| Common variants in FKBP5 gene and major depressive disorder (MDD) susceptibility: a comprehensive meta-analysis S Rao, Y Yao, J Ryan, T Li, D Wang, C Zheng, Y Xu, Q Xu Scientific reports 6 (1), 32687, 2016 | 67 | 2016 |
| Editing GWAS: experimental approaches to dissect and exploit disease-associated genetic variation S Rao, Y Yao, DE Bauer Genome Medicine 13 (1), 41, 2021 | 57 | 2021 |
| Accelerated leukocyte telomere erosion in schizophrenia: evidence from the present study and a meta-analysis S Rao, LN Kota, Z Li, Y Yao, J Tang, C Mao, S Jain, Y Xu, Q Xu Journal of psychiatric research 79, 50-56, 2016 | 53 | 2016 |
| Missense variants in HIF1A and LACC1 contribute to leprosy risk in Han Chinese D Wang, Y Fan, M Malhi, R Bi, Y Wu, M Xu, XF Yu, H Long, YY Li, ... The American Journal of Human Genetics 102 (5), 794-805, 2018 | 50 | 2018 |
| Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program Y Hu, AM Stilp, CP McHugh, S Rao, D Jain, X Zheng, J Lane, ... The American Journal of Human Genetics 108 (5), 874-893, 2021 | 49 | 2021 |
| Genome and epigenome editing identify CCR9 and SLC6A20 as target genes at the 3p21.31 locus associated with severe COVID-19 Y Yao, F Ye, K Li, P Xu, W Tan, Q Feng, S Rao Signal Transduction and Targeted Therapy 6 (1), 85, 2021 | 45 | 2021 |
| Common variants in CACNA1C and MDD susceptibility: A comprehensive meta‐analysis S Rao, Y Yao, C Zheng, J Ryan, C Mao, F Zhang, D Meyre, Q Xu American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 171 …, 2016 | 44 | 2016 |
| Genetic relationships between attention-deficit/hyperactivity disorder, autism spectrum disorder, and intelligence S Rao, A Baranova, Y Yao, J Wang, F Zhang Neuropsychobiology 81 (6), 484-496, 2022 | 34 | 2022 |
| Dissecting ELANE neutropenia pathogenicity by human HSC gene editing S Rao, Y Yao, JS de Brito, Q Yao, AH Shen, RE Watkinson, AL Kennedy, ... Cell Stem Cell 28 (5), 833-845. e5, 2021 | 33 | 2021 |
| Peripheral blood nerve growth factor levels in major psychiatric disorders S Rao, M Martinez-Cengotitabengoa, Y Yao, Z Guo, Q Xu, S Li, X Zhou, ... Journal of Psychiatric Research 86, 39-45, 2017 | 33 | 2017 |
| An APOE-independent cis-eSNP on chromosome 19q13. 32 influences tau levels and late-onset Alzheimer's disease risk S Rao, M Ghani, Z Guo, Y Deming, K Wang, R Sims, C Mao, Y Yao, ... Neurobiology of aging 66, 178. e1-178. e8, 2018 | 19 | 2018 |
| Genetic association of rs1344706 in ZNF804A with bipolar disorder and schizophrenia susceptibility in Chinese populations S Rao, Y Yao, J Ryan, C Jin, Y Xu, X Huang, J Guo, Y Wen, C Mao, ... Scientific reports 7 (1), 41140, 2017 | 14 | 2017 |
| Convergent lines of evidence supporting involvement of NFKB1 in schizophrenia J Long, L Tian, A Baranova, H Cao, Y Yao, S Rao, F Zhang Psychiatry research 312, 114588, 2022 | 10 | 2022 |
| No evidence for widespread positive selection signatures in common risk alleles associated with schizophrenia Y Yao, J Yang, Y Xie, H Liao, B Yang, Q Xu, S Rao Schizophrenia Bulletin 46 (3), 603-611, 2020 | 9 | 2020 |
| Genetic predisposition to blood cell indices in relation to severe COVID‐19 Y Yao, H Song, F Zhang, J Liu, D Wang, Q Feng, S Rao, C Jiang Journal of Medical Virology 95 (1), e28104, 2023 | 8 | 2023 |
| Multi-trait analysis for genome-wide association study of five psychiatric disorders. Transl Psychiatry. 2020; 10 (1): 209 Y Wu, H Cao, A Baranova, H Huang, S Li, L Cai, S Rao, M Dai, M Xie, ... Epub 2020/07/02. https://doi. org/10.1038/s41398-020-00902-6 PMID: 32606422, 0 | 7 | |
| NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium. Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program Y Hu, AM Stilp, CP McHugh, S Rao, D Jain, X Zheng, J Lane, ... Am J Hum Genet 108 (5), 874-893, 2021 | 6 | 2021 |
| Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program MM Wheeler, AM Stilp, S Rao, BV Halldórsson, D Beyter, J Wen, ... Nature communications 13 (1), 7592, 2022 | 4 | 2022 |
| Whole genome sequencing identifies common and rare structural variants contributing to hematologic traits in the NHLBI TOPMed program MM Wheeler, AM Stilp, S Rao, BV Halldórsson, D Beyter, J Wen, ... Medrxiv, 2021.12. 16.21267871, 2021 | 4 | 2021 |
| Recent advances in CRISPR/Cas-based genome insertion technologies X Chen, J Du, S Yun, C Xue, Y Yao, S Rao Molecular Therapy-Nucleic Acids, 2024 | 3 | 2024 |
Shuquan RaoChinese Academy of Medical Sciences and Peking Union Medical College; Harvard Medical School在 ihcams.ac.cn 的电子邮件经过验证
