GCAC: galaxy workflow system for predictive model building for virtual screening

Por Bharti, Deepak R., Hemrom, Anmol J., Lynn, Andrew M.
Publicado no BMC Bioinformatics (2019)

The New Normal: Key Considerations for Effective Serious Illness Communication Over Video or Telephone During the Coronavirus Disease 2019 (COVID-19) Pandemic

Por Flint, Lynn, Kotwal, Ashwin
Publicado no Ann Intern Med (2020)

Identifying medical terms in patient-authored text: a crowdsourcing-based approach

Por MacLean, Diana Lynn, Heer, Jeffrey
Publicado em 2013

PhosphoregDB: The tissue and sub-cellular distribution of mammalian protein kinases and phosphatases

Por Forrest, Alistair RR, Taylor, Darrin F, Fink, J Lynn, Gongora, M Milena, Flegg, Cameron, Teasdale, Rohan D, Suzuki, Harukazu, Kanamori, Mutsumi, Kai, Chikatoshi, Hayashizaki, Yoshihide, Grimmond, Sean M
Publicado em 2006

Clonal replacement of tumor-specific T cells following PD-1 blockade

Por Yost, Kathryn E., Satpathy, Ansuman T., Wells, Daniel K., Qi, Yanyan, Wang, Chunlin, Kageyama, Robin, McNamara, Katherine, Granja, Jeffrey M., Sarin, Kavita Y., Brown, Ryanne A., Gupta, Rohit K., Curtis, Christina, Bucktrout, Samantha L., Davis, Mark M., Chang, Anne Lynn S., Chang, Howard Y.
Publicado no Nat Med (2019)

Exome Sequencing Identifies Rare Variants in Multiple Genes in Atrioventricular Septal Defect

Por D’Alessandro, Lisa C.A., Al Turki, Saeed, Manickaraj, Ashok Kumar, Manase, Dorin, Mulder, Barbara J.M., Bergin, Lynn, Rosenberg, Herschel C., Mondal, Tapas, Gordon, Elaine, Lougheed, Jane, Smythe, John, Devriendt, Koen, Bhattacharya, Shoumo, Watkins, Hugh, Bentham, Jamie, Bowdin, Sarah, Hurles, Matthew E., Mital, Seema
Publicado no Genet Med (2015)

PK/PD Disconnect Observed with a Reversible Endothelial Lipase Inhibitor

Por Hangeland, Jon J., Abell, Lynn M., Adam, Leonard P., Jiang, Ji, Friends, Todd J., Haque, Lauren E., Neels, James, Onorato, Joelle M., Chen, Alice Ye A., Taylor, David S., Yin, Xiaohong, Harrity, Thomas W., Basso, Michael D., Yang, Richard, Sleph, Paul G., Gordon, David A., Huang, Christine S., Wexler, Ruth R., Finlay, Heather J., Lawrence, R. Michael
Publicado no ACS Med Chem Lett (2018)

A Single Dose of Neoadjuvant PD-1 Blockade Predicts Clinical Outcomes in Resectable Melanoma

Por Huang, Alexander C., Orlowski, Robert J., Xu, Xiaowei, Mick, Rosemarie, George, Sangeeth M., Yan, Patrick K., Manne, Sasikanth, Kraya, Adam A., Wubbenhorst, Bradley, Dorfman, Liza, D’Andrea, Kurt, Wenz, Brandon M., Liu, Shujing, Chilukuri, Lakshmi, Kozlov, Andrew, Carberry, Mary, Giles, Lydia, Kier, Melanie W., Quagliarello, Felix, McGettigan, Suzanne, Kreider, Kristin, Annamalai, Lakshmanan, Zhao, Qing, Mogg, Robin, Xu, Wei, Blumenschein, Wendy M., Yearley, Jennifer H., Linette, Gerald P., Amaravadi, Ravi K., Schuchter, Lynn M., Herati, Ramin S., Bengsch, Bertram, Nathanson, Katherine L., Farwell, Michael D., Karakousis, Giorgos C., John Wherry, E., Mitchell, Tara C.
Publicado no Nat Med (2019)

Viral variants that initiate and drive maturation of V1V2-directed HIV-1 broadly neutralizing antibodies

Por Bhiman, Jinal N., Anthony, Colin, Doria-Rose, Nicole A., Karimanzira, Owen, Schramm, Chaim A., Khoza, Thandeka, Kitchin, Dale, Botha, Gordon, Gorman, Jason, Garrett, Nigel J., Abdool Karim, Salim S., Shapiro, Lawrence, Williamson, Carolyn, Kwong, Peter D., Mascola, John R., Morris, Lynn, Moore, Penny L.
Publicado no Nat Med (2015)

Multi-site investigation of strategies for the clinical implementation of CYP2D6 genotyping to guide drug prescribing

Por Cavallari, Larisa H., Van Driest, Sara L., Prows, Cynthia A., Bishop, Jeffrey R., Limdi, Nita A., Pratt, Victoria M., Ramsey, Laura B., Smith, D. Max, Tuteja, Sony, Duong, Benjamin Q., Hicks, J. Kevin, Lee, James C., Obeng, Aniwaa Owusu, Beitelshees, Amber L., Bell, Gillian C., Blake, Kathryn, Crona, Daniel J., Dressler, Lynn, Gregg, Ryan A., Hines, Lindsay J., Scott, Stuart A., Shelton, Richard C., Weitzel, Kristin Wiisanen, Johnson, Julie A., Peterson, Josh F., Empey, Philip E., Skaar, Todd C.
Publicado no Genet Med (2019)

Genetic variants at CD28, PRDM1, and CD2/CD58 are associated with rheumatoid arthritis risk

Por Raychaudhuri, Soumya, Thomson, Brian P., Remmers, Elaine F., Eyre, Stephen, Hinks, Anne, Guiducci, Candace, Catanese, Joseph J., Xie, Gang, Stahl, Eli A., Chen, Robert, Alfredsson, Lars, Amos, Christopher I., Ardlie, Kristin G., Barton, Anne, Bowes, John, Burtt, Noel P., Chang, Monica, Coblyn, Jonathan, Costenbader, Karen H., Criswell, Lindsey A., Crusius, J. Bart A., Cui, Jing, De Jager, Phillip L., Ding, Bo, Emery, Paul, Flynn, Edward, Harrison, Pille, Hocking, Lynne J., Huizinga, Tom W. J., Kastner, Daniel L., Ke, Xiayi, Kurreeman, Fina A. S., Lee, Annette T., Liu, Xiangdong, Li, Yonghong, Martin, Paul, Morgan, Ann W., Padyukov, Leonid, Reid, David M., Seielstad, Mark, Seldin, Michael F., Shadick, Nancy A., Steer, Sophia, Tak, Paul P., Thomson, Wendy, van der Helm-van Mil, Annette H. M., van der Horst-Bruinsma, Irene E., Weinblatt, Michael E., Wilson, Anthony G., Wolbink, Gert Jan, Wordsworth, Paul, Altshuler, David, Karlson, Elizabeth W., Toes, Rene E. M., de Vries, Niek, Begovich, Ann B., Siminovitch, Katherine A., Worthington, Jane, Klareskog, Lars, Gregersen, Peter K., Daly, Mark J., Plenge, Robert M.
Publicado em 2009

Genetic identification of thiosulfate sulfurtransferase as an adipocyte-expressed anti-diabetic target in mice selected for leanness

Por Morton, Nicholas M., Beltram, Jasmina, Carter, Roderick N., Michailidou, Zoi, Gorjanc, Gregor, Fadden, Clare Mc, Barrios-Llerena, Martin E., Rodriguez-Cuenca, Sergio, Gibbins, Matthew T. G., Aird, Rhona E., Moreno-Navarrete, José Maria, Munger, Steven C., Svenson, Karen L., Gastaldello, Annalisa, Ramage, Lynne, Naredo, Gregorio, Zeyda, Maximilian, Wang, Zhao V., Howie, Alexander F., Saari, Aila, Sipilä, Petra, Stulnig, Thomas M., Gudnason, Vilmundur, Kenyon, Christopher J., Seckl, Jonathan R., Walker, Brian R., Webster, Scott P., Dunbar, Donald R., Churchill, Gary A., Vidal-Puig, Antonio, Fernandez-Real, José Manuel, Emilsson, Valur, Horvat, Simon
Publicado no Nat Med (2016)

Defining the clinical phenotype of Saul-Wilson syndrome.

Por Ferreira, Carlos R., Zein, Wadih M., Huryn, Laryssa A., Merker, Andrea, Berger, Seth I., Wilson, William G., Tiller, George E., Wolfe, Lynne A., Merideth, Melissa, Carvalho, Daniel R., Duker, Angela L., Bratke, Heiko, Haug, Marte Gjøl, Rohena, Luis, Hove, Hanne B., Xia, Zhi-Jie, Ng, Bobby G., Freeze, Hudson H., Gabriel, Melissa, Russi, Alvaro H. Serrano, Brick, Lauren, Kozenko, Mariya, Earl, Dawn L., Tham, Emma, Nishimura, Gen, Phillips, John A., Gahl, William A., Hamid, Rizwan, Jackson, Andrew P., Grigelioniene, Giedre, Bober, Michael B.
Publicado no Genet Med (2020)