Genome-scale network model of metabolism and histone acetylation reveals metabolic dependencies of histone deacetylase inhibitors

por Shen, Fangzhou, Boccuto, Luigi, Pauly, Rini, Srikanth, Sujata, Chandrasekaran, Sriram
Publicado 2019

Identification of condition-specific biomarker systems in uterine cancer

por Hickman, Allison R, Hang, Yuqing, Pauly, Rini, Feltus, Frank A
Publicado 2021

Insect Innate Immunity Database (IIID): An Annotation Tool for Identifying Immune Genes in Insect Genomes

por Brucker, Robert M., Funkhouser, Lisa J., Setia, Shefali, Pauly, Rini, Bordenstein, Seth R.
Publicado 2012

Discovery of eQTL Alleles Associated with Autism Spectrum Disorder: A Case–Control Study

por Hickman, Allison R., Selee, Bradley, Pauly, Rini, Husain, Benafsh, Hang, Yuqing, Feltus, Frank Alex
Publicado 2022

Identification of condition-specific regulatory mechanisms in normal and cancerous human lung tissue

por Hang, Yuqing, Burns, Josh, Shealy, Benjamin T., Pauly, Rini, Ficklin, Stephen P., Feltus, Frank A.
Publicado 2022

Named Data Networking for Genomics Data Management and Integrated Workflows

por Ogle, Cameron, Reddick, David, McKnight, Coleman, Biggs, Tyler, Pauly, Rini, Ficklin, Stephen P., Feltus, F. Alex, Shannigrahi, Susmit
Publicado 2021

Farewell to GBM-O: Genomic and transcriptomic profiling of glioblastoma with oligodendroglioma component reveals distinct molecular subgroups

por Hinrichs, Benjamin H., Newman, Scott, Appin, Christina L., Dunn, William, Cooper, Lee, Pauly, Rini, Kowalski, Jeanne, Rossi, Michael R., Brat, Daniel J.
Publicado 2016

Abnormalities in the genes that encode Large Amino Acid Transporters increase the risk of Autism Spectrum Disorder

por Cascio, Lauren, Chen, Chin‐Fu, Pauly, Rini, Srikanth, Sujata, Jones, Kelly, Skinner, Cindy D., Stevenson, Roger E., Schwartz, Charles E., Boccuto, Luigi
Publicado 2019

Position effects of 22q13 rearrangements on candidate genes in Phelan-McDermid syndrome

por Srikanth, Sujata, Jain, Lavanya, Zepeda-Mendoza, Cinthya, Cascio, Lauren, Jones, Kelly, Pauly, Rini, DuPont, Barb, Rogers, Curtis, Sarasua, Sara, Phelan, Katy, Morton, Cynthia, Boccuto, Luigi
Publicado 2021

A new test for autism spectrum disorder: Metabolic data from different cell types

por Srikanth, Sujata, Cascio, Lauren, Pauly, Rini, Jones, Kelly, Sorrow, Skylar, Cubillan, Rossana, Chen, Chin-Fu, Skinner, Cindy D., Champaigne, Kevin, Stevenson, Roger E., Schwartz, Charles E., Boccuto, Luigi
Publicado 2021

A Rare De Novo RAI1 Gene Mutation Affecting BDNF-Enhancer-Driven Transcription Activity Associated with Autism and Atypical Smith-Magenis Syndrome Presentation

por Abad, Clemer, Cook, Melissa M., Cao, Lei, Jones, Julie R., Rao, Nalini R., Dukes-Rimsky, Lynn, Pauly, Rini, Skinner, Cindy, Wang, Yunsheng, Luo, Feng, Stevenson, Roger E., Walz, Katherina, Srivastava, Anand K.
Publicado 2018

Gene integrated set profile analysis: a context-based approach for inferring biological endpoints

por Kowalski, Jeanne, Dwivedi, Bhakti, Newman, Scott, Switchenko, Jeffery M., Pauly, Rini, Gutman, David A., Arora, Jyoti, Gandhi, Khanjan, Ainslie, Kylie, Doho, Gregory, Qin, Zhaohui, Moreno, Carlos S., Rossi, Michael R., Vertino, Paula M., Lonial, Sagar, Bernal-Mizrachi, Leon, Boise, Lawrence H.
Publicado 2016

Spermine synthase deficiency causes lysosomal dysfunction and oxidative stress in models of Snyder-Robinson syndrome

por Li, Chong, Brazill, Jennifer M., Liu, Sha, Bello, Christofer, Zhu, Yi, Morimoto, Marie, Cascio, Lauren, Pauly, Rini, Diaz-Perez, Zoraida, Malicdan, May Christine V., Wang, Hongbo, Boccuto, Luigi, Schwartz, Charles E., Gahl, William A., Boerkoel, Cornelius F., Zhai, R. Grace
Publicado 2017

Publisher Correction: Spermine synthase deficiency causes lysosomal dysfunction and oxidative stress in models of Snyder-Robinson syndrome

por Li, Chong, Brazill, Jennifer M., Liu, Sha, Bello, Christofer, Zhu, Yi, Morimoto, Marie, Cascio, Lauren, Pauly, Rini, Diaz-Perez, Zoraida, Malicdan, May Christine V., Wang, Hongbo, Boccuto, Luigi, Schwartz, Charles E., Gahl, William A., Boerkoel, Cornelius F., Zhai, R. Grace
Publicado 2018

DIPG-47. TSO500ctDNA sequencing reveals oncogenic mutations and copy number variations in the liquid biome of children with diffuse midline glioma

por Bonner, Erin R, Harrington, Robin, Eze, Augustine, Bornhorst, Miriam, Kline, Cassie N, Dawood, Adam, Das, Biswajit, Chen, Li, Pauly, Rini, Williams, P Mickey, Karlovich, Chris, Peach, Amanda, Howell, D'Andra, Doroshow, James, Kilburn, Lindsay, Packer, Roger J, Mueller, Sabine, Nazarian, Javad
Publicado 2022

Circulating tumor DNA sequencing provides comprehensive mutation profiling for pediatric central nervous system tumors

por Bonner, Erin R., Harrington, Robin, Eze, Augustine, Bornhorst, Miriam, Kline, Cassie N., Gordish-Dressman, Heather, Dawood, Adam, Das, Biswajit, Chen, Li, Pauly, Rini, Williams, P. Mickey, Karlovich, Chris, Peach, Amanda, Howell, D’andra, Doroshow, James, Kilburn, Lindsay, Packer, Roger J., Mueller, Sabine, Nazarian, Javad
Publicado 2022