Fabien Touzot - Concepedia

Author

Fabien Touzot

Assistance Publique – Hôpitaux de Paris ORCID

Also Known As

Dewton F.P. Vasconcelos, F Touzot, F. Touzot, Fabien Touzot, Touzot, F, Touzot, Fabien

119

Publications

4.5K

Citations

H-Index

Concepts

All Affiliations

Assistance Publique – Hôpitaux de Paris Université Paris Cité Inserm Hôpital Necker-Enfants Malades Sorbonne Paris Cité

About

Fabien Touzot is an author at Assistance Publique – Hôpitaux de Paris specializing in medicine, immunology, and hematology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	20	1.4K
2	Cell Biology	6	6	308
3	Health Sciences	4	4	247
4	Blood Transplantation	3	3	222
5	Allergy	2	2	336

Fabien Touzot

Publications

3.9K

Citations

H-Index

Page 1

	Year	Citations
Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndrome: A large patient cohort study Tanya Coulter, Anita Chandra, Chris M. Bacon, Journal of Allergy and Clinical Immunology	2016	432
A Modified γ-Retrovirus Vector for X-Linked Severe Combined Immunodeficiency Salima Hacein‐Bey‐Abina, Sung‐Yun Pai, H. Bobby Gaspar, New England Journal of Medicine	2014	402
Outcomes Following Gene Therapy in Patients With Severe Wiskott-Aldrich Syndrome Salima Hacein-Bey Abina, H. Bobby Gaspar, Johanna Blondeau, JAMA	2015	374
Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency) Jana Pachlopnik Schmid, Danielle Canioni, Despina Moshous, Blood	2010	364
Evidence of innate lymphoid cell redundancy in humans Frédéric Vely, Vincent Barlogis, Blandine Vallentin, Nature Immunology ImmunogeneticsAutoimmune DiseaseAllergyLymphocyte DevelopmentImmunology	2016	303
Human RTEL1 deficiency causes Hoyeraal–Hreidarsson syndrome with short telomeres and genome instability Tangui Le Guen, Laurent Jullien, Fabien Touzot, Human Molecular Genetics	2013	191
Inherited CD70 deficiency in humans reveals a critical role for the CD70–CD27 pathway in immunity to Epstein-Barr virus infection Kazushi Izawa, Emmanuel Martin, Claire Soudais, The Journal of Experimental Medicine	2016	147
Major histocompatibility complex class II expression deficiency caused by a RFXANK founder mutation: a survey of 35 patients Monia Ouederni, Quentin B. Vincent, Pierre Frange, Blood	2011	117
Primary T-cell immunodeficiency with immunodysregulation caused by autosomal recessive LCK deficiency Fabian Hauck, Clotilde Randriamampita, Emmanuel Martin, Journal of Allergy and Clinical Immunology Primary ImmunodeficiencyAutoimmune DiseasePrimary T-cell ImmunodeficiencyImmunodeficienciesT-regulatory Cell	2012	110
An in vivo genetic reversion highlights the crucial role of Myb-Like, SWIRM, and MPN domains 1 (MYSM1) in human hematopoiesis and lymphocyte differentiation Tangui Le Guen, Fabien Touzot, Isabelle André‐Schmutz, Journal of Allergy and Clinical Immunology Hematological MalignancyImmunogeneticsMedicineCrucial RoleImmunology	2015	110

Page 1