Siri Atma W Greeley

Summary

Affiliation: University of Chicago
Country: USA

Publications

  1. pmc Creation of the Web-based University of Chicago Monogenic Diabetes Registry: using technology to facilitate longitudinal study of rare subtypes of diabetes
    Siri Atma W Greeley
    Department of Pediatrics, Section of Adult and Pediatric Endocrinology, Diabetes and Metabolism, The University of Chicago, Chicago, Illinois 60637, USA
    J Diabetes Sci Technol 5:879-86. 2011
  2. pmc Neonatal diabetes mellitus: a model for personalized medicine
    Siri Atma W Greeley
    Department of Pediatrics, Section of Adult and Pediatric Endocrinology, Diabetes and Metabolism, University of Chicago Pritzker School of Medicine, 5841 S Maryland Ave, MC 1027, Chicago, IL 60637, USA
    Trends Endocrinol Metab 21:464-72. 2010
  3. pmc Neonatal diabetes: an expanding list of genes allows for improved diagnosis and treatment
    Siri Atma W Greeley
    Section of Adult and Pediatric Endocrinology, Diabetes and Metabolism, Kovler Diabetes Center, The University of Chicago, Chicago, IL 60637, USA
    Curr Diab Rep 11:519-32. 2011
  4. pmc Diagnosis and treatment of neonatal diabetes: a United States experience
    Julie Støy
    Department of Medicine, The University of Chicago, Chicago, IL 60637, USA
    Pediatr Diabetes 9:450-9. 2008
  5. doi request reprint Update in neonatal diabetes
    Siri Atma W Greeley
    Department of Medicine, The University of Chicago, Chicago, Illinois 60637, USA
    Curr Opin Endocrinol Diabetes Obes 17:13-9. 2010
  6. doi request reprint Continued lessons from the INS gene: an intronic mutation causing diabetes through a novel mechanism
    David Carmody
    Departments of Medicine and Pediatrics, Section of Adult and Pediatric Endocrinology, Diabetes, and Metabolism, The University of Chicago, Chicago, Illinois, USA
    J Med Genet 52:612-6. 2015
  7. pmc Visuomotor performance in KCNJ11-related neonatal diabetes is impaired in children with DEND-associated mutations and may be improved by early treatment with sulfonylureas
    Reshma P Shah
    Section of Developmental and Behavioral Pediatrics and John P Kennedy Jr Intellectual and Developmental Disabilities Research Center, Department of Pediatrics, Comer Children s Hospital and Pritzer School of Medicine, The University of Chicago, Chicago, Illinois, USA
    Diabetes Care 35:2086-8. 2012
  8. pmc The cost-effectiveness of personalized genetic medicine: the case of genetic testing in neonatal diabetes
    Siri Atma W Greeley
    Department of Pediatrics, Section of Adult and Pediatric Endocrinology, Diabetes and Metabolism, University of Chicago, Chicago, Illinois, USA
    Diabetes Care 34:622-7. 2011
  9. doi request reprint Age at the time of sulfonylurea initiation influences treatment outcomes in KCNJ11-related neonatal diabetes
    Brian W Thurber
    Departments of Pediatrics and Medicine, Section of Adult and Pediatric Endocrinology, Diabetes, and Metabolism, University of Chicago, 5841 S Maryland Ave, MC 1027, Chicago, IL, 60637, USA
    Diabetologia 58:1430-5. 2015
  10. doi request reprint An online monogenic diabetes discussion group: supporting families and fueling new research
    Marie E Perrone
    Department of Medicine, Section of Adult and Pediatric Endocrinology, Diabetes, and Metabolism, The University of Chicago, Chicago, Ill Department of Pediatrics, Section of Adult and Pediatric Endocrinology, Diabetes, and Metabolism, The University of Chicago, Chicago, Ill
    Transl Res 166:425-31. 2015

Collaborators

  • Michael E Msall
  • Karen Spruyt
  • Elbert S Huang
  • Kirstie K Danielson
  • Sarah E Flanagan
  • Rebecca B Lipton
  • Louis H Philipson
  • David Carmody
  • Marie E Perrone
  • Julie Støy
  • Honggang Ye
  • Graeme I Bell
  • Brian W Thurber
  • Reshma P Shah
  • Ashley N Pastore
  • Veronica P Paz
  • Rochelle N Naylor
  • Soo Young Park
  • Heather M Highland
  • Jazzmyne T Dickens
  • G Alkorta-Aranburu
  • Elizabeth C Tadie
  • Kristen E Wroblewski
  • Craig L Hanis
  • Brigette C Kragie
  • W Zipf
  • M Swinyard
  • S Wentworth
  • Fran R Cogen
  • J Atchison
  • W P Zeller
  • S Day
  • D Edidin
  • M Vaccarello-Cruz
  • A Perelman
  • Kinga B Skowron
  • Anna Pluzhnikov
  • Jennifer E Below
  • Ann Marie Patch
  • Gregory M Lipkind
  • Nancy J Cox
  • Emma L Edghill
  • M Geoffrey Hayes
  • Donald F Steiner
  • Sian Ellard
  • Andrew T Hattersley

Detail Information

Publications12

  1. pmc Creation of the Web-based University of Chicago Monogenic Diabetes Registry: using technology to facilitate longitudinal study of rare subtypes of diabetes
    Siri Atma W Greeley
    Department of Pediatrics, Section of Adult and Pediatric Endocrinology, Diabetes and Metabolism, The University of Chicago, Chicago, Illinois 60637, USA
    J Diabetes Sci Technol 5:879-86. 2011
    ..kovlerdiabetescenter.org/registry/) for individuals with either neonatal diabetes diagnosed before 1 year of age or with a phenotype suggestive of maturity-onset diabetes of the young...
  2. pmc Neonatal diabetes mellitus: a model for personalized medicine
    Siri Atma W Greeley
    Department of Pediatrics, Section of Adult and Pediatric Endocrinology, Diabetes and Metabolism, University of Chicago Pritzker School of Medicine, 5841 S Maryland Ave, MC 1027, Chicago, IL 60637, USA
    Trends Endocrinol Metab 21:464-72. 2010
    ..It remains to be determined what is the most appropriate treatment of other causes. The diagnosis and treatment of neonatal diabetes, therefore, represents a model for personalized medicine...
  3. pmc Neonatal diabetes: an expanding list of genes allows for improved diagnosis and treatment
    Siri Atma W Greeley
    Section of Adult and Pediatric Endocrinology, Diabetes and Metabolism, Kovler Diabetes Center, The University of Chicago, Chicago, IL 60637, USA
    Curr Diab Rep 11:519-32. 2011
    ..This compelling example of personalized genetic medicine leading to improved glucose regulation and quality of life may-with continued research-be repeated for other forms of neonatal diabetes in the future...
  4. pmc Diagnosis and treatment of neonatal diabetes: a United States experience
    Julie Støy
    Department of Medicine, The University of Chicago, Chicago, IL 60637, USA
    Pediatr Diabetes 9:450-9. 2008
    ..The aim of this study was to identify the genetic cause of diabetes in 77 consecutive patients referred to the University of Chicago with diabetes diagnosed before 1 yr of age...
  5. doi request reprint Update in neonatal diabetes
    Siri Atma W Greeley
    Department of Medicine, The University of Chicago, Chicago, Illinois 60637, USA
    Curr Opin Endocrinol Diabetes Obes 17:13-9. 2010
    ..Identification of these mutations allows patients treated with insulin to be transferred to sulfonylureas, but associated conditions and other causes must be considered...
  6. doi request reprint Continued lessons from the INS gene: an intronic mutation causing diabetes through a novel mechanism
    David Carmody
    Departments of Medicine and Pediatrics, Section of Adult and Pediatric Endocrinology, Diabetes, and Metabolism, The University of Chicago, Chicago, Illinois, USA
    J Med Genet 52:612-6. 2015
    ..Diabetes in neonates usually has a monogenic aetiology; however, the cause remains unknown in 20-30%. Heterozygous INS mutations represent one of the most common gene causes of neonatal diabetes mellitus...
  7. pmc Visuomotor performance in KCNJ11-related neonatal diabetes is impaired in children with DEND-associated mutations and may be improved by early treatment with sulfonylureas
    Reshma P Shah
    Section of Developmental and Behavioral Pediatrics and John P Kennedy Jr Intellectual and Developmental Disabilities Research Center, Department of Pediatrics, Comer Children s Hospital and Pritzer School of Medicine, The University of Chicago, Chicago, Illinois, USA
    Diabetes Care 35:2086-8. 2012
    ..To assess performance on an age-standardized neuromotor coordination task among sulfonylurea-treated KCNJ11-related neonatal diabetic patients...
  8. pmc The cost-effectiveness of personalized genetic medicine: the case of genetic testing in neonatal diabetes
    Siri Atma W Greeley
    Department of Pediatrics, Section of Adult and Pediatric Endocrinology, Diabetes and Metabolism, University of Chicago, Chicago, Illinois, USA
    Diabetes Care 34:622-7. 2011
    ..Although treatment conversion has dramatic benefits, the cost-effectiveness of routine genetic testing is unknown...
  9. doi request reprint Age at the time of sulfonylurea initiation influences treatment outcomes in KCNJ11-related neonatal diabetes
    Brian W Thurber
    Departments of Pediatrics and Medicine, Section of Adult and Pediatric Endocrinology, Diabetes, and Metabolism, University of Chicago, 5841 S Maryland Ave, MC 1027, Chicago, IL, 60637, USA
    Diabetologia 58:1430-5. 2015
    ....
  10. doi request reprint An online monogenic diabetes discussion group: supporting families and fueling new research
    Marie E Perrone
    Department of Medicine, Section of Adult and Pediatric Endocrinology, Diabetes, and Metabolism, The University of Chicago, Chicago, Ill Department of Pediatrics, Section of Adult and Pediatric Endocrinology, Diabetes, and Metabolism, The University of Chicago, Chicago, Ill
    Transl Res 166:425-31. 2015
    ..Participation by researchers and care providers can inform future research directions and highlight issues of patient concern...
  11. pmc HLA-DQ haplotypes differ by ethnicity in patients with childhood-onset diabetes
    Rebecca B Lipton
    Department of Pediatrics, University of Chicago, Chicago, IL 60637, USA
    Pediatr Diabetes 12:388-95. 2011
    ..To understand the etiology of childhood-onset diabetes, we examined genetic risk markers, autoantibodies, and β-cell function in a mixed race group of young patients...
  12. pmc Insulin gene mutations as a cause of permanent neonatal diabetes
    Julie Støy
    Department of Medicine, University of Chicago, 5841 South Maryland Avenue, Chicago, IL 60637, USA
    Proc Natl Acad Sci U S A 104:15040-4. 2007
    ..One of the human mutations we report here is identical to that in the Akita mouse. The identification of insulin mutations as a cause of neonatal diabetes will facilitate the diagnosis and possibly, in time, treatment of this disorder...