Paul D P Pharoah

发表

Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade.

Jane E. Carpenter, Kyriaki Michailidou, France Labrèche, 2014, Human molecular genetics.

Neither off the peg nor made to measure calculations are fit for purpose

Paul D P Pharoah, 2012, BMJ : British Medical Journal.

Science is like a vast jigsaw

Paul D P Pharoah, 2013, BMJ.

IGF1 and IGFBP3 tagging polymorphisms are associated with circulating levels of IGF1, IGFBP3 and risk of breast cancer.

Nicholas J Wareham, Alison M Dunning, Paul D P Pharoah, 2006, Human molecular genetics.

Multiple loci with different cancer specificities within the 8q24 gene desert.

John L Hopper, Honglin Song, Thibaud Koessler, 2008, Journal of the National Cancer Institute.

Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types.

Peter Kraft, Todd L Edwards, Nazneen Rahman, 2016, Cancer discovery.

Variants in DNA double-strand break repair genes and breast cancer susceptibility.

Paul D P Pharoah, Douglas F Easton, Nicholas E Day, 2002, Human molecular genetics.

Single nucleotide polymorphisms in the TP53 region and susceptibility to invasive epithelial ovarian cancer.

Mark Sherman, Honglin Song, Rebecca Sutphen, 2009, Cancer research.

Cost effectiveness of the NHS breast screening programme: life table model

Paul D P Pharoah, Nora Pashayan, Deborah Fitzsimmons, 2013, BMJ.

Association of ESR1 gene tagging SNPs with breast cancer risk.

Julian Peto, Ute Hamann, Peter Devilee, 2009, Human molecular genetics.

Consortium analysis of gene and gene-folate interactions in purine and pyrimidine metabolism pathways with ovarian carcinoma risk.

Dong Liang, Thilo Dörk, Natalia Bogdanova, 2014, Molecular nutrition & food research.

Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers.

Christiana Kartsonaki, Mads Thomassen, Etienne Rouleau, 2011, Human molecular genetics.

A Transcriptome-Wide Association Study Among 97,898 Women to Identify Candidate Susceptibility Genes for Epithelial Ovarian Cancer Risk.

Harvey Risch, Yian A Chen, Mads Thomassen, 2018, Cancer research.

Genome-wide association study identifies five new breast cancer susceptibility loci

Deborah Hughes, Nazneen Rahman, William Tapper, 2010, Nature Genetics.

Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium.

Patrick Neven, Päivi Heikkilä, Giu-Cheng Hsu, 2011, Human molecular genetics.

Variation in NF-κB Signaling Pathways and Survival in Invasive Epithelial Ovarian Cancer

Hannah Yang, James Paul, Honglin Song, 2014, Cancer Epidemiology, Biomarkers & Prevention.

A Genome-Wide Association Study of Prognosis in Breast Cancer

Peter Kraft, Stephen J Chanock, Paul D P Pharoah, 2010, Cancer Epidemiology, Biomarkers & Prevention.

Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array

Peter Kraft, Anssi Auvinen, Henrik Gronberg, 2013, Nature Genetics.

Tagging single nucleotide polymorphisms in cell cycle control genes and susceptibility to invasive epithelial ovarian cancer.

Francesmary Modugno, Honglin Song, Danielle Shadforth, 2007, Cancer research.

Polymorphism in the GALNT1 Gene and Epithelial Ovarian Cancer in Non-Hispanic White Women: The Ovarian Cancer Association Consortium

Hannah Yang, Shan Wang-Gohrke, Honglin Song, 2010, Cancer Epidemiology, Biomarkers & Prevention.

Gene-panel sequencing and the prediction of breast-cancer risk.

Nazneen Rahman, Peter Devilee, Alfons Meindl, 2015, The New England journal of medicine.

Association Between BRCA1 and BRCA2 Mutations and Survival in Women With Invasive Epithelial Ovarian Cancer

Gord Glendon, Lesley McGuffog, Daniel Barrowdale, 2012 .

Patterns of Immune Infiltration in Breast Cancer and Their Clinical Implications: A Gene-Expression-Based Retrospective Study

Carlos Caldas, Florian Markowetz, Paul D P Pharoah, 2016, PLoS medicine.

A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46,450 cases and 42,461 controls from the breast cancer association consortium.

Julian Peto, Kyriaki Michailidou, Thomas Brüning, 2014, Human molecular genetics.

Investigation of gene‐environment interactions between 47 newly identified breast cancer susceptibility loci and environmental risk factors

Thomas Brüning, Kamila Czene, Ute Hamann, 2015, International journal of cancer.

Association between invasive ovarian cancer susceptibility and 11 best candidate SNPs from breast cancer genome-wide association study.

Shan Wang-Gohrke, Honglin Song, Georgia Chenevix-Trench, 2009, Human molecular genetics.

Five endometrial cancer risk loci identified through genome-wide association analysis

Hui Zhao, Mark McEvoy, Julian Peto, 2016, Nature Genetics.

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

Jane E. Carpenter, Peter Kraft, Gary K. Chen, 2011, Nature Genetics.

ESR1/SYNE1 Polymorphism and Invasive Epithelial Ovarian Cancer Risk: An Ovarian Cancer Association Consortium Study

Shan Wang-Gohrke, Honglin Song, Malcolm C Pike, 2010, Cancer Epidemiology, Biomarkers & Prevention.

Discovery of common and rare genetic risk variants for colorectal cancer

Mathieu Lemire, Steven Gallinger, Michael Wainberg, 2018, Nature Genetics.

A transcriptome-wide association study of high grade serous epithelial ovarian cancer identifies novel susceptibility genes and splice variants

Alexander Gusev, Bogdan Pasaniuc, Paul D P Pharoah, 2019, Nature Genetics.

Inherited genetic susceptibility to breast cancer: the beginning of the end or the end of the beginning?

Paul D P Pharoah, Douglas F Easton, Maya Ghoussaini, 2013, The American journal of pathology.

Molecular Classification of Breast Carcinomas Using Tissue Microarrays

Carlos Caldas, Paul D P Pharoah, Grace Callagy, 2003, Diagnostic molecular pathology : the American journal of surgical pathology, part B.

Age- and Tumor Subtype-Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers.

Michael Jones, Julian Peto, Thomas Brüning, 2016, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

GWAS meta-analysis of 16 852 women identifies new susceptibility locus for endometrial cancer.

Harvey Risch, Peter Kraft, Mark McEvoy, 2016, Human molecular genetics.

Identification of nine new susceptibility loci for endometrial cancer

Peter Kraft, Mark McEvoy, Julian Peto, 2018, Nature Communications.

The admixture maximum likelihood test: a novel experiment‐wise test of association between disease and multiple SNPs

Paul D P Pharoah, Douglas F Easton, D. Easton, 2006, Genetic epidemiology.

Genetic variation in insulin-like growth factor 2 may play a role in ovarian cancer risk.

David V Conti, Honglin Song, Malcolm C Pike, 2011, Human molecular genetics.

Assessment of Automated Image Analysis of Breast Cancer Tissue Microarrays for Epidemiologic Studies

Sean Davis, Jonine D Figueroa, Paul D P Pharoah, 2010, Cancer Epidemiology, Biomarkers & Prevention.