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Correction: Corrigendum: Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk

Sara Lindström
Deborah J. Thompson
Rulla M. Tamimi
Amendments and Corrections09 Sept 2015
Nature Communications

Volume: 6, P: 1
Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

Fine-mapping of causal variants and integration of epigenetic and chromatin conformation data identify likely target genes for 150 breast cancer risk regions.

Laura Fachal
Hugues Aschard
Alison M. Dunning
Research07 Jan 2020
Nature Genetics

Volume: 52, P: 56-73
Common variants in ZNF365 are associated with both mammographic density and breast cancer risk

Rulla Tamimi and colleagues report a meta-analysis of five genome-wide association studies for percent mammographic density. They identify an associated locus at ZNF365, which has also been associated with susceptibility to breast cancer.

Sara Lindström
Celine M Vachon
Rulla M Tamimi
Research30 Jan 2011
Nature Genetics

Volume: 43, P: 185-187
Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk

Mammographic density is a strong risk factor for breast cancer. Here, the authors identify several new loci associated dense area, non-dense area and percent density, and highlight a shared genetic basis for mammographic density and breast cancer.

Sara Lindström
Deborah J. Thompson
Rulla M. Tamimi
Research24 Oct 2014
Nature Communications

Volume: 5, P: 1-8
Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

Denise Harold
Richard Abraham
Julie Williams
Amendments and Corrections01 Oct 2009
Nature Genetics

Volume: 41, P: 1156
Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

Denise Harold
Richard Abraham
Julie Williams
Amendments and Corrections29 May 2013
Nature Genetics

Volume: 45, P: 712
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

Roger Milne and colleagues conduct a genome-wide association study for estrogen receptor (ER)-negative breast cancer combined with BRCA1 mutation carriers in a large cohort. They identify ten new risk variants and find high genetic correlation between breast cancer risk for BRCA1 mutation carriers and risk of ER-negative breast cancer in the general population.

Roger L Milne
Karoline B Kuchenbaecker
Jacques Simard
Research23 Oct 2017
Nature Genetics

Volume: 49, P: 1767-1778
Association analysis identifies 65 new breast cancer risk loci

Association analysis identifies 65 new breast cancer risk loci, predicts target genes for known risk loci and demonstrates a strong overlap with somatic driver genes in breast tumours.

Kyriaki Michailidou
Sara Lindström
Douglas F. Easton
Research23 Oct 2017
Nature

Volume: 551, P: 92-94
Defining stroke risks in sickle cell anemia

Children and young adults with sickle cell anemia at risk for stroke are identified principally by screening for cerebral vasculopathy using transcranial Doppler ultrasonography. Investigators now show how Bayesian networks can generate useful predictive models and highlight relationships between genes and the occurrence of stroke in those with sickle cell anemia.

James F Meschia
V Shane Pankratz
News & Views01 Apr 2005
Nature Genetics

Volume: 37, P: 340-341
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

Julie Williams and colleagues report a genome-wide association study for Alzheimer's disease. They identify variants at the CLU and PICALM loci associated with susceptibility to late-onset Alzheimer's disease.

Denise Harold
Richard Abraham
Julie Williams
Research06 Sept 2009
Nature Genetics

Volume: 41, P: 1088-1093
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

Julie Williams, Michael Owen and colleagues report staged follow-up and meta-analyses of genome-wide association studies for Alzheimer's disease from the GERAD+ consortium. They identify common variants at ABCA7 and MS4A6A/MS4A4E associated with Alzheimer's disease and support for several additional susceptibility loci.

Paul Hollingworth
Denise Harold
Julie Williams
Research03 Apr 2011
Nature Genetics

Volume: 43, P: 429-435
A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor–negative breast cancer in the general population

Fergus Couch and colleagues report a genome-wide association study for modifiers of breast cancer susceptibility in BRCA1 mutation carriers. They identify a locus at 19p13 associated with breast cancer risk in BRCA1 mutation carriers, and further replication studies identify this locus as associated with estrogen receptor–negative breast cancer in the general population.

Antonis C Antoniou
Xianshu Wang
Fergus J Couch
Research19 Sept 2010
Nature Genetics

Volume: 42, P: 885-892
Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease

Steve Younkin and colleagues report the results of a genome-wide association study for late-onset Alzheimer's disease. A variant on the X chromosome in PCDH11X is associated with increased risk of the disorder. PCDH11X encodes a protocadherin and is a member of a cell surface receptor molecule family.

Minerva M Carrasquillo
Fanggeng Zou
Steven G Younkin
Research11 Jan 2009
Nature Genetics

Volume: 41, P: 192-198
Pathologic Features, Proliferative Activity, and Cyclin D1 Expression in Hurthle Cell Neoplasms of the Thyroid

Lori A Erickson
Long Jin
Ricardo V Lloyd
Research01 Feb 2000
Modern Pathology

Volume: 13, P: 186-192
p27^kip1 Expression Distinguishes Papillary Hyperplasia in Graves’ Disease from Papillary Thyroid Carcinoma

Lori A Erickson
Omar M Yousef
Ricardo V Lloyd
Research01 Sept 2000
Modern Pathology

Volume: 13, P: 1014-1019
Factors That Influence the Measurement of Prostate Cancer DNA Ploidy and Proliferation in Paraffin Embedded Tissue Evaluated by Flow Cytometry

Mathew J. So
John C. Cheville
Thomas J. Sebo
Research01 Sept 2001
Modern Pathology

Volume: 14, P: 906-912
Genome-wide association study of germline variants and breast cancer-specific mortality

Maria Escala-Garcia
Qi Guo
Marjanka K. Schmidt
ResearchOpen Access21 Feb 2019
British Journal of Cancer

Volume: 120, P: 647-657
Lymphocyte-Rich Gastric Cancer: Associations with Epstein-Barr Virus, Microsatellite Instability, Histology, and Survival

Karen L Grogg
Christine M Lohse
Thomas C Smyrk
Research01 Jul 2003
Modern Pathology

Volume: 16, P: 641-651

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Correction: Corrigendum: Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk

Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

Common variants in ZNF365 are associated with both mammographic density and breast cancer risk

Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk

Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

Association analysis identifies 65 new breast cancer risk loci

Defining stroke risks in sickle cell anemia

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor–negative breast cancer in the general population

Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease

Pathologic Features, Proliferative Activity, and Cyclin D1 Expression in Hurthle Cell Neoplasms of the Thyroid

p27^kip1 Expression Distinguishes Papillary Hyperplasia in Graves’ Disease from Papillary Thyroid Carcinoma

Factors That Influence the Measurement of Prostate Cancer DNA Ploidy and Proliferation in Paraffin Embedded Tissue Evaluated by Flow Cytometry

Genome-wide association study of germline variants and breast cancer-specific mortality

Lymphocyte-Rich Gastric Cancer: Associations with Epstein-Barr Virus, Microsatellite Instability, Histology, and Survival

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