Gregory M Findlay

6PUBLICATIONS

66CO-AUTHORS

NeurogeneticsCell and nuclear divisionGene expression (incl. microarray and other genome-wide approaches)Micro- and nanosystems

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Publications (6)

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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.

|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

|Apr 29, 2025

Saturation genome editing of <i>RNU4-2</i> reveals distinct dominant and recessive neurodevelopmental disorders.

Joachim De Jonghe, Hyung Chul Kim, Ayanfeoluwa Adedeji

|Jul 05, 2024

Saturation genome editing maps the functional spectrum of pathogenic VHL alleles.

Megan Buckley, Chloé Terwagne, Athina Ganner

|Aug 08, 2023

spinDrop: a droplet microfluidic platform to maximise single-cell sequencing information content.

Joachim De Jonghe, Tomasz S Kaminski, David B Morse

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Frequent Collaborators

Joachim De Jonghe

Alexander Jm Blakes

Ruebena Dawes

Chloe A Cunningham

Rocio Rius

Christel Thauvin-Robinetvin

Cas Simons

Yuyang Chen

Salima El Chehadeh

Hyung Chul Kim

Frequent Collaborators

Joachim De Jonghe

Alexander Jm Blakes

Ruebena Dawes

Chloe A Cunningham