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1. Pernasetti, F; Toledo, SPA; Vasilyev, VV; Hayashida, CY; Cogan, JD; Ferrari, C; Lourenco, DM; Mellon, PL
   Impaired adrenocorticotropin-adrenal axis in combined pituitary hormone deficiency caused by a two-base pair deletion (301-302delAG) in the Prophet of Pit-1 gene
   JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
   
   F. Pernasetti et al., "Impaired adrenocorticotropin-adrenal axis in combined pituitary hormone deficiency caused by a two-base pair deletion (301-302delAG) in the Prophet of Pit-1 gene", J CLIN END, 85(1), 2000, pp. 390-397
2. Cogan, JD; Phillips, JA
   Molecular defects in the growth hormone axis
   MOLECULAR AND CELLULAR PEDIATRIC ENDOCRINOLOGY
   
   J.D. Cogan e J.A. Phillips, "Molecular defects in the growth hormone axis", CONT ENDOC, 10, 1999, pp. 23-38
3. WU W; COGAN JD; PFAFFLE RW; DASEN JS; FRISCH H; OCONNELL SM; FLYNN SE; BROWN MR; MULLIS PE; PARKS JS; PHILLIPS JA; ROSENFELD MG
   MUTATIONS IN PROP1 CAUSE FAMILIAL COMBINED PITUITARY-HORMONE DEFICIENCY
   Nature genetics
   
   W. Wu et al., "MUTATIONS IN PROP1 CAUSE FAMILIAL COMBINED PITUITARY-HORMONE DEFICIENCY", Nature genetics, 18(2), 1998, pp. 147-149
4. ARNHOLD IJP; OSORIO MGF; OLIVEIRA SB; ESTEFAN V; KAMIJO T; KRISHNAMANI MRS; COGAN JD; PHILLIPS JA; MENDONCA BB
   CLINICAL AND MOLECULAR CHARACTERIZATION OF BRAZILIAN PATIENTS WITH GROWTH-HORMONE GENE DELETIONS
   Brazilian journal of medical and biological research
   
   I.J.P. Arnhold et al., "CLINICAL AND MOLECULAR CHARACTERIZATION OF BRAZILIAN PATIENTS WITH GROWTH-HORMONE GENE DELETIONS", Brazilian journal of medical and biological research, 31(4), 1998, pp. 491-497
5. COGAN JD; WU W; PHILLIPS JA; ARNHOLD IJP; AGAPITO A; FOFANOVA OV; OSORIO MGF; BIRCAN I; MORENO A; MENDONCA BB
   THE PROP1 2-BASE PAIR DELETION IS A COMMON-CAUSE OF COMBINED PITUITARY-HORMONE DEFICIENCY
   The Journal of clinical endocrinology and metabolism
   
   J.D. Cogan et al., "THE PROP1 2-BASE PAIR DELETION IS A COMMON-CAUSE OF COMBINED PITUITARY-HORMONE DEFICIENCY", The Journal of clinical endocrinology and metabolism, 83(9), 1998, pp. 3346-3349
6. COGAN JD; PRINCE MA; LEKHAKULA S; BUNDEY S; FUTRAKUL A; MCCARTHY EMS; PHILLIPS JA
   A NOVEL MECHANISM OF ABERRANT PRE-MESSENGER-RNA SPLICING IN HUMANS
   Human molecular genetics
   
   J.D. Cogan et al., "A NOVEL MECHANISM OF ABERRANT PRE-MESSENGER-RNA SPLICING IN HUMANS", Human molecular genetics, 6(6), 1997, pp. 909-912
7. MIYATA I; COGAN JD; PRINCE MA; KAMIJO T; OGAWA M; PHILLIPS JA
   DETECTION OF GROWTH-HORMONE GENE DEFECTS BY DIDEOXY FINGERPRINTING (DDF)
   Endocrine journal
   
   I. Miyata et al., "DETECTION OF GROWTH-HORMONE GENE DEFECTS BY DIDEOXY FINGERPRINTING (DDF)", Endocrine journal, 44(1), 1997, pp. 149-154
8. WAGNER JK; EBLE A; COGAN JD; PRINCE MA; PHILLIPS JA; MULLIS PE
   ALLELIC VARIATIONS IN THE HUMAN GROWTH HORMONE-1 GENE PROMOTER OF GROWTH HORMONE-DEFICIENT PATIENTS AND NORMAL CONTROLS
   European journal of endocrinology
   
   J.K. Wagner et al., "ALLELIC VARIATIONS IN THE HUMAN GROWTH HORMONE-1 GENE PROMOTER OF GROWTH HORMONE-DEFICIENT PATIENTS AND NORMAL CONTROLS", European journal of endocrinology, 137(5), 1997, pp. 474-481
9. RASKIN S; COGAN JD; SUMMAR ML; MORENO A; KRISHNAMANI MRS; PHILLIPS JA
   GENETIC-MAPPING OF THE HUMAN PITUITARY-SPECIFIC TRANSCRIPTIONAL FACTOR GENE AND ITS ANALYSIS IN FAMILIAL PANHYPOPITUITARY DWARFISM
   Human genetics
   
   S. Raskin et al., "GENETIC-MAPPING OF THE HUMAN PITUITARY-SPECIFIC TRANSCRIPTIONAL FACTOR GENE AND ITS ANALYSIS IN FAMILIAL PANHYPOPITUITARY DWARFISM", Human genetics, 98(6), 1996, pp. 703-705
10. HAMID R; COGAN JD; JONES SN; TIBBETTS C
    PHENOTYPIC DETERMINANTS OF ADENOVIRUS E1A GENE AUTOREGULATION - VARIABLE REGION BETWEEN CONSERVED CODING DOMAIN-2 AND DOMAIN-3
    Virology
    
    R. Hamid et al., "PHENOTYPIC DETERMINANTS OF ADENOVIRUS E1A GENE AUTOREGULATION - VARIABLE REGION BETWEEN CONSERVED CODING DOMAIN-2 AND DOMAIN-3", Virology, 213(2), 1995, pp. 666-670
11. COGAN JD; RAMEL B; LEHTO M; PHILLIPS J; PRINCE M; BLIZZARD RM; DERAVEL TJL; BRAMMERT M; GROOP L
    A RECURRING DOMINANT-NEGATIVE MUTATION CAUSES AUTOSOMAL-DOMINANT GROWTH-HORMONE DEFICIENCY - A CLINICAL RESEARCH-CENTER STUDY
    The Journal of clinical endocrinology and metabolism
    
    J.D. Cogan et al., "A RECURRING DOMINANT-NEGATIVE MUTATION CAUSES AUTOSOMAL-DOMINANT GROWTH-HORMONE DEFICIENCY - A CLINICAL RESEARCH-CENTER STUDY", The Journal of clinical endocrinology and metabolism, 80(12), 1995, pp. 3591-3595
12. COGAN JD; PHILLIPS JA; SCHENKMAN SS; MILNER RDG; SAKATI N
    FAMILIAL GROWTH-HORMONE DEFICIENCY - A MODEL OF DOMINANT AND RECESSIVE MUTATIONS AFFECTING A MONOMERIC PROTEIN
    The Journal of clinical endocrinology and metabolism
    
    J.D. Cogan et al., "FAMILIAL GROWTH-HORMONE DEFICIENCY - A MODEL OF DOMINANT AND RECESSIVE MUTATIONS AFFECTING A MONOMERIC PROTEIN", The Journal of clinical endocrinology and metabolism, 79(5), 1994, pp. 1261-1265
13. PHILLIPS JA; COGAN JD
    GENETIC-BASIS OF ENDOCRINE DISEASE-6 - MOLECULAR-BASIS OF FAMILIAL HUMAN GROWTH-HORMONE DEFICIENCY
    The Journal of clinical endocrinology and metabolism
    
    J.A. Phillips e J.D. Cogan, "GENETIC-BASIS OF ENDOCRINE DISEASE-6 - MOLECULAR-BASIS OF FAMILIAL HUMAN GROWTH-HORMONE DEFICIENCY", The Journal of clinical endocrinology and metabolism, 78(1), 1994, pp. 11-16
14. COGAN JD; PHILLIPS JA; SAKATI N; FRISCH H; SCHOBER E; MILNER RDG
    HETEROGENEOUS GROWTH-HORMONE (GH) GENE-MUTATIONS IN FAMILIAL GH DEFICIENCY
    The Journal of clinical endocrinology and metabolism
    
    J.D. Cogan et al., "HETEROGENEOUS GROWTH-HORMONE (GH) GENE-MUTATIONS IN FAMILIAL GH DEFICIENCY", The Journal of clinical endocrinology and metabolism, 76(5), 1993, pp. 1224-1228
15. PHILLIPS JA; COGAN JD; MILLENDAVIS S; MILNER RDG; SAKATI NA; SCHENKMAN SS; BUNDEY SE
    MOLECULAR-BASIS OF AUTOSOMAL RECESSIVE AND AUTOSOMAL-DOMINANT INHERITANCE OF FAMILIAL GH DEFICIENCY
    American journal of human genetics
    
    J.A. Phillips et al., "MOLECULAR-BASIS OF AUTOSOMAL RECESSIVE AND AUTOSOMAL-DOMINANT INHERITANCE OF FAMILIAL GH DEFICIENCY", American journal of human genetics, 53(3), 1993, pp. 6-6