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Medicine

D-Index
102
Citations
37203
World Ranking
7682
National Ranking
4000

Research.com Recognitions

  • 1996 - E. Mead Johnson Award, Society for Pediatric Research

Overview

Perrin C. White is affiliated with The University of Texas Southwestern Medical Center in the United States. Their research primarily spans the fields of Medicine and Biochemistry, Genetics and Molecular Biology, with a focus on Endocrinology, Diabetes and Metabolism, Genetics, Molecular Biology, Surgery, and Clinical Biochemistry.

The scientist's work covers multiple main topics including Diabetes Management and Research, Diabetes and associated disorders, Sexual Differentiation and Disorders, Pancreatic function and diabetes, Adrenal Hormones and Disorders, Metabolism and Genetic Disorders, as well as Diabetes Treatment and Management.

Recent significant publications by Perrin C. White include:

  • Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management, 2021, Endocrine Reviews
  • Multicenter, Randomized Trial of a Bionic Pancreas in Type 1 Diabetes, 2022, New England Journal of Medicine
  • Positive Impact of the Bionic Pancreas on Diabetes Control in Youth 6-17 Years Old with Type 1 Diabetes: A Multicenter Randomized Trial, 2022, Diabetes Technology & Therapeutics
  • History of Adrenal Research: From Ancient Anatomy to Contemporary Molecular Biology, 2022, Endocrine Reviews
  • Impact of the COVID-19 pandemic on management of children and adolescents with Type 1 diabetes, 2022, BMC Pediatrics

Perrin C. White frequently publishes in venues such as:

  • Diabetes Care
  • The Journal of Clinical Endocrinology & Metabolism
  • Diabetes
  • Endocrine Reviews
  • Journal of the Endocrine Society

Collaborations are notable with several researchers including:

  • Soumya Adhikari
  • Phyllis Speiser
  • Richard J. Auchus
  • Andrew Muir
  • Abha Choudhary

Perrin C. White received the E. Mead Johnson Award from the Society for Pediatric Research in 1996.

Best Publications

  • Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

    Perrin C. White;Phyllis W. Speiser

  • Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline

    Phyllis W. Speiser;Ricardo Azziz;Laurence S. Baskin;Lucia Ghizzoni

  • Congenital adrenal hyperplasia

    Phyllis W. Speiser;Phyllis W. Speiser;Perrin C. White

  • Human hypertension caused by mutations in the kidney isozyme of 11β–hydroxysteroid dehydrogenase

    Tomoatsu Mune;Fraser M. Rogerson;Heli Nikkilä;Anil K. Agarwal

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

    Damien Chaussabel;Charles Quinn;Jing Shen;Pinakeen Patel

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

    Perrin C. White;Tomoatsu Mune;Tomoatsu Mune;Anil K. Agarwal

  • Structure of human steroid 21-hydroxylase genes

    Perrin C. White;Maria I. New;Bo Dupont

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

    Phyllis W. Speiser;Jakob Dupont;Deguang Zhu;Jorge Serrat

  • Characterization of two genes encoding human steroid 11 beta-hydroxylase (P-450(11) beta).

    E. Mornet;J. Dupont;A. Vitek;Perrin C White

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

    Speiser Pw;Arlt W;Auchus Rj;Baskin Ls

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

    Perrin C. White;Dario Grossberger;Barbara J. Onufer;David D. Chaplin

  • Cloning and expression of rat cDNA encoding corticosteroid 11 beta-dehydrogenase.

    Anil K Agarwal;C. Monder;B. Eckstein;Perrin C White

  • The human gene for 11 beta-hydroxysteroid dehydrogenase. Structure, tissue distribution, and chromosomal localization.

    Grace M. Tannin;Anil K. Agarwal;Carl Monder;Maria I. New

  • Chemical characterization of a neural cell adhesion molecule purified from embryonic brain membranes.

    S Hoffman;B C Sorkin;P C White;R Brackenbury

  • The Product of the CYP11B2 Gene Is Required for Aldosterone Biosynthesis in the Human Adrenal Cortex

    Kathleen M. Curnow;Maria Teresa Tusie-Luna;Leigh Pascoe;Rama Natarajan

  • Disorders of steroid 11β-hydroxylase isozymes

    Perrin C. White;Kathleen M. Curnow;Leigh Pascoe

  • Congenital adrenal hyperplasia. (1).

    Perrin C White;M. I. New;B. Dupont

  • Minireview: Steroidogenic Factor 1: Its Roles in Differentiation, Development, and Disease

    Bernard P. Schimmer;Perrin C. White

  • Associations Between Human Aldosterone Synthase (CYP11B2) Gene Polymorphisms and Left Ventricular Size, Mass, and Function

    Markku Kupari;Aarno Hautanen;Laura Lankinen;Pekka Koskinen

  • NAD(+)-dependent isoform of 11 beta-hydroxysteroid dehydrogenase. Cloning and characterization of cDNA from sheep kidney.

    Anil K. Agarwal;Tomoatsu Mune;Tomoatsu Mune;Carl Monder;Perrin C. White

Frequent Co-Authors

Maria I. New
Maria I. New Icahn School of Medicine at Mount Sinai
Bo Dupont
Bo Dupont Memorial Sloan Kettering Cancer Center
Deborah J. Wiebe
Deborah J. Wiebe University of Pennsylvania
Sunita M. Stewart
Sunita M. Stewart The University of Texas Southwestern Medical Center
Bo Dupont
Bo Dupont Kettering University
Paul M. Stewart
Paul M. Stewart University of Leeds
Walter L. Miller
Walter L. Miller University of California, San Francisco
Yana Suchy
Yana Suchy University of Utah
Cynthia A. Berg
Cynthia A. Berg University of Utah
Jonathan Butner
Jonathan Butner University of Utah

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