Mana Momenilandi

Imagine Institute for Genetic Diseases

France

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Articles (10)

Year:

2025

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Year:

2022

Collaborators (14)

Charlotte Slade

Walter and Eliza Hall Institute of Medical Research

AUSTRALIA

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Asbjørg Stray-Pedersen

NORWAY

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Elze Rackaityte

University of California, San Francisco

UNITED STATES

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Geraldine Blanchard-Rohner

University Hospital of Geneva

SWITZERLAND

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Ahmad Yatim

Rockefeller University

UNITED STATES

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Hideaki Morita

National Institute of Child Health and Human Development

JAPAN

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Rémi Duclaux-Loras

INSERM

FRANCE

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Bernard Malissen

FRANCE

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Rachael Philips

National Institutes of Health

UNITED STATES

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David Langlais

Assistant Professor / Principal Investigator

CANADA

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Johannes Raedler

GERMANY

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Venetia Bigley

MRC Senior Clinical Fellow, Clinical Senior Lecturer in Haematology

Newcastle University

UNITED KINGDOM

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qiang pan-hammarstrom

Karolinska University Hospital

SWEDEN

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Hassan Vahidnezhad

Incoming Associate professor

Children's Hospital of Philadelphia

UNITED STATES

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Mana Momenilandi

Research Interests

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Articles (10)

Serological diagnosis of chronic skin granulomas caused by wild-type or vaccine-derived rubella virus in patients with inherited HLA class I deficiency

The immunopathological landscape of human pre-TCRα deficiency: From rare to common variants

FLT3L governs the development of partially overlapping hematopoietic lineages in humans and mice

Human inherited CCR2 deficiency underlies progressive polycystic lung disease

Human germline gain-of-function in STAT6: from severe allergic disease to lymphoma and beyond

Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease.

Human inherited complete STAT2 deficiency underlies inflammatory viral diseases

Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency

Inherited human ZNF341 deficiency

Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency.

Collaborators (14)

Charlotte Slade

Asbjørg Stray-Pedersen

Elze Rackaityte

Geraldine Blanchard-Rohner

Ahmad Yatim

Hideaki Morita

Rémi Duclaux-Loras

Bernard Malissen

Rachael Philips

David Langlais

Johannes Raedler

Venetia Bigley

qiang pan-hammarstrom

Hassan Vahidnezhad

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