S. Yao

发表

Phenome-wide investigation of the causal associations between childhood BMI and adult outcomes: A two-sample Mendelian randomization study

Tie-Lin Yang, Yan Guo, Shan-Shan Dong, 2020, bioRxiv.

Modeling circRNAs expression pattern with integrated sequence and epigenetic features identifies H3K79me2 as regulators for circRNAs expression

Hlaing Nwe Thynn, Tie-Lin Yang, Yan Guo, 2018, bioRxiv.

Enhancer-Gene Interaction Analyses Identified the Epidermal Growth Factor Receptor as a Susceptibility Gene for Type 2 Diabetes Mellitus

Yan Guo, Jing-Miao Ding, S. Yao, 2020, Diabetes & metabolism journal.

Associations of Serum Uromodulin and Its Genetic Variants With Blood Pressure and Hypertension in Chinese Adults

Hao Li, J Zhang, J. Mu, 2021, Frontiers in Cardiovascular Medicine.

3D chromatin organization changes modulate adipogenesis and osteogenesis

Tie-Lin Yang, Yan Guo, Shan-Shan Dong, 2020, bioRxiv.

Sex‐specific SNP‐SNP interaction analyses within topologically associated domains reveals ANGPT1 as a novel tumor suppressor gene for lung cancer

Yan Guo, Shan-Shan Dong, Jing-Miao Ding, 2020, Genes, chromosomes & cancer.

Associations of plasma PAPP-A2 and genetic variations with salt sensitivity, blood pressure changes and hypertension incidence in Chinese adults

J Zhang, J. Mu, Tie-Lin Yang, 2021, Journal of hypertension.

Epigenetic Element-Based Transcriptome-Wide Association Study Identifies Novel Genes for Bipolar Disorder

Tie-Lin Yang, Yan Guo, Shan-Shan Dong, 2020, medRxiv.

Associations of corin genetic polymorphisms with salt sensitivity, blood pressure changes, and hypertension incidence in Chinese adults

Hao Li, J. Mu, Tie-Lin Yang, 2021, Journal of clinical hypertension.

Individualized pathway activity algorithm identifies oncogenic pathways in pan-cancer analysis

Tie-Lin Yang, Huafeng Kang, Shan-Shan Dong, 2022, EBioMedicine.

Transcription Factor Enrichment Analysis in Enhancers Identifies EZH2 as A Susceptibility Gene for Osteoporosis.

M. Li, Tie-Lin Yang, Yan Guo, 2019, The Journal of clinical endocrinology and metabolism.

Association of Vitamin D Binding Protein Variants with Susceptibility to Chronic Obstructive Pulmonary Disease

S. Yao, Bo Yu, F-Z Lu, 2010, The Journal of international medical research.

Bidirectional two-sample Mendelian randomization analysis identifies causal associations between relative carbohydrate intake and depression

Tie-Lin Yang, Yan Guo, Shan-Shan Dong, 2022, Nature Human Behaviour.

Lineage-specific rearrangement of chromatin loops and epigenomic features during adipocytes and osteoblasts commitment.

Hao Chen, Tie-Lin Yang, Yan Guo, 2022, Cell death and differentiation.

Mendelian randomization analyses support causal relationships between brain imaging-derived phenotypes and risk of psychiatric disorders

K. Yu, Tie-Lin Yang, Yan Guo, 2022, Nature Neuroscience.

Multi-Tissue Integrative Analysis Identifies Susceptibility Genes for Atopic Dermatitis.

Shan-Shan Dong, S. Yao, Hao Wu, 2022, The Journal of investigative dermatology.

Associations of plasma uromodulin and genetic variants with blood pressure responses to dietary salt interventions

Hao Li, J. Mu, Tie-Lin Yang, 2021, Journal of clinical hypertension.

Phenome-wide investigation of the causal associations between childhood BMI and adult trait outcomes: a two-sample Mendelian randomization study

Tie-Lin Yang, Yan Guo, Shan-Shan Dong, 2021, Genome Medicine.

A transcriptome-wide association study identifies susceptibility genes for Parkinson’s disease

Yan Guo, Weiping Kuang, S. Yao, 2021, npj Parkinson's Disease.

Detecting epistasis within chromatin regulatory circuitry reveals CAND2 as a novel susceptibility gene for obesity

Hui Shen, H. Deng, Q. Tian, 2019, International Journal of Obesity.

A transcriptome-wide association study identifies novel susceptibility genes for psoriasis.

Tie-Lin Yang, Yan Guo, Shan-Shan Dong, 2021, Human molecular genetics.

Transcriptome-wide association study identifies multiple genes associated with childhood body mass index

Yan Guo, Shan-Shan Dong, Jing-Miao Ding, 2021, International Journal of Obesity.

Comprehensive functional annotation of susceptibility SNPs prioritized 10 genes for schizophrenia

Ping Yang, Tie-Lin Yang, Yan Guo, 2019, Translational Psychiatry.

An Osteoporosis Risk SNP at 1p36.12 Acts as an Allele-Specific Enhancer to Modulate LINC00339 Expression via Long-Range Loop Formation.

Yan Guo, Tie-Lin Yang, Jia-Bin Chen, 2018, American journal of human genetics.

Brain image-derived phenotypes yield insights into causal risk of psychiatric disorders using a Mendelian randomization study

K. Yu, Tie-Lin Yang, Yan Guo, 2021, bioRxiv.

Comprehensive review and annotation of susceptibility SNPs associated with obesity‐related traits

Tie-Lin Yang, Yan Guo, Shan-Shan Dong, 2018, Obesity reviews : an official journal of the International Association for the Study of Obesity.

Causally Associations of Blood Lipids Levels with COVID-19 Risk: Mendelian Randomization Study

Tie-Lin Yang, Yan Guo, Shan-Shan Dong, 2020, medRxiv.

Causal Associations Between Blood Lipids and COVID-19 Risk: A Two-Sample Mendelian Randomization Study

Tie-Lin Yang, Yan Guo, Shan-Shan Dong, 2021, Arteriosclerosis, thrombosis, and vascular biology.

Runs of homozygosity associate with decreased risks of lung cancer in never-smoking East Asian females

Hlaing Nwe Thynn, Tie-Lin Yang, Yan Guo, 2018, Journal of Cancer.

Modeling circRNA expression pattern with integrated sequence and epigenetic features demonstrates the potential involvement of H3K79me2 in circRNA expression

Shan-Shan Dong, Yan Guo, Tie-Lin Yang, 2020, Bioinform..

Gene expression profiles indicate tissue-specific obesity regulation changes and strong obesity relevant tissues

Tie-Lin Yang, Shan-Shan Dong, S. Yao, 2018, International Journal of Obesity.

A transcriptome-wide association study identifies susceptibility genes for Parkinson’s disease

Yan Guo, Weiping Kuang, S. Yao, 2021, npj Parkinson's Disease.

Regulatory element-based prediction identifies new susceptibility regulatory variants for osteoporosis

H. Deng, Q. Tian, Tie-Lin Yang, 2017, Human Genetics.

Mendelian Randomization analyses identify causal associations of human gut microbiome composition on intelligence

Shan-Shan Dong, S. Yao, Li Qian, 2023, medRxiv.

Associations of SGLT2 genetic polymorphisms with salt sensitivity, blood pressure changes and hypertension incidence in Chinese adults

J. Mu, Hao Li, Xi Zhang, 2023, Hypertension Research.

Associations of genetic variations in NEDD4L with salt sensitivity, blood pressure changes and hypertension incidence in Chinese adults

J Zhang, J. Mu, Hao Li, 2022, Journal of clinical hypertension.

Multi‐tissue transcriptome‐wide association study reveals susceptibility genes and drug targets for insulin resistance‐relevant phenotypes

Tie-Lin Yang, Yan Guo, S. Yao, 2023, Diabetes, obesity & metabolism.

Integrating regulatory features data for prediction of functional disease-associated SNPs

Yan Guo, Shi Yao, Yu-Jie Zhang, 2019, Briefings Bioinform..

Detecting epistasis within chromatin regulatory circuitry reveals CAND2 as a novel susceptibility gene for obesity

Hui Shen, H. Deng, Q. Tian, 2019, International Journal of Obesity.

Unveiling Promising Neuroimaging Biomarkers for Schizophrenia Through Clinical and Genetic Perspectives.

Tie-Lin Yang, S. Yao, Jing Guo, 2024, Neuroscience bulletin.

The Causal Relationships Between Gut Microbiota, Brain Volume, and Intelligence: A Two-Step Mendelian Randomization Analysis

Tie-Lin Yang, S. Yao, Hao Wu, 2024, Biological Psychiatry.

Two-sample Mendelian randomization analysis reveals causal relationships between blood lipids and venous thromboembolism

Tie-Lin Yang, Kun Zhang, S. Yao, 2024, Haematologica.

A genome-wide cross-trait analysis identifies causal relationship and shared loci of food preference with obesity

Tie-Lin Yang, S. Yao, Hao Wu, 2024, medRxiv.