Hoda Anton-Culver

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.

Genotype determination for polymorphisms in linkage disequilibrium

Zhaoxia Yu, Argyrios Ziogas, Hoda Anton-Culver, 2008, BMC Bioinformatics.

Accurate classification of MLH1

Steven M. Lipkin, Hoda Anton-Culver, Laura S. Rozek, 2008 .

Training data used to generate predictive model

Gillian R. Hayes, Oliver L. Haimson, Hoda Anton-Culver, 2015 .

Tobacco control—debate on harm reduction enters new phase as India implements public smoking ban

James Hess, Argyrios Ziogas, Hoda Anton-Culver, 2008 .

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.

The Breast Cancer Family Registry: an infrastructure for cooperative multinational, interdisciplinary and translational studies of the genetic epidemiology of breast cancer

Norman Boyd, John L Hopper, Irene L Andrulis, 2004, Breast Cancer Research.

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

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

Common Genetic Variation in Circadian Rhythm Genes and Risk of Epithelial Ovarian Cancer (EOC)

Dong Liang, Brooke L. Fridley, Jennifer A. Doherty, 2015, Journal of genetics and genome research.

Population-based study of the risk of second primary contralateral breast cancer associated with carrying a mutation in BRCA1 or BRCA2.

Hoda Anton-Culver, Colin B Begg, Marinela Capanu, 2010, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

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

Michael Jones, Peter Kraft, Arnaud Droit, 2017, Nature Genetics.

Study design: Evaluating gene–environment interactions in the etiology of breast cancer – the WECARE study

Bryan Langholz, John D Boice, Hoda Anton-Culver, 2004, Breast Cancer Research.

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.

Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen-Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation

Matthias W. Beckmann, Peter A. Fasching, Simon S. Cross, 2016, American journal of human genetics.

19p13.1 is a triple-negative-specific breast cancer susceptibility locus.

Daniel J. Park, Julian Peto, Kamila Czene, 2012, Cancer research.

Meeting report: NCI think tanks in cancer biology.

Hoda Anton-Culver, Dinah S Singer, H. Anton-Culver, 2005, Cancer research.

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.

A network analysis to identify mediators of germline-driven differences in breast cancer prognosis

Gary D. Bader, Christine L. Clarke, Gary D Bader, 2020, Nature Communications.

Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer

Wei Lu, Wei Zheng, Mads Thomassen, 2013, Nature Genetics.

BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers.

Dong Liang, Patrick Neven, Harvey Risch, 2016, Journal of the National Cancer Institute.

The Cancer Genetics Network: Recruitment Results and Pilot Studies

Prakash Nadkarni, Argyrios Ziogas, Hoda Anton-Culver, 2003, Public Health Genomics.

Genome-wide Analysis Identifies Novel Loci Associated with Ovarian Cancer Outcomes: Findings from the Ovarian Cancer Association Consortium

Francesmary Modugno, James Paul, Honglin Song, 2015 .

Validity of Models for Predicting BRCA1 and BRCA2 Mutations

Leif E. Peterson, Giovanni Parmigiani, Li Hsu, 2007, Annals of Internal Medicine.

Extending Mendelian Risk Prediction Models to Handle Misreported Family History

Danielle Braun, Malka Gorfine, Giovanni Parmigiani, 2014 .

Residential proximity to agricultural pesticide use and incidence of breast cancer in the California Teachers Study cohort.

Argyrios Ziogas, Hoda Anton-Culver, Peggy Reynolds, 2004, Environmental research.

Breast cancer risk variants at 6 q 25 display different phenotype associations and regulate ESR 1 , RMND 1 and CCDC 170

Wei Zheng, Mads Thomassen, Nicholas A. Sinnott-Armstrong, 2016 .

Validation of family history data in cancer family registries.

Argyrios Ziogas, Hoda Anton-Culver, A. Ziogas, 2003, American journal of preventive medicine.

Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)

Patrick Neven, Hui Zhao, Nazneen Rahman, 2012, PloS one.

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.

Accurate classification of MLH1/MSH2 missense variants with multivariate analysis of protein polymorphisms–mismatch repair (MAPP‐MMR)

Stephen B Gruber, Hoda Anton-Culver, Jonathan L. Velasquez, 2008, Human mutation.

Body-mass index and mortality among 1.46 million white adults.

Yikyung Park, I-Min Lee, Jane A Hoppin, 2010, The New England journal of medicine.

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.

Duration of Adulthood Overweight, Obesity, and Cancer Risk in the Women’s Health Initiative: A Longitudinal Study from the United States

Thomas E Rohan, Oleg Zaslavsky, Hoda Anton-Culver, 2016, PLoS medicine.

GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer

Brooke L. Fridley, Matthias W. Beckmann, Peter A. Fasching, 2013, Nature Genetics.

Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium.

Michael Jones, Nazneen Rahman, Michael Bremer, 2011, Human molecular genetics.

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.

Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer

Patrick Neven, Peter Kraft, Nazneen Rahman, 2015 .

Laminin 332 expression and prognosis in breast cancer.

Argyrios Ziogas, Hoda Anton-Culver, A. Ziogas, 2018, Human pathology.

Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers.

Wei Lu, Päivi Heikkilä, Peter Kraft, 2013, American journal of human genetics.

Genome-wide association studies identify four ER negative–specific breast cancer risk loci

Patrick Neven, Michael Jones, Wei Lu, 2013, Nature Genetics.

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.

Network-Based Integration of GWAS and Gene Expression Identifies a HOX-Centric Network Associated with Serous Ovarian Cancer Risk

Dong Liang, Brooke L. Fridley, Jennifer A. Doherty, 2015, Cancer Epidemiology, Biomarkers & Prevention.

Supplementing Public Health Inspection via Social Media

Gillian R. Hayes, Oliver L. Haimson, Hoda Anton-Culver, 2016, PloS one.

Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study

Patrick Neven, Chiun-Sheng Huang, Julian Peto, 2014, Breast Cancer Research.

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.

The Athena Breast Health Network: developing a rapid learning system in breast cancer prevention, screening, treatment, and care

Arash Naeim, Michael Hogarth, Hoda Anton-Culver, 2013, Breast Cancer Research and Treatment.

PALB2,CHEK2 and ATM rare variants and cancer risk: Data from COGS

Dong Liang, Jane E. Carpenter, Peter Kraft, 2016 .

High breast cancer incidence rates among California teachers: results from the California Teachers Study (United States)

Hoda Anton-Culver, William Wright, Peggy Reynolds, 2002, Cancer Causes & Control.

Evidence of Gene–Environment Interactions between Common Breast Cancer Susceptibility Loci and Established Environmental Risk Factors

Patrick Neven, Daniel F. Schmidt, Julian Peto, 2013, PLoS genetics.

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.

Fine-scale mapping of the FGFR2 breast cancer risk locus: putative functional variants differentially bind FOXA1 and E2F1.

Wei Lu, Nina Ditsch, Julian Peto, 2013, American journal of human genetics.

Combined and interactive effects of environmental and GWAS-identified risk factors in ovarian cancer.

Harvey Risch, Malcolm C Pike, Georgia Chenevix-Trench, 2013, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

Robust Tests for Additive Gene-Environment Interaction in Case-Control Studies Using Gene-Environment Independence

Harvey Risch, Bhramar Mukherjee, Seunggeun Lee, 2018, American journal of epidemiology.

Genome-wide association analysis identifies three new breast cancer susceptibility loci

Michael Jones, Nazneen Rahman, Daniel J. Park, 2012, Nature Genetics.