Spatial normalization improves the quality of genotype calling for Affymetrix SNP 6.0 arrays

por Chai, High Seng, Therneau, Terry M, Bailey, Kent R, Kocher, Jean-Pierre A
Publicado 2010

GLOSSI: a method to assess the association of genetic loci-sets with complex diseases

por Chai, High-Seng, Sicotte, Hugues, Bailey, Kent R, Turner, Stephen T, Asmann, Yan W, Kocher, Jean-Pierre A
Publicado 2009

Copy number variation and cytidine analogue cytotoxicity: A genome-wide association approach

por Kalari, Krishna R, Hebbring, Scott J, Chai, High Seng, Li, Liang, Kocher, Jean-Pierre A, Wang, Liewei, Weinshilboum, Richard M
Publicado 2010

Batch effect correction for genome-wide methylation data with Illumina Infinium platform

por Sun, Zhifu, Chai, High Seng, Wu, Yanhong, White, Wendy M, Donkena, Krishna V, Klein, Christopher J, Garovic, Vesna D, Therneau, Terry M, Kocher, Jean-Pierre A
Publicado 2011

Concordance of Changes in Metabolic Pathways Based on Plasma Metabolomics and Skeletal Muscle Transcriptomics in Type 1 Diabetes

por Dutta, Tumpa, Chai, High Seng, Ward, Lawrence E., Ghosh, Aditya, Persson, Xuan-Mai T., Ford, G. Charles, Kudva, Yogish C., Sun, Zhifu, Asmann, Yan W., Kocher, Jean-Pierre A., Nair, K. Sreekumaran
Publicado 2012

A novel bioinformatics pipeline for identification and characterization of fusion transcripts in breast cancer and normal cell lines

por Asmann, Yan W., Hossain, Asif, Necela, Brian M., Middha, Sumit, Kalari, Krishna R., Sun, Zhifu, Chai, High-Seng, Williamson, David W., Radisky, Derek, Schroth, Gary P., Kocher, Jean-Pierre A., Perez, Edith A., Thompson, E. Aubrey
Publicado 2011

TREAT: a bioinformatics tool for variant annotations and visualizations in targeted and exome sequencing data

por Asmann, Yan W., Middha, Sumit, Hossain, Asif, Baheti, Saurabh, Li, Ying, Chai, High-Seng, Sun, Zhifu, Duffy, Patrick H., Hadad, Ahmed A., Nair, Asha, Liu, Xiaoyu, Zhang, Yuji, Klee, Eric W., Kalari, Krishna R., Kocher, Jean-Pierre A.
Publicado 2012

Deep Sequence Analysis of Non-Small Cell Lung Cancer: Integrated Analysis of Gene Expression, Alternative Splicing, and Single Nucleotide Variations in Lung Adenocarcinomas with an...

por Kalari, Krishna R., Rossell, David, Necela, Brian M., Asmann, Yan W., Nair, Asha, Baheti, Saurabh, Kachergus, Jennifer M., Younkin, Curtis S., Baker, Tiffany, Carr, Jennifer M., Tang, Xiaojia, Walsh, Michael P., Chai, High-Seng, Sun, Zhifu, Hart, Steven N., Leontovich, Alexey A., Hossain, Asif, Kocher, Jean-Pierre, Perez, Edith A., Reisman, David N., Fields, Alan P., Thompson, E. Aubrey
Publicado 2012

An Integrated Model of the Transcriptome of HER2-Positive Breast Cancer

por Kalari, Krishna R., Necela, Brian M., Tang, Xiaojia, Thompson, Kevin J., Lau, Melissa, Eckel-Passow, Jeanette E., Kachergus, Jennifer M., Anderson, S. Keith, Sun, Zhifu, Baheti, Saurabh, Carr, Jennifer M., Baker, Tiffany R., Barman, Poulami, Radisky, Derek C., Joseph, Richard W., McLaughlin, Sarah A., Chai, High-seng, Camille, Stephan, Rossell, David, Asmann, Yan W., Thompson, E. Aubrey, Perez, Edith A.
Publicado 2013

Late-onset Alzheimer disease risk variants mark brain regulatory loci

por Allen, Mariet, Kachadoorian, Michaela, Carrasquillo, Minerva M., Karhade, Aditya, Manly, Lester, Burgess, Jeremy D., Wang, Chen, Serie, Daniel, Wang, Xue, Siuda, Joanna, Zou, Fanggeng, Chai, High Seng, Younkin, Curtis, Crook, Julia, Medway, Christopher, Nguyen, Thuy, Ma, Li, Malphrus, Kimberly, Lincoln, Sarah, Petersen, Ronald C., Graff-Radford, Neill R., Asmann, Yan W., Dickson, Dennis W., Younkin, Steven G., Ertekin-Taner, Nilüfer
Publicado 2015

Human whole genome genotype and transcriptome data for Alzheimer’s and other neurodegenerative diseases

por Allen, Mariet, Carrasquillo, Minerva M., Funk, Cory, Heavner, Benjamin D., Zou, Fanggeng, Younkin, Curtis S., Burgess, Jeremy D., Chai, High-Seng, Crook, Julia, Eddy, James A., Li, Hongdong, Logsdon, Ben, Peters, Mette A., Dang, Kristen K., Wang, Xue, Serie, Daniel, Wang, Chen, Nguyen, Thuy, Lincoln, Sarah, Malphrus, Kimberly, Bisceglio, Gina, Li, Ma, Golde, Todd E., Mangravite, Lara M., Asmann, Yan, Price, Nathan D., Petersen, Ronald C., Graff-Radford, Neill R., Dickson, Dennis W., Younkin, Steven G., Ertekin-Taner, Nilüfer
Publicado 2016

Brain Expression Genome-Wide Association Study (eGWAS) Identifies Human Disease-Associated Variants

por Zou, Fanggeng, Chai, High Seng, Younkin, Curtis S., Allen, Mariet, Crook, Julia, Pankratz, V. Shane, Carrasquillo, Minerva M., Rowley, Christopher N., Nair, Asha A., Middha, Sumit, Maharjan, Sooraj, Nguyen, Thuy, Ma, Li, Malphrus, Kimberly G., Palusak, Ryan, Lincoln, Sarah, Bisceglio, Gina, Georgescu, Constantin, Kouri, Naomi, Kolbert, Christopher P., Jen, Jin, Haines, Jonathan L., Mayeux, Richard, Pericak-Vance, Margaret A., Farrer, Lindsay A., Schellenberg, Gerard D., Petersen, Ronald C., Graff-Radford, Neill R., Dickson, Dennis W., Younkin, Steven G., Ertekin-Taner, Nilüfer
Publicado 2012

Association of MAPT haplotypes with Alzheimer’s disease risk and MAPT brain gene expression levels

por Allen, Mariet, Kachadoorian, Michaela, Quicksall, Zachary, Zou, Fanggeng, Chai, High Seng, Younkin, Curtis, Crook, Julia E, Pankratz, V Shane, Carrasquillo, Minerva M, Krishnan, Siddharth, Nguyen, Thuy, Ma, Li, Malphrus, Kimberly, Lincoln, Sarah, Bisceglio, Gina, Kolbert, Christopher P, Jen, Jin, Mukherjee, Shubhabrata, Kauwe, John K, Crane, Paul K, Haines, Jonathan L, Mayeux, Richard, Pericak-Vance, Margaret A, Farrer, Lindsay A, Schellenberg, Gerard D, Parisi, Joseph E, Petersen, Ronald C, Graff-Radford, Neill R, Dickson, Dennis W, Younkin, Steven G, Ertekin-Taner, Nilüfer
Publicado 2014

Glutathione S-transferase omega genes in Alzheimer and Parkinson disease risk, age-at-diagnosis and brain gene expression: an association study with mechanistic implications

por Allen, Mariet, Zou, Fanggeng, Chai, High Seng, Younkin, Curtis S, Miles, Richard, Nair, Asha A, Crook, Julia E, Pankratz, V Shane, Carrasquillo, Minerva M, Rowley, Christopher N, Nguyen, Thuy, Ma, Li, Malphrus, Kimberly G, Bisceglio, Gina, Ortolaza, Alexandra I, Palusak, Ryan, Middha, Sumit, Maharjan, Sooraj, Georgescu, Constantin, Schultz, Debra, Rakhshan, Fariborz, Kolbert, Christopher P, Jen, Jin, Sando, Sigrid B, Aasly, Jan O, Barcikowska, Maria, Uitti, Ryan J, Wszolek, Zbigniew K, Ross, Owen A, Petersen, Ronald C, Graff-Radford, Neill R, Dickson, Dennis W, Younkin, Steven G, Ertekin-Taner, Nilüfer
Publicado 2012

Genome-wide study of resistant hypertension identified from electronic health records

por Dumitrescu, Logan, Ritchie, Marylyn D., Denny, Joshua C., El Rouby, Nihal M., McDonough, Caitrin W., Bradford, Yuki, Ramirez, Andrea H., Bielinski, Suzette J., Basford, Melissa A., Chai, High Seng, Peissig, Peggy, Carrell, David, Pathak, Jyotishman, Rasmussen, Luke V., Wang, Xiaoming, Pacheco, Jennifer A., Kho, Abel N., Hayes, M. Geoffrey, Matsumoto, Martha, Smith, Maureen E., Li, Rongling, Cooper-DeHoff, Rhonda M., Kullo, Iftikhar J., Chute, Christopher G., Chisholm, Rex L., Jarvik, Gail P., Larson, Eric B., Carey, David, McCarty, Catherine A., Williams, Marc S., Roden, Dan M., Bottinger, Erwin, Johnson, Julie A., de Andrade, Mariza, Crawford, Dana C.
Publicado 2017