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Chromatin Structural Changes in the Innate Immune Response
Genetic Association Between Personality and Major Depression or Bipolar Disorder. A          Polygenic Score Analysis Using Genome-wide Association Data
GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational          Attainment
Visualizing phylogenetic tree landscapes.
Pleiotropy, constraint, and modularity in the evolution of life histories
Molecular Genetic Architecture of Self-Employment
Zymosan Fungal Infection Induces Nucleosome Redistributions During the Innate Immune          Response
Promoter Capture Hi-C
Alternative to the Search for Single Polymorphisms
Genome-Wide Association Scan of Trait Depression
Heritability of Cardiovascular and Personality Traits in 6,148 Sardinians
Increased Genetic Vulnerability to Smoking at CHRNA5 in Early-Onset Smokers
Meta-Analysis of Genome-Wide Association Studies for Personality
Meta-Analysis and Imputation Refines the Association of 15q25 with Smoking          Quantity
Visual Perspective and Genetics
BDNF Val66Met is Associated with Introversion and Interacts with 5-HTTLPR to Influence          Neuroticism
Utilizing Cutting-Edge Computational Biology Methods in the Genomic Analysis of Florida Endangered Species
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.
Expanding anchored hybrid enrichment to resolve both deep and shallow relationships within the spider tree of life.
Longevity Candidate Genes and Their Association with Personality Traits in the          Elderly
Variants of the Serotonin Transporter Gene and NEO-PI-R Neuroticism
Replication timing and transcriptional control
Advancing behavioural genomics by considering timescale.
Anchored enrichment dataset for true flies (order Diptera) reveals insights into the phylogeny of flower flies (family Syrphidae).
Label-Free Relative Quantitation of Isobaric and Isomeric Human Histone H2A and H2B Variants by Fourier Transform Ion Cyclotron Resonance Top-Down MS/MS.
Resolving Cypriniformes relationships using an anchored enrichment approach.
Plasma BDNF Concentration, Val66Met Genetic Variant and Depression-Related Personality          Traits
Rapid automated landmarking for morphometric analysis of three-dimensional facial scans.
Meta-analysis of Genome-Wide Association Studies for Extraversion
Replicating Large Genomes
estrous cycle surpasses sex differences in regulating the transcriptome in the rat medial prefrontal cortex and reveals an underlying role of early growth response 1.
Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology.
GINOM
Deletion of DXZ4 on the human inactive X chromosome alters higher-order genome architecture.
Open chromatin reveals the functional maize genome.
Genome-Wide Association and Exome Sequencing Study of Language Disorder in an Isolated Population.
Excess histone levels mediate cytotoxicity via multiple mechanisms.
Histone tyrosine phosphorylation comes of age.
Identification of G1-regulated genes in normally cycling human cells.
Behavior, brain, and genome in genomic disorders
Childhood adversity and DNA methylation of genes involved in the hypothalamus-pituitary-adrenal axis and immune system
application of the elastic net for an endophenotype analysis.
Integrative Comparison of mRNA Expression Patterns in Breast Cancers from Caucasian and Asian Americans with Implications for Precision Medicine.
Genome-wide association study identifies 74 loci associated with educational attainment.
Influence of ATM-Mediated DNA Damage Response on Genomic Variation in Human Induced Pluripotent Stem Cells.
Genomewide Association Study of African Children Identifies Association of SCHIP1 and PDE8A with Facial Size and Shape.
Competing scaffolding proteins determine capsid size during mobilization of  pathogenicity islands.
DNA replication timing alterations identify common markers between distinct progeroid diseases.
DNA sequences proximal to human mitochondrial DNA deletion breakpoints prevalent in human disease form G-quadruplexes, a class of DNA structures inefficiently unwound by the mitochondrial replicative Twinkle helicase.