• 20084 Citations
  • 77 h-Index
1976 …2020

Research output per year

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Research Output

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

Endocrine hypertension

White, P. C., Jan 1 2013, Pediatric Hypertension: Third Edition. Humana Press Inc., p. 379-394 16 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

1 Scopus citations

Endocrine hypertension

White, P. C., Jan 1 2018, Pediatric Hypertension. Springer International Publishing, p. 517-537 21 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

Erratum: Congenital adrenal hyperplasia due to 21-hydroxylase deficiency (Endocrine Reviews (2000) 21 (245-291))

White, P. C. & Speiser, P. W., Dec 7 2000, In : Endocrine reviews. 21, 5, 1 p.

Research output: Contribution to journalComment/debate

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

Fertility in patients with congenital adrenal hyperplasia

Reichman, D. E., White, P. C., New, M. I. & Rosenwaks, Z., Feb 1 2014, In : Fertility and sterility. 101, 2, p. 301-309 9 p.

Research output: Contribution to journalReview article

40 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

Fluid Infusion Rates for Pediatric Diabetic Ketoacidosis

White, P. C., Sep 20 2018, In : The New England journal of medicine. 379, 12, p. 1182-1183 2 p.

Research output: Contribution to journalLetter

1 Scopus citations

Four is not more than two

Russell, D. W. & White, P. C., Jan 1 1995, In : American Journal of Human Genetics. 57, 5, p. 1002-1005 4 p.

Research output: Contribution to journalEditorial

6 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 adrenal zonation and regulation of aldosterone biosynthesis

Rainey, W. E. & White, P., Jan 1 1998, In : Current Opinion in Endocrinology and Diabetes. 5, 3, p. 175-182 8 p.

Research output: Contribution to journalReview article

7 Scopus citations

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

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

Genetics of steroid 21-hydroxylase deficiency.

White, P. C., 1987, In : Recent progress in hormone research. 43, p. 305-336 32 p.

Research output: Contribution to journalReview article

19 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 (H6PD) and corticosteroid metabolism

White, P. C., Rogoff, D., McMillan, D. R. & Lavery, G. G., Feb 1 2007, In : Molecular and Cellular Endocrinology. 265-266, SUPPL., p. 89-92 4 p.

Research output: Contribution to journalReview article

30 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