Author

Sarah cohen Beaussant

Observed names: COHEN-BEAUSSANT, Sarah, S Beaussant-Cohen, S. Beaussant Cohen, S. Beaussant-Cohen, S. Cohen Beaussant, Sarah Beaussant Cohen, Sarah Beaussant-Cohen, Sarah Cohen Beaussant, Sarah Cohen-Beaussant, Sarah L. Beaussant-Cohen

Observed institutions: Hôpital Necker-Enfants Malades, Boston Children's Hospital, Harvard University, Inserm, Collège de France, Hôpital Armand-Trousseau, Centre Hospitalier Universitaire de Besançon, Centre de Référence Déficits Immunitaires Héréditaires, Assistance Publique – Hôpitaux de Paris, MRC Biostatistics Unit, CRISPR Therapeutics (Switzerland), Human Genetic of Infectious Diseases, Institut des Maladies Génétiques Imagine, X4 Pharmaceuticals, Inc. (United States), Université de Franche-Comté

ORCID: 0000-0002-5591-9730

Observed ORCID: 0000-0002-5591-9730

OpenAlex ID: A5058698478

The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity

2019 · Markus G. Seidel, Gerhard Kindle, et al. · The Journal of Allergy and Clinical Immunology In Practice · 640

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Autoimmune and inflammatory manifestations occur frequently in patients with primary immunodeficiencies

2017 · Alain Fischer, Johan Provot, et al. · Journal of Allergy and Clinical Immunology · 320

Description and outcome of a cohort of 8 patients with WHIM syndrome from the French Severe Chronic Neutropenia Registry

2012 · Sarah Beaussant Cohen, Odile Fenneteau, et al. · Orphanet Journal of Rare Diseases · 134

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Results of a phase 2 trial of an oral CXCR4 antagonist, mavorixafor, for treatment of WHIM syndrome

2020 · David C. Dale, Frank Firkin, et al. · Blood · 78

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CTX110 Allogeneic CRISPR-Cas9-Engineered CAR T Cells in Patients (Pts) with Relapsed or Refractory (R/R) Large B-Cell Lymphoma (LBCL): Results from the Phase 1 Dose Escalation Carbon Study

2022 · Joseph P. McGuirk, Constantine S. Tam, et al. · Blood · 61

Lymphoid differentiation of hematopoietic stem cells requires efficient Cxcr4 desensitization

2017 · Christelle Freitas, Monika Wittner, et al. · The Journal of Experimental Medicine · 56

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Disease Progression of WHIM Syndrome in an International Cohort of 66 Pediatric and Adult Patients

2022 · Christoph B. Geier, Maryssa Ellison, et al. · Journal of Clinical Immunology · 51

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Combined immunodeficiency in a patient with c-Rel deficiency

2019 · Sarah Beaussant-Cohen, Faris Jaber, et al. · Journal of Allergy and Clinical Immunology · 40

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Paediatric Strategy Forum for medicinal product development of chimeric antigen receptor T-cells in children and adolescents with cancer

2021 · Andrew DJ. Pearson, Claudia Rossig, et al. · European Journal of Cancer · 39

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Human primary immunodeficiency caused by expression of a kinase-dead p110δ mutant

2018 · Sarah Beaussant Cohen, Wayne Bainter, et al. · Journal of Allergy and Clinical Immunology · 37

F-BAR domain only protein 1 (FCHO1) deficiency is a novel cause of combined immune deficiency in human subjects

2019 · Enrica Calzoni, Craig D. Platt, et al. · Journal of Allergy and Clinical Immunology · 30

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Combined immunodeficiency due to a mutation in the γ1 subunit of the coat protein I complex

2021 · Wayne Bainter, Craig D. Platt, et al. · Journal of Clinical Investigation · 25

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Genetic diagnosis of primary immunodeficiencies: A survey of the French national registry

2019 · Nizar Mahlaoui, Capucine Picard, et al. · Journal of Allergy and Clinical Immunology · 25

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CXCR4 WHIM syndrome is a cancer predisposition condition for virus‐induced malignancies

2024 · Clémentine Moulin, Blandine Beaupain, et al. · British Journal of Haematology · 14

ITK deficiency presenting as autoimmune lymphoproliferative syndrome

2020 · Jacqueline G. Wallace, Mohammed F. Alosaimi, et al. · Journal of Allergy and Clinical Immunology · 14

How Many Patients Have Congenital Neutropenia? a Population-Based Estimation from the Nationwide French Severe Chronic Neutropenia Registry

2020 · Jean Donadieu, Blandine Beaupain, et al. · Blood · 7

MR imaging features of peritoneal alveolar echinococcosis

2018 · S. Beaussant-Cohen, C. Richou, et al. · Diagnostic and Interventional Imaging · 7

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DOCK8 Mutation Syndrome: A Diagnostic Challenge for Dermatologists

2015 · J Moreau, S Beaussant-Cohen, et al. · Acta Dermato Venereologica · 6

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Safety and efficacy of allogeneic CD19-directed CAR-T therapy CTX110 in relapsed/refractory B-cell non-Hodgkin lymphoma

2026 · Joseph P. McGuirk, Armin Ghobadi, et al. · Blood Advances · 2

Congenital Neutropenia Is Also Associated with a High Cancer Risk: A Study from the French Severe Chronic Neutropenia Registry

2020 · Jean Donadieu, Fares bou Mitri, et al. · Blood · 2

Neutropénie en dehors d’un contexte de chimiothérapie : bilan et prise en charge-recommandations du centre de référence

2020 · F. Bou Mitri, B. Beaupain, et al. · Perfectionnement en Pédiatrie · 1

Abstract C004: The CXCR4 inhibitor X4-136 enhances the in vivo efficacy of established drugs against preclinical models of aggressive pediatric acute lymphoblastic leukemia

2019 · Richard B Lock, Kathryn Evans, et al. · Molecular Cancer Therapeutics

P-524 – Polyarthrite fébrile et thrombopénie révélant un VIH en pédiatrie

2015 · M. Granjon, M. Koudzi, et al. · Archives de Pédiatrie

P-253 – Un diagnostic tiré par les cheveux !

2015 · S. Beaussant Cohen, N. Cheik, et al. · Archives de Pédiatrie

Mutation DOCK 8 : une nouvelle cause du syndrome hyper-IgE

2013 · J. Moreau, E. Puzenat, et al. · Annales de Dermatologie et de Vénéréologie

Works count: 28

Citation count: 1,589

H-index: 14

I10-index: 15