Publications by authors named "Caroline Baynes"

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Analysis of more than 400,000 women provides case-control evidence for BRCA1 and BRCA2 variant classification.
Maria Zanti, Denise G O'Mahony, Michael T Parsons, Leila Dorling, Joe Dennis, Caroline Baynes

Nat Commun· May 2025

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Analysis of more than 400,000 women provides case-control evidence for and variant classification.
Maria Zanti, Denise G O'Mahony, Michael T Parsons, Leila Dorling, Joe Dennis, Caroline Baynes

medRxiv· September 2024

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Author Correction: Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk.
Naomi Wilcox, Martine Dumont, Anna González-Neira, Sara Carvalho, Charles Joly Beauparlant, Caroline Baynes

Nat Genet· November 2023

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Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk.
Naomi Wilcox, Martine Dumont, Anna González-Neira, Sara Carvalho, Charles Joly Beauparlant, Caroline Baynes

Nat Genet· September 2023

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Breast Cancer Risk in Women from Ghana Carrying Rare Germline Pathogenic Mutations.
Thomas U Ahearn, Parichoy Pal Choudhury, Andriy Derkach, Beatrice Wiafe-Addai, Baffour Awuah, Caroline Baynes

Cancer Epidemiol Biomarkers Prev· August 2022

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Characterisation of protein-truncating and missense variants in in 15 768 women from Malaysia and Singapore.
Pei Sze Ng, Rick Acm Boonen, Eldarina Wijaya, Chan Eng Chong, Milan Sharma, Caroline Baynes

J Med Genet· May 2022

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Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.
Juliette Coignard, Michael Lush, Jonathan Beesley, Tracy A O'Mara, Joe Dennis, Caroline Baynes

Nat Commun· May 2021

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Breast Cancer Risk Genes - Association Analysis in More than 113,000 Women.

N Engl J Med· February 2021

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CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers.
Nichola Johnson, Sarah Maguire, Anna Morra, Pooja Middha Kapoor, Katarzyna Tomczyk, Caroline Baynes

Br J Cancer· February 2021

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A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.
Juliette Coignard, Michael Lush, Jonathan Beesley, Tracy A O'Mara, Joe Dennis, Caroline Baynes

Nat Commun· February 2021

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Targeted Resequencing of the Coding Sequence of 38 Genes Near Breast Cancer GWAS Loci in a Large Case-Control Study.
Brennan Decker, Jamie Allen, Craig Luccarini, Karen A Pooley, Mitul Shah, Caroline Baynes

Cancer Epidemiol Biomarkers Prev· April 2019

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Low risk of invasive lobular carcinoma of the breast in carriers of BRCA1 (hereditary breast and ovarian cancer) and TP53 (Li-Fraumeni syndrome) germline mutations.
Yoan Ditchi, Chloé Broudin, Yolla El Dakdouki, Marie Muller, Pernelle Lavaud, Caroline Baynes

Breast J· January 2019

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A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer.
Lang Wu, Wei Shi, Jirong Long, Xingyi Guo, Kyriaki Michailidou, Caroline Baynes

Nat Genet· July 2018

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Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation.
Maya Ghoussaini, Stacey L Edwards, Kyriaki Michailidou, Silje Nord, Richard Cowper-Sal Lari, Caroline Baynes

Nat Commun· April 2018

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Inherited mutations in and in an unselected multiethnic cohort of Asian patients with breast cancer and healthy controls from Malaysia.
Wei Xiong Wen, Jamie Allen, Kah Nyin Lai, Shivaani Mariapun, Siti Norhidayu Hasan, Caroline Baynes

J Med Genet· February 2018

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Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer.
Roger L Milne, Karoline B Kuchenbaecker, Kyriaki Michailidou, Jonathan Beesley, Siddhartha Kar, Caroline Baynes

Nat Genet· December 2017

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Rare, protein-truncating variants in , and , but not , are associated with increased breast cancer risks.
Brennan Decker, Jamie Allen, Craig Luccarini, Karen A Pooley, Mitul Shah, Caroline Baynes

J Med Genet· November 2017

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Association analysis identifies 65 new breast cancer risk loci.
Kyriaki Michailidou, Sara Lindström, Joe Dennis, Jonathan Beesley, Shirley Hui, Caroline Baynes

Nature· November 2017

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Fine-Mapping of the 1p11.2 Breast Cancer Susceptibility Locus.
Hisani N Horne, Charles C Chung, Han Zhang, Kai Yu, Ludmila Prokunina-Olsson, Caroline Baynes

PLoS One· July 2017

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PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS.
Melissa C Southey, David E Goldgar, Robert Winqvist, Katri Pylkäs, Fergus Couch, Caroline Baynes

J Med Genet· December 2016

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Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21.
Yosr Hamdi, Penny Soucy, Véronique Adoue, Kyriaki Michailidou, Sander Canisius, Caroline Baynes

Oncotarget· December 2016

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Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus.
Chenjie Zeng, Xingyi Guo, Jirong Long, Karoline B Kuchenbaecker, Arnaud Droit, Caroline Baynes

Breast Cancer Res· June 2016

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No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing.
Douglas F Easton, Fabienne Lesueur, Brennan Decker, Kyriaki Michailidou, Jun Li, Caroline Baynes

J Med Genet· May 2016

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PPM1D Mosaic Truncating Variants in Ovarian Cancer Cases May Be Treatment-Related Somatic Mutations.
Paul D P Pharoah, Honglin Song, Ed Dicks, Maria P Intermaggio, Patricia Harrington, Caroline Baynes

J Natl Cancer Inst· March 2016

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Height and Breast Cancer Risk: Evidence From Prospective Studies and Mendelian Randomization.
Ben Zhang, Xiao-Ou Shu, Ryan J Delahanty, Chenjie Zeng, Kyriaki Michailidou, Caroline Baynes

J Natl Cancer Inst· November 2015

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