Publications by authors named "Franck Rapaport"

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Development of an AAV-delivered microRNA gene therapy for myotonic dystrophy type 1.
Giulio S Tomassy, Wei Fan, Shuwen Cao, Zhengyu Luo, Alessandro Magli, Franck Rapaport

Mol Ther· December 2025

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Artificial miRNA-mediated reduction of SNCA for the treatment of α-synucleinopathies.
Bradford Elmer, Erik Wischhof, Tiffany Chan, Thanga Aishwarya Mahendran, Jeff Ardinger, Franck Rapaport

Mol Ther· November 2025

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SciLinker: a large-scale text mining framework for mapping associations among biological entities.
Dongyu Liu, Cora Ames, Shameer Khader, Franck Rapaport

Front Artif Intell· March 2025

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Tuberculosis in otherwise healthy adults with inherited TNF deficiency.
Andrés A Arias, Anna-Lena Neehus, Masato Ogishi, Vincent Meynier, Adam Krebs, Franck Rapaport

Nature· September 2024

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Inherited human RelB deficiency impairs innate and adaptive immunity to infection.
Tom Le Voyer, Majistor Raj Luxman Maglorius Renkilaraj, Kunihiko Moriya, Malena Pérez Lorenzo, Tina Nguyen, Franck Rapaport

Proc Natl Acad Sci U S A· September 2024

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Helper T cell immunity in humans with inherited CD4 deficiency.
Antoine Guérin, Marcela Moncada-Vélez, Katherine Jackson, Masato Ogishi, Jérémie Rosain, Franck Rapaport

J Exp Med· May 2024

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Correction: Integrative analysis identifies an older female-linked AML patient group with better risk in ECOG-ACRIN Cancer Research Group's clinical trial E3999.
Franck Rapaport, Kenneth Seier, Yaseswini Neelamraju, Duane Hassane, Timour Baslan

Blood Cancer J· July 2023

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DiSiR: fast and robust method to identify ligand-receptor interactions at subunit level from single-cell RNA-sequencing data.
Milad R Vahid, Andre H Kurlovs, Tommaso Andreani, Franck Augé, Reza Olfati-Saber, Franck Rapaport

NAR Genom Bioinform· March 2023

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Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency.
Romain Lévy, Florian Gothe, Mana Momenilandi, Thomas Magg, Marie Materna, Franck Rapaport

J Exp Med· February 2023

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Human IRF1 governs macrophagic IFN-γ immunity to mycobacteria.
Jérémie Rosain, Anna-Lena Neehus, Jérémy Manry, Rui Yang, Jérémie Le Pen, Franck Rapaport

Cell· February 2023

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Integrative analysis identifies an older female-linked AML patient group with better risk in ECOG-ACRIN Cancer Research Group's clinical trial E3999.
Franck Rapaport, Kenneth Seier, Yaseswini Neelamraju, Duane Hassane, Timour Baslan

Blood Cancer J· September 2022

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Human OTULIN haploinsufficiency impairs cell-intrinsic immunity to staphylococcal α-toxin.
András N Spaan, Anna-Lena Neehus, Emmanuel Laplantine, Frederik Staels, Masato Ogishi, Franck Rapaport

Science· June 2022

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Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency.
Juan Li, Wei-Te Lei, Peng Zhang, Franck Rapaport, Yoann Seeleuthner

J Exp Med· November 2021

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Genomic and evolutionary portraits of disease relapse in acute myeloid leukemia.
Franck Rapaport, Yaseswini Neelamraju, Timour Baslan, Duane Hassane, Agata Gruszczynska

Leukemia· September 2021

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Inherited PD-1 deficiency underlies tuberculosis and autoimmunity in a child.
Masato Ogishi, Rui Yang, Caner Aytekin, David Langlais, Mathieu Bourgey, Franck Rapaport

Nat Med· September 2021

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Inherited human c-Rel deficiency disrupts myeloid and lymphoid immunity to multiple infectious agents.
Romain Lévy, David Langlais, Vivien Béziat, Franck Rapaport, Geetha Rao

J Clin Invest· September 2021

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Human STAT3 variants underlie autosomal dominant hyper-IgE syndrome by negative dominance.
Takaki Asano, Joëlle Khourieh, Peng Zhang, Franck Rapaport, András N Spaan

J Exp Med· August 2021

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Recurrent Mutations in Cyclin D3 Confer Clinical Resistance to FLT3 Inhibitors in Acute Myeloid Leukemia.
Catherine C Smith, Aaron D Viny, Evan Massi, Cyriac Kandoth, Nicholas D Socci, Franck Rapaport

Clin Cancer Res· July 2021

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Humans with inherited T cell CD28 deficiency are susceptible to skin papillomaviruses but are otherwise healthy.
Vivien Béziat, Franck Rapaport, Jiafen Hu, Matthias Titeux, Mathilde Bonnet des Claustres

Cell· July 2021

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Inherited GATA2 Deficiency Is Dominant by Haploinsufficiency and Displays Incomplete Clinical Penetrance.
Carmen Oleaga-Quintas, Edgar Borges de Oliveira-Júnior, Jérémie Rosain, Franck Rapaport, Caroline Deswarte

J Clin Immunol· April 2021

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Inherited deficiency of stress granule ZNFX1 in patients with monocytosis and mycobacterial disease.
Tom Le Voyer, Anna-Lena Neehus, Rui Yang, Masato Ogishi, Jérémie Rosain, Franck Rapaport

Proc Natl Acad Sci U S A· April 2021

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Negative selection on human genes underlying inborn errors depends on disease outcome and both the mode and mechanism of inheritance.
Franck Rapaport, Bertrand Boisson, Anne Gregor, Vivien Béziat, Stéphanie Boisson-Dupuis

Proc Natl Acad Sci U S A· January 2021

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Targeted genomic analysis of cutaneous T cell lymphomas identifies a subset with aggressive clinicopathological features.
Kimon V Argyropoulos, Melissa Pulitzer, Francesco Maura, Abhinita Mohanty, Patrizia Mondello, Franck Rapaport

Blood Cancer J· November 2020

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Inborn errors of type I IFN immunity in patients with life-threatening COVID-19.
Qian Zhang, Paul Bastard, Zhiyong Liu, Jérémie Le Pen, Marcela Moncada-Velez, Franck Rapaport

Science· October 2020

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Common homozygosity for predicted loss-of-function variants reveals both redundant and advantageous effects of dispensable human genes.
Antonio Rausell, Yufei Luo, Marie Lopez, Yoann Seeleuthner, Franck Rapaport

Proc Natl Acad Sci U S A· June 2020

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