Moon Ley Tung

6PUBLICATIONS
70CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)People with disabilityEpigenetics (incl. genome methylation and epigenomics)Cardiology (incl. cardiovascular diseases)Nanomedicine
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Publications (6)

|Jul 03, 2026
Leveraging Next-Generation Phenotyping in Dysmorphology to Support Variant Interpretation in Mowat-Wilson Syndrome.

|Jun 21, 2024
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases.

Hellen Lesmann, Alexander Hustinx, Shahida Moosa

|Mar 27, 2024
Iowa Newborn Screening Program Experience with Hemoglobinopathy Screening over the Last Two Decades and Its Increasing Global Relevance.

Ryan Jilek, Jennifer Marcy, Carol Johnson

|Sep 23, 2022
TBX3 and EFNA4 Variant in a Family with Ulnar-Mammary Syndrome and Sagittal Craniosynostosis.

Moon Ley Tung, Bharatendu Chandra, Jaclyn Kotlarek

|Feb 22, 2021
Anti-phospholipid syndrome and COVID-19 thrombosis: connecting the dots.

Moon Ley Tung, Bryce Tan, Robin Cherian

|Jul 18, 2020
COVID-19 conundrum: clinical phenotyping based on pathophysiology as a promising approach to guide therapy in a novel illness.

Robin Cherian, Bharatendu Chandra, Moon Ley Tung

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Frequent Collaborators

2 joint publications

Hannah Klinkhammer

2 joint publications

Tzung-Chien Hsieh

1 joint publications

Robin Cherian

1 joint publications

Alain Vuylsteke