Jenny Chang-Claude

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.

Pathway-Based Kernel Boosting for the Analysis of Genome-Wide Association Studies

Benjamin Hofner, Christopher I. Amos, Juliane Manitz, 2017, Comput. Math. Methods Medicine.

Additional file 3: of Prognostic value of automated KI67 scoring in breast cancer: a centralised evaluation of 8088 patients from 10 study groups

Stephen Hewitt, Qin Wang, John W. M. Martens, 2016 .

Der Einfluß fehlspezifizierter Modellparameter of Lod-Score und Rekombinationsfrequenz am Beispiel einer Familienstudie zu Brust- und Ovarialkrebs

Jenny Chang-Claude, Silke Schmidt, Heiko Becher, 1996, GMDS.

A data science approach for early-stage prediction of Patient's susceptibility to acute side effects of advanced radiotherapy

Daniele Soria, Thierry J. Chaussalet, Barry S. Rosenstein, 2021, Comput. Biol. Medicine.

Genetic Predisposition to In Situ and Invasive Lobular Carcinoma of the Breast

Julian Peto, Matthias W. Beckmann, Peter A. Fasching, 2014, PLoS genetics.

Genome-wide association study identifies multiple loci associated with bladder cancer risk.

William Wheeler, Paolo Vineis, Peter Kraft, 2014, Human molecular genetics.

Menarche, menopause, and breast cancer risk: individual participant meta-analysis, including 118 964 women with breast cancer from 117 epidemiological studies

Heather Eliassen, Karen Canfell, Julian Peto, 2012, The Lancet. Oncology.

Comparison of Different Haplotype-Based Haplotype-Based Association Methods for Gene-Environment (G×E) Interactions in Case-Control Studies when Haplotype-Phase Is Ambiguous

Jenny Chang-Claude, Rebecca Hein, Lars Beckmann, 2009, Human Heredity.

Whole-Genome Amplification Enables Accurate Genotyping for Microarray-Based High-Density Single Nucleotide Polymorphism Array

Muhammad G. Kibriya, Jenny Chang-Claude, Habibul Ahsan, 2008, Cancer Epidemiology Biomarkers & Prevention.

Diagnostics for Pleiotropy in Mendelian Randomization Studies: Global and Individual Tests for Direct Effects

Mathieu Lemire, Mingyang Song, Li Hsu, 2018, American journal of epidemiology.

Individual patient data meta-analysis shows a significant association between the ATM rs1801516 SNP and toxicity after radiotherapy in 5456 breast and prostate cancer patients.

Petra Seibold, Hubert Thierens, Alison M Dunning, 2016, Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology.

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.

Predicting survival from colorectal cancer histology slides using deep learning: A retrospective multicenter study

Constantino Carlos Reyes-Aldasoro, Jakob Nikolas Kather, Hermann Brenner, 2019, PLoS medicine.

Identification of Novel Genetic Markers of Breast Cancer Survival

Peter Kraft, Nazneen Rahman, Janet A. Dunn, 2015, Journal of the National Cancer Institute.

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.

Genetic polymorphisms of MPO, GSTT1, GSTM1, GSTP1, EPHX1 and NQO1 as risk factors of early‐onset lung cancer

Jenny Chang-Claude, Kirstin Mittelstrass, Thomas Illig, 2010, International journal of cancer.

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

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

Heterogeneity of Breast Cancer Associations with Five Susceptibility Loci by Clinical and Pathological Characteristics

Peter Kraft, Michael Bremer, Simon S. Cross, 2008, PLoS 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.

Repeat physical activity measurement by accelerometry among colorectal cancer patients—feasibility and minimal number of days of monitoring

Jürgen Böhm, Jenny Chang-Claude, Karen Steindorf, 2015, BMC Research Notes.

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

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

CD24 polymorphisms in breast cancer: impact on prognosis and risk

Barbara Burwinkel, Petra Seibold, Andreas Schneeweiss, 2013, Breast Cancer Research and Treatment.

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.

A Genome-wide Association Study of Early-Onset Breast Cancer Identifies PFKM as a Novel Breast Cancer Gene and Supports a Common Genetic Spectrum for Breast Cancer at Any Age

Jianxin Shi, Daniel F. Schmidt, Nazneen Rahman, 2014, Cancer Epidemiology, Biomarkers & Prevention.

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.

Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility.

Michael Krawczak, Henry Völzke, Barbara Burwinkel, 2010, Carcinogenesis.

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 .

Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk

Mads Thomassen, Julian Peto, Peter A. Fasching, 2013, PLoS genetics.

Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer

Steven Gallinger, Henry Völzke, Brent W Zanke, 2008, Nature Genetics.

Evaluation of human papillomavirus antibodies and risk of subsequent head and neck cancer.

Paolo Vineis, Salvatore Panico, Mattias Johansson, 2013, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Low-penetrance susceptibility to breast cancer due to CHEK2*1100delC in noncarriers of BRCA1 or BRCA2 mutations

Nazneen Rahman, Carel Meijers, Julian Peto, 2002, Nature Genetics.

SNP-SNP interaction analysis of NF-κB signaling pathway on breast cancer survival

Bernd Holleczek, Peter A. Fasching, Simon S. Cross, 2015, Oncotarget.

Reproductive factors and familial predisposition for breast cancer by age 50 years. A case-control-family study for assessing main effects and possible gene-environment interaction.

Silke Schmidt, Jenny Chang-Claude, Heiko Becher, 2003, International journal of epidemiology.

Prediction of BRCA1 Status in Patients with Breast Cancer Using Estrogen Receptor and Basal Phenotype

Julian Peto, Ute Hamann, Peter Devilee, 2005, Clinical Cancer Research.

Association of aspirin and NSAID use with risk of colorectal cancer according to genetic variants.

Mathieu Lemire, John D Potter, Conghui Qu, 2015, JAMA.

A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma.

Ying Wang, William Wheeler, Andres Metspalu, 2009, American journal of human genetics.

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 .

Gene–Environment Interaction Involving Recently Identified Colorectal Cancer Susceptibility Loci

Mathieu Lemire, Jing Ma, Mengmeng Du, 2014, Cancer Epidemiology, Biomarkers & Prevention.

Genome-wide interaction study of smoking and bladder cancer risk.

William Wheeler, Paolo Vineis, Peter Kraft, 2014, Carcinogenesis.

Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for Thirteen Cancer Types.

Jian Su, Wen Tan, Paolo Vineis, 2015, Journal of the National Cancer Institute.

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.

STROGAR – STrengthening the Reporting Of Genetic Association studies in Radiogenomics

Joseph O Deasy, Alison M Dunning, Jenny Chang-Claude, 2013, Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology.

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

Christiana Kartsonaki, Mads Thomassen, Julian Peto, 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.

Post-GWAS gene-environment interplay in breast cancer: results from the Breast and Prostate Cancer Cohort Consortium and a meta-analysis on 79,000 women.

Peter Kraft, Sara Lindström, I-Min Lee, 2014, Human molecular genetics.

Radiogenomics: radiobiology enters the era of big data and team science.

Andre Dekker, Michael Baumann, Karin Haustermans, 2014, International journal of radiation oncology, biology, physics.

Differential effect of NAT2 on the association between active and passive smoke exposure and breast cancer risk.

Jenny Chang-Claude, Angela Risch, J. Chang-Claude, 2002, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

Individual patient data meta-analysis shows no association between the SNP rs1800469 in TGFB and late radiotherapy toxicity.

Petra Seibold, Frederik Wenz, Alison M Dunning, 2012, Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology.

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.

Predictive factors for late normal tissue complications following radiotherapy for breast cancer

Frederik Wenz, Jenny Chang-Claude, Christine B. Ambrosone, 2007, Breast Cancer Research and Treatment.

Reduced risk of colorectal cancer up to 10 years after screening, surveillance, or diagnostic colonoscopy.

Christian Stock, Phillip Knebel, Hermann Brenner, 2014, Gastroenterology.

Gene–environment interactions for complex traits: definitions, methodological requirements and challenges

Jenny Chang-Claude, Astrid Dempfle, André Scherag, 2008, European Journal of Human Genetics.

Colorectal cancer and polymorphisms in DNA repair genes WRN, RMI1 and BLM.

Hermann Brenner, Jenny Chang-Claude, Thomas Illig, 2010, Carcinogenesis.

Estimating the heritability of colorectal cancer.

John D Potter, Jian Gong, Sonja Berndt, 2014, Human molecular genetics.

Intrinsic breast cancer subtypes defined by estrogen receptor signalling—prognostic relevance of progesterone receptor loss

Petra Seibold, Andreas Schneeweiss, Jenny Chang-Claude, 2013, Modern Pathology.

A Network-Based Kernel Machine Test for the Identification of Risk Pathways in Genome-Wide Association Studies

Christopher I. Amos, Thomas Kneib, Jenny Chang-Claude, 2014, Human Heredity.

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 .

Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations.

Steven Gallinger, Peter Kraft, Nazneen Rahman, 2016, Cancer research.

Epigenetic regulation of diacylglycerol kinase alpha promotes radiation-induced fibrosis

Axel Benner, Petra Seibold, Frederik Wenz, 2016, Nature Communications.

Circulating miRNAs with prognostic value in metastatic breast cancer and for early detection of metastasis.

Andreas Trumpp, Barbara Burwinkel, Manuela Zucknick, 2016, Carcinogenesis.

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.

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.

Sample size requirements for indirect association studies of gene–environment interactions (G × E)

Jenny Chang-Claude, Rebecca Hein, J. Chang-Claude, 2008, Genetic epidemiology.

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.

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

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

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.

Case-control study of physical activity and breast cancer risk among premenopausal women in Germany.

Jenny Chang-Claude, Karen Steindorf, J. Chang-Claude, 2003, American journal of epidemiology.

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.

Quantifying the Genetic Correlation between Multiple Cancer Types

Harvey Risch, Peter Kraft, Benjamin Neale, 2017, Cancer Epidemiology, Biomarkers & Prevention.

Age at Menarche and Menopause and Breast Cancer Risk in the International BRCA1/2 Carrier Cohort Study

Douglas F. Easton, Antonis C. Antoniou, Ana Osorio, 2007, Cancer Epidemiology Biomarkers & Prevention.

Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33.

William Wheeler, Hideo Tanaka, Jianxin Shi, 2014, Human molecular genetics.

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

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

Enrichment of colorectal cancer associations in functional regions: Insight for using epigenomics data in the analysis of whole genome sequence-imputed GWAS data

Mathieu Lemire, Steven Gallinger, Anshul Kundaje, 2017, PloS one.

Topography of cancer-associated immune cells in human solid tumors

Jakob Nikolas Kather, Jenny Chang-Claude, Niels Halama, 2018, eLife.

Intron 3 16 bp duplication polymorphism of p53 is associated with an increased risk for breast cancer by the age of 50 years.

Shan Wang-Gohrke, Jenny Chang-Claude, Heiko Becher, 2002, Pharmacogenetics.

Test-retest reliability of self-reported reproductive and lifestyle data in the context of a German case-control study on breast cancer and postmenopausal hormone therapy.

Dieter Flesch-Janys, Jenny Chang-Claude, J. Chang-Claude, 2007, Annals of epidemiology.

Clinical-grade Detection of Microsatellite Instability in Colorectal Tumors by Deep Learning.

Alexander T. Pearson, Philip Quirke, Jakob Nikolas Kather, 2020, Gastroenterology.

American Journal of Epidemiology Original Contribution Helicobacter Pylori Infection and Colorectal Cancer Risk: Evidence from a Large Population-based Case-control Study in Germany

Hermann Brenner, Jenny Chang-Claude, Michael Hoffmeister, 2022 .

Haplotype sharing analysis with SNPs in candidate genes: the genetic analysis workshop 12 example

Jenny Chang-Claude, Paul Majoram, Christine Fischer, 2003, Genetic epidemiology.

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.

Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk

Yan Guo, Ben Zhang, Min-Ho Shin, 2014, Nature 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.

Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for 13 Cancer Types

Alison P. Klein, William Wheeler, Li Jin, 2015 .

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.

2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy

Matthias W. Beckmann, Peter A. Fasching, Nur Aishah Mohd Taib, 2014, Nature Communications.

A model to determine colorectal cancer risk using common genetic susceptibility loci.

Mengmeng Du, Yingye Zheng, Jian Gong, 2015, Gastroenterology.

Assessment of polygenic architecture and risk prediction based on common variants across fourteen cancers

Alison P. Klein, Yan Zhang, Peter Kraft, 2019, bioRxiv.

Establishment of a Radiogenomics Consortium.

Andrzej Polanski, Karin Haustermans, Barry Rosenstein, 2010, International journal of radiation oncology, biology, physics.

The UGT1A6_19_GG genotype is a breast cancer risk factor

Peter A. Fasching, Thomas Brüning, Beate Pesch, 2013, Front. Genet..

Assessment of polygenic architecture and risk prediction based on common variants across fourteen cancers

Alison P. Klein, Peter Kraft, Florence Demenais, 2020, Nature Communications.

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.

Haplotype Misclassification Resulting from Statistical Reconstruction and Genotype Error, and Its Impact on Association Estimates

Florian Kronenberg, Jenny Chang-Claude, Helmut Küchenhoff, 2010, Annals of human genetics.

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.

Matrix Metalloproteinase 1 (MMP1) Is Associated with Early-Onset Lung Cancer

Florian Kronenberg, Jenny Chang-Claude, Kirstin Mittelstrass, 2008, Cancer Epidemiology Biomarkers & Prevention.

SBERIA: Set‐Based Gene‐Environment Interaction Test for Rare and Common Variants in Complex Diseases

Mathieu Lemire, Li Hsu, Hermann Brenner, 2013, Genetic epidemiology.

Material Supplementary Cited Articles E-mail Alerts Characterization of Gene–environment Interactions for Colorectal Cancer Susceptibility Loci American Association for Cancer Research

Mathieu Lemire, Steven Gallinger, Yan Liu, 2022 .