• 20084 Citations
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1976 …2020

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Article

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 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 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 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

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

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 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

Effects of residential summer camp on body mass index and body composition in type 1 diabetes

Oden, J. D., Franklin, B., Fernandez, E., Adhikari, S. & White, P. C., Jun 1 2018, In : Pediatric Diabetes. 19, 4, p. 782-787 6 p.

Research output: Contribution to journalArticle

Elevated expression of luteinizing hormone receptor in aldosterone- producing adenomas

Saner-Amigh, K., Mayhew, B. A., Mantero, F., Schiavi, F., White, P. C., Rao, C. V. & Rainey, W. E., Mar 2006, In : Journal of Clinical Endocrinology and Metabolism. 91, 3, p. 1136-1142 7 p.

Research output: Contribution to journalArticle

74 Scopus citations

Executive function predicting longitudinal change in type 1 diabetes management during the transition to emerging adulthood

Berg, C. A., Wiebe, D. J., Suchy, Y., Turner, S. L., Butner, J., Munion, A., Lansing, A. H., White, P. C. & Murray, M., Nov 1 2018, In : Diabetes care. 41, 11, p. 2281-2288 8 p.

Research output: Contribution to journalArticle

12 Scopus citations

Expression of 11β-hydroxysteroid dehydrogenase using recombinant vaccinia virus

Agarwal, A. K., Tusie-Luna, M. T., Monder, C. & White, P. C., Dec 1990, In : Molecular Endocrinology. 4, 12, p. 1827-1832 6 p.

Research output: Contribution to journalArticle

Open Access
162 Scopus citations

Expression of human kidney 11β-hydroxysteroid dehydrogenase (11-HSD2) in bacteria

Nunez, B. S., Mune, T. & White, P. C., Feb 24 1999, In : Biochemical and Biophysical Research Communications. 255, 3, p. 652-656 5 p.

Research output: Contribution to journalArticle

5 Scopus citations

Expression profiles for steroidogenic enzymes in adrenocortical disease

Bassett, M. H., Mayhew, B., Rehman, K., White, P. C., Mantero, F., Arnaldi, G., Stewart, P. M., Bujalska, I. & Rainey, W. E., Sep 2005, In : Journal of Clinical Endocrinology and Metabolism. 90, 9, p. 5446-5455 10 p.

Research output: Contribution to journalArticle

91 Scopus citations

First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency)

Speiser, P. W., Laforgia, N., Kato, K., Pareira, J., Khan, R., Yang, S. Y., Whorwood, C., White, P. C., Elias, S., Schriock, E., Schriock, E., Simpson, J. L., Taslimi, M., Najjar, J., May, S., Mills, G., Crawford, C. & New, M. I., Oct 1990, In : Obstetrical and Gynecological Survey. 45, 10, p. 707-709 3 p.

Research output: Contribution to journalArticle

First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency)

Speiser, P. W., Laforgia, N., Kato, K., Pareira, J., Khan, R., Yang, S. Y., Whorwood, C., White, P. C., Elias, S., Schriock, E., Schriock, E., Simpson, J. L., Taslimi, M., Najjar, J., May, S., Mills, G., Crawford, C. & New, M. I., Apr 1990, In : Journal of Clinical Endocrinology and Metabolism. 70, 4, p. 838-848 11 p.

Research output: Contribution to journalArticle

104 Scopus citations

Frequency deletion and duplication of the steroid 21-hydroxylase genes

Werkmeister, J. W., New, M. I., Dupont, B. & White, P. C., 1986, In : American Journal of Human Genetics. 39, 4, p. 461-469 9 p.

Research output: Contribution to journalArticle

95 Scopus citations

Frequent deletion and duplication of the steroid 21-hydroxylase genes

Werkmeister, J. W., New, M. I., Dupont, B. O. & White, P. C., 1987, In : Obstetrical and Gynecological Survey. 42, 9, p. 572-573 2 p.

Research output: Contribution to journalArticle

Functional analysis of four CYP21 mutations from Spanish patients with congenital adrenal hyperplasia

Nunez, B. S., Lobato, M. N., White, P. C. & Meseguer, A., Sep 7 1999, In : Biochemical and Biophysical Research Communications. 262, 3, p. 635-637 3 p.

Research output: Contribution to journalArticle

13 Scopus citations

Functional studies of 11β-hydroxysteroid dehydrogenase

White, P. C., Mune, T. & Agarwal, A. K., Jan 1995, In : Steroids. 60, 1, p. 65-68 4 p.

Research output: Contribution to journalArticle

7 Scopus citations

Gene conversion in salt-losing congenital adrenal hyperplasia with absent complement C4B protein

Donohoue, P. A., van Dop, C., McLean, R. H., White, P. C., Jospe, N. & Migeon, C. J., May 1986, In : Journal of Clinical Endocrinology and Metabolism. 62, 5, p. 995-1002 8 p.

Research output: Contribution to journalArticle

96 Scopus citations
Open Access
144 Scopus citations

Gene expression in peripheral blood mononuclear cells from children with diabetes

Kaizer, E. C., Glaser, C. L., Chaussabel, D., Banchereau, J., Pascual, V. & White, P. C., Sep 2007, In : Journal of Clinical Endocrinology and Metabolism. 92, 9, p. 3705-3711 7 p.

Research output: Contribution to journalArticle

134 Scopus citations

Gene structure and chromosomal localization of the human HSD11K gene encoding the kidney (Type 2) isozyme of 11β-hydroxysteroid dehydrogenase

Agarwal, A. K., Rogerson, F. M., Mune, T. & White, P. C., Sep 1 1995, In : Genomics. 29, 1, p. 195-199 5 p.

Research output: Contribution to journalArticle

106 Scopus citations

Genetic analysis of 11β-hydroxysteroid dehydrogenase

White, P. C., Obeid, J., Agarwal, A. K., Tannin, G. M. & Nikkila, H., Feb 1994, In : Steroids. 59, 2, p. 111-115 5 p.

Research output: Contribution to journalArticle

13 Scopus citations

Genetic analysis of the human type-1 angiotensin II receptor

Curnow, K. M., Pascoe, L. & White, P. C., Jul 1 1992, In : Molecular Endocrinology. 6, 7, p. 1113-1118 6 p.

Research output: Contribution to journalArticle

101 Scopus citations
90 Scopus citations