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Peng Chen
Peng Chen
Verified email at jlu.edu.cn
Title
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Year
The genetic architecture of type 2 diabetes
C Fuchsberger, J Flannick, TM Teslovich, A Mahajan, V Agarwala, ...
Nature 536 (7614), 41-47, 2016
12392016
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia
VJM Verhoeven, PG Hysi, R Wojciechowski, Q Fan, JA Guggenheim, ...
Nature genetics 45 (3), 314-318, 2013
5212013
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis
E Wheeler, A Leong, CT Liu, MF Hivert, RJ Strawbridge, C Podmore, M Li, ...
PLoS medicine 14 (9), e1002383, 2017
4022017
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
N Kato, M Loh, F Takeuchi, N Verweij, X Wang, W Zhang, TN Kelly, ...
Nature genetics 47 (11), 1282-1293, 2015
3552015
Meta-analysis identifies multiple loci associated with kidney function–related traits in east Asian populations
Y Okada, X Sim, MJ Go, JY Wu, D Gu, F Takeuchi, A Takahashi, S Maeda, ...
Nature genetics 44 (8), 904-909, 2012
3142012
Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease
W Zhao, A Rasheed, E Tikkanen, JJ Lee, AS Butterworth, JMM Howson, ...
Nature genetics 49 (10), 1450-1457, 2017
2572017
Deep whole-genome sequencing of 100 southeast Asian Malays
LP Wong, RTH Ong, WT Poh, X Liu, P Chen, R Li, KKY Lam, NE Pillai, ...
The American Journal of Human Genetics 92 (1), 52-66, 2013
1982013
FTO genetic variants, dietary intake and body mass index: insights from 177 330 individuals
Q Qi, TO Kilpeläinen, MK Downer, T Tanaka, CE Smith, I Sluijs, ...
Human molecular genetics 23 (25), 6961-6972, 2014
1932014
Genome-wide association study identifies three novel loci for type 2 diabetes
K Hara, H Fujita, TA Johnson, T Yamauchi, K Yasuda, M Horikoshi, ...
Human molecular genetics 23 (1), 239-246, 2014
1912014
New loci and coding variants confer risk for age-related macular degeneration in East Asians
CY Cheng, K Yamashiro, L Jia Chen, J Ahn, L Huang, L Huang, ...
Nature communications 6 (1), 6063, 2015
1852015
Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error
CY Cheng, M Schache, MK Ikram, TL Young, JA Guggenheim, V Vitart, ...
The American Journal of Human Genetics 93 (2), 264-277, 2013
1762013
Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels
CN Spracklen, P Chen, YJ Kim, X Wang, H Cai, S Li, J Long, Y Wu, ...
Human molecular genetics 26 (9), 1770-1784, 2017
1712017
Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia
J Simino, G Shi, JC Bis, DI Chasman, GB Ehret, X Gu, X Guo, SJ Hwang, ...
The American Journal of Human Genetics 95 (1), 24-38, 2014
1372014
Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium
Q Fan, X Guo, JWL Tideman, KM Williams, S Yazar, SM Hosseini, ...
Scientific reports 6 (1), 25853, 2016
1162016
Gold nanoparticles for high-throughput genotyping of long-range haplotypes
P Chen, D Pan, C Fan, J Chen, K Huang, D Wang, H Zhang, Y Li, G Feng, ...
Nature Nanotechnology 6 (10), 639-644, 2011
1152011
Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci
M He, M Xu, B Zhang, J Liang, P Chen, JY Lee, TA Johnson, H Li, X Yang, ...
Human molecular genetics 24 (6), 1791-1800, 2015
1122015
A genome-wide association study reveals association between common variants in an intergenic region of 4q25 and high-grade myopia in the Chinese Han population
Z Li, J Qu, X Xu, X Zhou, H Zou, N Wang, T Li, X Hu, Q Zhao, P Chen, W Li, ...
Human molecular genetics 20 (14), 2861-2868, 2011
1092011
Identification of four novel variants that influence central corneal thickness in multi-ethnic Asian populations
BK Cornes, CC Khor, ME Nongpiur, L Xu, WT Tay, Y Zheng, R Lavanya, ...
Human molecular genetics 21 (2), 437-445, 2012
972012
Common variants in major histocompatibility complex region and TCF4 gene are significantly associated with schizophrenia in Han Chinese
T Li, Z Li, P Chen, Q Zhao, T Wang, K Huang, JY Li, Y Li, J Liu, Z Zeng, ...
Biological psychiatry 68 (7), 671-673, 2010
912010
Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia
M Miyake, K Yamashiro, Y Tabara, K Suda, S Morooka, H Nakanishi, ...
Nature communications 6 (1), 6689, 2015
882015
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