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Author

Krishna Chatterjee

Observed names: Chatterjee K, Chatterjee, K, Chatterjee, Krishna, K Chatterjee
Observed institutions: University of Cambridge, Cambridge University Hospitals NHS Foundation Trust, Wellcome/MRC Institute of Metabolic Science, NIHR Cambridge Biomedical Research Centre, Wellcome Trust, Medical Research Council
ORCID: 0000-0002-2654-8854
Observed ORCID: 0000-0002-2654-8854
OpenAlex ID: A5073764267
A Mutation in the Thyroid Hormone Receptor Alpha Gene
2012 · Bochukova, E, Schoenmakers, N, et al. · UCL Discovery (University College London) · 327
Mapping variants in thyroid hormone transporter MCT8 to disease severity by genomic, phenotypic, functional, structural and deep learning integration
2026 · Stefan Groeneweg, van Geest Ferdy S., et al. · Yearbook of pediatric endocrinology · 2
Effectiveness and safety of the tri-iodothyronine analogue Triac in children and adults with MCT8 deficiency: an international, single-arm, open-label, phase 2 trial
2020 · Groeneweg S, Peeters RP, et al. · Yearbook of pediatric endocrinology · 2
Use of anti thyroid hormone receptor antibody (TRAB) in Graves Disease
2007 · Khin Swe Myint, Gayathridevisa Shankargall Andappa, et al. · Endocrine Abstracts · 2
Thyrotoxicosis in MCT8 deficiency
2026 · Kristien Boelaert, Andrew Bauer, et al. · The Journal of Clinical Endocrinology & Metabolism
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Damaging mutations in liver X receptor-α are hepatotoxic and implicate cholesterol sensing in liver health
2024 · Sam M. Lockhart, Milan Muso, et al. · Newcastle University ePrints (Newcastle Univesity)
Discordant Thyroid Function Tests Due to Dysalbuminemic Hyeprthyroxinemia Confounds Management of Thyroid Autoimmunity
2019 · Khoo SSK, Lyons G, et al. · Journal of the ASEAN Federation of Endocrine Societies
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Low-frequency variation in TP53 has large effects on head circumference and intracranial volume
2019 · Simon Haworth, Chin Yang Shapland, et al. · Newcastle University ePrints (Newcastle Univesity)
G450(P) An uncommon cause of deranged thyroid function in a family line
2016 · J Fordham, P Lwin, et al. · Archives of Disease in Childhood
G478(P) A case report of trbeta mutation leading to raised t4 levels
2015 · N Tomlinson, I Banerjee, et al. · Archives of Disease in Childhood
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Hypothalamic mTOR pathway mediates thyroid hormone-induced hyperphagia in hyperthyroidism
2012 · N Sanchez, Luis Varela, et al. · 15th International & 14th European Congress of Endocrinology
Hyperthyroxinaemia with non-suppressed TSH in a clinically euthyroid woman with an unusual sella mass
2009 · N Al-Ali, DJ Halsall, et al. · Society for Endocrinology BES 2009
Phenotype of mice harboring a thyroid hormone receptor alpha 1 gene with transdominant negative properties
2001 · Björn Vennström, Alexander A. Tinnikov, et al. · 192nd Meeting of the Society for Endocrinology
Thyrotoxicosis in MCT8 deficiency
· Boelaert K, Bauer A, et al. · Newcastle University ePrints (Newcastle Univesity)
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Works count: 16
Citation count: 333
H-index: 2
I10-index: 1
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