Automated screening for Fragile X premutation carriers based on linguistic and cognitive computational phenotypes

Por Movaghar, Arezoo, Mailick, Marsha, Sterling, Audra, Greenberg, Jan, Saha, Krishanu
Publicado no Sci Rep (2017)

High-Content Analysis of CRISPR-Cas9 Gene-Edited Human Embryonic Stem Cells

Por Carlson-Stevermer, Jared, Goedland, Madelyn, Steyer, Benjamin, Movaghar, Arezoo, Lou, Meng, Kohlenberg, Lucille, Prestil, Ryan, Saha, Krishanu
Publicado no Stem Cell Reports (2016)

Using Machine Learning to Identify Patterns of Lifetime Health Problems in Decedents with Autism Spectrum Disorder

Por Bishop-Fitzpatrick, Lauren, Movaghar, Arezoo, Greenberg, Jan S., Page, David, DaWalt, Leann S., Brilliant, Murray H., Mailick, Marsha R.
Publicado no Autism Res (2018)

Health Profiles of Mosaic Versus Non-mosaic FMR1 Premutation Carrier Mothers of Children With Fragile X Syndrome

Por Mailick, Marsha R., Movaghar, Arezoo, Hong, Jinkuk, Greenberg, Jan S., DaWalt, Leann S., Zhou, Lili, Jackson, Jonathan, Rathouz, Paul J., Baker, Mei W., Brilliant, Murray, Page, David, Berry-Kravis, Elizabeth
Publicado no Front Genet (2018)

Evolvix BEST Names for semantic reproducibility across code2brain interfaces

Por Loewe, Laurence, Scheuer, Katherine S., Keel, Seth A., Vyas, Vaibhav, Liblit, Ben, Hanlon, Bret, Ferris, Michael C., Yin, John, Dutra, Inês, Pietsch, Anthony, Javid, Christine G., Moog, Cecilia L., Meyer, Jocelyn, Dresel, Jerdon, McLoone, Brian, Loberger, Sonya, Movaghar, Arezoo, Gilchrist‐Scott, Morgaine, Sabri, Yazeed, Sescleifer, Dave, Pereda‐Zorrilla, Ivan, Zietlow, Andrew, Smith, Rodrigo, Pietenpol, Samantha, Goldfinger, Jacob, Atzen, Sarah L., Freiberg, Erika, Waters, Noah P., Nusbaum, Claire, Nolan, Erik, Hotz, Alyssa, Kliman, Richard M., Mentewab, Ayalew, Fregien, Nathan, Loewe, Martha
Publicado no Ann N Y Acad Sci (2016)