| 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 | 823 | 2017 |
| 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 | 338 | 2019 |
| 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 | 244 | 2013 |
| 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 | 235 | 2015 |
| 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 | 205 | 2019 |
| 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 | 204 | 2016 |
| 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 | 185 | 2017 |
| 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 | 176 | 2017 |
| Mutations disrupting neuritogenesis genes confer risk for cerebral palsy SC Jin, SA Lewis, S Bakhtiari, X Zeng, MC Sierant, S Shetty, SM Nordlie, ... Nature Genetics 52 (10), 1046-1056, 2020 | 154 | 2020 |
| SUPERGNOVA: local genetic correlation analysis reveals heterogeneous etiologic sharing of complex traits Y Zhang, Q Lu, Y Ye, K Huang, W Liu, Y Wu, X Zhong, B Li, Z Yu, ... Genome Biology 22 (1), 1-30, 2021 | 144* | 2021 |
| 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 | 143 | 2018 |
| Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus SC Jin, W Dong, AJ Kundishora, S Panchagnula, A Moreno-De-Luca, ... Nature medicine 26 (11), 1754-1765, 2020 | 132 | 2020 |
| Genetic Variants and Functional Pathways Associated with Resilience to Alzheimer's Disease L Dumitrescu, ER Mahoney, S Mukherjee, ML Lee, WS Bush, ... Brain 143 (8), 2561-2575, 2020 | 119 | 2020 |
| 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 | 112 | 2017 |
| 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 | 107 | 2016 |
| 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 | 93 | 2019 |
| Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations DJ Panyard, KM Kim, BF Darst, YK Deming, X Zhong, Y Wu, H Kang, ... Communications Biology 4 (1), 1-11, 2021 | 92 | 2021 |
| The socioeconomic gradient in epigenetic ageing clocks: evidence from the multi-ethnic study of atherosclerosis and the health and retirement study LL Schmitz, W Zhao, SM Ratliff, J Goodwin, J Miao, Q Lu, X Guo, ... Epigenetics 17 (6), 589-611, 2022 | 82 | 2022 |
| 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 | 80 | 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 | 75 | 2017 |
Hongyu ZhaoYale UniversityVerified email at yale.edu