SNPs2ChIP: Latent Factors of ChIP-seq to infer functions of non-coding SNPs

por Anand, Shankara, Kalesinskas, Laurynas, Smail, Craig, Tanigawa, Yosuke
Publicado 2019

Missed opportunities for improving practice performance in adult immunizations: a meta-narrative review of the literature

por Loskutova, Natalia, Smail, Craig, Webster, Brian, Ajayi, Kemi, Wood, Julie, Carroll, Jennifer
Publicado 2017

Protocol for the asthma tools study: a pragmatic practice-based research network trial

por Yawn, Barbara P, Bertram, Susan, Kurland, Margary, Wollan, Peter, Graham, Deborah, Littlefield, Dawn, Smail, Craig, Pace, Wilson
Publicado 2013

Effects of multicomponent primary care-based intervention on immunization rates and missed opportunities to vaccinate adults

por Loskutova, Natalia Y., Smail, Craig, Callen, Elisabeth, Staton, Elizabeth W., Nazir, Niaman, Webster, Brian, Pace, Wilson D.
Publicado 2020

Properties of structural variants and short tandem repeats associated with gene expression and complex traits

por Jakubosky, David, D’Antonio, Matteo, Bonder, Marc Jan, Smail, Craig, Donovan, Margaret K. R., Young Greenwald, William W., Matsui, Hiroko, D’Antonio-Chronowska, Agnieszka, Stegle, Oliver, Smith, Erin N., Montgomery, Stephen B., DeBoever, Christopher, Frazer, Kelly A.
Publicado 2020

Extravillous trophoblast cell lineage development is associated with active remodeling of the chromatin landscape

por Varberg, Kaela M., Dominguez, Esteban M., Koseva, Boryana, Varberg, Joseph M., McNally, Ross P., Moreno-Irusta, Ayelen, Wesley, Emily R., Iqbal, Khursheed, Cheung, Warren A., Schwendinger-Schreck, Carl, Smail, Craig, Okae, Hiroaki, Arima, Takahiro, Lydic, Michael, Holoch, Kristin, Marsh, Courtney, Soares, Michael J., Grundberg, Elin
Publicado 2023

Identification of rare and common regulatory variants in pluripotent cells using population-scale transcriptomics

por Bonder, Marc Jan, Smail, Craig, Gloudemans, Michael J., Frésard, Laure, Jakubosky, David, D’Antonio, Matteo, Li, Xin, Ferraro, Nicole M., Carcamo-Orive, Ivan, Mirauta, Bogdan, Seaton, Daniel D., Cai, Na, Vakili, Dara, Horta, Danilo, Zhao, Chunli, Zastrow, Diane B., Bonner, Devon E., Wheeler, Matthew T., Kilpinen, Helena, Knowles, Joshua W., Smith, Erin N., Frazer, Kelly A., Montgomery, Stephen B., Stegle, Oliver
Publicado 2021

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