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| A natural antisense transcript at the Huntington's disease repeat locus regulates HTT expression DW Chung, DD Rudnicki, L Yu, RL Margolis Human molecular genetics 20 (17), 3467-3477, 2011 | 212 | 2011 |
| Meta‐analysis Added Power to Identify Variants in FTO Associated With Type 2 Diabetes and Obesity in the Asian Population Y Liu, Z Liu, Y Song, D Zhou, D Zhang, T Zhao, Z Chen, L Yu, Y Yang, ... Obesity 18 (8), 1619-1624, 2010 | 140 | 2010 |
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| The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left … D Warburton, M Ronemus, J Kline, V Jobanputra, I Williams, ... Human genetics 133, 11-27, 2014 | 135 | 2014 |
| Genetic causes of congenital diaphragmatic hernia J Wynn, L Yu, WK Chung Seminars in Fetal and Neonatal Medicine 19 (6), 324-330, 2014 | 119 | 2014 |
| The E23K variation in the KCNJ11 gene is associated with type 2 diabetes in Chinese and East Asian population D Zhou, D Zhang, Y Liu, T Zhao, Z Chen, Z Liu, L Yu, Z Zhang, H Xu, L He Journal of human genetics 54 (7), 433-435, 2009 | 96 | 2009 |
| Intra-ethnic differences in genetic variants of the UGT-glucuronosyltransferase 1A1 gene in Chinese populations A Zhang, Q Xing, S Qin, J Du, L Wang, L Yu, X Li, L Xu, M Xu, G Feng, ... The pharmacogenomics journal 7 (5), 333-338, 2007 | 96 | 2007 |
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| De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders H Qi, L Yu, X Zhou, J Wynn, H Zhao, Y Guo, N Zhu, A Kitaygorodsky, ... PLoS genetics 14 (12), e1007822, 2018 | 89 | 2018 |
| The—1019 C/G polymorphism of the 5-HT1A receptor gene is associated with negative symptom response to risperidone treatment in schizophrenia patients L Wang, C Fang, A Zhang, J Du, L Yu, J Ma, G Feng, Q Xing, L He Journal of Psychopharmacology 22 (8), 904-909, 2008 | 89 | 2008 |
| Variants in GATA4 are a rare cause of familial and sporadic congenital diaphragmatic hernia L Yu, J Wynn, YH Cheung, Y Shen, GB Mychaliska, TM Crombleholme, ... Human Genetics, 1-8, 2012 | 88 | 2012 |
| Association of Leukocyte Telomere Length with Type 2 Diabetes in Mainland Chinese Populations Q Shen, X Zhao, L Yu, Z Zhang, D Zhou, M Kan, D Zhang, L Cao, Q Xing, ... Journal of Clinical Endocrinology & Metabolism, 2012 | 80 | 2012 |
| De novo copy number variants are associated with congenital diaphragmatic hernia L Yu, J Wynn, L Ma, S Guha, GB Mychaliska, TM Crombleholme, ... Journal of Medical Genetics 49 (10), 650-659, 2012 | 79 | 2012 |
| Increased burden of de novo predicted deleterious variants in complex congenital diaphragmatic hernia L Yu, AD Sawle, J Wynn, G Aspelund, CJ Stolar, MS Arkovitz, D Potoka, ... Human molecular genetics 24 (16), 4764-4773, 2015 | 75 | 2015 |
| Common variants near TERC are associated with leukocyte telomere length in the Chinese Han population Q Shen, Z Zhang, L Yu, L Cao, DZ Zhou, MY Kan, B Li, D Zhang, L He, ... European journal of human genetics 19 (6), 721-723, 2011 | 70 | 2011 |
| An association between polymorphisms of the interleukin-10 gene promoter and schizophrenia in the Chinese population L Yu, M Yang, J Zhao, Y Shi, X Zhao, J Yang, Z Liu, N Gu, G Feng, L He Schizophrenia research 71 (1), 179-183, 2004 | 70 | 2004 |
| Systematic screening for polymorphisms in the CYP3A4 gene in the Chinese population J Du, Q Xing, L Xu, M Xu, A Shu, Y Shi, L Yu, A Zhang, L Wang, H Wang, ... Future Medicine Ltd 7 (6), 831-841, 2006 | 68 | 2006 |
| Whole exome sequencing identifies de novo mutations in GATA6 associated with congenital diaphragmatic hernia L Yu, JT Bennett, J Wynn, GL Carvill, YH Cheung, Y Shen, GB Mychaliska, ... Journal of medical genetics 51 (3), 197-202, 2014 | 67 | 2014 |
| Positive association between variations in CDKAL1 and type 2 diabetes in Han Chinese individuals Y Liu, L Yu, D Zhang, Z Chen, DZ Zhou, T Zhao, S Li, T Wang, X Hu, ... Diabetologia 51, 2134-2137, 2008 | 67 | 2008 |
