Robert D Oates

Summary

Affiliation: Boston University School of Medicine
Country: USA

Publications

  1. doi request reprint The natural history of endocrine function and spermatogenesis in Klinefelter syndrome: what the data show
    Robert D Oates
    School of Medicine, Boston University, Boston, Massachusetts, USA
    Fertil Steril 98:266-73. 2012
  2. pmc Evaluation of the azoospermic male
    Robert Oates
    Boston University School of Medicine, MA 02118, USA
    Asian J Androl 14:82-7. 2012
  3. ncbi request reprint Clinical characterization of 42 oligospermic or azoospermic men with microdeletion of the AZFc region of the Y chromosome, and of 18 children conceived via ICSI
    Robert D Oates
    Department of Urology, Boston University School of Medicine, 720 Harrison Avenue, Boston, MA 02118, USA
    Hum Reprod 17:2813-24. 2002
  4. doi request reprint Clinical evaluation of the infertile male with respect to genetic etiologies
    Robert D Oates
    Department of Urology, Boston University School of Medicine, Boston Medical Center, Boston, MA 02118, USA
    Syst Biol Reprod Med 57:72-7. 2011
  5. doi request reprint The genetic basis of male reproductive failure
    Robert D Oates
    Department of Urology, Boston University School of Medicine, 720 Harrison Avenue, Suite 606, Boston, MA 02118, USA
    Urol Clin North Am 35:257-70, ix. 2008
  6. doi request reprint Ejaculatory dysfunction
    Elizabeth Phillips
    Division of Urology, Boston University School of Medicine, Shapiro Center, Suite 3B, 715 Albany Street, Boston, MA 02118, USA
    Urol Clin North Am 41:115-28. 2014
  7. ncbi request reprint Clinical and diagnostic features of patients with suspected Klinefelter syndrome
    Robert D Oates
    Boston University School of Medicine Department of Urology Boston, Massachusetts, USA
    J Androl 24:49-50. 2003
  8. ncbi request reprint A family of human Y chromosomes has dispersed throughout northern Eurasia despite a 1.8-Mb deletion in the azoospermia factor c region
    Sjoerd Repping
    Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Academic Medical Center, Amsterdam, The Netherlands
    Genomics 83:1046-52. 2004
  9. pmc Are sequence family variants useful for identifying deletions in the human Y chromosome?
    Sjoerd Repping
    Am J Hum Genet 75:514-7; author reply 517-9. 2004
  10. ncbi request reprint Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection
    Sjoerd Repping
    Howard Hughes Medical Institute, Whitehead Institute and Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02142, USA
    Nat Genet 35:247-51. 2003

Collaborators

  • David C Page
  • S J Silber
  • Judith Gianotten
  • Sjoerd Repping
  • Fulco van der Veen
  • Steve Rozen
  • Elizabeth Phillips
  • Cindy M Korver
  • Saskia K M van Daalen
  • Helen Skaletsky
  • Christina Carpenter
  • Janet D Marszalek
  • Laura G Brown
  • Jan W A de Vries
  • Tatyana Pyntikova
  • Laura Brown
  • Tomoko Kuroda-Kawaguchi
  • Julian Lange

Detail Information

Publications11

  1. doi request reprint The natural history of endocrine function and spermatogenesis in Klinefelter syndrome: what the data show
    Robert D Oates
    School of Medicine, Boston University, Boston, Massachusetts, USA
    Fertil Steril 98:266-73. 2012
    ....
  2. pmc Evaluation of the azoospermic male
    Robert Oates
    Boston University School of Medicine, MA 02118, USA
    Asian J Androl 14:82-7. 2012
    ..It is only with this information that a therapeutic plan can be made for the patient. As will be discussed, a targeted approach to testing is far more satisfying and cost-effective than a blind, shotgun approach...
  3. ncbi request reprint Clinical characterization of 42 oligospermic or azoospermic men with microdeletion of the AZFc region of the Y chromosome, and of 18 children conceived via ICSI
    Robert D Oates
    Department of Urology, Boston University School of Medicine, 720 Harrison Avenue, Boston, MA 02118, USA
    Hum Reprod 17:2813-24. 2002
    ..In this study, we have fully characterized 42 infertile men with a Y chromosome microdeletion strictly confined to the AZFc region, and we report on 18 children conceived through the use of ICSI...
  4. doi request reprint Clinical evaluation of the infertile male with respect to genetic etiologies
    Robert D Oates
    Department of Urology, Boston University School of Medicine, Boston Medical Center, Boston, MA 02118, USA
    Syst Biol Reprod Med 57:72-7. 2011
    ....
  5. doi request reprint The genetic basis of male reproductive failure
    Robert D Oates
    Department of Urology, Boston University School of Medicine, 720 Harrison Avenue, Suite 606, Boston, MA 02118, USA
    Urol Clin North Am 35:257-70, ix. 2008
    ..The author concentrates on some of the known causes of nonobstructive azoospermia and obstructive azoospermia with a well-established genetic cause such as congenital bilateral absence of the vas deferens...
  6. doi request reprint Ejaculatory dysfunction
    Elizabeth Phillips
    Division of Urology, Boston University School of Medicine, Shapiro Center, Suite 3B, 715 Albany Street, Boston, MA 02118, USA
    Urol Clin North Am 41:115-28. 2014
    ....
  7. ncbi request reprint Clinical and diagnostic features of patients with suspected Klinefelter syndrome
    Robert D Oates
    Boston University School of Medicine Department of Urology Boston, Massachusetts, USA
    J Androl 24:49-50. 2003
  8. ncbi request reprint A family of human Y chromosomes has dispersed throughout northern Eurasia despite a 1.8-Mb deletion in the azoospermia factor c region
    Sjoerd Repping
    Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Academic Medical Center, Amsterdam, The Netherlands
    Genomics 83:1046-52. 2004
    ..Our present findings suggest either that the b2/b3 deletion has at most a modest effect on fitness or that, within branch N, its effect has been counterbalanced by another genetic, possibly Y-linked, factor...
  9. pmc Are sequence family variants useful for identifying deletions in the human Y chromosome?
    Sjoerd Repping
    Am J Hum Genet 75:514-7; author reply 517-9. 2004
  10. ncbi request reprint Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection
    Sjoerd Repping
    Howard Hughes Medical Institute, Whitehead Institute and Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02142, USA
    Nat Genet 35:247-51. 2003
    ....
  11. pmc Recombination between palindromes P5 and P1 on the human Y chromosome causes massive deletions and spermatogenic failure
    Sjoerd Repping
    Howard Hughes Medical Institute, Whitehead Institute, and Department of Biology, Massachusetts Institute of Technology, Cambridge 02142, USA
    Am J Hum Genet 71:906-22. 2002
    ..The restriction of the associated phenotype to spermatogenic failure indicates the remarkable functional specialization of the affected regions of the Y chromosome...