The ubiquitin hydrolase OTUB1 promotes glioma cell stemness via suppressing ferroptosis through stabilizing SLC7A11 protein

por Zhao, Xinde, Zhou, Ming, Yang, Yong, Luo, Minjie
Publicado 2021

A highly sensitive and specific workflow for detecting rare copy-number variants from exome sequencing data

por Rajagopalan, Ramakrishnan, Murrell, Jill R., Luo, Minjie, Conlin, Laura K.
Publicado 2020

Congenital tumors of the central nervous system: an institutional review of 64 cases with emphasis on tumors with unique histologic and molecular characteristics

por Viaene, Angela N., Pu, Cunfeng, Perry, Arie, Li, Marilyn M., Luo, Minjie, Santi, Mariarita
Publicado 2020

CircUCP2 promotes the tumor progression of non-small cell lung cancer through the miR-149/UCP2 pathway

por DU, WEI, YIN, FANG, ZHONG, YATING, LUO, MINJIE, WANG, ZHEN, LIN, PENG, LIU, QING, YANG, HAN
Publicado 2023

Clinical impact of genomic characterization of 15 patients with acute megakaryoblastic leukemia–related malignancies

por Lalonde, Emilie, Rentas, Stefan, Wertheim, Gerald, Cao, Kajia, Surrey, Lea F., Lin, Fumin, Zhao, Xiaonan, Obstfeld, Amrom, Aplenc, Richard, Luo, Minjie, Li, Marilyn M.
Publicado 2021

AccuTyping: new algorithms for automated analysis of data from high-throughput genotyping with oligonucleotide microarrays

por Hu, Guohong, Wang, Hui-Yun, Greenawalt, Danielle M., Azaro, Marco A., Luo, Minjie, Tereshchenko, Irina V., Cui, Xiangfeng, Yang, Qifeng, Gao, Richeng, Shen, Li, Li, Honghua
Publicado 2006

Lipopolysaccharide (LPS) potentiates hydrogen peroxide toxicity in T98G astrocytoma cells by suppression of anti-oxidative and growth factor gene expression

por Yue, Gang, Shi, Guanfang, Azaro, Marco A, Yang, Qifeng, Hu, Guohong, Luo, Minjie, Yin, Kingsley, Nagele, Robert G, Fine, Daniel H, Yang, Jin-Ming, Li, Honghua
Publicado 2008

Glanzmann thrombasthenia: genetic basis and clinical correlates

por Botero, Juliana Perez, Lee, Kristy, Branchford, Brian R, Bray, Paul F, Freson, Kathleen, Lambert, Michele P., Luo, Minjie, Mohan, Shruthi, Ross, Justyne E., Bergmeier, Wolfgang, Di Paola, Jorge
Publicado 2020

Novel FGFR2-INA fusion identified in two low-grade mixed neuronal-glial tumors drives oncogenesis via MAPK and PI3K/mTOR pathway activation

por Jain, Payal, Surrey, Lea F., Straka, Joshua, Luo, Minjie, Lin, Fumin, Harding, Brian, Resnick, Adam C., Storm, Phillip B., Buccoliero, Anna Maria, Santi, Mariarita, Li, Marilyn M., Waanders, Angela J.
Publicado 2018

Case Report: Reversible Hyperglycemia Following Rapamycin Treatment for Atypical Choroid Plexus Papilloma in an Infant

por Liu, Jiale, Luo, Minjie, Lv, Siyuan, Tao, Shaohua, Wu, Zhu, Yu, Lihua, Lin, Danna, Huang, Lulu, Wu, Li, Liao, Xu, Zi, Juan, Lai, Xiaorong, Yuan, Yuting, Zhang, Wangming, Yang, Lihua
Publicado 2022

Identification of possible genetic alterations in the breast cancer cell line MCF-7 using high-density SNP genotyping microarray

por Wang, Hui-Yun, Greenawalt, Danielle, Cui, Xiangfeng, Tereshchenko, Irina V, Luo, Minjie, Yang, Qifeng, Azaro, Marco A, Hu, Guohong, Chu, Yi, Li, James Y, Shen, Li, Lin, Yong, Zhang, Lianjun, Li, Honghua
Publicado 2009

Patient specific circulating tumor DNA fingerprints to monitor treatment response across multiple tumors

por Li, Jiaping, Jiang, Wei, Wei, Jinwang, Zhang, Jianwei, Cai, Linbo, Luo, Minjie, Wang, Zhan, Sun, Wending, Wang, Shengzhou, Wang, Chen, Dai, Chun, Liu, Jun, Wang, Guan, Wang, Jiping, Xu, Qiang, Deng, Yanhong
Publicado 2020

Genetic Structures of Copy Number Variants Revealed by Genotyping Single Sperm

por Luo, Minjie, Cui, Xiangfeng, Fredman, David, Brookes, Anthony J., Azaro, Marco A., Greenawalt, Danielle M., Hu, Guohong, Wang, Hui-Yun, Tereshchenko, Irina V., Lin, Yong, Shentu, Yue, Gao, Richeng, Shen, Li, Li, Honghua
Publicado 2009

A germline PALB2 pathogenic variant identified in a pediatric high-grade glioma

por Zhong, Yiming, Schubert, Jeffrey, Wu, Jinhua, Xu, Feng, Lin, Fumin, Cao, Kajia, Zelley, Kristin, Luo, Minjie, Foster, Jessica B., Cole, Kristina A., MacFarland, Suzanne P., Resnick, Adam C., Storm, Phillip B., Li, Marilyn M.
Publicado 2020

Novel ATXN1/ATXN1L::NUTM2A fusions identified in aggressive infant sarcomas with gene expression and methylation patterns similar to CIC-rearranged sarcoma

por Xu, Feng, Viaene, Angela N., Ruiz, Jenny, Schubert, Jeffrey, Wu, Jinhua, Chen, Jiani, Cao, Kajia, Fu, Weixuan, Bagatell, Rochelle, Fan, Zhiqian, Long, Ariel, Pagliaroli, Luca, Zhong, Yiming, Luo, Minjie, Kreiger, Portia A., Surrey, Lea F., Wertheim, Gerald B., Cole, Kristina A., Li, Marilyn M., Santi, Mariarita, Storm, Phillip B.
Publicado 2022

NTRK Fusions Identified in Pediatric Tumors: The Frequency, Fusion Partners, and Clinical Outcome

por Zhao, Xiaonan, Kotch, Chelsea, Fox, Elizabeth, Surrey, Lea F., Wertheim, Gerald B., Baloch, Zubair W., Lin, Fumin, Pillai, Vinodh, Luo, Minjie, Kreiger, Portia A., Pogoriler, Jennifer E., Linn, Rebecca L., Russo, Pierre A., Santi, Mariarita, Resnick, Adam C., Storm, Phillip B., Hunger, Stephen P., Bauer, Andrew J., Li, Marilyn M.
Publicado 2021

A novel TP53 tandem duplication in a child with Li–Fraumeni syndrome

por Xu, Feng, Aref-Eshghi, Erfan, Wu, Jinhua, Schubert, Jeffrey, Wertheim, Gerald, Bhatti, Tricia, Pogoriler, Jennifer, Patel, Maha, Cao, Kajia, Long, Ariel, Fan, Zhiqian, Denenberg, Elizabeth H., Fanning, Elizabeth A., Wilmoth, Donna M., Luo, Minjie, Conlin, Laura K., Dain, Aleksandra S., Zelley, Kristin, Baldino, Sarah, Balamuth, Naomi, MacFarland, Suzanne, Li, Marilyn M., Zhong, Yiming
Publicado 2022

Utility and limitations of exome sequencing as a genetic diagnostic tool for children with hearing loss

por Sheppard, Sarah, Biswas, Sawona, Li, Mindy H., Jayaraman, Vijayakumar, Slack, Ian, Romasko, Edward J., Sasson, Ariella, Brunton, Joshua, Rajagopalan, Ramakrishnan, Sarmady, Mahdi, Abrudan, Jenica L., Jairam, Sowmya, DeChene, Elizabeth T., Ying, Xiahoan, Choi, Jiwon, Wilkens, Alisha, Raible, Sarah E., Scarano, Maria I., Santani, Avni, Pennington, Jeffrey W., Luo, Minjie, Conlin, Laura K., Devkota, Batsal, Dulik, Matthew C., Spinner, Nancy B., Krantz, Ian D.
Publicado 2018

Molecular Diagnostic Outcomes from 700 Cases: What Can We Learn from a Retrospective Analysis of Clinical Exome Sequencing?

por Murrell, Jill R., Nesbitt, Addie May I., Baker, Samuel W., Pechter, Kieran B., Balciuniene, Jorune, Zhao, Xiaonan, Denenberg, Elizabeth H., DeChene, Elizabeth T., Wu, Chao, Jayaraman, Pushkala, Cao, Kajia, Gonzalez, Michael, Devoto, Marcella, Testori, Alessandro, Monos, John D., Dulik, Matthew C., Conlin, Laura K., Luo, Minjie, McDonald Gibson, Kristin, Guan, Qiaoning, Sarmady, Mahdi, Bhoj, Elizabeth, Helbig, Ingo, Zackai, Elaine H., Bedoukian, Emma C., Wilkens, Alisha, Tarpinian, Jennifer, Izumi, Kosuke, Skraban, Cara M., Deardorff, Matthew A., Medne, Livija, Krantz, Ian D., Krock, Bryan L., Santani, Avni B.
Publicado 2022

Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel

por Shen, Jun, Oza, Andrea M., del Castillo, Ignacio, Duzkale, Hatice, Matsunaga, Tatsuo, Pandya, Arti, Kang, Hyunseok P., Mar-Heyming, Rebecca, Guha, Saurav, Moyer, Krista, Lo, Christine, Kenna, Margaret, Alexander, John J., Zhang, Yan, Hirsch, Yoel, Luo, Minjie, Cao, Ye, Choy, Kwong Wai, Cheng, Yen-Fu, Avraham, Karen B., Hu, Xinhua, Garrido, Gema, Moreno-Pelayo, Miguel A., Greinwald, John, Zhang, Kejian, Zeng, Yukun, Brownstein, Zippora, Basel-Salmon, Lina, Davidov, Bella, Frydman, Moshe, Weiden, Tzvi, Nagan, Narasimhan, Willis, Alecia, Hemphill, Sarah E., Grant, Andrew R., Siegert, Rebecca K., DiStefano, Marina T., Amr, Sami S., Rehm, Heidi L., Tayoun, Ahmad N. Abou
Publicado 2019