Das, Anirban; Sudhaman, Sumedha; Morgenstern, Daniel; Coblentz, Ailish; Chung, Jiil; Stone, Simone C.; Alsafwani, Noor; Liu, Zhihui Amy; Abu Al Karsaneh, Ola; Soleimani, Shirin; Ladany, Hagay; Chen, David; Zatzman, Matthew; Cabric, Vanja; Nobre, Liana; Bianchi, Vanessa; Edwards, Melissa; Nahum, Lauren C. Sambira; Ercan, Ayse B.; Nabbi, Arash; Constantini, Shlomi; Dvir, Rina; Yalon-Oren, Michal; Campino, Gadi Abebe; Caspi, Shani; Larouche, Valerie; Reddy, Alyssa; Osborn, Michael; Mason, Gary; Lindhorst, Scott; Bronsema, Annika; Magimairajan, Vanan; Opocher, Enrico; De Mola, Rebecca Loret; Sabel, Magnus; Frojd, Charlotta; Sumerauer, David; Samuel, David; Cole, Kristina; Chiaravalli, Stefano; Massimino, Maura; Tomboc, Patrick; Ziegler, David S.; George, Ben; Van Damme, An; Hijiya, Nobuko; Gass, David; McGee, Rose B.; Mordechai, Oz; Bowers, Daniel C.; Laetsch, Theodore W.; Lossos, Alexander; Blumenthal, Deborah T.; Sarosiek, Tomasz; Yen, Lee Yi; Knipstein, Jeffrey; Bendel, Anne; Hoffman, Lindsey M.; Luna-Fineman, Sandra; Zimmermann, Stefanie; Scheers, Isabelle; Nichols, Kim E.; Zapotocky, Michal; Hansford, Jordan R.; Maris, John M.; Dirks, Peter; Taylor, Michael D.; Kulkarni, Abhaya, V; Shroff, Manohar; Tsang, Derek S.; Villani, Anita; Xu, Wei; Aronson, Melyssa; Durno, Carol; Shlien, Adam; Malkin, David; Getz, Gad; Maruvka, Yosef E.; Ohashi, Pamela S.; Hawkins, Cynthia; Pugh, Trevor J.; Bouffet, Eric; Tabori, Uri

Genomes for Kids: The Scope of Pathogenic Mutations in Pediatric Cancer Revealed by Comprehensive DNA and RNA Sequencing

CANCER DISCOVERY

IF33.3

2021-07-23109

OAAI

Newman, Scott; Nakitandwe, Joy; Kesserwan, Chimene A.; Azzato, Elizabeth M.; Wheeler, David A.; Rusch, Michael; Shurtleff, Sheila; Hedges, Dale J.; Hamilton, Kayla, V; Foy, Scott G.; Edmonson, Michael N.; Thrasher, Andrew; Bahrami, Armita; Orr, Brent A.; Klco, Jeffery M.; Gu, Jiali; Harrison, Lynn W.; Wang, Lu; Clay, Michael R.; Ouma, Annastasia; Silkov, Antonina; Liu, Yanling; Zhang, Zhaojie; Liu, Yu; Brady, Samuel W.; Zhou, Xin; Chang, Ti-Cheng; Pande, Manjusha; Davis, Eric; Becksfort, Jared; Patel, Aman; Wilkinson, Mark R.; Rahbarinia, Delaram; Kubal, Manish; Maciaszek, Jamie L.; Pastor, Victor; Knight, Jay; Gout, Alexander M.; Wang, Jian; Gu, Zhaohui; Mullighan, Charles G.; McGee, Rose B.; Quinn, Emily A.; Nuccio, Regina; Mostafavi, Roya; Gerhardt, Elsie L.; Taylor, Leslie M.; Valdez, Jessica M.; Hines-Dowell, Stacy J.; Pappo, Alberto S.; Robinson, Giles; Johnson, Liza-Marie; Pui, Ching-Hon; Ellison, David W.; Downing, James R.; Zhang, Jinghui; Nichols, Kim E.

Diagnostic criteria for constitutional mismatch repair deficiency (CMMRD): recommendations from the international consensus working group

JOURNAL OF MEDICAL GENETICS

IF3.7

2021-02-2376

NCKAP1 Disruptive Variants Lead to a Neurodevelopmental Disorder with Core Features of Autism

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2020-11-0123

OAAI

Guo, Hui; Zhang, Qiumeng; Dai, Rujia; Yu, Bin; Hoekzema, Kendra; Tan, Jieqiong; Tan, Senwei; Jia, Xiangbin; Chung, Wendy K.; Hernan, Rebecca; Alkuraya, Fowzan S.; Alsulaiman, Ahood; Al-Muhaizea, Mohammad A.; Lesca, Gaetan; Pons, Linda; Labalme, Audrey; Laux, Linda; Bryant, Emily; Brown, Natasha J.; Savva, Elena; Ayres, Samantha; Eratne, Dhamidhu; Peeters, Hilde; Bilan, Frederic; Letienne-Cejudo, Lucile; Gilbert-Dussardier, Brigitte; Ruiz-Arana, Inge-Lore; Merlini, Jenny Meylan; Boizot, Alexia; Bartoloni, Lucia; Santoni, Federico; Karlowicz, Danielle; McDonald, Marie; Wu, Huidan; Hu, Zhengmao; Chen, Guodong; Ou, Jianjun; Brasch-Andersen, Charlotte; Fagerberg, Christina R.; Dreyer, Inken; Tsai, Anne Chun-hui; Slegesky, Valerie; McGee, Rose B.; Daniels, Brina; Sellars, Elizabeth A.; Carpenter, Lori A.; Schaefer, Bradley; Sacoto, Maria J. Guillen; Begtrup, Amber; Schnur, Rhonda E.; Punj, Sumit; Wentzensen, Ingrid M.; Rhodes, Lindsay; Pan, Qian; Bernier, Raphael A.; Chen, Chao; Eichler, Evan E.; Xia, Kun

Increased prevalence of germline monoallelic RECQL4 mutations in children with cancer

CANCER RESEARCH

IF16.6

2019-07-010

PRE

Speaking genomics to parents offered germline testing for cancer predisposition: Use of a 2-visit consent model

向父母讲基因组学提供了癌症易感性的种系检测: 使用2次访问同意模型

CANCER

IF5.1

2019-03-2231

OAAI

Clinical cancer genomic profiling by three-platform sequencing of whole genome, whole exome and transcriptome

通过全基因组，全外显子组和转录组的三平台测序进行临床癌症基因组分析

NATURE COMMUNICATIONS

IF15.7

2018-09-27151

OAAI

Rusch, Michael; Nakitandwe, Joy; Shurtleff, Sheila; Newman, Scott; Zhang, Zhaojie; Edmonson, Michael N.; Parker, Matthew; Jiao, Yuannian; Ma, Xiaotu; Liu, Yanling; Gu, Jiali; Walsh, Michael F.; Becksfort, Jared; Thrasher, Andrew; Li, Yongjin; McMurry, James; Hedlund, Erin; Patel, Aman; Easton, John; Yergeau, Donald; Vadodaria, Bhavin; Tatevossian, Ruth G.; Raimondi, Susana; Hedges, Dale; Chen, Xiang; Hagiwara, Kohei; McGee, Rose; Robinson, Giles W.; Klco, Jeffery M.; Gruber, Tanja A.; Ellison, David W.; Downing, James R.; Zhang, Jinghui

Rose B. McGee

个人简介

教育背景

工作经历

荣誉奖项

研究方向