Christopher I. Amos

22 papers Misc 4Journal 17Unranked 1
YearRankTypeTitle / Venue / Authors
2022 J jnl
Iam hiQ - a novel pair of accuracy indices for imputed genotypes.
BMC Bioinform.
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
2021 Misc conf
Lessons Learned from an Enterprise-Wide Clinical Datathon.
AMIA
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
2020 J jnl
Cancer prognosis prediction using somatic point mutation and copy number variation data: a comparison of gene-level and pathway-based models.
BMC Bioinform.
Xingyu Zheng, Christopher I. Amos, H. Robert Frost
2020 J jnl
Comparison of pathway and gene-level models for cancer prognosis prediction.
BMC Bioinform.
Xingyu Zheng, Christopher I. Amos, H. Robert Frost
2019 J jnl
An accurate and powerful method for copy number variation detection.
Bioinform.
Feifei Xiao, Xizhi Luo, Ning Hao, Yue Niu, Xiangjun Xiao, Guoshuai Cai, Christopher I. Amos, Heping Zhang
2018 J jnl
A multi-omics approach for identifying important pathways and genes in human cancer.
BMC Bioinform.
H. Robert Frost, Christopher I. Amos
2018 — conf
An Efficient Survival Multifactor Dimensionality Reduction Method for Detecting Gene-Gene Interactions of Lung Cancer Onset Age.
BIBM
Jennifer Luyapan, Xuemei Ji, Dakai Zhu, Todd A. MacKenzie, Christopher I. Amos, Jiang Gui
2018 J jnl
Gene characteristics predicting missense, nonsense and frameshift mutations in tumor samples.
BMC Bioinform.
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
2017 J jnl
Pathway-Based Kernel Boosting for the Analysis of Genome-Wide Association Studies.
Comput. Math. Methods Medicine
Stefanie Friedrichs, Juliane Manitz, Patricia Burger, Christopher I. Amos, Angela Risch, Jenny Chang-Claude, Heinz-Erich Wichmann, Thomas Kneib, Heike Bickeböller, Benjamin Hofner
2017 J jnl
seXY: a tool for sex inference from genotype arrays.
Bioinform.
David C. Qian, Jonathan A. Busam, Xiangjun Xiao, Tracy A. O'Mara, Rosalind A. Eeles, Frederick R. Schumacher, Catherine M. Phelan, Christopher I. Amos
2016 J jnl
Component-wise gradient boosting and false discovery control in survival analysis with high-dimensional covariates.
Bioinform.
Kevin He, Yanming Li, Ji Zhu, Hongliang Liu, Jeffrey E. Lee, Christopher I. Amos, Terry Hyslop, Jiashun Jin, Huazhen Lin, Qinyi Wei, Yi Li
2016 J jnl
FastPop: a rapid principal component derived method to infer intercontinental ancestry using genetic data.
BMC Bioinform.
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
2016 J jnl
Unsupervised gene set testing based on random matrix theory.
BMC Bioinform.
H. Robert Frost, Christopher I. Amos
2014 J jnl
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.
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
2012 J jnl
Derived SNP Alleles are Used More Frequently than Ancestral Alleles as Risk-associated Variants in Common Human Diseases.
J. Bioinform. Comput. Biol.
Olga Y. Gorlova, Jun Ying, Christopher I. Amos, Margaret R. Spitz, Bo Peng, Ivan P. Gorlov
2011 J jnl
Genome-wide algorithm for detecting CNV associations with diseases.
BMC Bioinform.
Yaji Xu, Bo Peng, Yunxin Fu, Christopher I. Amos
2010 J jnl
Forward-time simulation of realistic samples for genome-wide association studies.
BMC Bioinform.
Bo Peng, Christopher I. Amos
2009 J jnl
Statistical genetics & statistical genomics: Where biology, epistemology, statistics, and computation collide.
Comput. Stat. Data Anal.
David B. Allison, Peter M. Visscher, Guilherme J. M. Rosa, Christopher I. Amos
2008 J jnl
Forward-time simulations of non-random mating populations using simuPOP.
Bioinform.
Bo Peng, Christopher I. Amos
2006 Misc conf
Strategies to Improve Healthcare Websites.
AMIA
Constance M. Johnson, Susan K. Peterson, James P. Turley, Joe Ensor, Christopher I. Amos, Margaret R. Spitz, Bernard Levin, Donald Berry
2005 Misc conf
An Informatics Tool to Assess Individualized Colon Cancer Risk.
AMIA
Constance M. Johnson, Joe Ensor, Christopher I. Amos, Margaret R. Spitz, Susan K. Peterson, Bernard Levin, Donald Berry
1999 Misc conf
KinSys: A Database Management Application.
AMIA
Constance M. Johnson, Christopher I. Amos