• 20084 Citations
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1976 …2020

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Article

Genetic diseases of steroid metabolism.

White, P. C., 1994, In : Vitamins and Hormones. 49, p. 131-195 65 p.

Research output: Contribution to journalArticle

42 Scopus citations

Genetic disorders affecting aldosterone synthesis and action

White, P. C., Jan 1 1996, In : Current Opinion in Endocrinology and Diabetes. 3, 3, p. 220-226 7 p.

Research output: Contribution to journalArticle

1 Scopus citations

Genetic disorders of steroid hormone synthesis and metabolism

New, M. I. & White, P. C., Jul 1995, In : Bailliere's Clinical Endocrinology and Metabolism. 9, 3, p. 525-554 30 p.

Research output: Contribution to journalArticle

37 Scopus citations

Genetic interaction among three genomic regions creates distinct contributions to early-and late-onset type 1 diabetes mellitus

Felner, E. I., Klitz, W., Ham, M., Lazaro, A. M., Stastny, P., Dupont, B. & White, P. C., Dec 2005, In : Pediatric Diabetes. 6, 4, p. 213-220 8 p.

Research output: Contribution to journalArticle

33 Scopus citations

Genomic organization and chromosomal location of the human gene encoding the B-lymphocyte activation antigen B7

Selvakumar, A., Mohanraj, B. K., Eddy, R. L., Shows, T. B., White, P. C. & Dupont, B., May 1992, In : Immunogenetics. 36, 3, p. 175-181 7 p.

Research output: Contribution to journalArticle

35 Scopus citations

Genomic organization of the mouse B-lymphocyte activation antigen B7

Selvakumar, A., White, P. C. & Dupont, B., Jun 1993, In : Immunogenetics. 38, 4, p. 292-295 4 p.

Research output: Contribution to journalArticle

23 Scopus citations

Genotype of Yupik Eskimos with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Speisere, P. W., New, M. I., Tannin, G. M., Pickering, D., Yang, S. Y. & White, P. C., Mar 1992, In : Human genetics. 88, 6, p. 647-648 2 p.

Research output: Contribution to journalArticle

32 Scopus citations

Genotype-phenotype correlations of mutations and polymorphisms in HSD11B2, the gene encoding the kidney isozyme of 11β-hydroxysteroid dehydrogenase

White, P. C., Agarwal, A. K., Nunez, B. S., Giacchetti, G., Mantero, F. & Stewart, P. M., Jan 1 2000, In : Endocrine Research. 26, 4, p. 771-780 10 p.

Research output: Contribution to journalArticle

25 Scopus citations
40 Scopus citations

Glucocorticoid-suppressible hyperaldosteronism: Effects of crossover site and parental origin of chimaeric gene on phenotypic expression

Jamieson, A., Slutsker, L., Inglis, G. C., Fraser, R., White, P. C. & Connell, J. M. C., Jan 1 1995, In : Clinical science. 88, 5, p. 563-570 8 p.

Research output: Contribution to journalArticle

48 Scopus citations

Glucocorticoid-suppressible hyperaldosteronism results from hybrid genes created by unequal crossovers between CYP11B1 and CYP11B2

Pascoe, L., Curnow, K. M., Slutsker, L., Connell, J. M. C., Speiser, P. W., New, M. I. & White, P. C., 1992, In : Proceedings of the National Academy of Sciences of the United States of America. 89, 17, p. 8327-8331 5 p.

Research output: Contribution to journalArticle

Open Access
215 Scopus citations

Graves' disease in children: long-term outcomes of medical therapy

Rabon, S., Burton, A. M. & White, P. C., Oct 1 2016, In : Clinical Endocrinology. 85, 4, p. 632-635 4 p.

Research output: Contribution to journalArticle

14 Scopus citations

Haplotype analysis of CYP11b2

White, P. C. & Slutsker, L., Jan 1 1995, In : Endocrine Research. 21, 1-2, p. 437-442 6 p.

Research output: Contribution to journalArticle

181 Scopus citations

Hexose-6-phosphate dehydrogenase confers oxo-reductase activity upon 11β-hydroxysteroid dehydrogenase type 1

Bujalska, I. J., Draper, N., Michailidou, Z., Tomlinson, J. W., White, P. C., Chapman, K. E., Walker, E. A. & Stewart, P. M., Jun 2005, In : Journal of molecular endocrinology. 34, 3, p. 675-684 10 p.

Research output: Contribution to journalArticle

143 Scopus citations

Hexose-6-phosphate dehydrogenase knock-out mice lack 11β- hydroxysteroid dehydrogenase type 1-mediated glucocorticoid generation

Lavery, G. G., Walker, E. A., Draper, N., Jeyasuria, P., Marcos, J., Shackleton, C. H. L., Parker, K. L., White, P. C. & Stewart, P. M., Mar 10 2006, In : Journal of Biological Chemistry. 281, 10, p. 6546-6551 6 p.

Research output: Contribution to journalArticle

161 Scopus citations
Open Access
196 Scopus citations

HSD11B2 CA-repeat and sodium balance

Mune, T., Morita, H., Takada, N., Yamamoto, Y., Isomura, Y., Suwa, T., Takeda, J., White, P. C. & Kaku, K., Jul 1 2013, In : Hypertension Research. 36, 7, p. 614-619 6 p.

Research output: Contribution to journalArticle

4 Scopus citations

Human hypertension caused by mutations in the kidney isozyme of 11β–hydroxysteroid dehydrogenase

Mune, T., Rogerson, F. M., Nikkilä, H., Agarwal, A. K. & White, P. C., Aug 1995, In : Nature genetics. 10, 4, p. 394-399 6 p.

Research output: Contribution to journalArticle

561 Scopus citations

Hypothyroidism in siblings due to a homozygous mutation of the TSH-β subunit gene

Felner, E. I., Dickson, B. A. & White, P. C., Jan 1 2004, In : Journal of Pediatric Endocrinology and Metabolism. 17, 4, p. 669-672 4 p.

Research output: Contribution to journalArticle

12 Scopus citations

Identification of non-amplifying CYP21 genes when using PCR-based diagnosis of 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH) affected pedigrees

Day, D. J., Speiser, P. W., Schulze, E., Bettendorf, M., Fitness, J., Barany, F. & White, P. C., Dec 1996, In : Human molecular genetics. 5, 12, p. 2039-2048 10 p.

Research output: Contribution to journalArticle

Open Access
117 Scopus citations

Immunohistochemical localization of cytochrome P-450C21 in human adrenal cortex and its relation to endocrine function

Sasano, H., White, P. C., New, M. I. & Sasano, N., Feb 1988, In : Human Pathology. 19, 2, p. 181-185 5 p.

Research output: Contribution to journalArticle

41 Scopus citations

Immunohistochemistry of cytochrome P-450 21-hydroxylase: Microscopic examination of the enzyme in the bovine adrenal cortex and kidney

Sasano, H., White, P. C., New, M. I. & Sasano, N., Jan 1988, In : Endocrinology. 122, 1, p. 291-295 5 p.

Research output: Contribution to journalArticle

19 Scopus citations

Impaired overnight counterregulatory hormone responses to spontaneous hypoglycemia in children with type 1 diabetes

Mauras, N., Chase, P. H., Fiallo-Scharer, R., Fisher, J. H., Tallant, B., Tsalikian, E., Tansey, M. J., Larson, L. F., Coffey, J., Wysocki, T., Mauras, N., Fox, L. A., Bird, K., Lofton, K. L., Buckingham, B. A., Wilson, D. M., Block, J. M., Clinton, P., Weinzimer, S. A., Tamborlane, W. V. & 22 others, Doyle, E. A., Sikes, K., Beck, R. W., Ruedy, K. J., Kollman, C., Xing, D., Kalajian, A., Stockdale, C. R., Steffes, M. W., Bucksa, J. M., Nowicki, M. L., Van Hale, C. A., Makky, V., Singh, R., Grave, G. D., Linder, B., Winer, K. K., Becker, D. M., Cox, C., Ryan, C. M., White, N. H. & White, P. C., Aug 2007, In : Pediatric Diabetes. 8, 4, p. 199-205 7 p.

Research output: Contribution to journalArticle

28 Scopus citations

Improved glycemic control in adolescents with type 1 diabetes mellitus who attend diabetes camp

Wang, Y. C. A., Stewart, S., Tuli, E. & White, P., Feb 1 2008, In : Pediatric Diabetes. 9, 1, p. 29-34 6 p.

Research output: Contribution to journalArticle

36 Scopus citations

Improving management of diabetic ketoacidosis in children

Felner, E. I. & White, P. C., 2001, In : Pediatrics. 108, 3, p. 735-740 6 p.

Research output: Contribution to journalArticle

64 Scopus citations

Individual differences and day-to-day fluctuations in perceived self-regulation associated with daily adherence in late adolescents with type 1 diabetes

Berg, C. A., Wiebe, D. J., Suchy, Y., Hughes, A. E., Anderson, J. H., Godbey, E. I., Butner, J., Tucker, C., Franchow, E. I., Pihlaskari, A. K., King, P. S., Murray, M. A. & White, P. C., 2014, In : Journal of pediatric psychology. 39, 9, p. 1038-1048 11 p.

Research output: Contribution to journalArticle

36 Scopus citations

Inherited forms of mineralocorticoid hypertension

White, P. C., Dec 1996, In : Hypertension. 28, 6, p. 927-936 10 p.

Research output: Contribution to journalArticle

72 Scopus citations

Institution of basal-bolus therapy at diagnosis for children with type 1 diabetes mellitus

Adhikari, S., Adams-Huet, B., Wang, Y. C. A., Marks, J. F. & White, P. C., Apr 2009, In : Pediatrics. 123, 4, p. e673-e678

Research output: Contribution to journalArticle

9 Scopus citations

Insulin-like growth factor-I and fibroblast growth factor, but not growth hormone, affect growth plate chondrocyte proliferation

Hutchison, M. R., Bassett, M. H. & White, P. C., Jul 2007, In : Endocrinology. 148, 7, p. 3122-3130 9 p.

Research output: Contribution to journalArticle

34 Scopus citations

Iowa Gambling Task Performance Prospectively Predicts Changes in Glycemic Control among Adolescents with Type 1 Diabetes

Suchy, Y., Queen, T. L., Huntbach, B., Wiebe, D. J., Turner, S. L., Butner, J., Kelly, C. S., White, P. C., Murray, M., Swinyard, M. & Berg, C. A., Mar 1 2017, In : Journal of the International Neuropsychological Society. 23, 3, p. 204-213 10 p.

Research output: Contribution to journalArticle

4 Scopus citations

Joint effects of an aldosterone synthase (CYP11B2) gene polymorphism and classic risk factors on risk of myocardial infarction

Hautanen, A., Toivanen, P., Mänttäri, M., Tenkanen, L., Kupari, M., Manninen, V., Kayes, K. M., Rosenfeld, S. & White, P. C., Nov 30 1999, In : Circulation. 100, 22, p. 2213-2218 6 p.

Research output: Contribution to journalArticle

Open Access
42 Scopus citations

Longer HSD11B2 CA-repeat in impaired glucose tolerance and type 2 diabetes

Mune, T., Suwa, T., Morita, H., Isomura, Y., Takada, N., Yamamoto, Y., Hayashi, M., Yamakita, N., Sasaki, A., Takeda, N., Takeda, J., White, P. C. & Kaku, K., Jun 7 2013, In : Endocrine Journal. 60, 5, p. 671-678 8 p.

Research output: Contribution to journalArticle

6 Scopus citations

Long-term consequences of childhood-onset congenital adrenal hyperplasia

White, P. C. & Speiser, P. W., Jan 1 2002, In : Best Practice and Research: Clinical Endocrinology and Metabolism. 16, 2, p. 273-288 16 p.

Research output: Contribution to journalArticle

24 Scopus citations
45 Scopus citations

Low morbidity and mortality in children with diabetic ketoacidosis treated with isotonic fluids

White, P. C. & Dickson, B. A., Sep 1 2013, In : Journal of Pediatrics. 163, 3, p. 761-766 6 p.

Research output: Contribution to journalArticle

21 Scopus citations

Maternal depressive symptoms predict adolescent healthcare utilization and charges in youth with type 1 diabetes (T1D)

Clayton, K. M., Stewart, S. M., Wiebe, D. J., McConnel, C. E., Hughes, C. W. & White, P. C., Sep 1 2013, In : Health Psychology. 32, 9, p. 1013-1022 10 p.

Research output: Contribution to journalArticle

11 Scopus citations

Molecular analysis of 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 1 1997, In : Steroids. 62, 1, p. 83-88 6 p.

Research output: Contribution to journalArticle

40 Scopus citations

Molecular biology of 11β-hydroxylase and 11β-hydroxysteroid dehydrogenase enzymes

White, P. C., Pascoe, L., Curnow, K. M., Tannin, G. & Rösler, A., Dec 1992, In : Journal of Steroid Biochemistry and Molecular Biology. 43, 8, p. 827-835 9 p.

Research output: Contribution to journalArticle

20 Scopus citations

Molecular cloning and expression of rat liver 3α-hydroxysteroid dehydrogenase

Cheng, K. C., White, P. C. & Qin, K. N., Jun 1 1991, In : Molecular Endocrinology. 5, 6, p. 823-828 6 p.

Research output: Contribution to journalArticle

Open Access
63 Scopus citations

Molecular cloning of an inducible serine esterase gene from human cytotoxic lymphocytes

Trapani, J. A., Klein, J. L., White, P. C. & Dupont, B., 1988, In : Proceedings of the National Academy of Sciences of the United States of America. 85, 18, p. 6924-6928 5 p.

Research output: Contribution to journalArticle

Open Access
83 Scopus citations

Molecular cloning of steroid 21-hydroxylase

White, P. C., Dupont, B. & New, M. I., 1984, In : Endocrine Research. 10, 3-4, p. 335-345 11 p.

Research output: Contribution to journalArticle

3 Scopus citations

Molecular Cloning of Steroid 21‐Hydroxylase

White, P. C., New, M. I. & Dupont, B., Nov 1985, In : Annals of the New York Academy of Sciences. 458, 1, p. 277-287 11 p.

Research output: Contribution to journalArticle

8 Scopus citations

Molecular Genetic Analysis of Nonclassic Steroid 21-Hydroxylase Deficiency Associated with HLA-B14,DR1

Speiser, P. W., New, M. I. & White, P. C., Jul 7 1988, In : New England Journal of Medicine. 319, 1, p. 19-23 5 p.

Research output: Contribution to journalArticle

166 Scopus citations

Molecular genetic analysis of nonclassic steroid 21 hydroxylase deficiency associated with hla b14 dri

Speiser, P. W., New, M. I. & White, P. C., 1988, In : Obstetrical and Gynecological Survey. 43, 11, p. 693-694 2 p.

Research output: Contribution to journalArticle

Molecular genetic prenatal diagnosis of congenital adrenalhyperplasia due to 21-hydroxylase deficiency by allele-specific hybridization

Speiser, P. W., White, P. C., Dupont, J., Zhu, D., Mercado, A. & New, M. I., Jan 1 1994, In : Recent progress in hormone research. 49, 1, p. 367-371 5 p.

Research output: Contribution to journalArticle

9 Scopus citations

Molecular linkage of the genes encoding adrenal steroid 21-hydroxylase to the S region of the murine major histocompatibility complex (MHC)

Chaplin, D., Parker, K., White, P. & Seidman, J., Jan 1 1985, In : Federation Proceedings. 44, 3, p. No. 2175

Research output: Contribution to journalArticle

2 Scopus citations

Molecular pathology of steroid 21-hydroxylase deficiency

Strachan, T. & White, P. C., 1991, In : Journal of Steroid Biochemistry and Molecular Biology. 40, 4-6, p. 537-543 7 p.

Research output: Contribution to journalArticle

9 Scopus citations

Mutants of 11-hydroxysteroid dehydrogenase (11-hsd2) with partial activity: Improved correlations between genotype and biochemical phenotype in apparent mineralocorticoid excess

Nunez, B. S., Rogerson, F. M., Mune, T., Igarashi, Y., Nakagawa, Y., Phillipov, G., Moudgil, A., Travis, L. B., Palermo, M., Shackleton, C. & White, P. C., Oct 1999, In : Hypertension. 34, 4, p. 638-642 5 p.

Research output: Contribution to journalArticle

Open Access
49 Scopus citations

Mutation in the CYP21B gene (Ile-172→Asn) causes steroid 21-hydroxylase deficiency

Amor, M., Parker, K. L., Globerman, H., New, M. I. & White, P. C., 1988, In : Proceedings of the National Academy of Sciences of the United States of America. 85, 5, p. 1600-1604 5 p.

Research output: Contribution to journalArticle

Open Access
199 Scopus citations