• 19997 Citations
  • 77 h-Index
1976 …2019

Research output per year

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Research Output

1997

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

Steroid 21-hydroxylase expression and activity in human lymphocytes

Zhou, Z., Agarwal, V. R., Dixit, N., White, P. & Speiser, P. W., Mar 14 1997, In : Molecular and Cellular Endocrinology. 127, 1, p. 11-18 8 p.

Research output: Contribution to journalArticle

24 Scopus citations

Variation in placental type 2 11β-hydroxysteroid dehydrogenase activity is not related to birth weight or placental weight

Rogerson, F. M., Kayes, K. M. & White, P. C., Apr 4 1997, In : Molecular and Cellular Endocrinology. 128, 1-2, p. 103-109 7 p.

Research output: Contribution to journalArticle

68 Scopus citations
1996
31 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

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

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., Oct 8 1996, In : Journal of Clinical Endocrinology and Metabolism. 81, 8, p. 2896-2901 6 p.

Research output: Contribution to journalArticle

101 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

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 1 1996, In : Human molecular genetics. 5, 12, p. 2039-2048 10 p.

Research output: Contribution to journalArticle

116 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
1995

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

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

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

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

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

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

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
Open Access
144 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 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

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

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

180 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

559 Scopus citations
44 Scopus citations
1994

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

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 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

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 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

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

Mutations in Steroid 21‐Hydroxylase (CYP21)

White, P. C., Tusie-Luna, M. T., New, M. I. & Speiser, P. W., 1994, In : Human mutation. 3, 4, p. 373-378 6 p.

Research output: Contribution to journalArticle

108 Scopus citations

NAD+-dependent isoform of 11β-hydroxysteroid dehydrogenase. Cloning and characterization of cDNA from sheep kidney

Agarwal, A. K., Mune, T., Monder, C. & White, P. C., Jan 1 1994, In : Journal of Biological Chemistry. 269, 42, p. 25959-25962 4 p.

Research output: Contribution to journalArticle

252 Scopus citations

Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by allele-specific hybridization and Southern blot

Speiser, P. W., White, P. C., Dupont, J., Zhu, D., Mercado, A. B. & New, M. I., Apr 1 1994, In : Human genetics. 93, 4, p. 424-428 5 p.

Research output: Contribution to journalArticle

49 Scopus citations

Steroid 11β-hydroxylase deficiency and related disorders

White, P. C. & Speiser, P. W., Jan 1 1994, In : Endocrinology and Metabolism Clinics of North America. 23, 2, p. 325-339 15 p.

Research output: Contribution to journalReview article

39 Scopus citations
1993

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

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

Genomic organization of the mouse B-lymphocyte activation antigen B7

Selvakumar, A., White, P. C. & Dupont, B., Jun 1 1993, In : Immunogenetics. 38, 4, p. 292-295 4 p.

Research output: Contribution to journalArticle

23 Scopus citations
19 Scopus citations

Mutations in the CYP11B1 gene causing congenital adrenal hyperplasia and hypertension cluster in exons 6, 7, and 8

Curnow, K. M., Slutsker, L., Vitek, J., Cole, T., Speiser, P. W., New, M. I., White, P. C. & Pascoe, L., Jan 1 1993, In : Proceedings of the National Academy of Sciences of the United States of America. 90, 10, p. 4552-4556 5 p.

Research output: Contribution to journalArticle

Open Access
170 Scopus citations

Transcripts originating in intron 1 of the HSD11 (11 β-hydroxysteroid dehydrogenase) gene encode a truncated polypeptide that is enzymatically inactive

Obeid, J., Curnow, K. M., Aisenberg, J. & White, P. C., Dec 1993, In : Molecular Endocrinology. 7, 2, p. 154-160 7 p.

Research output: Contribution to journalArticle

Open Access
34 Scopus citations
1992

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

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
464 Scopus citations

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

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

100 Scopus citations
89 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 1 1992, In : Immunogenetics. 36, 3, p. 175-181 7 p.

Research output: Contribution to journalArticle

35 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 1 1992, In : Human genetics. 88, 6, p. 647-648 2 p.

Research output: Contribution to journalArticle

32 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

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

Mutations in the human CYP11B2 (aldosterone synthase) gene causing corticosterone methyloxidase II deficiency

Pascoe, L., Curnow, K. M., Slutsker, L., Rösler, A. & White, P. C., Jun 15 1992, In : Proceedings of the National Academy of Sciences of the United States of America. 89, 11, p. 4996-5000 5 p.

Research output: Contribution to journalArticle

Open Access
158 Scopus citations