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Medicine

D-Index
74
Citations
23844
World Ranking
19331
National Ranking
1744

Overview

Simon H. S. Pearce is affiliated with Newcastle University in the United Kingdom. Their research activities primarily focus on the field of medicine, with a significant concentration in endocrinology, diabetes, and metabolism. Additional subfields include genetics, pathology and forensic medicine, molecular biology, and immunology.

They have explored a variety of topics related to endocrine disorders and treatments. Key topics addressed in their work are:

  • Thyroid Disorders and Treatments
  • Adrenal Hormones and Disorders
  • Hormonal Regulation and Hypertension
  • Pituitary Gland Disorders and Treatments
  • Thyroid Cancer Diagnosis and Treatment
  • Ophthalmology and Eye Disorders
  • Diabetes and associated disorders

Among their recent papers are:

  • The 2021 European Group on Graves' orbitopathy (EUGOGO) clinical practice guidelines for the medical management of Graves' orbitopathy, 2021, European Journal of Endocrinology
  • Adrenal insufficiency, 2021, The Lancet
  • Primary hypothyroidism and quality of life, 2022, Nature Reviews Endocrinology
  • ENDOCRINOLOGY IN THE TIME OF COVID-19: Management of adrenal insufficiency, 2020, European Journal of Endocrinology
  • New Therapeutic Horizons for Graves' Hyperthyroidism, 2020, Endocrine Reviews

The scientist frequently publishes in several academic venues. These include:

  • Endocrine Abstracts
  • European Journal of Endocrinology
  • The Journal of Clinical Endocrinology & Metabolism
  • European Thyroid Journal
  • Clinical Endocrinology

Frequent collaborators within their research network include:

  • Anna L. Mitchell
  • Salman Razvi
  • Laura Lane
  • Catherine Napier
  • Petros Perros

Best Publications

  • Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

    Paul R Burton;David G Clayton;Lon R Cardon;Nick Craddock

  • 2013 ETA Guideline: Management of Subclinical Hypothyroidism

    Simon H.S. Pearce;Georg Brabant;Leonidas H. Duntas;Fabio Monzani

  • Consensus statement of the European Group on Graves' orbitopathy (EUGOGO) on management of GO.

    Luigi Bartalena;Lelio Baldeschi;Alison Dickinson;Anja Eckstein

  • A common molecular basis for three inherited kidney stone diseases

    Sarah E. Lloyd;Simon H. S. Pearce;Simon E. Fisher;Klaus Steinmeyer

  • Diagnosis and management of vitamin D deficiency

    Simon H S Pearce;Tim D Cheetham

  • 2018 European Thyroid Association Guideline for the Management of Graves' Hyperthyroidism

    George G.J. Kahaly;Luigi Bartalena;Lazlo Hegedüs;Laurence Leenhardt

  • Thyroid hormones and cardiovascular disease

    Avais Jabbar;Alessandro Pingitore;Simon H. S. Pearce;Simon H. S. Pearce;Azfar Zaman;Azfar Zaman

  • Expression and Characterization of Inactivating and Activating Mutations in the Human Ca2+o-sensing Receptor

    Mei Bai;Steven Quinn;Sunita Trivedi;Olga Kifor

  • A Familial Syndrome of Hypocalcemia with Hypercalciuria Due to Mutations in the Calcium-Sensing Receptor

    Simon H.S. Pearce;Catherine Williamson;Olga Kifor;Mei Bai

  • FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity

    Manuela Fanciulli;Penny J Norsworthy;Enrico Petretto;Rong Dong

  • Consensus statement of the European group on Graves' orbitopathy (EUGOGO) on management of Graves' orbitopathy.

    Luigi Bartalena;Lelio Baldeschi;Alison J Dickinson;Anja Eckstein

  • The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves' disease.

    M. R. Velaga;V. Wilson;C. E. Jennings;C. J. Owen

  • Prevalence and Relative Risk of Other Autoimmune Diseases in Subjects with Autoimmune Thyroid Disease

    Kristien Boelaert;Paul R. Newby;Matthew J. Simmonds;Roger L. Holder

  • Consensus statement on the diagnosis, treatment and follow-up of patients with primary adrenal insufficiency.

    E. S. Husebye;B. Allolio;W. Arlt;K. Badenhoop

  • Reversal of Idiopathic Hypogonadotropic Hypogonadism

    Taneli Raivio;John Falardeau;Andrew Dwyer;Richard Quinton

  • Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice

    John Falardeau;Wilson C.J. Chung;Andrew Beenken;Taneli Raivio

  • Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism

    Nelly Pitteloud;Richard Quinton;Simon Pearce;Taneli Raivio

  • The influence of age on the relationship between subclinical hypothyroidism and ischemic heart disease: a metaanalysis.

    Salman Razvi;Abdul Shakoor;Mark Vanderpump;Jolanta U. Weaver

  • Calcium-sensing receptor mutations in familial benign hypercalcemia and neonatal hyperparathyroidism.

    S H Pearce;D Trump;C Wooding;G M Besser

  • The Incidence of Ischemic Heart Disease and Mortality in People with Subclinical Hypothyroidism: Reanalysis of the Whickham Survey Cohort

    Salman Razvi;Jola U. Weaver;Jola U. Weaver;Mark P. Vanderpump;Simon H. S. Pearce

Frequent Co-Authors

Eystein S. Husebye
Eystein S. Husebye University of Bergen
Rajesh V. Thakker
Rajesh V. Thakker University of Oxford
Heather J. Cordell
Heather J. Cordell Newcastle University
Michael P. Whyte
Michael P. Whyte Washington University in St. Louis
Wiebke Arlt
Wiebke Arlt University of Birmingham
George J. Kahaly
George J. Kahaly Johannes Gutenberg University of Mainz
Jayne A. Franklyn
Jayne A. Franklyn University of Birmingham
Tony R. Merriman
Tony R. Merriman University of Otago
I. Nicol Ferrier
I. Nicol Ferrier Newcastle University
Wilmar M. Wiersinga
Wilmar M. Wiersinga University of Amsterdam

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