Christopher A. Haiman

发表

Refined histopathological predictors of BRCA1 and BRCA2 mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia | NOVA. The University of Newcastle's Digital Repository

Rosemary L. Balleine, Christine L. Clarke, D. Gareth Evans, 2014 .

Analysis of case-control association studies with known risk variants

Peter Kraft, Alkes L. Price, Noah Zaitlen, 2012, Bioinform..

Transferability of Tag SNPs to Capture Common Genetic Variation in DNA Repair Genes Across Multiple Populations

Christopher A. Haiman, Paul I. W. de Bakker, Robert R. Graham, 2005, Pacific Symposium on Biocomputing.

AA9int: SNP interaction pattern search using non‐hierarchical additive model set

Hardev Pandha, Graham G. Giles, Christopher A. Haiman, 2018, Bioinform..

Analysis of Latino populations from GALA and MEC studies reveals genomic loci with biased local ancestry estimation

Pedro C. Avila, Eran Halperin, Gary K. Chen, 2013, Bioinform..

SNP interaction pattern identifier (SIPI): an intensive search for SNP‐SNP interaction patterns

Zhide Fang, Hardev Pandha, Christopher A. Haiman, 2016, Bioinform..

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..

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

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

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.

Detectable clonal mosaicism from birth to old age and its relationship to cancer

Ingo Ruczinski, Li-e Wang, William L. Lowe, 2012, Nature Genetics.

Genome-Wide Testing of Putative Functional Exonic Variants in Relationship with Breast and Prostate Cancer Risk in a Multiethnic Population

Christopher A. Haiman, Lucy Xia, Daniel O. Stram, 2013, PLoS genetics.

Identification of Novel Genetic Markers of Breast Cancer Survival

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

Population specific reference panels are crucial for the genetic analyses of Native Hawai’ians: an example of the CREBRF locus

Maarit Tiirikainen, Christopher A. Haiman, Xin Sheng, 2019 .

Use of weighted reference panels based on empirical estimates of ancestry for capturing untyped variation

Christopher A. Haiman, Brian E. Henderson, Loic Le Marchand, 2009, Human Genetics.

Mapping adipose and muscle tissue expression quantitative trait loci in African Americans to identify genes for type 2 diabetes and obesity

Donald W. Bowden, Barry I. Freedman, Nisa M. Maruthur, 2016, Human Genetics.

The landscape of recombination in African Americans

Xiaofeng Zhu, Alex P. Reiner, Jasmin Divers, 2011, Nature.

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

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

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

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

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.

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.

Admixture Mapping of 15,280 African Americans Identifies Obesity Susceptibility Loci on Chromosomes 5 and X

Ching-Yu Cheng, Christopher A. Haiman, Matthew L. Freedman, 2009, PLoS 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.

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.

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

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

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

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

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

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

Common Genetic Variants in Prostate Cancer Risk Prediction—Results from the NCI Breast and Prostate Cancer Cohort Consortium (BPC3)

Peter Kraft, Jing Ma, Mattias Johansson, 2012, Cancer Epidemiology, Biomarkers & Prevention.

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 .

Characterizing Associations and SNP-Environment Interactions for GWAS-Identified Prostate Cancer Risk Markers—Results from BPC3

Peter Kraft, Jing Ma, Mattias Johansson, 2011, PloS one.

Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes

William S. Bush, Bin Zhu, Angeline S. Andrew, 2017, Nature Genetics.

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 Association Study of Coronary Heart Disease and Its Risk Factors in 8,090 African Americans: The NHLBI CARe Project

Donald W. Bowden, Eric Boerwinkle, Christopher A. Haiman, 2011, PLoS genetics.

Choosing Haplotype-Tagging SNPS Based on Unphased Genotype Data Using a Preliminary Sample of Unrelated Subjects with an Example from the Multiethnic Cohort Study

Christopher A. Haiman, Daniel O. Stram, Malcolm C. Pike, 2003, Human Heredity.

Association of Genes, Pathways, and Haplogroups of the Mitochondrial Genome with the Risk of Colorectal Cancer: The Multiethnic Cohort

Richa Saxena, Christopher A. Haiman, Daniel O. Stram, 2015, PloS one.

Quantifying the Genetic Correlation between Multiple Cancer Types

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

Genome-Wide Association of Body Fat Distribution in African Ancestry Populations Suggests New Loci

Mary K. Wojczynski, Charles Kooperberg, Lewis H. Kuller, 2013, PLoS genetics.

Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression

Peter Kraft, Elaine A. Ostrander, Henrik Gronberg, 2013, Human molecular genetics.

A polygenic risk score for breast cancer in U.S. Latinas and Latin-American women

Christopher A. Haiman, Luis G. Carvajal-Carmona, Lawrence H. Kushi, 2019, bioRxiv.

Haplotype-Based Association Studies of IGFBP1 and IGFBP3 with Prostate and Breast Cancer Risk: The Multiethnic Cohort

Christopher A. Haiman, Matthew L. Freedman, Daniel O. Stram, 2006, Cancer Epidemiology Biomarkers & Prevention.

The 8q24 cancer risk variant rs6983267 demonstrates long-range interaction with MYC in colorectal cancer

Christopher A. Haiman, Li Jia, Matthew L. Freedman, 2009, Nature Genetics.

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.

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.

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

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

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.

Identification of a Functional Genetic Variant at 16q12.1 for Breast Cancer Risk: Results from the Asia Breast Cancer Consortium

Wei Lu, Chiun-Sheng Huang, Guoliang Li, 2010, 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.

Phenome-Wide Association Study (PheWAS) for Detection of Pleiotropy within the Population Architecture using Genomics and Epidemiology (PAGE) Network

Marylyn D. Ritchie, Dana C. Crawford, Ewa Deelman, 2013, PLoS genetics.