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V. Krishna K. Chatterjee

University of Cambridge

53

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Germline mutations in the thyroid hormone receptor alpha gene predispose to cutaneous tags and melanocytic nevi.

2021 Thyroid
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Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism

2018 JCI insight
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Digenic DUOX1 and DUOX2 Mutations in Cases With Congenital Hypothyroidism

2017 The Journal of Clinical Endocrinology and Metabolism
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The Hypercoagulable state in Hyperthyroidism is mediated via the Thyroid Hormone β Receptor pathway

2016 European Journal of Endocrinology
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Comprehensive screening of eight known causative genes in congenital hypothyroidism with gland-in-situ

2016 The Journal of Clinical Endocrinology and Metabolism
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Thyroid gland: TSHR mutations and subclinical congenital hypothyroidism

2015 Nature Reviews Endocrinology
- Nadia Schoenmakers
- V. Krishna K. Chatterjee
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Investigating the genetic architecture of gland-in-situ congenital hypothyroidism by comprehensive screening of eight known causative genes

2015
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Congenital central hypothyroidism due to a TSHB mutation with uniparental inheritance

2014
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Thyroid dyshormonogenesis is mainly caused by TPO mutations in consanguineous community

2013 Clinical Endocrinology
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Loss-of-function mutations in IGSF1 cause a novel, X-linked syndrome of central hypothyroidism and testicular enlargement

2013
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