| 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 | 304 | 2015 |
| 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 | 195 | 2019 |
| 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 | 127 | 2014 |
| 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 | 94 | 2018 |
| 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 | 90 | 2013 |
| 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 | 80 | 2014 |
| 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), 44, 2018 | 63 | 2018 |
| 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 | 60 | 2017 |
| 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 | 55 | 2014 |
| 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 | 42 | 2014 |
| A genome-wide association meta-analysis identifies new eosinophilic esophagitis loci X Chang, M March, F Mentch, K Nguyen, J Glessner, H Qu, Y Liu, ... Journal of Allergy and Clinical Immunology 149 (3), 988-998, 2022 | 40 | 2022 |
| 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 | 38 | 2017 |
| Common and rare genetic risk factors converge in protein interaction networks underlying schizophrenia X Chang, LA Lima, Y Liu, J Li, Q Li, PMA Sleiman, H Hakonarson Frontiers in genetics 9, 434, 2018 | 37 | 2018 |
| 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 | 37 | 2017 |
| The Long Noncoding RNA Landscape in Amygdala Tissues from Schizophrenia Patients T Tian, Z Wei, X Chang, Y Liu, RE Gur, PMA Sleiman, H Hakonarson EBioMedicine 34, 171-181, 2018 | 36 | 2018 |
| 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 | 35 | 2015 |
| Expression Pattern of the SARS-CoV-2 Entry Genes ACE2 and TMPRSS2 in the Respiratory Tract Y Liu, HQ Qu, J Qu, L Tian, H Hakonarson Viruses 12 (10), 1174, 2020 | 34 | 2020 |
| Expression Pattern of the SARS-CoV-2 Entry Genes ACE2 and TMPRSS2 in the Respiratory Tract Y Liu, HQ Qu, J Qu, L Tian, H Hakonarson Viruses 12 (10), 1174, 2020 | 34 | 2020 |
| Combining targeted panel-based resequencing and copy-number variation analysis for the diagnosis of inherited syndromic retinopathies and associated ciliopathies I Sanchez-Navarro, L RJ da Silva, F Blanco-Kelly, O Zurita, ... Scientific reports 8 (1), 5285, 2018 | 33 | 2018 |
| Application of deep learning algorithm on whole genome sequencing data uncovers structural variants associated with multiple mental disorders in African American patients Y Liu, HQ Qu, FD Mentch, J Qu, X Chang, K Nguyen, L Tian, J Glessner, ... Molecular psychiatry 27 (3), 1469-1478, 2022 | 28 | 2022 |
Hakon HakonarsonDirector, Center for Applied Genomics, CHOP, UPENNEmail được xác minh tại email.chop.edu
