Prenatal cytogenomic identification and molecular refinement of compound heterozygous STRC deletion breakpoints

por Shi, Lisong, Bai, Yan, Kharbutli, Yara, Oza, Andrea M., Amr, Sami S., Edelmann, Lisa, Mehta, Lakshmi, Scott, Stuart A.
Publicado 2019

Genome-Wide Analysis of nsLTP Gene Family and Identification of SiLTPs Contributing to High Oil Accumulation in Sesame (Sesamum indicum L.)

por Song, Shengnan, You, Jun, Shi, Lisong, Sheng, Chen, Zhou, Wangyi, Dossou, Senouwa Segla Koffi, Dossa, Komivi, Wang, Linhai, Zhang, Xiurong
Publicado 2021

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 2011

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 2018

Deletion of ERF and CIC causes abnormal skull morphology and global developmental delay

por Singh, Ram, Cohen, Ana S.A., Poulton, Cathryn, Hjortshøj, Tina Duelund, Akahira-Azuma, Moe, Mendiratta, Geetu, Khan, Wahab A., Azmanov, Dimitar N., Woodward, Karen J., Kirchhoff, Maria, Shi, Lisong, Edelmann, Lisa, Baynam, Gareth, Scott, Stuart A., Jabs, Ethylin Wang
Publicado 2021

Development and Analytical Validation of a 29 Gene Clinical Pharmacogenetic Genotyping Panel: Multi‐Ethnic Allele and Copy Number Variant Detection

por Scott, Stuart A., Scott, Erick R., Seki, Yoshinori, Chen, Annette J., Wallsten, Richard, Owusu Obeng, Aniwaa, Botton, Mariana R., Cody, Neal, Shi, Huanzhi, Zhao, Geping, Brake, Paul, Nicoletti, Paola, Yang, Yao, Delio, Maria, Shi, Lisong, Kornreich, Ruth, Schadt, Eric E., Edelmann, Lisa
Publicado 2020

Lessons learned from expanded reproductive carrier screening in self‐reported Ashkenazi, Sephardi, and Mizrahi Jewish patients

por Akler, Gidon, Birch, Ashley H., Schreiber‐Agus, Nicole, Cai, Xiaoqiang, Cai, Guiqing, Shi, Lisong, Yu, Chunli, Larmore, Anastasia M., Mendiratta‐Vij, Geetu, Elkhoury, Lama, Dillon, Mitchell W., Zhu, Jun, Mclellan, Andrew S., Suer, Funda E., Webb, Bryn D., Schadt, Eric E., Kornreich, Ruth, Edelmann, Lisa
Publicado 2019

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 2011