Digital game based learning. Proceedings of the 4th International Symposium for Information Design, 2nd of June 2005 at Stuttgart Media University

Por Burmester, MichaelGerhard, DanielaThissen, Frank [Hrsg.]
Publicado em 2006

A 3-Mb Contig from D11S987 to MLK3, a Gene-Rich Region in 11q13

Por Smith, Carissa M., Ma, Nancy S., Nowak, Norma J., Shows, Thomas B., Gerhard, Daniela S.
Publicado em 1997

Denaturing High-Performance Liquid Chromatography for Detecting and Typing Genital Human Papillomavirus

Por Li, Jianduan, Gerhard, Daniela S., Zhang, Zhengyan, Huettner, Phyllis C., Wright, Jason, Nguyen, Loan, Lu, Danielle, Rader, Janet S.
Publicado em 2003

A Gene Map of the Best’s Vitelliform Macular Dystrophy Region in Chromosome 11q12–q13.1

Por Stöhr, Heidi, Marquardt, Andreas, Rivera, Andrea, Cooper, Paul R., Nowak, Norma J., Shows, Thomas B., Gerhard, Daniela S., Weber, Bernhard H.F.
Publicado em 1998

Somatic sequence alterations in twenty-one genes selected by expression profile analysis of breast carcinomas

Por Chanock, Stephen J, Burdett, Laurie, Yeager, Meredith, Llaca, Victor, Langerød, Anita, Presswalla, Shafaq, Kaaresen, Rolf, Strausberg, Robert L, Gerhard, Daniela S, Kristensen, Vessela, Perou, Charles M, Børresen-Dale, Anne-Lise
Publicado em 2007

SNP500Cancer: a public resource for sequence validation, assay development, and frequency analysis for genetic variation in candidate genes

Por Packer, Bernice R., Yeager, Meredith, Burdett, Laura, Welch, Robert, Beerman, Michael, Qi, Liqun, Sicotte, Hugues, Staats, Brian, Acharya, Mekhala, Crenshaw, Andrew, Eckert, Andrew, Puri, Vinita, Gerhard, Daniela S., Chanock, Stephen J.
Publicado em 2006

Targeted discovery of novel human exons by comparative genomics

Por Siepel, Adam, Diekhans, Mark, Brejová, Broňa, Langton, Laura, Stevens, Michael, Comstock, Charles L.G., Davis, Colleen, Ewing, Brent, Oommen, Shelly, Lau, Christopher, Yu, Hung-Chun, Li, Jianfeng, Roe, Bruce A., Green, Phil, Gerhard, Daniela S., Temple, Gary, Haussler, David, Brent, Michael R.
Publicado em 2007

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)

Key pathways are frequently mutated in high-risk childhood acute lymphoblastic leukemia: a report from the Children's Oncology Group

Por Zhang, Jinghui, Mullighan, Charles G., Harvey, Richard C., Wu, Gang, Chen, Xiang, Edmonson, Michael, Buetow, Kenneth H., Carroll, William L., Chen, I-Ming, Devidas, Meenakshi, Gerhard, Daniela S., Loh, Mignon L., Reaman, Gregory H., Relling, Mary V., Camitta, Bruce M., Bowman, W. Paul, Smith, Malcolm A., Willman, Cheryl L., Downing, James R., Hunger, Stephen P.
Publicado em 2011

JAK mutations in high-risk childhood acute lymphoblastic leukemia

Por Mullighan, Charles G., Zhang, Jinghui, Harvey, Richard C., Collins-Underwood, J. Racquel, Schulman, Brenda A., Phillips, Letha A., Tasian, Sarah K., Loh, Mignon L., Su, Xiaoping, Liu, Wei, Devidas, Meenakshi, Atlas, Susan R., Chen, I-Ming, Clifford, Robert J., Gerhard, Daniela S., Carroll, William L., Reaman, Gregory H., Smith, Malcolm, Downing, James R., Hunger, Stephen P., Willman, Cheryl L.
Publicado em 2009

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)

Tyrosine kinome sequencing of pediatric acute lymphoblastic leukemia: a report from the Children's Oncology Group TARGET Project

Por Loh, Mignon L., Zhang, Jinghui, Harvey, Richard C., Roberts, Kathryn, Payne-Turner, Debbie, Kang, Huining, Wu, Gang, Chen, Xiang, Becksfort, Jared, Edmonson, Michael, Buetow, Kenneth H., Carroll, William L., Chen, I-Ming, Wood, Brent, Borowitz, Michael J., Devidas, Meenakshi, Gerhard, Daniela S., Bowman, Paul, Larsen, Eric, Winick, Naomi, Raetz, Elizabeth, Smith, Malcolm, Downing, James R., Willman, Cheryl L., Mullighan, Charles G., Hunger, Stephen P.
Publicado em 2013

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)

LongSAGE profiling of nine human embryonic stem cell lines

Por Hirst, Martin, Delaney, Allen, Rogers, Sean A, Schnerch, Angelique, Persaud, Deryck R, O'Connor, Michael D, Zeng, Thomas, Moksa, Michelle, Fichter, Keith, Mah, Diana, Go, Anne, Morin, Ryan D, Baross, Agnes, Zhao, Yongjun, Khattra, Jaswinder, Prabhu, Anna-Liisa, Pandoh, Pawan, McDonald, Helen, Asano, Jennifer, Dhalla, Noreen, Ma, Kevin, Lee, Stephanie, Ally, Adrian, Chahal, Neil, Menzies, Stephanie, Siddiqui, Asim, Holt, Robert, Jones, Steven, Gerhard, Daniela S, Thomson, James A, Eaves, Connie J, Marra, Marco A
Publicado em 2007

Deletion of IKZF1 and Prognosis in Acute Lymphoblastic Leukemia

Por Mullighan, Charles G., Su, Xiaoping, Zhang, Jinghui, Radtke, Ina, Phillips, Letha A.A., Miller, Christopher B., Ma, Jing, Liu, Wei, Cheng, Cheng, Schulman, Brenda A., Harvey, Richard C., Chen, I-Ming, Clifford, Robert J., Carroll, William L., Reaman, Gregory, Bowman, W. Paul, Devidas, Meenakshi, Gerhard, Daniela S., Yang, Wenjian, Relling, Mary V., Shurtleff, Sheila A., Campana, Dario, Borowitz, Michael J., Pui, Ching-Hon, Smith, Malcolm, Hunger, Stephen P., Willman, Cheryl L., Downing, James R.
Publicado em 2009

A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer

Por Hunter, David J., Kraft, Peter, Jacobs, Kevin B., Cox, David G., Yeager, Meredith, Hankinson, Susan E., Wacholder, Sholom, Wang, Zhaoming, Welch, Robert, Hutchinson, Amy, Yu, Kai, Chatterjee, Nilanjan, Orr, Nick, Willett, Walter C., Colditz, Graham A., Ziegler, Regina G., Berg, Christine D., Buys, Saundra S., McCarty, Catherine A., Feigelson, Heather Spencer, Calle, Eugenia E., Thun, Michael J., Hayes, Richard B., Tucker, Margaret, Gerhard, Daniela S., Fraumeni, Joseph F., Hoover, Robert N., Thomas, Gilles, Chanock, Stephen J
Publicado em 2007

Rise and fall of subclones from diagnosis to relapse in pediatric B-acute lymphoblastic leukaemia

Por Ma, Xiaotu, Edmonson, Michael, Yergeau, Donald, Muzny, Donna M., Hampton, Oliver A., Rusch, Michael, Song, Guangchun, Easton, John, Harvey, Richard C., Wheeler, David A., Ma, Jing, Doddapaneni, HarshaVardhan, Vadodaria, Bhavin, Wu, Gang, Nagahawatte, Panduka, Carroll, William L., Chen, I-Ming, Gastier-Foster, Julie M., Relling, Mary V., Smith, Malcolm A., Devidas, Meenakshi, Auvil, Jaime M. Guidry, Downing, James R., Loh, Mignon L., Willman, Cheryl L., Gerhard, Daniela S., Mullighan, Charles G., Hunger, Stephen P., Zhang, Jinghui
Publicado no Nat Commun (2015)

Recurrent DGCR8, DROSHA, and SIX Homeodomain Mutations in Favorable Histology Wilms Tumors

Por Walz, Amy L., Ooms, Ariadne, Gadd, Samantha, Gerhard, Daniela S., Smith, Malcolm A., Guidry Auvil, Jamie M., Meerzaman, Daoud, Chen, Qing-Rong, Hsu, Chih Hao, Yan, Chunhua, Nguyen, Cu, Hu, Ying, Bowlby, Reanne, Brooks, Denise, Ma, Yussanne, Mungall, Andrew J., Moore, Richard A., Schein, Jacqueline, Marra, Marco A., Huff, Vicki, Dome, Jeffrey S., Chi, Yueh-Yun, Mullighan, Charles G., Ma, Jing, Wheeler, David A., Hampton, Oliver A., Jafari, Nadereh, Ross, Nicole, Gastier-Foster, Julie M., Perlman, Elizabeth J.
Publicado no Cancer Cell (2015)