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| TCF7L2 is not a major susceptibility gene for type 2 diabetes in Pima Indians: analysis of 3,501 individuals T Guo, RL Hanson, M Traurig, Y Li Muller, L Ma, J Mack, S Kobes, ... Diabetes 56 (12), 3082-3088, 2007 | 117 | 2007 |
| Positive association of the DIO2 (deiodinase type 2) gene with mental retardation in the iodine-deficient areas of China TW Guo, FC Zhang, MS Yang, XC Gao, L Bian, SW Duan, ZJ Zheng, ... Journal of medical genetics 41 (8), 585-590, 2004 | 110 | 2004 |
| Rare genome-wide copy number variation and expression of schizophrenia in 22q11. 2 deletion syndrome AS Bassett, C Lowther, D Merico, G Costain, EWC Chow, ... American Journal of Psychiatry 174 (11), 1054-1063, 2017 | 101 | 2017 |
| Enhanced maternal origin of the 22q11. 2 deletion in velocardiofacial and DiGeorge syndromes M Delio, T Guo, DM McDonald-McGinn, E Zackai, S Herman, ... The American Journal of Human Genetics 92 (3), 439-447, 2013 | 89 | 2013 |
| Association of AKT1 gene polymorphisms with risk of schizophrenia and with response to antipsychotics in the Chinese population. MQ Xu, QH Xing, YL Zheng, S Li, JJ Gao, G He, TW Guo, GY Feng, F Xu, ... Journal of Clinical Psychiatry 68 (9), 1358-1367, 2007 | 88 | 2007 |
| SNPs and haplotypes in the S100B gene reveal association with schizophrenia J Liu, Y Shi, J Tang, T Guo, X Li, Y Yang, Q Chen, X Zhao, G He, G Feng, ... Biochemical and biophysical research communications 328 (1), 335-341, 2005 | 88 | 2005 |
| Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo‐cardio‐facial/digeorge/22q11.2 deletion syndrome patients T Guo, D McDonald‐McGinn, A Blonska, A Shanske, AS Bassett, E Chow, ... Human mutation 32 (11), 1278-1289, 2011 | 85 | 2011 |
| A Genome-Wide Association Study in American Indians Implicates DNER as a Susceptibility Locus for Type 2 Diabetes RL Hanson, YL Muller, S Kobes, T Guo, L Bian, V Ossowski, K Wiedrich, ... Diabetes 63 (1), 369-376, 2014 | 81 | 2014 |
| Further evidence for the association between G72/G30 genes and schizophrenia in two ethnically distinct populations J Ma, W Qin, XY Wang, TW Guo, L Bian, SW Duan, XW Li, FG Zou, ... Molecular psychiatry 11 (5), 479-487, 2006 | 79 | 2006 |
| SIRT1 is associated with a decrease in acute insulin secretion and a sex specific increase in risk for type 2 diabetes in Pima Indians Y Dong, T Guo, M Traurig, CC Mason, S Kobes, J Perez, WC Knowler, ... Molecular genetics and metabolism 104 (4), 661-665, 2011 | 78 | 2011 |
| Population-based and family-based association studies of ZNF804A locus and schizophrenia R Zhang, SM Lu, C Qiu, XG Liu, CG Gao, TW Guo, RK Valenzuela, ... Molecular psychiatry 16 (4), 360-361, 2011 | 78 | 2011 |
| Copy-number variation of the glucose transporter gene SLC2A3 and congenital heart defects in the 22q11. 2 deletion syndrome EE Mlynarski, MB Sheridan, M Xie, T Guo, SE Racedo, ... The American Journal of Human Genetics 96 (5), 753-764, 2015 | 77 | 2015 |
| Strong Parent-of-Origin Effects in the Association of KCNQ1 Variants With Type 2 Diabetes in American Indians RL Hanson, T Guo, YL Muller, J Fleming, WC Knowler, S Kobes, ... Diabetes 62 (8), 2984-2991, 2013 | 70 | 2013 |
| Rare copy number variants and congenital heart defects in the 22q11. 2 deletion syndrome EE Mlynarski, M Xie, D Taylor, MB Sheridan, T Guo, SE Racedo, ... Human genetics 135, 273-285, 2016 | 67 | 2016 |
| Histone modifier genes alter conotruncal heart phenotypes in 22q11. 2 deletion syndrome T Guo, JH Chung, T Wang, DM McDonald-McGinn, WR Kates, W Hawuła, ... The American Journal of Human Genetics 97 (6), 869-877, 2015 | 67 | 2015 |
| Complete sequence of the 22q11. 2 allele in 1,053 subjects with 22q11. 2 deletion syndrome reveals modifiers of conotruncal heart defects Y Zhao, A Diacou, HR Johnston, FI Musfee, DM McDonald-McGinn, ... The American Journal of Human Genetics 106 (1), 26-40, 2020 | 62 | 2020 |
| Insulin-degrading enzyme and Alzheimer disease: a genetic association study in the Han Chinese L Bian, JD Yang, TW Guo, Y Sun, SW Duan, WY Chen, YX Pan, GY Feng, ... Neurology 63 (2), 241-245, 2004 | 62 | 2004 |
| No association between the promoter variants of tumor necrosis factor alpha (TNF-α) and schizophrenia in Chinese Han population S Duan, Y Xu, W Chen, Z Liu, T Guo, J Gao, L Bian, Y Zhen, X Li, X Zhang, ... Neuroscience letters 366 (2), 139-143, 2004 | 56 | 2004 |
| Pharacogenetic effects of dopamine transporter gene polymorphisms on response to chlorpromazine and clozapine and on extrapyramidal syndrome in schizophrenia M Xu, Q Xing, S Li, Y Zheng, S Wu, R Gao, L Yu, T Guo, Y Yang, J Liu, ... Progress in Neuro-Psychopharmacology and Biological Psychiatry 34 (6), 1026-1032, 2010 | 51 | 2010 |
Jianjun GaoGenentech在 gene.com 的电子邮件经过验证
