| RET germline mutations identified by exome sequencing in a Chinese multiple endocrine neoplasia type 2A/familial medullary thyroid carcinoma family XP Qi, JM Ma, ZF Du, RB Ying, J Fei, HY Jin, JS Han, JQ Wang, XL Chen, ... PloS one 6 (5), e20353, 2011 | 63 | 2011 |
| LncRNA-HOTAIR activates autophagy and promotes the imatinib resistance of gastrointestinal stromal tumor cells through a mechanism involving the miR-130a/ATG2B pathway J Zhang, K Chen, Y Tang, X Luan, X Zheng, X Lu, J Mao, L Hu, S Zhang, ... Cell death & disease 12 (4), 367, 2021 | 47 | 2021 |
| Genetic diagnosis of autosomal dominant polycystic kidney disease by targeted capture and next-generation sequencing: utility and limitations XP Qi, ZF Du, JM Ma, XL Chen, Q Zhang, J Fei, XM Wei, D Chen, HP Ke, ... Gene 516 (1), 93-100, 2013 | 46 | 2013 |
| Gut microbiota in children with juvenile idiopathic arthritis: characteristics, biomarker identification, and usefulness in clinical prediction X Qian, YX Liu, X Ye, W Zheng, S Lv, M Mo, J Lin, W Wang, W Wang, ... BMC genomics 21, 1-13, 2020 | 45 | 2020 |
| RET proto-oncogene genetic screening of families with multiple endocrine neoplasia type 2 optimizes diagnostic and clinical management in China XP Qi, XL Chen, JM Ma, ZF Du, J Fei, CP Yang, J Cheng, QZ Song, ... Thyroid 22 (12), 1257-1265, 2012 | 40 | 2012 |
| Prophylactic thyroidectomy for MEN 2-related medullary thyroid carcinoma based on predictive testing for RET proto-oncogene mutation and basal serum calcitonin in China XP Qi, JQ Zhao, ZF Du, RR Yang, JM Ma, J Fei, J Cheng, JS Han, HY Jin, ... European Journal of Surgical Oncology (EJSO) 39 (9), 1007-1012, 2013 | 30 | 2013 |
| Cloning and mapping of a novel human serum/glucocorticoid regulated kinase-like gene, SGKL, to chromosome 8q12. 3–q13. 1 F Dai, L Yu, H He, Y Zhao, J Yang, X Zhang, S Zhao Genomics 62 (1), 95-97, 1999 | 30 | 1999 |
| Eukaryotic translation initiation factor 5A2 regulates the migration and invasion of hepatocellular carcinoma cells via pathways involving reactive oxygen species RR Liu, YS Lv, YX Tang, YF Wang, XL Chen, XX Zheng, SZ Xie, Y Cai, ... Oncotarget 7 (17), 24348, 2016 | 29 | 2016 |
| 102T/C SNP in the 5‐hydroxytryptamine receptor 2A (HTR2A) gene and schizophrenia in two southern han chinese populations: Lack of association XN Zhang, SD Jiang, XH He, LN Zhang American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 126 …, 2004 | 29 | 2004 |
| A novel mutation of keratin 9 in a large Chinese family with epidermolytic palmoplantar keratoderma XH He, XN Zhang, W Mao, HP Chen, LR Xu, H Chen, XL He, YP Le British Journal of Dermatology 150 (4), 647-651, 2004 | 27 | 2004 |
| Whole exome sequencing implicates PTCH1 and COL17A1 genes in ossification of the posterior longitudinal ligament of the cervical spine in Chinese patients W Wei, HL He, CY Chen, Y Zhao, HL Jiang, WT Liu, ZF Du, XL Chen, ... Genet Mol Res 13 (1), 1794-1804, 2014 | 26 | 2014 |
| Deletion analysis of SMN1 and NAIP genes in Southern Chinese children with spinal muscular atrophy Y Liang, X Chen, Z Yu, C Chen, S Bi, L Mao, B Zhou, X Zhang Journal of Zhejiang University SCIENCE B 10 (1), 29-34, 2009 | 25 | 2009 |
| CRISPR/Cas9-mediated treatment ameliorates the phenotype of the epidermolytic palmoplantar keratoderma-like mouse XR Luan, XL Chen, YX Tang, JY Zhang, X Gao, HP Ke, ZY Lin, XN Zhang Molecular Therapy-Nucleic Acids 12, 220-228, 2018 | 24 | 2018 |
| A novel mutation within the 2B rod domain of keratin 9 in a Chinese pedigree with epidermolytic palmoplantar keratoderma combined with knuckle pads and camptodactyly ZF Du, W Wei, YF Wang, XL Chen, CY Chen, WT Liu, JJ Lu, LG Mao, ... European Journal of Dermatology 21 (5), 675-679, 2011 | 24 | 2011 |
| Complete mitochondrial DNA sequence analysis in two southern Chinese pedigrees with Leber hereditary optic neuropathy revealed secondary mutations along with the primary mutation L Shu, YM Zhang, XX Huang, CY Chen, XN Zhang International Journal of Ophthalmology 5 (1), 28, 2012 | 23 | 2012 |
| Genetic Analysis of RET, EDNRB, and EDN3 Genes and Three SNPs in MCS + 9.7 in Chinese Patients with Isolated Hirschsprung Disease XN Zhang, MN Zhou, YQ Qiu, SP Ding, M Qi, JC Li Biochemical genetics 45, 523-527, 2007 | 20 | 2007 |
| Association analysis of COMT polymorphisms and schizophrenia in a Chinese Han population: A case‐control study R Yu, XN Zhang, XX Huang, SP Ding, JC Li American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 144 …, 2007 | 20 | 2007 |
| Association analysis between attention-deficit hyperactivity disorder and Val158Met polymorphism of catechol-O-methyltransferase gene XN Zhang, LM Ruan, YP Le, Y Zhang Zhonghua yi xue yi chuan xue za zhi= Zhonghua yixue yichuanxue zazhi …, 2003 | 19 | 2003 |
| Case report: a p.C618S RET proto-oncogene germline mutation in a large Chinese pedigree with familial medullary thyroid carcinoma XP Qi, RB Ying, JM Ma, WT Liu, ZF Du, J Fei, CP Yang, QZ Song, HY Jin, ... Familial cancer 11, 131-136, 2012 | 18 | 2012 |
| Study on the forming of ‘‘small olded tree” and the transforming way in the loess plateau QC Hou, X Huang, SF Han, X Zhang J. Soil Water Conserv 5, 64-72, 1991 | 18 | 1991 |
