| scholarly article | Q13442814 |
| P2093 | author name string | Gang Chen | |
| Jun Zhu | |||
| Wen-da Xue | |||
| P2860 | cites work | Use of genome-wide expression data to mine the "Gray Zone" of GWA studies leads to novel candidate obesity genes | Q21144978 |
| Finding the missing heritability of complex diseases | Q22122198 | ||
| Personalized medicine and human genetic diversity | Q26824838 | ||
| Progress in pharmacogenetics: consortiums and new strategies | Q28071652 | ||
| Complement factor H variant increases the risk of age-related macular degeneration | Q28239239 | ||
| The mystery of missing heritability: Genetic interactions create phantom heritability | Q28732355 | ||
| A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications | Q28943311 | ||
| Rare and low-frequency coding variants alter human adult height | Q29583867 | ||
| An Expanded View of Complex Traits: From Polygenic to Omnigenic | Q30322686 | ||
| Phenome-wide heritability analysis of the UK Biobank | Q33590424 | ||
| Genome-wide association studies of drug response and toxicity: an opportunity for genome medicine | Q33725390 | ||
| A genome-wide association study of alcohol dependence | Q33740277 | ||
| An Exploration of Gene-Gene Interactions and Their Effects on Hypertension | Q33795037 | ||
| Efficacy of prospective pharmacogenetic testing in the treatment of major depressive disorder: results of a randomized, double-blind clinical trial | Q33909349 | ||
| A novel, functional and replicable risk gene region for alcohol dependence identified by genome-wide association study | Q34077684 | ||
| Genome-wide association study of alcohol dependence:significant findings in African- and European-Americans including novel risk loci | Q34193319 | ||
| A whole-genome association study of major determinants for allopurinol-related Stevens-Johnson syndrome and toxic epidermal necrolysis in Japanese patients | Q34215820 | ||
| Replication of genome wide association studies of alcohol dependence: support for association with variation in ADH1C. | Q34630031 | ||
| Genetic architecture of circulating lipid levels | Q35108611 | ||
| Associations of genetic risk score with obesity and related traits and the modifying effect of physical activity in a Chinese Han population | Q35120190 | ||
| Pharmacogenetics of clozapine treatment response and side-effects in schizophrenia: an update | Q35771833 | ||
| Efficacy-oriented compatibility for component-based Chinese medicine | Q36123992 | ||
| Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium | Q36131514 | ||
| The genetics of alcohol dependence: advancing towards systems-based approaches | Q36314812 | ||
| PTPRD gene associated with blood pressure response to atenolol and resistant hypertension | Q36677516 | ||
| Development and clinical application of an integrative genomic approach to personalized cancer therapy | Q36954557 | ||
| Mixed Linear Model Approaches of Association Mapping for Complex Traits Based on Omics Variants | Q37502143 | ||
| Comparing GWAS Results of Complex Traits Using Full Genetic Model and Additive Models for Revealing Genetic Architecture | Q37581455 | ||
| A genome-wide gene-gene interaction analysis identifies an epistatic gene pair for lung cancer susceptibility in Han Chinese. | Q37616076 | ||
| Genomic Prediction of Genotypic Effects with Epistasis and Environment Interactions for Yield-Related Traits of Rapeseed (Brassica napus L.). | Q37653726 | ||
| Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci | Q37658904 | ||
| Functional genomics- and network-driven systems biology approaches for pharmacogenomics and toxicogenomics | Q38010493 | ||
| Genome-wide association study success in ophthalmology | Q38228460 | ||
| The promise of psychiatric pharmacogenomics | Q38284614 | ||
| The usefulness of genotyping cytochrome P450 enzymes in the treatment of depression | Q38305701 | ||
| Genetic and environmental contributions to alcohol abuse and dependence in a population-based sample of male twins | Q38469701 | ||
| Human genomics projects and precision medicine | Q38626087 | ||
| A comparison of methods for inferring causal relationships between genotype and phenotype using additional biological measurements. | Q38687014 | ||
| Regulatory element-based prediction identifies new susceptibility regulatory variants for osteoporosis. | Q38699581 | ||
| Novel translational approaches to the search for precision therapies for acute respiratory distress syndrome | Q38700713 | ||
| Genome-wide analysis of clopidogrel active metabolite levels identifies novel variants that influence antiplatelet response | Q38756642 | ||
| Multi-target therapeutics for neuropsychiatric and neurodegenerative disorders | Q38923198 | ||
| Precision medicine, genomics and drug discovery | Q38931024 | ||
| Association of Liver Injury From Specific Drugs, or Groups of Drugs, With Polymorphisms in HLA and Other Genes in a Genome-Wide Association Study | Q39043874 | ||
| From Peas to Disease: Modifier Genes, Network Resilience, and the Genetics of Health | Q39310748 | ||
| Genetics of Schizophrenia: Overview of Methods, Findings and Limitations | Q39424410 | ||
| Missing heritability: is the gap closing? An analysis of 32 complex traits in the Lifelines Cohort Study | Q40246378 | ||
| An association study revealed substantial effects of dominance, epistasis and substance dependence co-morbidity on alcohol dependence symptom count. | Q40766616 | ||
| A population-based twin study of alcoholism in women | Q41097114 | ||
| Adiposity amplifies the genetic risk of fatty liver disease conferred by multiple loci | Q42347122 | ||
| Fangjiomics: revealing adaptive omics pharmacological mechanisms of the myriad combination therapies to achieve personalized medicine | Q43232760 | ||
| Genome-wide epistasis and pleiotropy characterized by the bipartite human phenotype network | Q43892181 | ||
| Surveillance of certain health behaviors and conditions among states and selected local areas--Behavioral Risk Factor Surveillance System (BRFSS), United States, 2006. | Q44005429 | ||
| Missing heritability in genome-wide association study research | Q57152019 | ||
| Alcohol metabolism and cardiovascular response in an alcoholic patient homozygous for the ALDH2*2 variant gene allele | Q73343857 | ||
| Psoriasis genome-wide association study identifies susceptibility variants within LCE gene cluster at 1q21 | Q83237938 | ||
| P4510 | describes a project that uses | genome-wide association study | Q1098876 |
| P433 | issue | 6 | |
| P921 | main subject | traditional Chinese medicine | Q200253 |
| genome-wide association study | Q1098876 | ||
| P304 | page(s) | 906-911 | |
| P577 | publication date | 2018-02-08 | |
| P1433 | published in | Acta Pharmacologica Sinica | Q15749885 |
| P1476 | title | Full genetic analysis for genome-wide association study of Fangji: a powerful approach for effectively dissecting the molecular architecture of personalized traditional Chinese medicine | |
| P478 | volume | 39 |
| Q61450525 | Identification of differentially expressed non-coding RNAs and mRNAs involved in Qi stagnation and blood stasis syndrome |
| Q64975131 | New omic and network paradigms for deep understanding of therapeutic mechanisms for Fangji of traditional Chinese medicine. |
| Q91905688 | Pharmacokinetics of Active Ingredients of Salvia miltiorrhiza and Carthamus tinctorius in Compatibility in Normal and Cerebral Ischemia Rats: A Comparative Study |
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