Samar Ojaimi

8PUBLICATIONS
81CO-AUTHORS
Gene and molecular therapyMedical infection agents (incl. prions)AutoimmunityNeonatologyInnate immunity
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Publications (8)

|Aug 27, 2026
Iterative genetic testing identifies SAMHD1 deficiency caused by a homozygous balanced translocation.

|Aug 07, 2026
An autoinflammatory CDC42 variant M45L demonstrates the mechanism of pyrin inflammasome activation.

|Jul 24, 2026
Familial associations between ANCA-associated vasculitis and other immune-mediated inflammatory diseases: a case control study.

|Oct 19, 2024
Phenotype of patients with late diagnosis of 22q11 deletion: a review and retrospective study.

Marissa Loh, Tamar Schildkraut, Angela Byrnes

|Oct 22, 2020
Influenza-specific IgG1+ memory B-cell numbers increase upon booster vaccination in healthy adults but not in patients with predominantly antibody deficiency.

Gemma E Hartley, Emily S J Edwards, Julian J Bosco

|Aug 18, 2020
Beyond monogenetic rare variants: tackling the low rate of genetic diagnoses in predominantly antibody deficiency.

Emily S J Edwards, Julian J Bosco, Samar Ojaimi

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Frequent Collaborators

2 joint publications

Menno C van Zelm

2 joint publications

Seth L Masters

2 joint publications

Imogen Bishop

2 joint publications

Dhanya Lakshmi Narayanan