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Human Molecular Genetics|December 22, 2018
Molecular signatures of X chromosome inactivation and associations with clinical outcomes in epithelial ovarian cancerStacey J Winham, Nicholas B Larson, Sebastian M Armasu, et al.
Translational Cancer Research|September 23, 2014
Integrative clustering methods for high-dimensional molecular dataPrabhakar Chalise, Devin C Koestler, Milan Bimali, et al.
Plos One|February 28, 2018
Assessment of data transformations for model-based clustering of RNA-Seq dataJanelle R Noel-MacDonnell, Joseph Usset, Ellen L Goode, et al.
Scientific Reports|December 6, 2025
Reproducibility of digital pathology features extracted from deep learning and foundational AI models on sequential tissue slidesJagadheshwar Balan, Nicholas B Larson
Molecular Vision|January 4, 2011
Genome-wide association analyses of genetic, phenotypic, and environmental risks in the age-related eye disease studyEuijung Ryu, Brooke L Fridley, Nirubol Tosakulwong, et al.
Frontiers in Genetics|September 14, 2012
Localization of association signal from risk and protective variants in sequencing studiesAbra Brisbin, Gregory D Jenkins, Katarzyna A Ellsworth, et al.
Blood|November 17, 2007
Host genetic variation contributes to phenotypic diversity in myeloproliferative disordersAnimesh Pardanani, Brooke L Fridley, Terra L Lasho, et al.
Investigative Ophthalmology & Visual Science|February 24, 2009
Complement component 3 (C3) haplotypes and risk of advanced age-related macular degenerationKyu Hyung Park, Brooke L Fridley, Euijung Ryu, et al.
Plos One|June 15, 2010
Utilizing genotype imputation for the augmentation of sequence dataBrooke L Fridley, Gregory Jenkins, Matthew E Deyo-Svendsen, et al.
European Journal of Human Genetics : EJHG|December 15, 2011
Use of the gamma method for self-contained gene-set analysis of SNP dataJoanna M Biernacka, Gregory D Jenkins, Liewei Wang, et al.
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