Canlyniadau Chwilio - Quesnel-Vallières, Mathieu

Essential roles for the splicing regulator nSR100/SRRM4 during nervous system development gan Quesnel-Vallières, Mathieu, Irimia, Manuel, Cordes, Sabine P., Blencowe, Benjamin J.

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Rapid and Scalable Profiling of Nascent RNA with fastGRO gan Barbieri, Elisa, Hill, Connor, Quesnel-Vallières, Mathieu, Zucco, Avery J., Barash, Yoseph, Gardini, Alessandro

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Identifying common transcriptome signatures of cancer by interpreting deep learning models gan Jha, Anupama, Quesnel-Vallières, Mathieu, Wang, David, Thomas-Tikhonenko, Andrei, Lynch, Kristen W, Barash, Yoseph

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Seronegative Hepatitis C Virus Infection in a Child Infected via Mother-to-Child Transmission gan Larouche, Ariane, Gaëtan, Geneviève, El-Bilali, Nabil, Quesnel-Vallières, Mathieu, Martin, Steven R., Alvarez, Fernando, Shoukry, Naglaa H., Soudeyns, Hugo

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Alternative splicing redefines landscape of commonly mutated genes in acute myeloid leukemia gan Rivera, Osvaldo D., Mallory, Michael J., Quesnel-Vallières, Mathieu, Chatrikhi, Rakesh, Schultz, David C., Carroll, Martin, Barash, Yoseph, Cherry, Sara, Lynch, Kristen W.

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Novel HIV-1 Recombinant Forms in Antenatal Cohort, Montreal, Quebec, Canada gan Quesnel-Vallières, Mathieu, Kouzayha, Iman, Tran, Evelyne, Barry, Issatou, Lasgi, Charlène, Merindol, Natacha, Monteil, Vanessa, Ransy, Doris G., Boucher, Marc, Lapointe, Normand, Soudeyns, Hugo

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An atlas of alternative splicing profiles and functional associations reveals new regulatory programs and genes that simultaneously express multiple major isoforms gan Tapial, Javier, Ha, Kevin C.H., Sterne-Weiler, Timothy, Gohr, André, Braunschweig, Ulrich, Hermoso-Pulido, Antonio, Quesnel-Vallières, Mathieu, Permanyer, Jon, Sodaei, Reza, Marquez, Yamile, Cozzuto, Luca, Wang, Xinchen, Gómez-Velázquez, Melisa, Rayon, Teresa, Manzanares, Miguel, Ponomarenko, Julia, Blencowe, Benjamin J., Irimia, Manuel

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A highly conserved program of neuronal microexons is misregulated in autistic brains gan Irimia, Manuel, Weatheritt, Robert J., Ellis, Jonathan, Parikshak, Neelroop N., Gonatopoulos-Pournatzis, Thomas, Babor, Mariana, Quesnel-Vallières, Mathieu, Tapial, Javier, Raj, Bushra, O’Hanlon, Dave, Barrios-Rodiles, Miriam, Sternberg, Michael J.E., Cordes, Sabine P., Roth, Frederick P., Wrana, Jeffrey L., Geschwind, Daniel H., Blencowe, Benjamin J.

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Missense Mutations in NKAP Cause a Disorder of Transcriptional Regulation Characterized by Marfanoid Habitus and Cognitive Impairment gan Fiordaliso, Sarah K., Iwata-Otsubo, Aiko, Ritter, Alyssa L., Quesnel-Vallières, Mathieu, Fujiki, Katsunori, Nishi, Eriko, Hancarova, Miroslava, Miyake, Noriko, Morton, Jenny E.V., Lee, Sangmoon, Hackmann, Karl, Bando, Masashige, Masuda, Koji, Nakato, Ryuichiro, Arakawa, Michiko, Bhoj, Elizabeth, Li, Dong, Hakonarson, Hakon, Takeda, Ryojun, Harr, Margaret, Keena, Beth, Zackai, Elaine H., Okamoto, Nobuhiko, Mizuno, Seiji, Ko, Jung Min, Valachova, Alica, Prchalova, Darina, Vlckova, Marketa, Pippucci, Tommaso, Seiler, Christoph, Choi, Murim, Matsumoto, Naomichi, Di Donato, Nataliya, Barash, Yoseph, Sedlacek, Zdenek, Shirahige, Katsuhiko, Izumi, Kosuke

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