Yichuan Edward Liu
Yichuan Edward Liu
The Children's Hospital of Philadelphia, Center for Applied Genomics
Verified email at email.chop.edu
Title
Cited by
Cited by
Year
RNA-Seq identifies novel myocardial gene expression signatures of heart failure
Y Liu, M Morley, J Brandimarto, S Hannenhalli, Y Hu, EA Ashley, ...
Genomics 105 (2), 83-89, 2015
1372015
Comprehensive analysis of gene expression in human retina and supporting tissues
M Li, C Jia, KL Kazmierkiewicz, AS Bowman, L Tian, Y Liu, NA Gupta, ...
Human molecular genetics 23 (15), 4001-4014, 2014
992014
Tissue-specific RNA-Seq in human evoked inflammation identifies blood and adipose LincRNA signatures of cardiometabolic diseases
Y Liu, JF Ferguson, C Xue, RL Ballantyne, IM Silverman, SJ Gosai, ...
Arteriosclerosis, thrombosis, and vascular biology 34 (4), 902-912, 2014
652014
Evaluating the impact of sequencing depth on transcriptome profiling in human adipose
Y Liu, JF Ferguson, C Xue, IM Silverman, B Gregory, MP Reilly, M Li
PloS one 8 (6), e66883, 2013
612013
ARAF recurrent mutation causes central conducting lymphatic anomaly treatable with a MEK inhibitor
D Li, ME March, A Gutierrez-Uzquiza, C Kao, C Seiler, E Pinto, ...
Nature medicine 25 (7), 1116-1122, 2019
462019
PennSeq: accurate isoform-specific gene expression quantification in RNA-Seq by modeling non-uniform read distribution
Y Hu, Y Liu, X Mao, C Jia, JF Ferguson, C Xue, MP Reilly, H Li, M Li
Nucleic acids research 42 (3), e20-e20, 2014
372014
A functional synonymous coding variant in the IL1RN gene is associated with survival in septic shock
NJ Meyer, JF Ferguson, R Feng, F Wang, PN Patel, M Li, C Xue, L Qu, ...
American journal of respiratory and critical care medicine 190 (6), 656-664, 2014
332014
RNA-seq analysis of amygdala tissue reveals characteristic expression profiles in schizophrenia
X Chang, Y Liu, CG Hahn, RE Gur, PMA Sleiman, H Hakonarson
Translational psychiatry 7 (8), e1203-e1203, 2017
322017
Pathogenic variant in EPHB4 results in central conducting lymphatic anomaly
D Li, TL Wenger, C Seiler, ME March, A Gutierrez-Uzquiza, C Kao, E Bhoj, ...
Human molecular genetics 27 (18), 3233-3245, 2018
312018
Non-coding RNA dysregulation in the amygdala region of schizophrenia patients contributes to the pathogenesis of the disease
Y Liu, X Chang, CG Hahn, RE Gur, PAM Sleiman, H Hakonarson
Translational psychiatry 8 (1), 1-10, 2018
272018
Application of Whole Exome Sequencing in Six Families with an Initial Diagnosis of Autosomal Dominant Retinitis Pigmentosa: Lessons Learned
B Almoguera, J Li, P Fernandez-San Jose, Y Liu, M March, R Pellegrino, ...
PloS one 10 (7), e0133624, 2015
272015
Bayesian integration of genetics and epigenetics detects causal regulatory SNPs underlying expression variability
A Das, M Morley, CS Moravec, WHW Tang, H Hakonarson, EA Ashley, ...
Nature communications 6, 8555, 2015
232015
Common variants in MMP20 at 11q22. 2 predispose to 11q deletion and neuroblastoma risk
X Chang, Y Zhao, C Hou, J Glessner, L McDaniel, MA Diamond, ...
Nature communications 8 (1), 569, 2017
222017
Common and rare genetic risk factors converge in protein interaction networks underlying schizophrenia
X Chang, LA Lima, Y Liu, J Li, P Sleiman, H Hakonarson
Frontiers in genetics 9, 434, 2018
182018
Integrative genomics identifies 7p11. 2 as a novel locus for fever and clinical stress response in humans
JF Ferguson, NJ Meyer, L Qu, C Xue, Y Liu, SL DerOhannessian, ...
Human molecular genetics 24 (6), 1801-1812, 2015
182015
A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling
D Li, X Chang, JJ Connolly, L Tian, Y Liu, EJ Bhoj, N Robinson, D Abrams, ...
Scientific reports 7 (1), 3847, 2017
172017
Mapping Splicing Quantitative Trait Loci in RNA-Seq: Supplement Issue: Array Platform Modeling and Analysis (A)
C Jia, Y Hu, Y Liu, M Li
Cancer informatics 13, CIN. S13971, 2014
16*2014
Mapping Splicing Quantitative Trait Loci in RNA-Seq: Supplement Issue: Array Platform Modeling and Analysis (A)
C Jia, Y Hu, Y Liu, M Li
Cancer informatics 13, CIN. S13971, 2014
16*2014
Combining targeted panel-based resequencing and copy-number variation analysis for the diagnosis of inherited syndromic retinopathies and associated ciliopathies
I Sanchez-Navarro, LRJ Da Silva, F Blanco-Kelly, O Zurita, ...
Scientific reports 8 (1), 1-11, 2018
152018
Testing genetic association with rare variants in admixed populations
X Mao, Y Li, Y Liu, L Lange, M Li
Genetic epidemiology 37 (1), 38-47, 2013
142013
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Articles 1–20