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. 
  • Clinical-pathological correlations of BAV and the attendant thoracic aortopathies. Part 2: Pluridisciplinary perspective on their genetic and molecular origins. 
  • 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. 
  • Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility. 
  • 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. 
  • Treatment of steroid-resistant nephrotic syndrome in the genomic era. 
  • 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

  • Noor, Mohamed A. F., Professor of Biology, Duke Science & Society