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Xin Jin (金鑫)
Xin Jin (金鑫)
BGI & SCUT, China
Verified email at genomics.cn - Homepage
Title
Cited by
Cited by
Year
A global reference for human genetic variation
1000 Genomes Project Consortium
Nature 526 (7571), 68, 2015
14429*2015
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
82132012
Sequencing of 50 human exomes reveals adaptation to high altitude
X Yi, Y Liang, E Huerta-Sanchez, X Jin, ZXP Cuo, JE Pool, X Xu, H Jiang, ...
Science's STKE 329 (5987), 75, 2010
17092010
Altitude adaptation in Tibetans caused by introgression of Denisovan-like DNA
E Huerta-Sánchez, X Jin, Asan, Z Bianba, BM Peter, N Vinckenbosch, ...
Nature 512 (7513), 194-197, 2014
10172014
Whole-Genome Sequencing in Autism Identifies Hot Spots for De Novo Germline Mutation
JJ Michaelson, Y Shi, M Gujral, H Zheng, D Malhotra, X Jin, M Jian, G Liu, ...
Cell 151 (7), 1431-1442, 2012
6602012
Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing
Y Jiang, RKC Yuen, X Jin, M Wang, N Chen, X Wu, J Ju, J Mei, Y Shi, ...
The American Journal of Human Genetics 93 (2), 249-263, 2013
5322013
Lanosterol reverses protein aggregation in cataracts
L Zhao, XJ Chen, J Zhu, YB Xi, X Yang, LD Hu, H Ouyang, SH Patel, X Jin, ...
Nature 523 (7562), 607-611, 2015
4632015
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel
O Delaneau, J Marchini
Nature communications 5 (1), 3934, 2014
4322014
A common Greenlandic TBC1D4 variant confers muscle insulin resistance and type 2 diabetes
I Moltke, N Grarup, ME Jřrgensen, P Bjerregaard, JT Treebak, ...
Nature 512 (7513), 190-193, 2014
4042014
The DNA methylome of human peripheral blood mononuclear cells
Y Li, J Zhu, G Tian, N Li, Q Li, M Ye, H Zheng, J Yu, H Wu, J Sun, H Zhang, ...
PLoS biology 8 (11), e1000533, 2010
3912010
Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants
Y Li, N Vinckenbosch, G Tian, E Huerta-Sanchez, T Jiang, H Jiang, ...
Nature genetics 42 (11), 969-972, 2010
3762010
TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing
JL Wang, X Yang, K Xia, ZM Hu, L Weng, X Jin, H Jiang, P Zhang, L Shen, ...
Brain 133 (12), 3510-3518, 2010
3412010
Building the sequence map of the human pan-genome
R Li, Y Li, H Zheng, R Luo, H Zhu, Q Li, W Qian, Y Ren, G Tian, J Li, ...
Nature biotechnology 28 (1), 57-63, 2010
2882010
Exome sequencing identifies ZNF644 mutations in high myopia
Y Shi, Y Li, D Zhang, H Zhang, Y Li, F Lu, X Liu, F He, B Gong, L Cai, R Li, ...
PLoS genetics 7 (6), e1002084, 2011
2382011
A large-scale screen for coding variants predisposing to psoriasis
H Tang, X Jin, Y Li, H Jiang, X Tang, X Yang, H Cheng, Y Qiu, G Chen, ...
Nature genetics 46 (1), 45-50, 2014
2372014
Genome-wide characteristics of de novo mutations in autism
RKC Yuen, D Merico, H Cao, G Pellecchia, B Alipanahi, ...
NPJ genomic medicine 1 (1), 1-10, 2016
2312016
Genomic analyses from non-invasive prenatal testing reveal genetic associations, patterns of viral infections, and Chinese population history
S Liu, S Huang, F Chen, L Zhao, Y Yuan, SS Francis, L Fang, Z Li, L Lin, ...
Cell 175 (2), 347-359. e14, 2018
2112018
Initial whole-genome sequencing and analysis of the host genetic contribution to COVID-19 severity and susceptibility
F Wang, S Huang, R Gao, Y Zhou, C Lai, Z Li, W Xian, X Qian, Z Li, ...
Cell discovery 6 (1), 83, 2020
2062020
Deep sequencing of the MHC region in the Chinese population contributes to studies of complex disease
F Zhou, H Cao, X Zuo, T Zhang, X Zhang, X Liu, R Xu, G Chen, Y Zhang, ...
Nature genetics 48 (7), 740-746, 2016
1982016
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
1832015
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