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)

TCF21 hypermethylation in genetically quiescent clear cell sarcoma of the kidney

Por Gooskens, Saskia L., Gadd, Samantha, Guidry Auvil, Jaime M., Gerhard, Daniela S., Khan, Javed, Patidar, Rajesh, Meerzaman, Daoud, Chen, Qing-Rong, Hsu, Chih Hao, Yan, Chunhua, Nguyen, Cu, Hu, Ying, Mullighan, Charles G., Ma, Jing, Jennings, Lawrence J., de Krijger, Ronald R., van den Heuvel-Eibrink, Marry M., Smith, Malcolm A., Ross, Nicole, Gastier-Foster, Julie M., Perlman, Elizabeth J.
Publicado no Oncotarget (2015)

MLLT1 YEATS domain mutations in clinically distinctive Favourable Histology Wilms tumours

Por Perlman, Elizabeth J., Gadd, Samantha, Arold, Stefan T., Radhakrishnan, Anand, Gerhard, Daniela S., Jennings, Lawrence, Huff, Vicki, Guidry Auvil, Jaime M., Davidsen, Tanja M., Dome, Jeffrey S., Meerzaman, Daoud, Hsu, Chih Hao, Nguyen, Cu, Anderson, James, Ma, Yussanne, Mungall, Andrew J., Moore, Richard A., Marra, Marco A., Mullighan, Charles G., Ma, Jing, Wheeler, David A., Hampton, Oliver A., Gastier-Foster, Julie M., Ross, Nicole, Smith, Malcolm A.
Publicado no Nat Commun (2015)

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)

Genetic predisposition to neuroblastoma mediated by a LMO1 super-enhancer polymorphism

Por Oldridge, Derek A., Wood, Andrew C., Weichert-Leahey, Nina, Crimmins, Ian, Sussman, Robyn, Winter, Cynthia, McDaniel, Lee D., Diamond, Maura, Hart, Lori S., Zhu, Shizhen, Durbin, Adam D., Abraham, Brian J., Anders, Lars, Tian, Lifeng, Zhang, Shile, Wei, Jun S., Khan, Javed, Bramlett, Kelli, Rahman, Nazneen, Capasso, Mario, Iolascon, Achille, Gerhard, Daniela S., Guidry Auvil, Jaime M., Young, Richard A., Hakonarson, Hakon, Diskin, Sharon J., Look, A. Thomas, Maris, John M.
Publicado no Nature (2015)

Significance of TP53 Mutation in Wilms Tumors with Diffuse Anaplasia: A Report from the Children’s Oncology Group

Por Ooms, Ariadne H.A.G., Gadd, Samantha, Gerhard, Daniela S., Smith, Malcolm A., Guidry Auvil, Jaime M., Meerzaman, Daoud, Chen, Qing-Rong, Hsu, Chih Hao, Yan, Chunhua, Nguyen, Cu, Hu, Ying, Ma, Yussanne, Zong, Zusheng, Mungall, Andrew J., Moore, Richard A., Marra, Marco A., Huff, Vicki, Dome, Jeffrey S., Chi, Yueh-Yun, Tian, Jing, Geller, James I., Mullighan, Charles G., Ma, Jing, Wheeler, David A., Hampton, Oliver A., Walz, Amy L., van den Heuvel-Eibrink, Marry M., de Krijger, Ronald R., Ross, Nicole, Gastier-Foster, Julie M., Perlman, Elizabeth J.
Publicado no Clin Cancer Res (2016)

Relapsed neuroblastomas show frequent RAS-MAPK pathway mutations

Por Eleveld, Thomas F., Oldridge, Derek A., Bernard, Virginie, Koster, Jan, Daage, Leo Colmet, Diskin, Sharon J., Schild, Linda, Bentahar, Nadia Bessoltane, Bellini, Angela, Chicard, Mathieu, Lapouble, Eve, Combaret, Valérie, Legoix-Né, Patricia, Michon, Jean, Pugh, Trevor J., Hart, Lori S., Rader, JulieAnn, Attiyeh, Edward F., Wei, Jun S., Zhang, Shile, Naranjo, Arlene, Gastier-Foster, Julie M., Hogarty, Michael D., Asgharzadeh, Shahab, Smith, Malcolm A., Guidry Auvil, Jaime M., Watkins, Thomas B. K., Zwijnenburg, Danny A., Ebus, Marli E., van Sluis, Peter, Hakkert, Anne, van Wezel, Esther, van der Schoot, C. Ellen, Westerhout, Ellen M., Schulte, Johannes H., Tytgat, Godelieve A., Dolman, M. Emmy M., Janoueix-Lerosey, Isabelle, Gerhard, Daniela S., Caron, Huib N., Delattre, Olivier, Khan, Javed, Versteeg, Rogier, Schleiermacher, Gudrun, Molenaar, Jan J., Maris, John M.
Publicado no Nat Genet (2015)