scholarly article | Q13442814 |
P50 | author | Eric R. Gamazon | Q37616152 |
Joshua C. Denny | Q56425939 | ||
Dan Roden | Q58973971 | ||
Nancy J Cox | Q67954217 | ||
Lisa Bastarache | Q88032983 | ||
Gokhan Unlu | Q89356673 | ||
Ela W. Knapik | Q89356674 | ||
P2093 | author name string | Daniel S Levic | |
Andrey Rzhetsky | |||
Xue Zhong | |||
Xinzi Qi | |||
Anuar I Konkashbaev | |||
Ilya Mayzus | |||
Max Breyer | |||
P2860 | cites work | Multiplex genome engineering using CRISPR/Cas systems | Q24609428 |
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Stable vascular connections and remodeling require full expression of VE-cadherin in zebrafish embryos | Q27348907 | ||
Principal components analysis corrects for stratification in genome-wide association studies | Q27860975 | ||
Characterizing the genetic basis of transcriptome diversity through RNA-sequencing of 922 individuals | Q28299787 | ||
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Extracting research-quality phenotypes from electronic health records to support precision medicine | Q28648163 | ||
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The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future | Q28674604 | ||
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A Nondegenerate Code of Deleterious Variants in Mendelian Loci Contributes to Complex Disease Risk | Q30002401 | ||
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High-throughput gene targeting and phenotyping in zebrafish using CRISPR/Cas9. | Q30407556 | ||
Sema3E-PlexinD1 signaling selectively suppresses disoriented angiogenesis in ischemic retinopathy in mice | Q30499914 | ||
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine | Q30840255 | ||
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Network-based bioinformatics analysis of spatio-temporal RNA-Seq data reveals transcriptional programs underpinning normal and aberrant retinal development | Q31126223 | ||
In vivo cell biology in zebrafish - providing insights into vertebrate development and disease | Q33557669 | ||
PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene-disease associations | Q33808357 | ||
Sec24D-dependent transport of extracellular matrix proteins is required for zebrafish skeletal morphogenesis | Q33815925 | ||
Using probabilistic estimation of expression residuals (PEER) to obtain increased power and interpretability of gene expression analyses | Q34255194 | ||
Human genomics. The Genotype-Tissue Expression (GTEx) pilot analysis: multitissue gene regulation in humans | Q34475541 | ||
Structural architecture of SNP effects on complex traits | Q34478069 | ||
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Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies | Q35286565 | ||
Partitioning heritability by functional annotation using genome-wide association summary statistics | Q36225291 | ||
Presynaptic localization of GluK5 in rod photoreceptors suggests a novel function of high affinity glutamate receptors in the mammalian retina | Q36290014 | ||
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants | Q36556369 | ||
Endothelial cell whole genome expression analysis in a mouse model of early-onset Fuchs' endothelial corneal dystrophy | Q36706740 | ||
Electronic medical records for genetic research: results of the eMERGE consortium | Q36948611 | ||
Efficient multiplex biallelic zebrafish genome editing using a CRISPR nuclease system | Q37117695 | ||
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Systems-level analysis of proteolytic events in increased vascular permeability and complement activation in skin inflammation | Q37412450 | ||
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Animal model of Sar1b deficiency presents lipid absorption deficits similar to Anderson disease. | Q38301880 | ||
The feelgood mutation in zebrafish dysregulates COPII-dependent secretion of select extracellular matrix proteins in skeletal morphogenesis | Q38965381 | ||
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Genetic Analysis of Venous Thromboembolism in UK Biobank Identifies the ZFPM2 Locus and Implicates Obesity as a Causal Risk Factor | Q40260213 | ||
FoxH1 negatively modulates flk1 gene expression and vascular formation in zebrafish | Q42775785 | ||
The mother superior mutation ablates foxd3 activity in neural crest progenitor cells and depletes neural crest derivatives in zebrafish | Q47073110 | ||
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Zebrafish as a model for hemorrhagic stroke. | Q51852686 | ||
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MicroRNAs Establish Uniform Traits during the Architecture of Vertebrate Embryos. | Q54137723 | ||
Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation | Q59784158 | ||
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No unexpected CRISPR-Cas9 off-target activity revealed by trio sequencing of gene-edited mice | Q89475108 | ||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Danio rerio | Q169444 |
transcriptome | Q252857 | ||
biobank | Q864217 | ||
eye disease | Q3041498 | ||
electronic health records | Q10871684 | ||
P304 | page(s) | 503-519 | |
P577 | publication date | 2019-02-28 | |
P1433 | published in | American Journal of Human Genetics | Q4744249 |
P1476 | title | GRIK5 Genetically Regulated Expression Associated with Eye and Vascular Phenomes: Discovery through Iteration among Biobanks, Electronic Health Records, and Zebrafish | |
P478 | volume | 104 |
Q92794386 | Disease Models & Mechanisms in the Age of Big Data |
Q99371201 | Identifying the RNA signatures of coronary artery disease from combined lncRNA and mRNA expression profiles |
Q97643603 | Metabolic coessentiality mapping identifies C12orf49 as a regulator of SREBP processing and cholesterol metabolism |
Q92611220 | Phenome-based approach identifies RIC1-linked Mendelian syndrome through zebrafish models, biobank associations and clinical studies |
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