Lyon Gholson

40PUBLICATIONS
214CO-AUTHORS
Foetal development and medicineEpigenetics (incl. genome methylation and epigenomics)Gene mappingClinical nutritionChild and adolescent development
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Publications (40)

|Jun 19, 2026
<i>Letter:</i> Psychosis Following Hormonal Therapy in NAA15-Related Neurodevelopmental Disorder.

|Mar 30, 2026
Pathogenic variants in the cohesin loader subunit MAU2 underlie a distinct Cornelia de Lange Syndrome subtype.

Ilaria Parenti, Alina Hesters, Marta Gil-Salvador

|Mar 05, 2026
Functional Data Strengthen Clinical Validation of PhenoScore Phenotype-Guided AI for ANKRD11 Missense Variants.

Evi Andriessen, Elke de Boer, Gholson J Lyon

|Jul 17, 2025
Growth Hormone Treatment in Patients With KBG Syndrome: Novel Insights, Challenges and Recommendations From Six New Patients and Literature Review.

Sietse M Aukema, Kim Vandenput, Emanuela Scarano

|May 29, 2025
Addressing the Diagnostic Odyssey for Adults With Neurodevelopmental Disabilities: Case Study of an Individual With Mandibulofacial Dysostosis With Microcephaly.

Ruhi Shah, Neora Shifrin, Mary Ellen Keogh

|Apr 16, 2025
The Cardiovascular Manifestations and Management Recommendations for Ogden Syndrome.

Rikhil Makwana, Rahi Patel, Rosemary O'Neill

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Frequent Collaborators

4 joint publications

Hannah Klinkhammer

3 joint publications

Charlotte W Ockeloen

3 joint publications

Jean Tori Pantel

3 joint publications

Shahida Moosa