| P50 | author | Nancy J Cox | Q67954217 |
| | Eric R. Gamazon | Q37616152 |
| | Hae Kyung Im | Q47327124 |
| P2093 | author name string | R Stephanie Huang | |
| | Dana Ziliak | |
| | Bonnie LaCroix | |
| | Danny S Park | |
| P2860 | cites work | DNA methylation patterns associate with genetic and gene expression variation in HapMap cell lines | Q21184030 |
| | Polymorphisms in the estrogen receptor 1 and vitamin C and matrix metalloproteinase gene families are associated with susceptibility to lymphoma | Q21562611 |
| | Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS | Q21563317 |
| | Genome-wide identification of SNPs in microRNA genes and the SNP effects on microRNA target binding and biogenesis | Q82299247 |
| | Potential etiologic and functional implications of genome-wide association loci for human diseases and traits | Q22066284 |
| | The C-terminal domains of human TNRC6A, TNRC6B, and TNRC6C silence bound transcripts independently of Argonaute proteins | Q24318187 |
| | miRBase: microRNA sequences, targets and gene nomenclature | Q24538656 |
| | A map of human genome variation from population-scale sequencing | Q24617794 |
| | New loci associated with kidney function and chronic kidney disease | Q24630646 |
| | A second generation human haplotype map of over 3.1 million SNPs | Q24651939 |
| | Most mammalian mRNAs are conserved targets of microRNAs | Q24655061 |
| | PolymiRTS Database: linking polymorphisms in microRNA target sites with complex traits | Q24675631 |
| | A miR-24 microRNA binding-site polymorphism in dihydrofolate reductase gene leads to methotrexate resistance | Q24679991 |
| | Statistical significance for genomewide studies | Q24681264 |
| | Combinatorial microRNA target predictions | Q27860510 |
| | MicroRNA gene expression deregulation in human breast cancer | Q27860690 |
| | The International HapMap Project | Q27860695 |
| | Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources | Q27860739 |
| | Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists | Q28131785 |
| | CpG-rich islands and the function of DNA methylation | Q28131800 |
| | A defect in the Kv channel-interacting protein 2 (KChIP2) gene leads to a complete loss of I(to) and confers susceptibility to ventricular tachycardia | Q28211696 |
| | The let-7 microRNA represses cell proliferation pathways in human cells | Q28240833 |
| | Let-7 prevents early cancer progression by suppressing expression of the embryonic gene HMGA2 | Q28254493 |
| | Posttranscriptional regulation of microRNA biogenesis in animals | Q28282519 |
| | Genetic variation in the sodium-dependent vitamin C transporters, SLC23A1, and SLC23A2 and risk for preterm delivery | Q28287147 |
| | Genetic variation in the vitamin C transporter, SLC23A2, modifies the risk of HPV16-associated head and neck cancer | Q28389041 |
| | Genetic analysis of human traits in vitro: drug response and gene expression in lymphoblastoid cell lines | Q28474104 |
| | Mixed effects modeling of proliferation rates in cell-based models: consequence for pharmacogenomics and cancer | Q28480587 |
| | Specificity of microRNA target selection in translational repression | Q28776123 |
| | Genomewide association study for onset age in Parkinson disease | Q29417034 |
| | Understanding mechanisms underlying human gene expression variation with RNA sequencing | Q29614412 |
| | Transcriptome genetics using second generation sequencing in a Caucasian population | Q29614413 |
| | Population genomics of human gene expression | Q29614905 |
| | Gene silencing by microRNAs: contributions of translational repression and mRNA decay | Q29615825 |
| | MicroRNA-378 targets the myogenic repressor MyoR during myoblast differentiation | Q30426550 |
| | PARK3 influences age at onset in Parkinson disease: a genome scan in the GenePD study | Q30448742 |
| | A genome-wide approach to identify genetic variants that contribute to etoposide-induced cytotoxicity. | Q30479559 |
| | miRNA malfunction causes spinal motor neuron disease | Q30495998 |
| | A genome-wide survey for SNPs altering microRNA seed sites identifies functional candidates in GWAS. | Q31034509 |
| | MicroRNA-133a protects against myocardial fibrosis and modulates electrical repolarization without affecting hypertrophy in pressure-overloaded adult hearts | Q33580704 |
| | Patrocles: a database of polymorphic miRNA-mediated gene regulation in vertebrates | Q33601105 |
| | SCAN: SNP and copy number annotation | Q33779644 |
| | The landscape of genetic complexity across 5,700 gene expression traits in yeast | Q33818641 |
| | The Influence of 3'UTRs on MicroRNA Function Inferred from Human SNP Data | Q34081307 |
| | Genetic loci influencing kidney function and chronic kidney disease | Q34109552 |
| | Downregulation of microRNA-200 in EBV-associated gastric carcinoma | Q34116271 |
| | Genetic variation in microRNA networks: the implications for cancer research | Q34177121 |
| | Heritable and non-genetic factors as variables of pharmacologic phenotypes in lymphoblastoid cell lines | Q34288272 |
| | Genetic variation in sodium-dependent vitamin C transporters SLC23A1 and SLC23A2 and risk of advanced colorectal adenoma | Q34657155 |
| | A comparison of background correction methods for two-colour microarrays | Q34667581 |
| | A genome-wide approach identifies that the aspartate metabolism pathway contributes to asparaginase sensitivity. | Q34989475 |
| | Inferring causative variants in microRNA target sites | Q35198281 |
| | Population differences in microRNA expression and biological implications | Q35578546 |
| | Identification of genetic variants contributing to cisplatin-induced cytotoxicity by use of a genomewide approach | Q35946327 |
| | Evaluation of genetic variation contributing to differences in gene expression between populations | Q36718956 |
| | Genetic architecture of transcript-level variation in humans | Q37118371 |
| | Effect of population and gender on chemotherapeutic agent-induced cytotoxicity | Q37159518 |
| | The database of experimentally supported targets: a functional update of TarBase | Q37202497 |
| | Genetic variants contributing to daunorubicin-induced cytotoxicity | Q37271466 |
| | Genetic variants associated with carboplatin-induced cytotoxicity in cell lines derived from Africans. | Q37344425 |
| | Genetic variation in sodium-dependent ascorbic acid transporters and risk of gastric cancer in Poland | Q37354850 |
| | Discovery and genotyping of genome structural polymorphism by sequencing on a population scale | Q37390913 |
| | Small RNAs are on the move. | Q37791829 |
| | MicroRNA gene expression during retinoic acid-induced differentiation of human acute promyelocytic leukemia. | Q38305314 |
| | MicroRNAs play an essential role in the development of cardiac hypertrophy | Q39340872 |
| | The effects of EBV transformation on gene expression levels and methylation profiles | Q39598932 |
| | Epstein-Barr virus encoded LMP1 downregulates TCL1 oncogene through miR-29b | Q39766210 |
| | The micro-ribonucleic acid (miRNA) miR-206 targets the human estrogen receptor-alpha (ERalpha) and represses ERalpha messenger RNA and protein expression in breast cancer cell lines. | Q40168734 |
| | Modulation of cholinephosphotransferase activity in breast cancer cell lines by Ro5-4864, a peripheral benzodiazepine receptor agonist | Q40413401 |
| | KChIP2 attenuates cardiac hypertrophy through regulation of Ito and intracellular calcium signaling. | Q40447179 |
| | Mapping of the human genes (SLC23A2 and SLC23A1) coding for vitamin C transporters 1 and 2 (SVCT1 and SVCT2) to 5q23 and 20p12, respectively | Q43075692 |
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | transcriptome | Q252857 |
| | complex trait | Q55608248 |
| | microRNA expression | Q60681249 |
| P304 | page(s) | 1046-1063 | |
| P577 | publication date | 2012-05-31 | |
| P1433 | published in | American Journal of Human Genetics | Q4744249 |
| P1476 | title | Genetic architecture of microRNA expression: implications for the transcriptome and complex traits | |
| P478 | volume | 90 | |