Helen R Griffin

4PUBLICATIONS
95CO-AUTHORS
Haematological tumoursGene expression (incl. microarray and other genome-wide approaches)Molecular targetsEpigenetics (incl. genome methylation and epigenomics)
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Publications (4)

|Jul 30, 2026
Human GPR174 deficiency drives polyclonal lymphoproliferative disease via defects in T cell function.

|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

2 joint publications

Jarmila Stremenova Spegarova

2 joint publications

Sophie Hambleton

2 joint publications

Karin R Engelhardt

1 joint publications

Romance A Zendah