• 19997 Citations
  • 77 h-Index
1976 …2019

Research output per year

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Research Output

11Beta‐Hydroxysteroid Dehydrogenase Messenger Ribonucleic Acid Expression, Bioactivity and Immunoreactivity in Rat Cerebellum

Moisan, M. P., Seckl, J. R., Brett, L. P., Monder, C., Agarwal, A. K., White, P. C. & Edwards, C. R. W., Dec 1990, In : Journal of Neuroendocrinology. 2, 6, p. 853-858 6 p.

Research output: Contribution to journalArticle

39 Scopus citations

11-Ketotestosterone Is the Dominant Circulating Bioactive Androgen during Normal and Premature Adrenarche

Rege, J., Turcu, A. F., Kasa-Vubu, J. Z., Lerario, A. M., Auchus, G. C., Auchus, R. J., Smith, J. M., White, P. C. & Rainey, W. E., 2018, In : Journal of Clinical Endocrinology and Metabolism. 103, 12, p. 4589-4598 10 p.

Research output: Contribution to journalArticle

21 Scopus citations
45 Scopus citations

11β-Hydroxysteroid Dehydrogenase

Monder, C. & White, P. C., Jan 1 1993, In : Vitamins and Hormones. 47, C, p. 187-271 85 p.

Research output: Contribution to journalArticle

208 Scopus citations

11β-Hydroxysteroid dehydrogenase and its role in the syndrome of apparent mineralocorticoid excess

White, P. C., Mune, T., Rogerson, F. M., Kayes, K. M. & Agarwal, A. K., Jan 1997, In : Pediatric Research. 41, 1, p. 25-29 5 p.

Research output: Contribution to journalArticle

Open Access
37 Scopus citations

11β-Hydroxysteroid dehydrogenase and the syndrome of apparent mineralocorticoid excess

White, P. C., Mune, T. & Agarwal, A. K., Feb 24 1997, In : Endocrine reviews. 18, 1, p. 135-156 22 p.

Research output: Contribution to journalArticle

524 Scopus citations

6 Molecular genetics of congenital adrenal hyperplasia

White, P. C. & New, M. I., Nov 1988, In : Bailliere's Clinical Endocrinology and Metabolism. 2, 4, p. 941-965 25 p.

Research output: Contribution to journalArticle

17 Scopus citations

Abnormalities of aldosterone synthesis and action in children

White, P. C., Jan 1 1997, In : Current opinion in pediatrics. 9, 4, p. 424-430 7 p.

Research output: Contribution to journalShort survey

22 Scopus citations

Abnormalities of glucose homeostasis and the hypothalamic-pituitary-adrenal axis in mice lacking hexose-6-phosphate dehydrogenase

Rogoff, D., Ryder, J. W., Black, K., Yan, Z., Burgess, S. C., McMillan, D. R. & White, P. C., Oct 2007, In : Endocrinology. 148, 10, p. 5072-5080 9 p.

Research output: Contribution to journalArticle

34 Scopus citations

Adolescent Information Management and Parental Knowledge in Non-Latino White and Latino Youth Managing Type 1 Diabetes

Tucker, C., Wiebe, D. J., Main, A., Lee, A. G. & White, P. C., Mar 1 2018, In : Journal of Pediatric Psychology. 43, 2, p. 207-217 11 p.

Research output: Contribution to journalArticle

1 Scopus citations

Adrenal 21‐Hydroxylase Cytochrome P‐450 Genes within the MHC Class III Region

White, P. C., New, M. I. & Dupont, B., Oct 1985, In : Immunological Reviews. 87, 1, p. 123-150 28 p.

Research output: Contribution to journalArticle

25 Scopus citations

Adrenarche

Oberfield, S. E. & White, P. C., Mar 1 2009, In : Reviews in Endocrine and Metabolic Disorders. 10, 1 SPEC. ISS., p. 1-2 2 p.

Research output: Contribution to journalEditorial

4 Scopus citations

Age-dependent increases in adrenal cytochrome b5 and serum 5-androstenediol-3-sulfate

Rege, J., Karashima, S., Lerario, A. M., Smith, J. M., Auchus, R. J., Kasa-Vubu, J. Z., Sasano, H., Nakamura, Y., White, P. C. & Rainey, W. E., Dec 2016, In : Journal of Clinical Endocrinology and Metabolism. 101, 12, p. 4585-4593 9 p.

Research output: Contribution to journalArticle

17 Scopus citations

Aldosterone: Direct effects on and production by the heart

White, P. C., Jun 1 2003, In : Journal of Clinical Endocrinology and Metabolism. 88, 6, p. 2376-2383 8 p.

Research output: Contribution to journalReview article

Open Access
72 Scopus citations

Aldosterone synthase (CYP11B2) polymorphisms and cardiovascular function

White, P. C., Hautanen, A. & Kupari, M., Jan 1 1998, In : Endocrine Research. 24, 3-4, p. 797-804 8 p.

Research output: Contribution to journalArticle

15 Scopus citations

Aldosterone synthase (CYP11B2) polymorphisms and cardiovascular function

White, P. C., Hautanen, A. & Kupari, M., Apr 1 1999, In : Journal of Steroid Biochemistry and Molecular Biology. 69, 1-6, p. 409-412 4 p.

Research output: Contribution to journalArticle

27 Scopus citations

Aldosterone synthase deficiency and related disorders

White, P. C., Mar 31 2004, In : Molecular and Cellular Endocrinology. 217, 1-2, p. 81-87 7 p.

Research output: Contribution to journalArticle

66 Scopus citations

Aldosterone Synthase Promoter Polymorphism and Cardiovascular Phenotypes in a Large, Multiethnic Population-Based Study

Byrd, J. B., Auchus, R. J. & White, P. C., Oct 1 2015, In : Journal of Investigative Medicine. 63, 7, p. 862-866 5 p.

Research output: Contribution to journalArticle

1 Scopus citations

Aldosterone Synthesis in Salt-Wasting Congenital Adrenal Hyperplasia with Complete Absence of Adrenal 21-Hydroxylase

Speiser, P. W., Agdere, L., Ueshiba, H., White, P. C. & New, M. I., Jan 17 1991, In : New England Journal of Medicine. 324, 3, p. 145-149 5 p.

Research output: Contribution to journalArticle

67 Scopus citations

Alterations of Cortisol Metabolism in Human Disorders

White, P. C., May 29 2018, (Accepted/In press) In : Hormone Research in Paediatrics. p. 1-11 11 p.

Research output: Contribution to journalArticle

4 Scopus citations

Alternatively spliced human type 1 angiotensin II receptor mRNAs are translated at different efficiencies and encode two receptor isoforms

Curnow, K. M., Pascoe, L., Davies, E., White, P. C., Corvol, P. & Clauser, E., Sep 1 1995, In : Molecular Endocrinology. 9, 9, p. 1250-1262 13 p.

Research output: Contribution to journalArticle

Open Access
69 Scopus citations

A Modular Analysis Framework for Blood Genomics Studies: Application to Systemic Lupus Erythematosus

Chaussabel, D., Quinn, C., Shen, J., Patel, P., Glaser, C., Baldwin, N., Stichweh, D., Blankenship, D., Li, L., Munagala, I., Bennett, L., Allantaz, F., Mejias, A., Ardura, M., Kaizer, E., Monnet, L., Allman, W., Randall, H., Johnson, D., Lanier, A. & 9 others, Punaro, M., Wittkowski, K. M., White, P., Fay, J., Klintmalm, G., Ramilo, O., Palucka, A. K., Banchereau, J. & Pascual, V., Jul 18 2008, In : Immunity. 29, 1, p. 150-164 15 p.

Research output: Contribution to journalArticle

409 Scopus citations

A mutation (pro-30 to leu) in CYP21 represents a potential nonclassic steroid 21-hydroxylase deficiency allele

Tusie-Luna, M. T., Speiser, P. W., Dumic, M., New, M. I. & White, P. C., May 1 1991, In : Molecular Endocrinology. 5, 5, p. 685-692 8 p.

Research output: Contribution to journalArticle

Open Access
155 Scopus citations

A mutation in CYP11B1 (Arg-448 → His) associated with steroid 11β-hydroxylase deficiency in Jews of Moroccan origin

White, P. C., Dupont, J., New, M. I., Leiberman, E., Hochberg, Z. & Rösler, A., Jan 1 1991, In : Journal of Clinical Investigation. 87, 5, p. 1664-1667 4 p.

Research output: Contribution to journalArticle

Open Access
190 Scopus citations

Analysis of mutations causing steroid 21-hydroxylase deficiency

White, P. C., Jan 1 1989, In : Endocrine Research. 15, 1-2, p. 239-256 18 p.

Research output: Contribution to journalArticle

22 Scopus citations

Analysis of Steroid 21-Hydroxylase Gene in Five Unrelated Japanese Patients with 21-Hydroxylase Deficiency

Nakura, J., Miki, T., Fukuchi, K. I., Shimizu, K., Nose, O., Takai, S., White, P. C., Honjo, T. & Kumahara, Y., Jan 1 1987, In : Endocrinologia Japonica. 34, 3, p. 373-379 7 p.

Research output: Contribution to journalArticle

Open Access

Analysis of the human gene encoding the kidney isozyme of 11β-hydroxysteroid dehydrogenase

Agarwal, A. K., Rogerson, F. M., Mune, T. & White, P. C., Dec 1995, In : Journal of Steroid Biochemistry and Molecular Biology. 55, 5-6, p. 473-479 7 p.

Research output: Contribution to journalArticle

24 Scopus citations
31 Scopus citations

Analysis of the very large G-protein coupled receptor gene (Vlgr1/Mass1/USH2C) in zebrafish

Gibert, Y., McMillan, D. R., Kayes-Wandover, K., Meyer, A., Begemann, G. & White, P. C., Jul 4 2005, In : Gene. 353, 2, p. 200-206 7 p.

Research output: Contribution to journalArticle

12 Scopus citations

Angiotensin II and potassium regulate human CYP11B2 transcription through common cis-elements

Clyne, C. D., Zhang, Y., Slutsker, L., Mathis, J. M., White, P. C. & Rainey, W. E., 1997, In : Molecular Endocrinology. 11, 5, p. 638-649 12 p.

Research output: Contribution to journalArticle

Open Access
172 Scopus citations

An Inherited Defect in Aldosterone Biosynthesis Caused by a Mutation in or near the Gene for Steroid 11-Hydroxylase

Globerman, H., Rosler, A., Theodor, R., New, M. I. & White, P. C., Nov 3 1988, In : New England Journal of Medicine. 319, 18, p. 1193-1197 5 p.

Research output: Contribution to journalArticle

45 Scopus citations

A novel gene constitutively expressed in human lymphoid cells is inducible with interferon-γ in myeloid cells

Trapani, J. A., Browne, K. A., Dawson, M. J., Ramsay, R. G., Eddy, R. L., Shows, T. B., White, P. C. & Dupont, B., Sep 1 1992, In : Immunogenetics. 36, 6, p. 369-376 8 p.

Research output: Contribution to journalArticle

85 Scopus citations
2 Scopus citations

Apparent cortisone reductase deficiency: A functional defect in 11β-hydroxysteroid dehydrogenase type 1

Jamieson, A., Wallace, A. M., Andrew, R., Nunez, B. S., Walker, B. R., Fraser, R., White, P. C. & Connell, J. M. C., 1999, In : Journal of Clinical Endocrinology and Metabolism. 84, 10, p. 3570-3574 5 p.

Research output: Contribution to journalArticle

Open Access
98 Scopus citations

Apparent mineralocorticoid excess: Genotype is correlated with biochemical phenotype

Mune, T. & White, P. C., Jan 1 1996, In : Hypertension. 27, 6, p. 1193-1199 7 p.

Research output: Contribution to journalArticle

72 Scopus citations

A randomized controlled trial comparing motivational interviewing in education to structured diabetes education in teens with type 1 diabetes

Wang, Y. C. A., Stewart, S. M., Mackenzie, M., Nakonezny, P. A., Edwards, D. & White, P. C., Aug 1 2010, In : Diabetes care. 33, 8, p. 1741-1743 3 p.

Research output: Contribution to journalArticle

33 Scopus citations

A role for the NGFI-B family in adrenal zonation and adrenocortical disease

Bassett, M. H., White, P. C. & Rainey, W. E., Dec 1 2004, In : Endocrine Research. 30, 4, p. 567-574 8 p.

Research output: Contribution to journalArticle

40 Scopus citations

Association of Lys173Arg polymorphism with CYP11B2 expression in normal adrenal glands and aldosterone-producing adenomas

Tanahashi, H., Mune, T., Takahashi, Y., Isaji, M., Suwa, T., Morita, H., Yamakita, N., Yasuda, K., Deguchi, T., White, P. C. & Takeda, J., Nov 1 2005, In : Journal of Clinical Endocrinology and Metabolism. 90, 11, p. 6226-6231 6 p.

Research output: Contribution to journalArticle

24 Scopus citations

Associations between aldosterone synthase gene polymorphism and the adrenocortical function in males

Hautanena, A., Lankinen, L., Kupari, M., Jänne, O. A., Adlercreutz, H., Nikkilä, H. & White, P. C., Jul 22 1998, In : Journal of Internal Medicine. 244, 1, p. 11-18 8 p.

Research output: Contribution to journalArticle

86 Scopus citations

Associations between human aldosterone synthase (CYP11B2) gene polymorphisms and left ventricular size, mass, and function

Kupari, M., Hautanen, A., Lankinen, L., Koskinen, P., Virolainen, J., Nikkila, H. & White, P. C., Feb 17 1998, In : Circulation. 97, 6, p. 569-575 7 p.

Research output: Contribution to journalArticle

Open Access
202 Scopus citations

Associations between restriction fragment length polymorphisms detected with a probe for human 21-hydroxylase (21-OH) and two clinical forms of 21-OH deficiency

Mornet, E., Couillin, P., Kutten, F., Raux, M. C., White, P. C., Cohen, D., Boué, A. & Dausset, J., Dec 1 1986, In : Human genetics. 74, 4, p. 402-408 7 p.

Research output: Contribution to journalArticle

19 Scopus citations

Associations of parent-adolescent relationship quality with type 1 diabetes management and depressive symptoms in Latino and Caucasian youth

Main, A., Wiebe, D. J., Croom, A. R., Sardone, K., Godbey, E., Tucker, C. & White, P. C., 2014, In : Journal of pediatric psychology. 39, 10, p. 1104-1114 11 p.

Research output: Contribution to journalArticle

16 Scopus citations

Autosomal recessive familial neurohypophyseal diabetes insipidus: Onset in early infancy

Libdeh, A. A., Levy-Khademi, F., Abdulhadi-Atwan, M., Bosin, E., Korner, M., White, P. C. & Zangen, D. H., Feb 1 2010, In : European Journal of Endocrinology. 162, 2, p. 221-226 6 p.

Research output: Contribution to journalArticle

29 Scopus citations

Autosomal recessive familial neurohypophyseal diabetes insipidus with continued secretion of mutant weakly active vasopressin

Willcutts, M. D., Felner, E. & White, P. C., Jul 27 1999, In : Human molecular genetics. 8, 7, p. 1303-1307 5 p.

Research output: Contribution to journalArticle

72 Scopus citations

Baroreflex sensitivity and variants of the renin angiotensin system genes

Ylitalo, A., Juhani Airaksinen, K. E., Hautanen, A., Kupari, M., Carson, M., Virolainen, J., Savolainen, M., Kauma, H., Antero Kesäniemi, Y., White, P. C. & Huikuri, H. V., Jan 2000, In : Journal of the American College of Cardiology. 35, 1, p. 194-200 7 p.

Research output: Contribution to journalArticle

58 Scopus citations
36 Scopus citations

Bovine Steroid 21-Hydroxylase: Regulation of Biosynthesis

John, M. E., Okamura, T., Dee, A., Adler, B., John, M. C., White, P. C., Simpson, E. R. & Waterman, M. R., May 1986, In : Biochemistry. 25, 10, p. 2846-2853 8 p.

Research output: Contribution to journalArticle

49 Scopus citations

Calcium regulates human CYP11B2 transcription

Clyne, C. D., White, P. C. & Rainey, W. E., Jan 1 1996, In : Endocrine Research. 22, 4, p. 485-492 8 p.

Research output: Contribution to journalArticle

31 Scopus citations

Camp-based multi-component intervention for families of young children with type 1 diabetes: A pilot and feasibility study

Gupta, O. T., Mackenzie, M., Burris, A., Jenkins, B. B., Collins, N., Shade, M., Santa-Sosa, E., Stewart, S. M. & White, P. C., Jan 1 2018, (Accepted/In press) In : Pediatric Diabetes.

Research output: Contribution to journalArticle

3 Scopus citations

CA-repeat polymorphism in intron 1 of HSD11B2: Effects on gene expression and salt sensitivity

Agarwal, A. K., Giacchetti, G., Lavery, G., Nikkila, H., Palermo, M., Ricketts, M., McTernan, C., Bianchi, G., Manunta, P., Strazzullo, P., Mantero, F., White, P. C. & Stewart, P. M., 2000, In : Hypertension. 36, 2, p. 187-194 8 p.

Research output: Contribution to journalArticle

Open Access
123 Scopus citations