| scholarly article | Q13442814 |
| P2093 | author name string | Hao Liu | |
| Dong Hu | |||
| Lei Xiao | |||
| Lin He | |||
| Shiyang Li | |||
| Dao Wen Wang | |||
| Xinxin Zhang | |||
| Yang Sun | |||
| Yanghui Chen | |||
| P2860 | cites work | Genetic studies of body mass index yield new insights for obesity biology | Q22305005 |
| TM6SF2 is a regulator of liver fat metabolism influencing triglyceride secretion and hepatic lipid droplet content | Q24299190 | ||
| Biological, clinical and population relevance of 95 loci for blood lipids | Q24622541 | ||
| Six new loci associated with body mass index highlight a neuronal influence on body weight regulation | Q24646434 | ||
| A global reference for human genetic variation | Q25909434 | ||
| Growth Hormone-Releasing Hormone in Diabetes | Q28070104 | ||
| Molecular cloning of human cytosolic purine 5'-nucleotidase | Q28115764 | ||
| A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease | Q28267020 | ||
| Psychiatric genetics: progress amid controversy | Q28284253 | ||
| Characterizing the genetic basis of transcriptome diversity through RNA-sequencing of 922 individuals | Q28299787 | ||
| Increased cardiovascular mortality in people with schizophrenia: a 24-year national register study | Q38744157 | ||
| An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans | Q38752732 | ||
| The SETD8/PR-Set7 Methyltransferase Functions as a Barrier to Prevent Senescence-Associated Metabolic Remodeling | Q38935483 | ||
| The Genetic Architecture of Gene Expression in Peripheral Blood | Q39033496 | ||
| The genetic overlap between mood disorders and cardiometabolic diseases: a systematic review of genome wide and candidate gene studies | Q39100917 | ||
| Dynamic methylation of Numb by Set8 regulates its binding to p53 and apoptosis | Q39147711 | ||
| The proprotein convertase furin in tumour progression | Q39215671 | ||
| Proprotein convertase furin/PCSK3 and atherosclerosis: New insights and potential therapeutic targets | Q39235557 | ||
| Large-Scale Identification of Common Trait and Disease Variants Affecting Gene Expression | Q40196315 | ||
| Rare Loss-of-Function Variants in NPC1 Predispose to Human Obesity | Q40361341 | ||
| The Chromatin Remodeling Complex Chd4/NuRD Controls Striated Muscle Identity and Metabolic Homeostasis | Q40760059 | ||
| SREBP1 Contributes to Resolution of Pro-inflammatory TLR4 Signaling by Reprogramming Fatty Acid Metabolism | Q41501239 | ||
| Role for sterol regulatory element binding protein-1c activation in mediating skeletal muscle insulin resistance via repression of rat insulin receptor substrate-1 transcription | Q42247586 | ||
| Growth hormone improves body composition, fasting blood glucose, glucose tolerance and liver triacylglycerol in a mouse model of diet-induced obesity and type 2 diabetes. | Q45996949 | ||
| Genetic effects on gene expression across human tissues | Q46285732 | ||
| Functional mapping and annotation of genetic associations with FUMA. | Q47101248 | ||
| Furin promotes dendritic morphogenesis and learning and memory in transgenic mice. | Q47230764 | ||
| Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia | Q47602743 | ||
| Growth Hormone Control of Hepatic Lipid Metabolism | Q49329608 | ||
| Mapping the genetic architecture of gene expression in human liver | Q28472693 | ||
| Mechanism of TrkB-mediated hippocampal long-term potentiation | Q28592383 | ||
| Systematic identification of trans eQTLs as putative drivers of known disease associations | Q28659854 | ||
| Circos: an information aesthetic for comparative genomics | Q29547653 | ||
| A general framework for estimating the relative pathogenicity of human genetic variants | Q29615730 | ||
| Schizophrenia. | Q30251961 | ||
| CRL4(Cdt2) regulates cell proliferation and histone gene expression by targeting PR-Set7/Set8 for degradation | Q30430339 | ||
| Linkage disequilibrium in humans: models and data | Q30654298 | ||
| MAGMA: generalized gene-set analysis of GWAS data | Q30935493 | ||
| Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets | Q31063920 | ||
| Heritability and genomics of gene expression in peripheral blood | Q33575322 | ||
| Prevalence, incidence and mortality from cardiovascular disease in patients with pooled and specific severe mental illness: a large-scale meta-analysis of 3,211,768 patients and 113,383,368 controls | Q33670588 | ||
| Mutations in C12orf65 in patients with encephalomyopathy and a mitochondrial translation defect | Q33960447 | ||
| Evidence for disturbed insulin and growth hormone signaling as potential risk factors in the development of schizophrenia | Q34113374 | ||
| Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk | Q34213805 | ||
| Improved detection of common variants associated with schizophrenia by leveraging pleiotropy with cardiovascular-disease risk factors | Q34325802 | ||
| Sherlock: detecting gene-disease associations by matching patterns of expression QTL and GWAS | Q34342875 | ||
| Human genomics. The Genotype-Tissue Expression (GTEx) pilot analysis: multitissue gene regulation in humans | Q34475541 | ||
| Inactivation of Tm6sf2, a Gene Defective in Fatty Liver Disease, Impairs Lipidation but Not Secretion of Very Low Density Lipoproteins | Q34519771 | ||
| Physical illness in patients with severe mental disorders. I. Prevalence, impact of medications and disparities in health care. | Q34623350 | ||
| IUGR disrupts the PPARγ-Setd8-H4K20me(1) and Wnt signaling pathways in the juvenile rat hippocampus | Q34715551 | ||
| Delineation of C12orf65-related phenotypes: a genotype-phenotype relationship | Q35150496 | ||
| Biological interpretation of genome-wide association studies using predicted gene functions | Q35571093 | ||
| clusterProfiler: an R package for comparing biological themes among gene clusters. | Q35920061 | ||
| Hyperglycemia and a common variant of GCKR are associated with the levels of eight amino acids in 9,369 Finnish men | Q36047495 | ||
| BDNF-TrkB signaling and neuroprotection in schizophrenia | Q36589545 | ||
| Comprehensive analysis of schizophrenia-associated loci highlights ion channel pathways and biologically plausible candidate causal genes | Q36608885 | ||
| Trk B signaling in dopamine 1 receptor neurons regulates food intake and body weight | Q37093348 | ||
| Changes in insulin sensitivity and insulin release in relation to glycemia and glucose tolerance in 6,414 Finnish men | Q37163530 | ||
| KLF15 Enables Rapid Switching between Lipogenesis and Gluconeogenesis during Fasting. | Q37273150 | ||
| Gene expression elucidates functional impact of polygenic risk for schizophrenia | Q37372402 | ||
| A Functional Switch of NuRD Chromatin Remodeling Complex Subunits Regulates Mouse Cortical Development | Q37492060 | ||
| Considering a frame of reference for physical activity research related to the cardiometabolic risk profile in schizophrenia | Q37734656 | ||
| Brain-derived neurotrophic factor, food intake regulation, and obesity | Q37938323 | ||
| Structure and function insights into the NuRD chromatin remodeling complex | Q38386331 | ||
| Cardiovascular risk factors in 2011 and secular trends since 2007: the Cardiovascular Risk in Young Finns Study. | Q51318473 | ||
| Efficient pathway enrichment and network analysis of GWAS summary data using GSA-SNP2. | Q51556580 | ||
| Integrative analysis of omics summary data reveals putative mechanisms underlying complex traits. | Q51766041 | ||
| Histone methyltransferase KMT5A gene modulates oncogenesis and lipid metabolism of papillary thyroid cancer in vitro. | Q52728279 | ||
| Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood. | Q55341962 | ||
| A survey of genetic human cortical gene expression | Q57272923 | ||
| Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps | Q57295524 | ||
| Cohort Profile: The Cardiovascular Risk in Young Finns Study | Q57417503 | ||
| Mutations in the mitochondrial gene C12ORF65 lead to syndromic autosomal recessive intellectual disability and show genotype phenotype correlation | Q59698183 | ||
| Evidence for genetic contribution to the increased risk of type 2 diabetes in schizophrenia | Q59812789 | ||
| Exploring shared genetic bases and causal relationships of schizophrenia and bipolar disorder with 28 cardiovascular and metabolic traits | Q60460182 | ||
| Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids | Q64112276 | ||
| Influence of a Coronary Artery Disease-Associated Genetic Variant on FURIN Expression and Effect of Furin on Macrophage Behavior. | Q64972726 | ||
| SET8 is involved in the regulation of hyperglycemic memory in human umbilical endothelial cells | Q88677806 | ||
| Temporal Proteomic Analysis of Pancreatic β-Cells in Response to Lipotoxicity and Glucolipotoxicity | Q90785773 | ||
| Co-shared genetics and possible risk gene pathway partially explain the comorbidity of schizophrenia, major depressive disorder, type 2 diabetes, and metabolic syndrome | Q91392789 | ||
| Genetic deletion of soluble 5'-nucleotidase II reduces body weight gain and insulin resistance induced by a high-fat diet | Q91901757 | ||
| A statistical framework for cross-tissue transcriptome-wide association analysis | Q91908163 | ||
| The Psychiatric Risk Gene NT5C2 Regulates Adenosine Monophosphate-Activated Protein Kinase Signaling and Protein Translation in Human Neural Progenitor Cells | Q92087685 | ||
| Probabilistic fine-mapping of transcriptome-wide association studies | Q92709272 | ||
| Deficiency of sterol regulatory element-binding protein-1c induces schizophrenia-like behavior in mice | Q93087901 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P921 | main subject | schizophrenia | Q41112 |
| pleiotropy | Q1134884 | ||
| comorbidity | Q1414874 | ||
| P304 | page(s) | 256 | |
| P577 | publication date | 2020-04-17 | |
| P1433 | published in | Frontiers in Psychiatry | Q27723495 |
| P1476 | title | Integrated Analysis of Summary Statistics to Identify Pleiotropic Genes and Pathways for the Comorbidity of Schizophrenia and Cardiometabolic Disease | |
| P478 | volume | 11 |
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