Laureline Berteloot

14PUBLICATIONS
298CO-AUTHORS
Immunogenetics (incl. genetic immunology)Applied immunology (incl. antibody engineering, xenotransplantation and t-cell therapies)Respiratory diseasesHaematological tumoursInfant and child health
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Publications (14)

|Jul 16, 2026
Familial pulmonary alveolar proteinosis and type I interferonopathy by mutation of STAT2 (TIMS2).

|Jan 16, 2026
Somatic deficiency of the human E3 ubiquitin ligase CBL in leukocytes impairs B cell but not T cell development and function.

Taja Vatovec, Anna-Lena Neehus, Katherine J L Jackson

|Sep 01, 2025
Allogeneic haematopoietic stem cell transplantation for severe Still's disease: a retrospective report of three paediatric patients.

Muriel Schmutz, Jade Cognard, Alice Hadchouel

|Jan 15, 2025
Mutations disrupting the kinase domain of IKKα lead to immunodeficiency and immune dysregulation in humans.

Quentin Riller, Boris Sorin, Charline Courteille

|Nov 13, 2024
Rare genetic interstitial lung diseases: a pictorial essay.

Raphael Borie, Laureline Berteloot, Caroline Kannengiesser

|Oct 01, 2024
Incontinentia pigmenti underlies thymic dysplasia, autoantibodies to type I IFNs, and viral diseases.

Jérémie Rosain, Tom Le Voyer, Xian Liu

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Frequent Collaborators

7 joint publications

Jean-Laurent Casanova

6 joint publications

Tom Le Voyer

6 joint publications

Anne Puel

5 joint publications

Mélanie Migaud