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Genomic Architecture of Regional Measures of Cerebral Cortical Thickness
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A Genome-Wide Association Study of Resistance to Tuberculosis Infection in a Multi-Ancestry Brazilian Cohort
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Depression is associated with earlier onset of cognitive impairment in a population-based longitudinal cohort
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Exploring The Phenotypic Effects of Toll Signaling Pathways In Tumor Progression in EGFR-driven Glioblastoma Models
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Genome-wide TWAS of brain and blood tissues identifies novel risk genes for Alzheimer’s disease dementia
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Exploring the Genetics and Biological Pathways of Obesity through Computational Biology and Statistical Approaches
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A benchmark of rare cell type detection methods for single-cell RNA sequencing data
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Potential biomarkers for ALS/FTD as a consequence of TDP-43 loss of function
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Maltreatment and Epigenetic Aging in Infants – A DNA Methylation Analysis
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Cellular Transcriptional Profiling Reveals Multiple B Cell Differentiation Branching Points in Mus musculus Spleen Exposed to Lipopolysaccharides (LPS) and NP-4-Hydroxy-3- Nitrophenylacetic (NPF)
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Web Tool for Clinic Trio Based Sequence Data Analysis to Identify Potential Pathogenic Variants for Rare Genetic Diseases
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Molecular Epidemiology of a Type 4 Dengue Virus Outbreak in Paraguay, 2019-2020
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DNA Methylation as a Potential Mediator of the Association Between Prenatal Tobacco and Alcohol Exposure and Child Neurodevelopment in a South African Birth Cohort
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Characterizing the role of recurrent histone H3 mutations in cancer initiation
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Integrate Proteomics Data with GWAS Summary data for Studying Alzheimer’s Disease by Nonparametric Bayesian Method
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Bayesian Functional Genome-wide Association Study using Standardized Individual-level and Summary-level GWAS Data
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Pilot investigation of treatment effect modification by vitamin D binding protein isoforms on calcium and vitamin D effects on biomarkers of risk for colorectal cancer in the normal-appearing colorectal mucosa of colorectal adenoma patients
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Metabolomic alterations in Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS) premutation carriers
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Association between Maternal Depression during Pregnancy and Newborn DNA Methylation
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Epigenetic Associations of Circulating Interleukin 6 among People with HIV
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Associations of DNA methylation with biomarkers of liver function among male veterans living with HIV
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TIGAR-V2 with nonparametric Bayesian eQTL weights estimated from GTEx V8 & Leveraging multiple reference panels to improve TWAS power by ensemble machine learning
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EDClust: An EM-MM hybrid method for cell clustering in population-level single cell RNA sequencing
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Integrating human brain transcriptomes and proteomes with genome-wide association data identifies risk genes shared between depression and Alzheimer’s disease
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Cis-regulatory methylation of the VIP gene in the white-throated sparrow (Zonotrichia albicollis)
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DNA Methylation of CD4+ T-cells Reveals Association of ITGB7 in Pediatric Crohn’s Disease
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Genetic Technology and the Virtues: The Significance of Reason, Care and Accountability
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Genomic Scan of Recent Positive Selection Differentiating Aggression in Chimpanzees and Bonobos
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Associations of polygenic risk score and polybrominated biphenyl exposure on age at menarche in the Michigan polybrominated biphenyl registry
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Analysis of age, tumor-sidedness, and mismatch repair (MMR) gene with response to immune checkpoint inhibitors (ICIs) in MMR-deficient (dMMR) colorectal cancer (CRC) patients (pts): A multi-institutional study
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Identifying Genetic Modifiers for Left and Right Sided Orofacial Clefts
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Genome-wide DNA methylation profile change in cancer cell lines under stresses
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Applying Genome-Wide Association Study to Analyze Novel Variants That Potentially Relate to Alzheimer’s Disease
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Influence of CYP3A4 inhibition on the tamoxifen metabolic pathway and the implications for breast cancer recurrence in a pre-menopausal cohort
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Powerful variance-component method for TWAS identifies novel and known risk genes for Alzheimer’s dementia
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Diabetes-related DNA Methylation of TXNIP Independently Associated with Inflammation
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Gain of Chromosome 1q is Associated with Early Progression in Multiple Myeloma Patients Treated with Lenalidomide, Bortezomib, and Dexamethasone
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Investigating the Roles of ACLY in Multiple Myeloma Biology and Drug Sensitivity
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Associations between Neighborhood-Level Factors and DNA Methylation in Breast Tumor Tissue: Using Social Epigenomics to Explore Cancer Disparities
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Epigenetic prediction of smoking status using machine-learning methods
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Identifying the Genetic Drivers of 3q29 Deletion-Associated Phenotypes
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Impact of Predictive Ability on Identifying Higher-Risk Population for Common Diseases in Polygenic Risk Prediction
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Association of Colorectal Cancer Susceptibility Loci Alone and in Combination with Adherence to the WCRF/AICF Guidelines for Cancer Prevention on Colorectal Cancer Risk
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Evaluate the host genetic effects of tuberculosis-associated variants on diabetes
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Genotyping Ascaris nematodes from diverse geographic locations
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Maternal phenylketonuria: an update on intervention compliance, challenges to staying compliant, and child outcomes from patient-reported survey data in the Newborn Screening Connect patient registry
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Association of Body Mass Index with DNA Methylation Age Acceleration In African American Mothers: Cross-sectional Analysis from InterGEN Study
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3q29 Microdeletion Syndrome: Phenotypic Differences between Urban and Rural Populations
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Impact of dairy restriction of children with Duarte galactosemia on breastfeeding of unaffected younger siblings
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Cell-type specific alteration of DNA methylation in Alzheimer’s Disease
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