about
Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencingMutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencingThe International Gene Trap Consortium Website: a portal to all publicly available gene trap cell lines in mouseGenomic Views of Transcriptional Enhancers: Essential Determinants of Cellular Identity and Activity-Dependent Responses in the CNSGermline and somatic mutations in homologous recombination genes predict platinum response and survival in ovarian, fallopian tube, and peritoneal carcinomasA common VLDLR polymorphism interacts with APOE genotype in the prediction of carotid artery disease riskRare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophreniaGenomic duplication and overexpression of TJP2/ZO-2 leads to altered expression of apoptosis genes in progressive nonsyndromic hearing loss DFNA51.Genome-wide association study of plasma lipoprotein(a) levels identifies multiple genes on chromosome 6qPolymorphisms of the IL1-receptor antagonist gene (IL1RN) are associated with multiple markers of systemic inflammation.Genetic variation in LPAL2, LPA, and PLG predicts plasma lipoprotein(a) level and carotid artery disease risk.Fine tuning of craniofacial morphology by distant-acting enhancersSubpallial Enhancer Transgenic Lines: a Data and Tool Resource to Study Transcriptional Regulation of GABAergic Cell Fate.Modeling insertional mutagenesis using gene length and expression in murine embryonic stem cells.Comparison of tagging single-nucleotide polymorphism methods in association analysesFunction-based identification of mammalian enhancers using site-specific integration.Tissue-specific SMARCA4 binding at active and repressed regulatory elements during embryogenesis.Apolipoprotein E genotype modifies the risk of behavior problems after infant cardiac surgery.Perioperative stroke in infants undergoing open heart operations for congenital heart disease.Patient characteristics are important determinants of neurodevelopmental outcome at one year of age after neonatal and infant cardiac surgery52 Genetic Loci Influencing Myocardial Mass.Accurate and exact CNV identification from targeted high-throughput sequence data.Transcriptional regulation of enhancers active in protodomains of the developing cerebral cortexTissue-specific RNA expression marks distant-acting developmental enhancers.Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian familiesReduced transcript expression of genes affected by inherited and de novo CNVs in autismGenomic perspectives of transcriptional regulation in forebrain development.Is cardiac diagnosis a predictor of neurodevelopmental outcome after cardiac surgery in infancy?ColoSeq provides comprehensive lynch and polyposis syndrome mutational analysis using massively parallel sequencing.Pbx Regulates Patterning of the Cerebral Cortex in Progenitors and Postmitotic NeuronsA high-resolution enhancer atlas of the developing telencephalon.Formation of chimeric genes by copy-number variation as a mutational mechanism in schizophrenia.Transcriptional Networks Controlled by NKX2-1 in the Development of Forebrain GABAergic Neurons.Rapid and pervasive changes in genome-wide enhancer usage during mammalian development.Learning about mammalian gene regulation from functional enhancer assays in the mouse.A public gene trap resource for mouse functional genomicsSpectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents.Targeted capture and sequencing for detection of mutations causing early onset epileptic encephalopathy.Germline Chd8 haploinsufficiency alters brain development in mouse.Predictors of impaired neurodevelopmental outcomes at one year of age after infant cardiac surgery.
P50
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P50
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Alex S Nord
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Alex S Nord
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Alex S Nord
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Alex S Nord
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Alex S Nord
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Alex S Nord
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Alex S Nord
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Alex S Nord
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Alex S Nord
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Alex S Nord
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Alex S Nord
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Alex S Nord
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P106
P21
P31
P496
0000-0003-4259-7514