Camille Soudee

Paris, France

Last Updated: 09/26/2026

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Found 24 publications

Human inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneity.

Human inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneity.

Journal: medRxiv : the preprint server for health sciences
Published: August 01, 2026

Homozygosity for rare or common hypomorphic IL23R variants confers a predisposition to tuberculosis in humans.

Homozygosity for rare or common hypomorphic IL23R variants confers a predisposition to tuberculosis in humans.

Journal: bioRxiv : the preprint server for biology
Published: April 03, 2026

STAT2 R148 variant: A 16th-century founder mutation and clinical response to high-dose JAK inhibitor therapy.

STAT2 R148 variant: A 16th-century founder mutation and clinical response to high-dose JAK inhibitor therapy.

Journal: Journal of human immunity
Published: January 01, 2026

IRF4 haploinsufficiency in a multiplex family with Whipple's disease.

IRF4 haploinsufficiency in a multiplex family with Whipple's disease.

Journal: Journal of human immunity
Published: December 22, 2025

Chronic granulomatous disease: Clinical, microbial, and genetic findings in 39 Colombian patients.

Chronic granulomatous disease: Clinical, microbial, and genetic findings in 39 Colombian patients.

Journal: Journal of human immunity
Published: December 13, 2025

Humans homozygous for rare or common hypomorphic IL23R variants are prone to tuberculosis.

Humans homozygous for rare or common hypomorphic IL23R variants are prone to tuberculosis.

Journal: The Journal of experimental medicine
Published: October 27, 2025

Human-inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneity.

Human-inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneity.

Journal: The Journal of experimental medicine
Published: October 01, 2025

Familial pulmonary alveolar proteinosis and type I interferonopathy by mutation of STAT2 (TIMS2).

Familial pulmonary alveolar proteinosis and type I interferonopathy by mutation of STAT2 (TIMS2).

Journal: The Journal of experimental medicine
Published: July 01, 2025

Complete and partial forms of X-linked MCTS1 deficiency in patients with mycobacterial disease.

Complete and partial forms of X-linked MCTS1 deficiency in patients with mycobacterial disease.

Journal: Journal of human immunity
Published: May 02, 2025

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

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

Journal: Nature immunology
Published: December 16, 2024

Human inherited CCR2 deficiency underlies progressive polycystic lung disease.

Human inherited CCR2 deficiency underlies progressive polycystic lung disease.

Journal: Cell
Published: May 22, 2024

Autoinflammation in patients with leukocytic CBL loss of heterozygosity is caused by constitutive ERK-mediated monocyte activation.

Autoinflammation in patients with leukocytic CBL loss of heterozygosity is caused by constitutive ERK-mediated monocyte activation.

Journal: The Journal of clinical investigation
Published: April 02, 2024
Showing 1-12 of 24

Last Updated: 09/26/2026