• 20084 Citations
  • 77 h-Index
1976 …2020

Research output per year

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Research Output

Case 3: Hypoglycemia in an Infant with Cholestasis

Patni, N., Collins, K. & White, P., Sep 1 2019, In : Pediatrics in review. 40, 9, p. 488-490 3 p.

Research output: Contribution to journalArticle

Characterization of 11 β-hydroxysteroid dehydrogenase gene expression: Identification of multiple unique forms of messenger ribonucleic acid in the rat kidney

Krozowski, Z., Stuchbery, S., White, P., Monder, C. & Funder, J. W., Dec 1990, In : Endocrinology. 127, 6, p. 3009-3013 5 p.

Research output: Contribution to journalArticle

93 Scopus citations

Characterization of frequent deletions causing steroid 21-hydroxylase deficiency

White, P. C., Vitek, A., Dupont, B. & New, M. I., 1988, In : Proceedings of the National Academy of Sciences of the United States of America. 85, 12, p. 4436-4440 5 p.

Research output: Contribution to journalArticle

Open Access
199 Scopus citations

Characterization of two genes encoding human steroid 11β-hydroxylase (P-450(11β))

Mornet, E., Dupont, J., Vitek, A. & White, P. C., Dec 1 1989, In : Journal of Biological Chemistry. 264, 35, p. 20961-20967 7 p.

Research output: Contribution to journalArticle

418 Scopus citations

Classical and late-onset forms of congenital adrenal hyperplasia caused by 21-OH deficiency reveal different alterations in the C4/21-OH gene region

Boehm, B. O., Rosak, C., Boehm, T. L. J., Kuehnl, P., White, P. C. & Schöffling, K., Dec 1 1986, In : Molecular Biology and Medicine. 3, 5, p. 437-448 12 p.

Research output: Contribution to journalArticle

2 Scopus citations

Clinical, biochemical and genetic features of five extended kindred's with glucocorticoid-suppressible hyperaldosteronism

Jamieson, A., Slutsker, L., Inglis, G., Campbell, M., Fraser, R., White, P. & Connell, J., Jan 1 1995, In : Endocrine Research. 21, 1-2, p. 463-469 7 p.

Research output: Contribution to journalArticle

6 Scopus citations

Clinical and genetic characterization of nonclassic 21-hydroxylase deficiency

Speiser, P. W., New, M. I. & White, P. C., Jan 1 1989, In : Endocrine Research. 15, 1-2, p. 257-276 20 p.

Research output: Contribution to journalArticle

5 Scopus citations

Clinical case seminar: Type 1 aldosterone synthase deficiency presenting in a middle-aged man

Kayes-Wandover, K. M., Lee Schindler, R. E., Taylor, H. C. & White, P. C., Apr 30 2001, In : Journal of Clinical Endocrinology and Metabolism. 86, 3, p. 1008-1012 5 p.

Research output: Contribution to journalArticle

26 Scopus citations
Open Access
60 Scopus citations
2 Scopus citations

Cloning and expression of rat cDNA encoding corticosteroid 11β-dehydrogenase

Agarwal, A. K., Monder, C., Eckstein, B. & White, P. C., 1989, In : Journal of Biological Chemistry. 264, 32, p. 18939-18943 5 p.

Research output: Contribution to journalArticle

431 Scopus citations

Cloning of cDNA encoding an NAD+-dependent isoform of 11βhydroxysteroid dehydrogenase in sheep kidney

Agarwal, A. K., Mune, T., Monder, C. & White, P. C., Jan 1 1995, In : Endocrine Research. 21, 1-2, p. 389-397 9 p.

Research output: Contribution to journalArticle

20 Scopus citations

Cloning of cDNA encoding steroid 11 beta-hydroxylase (P450c11).

Chua, S. C., Szabo, P., Vitek, A., Grzeschik, K. H., John, M. & White, P. C., Oct 1987, In : Proceedings of the National Academy of Sciences of the United States of America. 84, 20, p. 7193-7197 5 p.

Research output: Contribution to journalArticle

Open Access
180 Scopus citations

Comparison of fingerstick hemoglobin A1c levels assayed by DCA 2000 with the DCCT/EDIC central laboratory assay: Results of a Diabetes Research in Children Network (DirecNet) Study

Chase, H. P., 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., Doyle, E. A. & 18 others, Sikes, K., Beck, R. W., Ruedy, K. J., Kollman, C., Xing, D., Silvester, C. R., Becker, D. M., Cox, C., Ryan, C. M., White, N. H., White, P. C., Steffes, M. W., Bucksa, J. M., Nowicki, M. L., Van Hale, C. A., Grave, G. D., Linder, B. & Winer, K. K., Mar 2005, In : Pediatric Diabetes. 6, 1, p. 13-16 4 p.

Research output: Contribution to journalArticle

101 Scopus citations

Congenital adrenal hyperplasia

Speiser, P. W. & White, P. C., Aug 21 2003, In : New England Journal of Medicine. 349, 8, p. 776-788 13 p.

Research output: Contribution to journalReview article

619 Scopus citations

Congenital Adrenal Hyperplasia

White, P. C., New, M. I. & Dupont, B., Jun 18 1987, In : New England Journal of Medicine. 316, 25, p. 1580-1586 7 p.

Research output: Contribution to journalReview article

194 Scopus citations

Congenital Adrenal Hyperplasia

Miller, W. L., White, P. C., New, M. & Dupont, B., Nov 26 1987, In : New England Journal of Medicine. 317, 22, p. 1413-1415 3 p.

Research output: Contribution to journalLetter

7 Scopus citations

Congenital Adrenal Hyperplasia

White, P. C., New, M. I. & Dupont, B., Jun 11 1987, In : New England Journal of Medicine. 316, 24, p. 1519-1524 6 p.

Research output: Contribution to journalReview article

161 Scopus citations

Congenital adrenal hyperplasia due to 21 hydroxylase deficiency: From birth to adulthood

White, P. & Bachega, T. S. S., Oct 9 2012, In : Seminars in reproductive medicine. 30, 5, p. 400-409 10 p.

Research output: Contribution to journalArticle

32 Scopus citations

Congenital adrenal hyperplasia due to 21-hydroxylase deficiency

White, P. C. & Speiser, P. W., Dec 1 2000, In : Endocrine reviews. 21, 3, p. 245-291 47 p.

Research output: Contribution to journalReview article

973 Scopus citations

Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: An Endocrine Society clinical practice guideline

Speiser, P. W., Azziz, R., Baskin, L. S., Ghizzoni, L., Hensle, T. W., Merke, D. P., Meyer-Bahlburg, H. F. L., Miller, W. L., Montori, V. M., Oberfield, S. E., Ritzen, M. & White, P. C., Sep 2010, In : Journal of Clinical Endocrinology and Metabolism. 95, 9, p. 4133-4160 28 p.

Research output: Contribution to journalReview article

703 Scopus citations

Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency

Speiser, P. W. & White, P. C., 1998, In : Clinical Endocrinology. 49, 4, p. 411-417 7 p.

Research output: Contribution to journalReview article

23 Scopus citations

Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: An endocrine society clinical practice guideline (The Journal of Clinical Endocrinology & Metabolism (2010) 95 (4133-4160))

Speiser, P. W., Azziz, R., Baskin, L. S., Ghizzoni, L., Hensle, T. W., Merke, D. P., Meyer-Bahlburg, H. F. L., Miller, W. L., Montori, V. M., Oberfield, S. E., Ritzen, M. & White, P. C., Nov 1 2010, In : Journal of Clinical Endocrinology and Metabolism. 95, 11, 1 p.

Research output: Contribution to journalComment/debate

1 Scopus citations

Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: An endocrine society* clinical practice guideline

Speiser, P. W., Arlt, W., Auchus, R. J., Baskin, L. S., Conway, G. S., Merke, D. P., Meyer-Bahlburg, H. F. L., Miller, W. L., Murad, M. H., Oberfield, S. E. & White, P. C., 2018, In : Journal of Clinical Endocrinology and Metabolism. 103, 11, p. 4043-4088 46 p.

Research output: Contribution to journalArticle

150 Scopus citations

Congenital adrenal hyperplasia owing to 11β-hydroxylase deficiency

White, P. C., Jul 29 2011, Hormonal and Genetic Basis of Sexual Differentiation Disorders and Hot Topics in Endocrinology: Proceedings of the 2nd World Conference. New, M. & Simpson, J. L. (eds.). p. 7-8 2 p. (Advances in Experimental Medicine and Biology; vol. 707).

Research output: Chapter in Book/Report/Conference proceedingChapter

3 Scopus citations

Congenital adrenal hyperplasias

White, P. C., Jan 1 2001, In : Best Practice and Research: Clinical Endocrinology and Metabolism. 15, 1, p. 17-41 25 p.

Research output: Contribution to journalArticle

22 Scopus citations

Congenital hyperreninemic hypoaldosteronism unlinked to the aldosterone synthase (CYP11B2) gene

Kayes-Wandover, K. M., Tannin, G. M., Shulman, D., Peled, D., Jones, K. L., Karaviti, L. & White, P. C., 2001, In : Journal of Clinical Endocrinology and Metabolism. 86, 11, p. 5379-5382 4 p.

Research output: Contribution to journalArticle

Open Access
17 Scopus citations

Contribution of hexose-6-phosphate dehydrogenase to NADPH content and redox environment in the endoplasmic reticulum

Rogoff, D., Black, K., Mcmillan, D. R. & White, P. C., Apr 1 2010, In : Redox Report. 15, 2, p. 64-70 7 p.

Research output: Contribution to journalArticle

9 Scopus citations

Correlation between left ventricular mass and urinary sodium excretion in specific genotypes of CYP11B2

Isaji, M., Mune, T., Takada, N., Yamamoto, Y., Suwa, T., Morita, H., Takeda, J. & White, P. C., Jun 2005, In : Journal of hypertension. 23, 6, p. 1149-1157 9 p.

Research output: Contribution to journalArticle

28 Scopus citations

CYP11B1 mutations causing congenital adrenal hyperplasia due to 11β- hydroxylase deficiency

Geley, S., Kapelari, K., Jöhrer, K., Peter, M., Glatzl, J., Vierhapper, H., Schwarz, S., Helmberg, A., Sippell, W. G., White, P. C. & Kofler, R., 1996, In : Journal of Clinical Endocrinology and Metabolism. 81, 8, p. 2896-2901 6 p.

Research output: Contribution to journalArticle

101 Scopus citations

CYP11B1 mutations causing non-classic adrenal hyperplasia due to 11β- hydroxylase deficiency

Joehrer, K., Geley, S., Strasser-Wozak, E. M. C., Azziz, R., Wollmann, H. A., Schmitt, K., Kofler, R. & White, P. C., Oct 1 1997, In : Human molecular genetics. 6, 11, p. 1829-1834 6 p.

Research output: Contribution to journalArticle

93 Scopus citations

Defects in cortisol metabolism causing low-renin hypertension

White, P. C., Jan 1 1991, In : Endocrine Research. 17, 1-2, p. 85-107 23 p.

Research output: Contribution to journalArticle

8 Scopus citations

Defects in the HSD11 gene encoding 11β-hydroxysteroid dehydrogenase are not found in patients with apparent mineralocorticoid excess or 11-oxoreductase deficiency

Nikkilä, H., Tannin, G. M., New, M. I., Taylor, N. F., Kalaitzoglou, G., Monder, C. & White, P. C., Jun 1 1994, In : Pediatric Nephrology. 8, 3, 1 p.

Research output: Contribution to journalArticle

Defects in the HSD11 gene encoding 11 β-hydroxysteroid dehydrogenase are not found in patients with apparent mineralocorticoid excess or 11-oxoreductase deficiency

Nikkilä, H., Tannin, G. M., New, M. I., Taylor, N. F., Kalaitzoglou, G., Monder, C. & White, P. C., Sep 1993, In : Journal of Clinical Endocrinology and Metabolism. 77, 3, p. 687-691 5 p.

Research output: Contribution to journalArticle

100 Scopus citations

Deletion of hexose-6-phosphate dehydrogenase activates the unfolded protein response pathway and induces skeletal myopathy

Lavery, G. G., Walker, E. A., Turan, N., Rogoff, D., Ryder, J. W., Shelton, J. M., Richardson, J. A., Falciani, F., White, P. C., Stewart, P. M., Parker, K. L. & McMillan, D. R., Mar 28 2008, In : Journal of Biological Chemistry. 283, 13, p. 8453-8461 9 p.

Research output: Contribution to journalArticle

61 Scopus citations

Depression and diabetes in children and adolescents

Stewart, S. M., Rao, U. & White, P., Oct 2005, In : Current opinion in pediatrics. 17, 5, p. 626-631 6 p.

Research output: Contribution to journalReview article

18 Scopus citations

Depressive symptoms predict hospitalization for adolescents with type 1 diabetes mellitus

Stewart, S. M., Rao, U., Emslie, G. J., Klein, D. & White, P. C., May 2005, In : Pediatrics. 115, 5, p. 1315-1319 5 p.

Research output: Contribution to journalArticle

104 Scopus citations

Detection of steroid 21-hydroxylase alleles using gene-specific PCR and a multiplexed ligation detection reaction

Day, D. J., Speiser, P. W., White, P. C. & Barany, F., Sep 1 1995, In : Genomics. 29, 1, p. 152-162 11 p.

Research output: Contribution to journalArticle

105 Scopus citations

Determination of functional effects of mutations in the steroid 21-hydroxylase gene (CYP21) using recombinant vaccinia virus

Tusie-Luna, M. T., Traktman, P. & White, P. C., 1990, In : Journal of Biological Chemistry. 265, 34, p. 20916-20922 7 p.

Research output: Contribution to journalArticle

190 Scopus citations

Developmental trajectories of metabolic control among white, black, and Hispanic youth with type 1 diabetes

Wang, J. T., Wiebe, D. J. & White, P. C., Oct 1 2011, In : Journal of Pediatrics. 159, 4, p. 571-576 6 p.

Research output: Contribution to journalArticle

25 Scopus citations

Differential regulation of aldosterone synthase and 11β-hydroxylase transcription by steroidogenic factor-1

Bassett, M. H., Zhang, Y., Clyne, C., White, P. C. & Rainey, W. E., 2002, In : Journal of molecular endocrinology. 28, 2, p. 125-135 11 p.

Research output: Contribution to journalReview article

126 Scopus citations

Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Speiser, P. W., Dupont, J., Zhu, D., Serrat, J., Buegeleisen, M., Tusie-Luna, M. T., Lesser, M., New, M. I. & White, P. C., 1992, In : Journal of Clinical Investigation. 90, 2, p. 584-595 12 p.

Research output: Contribution to journalArticle

Open Access
467 Scopus citations

Disorders of aldosterone biosynthesis and action

White, P. C., Jul 28 1994, In : New England Journal of Medicine. 331, 4, p. 250-258 9 p.

Research output: Contribution to journalReview article

162 Scopus citations

Disorders of Sexual Development

White, P. C., Jul 1 2011, Goldman's Cecil Medicine: Twenty Fourth Edition. Elsevier Inc., Vol. 2. p. 1511-1519 9 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

Disorders of steroid 11β-hydroxylase isozymes

White, P. C. & Pascoe, L., Aug 1992, In : Trends in Endocrinology and Metabolism. 3, 6, p. 229-234 6 p.

Research output: Contribution to journalReview article

8 Scopus citations

Disorders of Steroid 1lβ-Hydroxylase Isozymes*

White, P. C., Curnow, K. M. & Pascoe, L., Aug 1994, In : Endocrine reviews. 15, 4, p. 421-438 18 p.

Research output: Contribution to journalArticle

275 Scopus citations

Distribution of deletions and seven point mutations on CYP21B genes in three clinical forms of steroid 21-hydroxylase deficiency

Mornet, E., Crété, P., Kuttenn, F., Raux-Demay, M. C., Boué, J., White, P. C. & Boué, A., Feb 4 1991, In : American Journal of Human Genetics. 48, 1, p. 79-88 10 p.

Research output: Contribution to journalArticle

127 Scopus citations

DNA Polymerase Epsilon Deficiency Causes IMAGe Syndrome with Variable Immunodeficiency

SGP Consortium, Dec 6 2018, In : American Journal of Human Genetics. 103, 6, p. 1038-1044 7 p.

Research output: Contribution to journalArticle

12 Scopus citations

Editorial: Polymorphisms in CYP11B genes and 11-hydroxylase activity

White, P. C. & Rainey, W. E., Feb 2005, In : Journal of Clinical Endocrinology and Metabolism. 90, 2, p. 1252-1255 4 p.

Research output: Contribution to journalEditorial

33 Scopus citations