Chromosomes, Human, Pair 15

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  Subject Areas on Research

  • A Genome-Wide Functional Genomics Approach Identifies Susceptibility Pathways to Fungal Bloodstream Infection in Humans. 
  • A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25. 
  • A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14. 
  • A sex-specific association between a 15q25 variant and upper aerodigestive tract cancers. 
  • An analysis paradigm for investigating multi-locus effects in complex disease: examination of three GABA receptor subunit genes on 15q11-q13 as risk factors for autistic disorder. 
  • Analysis of centromeric activity in Robertsonian translocations: implications for a functional acrocentric hierarchy. 
  • Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder. 
  • Angelman syndrome: are the estimates too low? 
  • Application of a rank-based genetic association test to age-at-onset data from the Collaborative Study on the Genetics of Alcoholism study. 
  • Association analysis of chromosome 15 gabaa receptor subunit genes in autistic disorder. 
  • Autistic disorder and chromosome 15q11-q13: construction and analysis of a BAC/PAC contig. 
  • Autistic symptoms among children and young adults with isodicentric chromosome 15. 
  • Clinical heterogeneity of familial spastic paraplegia linked to chromosome 2p21. 
  • Common genetic variants associated with resting oxygenation in chronic obstructive pulmonary disease. 
  • Cytogenetic and molecular analysis of an unusual case of acute promyelocytic leukemia with a t(15;17;17)(q22;q23;q21). 
  • Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation. 
  • Early adult-onset POAG linked to 15q11-13 using ordered subset analysis. 
  • Equatorial segment protein defines a discrete acrosomal subcompartment persisting throughout acrosomal biogenesis. 
  • Estrogen excess associated with novel gain-of-function mutations affecting the aromatase gene. 
  • Evidence for structural heterogeneity from molecular cytogenetic analysis of dicentric Robertsonian translocations. 
  • Familial supernumerary marker chromosome evolution through three generations. 
  • Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes. 
  • Fine-mapping of the 5p15.33, 6p22.1-p21.31, and 15q25.1 regions identifies functional and histology-specific lung cancer susceptibility loci in African-Americans. 
  • Further clinical and molecular delineation of the 15q24 microdeletion syndrome. 
  • Gene by Environment Investigation of Incident Lung Cancer Risk in African-Americans. 
  • Genetic analysis of multiplex rheumatoid arthritis families. 
  • Genetic association of refractive error and axial length with 15q14 but not 15q25 in the Blue Mountains Eye Study cohort. 
  • Genetic studies in autistic disorder and chromosome 15. 
  • Genome-wide linkage scan for primary open angle glaucoma: influences of ancestry and age at diagnosis. 
  • Genome-wide linkage scan for prostate cancer susceptibility genes in men with aggressive disease: significant evidence for linkage at chromosome 15q12. 
  • Genome-wide linkage scan in fuchs endothelial corneal dystrophy. 
  • Genome-wide meta-analyses of smoking behaviors in African Americans. 
  • Identification of centromeric antigens in dicentric Robertsonian translocations: CENP-C and CENP-E are necessary components of functional centromeres. 
  • Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium. 
  • Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families. 
  • Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers. 
  • NF1-related locus on chromosome 15. 
  • Ordered-subset analysis of savant skills in autism for 15q11-q13. 
  • Ordered-subsets linkage analysis detects novel Alzheimer disease loci on chromosomes 2q34 and 15q22. 
  • Phenotypic definition of Chiari type I malformation coupled with high-density SNP genome screen shows significant evidence for linkage to regions on chromosomes 9 and 15. 
  • Regional rearrangements in chromosome 15q21 cause formation of cryptic promoters for the CYP19 (aromatase) gene. 
  • The role of lysyl oxidase-like 1 DNA copy number variants in exfoliation glaucoma. 
  • Three probands with autistic disorder and isodicentric chromosome 15. 
  • Trisomy 15 associated with nonimmune hydrops. 
  • Unbalanced translocation 46,XY,-15,+der(22)t(15;22)(q13;q11)pat: case report and review of the literature. 
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  Keywords of People

  • Liu, Yutao, Adjunct Assistant Professor in the Department of Medicine, Medicine, Medical Genetics