| scholarly article | Q13442814 |
| P50 | author | David B. Goldstein | Q15989762 |
| Erin L Heinzen | Q88428035 | ||
| Kevin V Shianna | Q114366502 | ||
| Dongliang Ge | Q115248929 | ||
| Jessica M Maia | Q115248947 | ||
| Thomas Denny | Q42939171 | ||
| P2093 | author name string | Christine M Hulette | |
| Kathleen A Welsh-Bohmer | |||
| Kenneth D Cronin | |||
| Willow N Gabriel | |||
| P2860 | cites work | A survey of genetic human cortical gene expression | Q57272923 |
| Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4 | Q28469186 | ||
| Mapping the genetic architecture of gene expression in human liver | Q28472693 | ||
| A genome-wide association study of global gene expression | Q29614592 | ||
| Risk alleles for multiple sclerosis identified by a genomewide study | Q29614890 | ||
| A whole-genome association study of major determinants for host control of HIV-1 | Q29614891 | ||
| Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma | Q29614903 | ||
| Listening to silence and understanding nonsense: exonic mutations that affect splicing | Q29618493 | ||
| Identification of common genetic variation that modulates alternative splicing | Q33287883 | ||
| Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma | Q34005664 | ||
| Mapping determinants of human gene expression by regional and genome-wide association | Q34421244 | ||
| Messenger RNA regulation: to translate or to degrade | Q36456597 | ||
| Evaluation of genetic variation contributing to differences in gene expression between populations | Q36718956 | ||
| Human genetics: the hidden text of genome-wide associations | Q44872002 | ||
| Genome-wide analysis of transcript isoform variation in humans | Q46809730 | ||
| Genome-wide midrange transcription profiles reveal expression level relationships in human tissue specification | Q48522151 | ||
| Genome-wide associations of gene expression variation in humans | Q21145274 | ||
| Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci | Q24306903 | ||
| Replication of putative candidate-gene associations with rheumatoid arthritis in >4,000 samples from North America and Sweden: association of susceptibility with PTPN22, CTLA4, and PADI4 | Q24538382 | ||
| Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls | Q24550675 | ||
| Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans | Q24643492 | ||
| Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants | Q24646663 | ||
| A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21 | Q24649802 | ||
| Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes | Q24652324 | ||
| Large recurrent microdeletions associated with schizophrenia | Q24654741 | ||
| PLINK: a tool set for whole-genome association and population-based linkage analyses | Q24677407 | ||
| Principal components analysis corrects for stratification in genome-wide association studies | Q27860975 | ||
| A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes | Q28248848 | ||
| Association between microdeletion and microduplication at 16p11.2 and autism | Q28264205 | ||
| Newly identified loci that influence lipid concentrations and risk of coronary artery disease | Q28264535 | ||
| Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX | Q28265206 | ||
| Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia | Q28274064 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 12 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | complex trait | Q55608248 |
| P304 | page(s) | e1 | |
| P577 | publication date | 2008-12-01 | |
| P1433 | published in | PLOS Biology | Q1771695 |
| P1476 | title | Tissue-specific genetic control of splicing: implications for the study of complex traits | |
| P478 | volume | 6 |
| Q41587969 | A New Genomewide Association Meta-Analysis of Alcohol Dependence |
| Q34077684 | A Novel, Functional and Replicable Risk Gene Region for Alcohol Dependence Identified by Genome-Wide Association Study |
| Q34743365 | A common HLA-DPA1 variant is a major determinant of hepatitis B virus clearance in Han Chinese. |
| Q28943556 | A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids |
| Q24644827 | A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB |
| Q35150211 | A meta-analysis of gene expression quantitative trait loci in brain |
| Q60290274 | A neurobiological pathway to smoking in adolescence: TTC12-ANKK1-DRD2 variants and reward response. |
| Q40437541 | A rare sequence variant in intron 1 of THAP1 is associated with primary dystonia |
| Q35541843 | ADAMTS-18: a metalloproteinase with multiple functions |
| Q21563315 | Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain |
| Q37408201 | Allele-specific chromatin remodeling in the ZPBP2/GSDMB/ORMDL3 locus associated with the risk of asthma and autoimmune disease. |
| Q36090387 | Alternative splicing: a potential source of functional innovation in the eukaryotic genome |
| Q50209263 | An APOE-independent cis-eSNP on chromosome 19q13.32 influences tau levels and late-onset Alzheimer's disease risk |
| Q33739437 | An independent component analysis confounding factor correction framework for identifying broad impact expression quantitative trait loci |
| Q37966594 | An integrative functional genomics approach for discovering biomarkers in schizophrenia |
| Q38089094 | Analytical strategies for large imaging genetic datasets: experiences from the IMAGEN study |
| Q40696309 | Association, characterisation and meta-analysis of SNPs linked to general reading ability in a German dyslexia case-control cohort |
| Q34779923 | Brain expression quantitative trait locus mapping informs genetic studies of psychiatric diseases |
| Q53377097 | CHRNA7 Gene and Response to Cholinesterase Inhibitors in an Italian Cohort of Alzheimer's Disease Patients. |
| Q40816230 | Common Regulatory Variants of CYFIP1 Contribute to Susceptibility for Autism Spectrum Disorder (ASD) and Classical Autism |
| Q35062523 | Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease |
| Q24603204 | Common genetic variants on 5p14.1 associate with autism spectrum disorders |
| Q34100294 | Common genetic variation in Neuregulin 3 (NRG3) influences risk for schizophrenia and impacts NRG3 expression in human brain |
| Q29614882 | Common regulatory variation impacts gene expression in a cell type-dependent manner |
| Q33714033 | Complementary metal oxide semiconductor compatible fabrication and characterization of parylene-C covered nanofluidic channels with integrated nanoelectrodes. |
| Q36994687 | Comprehensive promoter level expression quantitative trait loci analysis of the human frontal lobe |
| Q34597848 | Context-dependent robustness to 5′ splice site polymorphisms in human populations |
| Q47253637 | Converging evidence that sequence variations in the novel candidate gene MAP2K7 (MKK7) are functionally associated with schizophrenia |
| Q33727315 | Coronary Artery Disease-Associated LIPA Coding Variant rs1051338 Reduces Lysosomal Acid Lipase Levels and Activity in Lysosomes. |
| Q24643052 | DISC1 splice variants are upregulated in schizophrenia and associated with risk polymorphisms |
| Q38801880 | Decreased SMG7 expression associates with lupus-risk variants and elevated antinuclear antibody production |
| Q39301532 | Deep intronic mutations and human disease |
| Q43917227 | Differential effects of a common splice site polymorphism on the generation of OAS1 variants in human bronchial epithelial cells. |
| Q52809303 | Dyslexia risk variant rs600753 is linked with dyslexia-specific differential allelic expression of DYX1C1. |
| Q33858783 | Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations |
| Q37486720 | Epilepsy pharmacogenetics |
| Q35795392 | Evaluation of microRNA expression profiles and their associations with risk alleles in lymphoblastoid cell lines of familial ovarian cancer |
| Q51500567 | Evidence of Sex-Modulated Association of ZNF804A with Schizophrenia |
| Q37012632 | Exome-Wide Association Study of Replicable Nonsynonymous Variants Conferring Risk for Alcohol Dependence |
| Q89057809 | Exon Array Biomarkers for the Differential Diagnosis of Schizophrenia and Bipolar Disorder |
| Q21131248 | Exploiting Gene Expression Variation to Capture Gene-Environment Interactions for Disease |
| Q39807149 | Exploiting aberrant mRNA expression in autism for gene discovery and diagnosis. |
| Q36170457 | Expression QTL analysis of top loci from GWAS meta-analysis highlights additional schizophrenia candidate genes |
| Q37397399 | Expression quantitative trait loci detected in cell lines are often present in primary tissues |
| Q38104720 | Expression quantitative trait loci: present and future |
| Q34007854 | Expression quantitative trait loci: replication, tissue- and sex-specificity in mice |
| Q35921937 | Fine mapping of the uterine leiomyoma locus on 1q43 close to a lncRNA in the RGS7-FH interval |
| Q83567368 | From expression QTLs to personalized transcriptomics |
| Q64249673 | Functional SNPs in the Human Autoimmunity-Associated Locus 17q12-21 |
| Q37357992 | Functional transcriptomics in the post-ENCODE era |
| Q84969110 | G/A polymorphism in intronic sequence affects the processing of MAO‐B gene in patients with Parkinson disease |
| Q30656680 | GLiMMPS: robust statistical model for regulatory variation of alternative splicing using RNA-seq data |
| Q24289119 | GWAS of 126,559 individuals identifies genetic variants associated with educational attainment |
| Q34325576 | Gene expression profiles in Parkinson disease prefrontal cortex implicate FOXO1 and genes under its transcriptional regulation |
| Q37259600 | Gene × smoking interactions on human brain gene expression: finding common mechanisms in adolescents and adults. |
| Q37634121 | Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci |
| Q35153945 | Genetic Neuropathology of Schizophrenia: New Approaches to an Old Question and New Uses for Postmortem Human Brains |
| Q37511422 | Genetic associations with expression for genes implicated in GWAS studies for atherosclerotic cardiovascular disease and blood phenotypes |
| Q35791545 | Genetic control of gene expression in whole blood and lymphoblastoid cell lines is largely independent |
| Q36065523 | Genetic determinants of uterine fibroid size in the multiethnic NIEHS uterine fibroid study |
| Q34781864 | Genetic evidence for a pathogenic role for the vitamin D3 metabolizing enzyme CYP24A1 in multiple sclerosis |
| Q34398489 | Genetic variability in the regulation of gene expression in ten regions of the human brain |
| Q42321746 | Genetic variant rs763361 regulates multiple sclerosis CD226 gene expression |
| Q28290491 | Genetic variants in GPR126 are associated with adolescent idiopathic scoliosis |
| Q33955584 | Genetic variation in cholinergic muscarinic-2 receptor gene modulates M2 receptor binding in vivo and accounts for reduced binding in bipolar disorder. |
| Q26858897 | Genetic variation of pre-mRNA alternative splicing in human populations |
| Q33644491 | Genetically dependent ERBB3 expression modulates antigen presenting cell function and type 1 diabetes risk |
| Q33821365 | Genetics of focal segmental glomerulosclerosis and human immunodeficiency virus-associated collapsing glomerulopathy: the role of MYH9 genetic variation |
| Q28650280 | Genetics of gene expression in CNS |
| Q28740314 | Genetics of sputum gene expression in chronic obstructive pulmonary disease |
| Q33654995 | Genevar: a database and Java application for the analysis and visualization of SNP-gene associations in eQTL studies |
| Q38801250 | Genome-Wide and Gene-Based Meta-Analyses Identify Novel Loci Influencing Blood Pressure Response to Hydrochlorothiazide. |
| Q34220999 | Genome-wide association and functional follow-up reveals new loci for kidney function |
| Q27003168 | Genome-wide association discoveries of alcohol dependence |
| Q34270507 | Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women |
| Q29248524 | Genome-wide association meta-analyses identified 1q43 and 2q32.2 for hip Ward's triangle areal bone mineral density |
| Q34270522 | Genome-wide association of pericardial fat identifies a unique locus for ectopic fat |
| Q33713286 | Genome-wide association reveals genetic effects on human Aβ 42 and τ protein levels in cerebrospinal fluids: a case control study |
| Q35065065 | Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium |
| Q34855734 | Genome-wide association studies of maximum number of drinks |
| Q29417149 | Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder |
| Q40341088 | Genome-wide association study of HLA-DQB1*06:02 negative essential hypersomnia |
| Q28943436 | Genome-wide association study of alcohol dependence implicates KIAA0040 on chromosome 1q |
| Q92024813 | Genome-wide human brain eQTLs: In-depth analysis and insights using the UKBEC dataset |
| Q33535874 | Genome-wide mRNA expression correlates of viral control in CD4+ T-cells from HIV-1-infected individuals |
| Q28943297 | Genome-wide search for replicable risk gene regions in alcohol and nicotine co-dependence |
| Q36724501 | Genome-wide significant association signals in IPO11-HTR1A region specific for alcohol and nicotine codependence |
| Q36586562 | Genomics of ADME gene expression: mapping expression quantitative trait loci relevant for absorption, distribution, metabolism and excretion of drugs in human liver |
| Q34299704 | Genotype-Based Test in Mapping Cis-Regulatory Variants from Allele-Specific Expression Data |
| Q33560717 | Geographical genomics of human leukocyte gene expression variation in southern Morocco |
| Q34758225 | Global Properties and Functional Complexity of Human Gene Regulatory Variation |
| Q33809390 | Global analysis of the impact of environmental perturbation on cis-regulation of gene expression |
| Q52664095 | HT-eQTL: integrative expression quantitative trait loci analysis in a large number of human tissues |
| Q33640185 | Heritability in the efficiency of nonsense-mediated mRNA decay in humans. |
| Q64108136 | Identification of DNA-Methylated CpG Islands Associated With Gene Silencing in the Adult Body Tissues of the Ogye Chicken Using RNA-Seq and Reduced Representation Bisulfite Sequencing |
| Q64102087 | Identification of a Functional Non-coding Variant in the GABA Receptor α2 Subunit of the C57BL/6J Mouse Reference Genome: Major Implications for Neuroscience Research |
| Q30571934 | Identification of a novel Parkinson's disease locus via stratified genome-wide association study |
| Q36106984 | Identification of allele-specific alternative mRNA processing via transcriptome sequencing |
| Q48225633 | Identification of common genetic variants controlling transcript isoform variation in human whole blood |
| Q36792668 | Identification of common variants associated with human hippocampal and intracranial volumes |
| Q36791694 | Impact of a cis-associated gene expression SNP on chromosome 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performance |
| Q36466430 | Impact of common regulatory single-nucleotide variants on gene expression profiles in whole blood |
| Q34765325 | Impact of natural genetic variation on gene expression dynamics. |
| Q30419441 | Imputation of exome sequence variants into population- based samples and blood-cell-trait-associated loci in African Americans: NHLBI GO Exome Sequencing Project. |
| Q34789256 | Incorporating alternative splicing and mRNA editing into the genetic analysis of complex traits. |
| Q41095173 | Increased brain expression of GPNMB is associated with genome wide significant risk for Parkinson's disease on chromosome 7p15.3. |
| Q37856453 | Insights from GWAS into the quantitative genetics of transcription in humans |
| Q35980870 | Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brain |
| Q36714212 | Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function |
| Q37961088 | Integrative Genomics Strategies to Elucidate the Complexity of Drug Response |
| Q38345502 | Integrative genome-wide association analysis of cytoarchitectural abnormalities in the prefrontal cortex of psychiatric disorders |
| Q30278644 | Integrative pathway genomics of lung function and airflow obstruction |
| Q35804056 | Interplay between DISC1 and GABA signaling regulates neurogenesis in mice and risk for schizophrenia |
| Q90947276 | Linear isoforms of the long noncoding RNA CDKN2B-AS1 regulate the c-myc-enhancer binding factor RBMS1 |
| Q84597467 | Linking Variants from Genome-Wide Association Analysis to Function via Transcriptional Network Analysis |
| Q36853815 | Loci influencing blood pressure identified using a cardiovascular gene-centric array |
| Q55415905 | Loci influencing blood pressure identified using a cardiovascular gene-centric array. |
| Q86858193 | Mapping Splicing Quantitative Trait Loci in RNA-Seq |
| Q34444821 | Mapping Splicing Quantitative Trait Loci in RNA-Seq. |
| Q37597805 | Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci |
| Q34248904 | Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways |
| Q29417150 | Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1. |
| Q48131559 | MixupMapper: correcting sample mix-ups in genome-wide datasets increases power to detect small genetic effects |
| Q39043771 | Molecular mechanisms underlying noncoding risk variations in psychiatric genetic studies |
| Q39231609 | Most brain disease-associated and eQTL haplotypes are not located within transcription factor DNase-seq footprints in brain |
| Q36773254 | NKAIN1–SERINC2 is a functional, replicable and genome-wide significant risk gene region specific for alcohol dependence in subjects of European descent |
| Q91370397 | NT5C2 germline variants alter thiopurine metabolism and are associated with acquired NT5C2 relapse mutations in childhood acute lymphoblastic leukaemia |
| Q28674016 | Network models of genome-wide association studies uncover the topological centrality of protein interactions in complex diseases |
| Q44755824 | Neuropsychological effects of the CSMD1 genome-wide associated schizophrenia risk variant rs10503253. |
| Q37451936 | Next-generation sequencing approaches in genetic rodent model systems to study functional effects of human genetic variation |
| Q35193842 | Novel insights into the regulatory architecture of CD4+ T cells in rheumatoid arthritis |
| Q64387819 | Oncogenic splicing factor SRSF3 regulates ILF3 alternative splicing to promote cancer cell proliferation and transformation |
| Q33789101 | Overlap of expression quantitative trait loci (eQTL) in human brain and blood |
| Q34289136 | Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche |
| Q34453666 | Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins |
| Q37417346 | Population genomics in a disease targeted primary cell model |
| Q33702079 | Post genome-wide association studies functional characterization of prostate cancer risk loci |
| Q42584559 | Postmortem brain tissue for drug discovery in psychiatric research |
| Q34535007 | Prostatic alpha-linolenic acid (ALA) is positively associated with aggressive prostate cancer: a relationship which may depend on genetic variation in ALA metabolism |
| Q36158905 | Quantitative assessment of common genetic variations in HLA-DP with hepatitis B virus infection, clearance and hepatocellular carcinoma development |
| Q36782437 | RNA sequencing of cancer reveals novel splicing alterations |
| Q35849067 | RNA sequencing of transcriptomes in human brain regions: protein-coding and non-coding RNAs, isoforms and alleles |
| Q24630966 | RNA sequencing reveals the role of splicing polymorphisms in regulating human gene expression |
| Q34872499 | Rare SERINC2 variants are specific for alcohol dependence in individuals of European descent |
| Q64048496 | Rare high-impact disease variants: properties and identifications |
| Q30395065 | Replicated Risk Nicotinic Cholinergic Receptor Genes for Nicotine Dependence |
| Q90568230 | Reproductive period and epigenetic modifications of the oxidative phosphorylation pathway in the human prefrontal cortex |
| Q36769422 | Resolving the polymorphism-in-probe problem is critical for correct interpretation of expression QTL studies |
| Q37059645 | Review: The role of LOXL1 in exfoliation syndrome/glaucoma |
| Q45961884 | Revisiting DARPP-32 in postmortem human brain: changes in schizophrenia and bipolar disorder and genetic associations with t-DARPP-32 expression |
| Q35061264 | Rheumatoid arthritis-associated polymorphisms are not protective against Alzheimer's disease |
| Q44396456 | Role of genetic variation in the cannabinoid type 1 receptor gene (CNR1) in the pathophysiology of human obesity |
| Q34421408 | SRp20 is a proto-oncogene critical for cell proliferation and tumor induction and maintenance |
| Q33965942 | Screening the human exome: a comparison of whole genome and whole transcriptome sequencing |
| Q36853488 | Significant association between rare IPO11-HTR1A variants and attention deficit hyperactivity disorder in Caucasians |
| Q29614572 | Spatio-temporal transcriptome of the human brain |
| Q84357911 | Spatiotemporal expression pattern of gonad-stimulating substance-like peptide of the sea cucumber, Apostichopus japonicus |
| Q35997597 | Statistical colocalization of monocyte gene expression and genetic risk variants for type 1 diabetes |
| Q29417103 | Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases |
| Q33917269 | Synthesis of 53 tissue and cell line expression QTL datasets reveals master eQTLs |
| Q36435510 | Temporal dynamics and genetic control of transcription in the human prefrontal cortex |
| Q35050752 | The Alzheimer's associated 5' region of the SORL1 gene cis regulates SORL1 transcripts expression |
| Q28073441 | The Future is The Past: Methylation QTLs in Schizophrenia |
| Q36410191 | The Genetics of Sudden Cardiac Death |
| Q28645981 | The National NeuroAIDS Tissue Consortium (NNTC) Database: an integrated database for HIV-related studies |
| Q37614934 | The genetic basis for individual differences in mRNA splicing and APOBEC1 editing activity in murine macrophages. |
| Q38174431 | The genetics of gene expression in complex mouse crosses as a tool to study the molecular underpinnings of behavior traits |
| Q35328703 | The genetics of splicing in neuroblastoma |
| Q38323555 | The molecular genetic architecture of attention deficit hyperactivity disorder. |
| Q24617186 | The neuronal transporter gene SLC6A15 confers risk to major depression |
| Q37359270 | The splice site variant rs11078928 may be associated with a genotype-dependent alteration in expression of GSDMB transcripts |
| Q34152797 | The study of eQTL variations by RNA-seq: from SNPs to phenotypes |
| Q33493408 | Tissue effect on genetic control of transcript isoform variation |
| Q35551534 | Tissue-specific effects of genetic and epigenetic variation on gene regulation and splicing |
| Q28651272 | Trans-ethnic meta-analysis of white blood cell phenotypes |
| Q35499189 | Transcriptome of the human retina, retinal pigmented epithelium and choroid. |
| Q39733187 | Transcriptome-Wide Analysis Reveals Modulation of Human Macrophage Inflammatory Phenotype Through Alternative Splicing |
| Q35774358 | Translational studies of lipoprotein-associated phospholipase A₂ in inflammation and atherosclerosis |
| Q27309750 | Tyro3 Modulates Mertk-Associated Retinal Degeneration |
| Q37755970 | Uncovering the roles of rare variants in common disease through whole-genome sequencing |
| Q27012811 | Use of Functional Genomics to Identify Candidate Genes Underlying Human Genetic Association Studies of Vascular Diseases |
| Q34469030 | Variants affecting exon skipping contribute to complex traits. |
| Q37217280 | Variants in interferon-alpha pathway genes and response to pegylated interferon-Alpha2a plus ribavirin for treatment of chronic hepatitis C virus infection in the hepatitis C antiviral long-term treatment against cirrhosis trial |
| Q44800774 | ZNF804A and schizophrenia susceptibility in Asian populations. |
| Q36280814 | ulfasQTL: an ultra-fast method of composite splicing QTL analysis. |
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