Helen R Griffin
3PUBLICATIONS
70CO-AUTHORS
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Publications (3)
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|Feb 26, 2025
Rare disease gene association discovery in the 100,000 Genomes Project.Valentina Cipriani, Letizia Vestito, Emma F Magavern
|May 24, 2024
NUDCD3 deficiency disrupts V(D)J recombination to cause SCID and Omenn syndrome.Rui Chen, Elena Lukianova, Ina Schim van der Loeff
|Jun 13, 2020
RNA exosome mutations in pontocerebellar hypoplasia alter ribosome biogenesis and p53 levels.Juliane S Müller, David T Burns, Helen Griffin
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Frequent Collaborators
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Romance A Zendah
1 joint publications
Benjamin Munro
1 joint publications
Claudia Schneider
1 joint publications
Rita Horvath
1 joint publications
Rui Chen
1 joint publications
Elena Lukianova
1 joint publications
Ina Schim van der Loeff
1 joint publications
Jarmila Stremenova Spegarova
1 joint publications
Kieran D James
1 joint publications
Edward J Ryder
