Jeannie Visootsak

Summary

Affiliation: Emory University
Country: USA

Publications

  1. ncbi request reprint Behavioral phenotype of sex chromosome aneuploidies: 48,XXYY, 48,XXXY, and 49,XXXXY
    Jeannie Visootsak
    Department of Human Genetics and Pediatrics, Emory University School of Medicine, Atlanta, Georgia, USA
    Am J Med Genet A 143:1198-203. 2007
  2. pmc Klinefelter syndrome and other sex chromosomal aneuploidies
    Jeannie Visootsak
    Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30033, USA
    Orphanet J Rare Dis 1:42. 2006
  3. ncbi request reprint Neuropsychiatric and behavioral aspects of trisomy 21
    Jeannie Visootsak
    Curr Psychiatry Rep 9:135-40. 2007
  4. ncbi request reprint Fragile X syndrome: an update and review for the primary pediatrician
    Jeannie Visootsak
    Departments of Human Genetics and Pediatrics, Emory University School of Medicine, Atlanta, GA, USA
    Clin Pediatr (Phila) 44:371-81. 2005
  5. ncbi request reprint Clinical and behavioral features of patients with Borjeson-Forssman-Lehmann syndrome with mutations in PHF6
    Jeannie Visootsak
    Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia, USA
    J Pediatr 145:819-25. 2004
  6. ncbi request reprint Social function in multiple X and Y chromosome disorders: XXY, XYY, XXYY, XXXY
    Jeannie Visootsak
    Department of Human Genetics and Pediatrics, Emory University School of Medicine, Atlanta, Georgia, USA
    Dev Disabil Res Rev 15:328-32. 2009
  7. pmc Timing of diagnosis of 47,XXY and 48,XXYY: a survey of parent experiences
    Jeannie Visootsak
    Department of Human Genetics, Emory University, Atlanta, Georgia 30033, USA
    Am J Med Genet A 161:268-72. 2013
  8. ncbi request reprint Turner syndrome: an update and review for the primary pediatrician
    Brandy H Doswell
    Emory University School of Medicine, Atlanta, GA, USA
    Clin Pediatr (Phila) 45:301-13. 2006
  9. pmc Diagnosis of fragile X syndrome: a qualitative study of African American families
    Jeannie Visootsak
    Department of Human Genetics, Emory University, Atlanta, GA, USA
    J Genet Couns 21:845-53. 2012
  10. pmc Genome-wide analysis validates aberrant methylation in fragile X syndrome is specific to the FMR1 locus
    Reid S Alisch
    Departments of Human Genetics, Emory University School of Medicine, 615 Michael Street, Atlanta, GA 30322, USA
    BMC Med Genet 14:18. 2013

Detail Information

Publications17

  1. ncbi request reprint Behavioral phenotype of sex chromosome aneuploidies: 48,XXYY, 48,XXXY, and 49,XXXXY
    Jeannie Visootsak
    Department of Human Genetics and Pediatrics, Emory University School of Medicine, Atlanta, Georgia, USA
    Am J Med Genet A 143:1198-203. 2007
    ..Both groups display interests in helping others, but have a low tolerance for being rejected or teased. Specific recommendations and interventional strategies are provided for individuals with 48,XXYY, 48,XXXY, and 49,XXXXY...
  2. pmc Klinefelter syndrome and other sex chromosomal aneuploidies
    Jeannie Visootsak
    Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30033, USA
    Orphanet J Rare Dis 1:42. 2006
    ....
  3. ncbi request reprint Neuropsychiatric and behavioral aspects of trisomy 21
    Jeannie Visootsak
    Curr Psychiatry Rep 9:135-40. 2007
    ..Understanding the age-related changes in cognitive functioning and behavioral profiles in individuals with DS provides insight into clinical and treatment implications...
  4. ncbi request reprint Fragile X syndrome: an update and review for the primary pediatrician
    Jeannie Visootsak
    Departments of Human Genetics and Pediatrics, Emory University School of Medicine, Atlanta, GA, USA
    Clin Pediatr (Phila) 44:371-81. 2005
    ..Here the current state of knowledge is reviewed and a framework is provided for early recognition and diagnosis, along with counseling and treatment implications for the children and family members...
  5. ncbi request reprint Clinical and behavioral features of patients with Borjeson-Forssman-Lehmann syndrome with mutations in PHF6
    Jeannie Visootsak
    Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia, USA
    J Pediatr 145:819-25. 2004
    ..To describe clinical and behavioral features of 10 men from 2 families with Borjeson-Forssman-Lehmann syndrome (BFLS) and missense mutations in the PHF6 zinc-finger transcription factor gene...
  6. ncbi request reprint Social function in multiple X and Y chromosome disorders: XXY, XYY, XXYY, XXXY
    Jeannie Visootsak
    Department of Human Genetics and Pediatrics, Emory University School of Medicine, Atlanta, Georgia, USA
    Dev Disabil Res Rev 15:328-32. 2009
    ..g., 48,XXYY and 48,XXXY) and an additional Y (e.g., 47,XYY) is less common, but it is important to understand their social functioning as it provides insight into treatment implications...
  7. pmc Timing of diagnosis of 47,XXY and 48,XXYY: a survey of parent experiences
    Jeannie Visootsak
    Department of Human Genetics, Emory University, Atlanta, Georgia 30033, USA
    Am J Med Genet A 161:268-72. 2013
    ....
  8. ncbi request reprint Turner syndrome: an update and review for the primary pediatrician
    Brandy H Doswell
    Emory University School of Medicine, Atlanta, GA, USA
    Clin Pediatr (Phila) 45:301-13. 2006
    ....
  9. pmc Diagnosis of fragile X syndrome: a qualitative study of African American families
    Jeannie Visootsak
    Department of Human Genetics, Emory University, Atlanta, GA, USA
    J Genet Couns 21:845-53. 2012
    ....
  10. pmc Genome-wide analysis validates aberrant methylation in fragile X syndrome is specific to the FMR1 locus
    Reid S Alisch
    Departments of Human Genetics, Emory University School of Medicine, 615 Michael Street, Atlanta, GA 30322, USA
    BMC Med Genet 14:18. 2013
    ..Although a dramatic increase in DNA methylation of the FMR1 full mutation allele is well documented, the extent to which these changes affect DNA methylation throughout the rest of the genome has gone unexplored...
  11. pmc Neurodevelopmental outcomes in children with Down syndrome and congenital heart defects
    Jeannie Visootsak
    Department of Human Genetics, Emory University, Atlanta, Georgia, USA
    Am J Med Genet A 155:2688-91. 2011
    ..Since this is the first study to examine the early developmental outcomes of children with DS +‚ÄČAVSD, the findings may be useful for clinicians in providing anticipatory guidance...
  12. doi request reprint Fragile X syndrome
    Kathryn B Garber
    Department of Human Genetics, Emory University School of Medicine, 615 Michael Street, Atlanta, GA 30322, USA
    Eur J Hum Genet 16:666-72. 2008
    ..The resulting over abundance of certain proteins results in reduced synaptic strength due to AMPA receptor trafficking abnormalities that lead, at least in part, to the fragile X phenotype...
  13. ncbi request reprint Prader-Willi syndrome: an update and review for the primary pediatrician
    Christina Chen
    Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia, USA
    Clin Pediatr (Phila) 46:580-91. 2007
    ..They can also serve as a valuable source of support and advocacy for the family. This article reviews the current state of knowledge about Prader-Willi syndrome and discusses up-to-date understanding of the management of this condition...
  14. pmc A new look at XXYY syndrome: medical and psychological features
    Nicole Tartaglia
    Department of Pediatrics, University of Colorado Denver, School of Medicine, Aurora, Colorado, USA
    Am J Med Genet A 146:1509-22. 2008
    ..2%), autism spectrum disorders (28.3%), mood disorders (46.8%), and tic disorders (18.9%), were elevated with 55.9% on psychopharmacologic medication overall. Recommendations for evaluation and treatment are summarized...
  15. doi request reprint Brain magnetic resonance imaging findings in 49,XXXXY syndrome
    Trevor L Hoffman
    Section of Biochemical Genetics, Children s Hospital of Philadelphia, Philadelphia, Pennsylvania, USA
    Pediatr Neurol 38:450-3. 2008
    ....
  16. ncbi request reprint Midline defects in FG syndrome: does tethered spinal cord contribute to the phenotype?
    Raymond Wang
    Medical Genetics Institute, Steven Spielberg Pediatric Research Center, Cedars Sinai Medical Center, 444 South San Vicente Boulevard 1001, Los Angeles, CA 90048, USA
    J Pediatr 146:537-41. 2005
    ..Because tethered spinal cord syndrome (TCS) has similar symptoms, we evaluated imaging for TCS in patients with FG syndrome...
  17. ncbi request reprint Behavioral features of CHARGE syndrome (Hall-Hittner syndrome) comparison with Down syndrome, Prader-Willi syndrome, and Williams syndrome
    John M Graham
    Department of Pediatrics, Medical Genetics Birth Defects Center, David Geffen School of Medicine at UCLA, Los Angeles, California 90048, USA
    Am J Med Genet A 133:240-7. 2005
    ....