Christopher I. Amos

Publication Activity (10 Years)

Years Active: 1999-2022
Publications (10 Years): 13

Top Topics

Survival Analysis

Random Matrix Theory

Association Studies

Top Venues

Publications

Albert Rosenberger, Viola Tozzi, Heike Bickeböller, Rayjean J. Hung, David C. Christiani, Neil E. Caporaso, Geoffrey Liu, Stig E. Bojesen, Loic Le Marchand, Demetrios Albanes, Melinda C. Aldrich, Adonina Tardon, Guillermo Fernández-Tardón, Gad Rennert, John K. Field, Mike Davies, Triantafillos Liloglou, Lambertus A. Kiemeney, Philip Lazarus, Aage Haugen, Shanbeh Zienolddiny, Stephen Lam, Matthew B. Schabath, Angeline S. Andrew, Eric J. Duell, Susanne M. Arnold, Hans Brunnström, Olle Melander, Gary E. Goodman, Chu Chen, Jennifer A. Doherty, Marion Dawn Teare, Angela Cox, Penella J. Woll, Angela Risch, Thomas R. Muley, Mikael Johansson, Paul Brennan, Maria Teresa Landi, Sanjay Shete, Christopher I. Amos
Iam hiQ - a novel pair of accuracy indices for imputed genotypes. BMC Bioinform. 23 (1) (2022)
Andrew J. Zimolzak, Jessica A. Davila, Vamshi Punugoti, Katherine H. Sippel, Ashok Balasubramanyam, Paul Klotman, Laura A. Petersen, Ryan H. Rochat, Gloria Liao, Rory R. Laubscher, Lee Leiber, Christopher I. Amos
Lessons Learned from an Enterprise-Wide Clinical Datathon. AMIA (2021)
Xingyu Zheng, Christopher I. Amos, H. Robert Frost
Comparison of pathway and gene-level models for cancer prognosis prediction. BMC Bioinform. 21 (1) (2020)
Xingyu Zheng, Christopher I. Amos, H. Robert Frost
Cancer prognosis prediction using somatic point mutation and copy number variation data: a comparison of gene-level and pathway-based models. BMC Bioinform. 21 (1) (2020)
Feifei Xiao, Xizhi Luo, Ning Hao, Yue Niu, Xiangjun Xiao, Guoshuai Cai, Christopher I. Amos, Heping Zhang
An accurate and powerful method for copy number variation detection. Bioinform. 35 (17) (2019)
H. Robert Frost, Christopher I. Amos
A multi-omics approach for identifying important pathways and genes in human cancer. BMC Bioinform. 19 (1) (2018)
Jennifer Luyapan, Xuemei Ji, Dakai Zhu, Todd A. MacKenzie, Christopher I. Amos, Jiang Gui
An Efficient Survival Multifactor Dimensionality Reduction Method for Detecting Gene-Gene Interactions of Lung Cancer Onset Age. BIBM (2018)
Ivan P. Gorlov, Claudio W. Pikielny, Hildreth R. Frost, Stephanie C. Her, Michael D. Cole, Samuel D. Strohbehn, David Wallace-Bradley, Marek Kimmel, Olga Y. Gorlova, Christopher I. Amos
Gene characteristics predicting missense, nonsense and frameshift mutations in tumor samples. BMC Bioinform. 19 (1) (2018)
Stefanie Friedrichs, Juliane Manitz, Patricia Burger, Christopher I. Amos, Angela Risch, Jenny Chang-Claude, Heinz-Erich Wichmann, Thomas Kneib, Heike Bickeböller, Benjamin Hofner
Pathway-Based Kernel Boosting for the Analysis of Genome-Wide Association Studies. Comput. Math. Methods Medicine 2017 (2017)
David C. Qian, Jonathan A. Busam, Xiangjun Xiao, Tracy A. O'Mara, Rosalind A. Eeles, Frederick R. Schumacher, Catherine M. Phelan, Christopher I. Amos
seXY: a tool for sex inference from genotype arrays. Bioinform. 33 (4) (2017)
Kevin He, Yanming Li, Ji Zhu, Hongliang Liu, Jeffrey E. Lee, Christopher I. Amos, Terry Hyslop, Jiashun Jin, Huazhen Lin, Qinyi Wei, Yi Li
Component-wise gradient boosting and false discovery control in survival analysis with high-dimensional covariates. Bioinform. 32 (1) (2016)
Yafang Li, Jinyoung Byun, Guoshuai Cai, Xiangjun Xiao, Younghun Han, Olivier Cornelis, James E. Dinulos, Joe Dennis, Douglas F. Easton, Ivan P. Gorlov, Michael F. Seldin, Christopher I. Amos
FastPop: a rapid principal component derived method to infer intercontinental ancestry using genetic data. BMC Bioinform. 17 (2016)
H. Robert Frost, Christopher I. Amos
Unsupervised gene set testing based on random matrix theory. BMC Bioinform. 17 (2016)
Timothy H. Ciesielski, Sarah A. Pendergrass, Marquitta J. White, Nuri Kodaman, Rafal S. Sobota, Minjun Huang, Jacquelaine Bartlett, Jing Li, Qinxin Pan, Jiang Gui, Scott B. Selleck, Christopher I. Amos, Marylyn D. Ritchie, Jason H. Moore, Scott M. Williams
Diverse convergent evidence in the genetic analysis of complex disease: coordinating omic, informatic, and experimental evidence to better identify and validate risk factors. BioData Min. 7 (2014)
Olga Y. Gorlova, Jun Ying, Christopher I. Amos, Margaret R. Spitz, Bo Peng, Ivan P. Gorlov
Derived SNP Alleles are Used More Frequently than Ancestral Alleles as Risk-associated Variants in Common Human Diseases. J. Bioinform. Comput. Biol. 10 (2) (2012)
Yaji Xu, Bo Peng, Yunxin Fu, Christopher I. Amos
Genome-wide algorithm for detecting CNV associations with diseases. BMC Bioinform. 12 (2011)
Bo Peng, Christopher I. Amos
Forward-time simulation of realistic samples for genome-wide association studies. BMC Bioinform. 11 (2010)
David B. Allison, Peter M. Visscher, Guilherme J. M. Rosa, Christopher I. Amos
Statistical genetics & statistical genomics: Where biology, epistemology, statistics, and computation collide. Comput. Stat. Data Anal. 53 (5) (2009)
Bo Peng, Christopher I. Amos
Forward-time simulations of non-random mating populations using simuPOP. Bioinform. 24 (11) (2008)
Constance M. Johnson, Susan K. Peterson, James P. Turley, Joe Ensor, Christopher I. Amos, Margaret R. Spitz, Bernard Levin, Donald Berry
Strategies to Improve Healthcare Websites. AMIA (2006)
Constance M. Johnson, Joe Ensor, Christopher I. Amos, Margaret R. Spitz, Susan K. Peterson, Bernard Levin, Donald Berry
An Informatics Tool to Assess Individualized Colon Cancer Risk. AMIA (2005)
Constance M. Johnson, Christopher I. Amos
KinSys: A Database Management Application. AMIA (1999)