Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Patee Gesuwan"'
Autor:
Soheil Meshinchi, Daniela S. Gerhard, Malcolm A. Smith, David A. Wheeler, Alan S. Gamis, Lora R. Lewis, Navin Rustagi, Ninad Dewal, Donna M. Muzny, Leandro Hermida, Patee Gesuwan, Tanja M. Davidsen, Jaime M. Guidry Auvil, Todd A. Alonzo, Lisa R. Trevino, Oliver A. Hampton, Daniel Wai, Rhonda E. Ries, Heather L. Schuback, Jason E. Farrar
Demographic Information of Patient Cohort. A) Age category of patients. B) Cytogenetic category.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5073cf6db09b01277dbc1eb3e614631c
https://doi.org/10.1158/0008-5472.22410521.v1
https://doi.org/10.1158/0008-5472.22410521.v1
Autor:
Soheil Meshinchi, Daniela S. Gerhard, Malcolm A. Smith, David A. Wheeler, Alan S. Gamis, Lora R. Lewis, Navin Rustagi, Ninad Dewal, Donna M. Muzny, Leandro Hermida, Patee Gesuwan, Tanja M. Davidsen, Jaime M. Guidry Auvil, Todd A. Alonzo, Lisa R. Trevino, Oliver A. Hampton, Daniel Wai, Rhonda E. Ries, Heather L. Schuback, Jason E. Farrar
Patient Characteristics
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e1730c4808a820a6068d5be1f2e47d6
https://doi.org/10.1158/0008-5472.22410509
https://doi.org/10.1158/0008-5472.22410509
Autor:
Soheil Meshinchi, Daniela S. Gerhard, Malcolm A. Smith, David A. Wheeler, Alan S. Gamis, Lora R. Lewis, Navin Rustagi, Ninad Dewal, Donna M. Muzny, Leandro Hermida, Patee Gesuwan, Tanja M. Davidsen, Jaime M. Guidry Auvil, Todd A. Alonzo, Lisa R. Trevino, Oliver A. Hampton, Daniel Wai, Rhonda E. Ries, Heather L. Schuback, Jason E. Farrar
List of all segment variations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d21d77850adb8344d7aeb4f0c594fc83
https://doi.org/10.1158/0008-5472.22410503
https://doi.org/10.1158/0008-5472.22410503
Autor:
Soheil Meshinchi, Daniela S. Gerhard, Malcolm A. Smith, David A. Wheeler, Alan S. Gamis, Lora R. Lewis, Navin Rustagi, Ninad Dewal, Donna M. Muzny, Leandro Hermida, Patee Gesuwan, Tanja M. Davidsen, Jaime M. Guidry Auvil, Todd A. Alonzo, Lisa R. Trevino, Oliver A. Hampton, Daniel Wai, Rhonda E. Ries, Heather L. Schuback, Jason E. Farrar
Clonal cluster analysis. Mutations were clustered using DBSCAN based on the VAF and graphed according to timepoint. Panels A-T illustrate possible scenarios of how individual mutations may originate, evolve, and resolve based on VAF.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fa9f69b815765f6fabdb41f9b5be176
https://doi.org/10.1158/0008-5472.22410512
https://doi.org/10.1158/0008-5472.22410512
Autor:
Soheil Meshinchi, Daniela S. Gerhard, Malcolm A. Smith, David A. Wheeler, Alan S. Gamis, Lora R. Lewis, Navin Rustagi, Ninad Dewal, Donna M. Muzny, Leandro Hermida, Patee Gesuwan, Tanja M. Davidsen, Jaime M. Guidry Auvil, Todd A. Alonzo, Lisa R. Trevino, Oliver A. Hampton, Daniel Wai, Rhonda E. Ries, Heather L. Schuback, Jason E. Farrar
Clonal evolution of mutations from diagnosis to relapse. These graphs depict the Variant Allele Frequency (VAF) of each patient's mutations at diagnosis and relapse. Note: Mutations absent at diagnosis or relapse are depicted with VAF of zero. Gene n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ec810271ec787c2a63ed9eb89e084a4
https://doi.org/10.1158/0008-5472.22410515.v1
https://doi.org/10.1158/0008-5472.22410515.v1
Autor:
Soheil Meshinchi, Daniela S. Gerhard, Malcolm A. Smith, David A. Wheeler, Alan S. Gamis, Lora R. Lewis, Navin Rustagi, Ninad Dewal, Donna M. Muzny, Leandro Hermida, Patee Gesuwan, Tanja M. Davidsen, Jaime M. Guidry Auvil, Todd A. Alonzo, Lisa R. Trevino, Oliver A. Hampton, Daniel Wai, Rhonda E. Ries, Heather L. Schuback, Jason E. Farrar
List of all verified mutations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6022b2319c98a06948b71d603d02d9f9
https://doi.org/10.1158/0008-5472.22410506.v1
https://doi.org/10.1158/0008-5472.22410506.v1
Autor:
Samuel W. Brady, Kathryn G. Roberts, Zhaohui Gu, Lei Shi, Stanley Pounds, Deqing Pei, Cheng Cheng, Yunfeng Dai, Meenakshi Devidas, Chunxu Qu, Ashley N. Hill, Debbie Payne-Turner, Xiaotu Ma, Ilaria Iacobucci, Pradyuamna Baviskar, Lei Wei, Sasi Arunachalam, Kohei Hagiwara, Yanling Liu, Diane A. Flasch, Yu Liu, Matthew Parker, Xiaolong Chen, Abdelrahman H. Elsayed, Omkar Pathak, Yongjin Li, Yiping Fan, J. Robert Michael, Michael Rusch, Mark R. Wilkinson, Scott Foy, Dale J. Hedges, Scott Newman, Xin Zhou, Jian Wang, Colleen Reilly, Edgar Sioson, Stephen V. Rice, Victor Pastor Loyola, Gang Wu, Evadnie Rampersaud, Shalini C. Reshmi, Julie Gastier-Foster, Jaime M. Guidry Auvil, Patee Gesuwan, Malcolm A. Smith, Naomi Winick, Andrew J. Carroll, Nyla A. Heerema, Richard C. Harvey, Cheryl L. Willman, Eric Larsen, Elizabeth A. Raetz, Michael J. Borowitz, Brent L. Wood, William L. Carroll, Patrick A. Zweidler-McKay, Karen R. Rabin, Leonard A. Mattano, Kelly W. Maloney, Stuart S. Winter, Michael J. Burke, Wanda Salzer, Kimberly P. Dunsmore, Anne L. Angiolillo, Kristine R. Crews, James R. Downing, Sima Jeha, Ching-Hon Pui, William E. Evans, Jun J. Yang, Mary V. Relling, Daniela S. Gerhard, Mignon L. Loh, Stephen P. Hunger, Jinghui Zhang, Charles G. Mullighan
Publikováno v:
Nat Genet
Acute lymphoblastic leukemia (ALL) is the most common childhood cancer. Here, using whole-genome, exome and transcriptome sequencing of 2,754 childhood patients with ALL, we find that, despite a generally low mutation burden, ALL cases harbor a media
Autor:
Akinyemi I. Ojesina, Andrew J. Mungall, Corey Casper, Karen Mungall, Yussanne Ma, Nicholas B. Griner, Simon K. Chan, Jackson Orem, Vanessa L Porter, Martin Origa, Gordon B. Mills, Carolyn Nakisige, Luka Culibrk, Jay Bowen, Alessia Gagliardi, Zusheng Zong, Daniela S. Gerhard, Julie M. Gastier-Foster, Reanne Bowlby, Emma Titmuss, Steven J.M. Jones, Hilary Petrello, Janet S. Rader, Thomas C. Wright, Patee Gesuwan, Mark H. Stoler, Marco A. Marra, Karen Novik, Maureen A. Dyer, Teresa M. Darragh, Robert Yarchoan, Constance Namirembe
Publikováno v:
Nature genetics, vol 52, iss 8
Nature genetics
Nature genetics
Cervical cancer is the most common cancer affecting sub-Saharan African women and is prevalent among HIV-positive (HIV+) individuals. No comprehensive profiling of cancer genomes, transcriptomes or epigenomes has been performed in this population thu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa373ba24d7d29c6a93d8c251f780f06
https://escholarship.org/uc/item/2468c667
https://escholarship.org/uc/item/2468c667
Autor:
Pamela C. Birriel, Tanja Davidsen, Yiwen He, Daniela S. Gerhard, Cindy W. Kyi, Patee Gesuwan, Martin L. Ferguson, Eva Tonsing-Carter, Nicholas B. Griner, Julyann Perez-Mayoral
Publikováno v:
Cancer Research. 81:2224-2224
The mission of the Office of Cancer Genomics (OCG) at the National Cancer Institute (NCI) is to advance the understanding of cancers to improve clinical outcomes. To accomplish this goal, OCG supports innovative and complementary initiatives that cha
Autor:
Daoud Meerzaman, Stefan T. Arold, Malcolm A. Smith, Marco A. Marra, Richard A. Moore, Amy L. Walz, Qing Rong Chen, Jaime M. Guidry Auvil, Ariadne H. A. G. Ooms, Cu Nguyen, Andrew J. Mungall, Ying Hu, Yussanne Ma, Zusheng Zong, Patee Gesuwan, Jeffrey S. Dome, Vicki Huff, Jing Ma, David A. Wheeler, Samantha Gadd, Amy E. Armstrong, Tanja M. Davidsen, Chih Hao Hsu, Chunhua Yan, Oliver A. Hampton, Charles G. Mullighan, Elizabeth J. Perlman, Nicole Ross, Daniela S. Gerhard, Leandro C. Hermida, Julie M. Gastier-Foster
Publikováno v:
Nature Genetics. 49:1487-1494
We performed genome-wide sequencing and analyzed mRNA and miRNA expression, DNA copy number, and DNA methylation in 117 Wilms tumors, followed by targeted sequencing of 651 Wilms tumors. In addition to genes previously implicated in Wilms tumors (WT1