Pages that link to "Q36973621"

The following pages link to Maps of open chromatin highlight cell type-restricted patterns of regulatory sequence variation at hematological trait loci (Q36973621):

Displaying 26 items.

• Massively parallel sequencing: the new frontier of hematologic genomics (Q26830619) (← links)
• Joint analysis of functional genomic data and genome-wide association studies of 18 human traits (Q30794057) (← links)
• On the identification of potential regulatory variants within genome wide association candidate SNP sets (Q33789149) (← links)
• Platelet function is modified by common sequence variation in megakaryocyte super enhancers (Q33906387) (← links)
• Identification of a regulatory variant that binds FOXA1 and FOXA2 at the CDC123/CAMK1D type 2 diabetes GWAS locus (Q34165822) (← links)
• Missing heritability of common diseases and treatments outside the protein-coding exome (Q34212558) (← links)
• Transcriptional diversity during lineage commitment of human blood progenitors (Q34626417) (← links)
• Epigenetic modification of histone 3 lysine 27: mediator subunit MED25 is required for the dissociation of polycomb repressive complex 2 from the promoter of cytochrome P450 2C9 (Q35002929) (← links)
• A loss of function screen of identified genome-wide association study Loci reveals new genes controlling hematopoiesis (Q35204380) (← links)
• Lipid-induced epigenomic changes in human macrophages identify a coronary artery disease-associated variant that regulates PPAP2B Expression through Altered C/EBP-beta binding (Q35250745) (← links)
• Genetic variation at MECOM, TERT, JAK2 and HBS1L-MYB predisposes to myeloproliferative neoplasms (Q35407362) (← links)
• Genome-wide association study follow-up identifies cyclin A2 as a regulator of the transition through cytokinesis during terminal erythropoiesis (Q35537090) (← links)
• In-silico QTL mapping of postpubertal mammary ductal development in the mouse uncovers potential human breast cancer risk loci (Q35994508) (← links)
• Early developmental gene enhancers affect subcortical volumes in the adult human brain (Q36942388) (← links)
• Global analysis of DNA methylation variation in adipose tissue from twins reveals links to disease-associated variants in distal regulatory elements (Q37298169) (← links)
• Lessons and Implications from Genome-Wide Association Studies (GWAS) Findings of Blood Cell Phenotypes (Q37689829) (← links)
• Using chromatin marks to interpret and localize genetic associations to complex human traits and diseases. (Q38167223) (← links)
• A symbiotic liaison between the genetic and epigenetic code (Q38211430) (← links)
• Functional interpretation of non-coding sequence variation: concepts and challenges (Q38843497) (← links)
• CTCF mediates the TERT enhancer-promoter interactions in lung cancer cells: identification of a novel enhancer region involved in the regulation of TERT gene (Q39068532) (← links)
• Cyclin A2 regulates erythrocyte morphology and numbers (Q39362400) (← links)
• Priming of transcriptional memory responses via the chromatin accessibility landscape in T cells (Q40288456) (← links)
• Transcriptional, epigenetic and retroviral signatures identify regulatory regions involved in hematopoietic lineage commitment. (Q40370482) (← links)
• Disentangling the Effects of Colocalizing Genomic Annotations to Functionally Prioritize Non-coding Variants within Complex-Trait Loci. (Q42033919) (← links)
• Concise Review: Epigenetic Regulation of Hematopoiesis: Biological Insights and Therapeutic Applications (Q47147613) (← links)
• Common variants in signaling transcription-factor-binding sites drive phenotypic variability in red blood cell traits (Q102369493) (← links)