Space–Time Conservation Element and Solution Element Method

Por Wen, Chih-Yung, Jiang, Yazhong, Shi, Lisong
Publicado no Engineering Applications of Computational Methods (2023)

CADgene: a comprehensive database for coronary artery disease genes

Por Liu, Hui, Liu, Wei, Liao, Yifang, Cheng, Long, Liu, Qian, Ren, Xiang, Shi, Lisong, Tu, Xin, Wang, Qing Kenneth, Guo, An-Yuan
Publicado em 2011

A PTPN11 allele encoding a catalytically impaired SHP2 protein in a patient with a Noonan syndrome phenotype

Por Edwards, Jonathan J., Martinelli, Simone, Pannone, Luca, Lo, Ivan Fai-Man, Shi, Lisong, Edelmann, Lisa, Tartaglia, Marco, Luk, Ho-Ming, Gelb, Bruce D.
Publicado em 2014

AN INTEGRATIVE PIPELINE FOR MULTI-MODAL DISCOVERY OF DISEASE RELATIONSHIPS

Por Glicksberg, Benjamin S., Li, Li, Cheng, Wei-Yi, Shameer, Khader, Hakenberg, Jörg, Castellanos, Rafael, Ma, Meng, Shi, Lisong, Shah, Hardik, Dudley, Joel T., Chen, Rong
Publicado no Pac Symp Biocomput (2015)

Dual Diagnosis of Ellis-van Creveld Syndrome and Hearing Loss in a Consanguineous Family

Por Vona, Barbara, Maroofian, Reza, Mendiratta, Geetu, Croken, Matthew, Peng, Siwu, Ye, Xiaoqian, Rezazadeh, Jamileh, Bahena, Paulina, Lekszas, Caroline, Haaf, Thomas, Edelmann, Lisa, Shi, Lisong
Publicado no Mol Syndromol (2017)

Cytogenomic identification and long-read single molecule real-time (SMRT) sequencing of a Bardet–Biedl Syndrome 9 (BBS9) deletion

Por Reiner, Jennifer, Pisani, Laura, Qiao, Wanqiong, Singh, Ram, Yang, Yao, Shi, Lisong, Khan, Wahab A., Sebra, Robert, Cohen, Ninette, Babu, Arvind, Edelmann, Lisa, Jabs, Ethylin Wang, Scott, Stuart A.
Publicado no NPJ Genom Med (2018)

Identification of Rare Variants in TNNI3 with Atrial Fibrillation in a Chinese GeneID Population

Por Wang, Chuchu, Wu, Manman, Qian, Jin, Li, Bin, Tu, Xin, Xu, Chengqi, Li, Sisi, Chen, Shanshan, Zhao, Yuanyuan, Huang, Yufeng, Shi, Lisong, Cheng, Xiang, Liao, Yuhua, Chen, Qiuyun, Xia, Yunlong, Yao, Wei, Wu, Gang, Cheng, Mian, Wang, Qing K.
Publicado no Mol Genet Genomics (2015)

Functional dominant-negative mutation of sodium channel subunit gene SCN3B associated with atrial fibrillation in a Chinese GeneID population

Por Wang, Pengyun, Yang, Qinbo, Wu, Xiaofen, Yang, Yanzong, Shi, Lisong, Wang, Chuchu, Wu, Gang, Xia, Yunlong, Yang, Bo, Zhang, Rongfeng, Xu, Chengqi, Cheng, Xiang, Li, Sisi, Zhao, Yuanyuan, Fu, Fenfen, Liao, Yuhua, Fang, Fang, Chen, Qiuyun, Tu, Xin, Wang, Qing K.
Publicado em 2010

Significant association of SNP rs2106261 in the ZFHX3 gene with atrial fibrillation in a Chinese Han GeneID population

Por Li, Cong, Wang, Fan, Yang, Yanzong, Fu, Fenfen, Xu, Chengqi, Shi, Lisong, Li, Sisi, Xia, Yunlong, Wu, Gang, Cheng, Xiang, Liu, Hui, Wang, Chuchu, Wang, Pengyun, Hao, Jianjun, Ke, Yuhe, Zhao, Yuanyuan, Liu, Mugen, Zhang, Rongfeng, Gao, Lianjun, Yu, Bo, Zeng, Qiutang, Liao, Yuhua, Yang, Bo, Tu, Xin, Wang, Qing K.
Publicado no Hum Genet (2010)

The Same Chromosome 9p21.3 Locus Is Associated With Type 2 Diabetes and Coronary Artery Disease in a Chinese Han Population

Por Cheng, Xiang, Shi, Lisong, Nie, Shaofang, Wang, Fan, Li, Xiuchun, Xu, Chengqi, Wang, Pengyun, Yang, Baofeng, Li, Qingxian, Pan, Zhenwei, Li, Yue, Xia, Hao, Zheng, Chenhong, Ke, Yuhe, Wu, Yanxia, Tang, Tingting, Yan, Xinxin, Yang, Yan, Xia, Ni, Yao, Rui, Wang, Binbin, Ma, Xu, Zeng, Qiutang, Tu, Xin, Liao, Yuhua, Wang, Qing K.
Publicado em 2011

A genome-wide association study identifies susceptibility loci for non-syndromic sagittal craniosynostosis near BMP2 and within BBS9

Por Justice, Cristina M., Yagnik, Garima, Kim, Yoonhee, Peter, Inga, Jabs, Ethylin Wang, Erazo, Monica, Ye, Xiaoqian, Ainehsazan, Edmond, Shi, Lisong, Cunningham, Michael L., Kimonis, Virginia, Roscioli, Tony, Wall, Steven A., Wilkie, Andrew O.M., Stoler, Joan, Richtsmeier, Joan T., Heuzé, Yann, Sanchez-Lara, Pedro A., Buckley, Michael F., Druschel, Charlotte M., Mills, James L., Caggana, Michele, Romitti, Paul A., Kay, Denise M., Senders, Craig, Taub, Peter J., Klein, Ophir D., Boggan, James, Zwienenberg-Lee, Marike, Naydenov, Cyril, Kim, Jinoh, Wilson, Alexander F., Boyadjiev, Simeon A.
Publicado em 2012