Art Daniel

Summary

Affiliation: The Children's Hospital at Westmead
Country: Australia

Publications

  1. pmc Two mosaic terminal inverted duplications arising post-zygotically: Evidence for possible formation of neo-telomeres
    Art Daniel
    Department of Cytogenetics, Western Sydney Genetics Program, The Children s Hospital at Westmead, NSW 2145, Australia
    Cell Chromosome 7:1. 2008
  2. pmc Chromosome loops arising from intrachromosomal tethering of telomeres occur at high frequency in G1 (non-cycling) mitotic cells: Implications for telomere capture
    Art Daniel
    Department of Cytogenetics, Western Sydney Genetics Program, The Children s Hospital at Westmead, NSW 2145, Australia
    Cell Chromosome 3:3. 2004
  3. ncbi Karyotype, phenotype and parental origin in 19 cases of triploidy
    A Daniel
    Department of Cytogenetics, The Children s Hospital at Westmead, Parramatta, NSW 2145, Australia
    Prenat Diagn 21:1034-48. 2001
  4. ncbi An innocuous duplication of 11.2 Mb at 13q21 is gene poor: sub-bands of gene paucity and pervasive CNV characterize the chromosome anomalies
    Art Daniel
    Department of Cytogenetics, Western Sydney Genetics Program, The Children s Hospital at Westmead, Westmead, NSW, Australia
    Am J Med Genet A 143:2452-9. 2007
  5. ncbi Three different origins for apparent triploid/diploid mosaics
    Art Daniel
    Departments of Cytogenetics, Western Sydney Genetics Program, The Children s Hospital at Westmead, P O Box 3515, Parramatta, NSW 2124, Australia
    Prenat Diagn 23:529-34. 2003
  6. ncbi Prospective ranking of the sonographic markers for aneuploidy: data of 2143 prenatal cytogenetic diagnoses referred for abnormalities on ultrasound
    Art Daniel
    Department of Cytogenetics, Western Sydney Genetics Program, Children s Hospital at Westmead, NSW, Australia
    Aust N Z J Obstet Gynaecol 43:16-26. 2003
  7. ncbi A series of supernumerary small ring marker autosomes identified by FISH with chromosome probe arrays and literature review excluding chromosome 15
    Art Daniel
    Department of Cytogenetics, The Children s Hospital at Westmead, Hawkesbury Road, Westmead, New South Wales 2145, Australia
    Am J Med Genet A 117:212-22. 2003
  8. ncbi Recombinants of intrachromosomal transposition of subtelomeres in chromosomes 1 and 2: a cause of minute terminal chromosomal imbalances
    Art Daniel
    Cytogenetics Department, Western Sydney Genetics Program, The Children s Hospital at Westmead, Sydney, Australia
    Am J Med Genet A 117:57-64. 2003
  9. ncbi Issues arising from the prenatal diagnosis of some rare trisomy mosaics--the importance of cryptic fetal mosaicism
    Art Daniel
    Department of Cytogenetics, Western Sydney Genetics Program, The Children s Hospital at Westmead, NSW, Australia
    Prenat Diagn 24:524-36. 2004
  10. ncbi Isochromosome 5p mosaicism at prenatal diagnosis: observations and outcomes in six cases at chorionic villus sampling and one at amniocentesis
    Susan Clement Wilson
    Genetic Health Services Victoria, Royal Children s Hospital, Melbourne, Australia
    Prenat Diagn 22:681-5. 2002

Collaborators

Detail Information

Publications13

  1. pmc Two mosaic terminal inverted duplications arising post-zygotically: Evidence for possible formation of neo-telomeres
    Art Daniel
    Department of Cytogenetics, Western Sydney Genetics Program, The Children s Hospital at Westmead, NSW 2145, Australia
    Cell Chromosome 7:1. 2008
    ..To elucidate the structure of terminal inverted duplications and to investigate potential mechanisms of formation in two cases where there was mosaicism with cells of apparently normal karyotype...
  2. pmc Chromosome loops arising from intrachromosomal tethering of telomeres occur at high frequency in G1 (non-cycling) mitotic cells: Implications for telomere capture
    Art Daniel
    Department of Cytogenetics, Western Sydney Genetics Program, The Children s Hospital at Westmead, NSW 2145, Australia
    Cell Chromosome 3:3. 2004
    ....
  3. ncbi Karyotype, phenotype and parental origin in 19 cases of triploidy
    A Daniel
    Department of Cytogenetics, The Children s Hospital at Westmead, Parramatta, NSW 2145, Australia
    Prenat Diagn 21:1034-48. 2001
    ..This trisomy was probably of post-zygotic origin and we suggest the fetus was rescued by the prominence of the triploid line...
  4. ncbi An innocuous duplication of 11.2 Mb at 13q21 is gene poor: sub-bands of gene paucity and pervasive CNV characterize the chromosome anomalies
    Art Daniel
    Department of Cytogenetics, Western Sydney Genetics Program, The Children s Hospital at Westmead, Westmead, NSW, Australia
    Am J Med Genet A 143:2452-9. 2007
    ..0); 5q21.1 (43.6); 6q24.2 (41.4); 9p23 (38.8); 10q21.1 (36.5); 5q21.2 (35.4), and 11q14.3 (33.8). We argue that both gene paucity and pervasive CNV are major indicators of bands conforming to the Chromosome Anomaly phenomenon...
  5. ncbi Three different origins for apparent triploid/diploid mosaics
    Art Daniel
    Departments of Cytogenetics, Western Sydney Genetics Program, The Children s Hospital at Westmead, P O Box 3515, Parramatta, NSW 2124, Australia
    Prenat Diagn 23:529-34. 2003
    ..This fetus developed normally and a normal infant was born with no evidence of triploidy in newborn blood or cord blood at three months of age...
  6. ncbi Prospective ranking of the sonographic markers for aneuploidy: data of 2143 prenatal cytogenetic diagnoses referred for abnormalities on ultrasound
    Art Daniel
    Department of Cytogenetics, Western Sydney Genetics Program, Children s Hospital at Westmead, NSW, Australia
    Aust N Z J Obstet Gynaecol 43:16-26. 2003
    ....
  7. ncbi A series of supernumerary small ring marker autosomes identified by FISH with chromosome probe arrays and literature review excluding chromosome 15
    Art Daniel
    Department of Cytogenetics, The Children s Hospital at Westmead, Hawkesbury Road, Westmead, New South Wales 2145, Australia
    Am J Med Genet A 117:212-22. 2003
    ..The high proportion ( approximately 12.5%) of cases with multiple supernumerary small rings almost always of different centromeric origin is consistent with this concept...
  8. ncbi Recombinants of intrachromosomal transposition of subtelomeres in chromosomes 1 and 2: a cause of minute terminal chromosomal imbalances
    Art Daniel
    Cytogenetics Department, Western Sydney Genetics Program, The Children s Hospital at Westmead, Sydney, Australia
    Am J Med Genet A 117:57-64. 2003
    ..Other cases of this unusual mechanism may be detected with more common use of subtelomeric probes. It is suggested the bouquet associations of telomeres in early meiosis may facilitate such unusual rearrangements...
  9. ncbi Issues arising from the prenatal diagnosis of some rare trisomy mosaics--the importance of cryptic fetal mosaicism
    Art Daniel
    Department of Cytogenetics, Western Sydney Genetics Program, The Children s Hospital at Westmead, NSW, Australia
    Prenat Diagn 24:524-36. 2004
    ..To add to the knowledge of fetal mosaicism, confined placental mosaicism (CPM), and uniparental disomy (UPD), in rare trisomies detected at prenatal diagnosis...
  10. ncbi Isochromosome 5p mosaicism at prenatal diagnosis: observations and outcomes in six cases at chorionic villus sampling and one at amniocentesis
    Susan Clement Wilson
    Genetic Health Services Victoria, Royal Children s Hospital, Melbourne, Australia
    Prenat Diagn 22:681-5. 2002
    ..In addition, we report a case of the primary diagnosis of 47,+i(5p)/46 mosaicism at amniocentesis. The infant appeared normal at birth, but a brain malformation was subsequently identified...
  11. ncbi Molecular distinction between true centric fission and pericentric duplication-fission
    Jo Perry
    Chromosome Research Laboratory, Murdoch Childrens Research Institute and Department of Paediatrics, Royal Children s Hospital, Parkville, Vic, 3052, Australia
    Hum Genet 116:300-10. 2005
    ....
  12. ncbi Chromosome 13q neocentromeres: molecular cytogenetic characterization of three additional cases and clinical spectrum
    Shulan Li
    Department of Human Genetics Mount Sinai School of Medicine, New York, New York 10029, USA
    Am J Med Genet 110:258-67. 2002
    ..The complexity and variability of the phenotypes seen in these patients does not support a simple reductionist view of phenotype/genotype correlation with polysomy for certain chromosomal regions...
  13. ncbi Distortion of female meiotic segregation and reduced male fertility in human Robertsonian translocations: consistent with the centromere model of co-evolving centromere DNA/centromeric histone (CENP-A)
    Art Daniel
    Am J Med Genet 111:450-2. 2002