Faculty Appointments
Research Professor of Pediatrics
Education
Ph.D., Biochemistry, Vanderbilt University, Nashville, TennesseeA.B., Transylvania University, Lexington, Kentucky
Office Address
DD-2205 MCN
TN
TN
Publications
Cogan JD, Vnencak-Jones CL, Phillips JA, Lane KB, Wheeler LA, Robbins IM, Garrison G, Hedges LK, Loyd JE. Gross BMPR2 gene rearrangements constitute a new cause for primary pulmonary hypertension. Genet. Med. 2005 Mar; 7(3): 169-74. PMID: 15775752, PII: 00125817-200503000-00003, DOI: 10.109701.GIM.0000156525.09595.E9, ISSN: 1098-3600.
Cogan JD, Wu W, Phillips JA, Arnhold IJ, Agapito A, Fofanova OV, Osorio MG, Bircan I, Moreno A, Mendonca BB. The PROP1 2-base pair deletion is a common cause of combined pituitary hormone deficiency. J. Clin. Endocrinol. Metab. 1998 Sep; 83(9): 3346-9. PMID: 9745452, DOI: 10.1210/jcem.83.9.5142, ISSN: 0021-972X.
Cogan JD, Phillips JA. Growth disorders caused by genetic defects in the growth hormone pathway. Adv Pediatr. 1998; 45: 337-61. PMID: 9742308, ISSN: 0065-3101.
Cogan JD, Prince MA, Lekhakula S, Bundey S, Futrakul A, McCarthy EM, Phillips JA. A novel mechanism of aberrant pre-mRNA splicing in humans. Hum. Mol. Genet. 1997 Jun; 6(6): 909-12. PMID: 9175738, PII: dda120, ISSN: 0964-6906.
Miyata I, Cogan JD, Prince MA, Kamijo T, Ogawa M, Phillips JA. Detection of growth hormone gene defects by dideoxy fingerprinting (ddF). Endocr. J. 1997 Feb; 44(1): 149-54. PMID: 9152628, ISSN: 0918-8959.
Raskin S, Cogan JD, Summar ML, Moreno A, Krishnamani MR, Phillips JA. Genetic mapping of the human pituitary-specific transcriptional factor gene and its analysis in familial panhypopituitary dwarfism. Hum. Genet. 1996 Dec; 98(6): 703-5. PMID: 8931705, ISSN: 0340-6717.
Cogan JD, Ramel B, Lehto M, Phillips J, Prince M, Blizzard RM, de Ravel TJ, Brammert M, Groop L. A recurring dominant negative mutation causes autosomal dominant growth hormone deficiency--a clinical research center study. J. Clin. Endocrinol. Metab. 1995 Dec; 80(12): 3591-5. PMID: 8530604, DOI: 10.1210/jcem.80.12.8530604, ISSN: 0021-972X.
Hamid R, Cogan JD, Jones SN, Tibbetts C. Phenotypic determinants of adenovirus E1A gene autoregulation: variable region between conserved coding domains 2 and 3. Virology. 1995 Nov 11/10/1995; 213(2): 666-70. PMID: 7491791, PII: S0042-6822(85)70039-6, DOI: 10.1006/viro.1995.0039, ISSN: 0042-6822.
Cogan JD, Phillips JA, Schenkman SS, Milner RD, Sakati N. Familial growth hormone deficiency: a model of dominant and recessive mutations affecting a monomeric protein. J. Clin. Endocrinol. Metab. 1994 Nov; 79(5): 1261-5. PMID: 7962317, DOI: 10.1210/jcem.79.5.7962317, ISSN: 0021-972X.
Phillips JA, Cogan JD. Genetic basis of endocrine disease. 6. Molecular basis of familial human growth hormone deficiency. J. Clin. Endocrinol. Metab. 1994 Jan; 78(1): 11-6. PMID: 8288694, DOI: 10.1210/jcem.78.1.8288694, ISSN: 0021-972X.
Cogan JD, Phillips JA, Sakati N, Frisch H, Schober E, Milner RD. Heterogeneous growth hormone (GH) gene mutations in familial GH deficiency. J. Clin. Endocrinol. Metab. 1993 May; 76(5): 1224-8. PMID: 8496314, DOI: 10.1210/jcem.76.5.8496314, ISSN: 0021-972X.
Cogan JD, Jones SN, Hall RK, Tibbetts C. Functional diversity of E1A gene autoregulation among human adenoviruses. J. Virol. 1992 Jun; 66(6): 3833-45. PMID: 1533882, PMCID: PMC241169, ISSN: 0022-538X.
Cogan JD, Wu W, Phillips JA, Arnhold IJ, Agapito A, Fofanova OV, Osorio MG, Bircan I, Moreno A, Mendonca BB. The PROP1 2-base pair deletion is a common cause of combined pituitary hormone deficiency. J. Clin. Endocrinol. Metab. 1998 Sep; 83(9): 3346-9. PMID: 9745452, DOI: 10.1210/jcem.83.9.5142, ISSN: 0021-972X.
Cogan JD, Phillips JA. Growth disorders caused by genetic defects in the growth hormone pathway. Adv Pediatr. 1998; 45: 337-61. PMID: 9742308, ISSN: 0065-3101.
Cogan JD, Prince MA, Lekhakula S, Bundey S, Futrakul A, McCarthy EM, Phillips JA. A novel mechanism of aberrant pre-mRNA splicing in humans. Hum. Mol. Genet. 1997 Jun; 6(6): 909-12. PMID: 9175738, PII: dda120, ISSN: 0964-6906.
Miyata I, Cogan JD, Prince MA, Kamijo T, Ogawa M, Phillips JA. Detection of growth hormone gene defects by dideoxy fingerprinting (ddF). Endocr. J. 1997 Feb; 44(1): 149-54. PMID: 9152628, ISSN: 0918-8959.
Raskin S, Cogan JD, Summar ML, Moreno A, Krishnamani MR, Phillips JA. Genetic mapping of the human pituitary-specific transcriptional factor gene and its analysis in familial panhypopituitary dwarfism. Hum. Genet. 1996 Dec; 98(6): 703-5. PMID: 8931705, ISSN: 0340-6717.
Cogan JD, Ramel B, Lehto M, Phillips J, Prince M, Blizzard RM, de Ravel TJ, Brammert M, Groop L. A recurring dominant negative mutation causes autosomal dominant growth hormone deficiency--a clinical research center study. J. Clin. Endocrinol. Metab. 1995 Dec; 80(12): 3591-5. PMID: 8530604, DOI: 10.1210/jcem.80.12.8530604, ISSN: 0021-972X.
Hamid R, Cogan JD, Jones SN, Tibbetts C. Phenotypic determinants of adenovirus E1A gene autoregulation: variable region between conserved coding domains 2 and 3. Virology. 1995 Nov 11/10/1995; 213(2): 666-70. PMID: 7491791, PII: S0042-6822(85)70039-6, DOI: 10.1006/viro.1995.0039, ISSN: 0042-6822.
Cogan JD, Phillips JA, Schenkman SS, Milner RD, Sakati N. Familial growth hormone deficiency: a model of dominant and recessive mutations affecting a monomeric protein. J. Clin. Endocrinol. Metab. 1994 Nov; 79(5): 1261-5. PMID: 7962317, DOI: 10.1210/jcem.79.5.7962317, ISSN: 0021-972X.
Phillips JA, Cogan JD. Genetic basis of endocrine disease. 6. Molecular basis of familial human growth hormone deficiency. J. Clin. Endocrinol. Metab. 1994 Jan; 78(1): 11-6. PMID: 8288694, DOI: 10.1210/jcem.78.1.8288694, ISSN: 0021-972X.
Cogan JD, Phillips JA, Sakati N, Frisch H, Schober E, Milner RD. Heterogeneous growth hormone (GH) gene mutations in familial GH deficiency. J. Clin. Endocrinol. Metab. 1993 May; 76(5): 1224-8. PMID: 8496314, DOI: 10.1210/jcem.76.5.8496314, ISSN: 0021-972X.
Cogan JD, Jones SN, Hall RK, Tibbetts C. Functional diversity of E1A gene autoregulation among human adenoviruses. J. Virol. 1992 Jun; 66(6): 3833-45. PMID: 1533882, PMCID: PMC241169, ISSN: 0022-538X.