Home Self-Collection of Nasal Swabs for Diagnosis of Acute Respiratory Virus Infections in Children With Cystic Fibrosis

por Emerson, Julia, Cochrane, Elizabeth, McNamara, Sharon, Kuypers, Jane, Gibson, Ronald L., Campbell, Angela P.
Publicado 2013

Respiratory viruses in children with cystic fibrosis: viral detection and clinical findings

por Burns, Jane L., Emerson, Julia, Kuypers, Jane, Campbell, Angela P., Gibson, Ronald L., McNamara, Sharon, Worrell, Kelly, Englund, Janet A.
Publicado 2011

Exome Sequencing of Phenotypic Extremes Identifies CAV2 and TMC6 as Interacting Modifiers of Chronic Pseudomonas aeruginosa Infection in Cystic Fibrosis

por Emond, Mary J., Louie, Tin, Emerson, Julia, Chong, Jessica X., Mathias, Rasika A., Knowles, Michael R., Rieder, Mark J., Tabor, Holly K., Nickerson, Debbie A., Barnes, Kathleen C., GO, Lung, Gibson, Ronald L., Bamshad, Michael J.
Publicado 2015

Correction: Exome Sequencing of Phenotypic Extremes Identifies CAV2 and TMC6 as Interacting Modifiers of Chronic Pseudomonas aeruginosa Infection in Cystic Fibrosis

por Emond, Mary J., Louie, Tin, Emerson, Julia, Chong, Jessica X., Mathias, Rasika A., Knowles, Michael R., Rieder, Mark J., Tabor, Holly K., Nickerson, Debbie A., Barnes, Kathleen C., GO, Lung, Gibson, Ronald L., Bamshad, Michael J.
Publicado 2015

Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis

por Emond, Mary J, Louie, Tin, Emerson, Julia, Zhao, Wei, Mathias, Rasika A., Knowles, Michael R., Wright, Fred A., Rieder, Mark J., Tabor, Holly K., Nickerson, Debbie A., Barnes, Kathleen C., GO, Lung, Gibson, Ronald L., Bamshad, Michael J.
Publicado 2012

Testing the effects of combining azithromycin with inhaled tobramycin for P. aeruginosa in cystic fibrosis: a randomised, controlled clinical trial

por Nichols, David P, Singh, Pradeep K, Baines, Arthur, Caverly, Lindsay J, Chmiel, James F, GIbson, Ronald L, Lascano, Jorge, Morgan, Sarah J, Retsch-Bogart, George, Saiman, Lisa, Sadeghi, Hossein, Billings, Joanne L, Heltshe, Sonya L, Kirby, Shannon, Kong, Ada, Nick, Jerry A, Mayer-Hamblett, Nicole
Publicado 2022

MagicalRsq: Machine-learning-based genotype imputation quality calibration

por Sun, Quan, Yang, Yingxi, Rosen, Jonathan D., Jiang, Min-Zhi, Chen, Jiawen, Liu, Weifang, Wen, Jia, Raffield, Laura M., Pace, Rhonda G., Zhou, Yi-Hui, Wright, Fred A., Blackman, Scott M., Bamshad, Michael J., Gibson, Ronald L., Cutting, Garry R., Knowles, Michael R., Schrider, Daniel R., Fuchsberger, Christian, Li, Yun
Publicado 2022

US Cystic Fibrosis Foundation and European Cystic Fibrosis Society consensus recommendations for the management of non-tuberculous mycobacteria in individuals with cystic fibrosis

por Floto, R Andres, Olivier, Kenneth N, Saiman, Lisa, Daley, Charles L, Herrmann, Jean-Louis, Nick, Jerry A, Noone, Peadar G, Bilton, Diana, Corris, Paul, Gibson, Ronald L, Hempstead, Sarah E, Koetz, Karsten, Sabadosa, Kathryn A, Sermet-Gaudelus, Isabelle, Smyth, Alan R, van Ingen, Jakko, Wallace, Richard J, Winthrop, Kevin L, Marshall, Bruce C, Haworth, Charles S
Publicado 2016

US Cystic Fibrosis Foundation and European Cystic Fibrosis Society consensus recommendations for the management of non-tuberculous mycobacteria in individuals with cystic fibrosis:...

por Floto, R Andres, Olivier, Kenneth N, Saiman, Lisa, Daley, Charles L, Herrmann, Jean-Louis, Nick, Jerry A, Noone, Peadar G, Bilton, Diana, Corris, Paul, Gibson, Ronald L, Hempstead, Sarah E, Koetz, Karsten, Sabadosa, Kathryn A, Sermet-Gaudelus, Isabelle, Smyth, Alan R, van Ingen, Jakko, Wallace, Richard J, Winthrop, Kevin L, Marshall, Bruce C, Haworth, Charles S
Publicado 2016

A Phase 3 Open-Label Study of Elexacaftor/Tezacaftor/Ivacaftor in Children 6 through 11 Years of Age with Cystic Fibrosis and at Least One F508del Allele

por Zemanick, Edith T., Taylor-Cousar, Jennifer L., Davies, Jane, Gibson, Ronald L., Mall, Marcus A., McKone, Edward F., McNally, Paul, Ramsey, Bonnie W., Rayment, Jonathan H., Rowe, Steven M., Tullis, Elizabeth, Ahluwalia, Neil, Chu, Chenghao, Ho, Thang, Moskowitz, Samuel M., Noel, Sabrina, Tian, Simon, Waltz, David, Weinstock, Tanya G., Xuan, Fengjuan, Wainwright, Claire E., McColley, Susanna A.
Publicado 2021

Leveraging TOPMed imputation server and constructing a cohort-specific imputation reference panel to enhance genotype imputation among cystic fibrosis patients

por Sun, Quan, Liu, Weifang, Rosen, Jonathan D., Huang, Le, Pace, Rhonda G., Dang, Hong, Gallins, Paul J., Blue, Elizabeth E., Ling, Hua, Corvol, Harriet, Strug, Lisa J., Bamshad, Michael J., Gibson, Ronald L., Pugh, Elizabeth W., Blackman, Scott M., Cutting, Garry R., O'Neal, Wanda K., Zhou, Yi-Hui, Wright, Fred A., Knowles, Michael R., Wen, Jia, Li, Yun
Publicado 2022

CFTR bearing variant p.Phe312del exhibits function inconsistent with phenotype and negligible response to ivacaftor

por Raraigh, Karen S., Paul, Kathleen C., Goralski, Jennifer L., Worthington, Erin N., Faino, Anna V., Sciortino, Stanley, Wang, Yiting, Aksit, Melis A., Ling, Hua, Osorio, Derek L., Onchiri, Frankline M., Patel, Shivani U., Merlo, Christian A., Montemayor, Kristina, Gibson, Ronald L., West, Natalie E., Thakerar, Amita, Bridges, Robert J., Sheppard, David N., Sharma, Neeraj, Cutting, Garry R.
Publicado 2022

Accounting for population structure in genetic studies of cystic fibrosis

por Kingston, Hanley, Stilp, Adrienne M., Gordon, William, Broome, Jai, Gogarten, Stephanie M., Ling, Hua, Barnard, John, Dugan-Perez, Shannon, Ellinor, Patrick T., Gabriel, Stacey, Germer, Soren, Gibbs, Richard A., Gupta, Namrata, Rice, Kenneth, Smith, Albert V., Zody, Michael C., Blackman, Scott M., Cutting, Garry, Knowles, Michael R., Zhou, Yi-Hui, Rosenfeld, Margaret, Gibson, Ronald L., Bamshad, Michael, Fohner, Alison, Blue, Elizabeth E.
Publicado 2022