Ian Glass

21PUBLICATIONS

255CO-AUTHORS

NeurogeneticsEvolution of developmental systemsCell and nuclear divisionVision scienceInfant and child health

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Publications (21)

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|May 18, 2026

Author Correction: Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes.

|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

|Feb 13, 2026

A cell fate specification and transition mechanism for human foveolar cone subtype patterning.

Katarzyna A Hussey, Kiara C Eldred, Brian Guy

|Feb 04, 2026

Rete ridges form via evolutionarily distinct mechanisms in mammalian skin.

Sean M Thompson, Violet S Yaple, Gabriella H Searle

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Frequent Collaborators

Kimberly A Aldinger

Benjamin Cogné

Joachim De Jonghe

Yuyang Chen

Alexander J M Blakes

Terence D Capellini

Gayani Senevirathne

James R Lupski

Hyung Chul Kim

Ruebena Dawes

Frequent Collaborators

Kimberly A Aldinger

Benjamin Cogné

Joachim De Jonghe

Yuyang Chen