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A

Anath C. Lionel

university of texas m d anderson cancer center
H指数:35
被引数:1.1万

个人简介

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教育背景

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工作经历

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荣誉奖项

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Treatment and outcomes of progression of disease post-CAR T-cell therapy in mantle cell lymphoma: a multicenter analysis

CAR T细胞疗法后套细胞淋巴瘤疾病进展的治疗与结局：一项多中心分析

Blood Advances
IF7.1
2025-08-070
OAAI
Zachary D. Epstein-Peterson; Anath C. Lionel; Ashlee Joseph; Esther Drill; Suheil Albert Atallah-Yunes; Taylor R. Brooks; Elise A. Chong; Emeline R. Chong; Jamie Dela Cruz; Matthew J. Frank; Andrew Ip; Madiha Iqbal; Caron A. Jacobson; Manali K. Kamdar; Reem Karmali; Ofrat Beyar-Katz; Kami J. Maddocks; Matthew J. Matasar; Daniel McLoughlin; Reid W. Merryman
Cytokine Storms in COVID-19, Hemophagocytic Lymphohistiocytosis, and CAR-T Therapy

COVID-19中的细胞因子风暴、噬血细胞性淋巴组织细胞增生症，以及CAR-T疗法

JAMA NETWORK OPEN
IF9.7
2025-04-071
OA
Long, James P.; Prakash, Rishab; Edelkamp Jr, Paul; Knafl, Mark; Lionel, Anath C.; Nair, Ranjit; Ahmed, Sairah; Strati, Paolo; Castillo, Luis E. Malpica; Al-Zaki, Ajlan; Chien, Kelly; Westin, Jason; Khawaja, Fareed; Nastoupil, Loretta J.; Mulanovich, Victor; Futreal, Andrew; Woodman, Scott E.; Daver, Naval G.; Flowers, Christopher R.; Neelapu, Sattva; Manzano, Joanna-Grace; Iyer, Swaminathan P.
Treatment Patterns and Outcomes Following Progression of Disease Post-CAR-T Therapy in Relapsed or Refractory Mantle Cell Lymphoma: A Multicenter Analysis

CAR-T疗法后疾病进展的复发或难治性套细胞淋巴瘤患者的治疗方案与结局：一项多中心分析

BLOOD
IF23.1
2024-11-050
PRE
Epstein-Peterson, Zachary D.; Lionel, Anath C.; Joseph, Ashlee; Drill, Esther; Atallah-Yunes, Suheil Albert; Brooks, Taylor R.; Chong, Elise A.; Chong, Emeline R.; Dela Cruz, Jamie; Frank, Matthew J.; Ip, Andrew; Iqbal, Madiha; Jacobson, Caron A.; Kamdar, Manali K.; Karmali, Reem; Maddocks, Kami J.; Matasar, Matthew; Merryman, Reid W.; Munoz, Javier; Riedell, Peter A.; Ryan, Christine E.; Salles, Gilles; Sauter, Craig S.; Sawalha, Yazeed; Shouval, Roni; Shukla, Navika; Stanisic, Alexander, V; Therwhanger, Dylan; Van Besien, Herman; Wang, Yucai; Yamshon, Samuel; Zelenetz, Andrew D.; Palomba, Maria Lia; Jain, Preetesh; Kumar, Anita
Complete Disruption of Autism-Susceptibility Genes by Gene Editing Predominantly Reduces Functional Connectivity of Isogenic Human Neurons (vol 11, pg 1211, 2018)
STEM CELL REPORTS
IF5.1
2019-02-019
OAAI
Deneault, Eric; White, Sean H.; Rodrigues, Deivid C.; Ross, P. Joel; Faheem, Muhammad; Zaslavsky, Kirill; Wang, Zhuozhi; Alexandrova, Roumiana; Pellecchia, Giovanna; Wei, Wei; Piekna, Alina; Kaur, Gaganjot; Howe, Jennifer L.; Kwan, Vickie; Thiruvahindrapuram, Bhooma; Walker, Susan; Lionel, Anath C.; Pasceri, Peter; Merico, Daniele; Yuen, Ryan K. C.; Singh, Karun K.; Ellis, James; Scherer, Stephen W.
Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test
GENETICS IN MEDICINE
IF6.2
2018-04-01386
OAAI
Lionel, Anath C.; Costain, Gregory; Monfared, Nasim; Walker, Susan; Reuter, Miriam S.; Hosseini, S. Mohsen; Thiruvahindrapuram, Bhooma; Merico, Daniele; Jobling, Rebekah; Nalpathamkalam, Thomas; Pellecchia, Giovanna; Sung, Wilson W. L.; Wang, Zhuozhi; Bikangaga, Peter; Boelman, Cyrus; Carter, Melissa T.; Cordeiro, Dawn; Cytrynbaum, Cheryl; Dell, Sharon D.; Dhir, Priya; Dowling, James J.; Heon, Elise; Hewson, Stacy; Hiraki, Linda; Inbar-Feigenberg, Michal; Klatt, Regan; Kronick, Jonathan; Laxer, Ronald M.; Licht, Christoph; MacDonald, Heather; Mercimek-Andrews, Saadet; Mendoza-Londono, Roberto; Piscione, Tino; Schneider, Rayfel; Schulze, Andreas; Silverman, Earl; Siriwardena, Komudi; Snead, O. Carter; Sondheimer, Neal; Sutherland, Joanne; Vincent, Ajoy; Wasserman, Jonathan D.; Weksberg, Rosanna; Shuman, Cheryl; Carew, Chris; Szego, Michael J.; Hayeems, Robin Z.; Basran, Raveen; Stavropoulos, Dimitri J.; Ray, Peter N.; Bowdin, Sarah; Meyn, M. Stephen; Cohn, Ronald D.; Scherer, Stephen W.; Marshall, Christian R.
Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression
GENETICS IN MEDICINE
IF6.2
2017-01-0174
OAAI
Lowther, Chelsea; Speevak, Marsha; Armour, Christine M.; Goh, Elaine S.; Graham, Gail E.; Li, Chumei; Zeesman, Susan; Nowaczyk, Malgorzata J. M.; Schultz, Lee-Anne; Morra, Antonella; Nicolson, Rob; Bikangaga, Peter; Samdup, Dawa; Zaazou, Mostafa; Boyd, Kerry; Jung, Jack H.; Siu, Victoria; Rajguru, Manjulata; Goobie, Sharan; Tarnopolsky, Mark A.; Prasad, Chitra; Dick, Paul T.; Hussain, Asmaa S.; Walinga, Margreet; Reijenga, Renske G.; Gazzellone, Matthew; Lionel, Anath C.; Marshall, Christian R.; Scherer, Stephen W.; Stavropoulos, Dimitri J.; McCready, Elizabeth; Bassett, Anne S.
Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder

自闭症谱系障碍儿童染色体微阵列分析和全外显子组测序的分子诊断率

JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
IF55
2015-09-01311
PREAI
Tammimies, Kristiina; Marshall, Christian R.; Walker, Susan; Kaur, Gaganjot; Thiruvahindrapuram, Bhooma; Lionel, Anath C.; Yuen, Ryan K. C.; Uddin, Mohammed; Roberts, Wendy; Weksberg, Rosanna; Woodbury-Smith, Marc; Zwaigenbaum, Lonnie; Anagnostou, Evdokia; Wang, Zhuozhi; Wei, John; Howe, Jennifer L.; Gazzellone, Matthew J.; Lau, Lynette; Sung, Wilson W. L.; Whitten, Kathy; Vardy, Cathy; Crosbie, Victoria; Tsang, Brian; D'Abate, Lia; Tong, Winnie W. L.; Luscombe, Sandra; Doyle, Tyna; Carter, Melissa T.; Szatmari, Peter; Stuckless, Susan; Merico, Daniele; Stavropoulos, Dimitri J.; Scherer, Stephen W.; Fernandez, Bridget A.
A high-resolution copy-number variation resource for clinical and population genetics
GENETICS IN MEDICINE
IF6.2
2015-09-0169
OAAI
Uddin, Mohammed; Thiruvahindrapuram, Bhooma; Walker, Susan; Wang, Zhuozhi; Hu, Pingzhao; Lamoureux, Sylvia; Wei, John; MacDonald, Jeffrey R.; Pellecchia, Giovanna; Lu, Chao; Lionel, Anath C.; Gazzellone, Matthew J.; McLaughlin, John R.; Brown, Catherine; Andrulis, Irene L.; Knight, Julia A.; Herbrick, Jo-Anne; Wintle, Richard F.; Ray, Peter; Stavropoulos, Dimitri J.; Marshall, Christian R.; Scherer, Stephen W.
Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes
HUMAN GENETICS
IF3.6
2014-11-2917
PREAI
Woodbury-Smith, Marc; Paterson, Andrew D.; Thiruvahindrapduram, Bhooma; Lionel, Anath C.; Marshall, Christian R.; Merico, Daniele; Fernandez, Bridget A.; Duku, Eric; Sutcliffe, James S.; O'Conner, Irene; Chrysler, Christina; Thompson, Ann; Kellam, Barbara; Tammimies, Kristiina; Walker, Susan; Yuen, Ryan K. C.; Uddin, Mohammed; Howe, Jennifer L.; Parlier, Morgan; Whitten, Kathy; Szatmari, Peter; Vieland, Veronica J.; Piven, Joseph; Scherer, Stephen W.
CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems

CHD2单倍功能不全与发育迟缓，智力残疾，癫痫和神经行为问题有关

JOURNAL OF NEURODEVELOPMENTAL DISORDERS
IF4
2014-04-2289
OAAI
Chenier, Sebastien; Yoon, Grace; Argiropoulos, Bob; Lauzon, Julie; Laframboise, Rachel; Ahn, Joo Wook; Ogilvie, Caroline Mackie; Lionel, Anath C.; Marshall, Christian R.; Vaags, Andrea K.; Hashemi, Bita; Boisvert, Karine; Mathonnet, Geraldine; Tihy, Frederique; So, Joyce; Scherer, Stephen W.; Lemyre, Emmanuelle; Stavropoulos, Dimitri J.

研究方向

暂未获取到该数据
S
Stephen W. Scherer
H 指数:161论文数:1,092被引数:12.0万
C
Christian R. Marshall
H 指数:76论文数:339被引数:3.6万
D
Dimitri J. Stavropoulos
H 指数:43论文数:134被引数:9,983
B
Bridget A. Fernandez
H 指数:50论文数:98被引数:2.1万
B
Bhooma Thiruvahindrapuram
H 指数:39论文数:176被引数:1.0万
S
Susan Walker
H 指数:45论文数:139被引数:1.0万
D
Dalila Pinto
H 指数:62论文数:208被引数:3.6万
P
Péter Szatmári
H 指数:91论文数:280被引数:4.3万
W
Wendy Roberts
H 指数:76论文数:295被引数:2.6万
A
Anne S. Bassett
H 指数:73论文数:338被引数:2.0万