Nikolaos Settas

Children's National — United States

Medicine · Health Sciences

10h-index489citations27works1.02yr avg
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Research Topics

Adrenal and Paraganglionic Tumors(7), Neuroendocrine Tumor Research Advances(4), Cardiac tumors and thrombi(4), Reproductive Biology and Fertility(3), Cancer-related Molecular Pathways(3)

Publications27 total

Increased METTL3 Expression and m6A Methylation in Myoblasts of Facioscapulohumeral Muscular Dystrophy
International Journal of Molecular Sciences·2025· 1 citedOpen Access
HNF1A gene mutations and premature ovarian failure (POF): evidence from a clinical paradigm combining MODY 3 and POF
HORMONES·2024· 1 citedOpen Access
USP13 genetics and expression in a family with thyroid cancer
Endocrine·2022· 7 citedOpen Access
USP13 Genetics and Expression in a Family With Thyroid Cancer
Research Square (Research Square)·2022Open Access
Kisspeptin deficiency leads to abnormal adrenal glands and excess steroid hormone secretion
Yearbook of pediatric endocrinology·2021
Carney Triad, Carney-Stratakis Syndrome, 3PAS and Other Tumors Due to SDH Deficiency
Frontiers in Endocrinology·2021· 46 citedOpen Access
The PRKAR1B p.R115K Variant is Associated with Lipoprotein Profile in African American Youth with Metabolic Challenges
Journal of the Endocrine Society·2021· 6 citedOpen Access
Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain
Genetics in Medicine·2021· 27 citedOpen Access
Correction: Genomic and sequence variants of protein kinase A regulatory subunit type 1β (PRKAR1B) in patients with adrenocortical disease and Cushing syndrome
Genetics in Medicine·2020· 1 citedOpen Access
Kisspeptin deficiency leads to abnormal adrenal glands and excess steroid hormone secretion
Human Molecular Genetics·2020· 7 citedOpen Access
PRKACB variants in skeletal disease or adrenocortical hyperplasia: effects on protein kinase A
Endocrine Related Cancer·2020· 16 citedOpen Access
Genomic and sequence variants of protein kinase A regulatory subunit type 1β (PRKAR1B) in patients with adrenocortical disease and Cushing syndrome
Genetics in Medicine·2020· 20 citedOpen Access
ARMC5 variants in PRKAR1A-mutated patients modify cortisol levels and Cushing’s syndrome
Endocrine Related Cancer·2020· 9 citedOpen Access
OR24-06 USP8 Genetic Variants May Contribute to the Development of Bilateral Adrenal Hyperplasia and ACTH-Independent Cushing Syndrome
Journal of the Endocrine Society·2020· 1 citedOpen Access
MON-433 The Spectrum Of Growth Hormone Excess In Carney Complex: Characterizing A Common Finding In A Rare Syndrome
Journal of the Endocrine Society·2019Open Access
SGPL1 Deficiency: A Rare Cause of Primary Adrenal Insufficiency
The Journal of Clinical Endocrinology & Metabolism·2018· 52 citedOpen Access
A Novel Germline DICER1 Mutation in a Girl with Multinodular Goiter and Ovarian Sertoli-Leydig Cell Tumor
57th Annual ESPE·2018
The E3 ubiquitin ligase Siah1 regulates adrenal gland organization and aldosterone secretion
JCI Insight·2017· 11 citedOpen Access
Medullary thyroid cancer, leukemia, mesothelioma and meningioma associated with germline APC and RASAL1 variants: a new syndrome?
HORMONES·2017· 6 citedOpen Access
Succinate dehydrogenase (SDH) deficiency, Carney triad and the epigenome
Molecular and Cellular Endocrinology·2017· 60 cited
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Frequent Co-authors

Constantine A. Stratakis(19), Fábio R. Faucz(17), Catherine Dacou‐Voutetakis(7), Annabel Berthon(6), George P. Chrousos(6), Antonis Voutetakis(6), Edra London(5), Andréa Gutierrez Maria(5), Christina Tatsi(4), Ludivine Drougat(4), Kerstin Bathon(4), Anna Angelousi(3), Maya Lodish(3), Christina Kanaka‐Gantenbein(3), Davide Calebiro(3), Sara Haydar(3), Antonios Voutetakis(3), Andreas Giannakou(3), Emmanuel Kanavakis(3), Fady Hannah‐Shmouni(3)