Qiongshi Lu
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Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands
SC Jin, J Homsy, S Zaidi, Q Lu, S Morton, SR DePalma, X Zeng, H Qi, ...
Nature genetics 49 (11), 1593-1601, 2017
Computational prediction of associations between long non-coding RNAs and proteins
Q Lu, S Ren, M Lu, Y Zhang, D Zhu, X Zhang, T Li
BMC genomics 14 (1), 651, 2013
Two locus inheritance of non-syndromic midline craniosynostosis via rare SMAD6 and common BMP2 alleles
AT Timberlake, J Choi, S Zaidi, Q Lu, C Nelson-Williams, ED Brooks, ...
Elife 5, e20125, 2016
A statistical framework to predict functional non-coding regions in the human genome through integrated analysis of annotation data
Q Lu, Y Hu, J Sun, Y Cheng, KH Cheung, H Zhao
Scientific reports 5, 10576, 2015
Integrative tissue-specific functional annotations in the human genome provide novel insights on many complex traits and improve signal prioritization in genome wide …
Q Lu, RL Powles, Q Wang, BJ He, H Zhao
PLoS genetics 12 (4), e1005947, 2016
A statistical framework for cross-tissue transcriptome-wide association analysis
Y Hu, M Li, Q Lu, H Weng, J Wang, SM Zekavat, Z Yu, B Li, J Gu, ...
Nature genetics 51 (3), 568-576, 2019
A Review of Study Designs and Statistical Methods for Genomic Epidemiology Studies using Next Generation Sequencing
Q Wang, Q Lu, H Zhao
Frontiers in Genetics 6, 149, 2015
Leveraging functional annotations in genetic risk prediction for human complex diseases
Y Hu, Q Lu, R Powles, X Yao, C Yang, F Fang, X Xu, H Zhao
PLOS Computational Biology 13 (6), e1005589, 2017
Systematic tissue-specific functional annotation of the human genome highlights immune-related DNA elements for late-onset Alzheimer's disease
Q Lu, RL Powles, S Abdallah, D Ou, Q Wang, Y Hu, Y Lu, W Liu, B Li, ...
PLoS genetics 13 (7), e1006933, 2017
GenoWAP: GWAS signal prioritization through integrated analysis of genomic functional annotation
Q Lu, X Yao, Y Hu, H Zhao
Bioinformatics 32 (4), 542-548, 2016
De novo mutation in genes regulating neural stem cell fate in human congenital hydrocephalus
CG Furey, J Choi, SC Jin, X Zeng, AT Timberlake, C Nelson-Williams, ...
Neuron 99 (2), 302-314. e4, 2018
A powerful approach to estimating annotation-stratified genetic covariance via GWAS summary statistics
Q Lu, B Li, D Ou, M Erlendsdottir, RL Powles, T Jiang, Y Hu, D Chang, ...
The American Journal of Human Genetics 101 (6), 939-964, 2017
Genome-wide association study of post-traumatic stress disorder reexperiencing symptoms in> 165,000 US veterans
J Gelernter, N Sun, R Polimanti, R Pietrzak, DF Levey, J Bryois, Q Lu, ...
Nature neuroscience 22 (9), 1394-1401, 2019
Joint modeling of genetically correlated diseases and functional annotations increases accuracy of polygenic risk prediction
Y Hu, Q Lu, W Liu, Y Zhang, M Li, H Zhao
PLoS genetics 13 (6), e1006836, 2017
A genome-wide association study to identify single-nucleotide polymorphisms for acute kidney injury
B Zhao, Q Lu, Y Cheng, JM Belcher, ED Siew, DE Leaf, SC Body, AA Fox, ...
American journal of respiratory and critical care medicine 195 (4), 482-490, 2017
Genome-wide association study of maximum habitual alcohol intake in> 140,000 US European and African American veterans yields novel risk loci
J Gelernter, N Sun, R Polimanti, RH Pietrzak, DF Levey, Q Lu, Y Hu, B Li, ...
Biological psychiatry 86 (5), 365-376, 2019
Mutations in Chromatin Modifier and Ephrin Signaling Genes in Vein of Galen Malformation
D Duran, X Zeng, SC Jin, J Choi, C Nelson-Williams, B Yatsula, J Gaillard, ...
Neuron 101 (3), 429-443. e4, 2019
High frequency of mitochondrial DNA mutations in HIV‐infected treatment‐experienced individuals
M Li, Y Foli, Z Liu, G Wang, Y Hu, Q Lu, S Selvaraj, W Lam, E Paintsil
HIV medicine 18 (1), 45-55, 2017
Integrated analysis of genomics, longitudinal metabolomics, and Alzheimer's risk factors among 1,111 cohort participants
BF Darst, Q Lu, SC Johnson, CD Engelman
Genetic epidemiology 43 (6), 657-674, 2019
Genome-wide association study reveals sex-specific genetic architecture of facial attractiveness
B Hu, N Shen, JJ Li, H Kang, J Hong, J Fletcher, J Greenberg, MR Mailick, ...
PLOS Genetics 15 (4), e1007973, 2019
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