. Vajdic

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Giovanni M Ferri

Giovanni M. Ferri

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Logan G. Spector

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Angela Cox

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Anthony Staines

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Gianluca Severi

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Angel Carracedo

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Giovanna Masala

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Elias Campo

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Francine Laden

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Francine Laden

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Paolo Vineis

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Kenneth Offit

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Graham G. Giles

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Stephen J. Chanock

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Amy Hutchinson

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W. Ryan Diver

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Celine M. Vachon

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Bruce K. Armstrong

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Julie M. Cunningham

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Zhaoming Wang

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Kari E. North

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Sonja I. Berndt

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Lesley F. Tinker

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Stephanie Weinstein

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Susan L. Slager

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James R. Cerhan

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Lisa A. Cannon-Albright

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George J. Weiner

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Aaron D. Norman

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Kimberly A. Bertrand

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Roel C. H. Vermeulen

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Neil E. Caporaso

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Joseph F. Fraumeni, Jr.

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Joseph F. Fraumeni

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Laurie Burdette

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Charles C. Chung

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Tongzhang Zheng

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Paige M. Bracci

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Elizabeth A. Holly

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Sara S. Strom

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Pierluigi Cocco

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Simon Crouch

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Anne Kricker

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Mark Liebow

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Marc Maynadie

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Alain Monnereau

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Jacques Riby

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Jenny Turner

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Lucia Miligi

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Liming Liang

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Karen Curtin

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Lynn R. Goldin

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Mark C. Lanasa

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J. Brice Weinberg

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Silvia Bea

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Angela R. Brooks-Wilson

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Martha S. Linet

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Vicki A. Morrison

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Lindsay M. Morton

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Carlos Lopez-Otin

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Joshua Sampson

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Sophia S. Wang

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Rachel S. Kelly

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Qing Lan

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Yawei Zhang

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Charles Lawrence

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Alice H. Wang

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Martha Glenn

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Brandt Jones

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Lucia Conde

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Nikolaus Becker

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language of work or name

English

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publication date

1 August 2013

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page(s)

868–876

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describes a project that uses

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genome-wide association study

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on focus list of Wikimedia project

inferred from title

ScienceSource

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cites work

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16 March 2017

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16 March 2017

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16 March 2017

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16 March 2017

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16 March 2017

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Differential Noxa/Mcl-1 balance in peripheral versus lymph node chronic lymphocytic leukemia cells correlates with survival capacity

16 March 2017

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Principal components analysis corrects for stratification in genome-wide association studies

16 March 2017

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A role for Wnt signalling in self-renewal of haematopoietic stem cells

16 March 2017

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Inference of population structure using multilocus genotype data

16 March 2017

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Genome-wide association study identifies three new melanoma susceptibility loci

16 March 2017

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Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study

7 April 2017

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Common SNPs explain a large proportion of the heritability for human height

7 April 2017

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Genome-wide association study identifies five susceptibility loci for glioma

7 April 2017

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Sequence variants at the TERT-CLPTM1L locus associate with many cancer types

7 April 2017

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A genome-wide association study of global gene expression

7 April 2017

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Population genomics of human gene expression

7 April 2017

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PRRC2A and BCL2L11 gene variants influence risk of non-Hodgkin lymphoma: results from the InterLymph consortium

7 April 2017

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Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia

3 June 2018

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Significant evidence for a heritable contribution to cancer predisposition: a review of cancer familiality by site

3 June 2018

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Genotypic variants at 2q33 and risk of esophageal squamous cell carcinoma in China: a meta-analysis of genome-wide association studies

3 June 2018

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Improved imputation of common and uncommon SNPs with a new reference set.

3 June 2018

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A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer

3 June 2018

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C-T variant in a miRNA target site of BCL2 is associated with increased risk of human papilloma virus related cervical cancer--an in silico approach

3 June 2018

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Estimating missing heritability for disease from genome-wide association studies

3 June 2018

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Polymorphic Cis- and Trans-Regulation of Human Gene Expression

3 June 2018

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Germline variation in apoptosis pathway genes and risk of non-Hodgkin's lymphoma

3 June 2018

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Genetic susceptibility for chronic lymphocytic leukemia among Chinese in Hong Kong

3 June 2018

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InterLymph hierarchical classification of lymphoid neoplasms for epidemiologic research based on the WHO classification (2008): update and future directions

3 June 2018

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Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32.

3 June 2018

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LEF-1 is a prosurvival factor in chronic lymphocytic leukemia and is expressed in the preleukemic state of monoclonal B-cell lymphocytosis

3 June 2018

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Estimation of effect size distribution from genome-wide association studies and implications for future discoveries

3 June 2018

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Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk

3 June 2018

1 reference

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Elevated risk of chronic lymphocytic leukemia and other indolent non-Hodgkin's lymphomas among relatives of patients with chronic lymphocytic leukemia

3 June 2018

1 reference

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Genetic variants in apoptosis and immunoregulation-related genes are associated with risk of chronic lymphocytic leukemia

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3729927

Loss of the BH3-only protein Bmf impairs B cell homeostasis and accelerates gamma irradiation-induced thymic lymphoma development

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3729927

Proposed classification of lymphoid neoplasms for epidemiologic research from the Pathology Working Group of the International Lymphoma Epidemiology Consortium (InterLymph).

3 June 2018

1 reference

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Application of coalescent methods to reveal fine-scale rate variation and recombination hotspots

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3729927

Bim is a suppressor of Myc-induced mouse B cell leukemia

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3729927

Modeling linkage disequilibrium and identifying recombination hotspots using single-nucleotide polymorphism data

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3729927

Expression and transcriptional regulation of functionally distinct Bmf isoforms in B-chronic lymphocytic leukemia cells

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3729927

The development of lymphomas in families with autoimmune lymphoproliferative syndrome with germline Fas mutations and defective lymphocyte apoptosis

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3729927

Fas gene mutations in the Canale-Smith syndrome, an inherited lymphoproliferative disorder associated with autoimmunity

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3729927

Cloning and structural analysis of cDNAs for bcl-2 and a hybrid bcl-2/immunoglobulin transcript resulting from the t(14;18) translocation

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3729927

Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3729927

Dominant interfering Fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3729927

Common genetic variation at 15q25.2 impacts on chronic lymphocytic leukaemia risk

28 July 2018

1 reference

TERT polymorphisms modify the risk of acute lymphoblastic leukemia in Chinese children

21 January 2018

1 reference

In non-follicular lymphoproliferative disorders, IGH/BCL2-fusion is not restricted to chronic lymphocytic leukaemia.

21 January 2018

1 reference

BH3-only protein Noxa regulates apoptosis in activated B cells and controls high-affinity antibody formation.

21 January 2018

1 reference

A common coding variant in CASP8 is associated with breast cancer risk

21 January 2018

1 reference

Genetic variants in caspase genes and susceptibility to non-Hodgkin lymphoma.

21 January 2018

1 reference

SequenceLDhot: detecting recombination hotspots

21 January 2018

1 reference

snp.plotter: an R-based SNP/haplotype association and linkage disequilibrium plotting package.

21 January 2018

1 reference

Verification that common variation at 2q37.1, 6p25.3, 11q24.1, 15q23, and 19q13.32 influences chronic lymphocytic leukaemia risk.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3729927

E mu-bcl-2 transgene facilitates spontaneous transformation of early pre-B and immunoglobulin-secreting cells but not T cells.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3729927

Beckwith-Wiedemann syndrome

26 November 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/23770605

12 December 2020

inferred from PubMed ID database lookup

Polygenic susceptibility to breast cancer and implications for prevention

1 reference

https://pubmed.ncbi.nlm.nih.gov/23770605

12 December 2020

inferred from PubMed ID database lookup

Evidence for substantial fine-scale variation in recombination rates across the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/23770605

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1038/NG.2652

1 reference

1 reference

1 reference

1 reference