Joe Leigh Simpson

Summary

Affiliation: March of Dimes
Country: USA

Publications

  1. ncbi request reprint Birth defects and assisted reproductive technologies
    Joe Leigh Simpson
    March of Dimes, 1275 Mamaroneck Avenue, White Plains, NY 10605, USA Electronic address
    Semin Fetal Neonatal Med 19:177-82. 2014
  2. doi request reprint Cell-free fetal DNA and maternal serum analytes for monitoring embryonic and fetal status
    Joe Leigh Simpson
    March of Dimes Foundation, White Plains, New York 10605, USA
    Fertil Steril 99:1124-34. 2013
  3. doi request reprint Prenatal diagnosis and 47,XXY
    Joe Leigh Simpson
    March of Dimes Foundation, White Plains, NY 10605, USA
    Am J Med Genet C Semin Med Genet 163:64-70. 2013
  4. doi request reprint Preimplantation genetic diagnosis to improve pregnancy outcomes in subfertility
    Joe Leigh Simpson
    March of Dimes Foundation, White Plains, NY, USA
    Best Pract Res Clin Obstet Gynaecol 26:805-15. 2012
  5. doi request reprint Invasive procedures for prenatal diagnosis: any future left?
    Joe Leigh Simpson
    March of Dimes Foundation, White Plains, NY 10605, United States
    Best Pract Res Clin Obstet Gynaecol 26:625-38. 2012
  6. doi request reprint Integration of microarray technology into prenatal diagnosis: counselling issues generated during the NICHD clinical trial
    Ronald J Wapner
    Department of Obstetrics and Gynecology, Columbia University College of Physicians and Surgeons, New York, NY, USA
    Prenat Diagn 32:396-400. 2012

Detail Information

Publications6

  1. ncbi request reprint Birth defects and assisted reproductive technologies
    Joe Leigh Simpson
    March of Dimes, 1275 Mamaroneck Avenue, White Plains, NY 10605, USA Electronic address
    Semin Fetal Neonatal Med 19:177-82. 2014
    ..There is no additive risk in ART twins compared with non-ART twins, nor in embryos having been cryopreserved. The increased risk observed had not appeared to dissuade couples from attempting to have their own children. ..
  2. doi request reprint Cell-free fetal DNA and maternal serum analytes for monitoring embryonic and fetal status
    Joe Leigh Simpson
    March of Dimes Foundation, White Plains, New York 10605, USA
    Fertil Steril 99:1124-34. 2013
    ..Such detection rates are substantively higher than with maternal serum analytes, and are accompanied by a much lower (<1%) false-positive rate...
  3. doi request reprint Prenatal diagnosis and 47,XXY
    Joe Leigh Simpson
    March of Dimes Foundation, White Plains, NY 10605, USA
    Am J Med Genet C Semin Med Genet 163:64-70. 2013
    ..A further consideration is that ability of array CGH to detect microdeletions or microduplications below resolution of a karyotype could make return to direct testing using an invasive procedure attractive...
  4. doi request reprint Preimplantation genetic diagnosis to improve pregnancy outcomes in subfertility
    Joe Leigh Simpson
    March of Dimes Foundation, White Plains, NY, USA
    Best Pract Res Clin Obstet Gynaecol 26:805-15. 2012
    ..Current recommendations are for obligatory 24 chromosome testing, most readily using array comparative genome hybridisation...
  5. doi request reprint Invasive procedures for prenatal diagnosis: any future left?
    Joe Leigh Simpson
    March of Dimes Foundation, White Plains, NY 10605, United States
    Best Pract Res Clin Obstet Gynaecol 26:625-38. 2012
    ..Application of cell-free fetal DNA for aneuploidy screening may or may not narrow this difference. Irrespective, invasive procedures are currently required for application of array comparative genome hybridisation...
  6. doi request reprint Integration of microarray technology into prenatal diagnosis: counselling issues generated during the NICHD clinical trial
    Ronald J Wapner
    Department of Obstetrics and Gynecology, Columbia University College of Physicians and Surgeons, New York, NY, USA
    Prenat Diagn 32:396-400. 2012
    ..Of equal import is additional research into patient attitudes and desires, and a better understanding of the full phenotypic spectrum of copy number variants discovered in utero...