Therapy development for adult diffuse glioma is hindered by incomplete knowledge of somatic glioma driving alterations and suboptimal disease classification. We defined the complete set of genes associated with 1,122 diffuse grade II-III-IV gliomas from The Cancer Genome Atlas and used molecular profiles to improve disease classification, identify molecular correlations, and provide insights into the […]
Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma.
Primary open-angle glaucoma (POAG) is a leading cause of blindness worldwide. To identify new susceptibility loci, we performed meta-analysis on genome-wide association study (GWAS) results from eight independent studies from the United States (3,853 cases and 33,480 controls) and investigated the most significantly associated SNPs in two Australian studies (1,252 cases and 2,592 controls), three […]
Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records.
Large-scale DNA sequencing identifies incidental rare variants in established Mendelian disease genes, but the frequency of related clinical phenotypes in unselected patient populations is not well established. Phenotype data from electronic medical records (EMRs) may provide a resource to assess the clinical relevance of rare variants.To determine the clinical phenotypes from EMRs for individuals with […]
Time to Give Thanks for Good News
It’s the middle of the fall semester, so it’s time for some good news updates from the Crawford Crew! Both former Crawford Crew members Drs. Nicole Restrepo and Logan Dumitrescu recently received an NSF travel award to present work from the Crawford lab at the 2016 Pacific Symposium on Biocomputing. Also receiving a travel award […]
Towards a phenome-wide catalog of human clinical traits impacted by genetic ancestry.
Racial/ethnic differences for commonly measured clinical variables are well documented, and it has been postulated that population-specific genetic factors may play a role. The genetic heterogeneity of admixed populations, such as African Americans, provides a unique opportunity to identify genomic regions and variants associated with the clinical variability observed for diseases and traits across populations.To […]
American Society of Human Genetics (ASHG) 2015 in Baltimore, MD
There’s a chill in the air. Leaves have turned from bright green to brilliant red, yellow, and orange. The wind is picking up. You know what that means. Yes, it’s time for the annual American Society of Human Genetics (ASHG) meeting! ASHG is the professional organization for human genetics and has had an annual meeting […]
Estimating cumulative pathway effects on risk for age-related macular degeneration using mixed linear models.
Age-related macular degeneration (AMD) is the leading cause of irreversible visual loss in the elderly in developed countries and typically affects more than 10% of individuals over age 80. AMD has a large genetic component, with heritability estimated to be between 45% and 70%. Numerous variants have been identified and implicate various molecular mechanisms and […]
Estimating cumulative pathway effects on risk for age-related macular degeneration using mixed linear models.
Age-related macular degeneration (AMD) is the leading cause of irreversible visual loss in the elderly in developed countries and typically affects more than 10% of individuals over age 80. AMD has a large genetic component, with heritability estimated to be between 45% and 70%. Numerous variants have been identified and implicate various molecular mechanisms and […]
It’s aloha time in the Crawford lab!
The Pacific Symposium on Biocomputing is a unique mid-sized conference focused on computational methods with applications to the biomedical sciences. Hosted in Hawaii (Figures 1 and 2), PSB has been around since 1996, and many attendees have been to every single meeting. I had not heard of PSB until I met Dr. Marylyn Ritchie and […]
Gene expression in cell lines from propionic acidemia patients, carrier parents, and controls.
Propionic acidemia (PA) is an inborn of metabolism which usually presents with metabolic acidosis and accumulation of 3-hydroxypropionate among other toxins. Examining the gene expression in lymphoblastoid cell lines (LCLs) from PA patients, their carrier parents and age/sex-matched controls at normal glucose and low glucose growth conditions demonstrated differences among and between these groups. Using […]
Sex-Specific Parental Effects on Offspring Lipid Levels.
Plasma lipid levels are highly heritable traits, but known genetic loci can only explain a small portion of their heritability.In this study, we analyzed the role of parental levels of total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), and triglycerides (TGs) in explaining the values of the corresponding traits in adult offspring. […]