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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Constantine A. Stratakis

Section on Pediatric Endocrinology

National Institute of Child Health & Human Development

National Institutes of Health (NIH)

Bethesda

USA

[email]@cc1.nichd.nih.gov

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Section on Pediatric Endocrinology, National Institute of Child Health & Human Development, National Institutes of Health (NIH), Bethesda, USA. 1996 - 2005
  • Unit of Genetics & Endocrinology, DEB, NICHD, NIH, Bethesda, USA. 2000 - 2001
  • Unit on Genetics & Endocrinology, Section on Pediatric Endocrinology, Developmental Endocrinology Branch, National Institute of Child Health & Human Development, USA. 1998

References

  1. Applications of genomic medicine in endocrinology and post-genomic endocrine research. Stratakis, C.A. Hormones. (Athens) (2005) [Pubmed]
  2. Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit (PRKAR1A) in patients with the "complex of spotty skin pigmentation, myxomas, endocrine overactivity, and schwannomas" (Carney complex). Stratakis, C.A. Ann. N. Y. Acad. Sci. (2002) [Pubmed]
  3. Genetics of adrenocortical tumors: Carney complex. Stratakis, C.A. Ann. Endocrinol. (Paris) (2001) [Pubmed]
  4. Clinical genetics of multiple endocrine neoplasias, Carney complex and related syndromes. Stratakis, C.A. J. Endocrinol. Invest. (2001) [Pubmed]
  5. Clinical and molecular features of the Carney complex: diagnostic criteria and recommendations for patient evaluation. Stratakis, C.A., Kirschner, L.S., Carney, J.A. J. Clin. Endocrinol. Metab. (2001) [Pubmed]
  6. A concise genetic and clinical guide to multiple endocrine neoplasias and related syndromes. Stratakis, C.A., Ball, D.W. J. Pediatr. Endocrinol. Metab. (2000) [Pubmed]
  7. Anisomastia associated with interstitial duplication of chromosome 16, mental retardation, obesity, dysmorphic facies, and digital anomalies: molecular mapping of a new syndrome by fluorescent in situ hybridization and microsatellites to 16q13 (D16S419-D16S503). Stratakis, C.A., Lafferty, A., Taymans, S.E., Gafni, R.I., Meck, J.M., Blancato, J. J. Clin. Endocrinol. Metab. (2000) [Pubmed]
  8. Dysregulation of the hypothalamic-pituitary-adrenal axis in short children with and without growth hormone deficiency. Stratakis, C.A., Rusovici, D.E., Kulin, H.E., Finkelstein, J.W. J. Pediatr. Endocrinol. Metab. (2000) [Pubmed]
  9. Ovarian lesions in Carney complex: clinical genetics and possible predisposition to malignancy. Stratakis, C.A., Papageorgiou, T., Premkumar, A., Pack, S., Kirschner, L.S., Taymans, S.E., Zhuang, Z., Oelkers, W.H., Carney, J.A. J. Clin. Endocrinol. Metab. (2000) [Pubmed]
  10. Pituitary macroadenoma in a 5-year-old: an early expression of multiple endocrine neoplasia type 1. Stratakis, C.A., Schussheim, D.H., Freedman, S.M., Keil, M.F., Pack, S.D., Agarwal, S.K., Skarulis, M.C., Weil, R.J., Lubensky, I.A., Zhuang, Z., Oldfield, E.H., Marx, S.J. J. Clin. Endocrinol. Metab. (2000) [Pubmed]
  11. Genetics of Peutz-Jeghers syndrome, Carney complex and other familial lentiginoses. Stratakis, C.A. Horm. Res. (2000) [Pubmed]
  12. The aromatase excess syndrome is associated with feminization of both sexes and autosomal dominant transmission of aberrant P450 aromatase gene transcription. Stratakis, C.A., Vottero, A., Brodie, A., Kirschner, L.S., DeAtkine, D., Lu, Q., Yue, W., Mitsiades, C.S., Flor, A.W., Chrousos, G.P. J. Clin. Endocrinol. Metab. (1998) [Pubmed]
  13. Clinical and genetic analysis of primary bilateral adrenal diseases (micro- and macronodular disease) leading to Cushing syndrome. Stratakis, C.A., Kirschner, L.S. Horm. Metab. Res. (1998) [Pubmed]
  14. Skin manifestations of Cushing disease in children and adolescents before and after the resolution of hypercortisolemia. Stratakis, C.A., Mastorakos, G., Mitsiades, N.S., Mitsiades, C.S., Chrousos, G.P. Pediatr. Dermatol (1998) [Pubmed]
  15. Thyroid gland abnormalities in patients with the syndrome of spotty skin pigmentation, myxomas, endocrine overactivity, and schwannomas (Carney complex). Stratakis, C.A., Courcoutsakis, N.A., Abati, A., Filie, A., Doppman, J.L., Carney, J.A., Shawker, T. J. Clin. Endocrinol. Metab. (1997) [Pubmed]
  16. Carney complex, a familial multiple neoplasia and lentiginosis syndrome. Analysis of 11 kindreds and linkage to the short arm of chromosome 2. Stratakis, C.A., Carney, J.A., Lin, J.P., Papanicolaou, D.A., Karl, M., Kastner, D.L., Pras, E., Chrousos, G.P. J. Clin. Invest. (1996) [Pubmed]
  17. Cytogenetic and microsatellite alterations in tumors from patients with the syndrome of myxomas, spotty skin pigmentation, and endocrine overactivity (Carney complex). Stratakis, C.A., Jenkins, R.B., Pras, E., Mitsiadis, C.S., Raff, S.B., Stalboerger, P.G., Tsigos, C., Carney, J.A., Chrousos, G.P. J. Clin. Endocrinol. Metab. (1996) [Pubmed]
  18. Dideoxyfingerprinting (ddF) analysis of the type X collagen gene (COL10A1) and identification of a novel mutation (S671P) in a kindred with Schmid metaphyseal chondrodysplasia. Stratakis, C.A., Orban, Z., Burns, A.L., Vottero, A., Mitsiades, C.S., Marx, S.J., Abbassi, V., Chrousos, G.P. Biochem. Mol. Med. (1996) [Pubmed]
 
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