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Simon Pearce
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13
Kendall-Taylor, Pat
12
Vaidya, Bijay
11
Perros, Petros
11
Imrie, Helen
9
Owen, Catherine
8
Cheetham, Tim
7
Jennings, Claire
5
Kelly, William
5
Merriman, Tony
5
Wilson, Valerie
5
Young, ET
5
Toft, AD
5
Quinton, Richard
4
Sayer, John
4
James, Robert
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All Publications
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2009: McDonald David O; Pearce Simon H S
Thyroid peroxidase forms thionamide-sensitive homodimers: relevance for immunomodulation of thyroid autoimmunity.
Journal of molecular medicine (Berlin, Germany) 2009;87(10):971-80.
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2009: Pearce Simon H S; Merriman Tony R
Genetics of type 1 diabetes and autoimmune thyroid disease.
Endocrinology and metabolism clinics of North America 2009;38(2):289-301, vii-viii.
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2009: Pearce Simon H S
Autoimmune disorders are among the most frequently encountered conditions in endocrine practice. Preface.
Endocrinology and metabolism clinics of North America 2009;38(2):xvii-xviii.
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2009: Owen Catherine J; Habeb Abdul; Pearce Simon H S; Wright Michael; Ichikawa Shoji; Sorenson Andrea H; Econs Michael J; Cheetham Tim D
Discordance for X-linked hypophosphataemic rickets in identical twin girls.
Hormone research 2009;71(4):237-44.
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2008: Falardeau John; Chung Wilson C J; Beenken Andrew; Raivio Taneli; Plummer Lacey; Sidis Yisrael; Jacobson-Dickman Elka E; Eliseenkova Anna V; Ma Jinghong; Dwyer Andrew; Quinton Richard; Na Sandra; Hall Janet E; Huot Celine; Alois Natalie; Pearce Simon H S; Cole Lindsay W; Hughes Virginia; Mohammadi Moosa; Tsai Pei; Pitteloud Nelly
Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice.
The Journal of clinical investigation 2008;118(8):2822-31.
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2008: Razvi Salman; Shakoor Abdul; Vanderpump Mark; Weaver Jolanta U; Pearce Simon H S
The influence of age on the relationship between subclinical hypothyroidism and ischemic heart disease: a metaanalysis.
The Journal of clinical endocrinology and metabolism 2008;93(8):2998-3007.
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2008: Sievenpiper John L; McIntyre Elizabeth A; Verrill Mark; Quinton Richard; Pearce Simon H S
Unrecognised severe vitamin D deficiency.
BMJ (Clinical research ed.) 2008;336(7657):1371-4.
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2008: Vaidya Bijay; Williams Graham R; Abraham Prakash; Pearce Simon H S
Radioiodine treatment for benign thyroid disorders: results of a nationwide survey of UK endocrinologists.
Clinical endocrinology 2008;68(5):814-20.
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2008: Quinton Richard; Pearce Simon H S; Sievenpiper John L
Sun and melanoma: Time to go to get your hat.
BMJ (Clinical research ed.) 2008;337():a1130.
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2008: Vaidya Bijay; Pearce Simon H S
Management of hypothyroidism in adults.
BMJ (Clinical research ed.) 2008;337():a801.
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2007: Razvi Salman; Pearce Simon H S
Do antithyroid drugs influence outcome after radioiodine therapy for hyperthyroidism?
Nature clinical practice. Endocrinology & metabolism 2007;3(9):628-9.
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2007: Raivio Taneli; Falardeau John; Dwyer Andrew; Quinton Richard; Hayes Frances J; Hughes Virginia A; Cole Lindsay W; Pearce Simon H; Lee Hang; Boepple Paul; Crowley William F; Pitteloud Nelly
Reversal of idiopathic hypogonadotropic hypogonadism.
The New England journal of medicine 2007;357(9):863-73.
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2007: Sutherland Alison; Davies Jocelyn; Owen Catherine J; Vaikkakara Suresh; Walker Christine; Cheetham Timothy D; James R Andrew; Perros Petros; Donaldson Peter T; Cordell Heather J; Quinton Richard; Pearce Simon H S
Genomic polymorphism at the interferon-induced helicase (IFIH1) locus contributes to Graves' disease susceptibility.
The Journal of clinical endocrinology and metabolism 2007;92(8):3338-41.
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2007: Fanciulli Manuela; Norsworthy Penny J; Petretto Enrico; Dong Rong; Harper Lorraine; Kamesh Lavanya; Heward Joanne M; Gough Stephen C L; de Smith Adam; Blakemore Alexandra I F; Froguel Philippe; Owen Catherine J; Pearce Simon H S; Teixeira Luis; Guillevin Loic; Graham Deborah S Cunninghame; Pusey Charles D; Cook H Terence; Vyse Timothy J; Aitman Timothy J
FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity.
Nature genetics 2007;39(6):721-3.
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2007: Vaikkakara S; James R A; Pearce S H S; Talks S J
A second corneal arcus?
Postgraduate medical journal 2007;83(977):153.
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2007: Owen Catherine J; Kelly Hannah; Eden James A; Merriman Marilyn E; Pearce Simon H S; Merriman Tony R
Analysis of the Fc receptor-like-3 (FCRL3) locus in Caucasians with autoimmune disorders suggests a complex pattern of disease association.
The Journal of clinical endocrinology and metabolism 2007;92(3):1106-11.
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2007: Rossor Alexander M; Pearce Simon H S; Adams Philip C
Left ventricular apical ballooning (takotsubo cardiomyopathy) in thyrotoxicosis.
Thyroid : official journal of the American Thyroid Association 2007;17(2):181-2.
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2007: Adamson K A; Cheetham T D; Kendall-Taylor P; Seckl J R; Pearce S H S
The role of the IDDM2 locus in the susceptibility of UK APS1 subjects to type 1 diabetes mellitus.
International journal of immunogenetics 2007;34(1):17-21.
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2006: Manji N; Carr-Smith J D; Boelaert K; Allahabadia A; Armitage M; Chatterjee V K; Lazarus J H; Pearce S H S; Vaidya B; Gough S C; Franklyn J A
Influences of age, gender, smoking, and family history on autoimmune thyroid disease phenotype.
The Journal of clinical endocrinology and metabolism 2006;91(12):4873-80.
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2006: Owen Catherine J; Eden James A; Jennings Claire E; Wilson Valerie; Cheetham Tim D; Pearce Simon H S
Genetic association studies of the FOXP3 gene in Graves' disease and autoimmune Addison's disease in the United Kingdom population.
Journal of molecular endocrinology 2006;37(1):97-104.
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2006: Razvi Salman; Vaidya Bijay; Perros Petros; Pearce Simon H S
What is the evidence behind the evidence-base? The premature death of block-replace antithyroid drug regimens for Graves' disease.
European journal of endocrinology / European Federation of Endocrine Societies 2006;154(6):783-6.
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2006: Merriman Tony R; Pearce Simon H S
Genetic progress towards the molecular basis of common autoimmunity.
Discovery medicine 2006;6(31):40-5.
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2006: Pearce Simon H S; Merriman Tony R
Genetic progress towards the molecular basis of autoimmunity.
Trends in molecular medicine 2006;12(2):90-8.
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2005: Jennings C E; Owen C J; Wilson V; Pearce S H S
A haplotype of the CYP27B1 promoter is associated with autoimmune Addison's disease but not with Graves' disease in a UK population.
Journal of molecular endocrinology 2005;34(3):859-63.
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2005: Jennings Claire E; Owen Catherine J; Wilson Valerie; Pearce Simon H S
No association of the codon 55 methionine to valine polymorphism in the SUMO4 gene with Graves' disease.
Clinical endocrinology 2005;62(3):362-5.
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2004: Velaga M R; Wilson V; Jennings C E; Owen C J; Herington S; Donaldson P T; Ball S G; James R A; Quinton R; Perros P; Pearce S H S
The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves' disease.
The Journal of clinical endocrinology and metabolism 2004;89(11):5862-5.
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2004: Pearce Simon H S
Spontaneous reporting of adverse reactions to carbimazole and propylthiouracil in the UK.
Clinical endocrinology 2004;61(5):589-94.
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2004: Houston Fiona A; Wilson Valerie; Jennings Claire E; Owen Catherine J; Donaldson Peter; Perros Petros; Pearce Simon H S
Role of the CD40 locus in Graves' disease.
Thyroid : official journal of the American Thyroid Association 2004;14(7):506-9.
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2004: Pearce Simon H S; Leech Nicola J
Toward precise forecasting of autoimmune endocrinopathy.
The Journal of clinical endocrinology and metabolism 2004;89(2):544-7.
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2004: Adamson K A; Pearce S H S; Lamb J R; Seckl J R; Howie S E M
A comparative study of mRNA and protein expression of the autoimmune regulator gene (Aire) in embryonic and adult murine tissues.
The Journal of pathology 2004;202(2):180-7.
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2003: Owen Catherine J; Jennings Claire E; Imrie Helen; Lachaux Alain; Bridges Nicola A; Cheetham Tim D; Pearce Simon H S
Mutational analysis of the FOXP3 gene and evidence for genetic heterogeneity in the immunodysregulation, polyendocrinopathy, enteropathy syndrome.
The Journal of clinical endocrinology and metabolism 2003;88(12):6034-9.
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2003: Hall Richard J; Merriman Marilyn E; Green Rachel A; Markham Valerie H; Smyth Deborah J; Heward Joanne M; Jennings Claire E; Braithwaite Antony W; Cundy Tim; Darlow Brian A; Gow Peter J; Harrison Andrew A; Highton John; Hunt Penny J; Manning Patrick; Pokorny Violetta; Scott Russell S; Taylor Barry J; Willis Jinny A; Yeoman Sue; McLean Lachy; Gough Stephen C L; Pearce Simon H; Merriman Tony R
The deleted in colorectal carcinoma (DCC) gene 201 R --> G polymorphism: no evidence for genetic association with autoimmune disease.
European journal of human genetics : EJHG 2003;11(11):840-4.
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2003: Sayer John A; Pearce Simon H S
Extracellular calcium-sensing receptor dysfunction is associated with two new phenotypes.
Clinical endocrinology 2003;59(4):419-21.
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2003: Vaidya B; Oakes E J C; Imrie H; Dickinson A J; Perros P; Kendall-Taylor P; Pearce S H S
CTLA4 gene and Graves' disease: association of Graves' disease with the CTLA4 exon 1 and intron 1 polymorphisms, but not with the promoter polymorphism.
Clinical endocrinology 2003;58(6):732-5.
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2003: Singh J; Moghal N; Pearce S H S; Cheetham T
The investigation of hypocalcaemia and rickets.
Archives of disease in childhood 2003;88(5):403-7.
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2003: Sayer John A; Carr Georgina; Pearce Simon H S; Goodship Timothy H J; Simmons Nicholas L
Disordered calcium crystal handling in antisense CLC-5-treated collecting duct cells.
Biochemical and biophysical research communications 2003;300(2):305-10.
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2002: Vaidya Bijayeswar; Kendall-Taylor Pat; Pearce Simon H S
The genetics of autoimmune thyroid disease.
The Journal of clinical endocrinology and metabolism 2002;87(12):5385-97.
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2002: Vaidya B; Pearce S H S; Charlton S; Marshall N; Rowan A D; Griffiths I D; Kendall-Taylor P; Cawston T E; Young-Min S
An association between the CTLA4 exon 1 polymorphism and early rheumatoid arthritis with autoimmune endocrinopathies.
Rheumatology (Oxford, England) 2002;41(2):180-3.
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2002: Sibal Latika; Ugwu Paul; Kendall-Taylor Pat; Ball Steve G; James R Andy; Pearce Simon H S; Hall Keith; Quinton Richard
Medical therapy of macroprolactinomas in males: I. Prevalence of hypopituitarism at diagnosis. II. Proportion of cases exhibiting recovery of pituitary function.
Pituitary 2002;5(4):243-6.
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2002: Pearce Simon H S
Clinical disorders of extracellular calcium-sensing and the molecular biology of the calcium-sensing receptor.
Annals of medicine 2002;34(3):201-6.
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2001: Sayer J A; Stewart G S; Boese S H; Gray M A; Pearce S H; Goodship T H; Simmons N L
The voltage-dependent Cl(-) channel ClC-5 and plasma membrane Cl(-) conductances of mouse renal collecting duct cells (mIMCD-3).
The Journal of physiology 2001;536(Pt 3):769-83.
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2001: Sayer J A; Pearce S H
Diagnosis and clinical biochemistry of inherited tubulopathies.
Annals of clinical biochemistry 2001;38(Pt 5):459-70.
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2001: Pearce S H; Cheetham T D
Autoimmune polyendocrinopathy syndrome type 1: treat with kid gloves.
Clinical endocrinology 2001;54(4):433-5.
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2001: Imrie H; Vaidya B; Perros P; Kelly W F; Toft A D; Young E T; Kendall-Taylor P; Pearce S H
Evidence for a Graves' disease susceptibility locus at chromosome Xp11 in a United Kingdom population.
The Journal of clinical endocrinology and metabolism 2001;86(2):626-30.
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2000: Vaidya B; Imrie H; Perros P; Young E T; Kelly W F; Carr D; Large D M; Toft A D; Kendall-Taylor P; Pearce S H
Evidence for a new Graves disease susceptibility locus at chromosome 18q21.
American journal of human genetics 2000;66(5):1710-4.
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2000: Vaidya B; Imrie H; Geatch D R; Perros P; Ball S G; Baylis P H; Carr D; Hurel S J; James R A; Kelly W F; Kemp E H; Young E T; Weetman A P; Kendall-Taylor P; Pearce S H
Association analysis of the cytotoxic T lymphocyte antigen-4 (CTLA-4) and autoimmune regulator-1 (AIRE-1) genes in sporadic autoimmune Addison's disease.
The Journal of clinical endocrinology and metabolism 2000;85(2):688-91.
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1999: Pearce S H; Vaidya B; Imrie H; Perros P; Kelly W F; Toft A D; McCarthy M I; Young E T; Kendall-Taylor P
Further evidence for a susceptibility locus on chromosome 20q13.11 in families with dominant transmission of Graves disease.
American journal of human genetics 1999;65(5):1462-5.
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1999: Vaidya B; Imrie H; Perros P; Dickinson J; McCarthy M I; Kendall-Taylor P; Pearce S H
Cytotoxic T lymphocyte antigen-4 (CTLA-4) gene polymorphism confers susceptibility to thyroid associated orbitopathy.
Lancet 1999;354(9180):743-4.
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1999: Pearce S H
Mapping of a novel tumour suppressor gene with a role in neuroendocrine tumours.
Clinical endocrinology 1999;51(1):19-20.
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1999: Vaidya B; Imrie H; Perros P; Young E T; Kelly W F; Carr D; Large D M; Toft A D; McCarthy M I; Kendall-Taylor P; Pearce S H
The cytotoxic T lymphocyte antigen-4 is a major Graves' disease locus.
Human molecular genetics 1999;8(7):1195-9.
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1998: Pearce S H; Cheetham T; Imrie H; Vaidya B; Barnes N D; Bilous R W; Carr D; Meeran K; Shaw N J; Smith C S; Toft A D; Williams G; Kendall-Taylor P
A common and recurrent 13-bp deletion in the autoimmune regulator gene in British kindreds with autoimmune polyendocrinopathy type 1.
American journal of human genetics 1998;63(6):1675-84.
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1998: Kemp E H; Ajjan R A; Husebye E S; Peterson P; Uibo R; Imrie H; Pearce S H; Watson P F; Weetman A P
A cytotoxic T lymphocyte antigen-4 (CTLA-4) gene polymorphism is associated with autoimmune Addison's disease in English patients.
Clinical endocrinology 1998;49(5):609-13.
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1998: Pearce S H
Straightening out the renal tubule: advances in the molecular basis of the inherited tubulopathies.
QJM : monthly journal of the Association of Physicians 1998;91(1):5-12.
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1998: Pearce S H
Calcium homeostasis and disorders of the calcium-sensing receptor.
Journal of the Royal College of Physicians of London 1998;32(1):10-4.
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1997: Pearce S H; Foster D J; Imrie H; Myerscough N; Beckett G J; Thoday K L; Kendall-Taylor P
Mutational analysis of the thyrotropin receptor gene in sporadic and familial feline thyrotoxicosis.
Thyroid : official journal of the American Thyroid Association 1997;7(6):923-7.
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1997: Pearce S H
Multiple endocrine neoplasia type 1 (MEN1): recent advances.
Clinical endocrinology 1997;47(5):513-4.
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1997: Pearce S H; Thakker R V
The calcium-sensing receptor: insights into extracellular calcium homeostasis in health and disease.
The Journal of endocrinology 1997;154(3):371-8.
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