Ulrike Peters

发表

A Mixed-Effects Model for Powerful Association Tests in Integrative Functional Genomics.

Xinyuan Dong, Sonja Berndt, Li Hsu, 2018, American journal of human genetics.

Powerful Cocktail Methods for Detecting Genome‐Wide Gene‐Environment Interaction

Carolyn Hutter, Shuo Jiao, Li Hsu, 2012, Genetic epidemiology.

Imputation of coding variants in African Americans: better performance using data from the exome sequencing project

Yun Li, Goo Jun, Dana C. Crawford, 2013, Bioinform..

Powerful Set‐Based Gene‐Environment Interaction Testing Framework for Complex Diseases

Mathieu Lemire, John D Potter, Shuo Jiao, 2015, Genetic epidemiology.

Multivariate association analysis with somatic mutation data.

Yang Liu, Qianchuan He, Li Hsu, 2018, Biometrics.

Pleiotropic Associations of Risk Variants Identified for Other Cancers With Lung Cancer Risk: The PAGE and TRICL Consortia

Wei Chen, Dana C. Crawford, Ewa Deelman, 2014, Journal of the National Cancer Institute.

Abstract PR03: Genetic mechanisms of immune evasion in colorectal cancer

Benjamin J. Raphael, Matteo Pellegrini, Ming Yu, 2018, Systems Immuno-Oncology.

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.

Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome

William Wheeler, Nan Hu, Peter Kraft, 2016, Nature Communications.

Whole-exome imputation of sequence variants identified two novel alleles associated with adult body height in African Americans.

Mengmeng Du, Charles Kooperberg, Eric Boerwinkle, 2014, Human molecular genetics.

Is It Time to Abandon the Food Frequency Questionnaire?

Ulrike Peters, John D. Potter, Alan R. Kristal, 2005, Cancer Epidemiology Biomarkers & Prevention.

Fine-Mapping and Initial Characterization of QT Interval Loci in African Americans

Karen L. Mohlke, Praveen Sethupathy, Lucia A. Hindorff, 2012, PLoS genetics.

Genome-wide association study identifies multiple risk loci for renal cell carcinoma

Bin Tean Teh, Tony Fletcher, Peter Kraft, 2017, Nature Communications.

Association of Cancer Susceptibility Variants with Risk of Multiple Primary Cancers: The Population Architecture using Genomics and Epidemiology Study

Dana C. Crawford, Ewa Deelman, William S. Bush, 2014, Cancer Epidemiology, Biomarkers & Prevention.

Genome-wide association analyses in East Asians identify new susceptibility loci for colorectal cancer

Ben Zhang, Gong Yang, Keitaro Matsuo, 2012, Nature Genetics.

Genome-wide association study of glioma and meta-analysis

Melissa Bondy, Nilanjan Chatterjee, John K. Wiencke, 2012, Human Genetics.

A Meta-Analysis Identifies New Loci Associated with Body Mass index in Individuals of African Ancestry

Xiaofeng Zhu, Olufunmilayo I. Olopade, Alex P. Reiner, 2013, Nature Genetics.

Vitamin E and selenium supplementation and risk of prostate cancer in the Vitamins and lifestyle (VITAL) study cohort

Emily White, Ulrike Peters, John D. Potter, 2008, Cancer Causes & Control.

A Haplotype-Based Test of Association Using Data from Cohort and Nested Case-Control Epidemiologic Studies

Nilanjan Chatterjee, Jinbo Chen, Ulrike Peters, 2004, Human Heredity.

Fine Mapping and Identification of BMI Loci in African Americans.

Eric Farber-Eger, Dana C Crawford, Stephanie Rosse, 2013, American journal of human genetics.

Association of exome sequences with plasma C-reactive protein levels in >9000 participants.

Pierre Fontanillas, Charles Kooperberg, Eric Boerwinkle, 2015, Human molecular genetics.

Mapping and characterization of structural variation in 17,795 human genomes

Eric S. Lander, Haley J. Abel, Yeting Zhang, 2020, Nature.

Specialty Supplements and Prostate Cancer Risk in the VITamins And Lifestyle (VITAL) Cohort

Johanna W Lampe, Ruth E Patterson, Emily White, 2011, Nutrition and cancer.

Vitamin D pathway gene variants and prostate cancer prognosis

Joseph S Koopmeiners, Ziding Feng, Ulrike Peters, 2010, The Prostate.

Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits

Uwe Völker, Marie-Pierre Dubé, Alexander Teumer, 2014, Nature Genetics.

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

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

Analysis of Metabolic Syndrome Components in >15 000 African Americans Identifies Pleiotropic Variants: Results From the Population Architecture Using Genomics and Epidemiology Study

Chun-Nan Hsu, Nilanjan Chatterjee, Elizabeth Selvin, 2014, Circulation. Cardiovascular genetics.

Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project.

Eric Boerwinkle, Deborah A Nickerson, David Green, 2013, Blood.

Gene–Environment Interaction Involving Recently Identified Colorectal Cancer Susceptibility Loci

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

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.

Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer

Peter Kraft, Krzysztof Jamroziak, Pavel Soucek, 2018, Nature Communications.

A genome-wide association study of breast cancer in women of African ancestry

Clement Adebamowo, Olufunmilayo I. Olopade, Gary K. Chen, 2012, Human Genetics.

Pleiotropy of Cancer Susceptibility Variants on the Risk of Non-Hodgkin Lymphoma: The PAGE Consortium

Ewa Deelman, William S. Bush, Lucia A. Hindorff, 2014, PloS one.

Genome-wide physical activity interactions in adiposity. A meta-analysis of 200,452 adults

Claude Bouchard, Christian Gieger, Tuija Tammelin, 2017 .

Estimating the heritability of colorectal cancer.

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

Characterization of large structural genetic mosaicism in human autosomes.

William Wheeler, Nan Hu, Peter Kraft, 2015, American journal of human genetics.

Serum vitamin D concentration and prostate cancer risk: a nested case-control study.

Nilanjan Chatterjee, Christian C Abnet, Mark P Purdue, 2008, Journal of the National Cancer Institute.

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.

Long-Chain Omega-3 Polyunsaturated Fatty Acid Intake and Risk of Colorectal Cancer

Johanna W Lampe, Emily White, Ulrike Peters, 2014, Nutrition and cancer.

Serum Lycopene, Other Carotenoids, and Prostate Cancer Risk: a Nested Case-Control Study in the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial

Nilanjan Chatterjee, Richard B. Hayes, Elio Riboli, 2007, Cancer Epidemiology Biomarkers & Prevention.

Estimation of effect size distribution from genome-wide association studies and implications for future discoveries

Nilanjan Chatterjee, Stephen J Chanock, Mitchell H Gail, 2010, Nature Genetics.

Cross-cancer pleiotropic analysis of endometrial cancer: PAGE and E2C2 consortia.

Harvey Risch, Peter Kraft, Dana C Crawford, 2014, Carcinogenesis.

Detectable clonal mosaicism and its relationship to aging and cancer

William Wheeler, Nan Hu, Peter Kraft, 2012, Nature Genetics.

A reference panel of 64,976 haplotypes for genotype imputation

Laura J. Scott, He Zhang, Gonçalo Abecasis, 2015, bioRxiv.

Discovery of common and rare genetic risk variants for colorectal cancer

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

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.

Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project.

Sudha Seshadri, Deborah A Nickerson, Wei-Min Chen, 2015, JAMA neurology.

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.

Edinburgh Explorer Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture

Beth Wilmot, Joel Eriksson, Jie Huang, 2022 .

Genome-wide association study of body height in African Americans: the Women's Health Initiative SNP Health Association Resource (SHARe).

Nicholas A. Johnson, Carolyn M Hutter, Charles Kooperberg, 2012, Human molecular genetics.

Genotype Imputation of MetabochipSNPs Using a Study‐Specific Reference Panel of ∼4,000 Haplotypes in African Americans From the Women's Health Initiative

Wei Wang, Dana C Crawford, Eric Yi Liu, 2012, Genetic epidemiology.

Methods for etiologic and early marker investigations in the PLCO trial.

Robert N Hoover, Ulrike Peters, Paul Pinsky, 2005, Mutation research.

Joint Effects of Colorectal Cancer Susceptibility Loci, Circulating 25-Hydroxyvitamin D and Risk of Colorectal Cancer

Peter Kraft, Jing Ma, Elizabeth W. Karlson, 2014, PloS one.

Genetic susceptibility to cancer: the role of polymorphisms in candidate genes.

John D Potter, Emily White, Ulrike Peters, 2008, JAMA.

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

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

Three new pancreatic cancer susceptibility signals identified on chromosomes 1q32.1, 5p15.33 and 8q24.21

Alison P. Klein, Nan Hu, Peter Kraft, 2016, Oncotarget.

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

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

Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer

Yusuke Nakamura, Nan Hu, Peter Kraft, 2014, Nature Genetics.

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

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

A prospective study of meat and meat mutagens and prostate cancer risk.

Ulrike Peters, Rashmi Sinha, R. Sinha, 2005, Cancer research.

A Systematic Mapping Approach of 16q12.2/FTO and BMI in More Than 20,000 African Americans Narrows in on the Underlying Functional Variation: Results from the Population Architecture using Genomics and Epidemiology (PAGE) Study

Dana C. Crawford, Praveen Sethupathy, Lucia A. Hindorff, 2013, PLoS genetics.

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

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

Genome-wide association and population genetic analysis of C-reactive protein in African American and Hispanic American women.

Jennifer G. Robinson, Charles Kooperberg, Hua Tang, 2012, American journal of human genetics.

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

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

Confirmation of the Reported Association of Clonal Chromosomal Mosaicism with an Increased Risk of Incident Hematologic Cancer

Alex P. Reiner, David R. Crosslin, Gail P. Jarvik, 2013, PloS one.

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 .