Nipith Charoenngam

32PUBLICATIONS
15CO-AUTHORS
Cancer geneticsGenomicsMedical mycologyHaematologyEpigenetics (incl. genome methylation and epigenomics)
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Publications (32)

|Aug 25, 2026
Genotype-First Characterization of Familial Hypocalciuric Hypercalcemia Type 1: Prevalence, Serum Calcium and Clinical Associations.

|May 22, 2026
Global prevalence of genetic carriers for ARMC5- and KDM1A-associated primary bilateral macronodular adrenal hyperplasia: insights from a large multiethnic genomic database.

|Feb 13, 2026
Multiple endocrine neoplasia type 5: emerging evidence and clinical perspectives.

Nipith Charoenngam, Michael Mannstadt

|Feb 09, 2026
Disproportionate Decline in Trabecular Bone Score Compared to Bone Mineral Density in Southeast Asian Patients with Thalassemia: A Matched Control Study.

Chatlert Pongchaiyakul, Nattiya Teawtrakul, Daris Theerakulpisut

|Nov 29, 2025
Population-based estimates of the global prevalence and carrier frequency of apparent mineralocorticoid excess caused by 11β-hydroxysteroid dehydrogenase type 2 deficiency.

Nipith Charoenngam, Chalermkiat Kansuttiviwat, Palinee Chinsawangwatanakul

|Sep 20, 2025
Estimated global prevalence of genetic carriers of hereditary pheochromocytoma-paraganglioma syndrome in a large multiethnic genomic database.

Nipith Charoenngam, Taweesak Wannachalee

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Frequent Collaborators

5 joint publications

Michael Mannstadt

3 joint publications

Ben Ponvilawan

3 joint publications

Michael F Holick

2 joint publications

Patompong Ungprasert