Ian Glass

24PUBLICATIONS
294CO-AUTHORS
Neurology and neuromuscular diseasesGene mappingGene expression (incl. microarray and other genome-wide approaches)Evolution of developmental systemsNeurogenetics
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Publications (24)

|Sep 10, 2026
Nx3 Is a Z-Disk Structural and Signaling Hub That Is Reduced in Heart Failure.

|Aug 26, 2026
Heterozygous Variants in LRP1 Cause a Neurodevelopmental Disorder With Congenital Heart Defects.

|Jul 22, 2026
Mapping mesenchymal diversity in the human small intestine and organoids.

|May 12, 2026
Modular genetic architecture underlies human hand and foot evolution.

|Apr 08, 2026
Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes.

Rocio Rius, Alexander J M Blakes, Yuyang Chen

|Apr 08, 2026
Saturation editing of RNU4-2 reveals distinct dominant and recessive disorders.

Joachim De Jonghe, Hyung Chul Kim, Ayanfeoluwa Adedeji

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Frequent Collaborators

4 joint publications

Benjamin Cogné

4 joint publications

Kimberly A Aldinger

3 joint publications

Ruebena Dawes

3 joint publications

Yuyang Chen