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)

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|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

Hannah Klinkhammer

Charlotte W Ockeloen

Jean Tori Pantel

Shahida Moosa

Peter M Krawitz

Heidi Beate Bentzen

Sébastien Küry

Bernd Wollnik

Tzung-Chien Hsieh

Koenraad Devriendt

Frequent Collaborators

Hannah Klinkhammer

Charlotte W Ockeloen

Jean Tori Pantel

Shahida Moosa