Sample processing obscures cancer-specific alterations in leukemic transcriptomes

Por Dvinge, Heidi, Ries, Rhonda E., Ilagan, Janine O., Stirewalt, Derek L., Meshinchi, Soheil, Bradley, Robert K.
Publicado no Proc Natl Acad Sci U S A (2014)

Expression of a bcr-1 isoform of RARα-PML does not affect the penetrance of acute promyelocytic leukemia or the acquisition of an interstitial deletion on mouse chromosome 2

Por Walter, Matthew J., Ries, Rhonda E., Armstrong, Jon R., Park, John S., Mardis, Elaine R., Ley, Timothy J.
Publicado em 2007

Reduced PU.1 expression causes myeloid progenitor expansion and increased leukemia penetrance in mice expressing PML-RARα

Por Walter, Matthew J., Park, John S., Ries, Rhonda E., Lau, Steven K. M., McLellan, Michael, Jaeger, Sara, Wilson, Richard K., Mardis, Elaine R., Ley, Timothy J.
Publicado em 2005

Transcriptome Profiling of Pediatric Core Binding Factor AML

Por Hsu, Chih-Hao, Nguyen, Cu, Yan, Chunhua, Ries, Rhonda E., Chen, Qing-Rong, Hu, Ying, Ostronoff, Fabiana, Stirewalt, Derek L., Komatsoulis, George, Levy, Shawn, Meerzaman, Daoud, Meshinchi, Soheil
Publicado no PLoS One (2015)

Expression and functional characterization of CD33 transcript variants in human acute myeloid leukemia

Por Laszlo, George S., Harrington, Kimberly H., Gudgeon, Chelsea J., Beddoe, Mary E., Fitzgibbon, Matthew P., Ries, Rhonda E., Lamba, Jatinder K., McIntosh, Martin W., Meshinchi, Soheil, Walter, Roland B.
Publicado no Oncotarget (2016)

High Expression of Suppressor of Cytokine Signaling-2 Predicts Poor Outcome in Pediatric Acute Myeloid Leukemia: A Report from the Children's Oncology Group

Por Laszlo, George S., Ries, Rhonda E., Gudgeon, Chelsea J., Harrington, Kimberly H., Alonzo, Todd A., Gerbing, Robert B., Raimondi, Susana C., Hirsch, Betsy A., Gamis, Alan S., Meshinchi, Soheil, Walter, Roland B.
Publicado no Leuk Lymphoma (2014)

Multimerin-1 (MMRN1) as Novel Adverse Marker in Pediatric Acute Myeloid Leukemia: A Report from the Children’s Oncology Group

Por Laszlo, George S., Alonzo, Todd A., Gudgeon, Chelsea J., Harrington, Kimberly H., Gerbing, Robert B., Wang, Yi-Cheng, Ries, Rhonda E., Raimondi, Susana C., Hirsch, Betsy A., Gamis, Alan S., Meshinchi, Soheil, Walter, Roland B.
Publicado no Clin Cancer Res (2015)

Concordance of copy number alterations using a common analytic pipeline for genome-wide analysis of Illumina and Affymetrix genotyping data: A report from the Children’s Oncology G...

Por Vujkovic, Marijana, Attiyeh, Edward F., Ries, Rhonda E., Horn, Michelle, Goodman, Elizabeth K., Ding, Yang, Kavcic, Marko, Alonzo, Todd A., Gerbing, Robert B., Hirsch, Betsy, Raimondi, Susana, Gamis, Alan S., Meshinchi, Soheil, Aplenc, Richard
Publicado no Cancer Genet (2015)

High expression of myocyte enhancer factor 2C (MEF2C) is associated with adverse-risk features and poor outcome in pediatric acute myeloid leukemia: a report from the Children’s On...

Por Laszlo, George S., Alonzo, Todd A., Gudgeon, Chelsea J., Harrington, Kimberly H., Kentsis, Alex, Gerbing, Robert B., Wang, Yi-Cheng, Ries, Rhonda E., Raimondi, Susana C., Hirsch, Betsy A., Gamis, Alan S., Meshinchi, Soheil, Walter, Roland B.
Publicado no J Hematol Oncol (2015)

Erratum to: High expression of myocyte enhancer factor 2C (MEF2C) is associated with adverse-risk features and poor outcome in pediatric acute myeloid leukemia: a report from the C...

Por Laszlo, George S., Alonzo, Todd A., Gudgeon, Chelsea J., Harrington, Kimberly H., Kentsis, Alex, Gerbing, Robert B., Wang, Yi-Cheng, Ries, Rhonda E., Raimondi, Susana C., Hirsch, Betsy A., Gamis, Alan S., Meshinchi, Soheil, Walter, Roland B.
Publicado no J Hematol Oncol (2016)

Significance of Expression of ITGA5 and its Splice Variants in Acute Myeloid Leukemia: A Report from the Children’s Oncology Group

Por Walter, Roland B., Laszlo, George S., Alonzo, Todd A., Gerbing, Robert B., Levy, Shawn, Fitzgibbon, Matthew P., Gudgeon, Chelsea J., Ries, Rhonda E., Harrington, Kimberly H., Raimondi, Susana C., Hirsch, Betsy A., Gamis, Alan S., McIntosh, Martin W., Meshinchi, Soheil
Publicado em 2013

Genomic profiling of pediatric acute myeloid leukemia reveals a changing mutational landscape from disease diagnosis to relapse

Por Farrar, Jason E., Schuback, Heather L., Ries, Rhonda E., Wai, Daniel, Hampton, Oliver A., Trevino, Lisa R., Alonzo, Todd A., Guidry Auvil, Jaime M., Davidsen, Tanja M., Gesuwan, Patee, Hermida, Leandro, Muzny, Donna M., Dewal, Ninad, Rustagi, Navin, Lewis, Lora R., Gamis, Alan S., Wheeler, David A., Smith, Malcolm A., Gerhard, Daniela S., Meshinchi, Soheil
Publicado no Cancer Res (2016)

Identification of somatic JAK1 mutations in patients with acute myeloid leukemia

Por Xiang, Zhifu, Zhao, Yu, Mitaksov, Vesselin, Fremont, Daved H., Kasai, Yumi, Molitoris, AnnaLynn, Ries, Rhonda E., Miner, Tracie L., McLellan, Michael D., DiPersio, John F., Link, Daniel C., Payton, Jacqueline E., Graubert, Timothy A., Watson, Mark, Shannon, William, Heath, Sharon E., Nagarajan, Rakesh, Mardis, Elaine R., Wilson, Richard K., Ley, Timothy J., Tomasson, Michael H.
Publicado em 2008

A pilot study of high-throughput, sequence-based mutational profiling of primary human acute myeloid leukemia cell genomes

Por Ley, Timothy J., Minx, Patrick J., Walter, Matthew J., Ries, Rhonda E., Sun, Hui, McLellan, Michael, DiPersio, John F., Link, Daniel C., Tomasson, Michael H., Graubert, Timothy A., McLeod, Howard, Khoury, Hanna, Watson, Mark, Shannon, William, Trinkaus, Kathryn, Heath, Sharon, Vardiman, James W., Caligiuri, Michael A., Bloomfield, Clara D., Milbrandt, Jeffrey D., Mardis, Elaine R., Wilson, Richard K.
Publicado em 2003

Somatic mutations and germline sequence variants in the expressed tyrosine kinase genes of patients with de novo acute myeloid leukemia

Por Tomasson, Michael H., Xiang, Zhifu, Walgren, Richard, Zhao, Yu, Kasai, Yumi, Miner, Tracie, Ries, Rhonda E., Lubman, Olga, Fremont, Daved H., McLellan, Michael D., Payton, Jacqueline E., Westervelt, Peter, DiPersio, John F., Link, Daniel C., Walter, Matthew J., Graubert, Timothy A., Watson, Mark, Baty, Jack, Heath, Sharon, Shannon, William D., Nagarajan, Rakesh, Bloomfield, Clara D., Mardis, Elaine R., Wilson, Richard K., Ley, Timothy J.
Publicado em 2008

Prognostic implications of the IDH1 synonymous SNP rs11554137 in pediatric and adult AML: a report from the Children's Oncology Group and SWOG

Por Ho, Phoenix A., Kopecky, Kenneth J., Alonzo, Todd A., Gerbing, Robert B., Miller, Kristen L., Kuhn, Julia, Zeng, Rong, Ries, Rhonda E., Raimondi, Susana C., Hirsch, Betsy A., Oehler, Vivian, Hurwitz, Craig A., Franklin, Janet L., Gamis, Alan S., Petersdorf, Stephen H., Anderson, Jeanne E., Godwin, John E., Reaman, Gregory H., Willman, Cheryl L., Bernstein, Irwin D., Radich, Jerald P., Appelbaum, Frederick R., Stirewalt, Derek L., Meshinchi, Soheil
Publicado em 2011

CSF3R mutations have a high degree of overlap with CEBPA mutations in pediatric AML

Por Maxson, Julia E., Ries, Rhonda E., Wang, Yi-Cheng, Gerbing, Robert B., Kolb, E. Anders, Thompson, Sarah L., Guidry Auvil, Jaime M., Marra, Marco A., Ma, Yussanne, Zong, Zusheng, Mungall, Andrew J., Moore, Richard, Long, William, Gesuwan, Patee, Davidsen, Tanja M., Hermida, Leandro C., Hughes, Seamus B., Farrar, Jason E., Radich, Jerald P., Smith, Malcolm A., Gerhard, Daniela S., Gamis, Alan S., Alonzo, Todd A., Meshinchi, Soheil
Publicado no Blood (2016)

Distinct patterns of mutations occurring in de novo AML versus AML arising in the setting of severe congenital neutropenia

Por Link, Daniel C., Kunter, Ghada, Kasai, Yumi, Zhao, Yu, Miner, Tracie, McLellan, Michael D., Ries, Rhonda E., Kapur, Deepak, Nagarajan, Rakesh, Dale, David C., Bolyard, Audrey Anna, Boxer, Laurence A., Welte, Karl, Zeidler, Cornelia, Donadieu, Jean, Bellanné-Chantelot, Christine, Vardiman, James W., Caligiuri, Michael A., Bloomfield, Clara D., DiPersio, John F., Tomasson, Michael H., Graubert, Timothy A., Westervelt, Peter, Watson, Mark, Shannon, William, Baty, Jack, Mardis, Elaine R., Wilson, Richard K., Ley, Timothy J.
Publicado em 2007

Acquired copy number alterations in adult acute myeloid leukemia genomes

Por Walter, Matthew J., Payton, Jacqueline E., Ries, Rhonda E., Shannon, William D., Deshmukh, Hrishikesh, Zhao, Yu, Baty, Jack, Heath, Sharon, Westervelt, Peter, Watson, Mark A., Tomasson, Michael H., Nagarajan, Rakesh, O'Gara, Brian P., Bloomfield, Clara D., Mrózek, Krzysztof, Selzer, Rebecca R., Richmond, Todd A., Kitzman, Jacob, Geoghegan, Joel, Eis, Peggy S., Maupin, Rachel, Fulton, Robert S., McLellan, Michael, Wilson, Richard K., Mardis, Elaine R., Link, Daniel C., Graubert, Timothy A., DiPersio, John F., Ley, Timothy J.
Publicado em 2009

Sequencing a mouse acute promyelocytic leukemia genome reveals genetic events relevant for disease progression

Por Wartman, Lukas D., Larson, David E., Xiang, Zhifu, Ding, Li, Chen, Ken, Lin, Ling, Cahan, Patrick, Klco, Jeffery M., Welch, John S., Li, Cheng, Payton, Jacqueline E., Uy, Geoffrey L., Varghese, Nobish, Ries, Rhonda E., Hoock, Mieke, Koboldt, Daniel C., McLellan, Michael D., Schmidt, Heather, Fulton, Robert S., Abbott, Rachel M., Cook, Lisa, McGrath, Sean D., Fan, Xian, Dukes, Adam F., Vickery, Tammi, Kalicki, Joelle, Lamprecht, Tamara L., Graubert, Timothy A., Tomasson, Michael H., Mardis, Elaine R., Wilson, Richard K., Ley, Timothy J.
Publicado em 2011