Year |
Citation |
Score |
2021 |
Hu Y, Stilp AM, McHugh CP, Rao S, Jai D, Zheng X, Lane J, Méric de Bellefon S, Raffield LM, Chen MH, Yanek LR, Wheeler M, Yao Y, Ren C, Broome J, et al. Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program. American Journal of Human Genetics. PMID 33887194 DOI: 10.1016/j.ajhg.2021.04.003 |
0.389 |
|
2020 |
Yao Y, Yang J, Qin Q, Tang C, Li Z, Chen L, Li K, Ren C, Chen L, Rao S. Functional annotation of genetic associations by transcriptome-wide association analysis provides insights into neutrophil development regulation. Communications Biology. 3: 790. PMID 33340029 DOI: 10.1038/s42003-020-01527-7 |
0.3 |
|
2020 |
Wu Y, Cao H, Baranova A, Huang H, Li S, Cai L, Rao S, Dai M, Xie M, Dou Y, Hao Q, Zhu L, Zhang X, Yao Y, Zhang F, et al. Correction: Multi-trait analysis for genome-wide association study of five psychiatric disorders. Translational Psychiatry. 10: 234. PMID 32665544 DOI: 10.1038/S41398-020-00924-0 |
0.381 |
|
2020 |
Wu Y, Cao H, Baranova A, Huang H, Li S, Cai L, Rao S, Dai M, Xie M, Dou Y, Hao Q, Zhu L, Zhang X, Yao Y, Xu M, et al. Multi-trait analysis for genome-wide association study of five psychiatric disorders. Translational Psychiatry. 10: 209. PMID 32606422 DOI: 10.1038/S41398-020-00902-6 |
0.428 |
|
2019 |
Yang Z, Zhang S, Zhang F, Yao Y, Kim K, Meyre D, Zhang H, Liao H, Rao S, Huang X. Allelic frequency differences of DAOA variants between Caucasians and Asians and their association with major mood disorders. Signal Transduction and Targeted Therapy. 4: 39. PMID 33009365 DOI: 10.1038/S41392-019-0066-5 |
0.406 |
|
2019 |
Liu S, Rao S, Xu Y, Li J, Huang H, Zhang X, Fu H, Wang Q, Cao H, Baranova A, Jin C, Zhang F. Identifying common genome-wide risk genes for major psychiatric traits. Human Genetics. PMID 31813014 DOI: 10.1007/S00439-019-02096-4 |
0.451 |
|
2019 |
Yang Z, Zhang S, Zhang F, Yao Y, Kim K, Meyre D, Zhang H, Liao H, Rao S, Huang X. Allelic frequency differences of variants between Caucasians and Asians and their association with major mood disorders. Signal Transduction and Targeted Therapy. 4: 39. PMID 31637017 DOI: 10.1038/s41392-019-0066-5 |
0.33 |
|
2019 |
Luo N, Tian L, Calhoun VD, Chen J, Lin D, Vergara VM, Rao S, Yang J, Zhuo C, Xu Y, Turner JA, Zhang F, Sui J. Brain function, structure and genomic data are linked but show different sensitivity to duration of illness and disease stage in schizophrenia. Neuroimage. Clinical. 23: 101887. PMID 31176952 DOI: 10.1016/J.Nicl.2019.101887 |
0.411 |
|
2019 |
Yao Y, Yang J, Xie Y, Liao H, Yang B, Xu Q, Rao S. No Evidence for Widespread Positive Selection Signatures in Common Risk Alleles Associated with Schizophrenia. Schizophrenia Bulletin. PMID 31150552 DOI: 10.1093/Schbul/Sbz048 |
0.417 |
|
2018 |
Rao S, Luo N, Sui J, Xu Q, Zhang F. Effect of the SIRT1 gene on regional cortical grey matter density in the Han Chinese population. The British Journal of Psychiatry : the Journal of Mental Science. 1-5. PMID 30567608 DOI: 10.1192/Bjp.2018.270 |
0.441 |
|
2018 |
Luo N, Tian L, Calhoun VD, Chen J, Lin D, Vergara VM, Rao S, Zhang F, Sui J. Exploring different impaired speed of genetic-related brain function and structures in schizophrenic progress using multimodal analysis. Conference Proceedings : ... Annual International Conference of the Ieee Engineering in Medicine and Biology Society. Ieee Engineering in Medicine and Biology Society. Annual Conference. 2018: 4126-4129. PMID 30441263 DOI: 10.1109/EMBC.2018.8513313 |
0.336 |
|
2018 |
Rao S, Ghani M, Guo Z, Deming Y, Wang K, Sims R, Mao C, Yao Y, Cruchaga C, Stephan DA, Rogaeva E. An APOE-independent cis-eSNP on chromosome 19q13.32 influences tau levels and late-onset Alzheimer's disease risk. Neurobiology of Aging. PMID 29395286 DOI: 10.1016/J.Neurobiolaging.2017.12.027 |
0.418 |
|
2017 |
Liu Y, Rao S, Xu Y, Zhang F, Wang Z, Zhao X. Changes in the level of Long Non-Coding RNA Gomafu gene expression in schizophrenia patients before and after antipsychotic medication. Schizophrenia Research. PMID 28911914 DOI: 10.1016/J.Schres.2017.08.025 |
0.34 |
|
2017 |
Xu Y, Wang J, Rao S, Ritter M, Manor LC, Backer R, Cao H, Cheng Z, Liu S, Liu Y, Tian L, Dong K, Yao Shugart Y, Wang G, Zhang F. An Integrative Computational Approach to Evaluate Genetic Markers for Bipolar Disorder. Scientific Reports. 7: 6745. PMID 28751646 DOI: 10.1038/S41598-017-05846-4 |
0.365 |
|
2017 |
Rao S, Yao Y, Ryan J, Jin C, Xu Y, Huang X, Guo J, Wen Y, Mao C, Meyre D, Zhang F. Genetic association of rs1344706 in ZNF804A with bipolar disorder and schizophrenia susceptibility in Chinese populations. Scientific Reports. 7: 41140. PMID 28120939 DOI: 10.1038/Srep41140 |
0.513 |
|
2016 |
Ye N, Rao S, Du T, Hu H, Liu Z, Shen Y, Xu Q. Intergenic variants may predispose to major depression disorder through regulation of long non-coding RNA expression. Gene. PMID 27940106 DOI: 10.1016/J.Gene.2016.11.041 |
0.476 |
|
2016 |
Rao S, Martínez-Cengotitabengoa M, Yao Y, Guo Z, Xu Q, Li S, Zhou X, Zhang F. Peripheral blood nerve growth factor levels in major psychiatric disorders. Journal of Psychiatric Research. 86: 39-45. PMID 27898323 DOI: 10.1016/J.Jpsychires.2016.11.012 |
0.389 |
|
2016 |
Rao S, Yao Y, Ryan J, Li T, Wang D, Zheng C, Xu Y, Xu Q. Common variants in FKBP5 gene and major depressive disorder (MDD) susceptibility: a comprehensive meta-analysis. Scientific Reports. 6: 32687. PMID 27601205 DOI: 10.1038/Srep32687 |
0.493 |
|
2016 |
Ren Z, Qiu A, Zhang A, Huang L, Rao S. A cis-eQTL in AHI1 confers risk to schizophrenia in European populations. Neuroscience Letters. PMID 27585752 DOI: 10.1016/j.neulet.2016.08.050 |
0.427 |
|
2016 |
Wang D, Xie T, Xu J, Wang H, Zeng W, Rao S, Zhou K, Pei F, Zhou Z. Genetic association between NFKB1 -94 ins/del ATTG Promoter Polymorphism and cancer risk: a meta-analysis of 42 case-control studies. Scientific Reports. 6: 30220. PMID 27443693 DOI: 10.1038/Srep30220 |
0.394 |
|
2016 |
Rao S, Yao Y, Zheng C, Ryan J, Mao C, Zhang F, Meyre D, Xu Q. Common variants in CACNA1C and MDD susceptibility: A comprehensive meta-analysis. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 27260792 DOI: 10.1002/Ajmg.B.32466 |
0.508 |
|
2016 |
Rao S, Kota LN, Li Z, Yao Y, Tang J, Mao C, Jain S, Xu Y, Xu Q. Accelerated leukocyte telomere erosion in schizophrenia: Evidence from the present study and a meta-analysis. Journal of Psychiatric Research. 79: 50-56. PMID 27174400 DOI: 10.1016/J.Jpsychires.2016.04.010 |
0.404 |
|
2016 |
Rao S, Ye N, Hu H, Shen Y, Xu Q. Variants in TERT influencing telomere length are associated with paranoid schizophrenia risk. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 26799699 DOI: 10.1002/Ajmg.B.32403 |
0.502 |
|
2016 |
Rao S, Kota LN, Li Z, Yao Y, Tang J, Mao C, Jain S, Xu Y, Xu Q. Accelerated leukocyte telomere erosion in schizophrenia: Evidence from the present study and a meta-analysis Journal of Psychiatric Research. 79: 50-56. DOI: 10.1016/j.jpsychires.2016.04.010 |
0.33 |
|
2016 |
Yao Y, Wen Y, Du T, Sun N, Deng H, Ryan J, Rao S. Meta-analysis indicates that SNP rs9939609 within FTO is not associated with major depressive disorder (MDD) in Asian population Journal of Affective Disorders. 193: 27-30. DOI: 10.1016/j.jad.2015.12.048 |
0.378 |
|
2015 |
Yao Y, Wen Y, Du T, Sun N, Deng H, Ryan J, Rao S. Meta-analysis indicates that SNP rs9939609 within FTO is not associated with major depressive disorder (MDD) in Asian population. Journal of Affective Disorders. 193: 27-30. PMID 26766031 DOI: 10.1016/J.Jad.2015.12.048 |
0.48 |
|
2015 |
Du T, Rao S, Wu L, Ye N, Liu Z, Hu H, Xiu J, Shen Y, Xu Q. An association study of the m6A genes with major depressive disorder in Chinese Han population. Journal of Affective Disorders. 183: 279-86. PMID 26047305 DOI: 10.1016/J.Jad.2015.05.025 |
0.398 |
|
2015 |
Rao SQ, Hu HL, Ye N, Shen Y, Xu Q. Genetic variants in long non-coding RNA MIAT contribute to risk of paranoid schizophrenia in a Chinese Han population. Schizophrenia Research. 166: 125-30. PMID 26004688 DOI: 10.1016/J.Schres.2015.04.032 |
0.485 |
|
2015 |
Rao S, Lang J, Zhu L, Chen J. Exome sequencing identifies a novel gene, WNK1, for susceptibility to pelvic organ prolapse (POP). Plos One. 10: e0119482. PMID 25739019 DOI: 10.1371/Journal.Pone.0119482 |
0.336 |
|
Show low-probability matches. |