Redefining tissue specificity of genetic regulation of gene expression in the presence of allelic heterogeneity

por Arvanitis, Marios, Tayeb, Karl, Strober, Benjamin J., Battle, Alexis
Publicado 2022

Fine-mapping causal tissues and genes at disease-associated loci

por Strober, Benjamin J., Zhang, Martin Jinye, Amariuta, Tiffany, Rossen, Jordan, Price, Alkes L.
Publicado 2023

Single-cell allele-specific expression analysis reveals dynamic and cell-type-specific regulatory effects

por Qi, Guanghao, Strober, Benjamin J., Popp, Joshua M., Keener, Rebecca, Ji, Hongkai, Battle, Alexis
Publicado 2023

Human embryoid bodies as a novel system for genomic studies of functionally diverse cell types

por Rhodes, Katherine, Barr, Kenneth A, Popp, Joshua M, Strober, Benjamin J, Battle, Alexis, Gilad, Yoav
Publicado 2022

Single-cell sequencing reveals lineage-specific dynamic genetic regulation of gene expression during human cardiomyocyte differentiation

por Elorbany, Reem, Popp, Joshua M., Rhodes, Katherine, Strober, Benjamin J., Barr, Kenneth, Qi, Guanghao, Gilad, Yoav, Battle, Alexis
Publicado 2022

A method to predict the impact of regulatory variants from DNA sequence

por Lee, Dongwon, Gorkin, David U., Baker, Maggie, Strober, Benjamin J., Asoni, Alessandro L., McCallion, Andrew S., Beer, Michael A.
Publicado 2015

The impact of rare variation on gene expression across tissues

por Li, Xin, Kim, Yungil, Tsang, Emily K., Davis, Joe R., Damani, Farhan N., Chiang, Colby, Hess, Gaelen T., Zappala, Zachary, Strober, Benjamin J., Scott, Alexandra J., Li, Amy, Ganna, Andrea, Bassik, Michael C., Merker, Jason D., Hall, Ira M., Battle, Alexis, Montgomery, Stephen B.
Publicado 2017

Merkel cell polyomavirus recruits MYCL to the EP400 complex to promote oncogenesis

por Cheng, Jingwei, Park, Donglim Esther, Berrios, Christian, White, Elizabeth A., Arora, Reety, Yoon, Rosa, Branigan, Timothy, Xiao, Tengfei, Westerling, Thomas, Federation, Alexander, Zeid, Rhamy, Strober, Benjamin, Swanson, Selene K., Florens, Laurence, Bradner, James E., Brown, Myles, Howley, Peter M., Padi, Megha, Washburn, Michael P., DeCaprio, James A.
Publicado 2017

Identification of rare-disease genes using blood transcriptome sequencing and large control cohorts

por Frésard, Laure, Smail, Craig, Ferraro, Nicole M., Teran, Nicole A., Li, Xin, Smith, Kevin S., Bonner, Devon, Kernohan, Kristin D., Marwaha, Shruti, Zappala, Zachary, Balliu, Brunilda, Davis, Joe R., Liu, Boxiang, Prybol, Cameron J., Kohler, Jennefer N., Zastrow, Diane B., Reuter, Chloe M., Fisk, Dianna G., Grove, Megan E., Davidson, Jean M., Hartley, Taila, Joshi, Ruchi, Strober, Benjamin J., Utiramerur, Sowmithri, Lind, Lars, Ingelsson, Erik, Battle, Alexis, Bejerano, Gill, Bernstein, Jonathan A., Ashley, Euan A., Boycott, Kym M., Merker, Jason D., Wheeler, Matthew T., Montgomery, Stephen B.
Publicado 2019

The functional impact of rare variation across the regulatory cascade

por Li, Taibo, Ferraro, Nicole, Strober, Benjamin J., Aguet, Francois, Kasela, Silva, Arvanitis, Marios, Ni, Bohan, Wiel, Laurens, Hershberg, Elliot, Ardlie, Kristin, Arking, Dan E., Beer, Rebecca L., Brody, Jennifer, Blackwell, Thomas W., Clish, Clary, Gabriel, Stacey, Gerszten, Robert, Guo, Xiuqing, Gupta, Namrata, Johnson, W. Craig, Lappalainen, Tuuli, Lin, Henry J., Liu, Yongmei, Nickerson, Deborah A., Papanicolaou, George, Pritchard, Jonathan K., Qasba, Pankaj, Shojaie, Ali, Smith, Josh, Sotoodehnia, Nona, Taylor, Kent D., Tracy, Russell P., Van Den Berg, David, Wheeler, Matthew T., Rich, Stephen S., Rotter, Jerome I., Battle, Alexis, Montgomery, Stephen B.
Publicado 2023