Articles with public access mandates - Xin Jin (金鑫)Learn more
OverallNSFCNIHMRCWellcomeCASBHFHHMINHMRCCIHRDFFAutism Speaks Inc, USAGenome CanadaSwedish Research CouncilBBSRCNIHREuropean CommissionHealth Data Research, UKNSFSNSFFRQSDCTIINSERMA*StarVersus Arthritis, UKCancer Research UKInnovation Fund DenmarkNational Research Foundation, SingaporeRoyal Society UKOICR
Not available anywhere: 2
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
Mandates: US National Institutes of Health
Metagenomic analysis of individual mosquito viromes reveals the geographical patterns and drivers of viral diversity
YF Pan, H Zhao, QY Gou, PB Shi, JH Tian, Y Feng, K Li, WH Yang, D Wu, ...
Nature Ecology & Evolution 8 (5), 947-959, 2024
Mandates: National Health and Medical Research Council, Australia
Available somewhere: 72
A global reference for human genetic variation
1000 Genomes Project Consortium
Nature 526 (7571), 68, 2015
Mandates: US National Institutes of Health, Howard Hughes Medical Institute, Canadian …
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
Mandates: US National Institutes of Health, Howard Hughes Medical Institute, British …
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
Mandates: Swiss National Science Foundation, US National Institutes of Health
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
Mandates: US National Institutes of Health, National Natural Science Foundation of China
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
Mandates: US National Institutes of Health, National Health and Medical Research …
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
Mandates: US National Institutes of Health, Canadian Institutes of Health Research …
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
Mandates: National Natural Science Foundation of China
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
Mandates: US National Institutes of Health, UK Biotechnology and Biological Sciences …
A common Greenlandic TBC1D4 variant confers muscle insulin resistance and type 2 diabetes
I Moltke, N Grarup, ME Jørgensen, P Bjerregaard, JT Treebak, ...
Nature 512 (7513), 190-193, 2014
Mandates: Danish Council for Independent Research, UK Medical Research Council
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
Mandates: US National Institutes of Health, Canadian Institutes of Health Research …
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
Mandates: US National Institutes of Health, Howard Hughes Medical Institute, UK …
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
Mandates: National Natural Science Foundation of China
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
Mandates: National Natural Science Foundation of China
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
Mandates: US National Institutes of Health, National Natural Science Foundation of …
Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes
A Albrechtsen, N Grarup, Y Li, T Sparsø, G Tian, H Cao, T Jiang, SY Kim, ...
Diabetologia, 1-13, 2012
Mandates: Danish Council for Technology and Innovation, Danish Council for Independent …
Whole-genome sequencing uncovers the genetic basis of chronic mountain sickness in Andean highlanders
D Zhou, N Udpa, R Ronen, T Stobdan, J Liang, O Appenzeller, HW Zhao, ...
The American Journal of Human Genetics 93 (3), 452-462, 2013
Mandates: US National Institutes of Health
Distinct biological ages of organs and systems identified from a multi-omics study
C Nie, Y Li, R Li, Y Yan, D Zhang, T Li, Z Li, Y Sun, H Zhen, J Ding, Z Wan, ...
Cell reports 38 (10), 2022
Mandates: National Natural Science Foundation of China
The trans-omics landscape of COVID-19
P Wu, D Chen, W Ding, P Wu, H Hou, Y Bai, Y Zhou, K Li, S Xiang, P Liu, ...
Nature Communications 12 (1), 4543, 2021
Mandates: National Natural Science Foundation of China
Publication and funding information is determined automatically by a computer program