Fragile X-Associated Primary Ovarian Insufficiency (FXPOI): Scientific Articles

Featured Articles

The following featured articles include those from NICHD researchers or NICHD-supported researchers.

  • Loomis, E. W., Eid, J. S., Peluso, P., Yin, J., Hickey, L., Rank, D., et al. (2013). Sequencing the unsequenceable: expanded CGG-repeat alleles of the fragile X gene. Genome Research, 23(1), 121–128. PMID: 23064752
  • Sterling, A. M., Mailick, M., Greenberg, J. Warren, S. F., & Brady, N. (2013). Language dysfluencies in females with the FMR1 premutation. Brain and Cognition, 82(1), 84–89. PMID: 23523717
  • Seltzer, M. M., Barker, E. T., Greenberg, J. S., Hong, J., Coe, C., & Almeida, D. (2012). Differential sensitivity to life stress in FMR1 premutation carrier mothers of children with fragile X syndrome. Health Psychology, 31(5), 612–622. PMID: 22149120
  • Seltzer, M. M., Baker, M. W., Hong, J., Maenner, M., Greenberg, J., & Mandel, D. (2012). Prevalence of CGG expansions of the FMR1 gene in a US population-based sample. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics, 159B(5), 589–597. PMID: 22619118
  • Winarni, T. I., Chonchaiya, W., Sumekar, T. A., Ashwood, P., Morales, G. M., Tassone, F., et al. (2012). Immune-mediated disorders among women carriers of fragile X premutation alleles. American Journal of Medical Genetics. Part A, 158A(10), 2473–2481. PMID: 22903889
  • Willemsen, R., Levenga, J., & Oostra, B. A. (2011). CGG repeat in the FMR1 gene. Clinical Genetics, 80, 214–225. PMID: 21651511
  • Hunter, J. E., Rohr, J. K., & Sherman, S. L. (2010). Co-occurring diagnoses among FMR1 premutation allele carriers. Clinical Genetics, 77, 374–381. PMID: 20059484

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