Inheritance Patterns
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Subject Areas on Research
- A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.
- A longitudinal study of epigenetic variation in twins.
- Beyond Mendel: an evolving view of human genetic disease transmission.
- De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
- Finding the missing heritability of complex diseases.
- Genetic and physiological basis of adaptive salt tolerance divergence between coastal and inland Mimulus guttatus.
- Genetic basis of adaptive evolution of a polyphenism by genetic accommodation.
- Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.
- Genetics and evolution: an iOS application to supplement introductory courses in transmission and evolutionary genetics.
- Genetics of resistance to the rust fungus Coleosporium ipomoeae in three species of morning glory (Ipomoea).
- Geographical variation in postzygotic isolation and its genetic basis within and between two Mimulus species.
- High heritability of metabolomic profiles in families burdened with premature cardiovascular disease.
- High-throughput imaging and analysis of root system architecture in Brachypodium distachyon under differential nutrient availability.
- Inter-chromosomal level of genome organization and longevity-related phenotypes in humans.
- Late-onset hereditary axonal neuropathies.
- Molecular and clinical analysis of ALPL in a cohort of patients with suspicion of Hypophosphatasia.
- Mutations in Either TUBB or MAPRE2 Cause Circumferential Skin Creases Kunze Type.
- Parental origin impairment of synaptic functions and behaviors in cytoplasmic FMRP interacting protein 1 (Cyfip1) deficient mice.
- Phenotypic stability of Pro347Leu rhodopsin transgenic pigs as indicated by photoreceptor cell degeneration.
- Polymorphic mimicry in Papilio dardanus: mosaic dominance, big effects, and origins.
- Polymorphisms of large effect explain the majority of the host genetic contribution to variation of HIV-1 virus load.
- Putative digenic inheritance of heterozygous RP1L1 and C2orf71 null mutations in syndromic retinal dystrophy.
- RNAi-mediated allelic trans-interaction at the imprinted Rtl1/Peg11 locus.
- Separating the domains of oppositional behavior: comparing latent models of the conners' oppositional subscale.
- Sex in fungi.
- Sex-specific incompatibility generates locus-specific rates of introgression between species.
- Shared heritability and functional enrichment across six solid cancers.
- TAF1 Variants Are Associated with Dysmorphic Features, Intellectual Disability, and Neurological Manifestations.
- The quick and the dead: microbial demography at the yeast thermal limit.
- Truncating CLCN1 mutations in myotonia congenita: variable patterns of inheritance.
- Unraveling genetic origin of aging-related traits: evolving concepts.
- Why some women look young for their age.
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Keywords of People
- Davis, Erica Ellen, Associate Professor of Pediatrics, Cell Biology
- Noor, Mohamed A. F., Professor of Biology, Duke Science & Society