BRIEF REPORT: Housestaff Adherence to Cervical Cancer Screening Recommendations

由 Ross, Joseph S, Forsyth, Beverly A, Rosenbaum, Julie R
出版 2006

Resident Career Planning Needs in Internal Medicine: A Qualitative Assessment

由 Garcia, Rina L., Windish, Donna M., Rosenbaum, Julie R.
出版 2010

Racial and ethnic differences in personal cervical cancer screening amongst post-graduate physicians: Results from a cross-sectional survey

由 Ross, Joseph S, Nuñez-Smith, Marcella, Forsyth, Beverly A, Rosenbaum, Julie R
出版 2008

Trk-signaling endosomes are generated by Rac-dependent macroendocytosis

由 Valdez, Gregorio, Philippidou, Polyxeni, Rosenbaum, Julie, Akmentin, Wendy, Shao, Yufang, Halegoua, Simon
出版 2007

Physicians Should Play a Role in Ensuring Safe Firearm Ownership

由 Holt, Stephen R., Rosenbaum, Julie, Ellman, Matthew, Doolittle, Benjamin, Tobin, Daniel G.
發表在 J Gen Intern Med (2019)

Partial bisulfite conversion for unique template sequencing

由 Kumar, Vijay, Rosenbaum, Julie, Wang, Zihua, Forcier, Talitha, Ronemus, Michael, Wigler, Michael, Levy, Dan
發表在 Nucleic Acids Res (2018)

Discrepancy Between Patient Health Literacy Levels and Readability of Patient Education Materials from an Electronic Health Record

由 Imoisili, Omoye E., Levinsohn, Erik, Pan, Cassie, Howell, Benjamin A., Streiter, Shoshana, Rosenbaum, Julie R.
發表在 Health Lit Res Pract (2017)

A Systematic Review of Advocacy Curricula in Graduate Medical Education

由 Howell, Benjamin A., Kristal, Ross B., Whitmire, Lacey R., Gentry, Mark, Rabin, Tracy L., Rosenbaum, Julie
發表在 J Gen Intern Med (2019)

Pincher, a pinocytic chaperone for nerve growth factor/TrkA signaling endosomes

由 Shao, Yufang, Akmentin, Wendy, Toledo-Aral, Juan Jose, Rosenbaum, Julie, Valdez, Gregorio, Cabot, John B., Hilbush, Brian S., Halegoua, Simon
出版 2002

Reducing INDEL calling errors in whole genome and exome sequencing data

由 Fang, Han, Wu, Yiyang, Narzisi, Giuseppe, O’Rawe, Jason A, Barrón, Laura T Jimenez, Rosenbaum, Julie, Ronemus, Michael, Iossifov, Ivan, Schatz, Michael C, Lyon, Gholson J
發表在 Genome Med (2014)

Indel variant analysis of short-read sequencing data with Scalpel

由 Fang, Han, Bergmann, Ewa A, Arora, Kanika, Vacic, Vladimir, Zody, Michael C, Iossifov, Ivan, O’Rawe, Jason A, Wu, Yiyang, Barron, Laura T Jimenez, Rosenbaum, Julie, Ronemus, Michael, Lee, Yoon-ha, Wang, Zihua, Dikoglu, Esra, Jobanputra, Vaidehi, Lyon, Gholson J, Wigler, Michael, Schatz, Michael C, Narzisi, Giuseppe
發表在 Nat Protoc (2016)

De Novo Gene Disruptions in Children on the Autistic Spectrum

由 Iossifov, Ivan, Ronemus, Michael, Levy, Dan, Wang, Zihua, Hakker, Inessa, Rosenbaum, Julie, Yamrom, Boris, Lee, Yoon-ha, Narzisi, Giuseppe, Leotta, Anthony, Kendall, Jude, Grabowska, Ewa, Ma, Beicong, Marks, Steven, Rodgers, Linda, Stepansky, Asya, Troge, Jennifer, Andrews, Peter, Bekritsky, Mitchell, Pradhan, Kith, Ghiban, Elena, Kramer, Melissa, Parla, Jennifer, Demeter, Ryan, Fulton, Lucinda L., Fulton, Robert S., Magrini, Vincent J., Ye, Kenny, Darnell, Jennifer C., Darnell, Robert B., Mardis, Elaine R., Wilson, Richard K., Schatz, Michael C., McCombie, W. Richard, Wigler, Michael
出版 2012

The contribution of de novo coding mutations to autism spectrum disorder

由 Iossifov, Ivan, O’Roak, Brian J., Sanders, Stephan J., Ronemus, Michael, Krumm, Niklas, Levy, Dan, Stessman, Holly A., Witherspoon, Kali, Vives, Laura, Patterson, Karynne E., Smith, Joshua D., Paeper, Bryan, Nickerson, Deborah A., Dea, Jeanselle, Dong, Shan, Gonzalez, Luis E., Mandell, Jefferey D., Mane, Shrikant M., Murtha, Michael T., Sullivan, Catherine A., Walker, Michael F., Waqar, Zainulabedin, Wei, Liping, Willsey, A. Jeremy, Yamrom, Boris, Lee, Yoon-ha, Grabowska, Ewa, Dalkic, Ertugrul, Wang, Zihua, Marks, Steven, Andrews, Peter, Leotta, Anthony, Kendall, Jude, Hakker, Inessa, Rosenbaum, Julie, Ma, Beicong, Rodgers, Linda, Troge, Jennifer, Narzisi, Giuseppe, Yoon, Seungtai, Schatz, Michael C., Ye, Kenny, McCombie, W. Richard, Shendure, Jay, Eichler, Evan E., State, Matthew W., Wigler, Michael
發表在 Nature (2014)