White, Perrin C.

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., et al. (2010) · The Journal of Clinical Endocrinology & Metabolism

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 1,468

Congenital adrenal hyperplasia due to 21-hydroxylase deficiency*

White, P. C., & Speiser, P. W. (2000) · Endocrine Reviews

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 1,432

Congenital adrenal hyperplasia

Speiser, P. W., & White, P. C. (2003) · New England Journal of Medicine

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 1,405

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., et al. (2018) · The Journal of Clinical Endocrinology & Metabolism

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 1,234

A Modular Analysis Framework for Blood Genomics Studies: Application to Systemic Lupus Erythematosus

Chaussabel, D., Quinn, C., Shen, J., Patel, P., Glaser, C., Baldwin, N., Stichweh, D., Blankenship, D., Li, L., Munagala, I., et al. (2008) · Immunity

Gene expression and cancer classificationSystemic Lupus Erythematosus Research

Cited by 649

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. (1995) · Nature Genetics

Hormonal Regulation and HypertensionRenin-Angiotensin System Studies

Cited by 619

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) · Journal of Clinical Investigation

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 572

Structure of human steroid 21-hydroxylase genes.

White, P. C., New, M. I., & Dupont, B. (1986) · Proceedings of the National Academy of Sciences

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 569

Congenital Adrenal Hyperplasia—Current Insights in Pathophysiology, Diagnostics, and Management

Claahsen - van der Grinten, H. L., Speiser, P. W., Ahmed, S. F., Arlt, W., Auchus, R. J., Falhammar, H., Flück, C. E., Guasti, L., Huebner, A., Kortmann, B. B. M., et al. (2022) · Endocrine Reviews

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 556

11β-Hydroxysteroid Dehydrogenase and the Syndrome of Apparent Mineralocorticoid Excess*

White, P. C., Mune, T., & Agarwal, A. K. (1997) · Endocrine Reviews

Hormonal Regulation and HypertensionAdrenal Hormones and Disorders

Cited by 517

Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man

White, P. C., Grossberger, D., Onufer, B. J., Chaplin, D. D., New, M. I., Dupont, B., & Strominger, J. L. (1985) · Proceedings of the National Academy of Sciences

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 490

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

Agarwal, A. K., Monder, C., Eckstein, B., & White, P. C. (1989) · Journal of Biological Chemistry

Hormonal Regulation and HypertensionAdrenal Hormones and Disorders

Cited by 455

Characterization of Two Genes Encoding Human Steroid 11β-Hydroxylase (P-45011β)

Mornet, E., Dupont, J., Vitek, A., & White, P. C. (1989) · Journal of Biological Chemistry

Hormonal Regulation and HypertensionAdrenal Hormones and Disorders

Cited by 405

The product of the CYP11B2 gene is required for aldosterone biosynthesis in the human adrenal cortex

Curnow, K. M., Tusie-Luna, M.-T., Pascoe, L., Natarajan, R., Gu, J.-L., Nadler, J. L., & White, P. C. (1991) · Molecular Endocrinology

Hormonal Regulation and HypertensionAdrenal Hormones and Disorders

Cited by 362

HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation.

White, P. C., New, M. I., & Dupont, B. (1984) · Proceedings of the National Academy of Sciences

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 292

Mutations in the genes encoding 11β-hydroxysteroid dehydrogenase type 1 and hexose-6-phosphate dehydrogenase interact to cause cortisone reductase deficiency

Draper, N., Walker, E. A., Bujalska, I. J., Tomlinson, J. W., Chalder, S. M., Arlt, W., Lavery, G. G., Bedendo, O., Ray, D. W., Laing, I., et al. (2003) · Nature Genetics

Adrenal Hormones and DisordersSexual Differentiation and Disorders

Cited by 285

Disorders of Steroid 11β-Hydroxylase Isozymes*

WHITE, P. C., CURNOW, K. M., & PASCOE, L. (1994) · Endocrine Reviews

Hormonal Regulation and HypertensionAdrenal Hormones and Disorders

Cited by 271

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., Speiser, P. W., New, M. I., & White, P. C. (1992) · Proceedings of the National Academy of Sciences

Hormonal Regulation and HypertensionRenin-Angiotensin System Studies

Cited by 271

Minireview: steroidogenic factor 1: its roles in differentiation, development, and disease

Schimmer, B. P., & White, P. C. (2010) · Molecular Endocrinology

Adrenal Hormones and DisordersSexual Differentiation and Disorders

Cited by 268

A mutation in CYP11B1 (Arg-448----His) associated with steroid 11 beta-hydroxylase deficiency in Jews of Moroccan origin.

White, P. C., Dupont, J., New, M. I., Leiberman, E., Hochberg, Z., & Rösler, A. (1991) · Journal of Clinical Investigation

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 267

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) · Journal of Biological Chemistry

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 254

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) · Proceedings of the National Academy of Sciences

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 251

Neonatal screening for congenital adrenal hyperplasia

White, P. C. (2009) · Nature Reviews Endocrinology

Sexual Differentiation and DisordersMetabolism and Genetic Disorders

Cited by 240

Characterization of frequent deletions causing steroid 21-hydroxylase deficiency

White, P. C., Vitek, A., Dupont, B., & New, M. I. (1988) · Proceedings of the National Academy of Sciences

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 229