1. Anatomical versus non‐anatomical resection for solitary hepatocellular carcinoma without macroscopic vascular invasion: A propensity score matching analysis. Issue 4 (April 2017) Authors: Zhao, Hui; Chen, Chuang; Gu, Shen; Yan, Xiaopeng; Jia, Wenjun; Mao, Liang; Qiu, Yudong Journal: Journal of gastroenterology and hepatology Issue: Volume 32:Issue 4(2017) Page Start: 870 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Chromosomal microarray analysis on uncultured chorionic villus sampling can be complicated by confined placental mosaicism for aneuploidy and microdeletions. (5th September 2018) Authors: Gu, Shen; Jernegan, Madison; Van den Veyver, Ignatia B.; Peacock, Sandra; Smith, Janice; Breman, Amy Journal: Prenatal diagnosis Issue: Volume 38:Number 11(2018) Page Start: 858 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Exome sequencing in mostly consanguineous Arab families with neurologic disease provides a high potential molecular diagnosis rate. Issue 1 (December 2016) Authors: Charng, Wu-Lin; Karaca, Ender; Coban Akdemir, Zeynep; Gambin, Tomasz; Atik, Mehmed; Gu, Shen; Posey, Jennifer; Jhangiani, Shalini; Muzny, Donna; Doddapaneni, Harsha; Hu, Jianhong; Boerwinkle, Eric; Gibbs, Richard; Rosenfeld, Jill; Cui, Hong; Xia, Fan; Manickam, Kandamurugu; Yang, Yaping; Faqeih, ... Journal: BMC medical genomics Issue: Volume 9:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Higher content of microcystin‐leucine‐arginine promotes the survival of intrahepatic cholangiocarcinoma cells via regulating SET resulting in the poorer prognosis of patients. (25th November 2020) Authors: Gu, Shen; He, Wei; Yan, Minghao; He, Jian; Zhou, Qun; Yan, Xiaopeng; Fu, Xiao; Chen, Jun; Han, Xiaodong; Qiu, Yudong Journal: Cell proliferation Issue: Volume 54:Number 2(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Hutterite‐type cataract maps to chromosome 6p21.32‐p21.31, cosegregates with a homozygous mutation in LEMD2, and is associated with sudden cardiac death. Issue 1 (14th November 2015) Authors: Boone, Philip M.; Yuan, Bo; Gu, Shen; Ma, Zhiwei; Gambin, Tomasz; Gonzaga‐Jauregui, Claudia; Jain, Mahim; Murdock, Todd J.; White, Janson J.; Jhangiani, Shalini N.; Walker, Kimberly; Wang, Qiaoyan; Muzny, Donna M.; Gibbs, Richard A.; Hejtmancik, J. Fielding; Lupski, James R.; Posey, Jennifer E.; ... Journal: Molecular genetics & genomic medicine Issue: Volume 4:Issue 1(2016) Page Start: 77 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Identification of a RAI1-associated disease network through integration of exome sequencing, transcriptomics, and 3D genomics. Issue 1 (December 2016) Authors: Loviglio, Maria; Beck, Christine; White, Janson; Leleu, Marion; Harel, Tamar; Guex, Nicolas; Niknejad, Anne; Bi, Weimin; Chen, Edward; Crespo, Isaac; Yan, Jiong; Charng, Wu-Lin; Gu, Shen; Fang, Ping; Coban-Akdemir, Zeynep; Shaw, Chad; Jhangiani, Shalini; Muzny, Donna; Gibbs, Richard; Rougemont, J... Journal: Genome medicine Issue: Volume 8:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Integrated sequencing and array comparative genomic hybridization in familial Parkinson disease. (October 2020) Authors: Robak, Laurie A.; Du, Renqian; Yuan, Bo; Gu, Shen; Alfradique-Dunham, Isabel; Kondapalli, Vismaya; Hinojosa, Evelyn; Stillwell, Amanda; Young, Emily; Zhang, Chaofan; Song, Xiaofei; Du, Haowei; Gambin, Tomasz; Jhangiani, Shalini N.; Coban Akdemir, Zeynep; Muzny, Donna M.; Tejomurtula, Anusha; Ross... Journal: Neurology Issue: Volume 6:Number 5(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Mechanisms for the Generation of Two Quadruplications Associated with Split‐Hand Malformation. Issue 2 (2nd December 2015) Authors: Gu, Shen; Posey, Jennifer E.; Yuan, Bo; Carvalho, Claudia M.B.; Luk, H.M.; Erikson, Kelly; Lo, Ivan F.M.; Leung, Gordon K.C.; Pickering, Curtis R.; Chung, Brian H.Y.; Lupski, James R. Journal: Human mutation Issue: Volume 37:Issue 2(2016) Page Start: 160 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. MED27 Variants Cause Developmental Delay, Dystonia, and Cerebellar Hypoplasia. Issue 4 (8th February 2021) Authors: Meng, Linyan; Isohanni, Pirjo; Shao, Yunru; Graham, Brett H.; Hickey, Scott E.; Brooks, Stephanie; Suomalainen, Anu; Joset, Pascal; Steindl, Katharina; Rauch, Anita; Hackenberg, Annette; High, Frances A.; Armstrong‐Javors, Amy; Mencacci, Niccolò E.; Gonzàlez‐Latapi, Paulina; Kamel, Walaa A.; Al‐H... Journal: Annals of neurology Issue: Volume 89:Issue 4(2021) Page Start: 828 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile death. Issue 1 (December 2016) Authors: Eldomery, Mohammad; Akdemir, Zeynep; Vögtle, F.-Nora; Charng, Wu-Lin; Mulica, Patrycja; Rosenfeld, Jill; Gambin, Tomasz; Gu, Shen; Burrage, Lindsay; Al Shamsi, Aisha; Penney, Samantha; Jhangiani, Shalini; Zimmerman, Holly; Muzny, Donna; Wang, Xia; Tang, Jia; Medikonda, Ravi; Ramachandran, Prasann... Journal: Genome medicine Issue: Volume 8:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗