Gregory M Findlay

7PUBLICATIONS
85CO-AUTHORS
Cancer geneticsNeurogeneticsCell and nuclear divisionGene expression (incl. microarray and other genome-wide approaches)Micro- and nanosystems
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Publications (7)

|Jul 30, 2026
'Truthsets' for clinical validation of large-scale functional assays: Practice recommendations from Cancer Variant Interpretation Group UK (CanVIG-UK).

|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 RNU4-2 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

6 joint publications

Joachim De Jonghe

4 joint publications

Alexander Jm Blakes

4 joint publications

Ruebena Dawes

4 joint publications

Chloe A Cunningham