Lista de obras - Guillaume Vogt - Dominio Público Uruguay

23andMe: a new two-sided data-banking market model

artículo científico publicado en 2016

A novel X-linked recessive form of Mendelian susceptibility to mycobaterial disease

artículo científico publicado en 2007

A novel form of cell type-specific partial IFN-gammaR1 deficiency caused by a germ line mutation of the IFNGR1 initiation codon

artículo científico publicado en 2009

A partial form of recessive STAT1 deficiency in humans

artículo científico publicado en 2009

Artificial intelligence in internal medicine: Between science and pseudoscience.

artículo científico publicado en 2018

Auto-antibodies against type I IFNs in patients with life-threatening COVID-19

artículo científico publicado en 2020

BCG-osis and tuberculosis in a child with chronic granulomatous disease

scholarly article by Jacinta Bustamante et al published July 2007 in The Journal of Allergy and Clinical Immunology

Complementation of a pathogenic IFNGR2 misfolding mutation with modifiers of N-glycosylation

Complementation of a pathogenic IFNGR2 misfolding mutation with modifiers of N-glycosylation.

artículo científico publicado en 2008

Corrigendum to “Inborn errors of IL-12/23- and IFN-γ-mediated immunity: Molecular, cellular, and clinical features” [Semin. Immunol. 18 (2006) 347–361]

scholarly article published in Seminars in Immunology

French-style genetics v. 2.0: The "e-CohortE" project

artículo científico publicado en 2019

Gain-of-glycosylation mutations

artículo científico publicado en 2007

Gains of glycosylation comprise an unexpectedly large group of pathogenic mutations

artículo científico publicado en 2005

Gains of glycosylation mutations

artículo científico publicado en 2006

Genetic Data, Two-Sided Markets and Dynamic Consent: United States Versus France

artículo científico publicado en 2019

Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease

artículo científico publicado en 2011

Glycosylation-Dependent IFN-γR Partitioning in Lipid and Actin Nanodomains Is Critical for JAK Activation.

artículo científico publicado en 2016

Haploinsufficiency at the human IFNGR2 locus contributes to mycobacterial disease

artículo científico publicado en 2012

Herpes simplex virus encephalitis in a patient with complete TLR3 deficiency: TLR3 is otherwise redundant in protective immunity

artículo científico publicado en 2011

IFN-gamma mediates the rejection of haematopoietic stem cells in IFN-gammaR1-deficient hosts

artículo científico publicado en 2008

IRF4 haploinsufficiency in a family with Whipple's disease.

artículo científico publicado en 2018

In vitro differentiation of human macrophages with enhanced antimycobacterial activity

artículo científico publicado en 2011

Inborn errors of IL-12/23- and IFN-gamma-mediated immunity: molecular, cellular, and clinical features

artículo científico publicado en 2006

Inherited disorders of the IL-12-IFN-gamma axis in patients with disseminated BCG infection

artículo científico publicado en 2005

Inhibitors selective for mycobacterial versus human proteasomes

artículo científico publicado en 2009

Molecular Tumor Boards: Ethical Issues in the New Era of Data Medicine.

artículo científico publicado en 2017

Multiple cutaneous squamous cell carcinomas in a patient with interferon gamma receptor 2 (IFN gamma R2) deficiency

artículo científico publicado en 2010

Mycobacterial disease and impaired IFN-γ immunity in humans with inherited ISG15 deficiency

artículo científico publicado en 2012

Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases.

artículo científico publicado en 2016

Mycobacterium simiae infection in two unrelated patients with different forms of inherited IFN-γR2 deficiency

artículo científico publicado en 2014

Novel STAT1 alleles in otherwise healthy patients with mycobacterial disease

artículo científico publicado en 2006

Partial IFN-γR2 deficiency is due to protein misfolding and can be rescued by inhibitors of glycosylation

artículo científico publicado en 2013

Prédisposition génétique et infections de l'enfant

artículo científico publicado en 2006

Recurrent non-typhoidal salmonella bacteremia in a patient with interleukin -12p40 deficiency.

artículo científico publicado en 2004

T cell-dependent activation of dendritic cells requires IL-12 and IFN-gamma signaling in T cells

artículo científico publicado en 2006

The human gene connectome as a map of short cuts for morbid allele discovery

artículo científico publicado en 2013

Toward dynamic informed consent

artículo científico publicado en 2017

X-linked susceptibility to mycobacteria is caused by mutations in NEMO impairing CD40-dependent IL-12 production

artículo científico publicado en 2006

[Genetic data sharing: a new type of capital]

scientific article published on 01 August 2018

[The ownership of genetic data: from data to information]

scientific article published on 01 December 2018

Lista de obras de Guillaume Vogt

23andMe: a new two-sided data-banking market model

A novel X-linked recessive form of Mendelian susceptibility to mycobaterial disease

A novel form of cell type-specific partial IFN-gammaR1 deficiency caused by a germ line mutation of the IFNGR1 initiation codon

A partial form of recessive STAT1 deficiency in humans

Artificial intelligence in internal medicine: Between science and pseudoscience.

Auto-antibodies against type I IFNs in patients with life-threatening COVID-19

BCG-osis and tuberculosis in a child with chronic granulomatous disease

Complementation of a pathogenic IFNGR2 misfolding mutation with modifiers of N-glycosylation

Complementation of a pathogenic IFNGR2 misfolding mutation with modifiers of N-glycosylation.

Corrigendum to “Inborn errors of IL-12/23- and IFN-γ-mediated immunity: Molecular, cellular, and clinical features” [Semin. Immunol. 18 (2006) 347–361]

French-style genetics v. 2.0: The "e-CohortE" project

Gain-of-glycosylation mutations

Gains of glycosylation comprise an unexpectedly large group of pathogenic mutations

Gains of glycosylation mutations

Genetic Data, Two-Sided Markets and Dynamic Consent: United States Versus France

Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease

Glycosylation-Dependent IFN-γR Partitioning in Lipid and Actin Nanodomains Is Critical for JAK Activation.

Haploinsufficiency at the human IFNGR2 locus contributes to mycobacterial disease

Herpes simplex virus encephalitis in a patient with complete TLR3 deficiency: TLR3 is otherwise redundant in protective immunity

IFN-gamma mediates the rejection of haematopoietic stem cells in IFN-gammaR1-deficient hosts

IRF4 haploinsufficiency in a family with Whipple's disease.

In vitro differentiation of human macrophages with enhanced antimycobacterial activity

Inborn errors of IL-12/23- and IFN-gamma-mediated immunity: molecular, cellular, and clinical features

Inherited disorders of the IL-12-IFN-gamma axis in patients with disseminated BCG infection

Inhibitors selective for mycobacterial versus human proteasomes

Molecular Tumor Boards: Ethical Issues in the New Era of Data Medicine.

Multiple cutaneous squamous cell carcinomas in a patient with interferon gamma receptor 2 (IFN gamma R2) deficiency

Mycobacterial disease and impaired IFN-γ immunity in humans with inherited ISG15 deficiency

Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases.

Mycobacterium simiae infection in two unrelated patients with different forms of inherited IFN-γR2 deficiency

Novel STAT1 alleles in otherwise healthy patients with mycobacterial disease

Partial IFN-γR2 deficiency is due to protein misfolding and can be rescued by inhibitors of glycosylation

Prédisposition génétique et infections de l'enfant

Recurrent non-typhoidal salmonella bacteremia in a patient with interleukin -12p40 deficiency.

T cell-dependent activation of dendritic cells requires IL-12 and IFN-gamma signaling in T cells

The human gene connectome as a map of short cuts for morbid allele discovery

Toward dynamic informed consent

X-linked susceptibility to mycobacteria is caused by mutations in NEMO impairing CD40-dependent IL-12 production

[Genetic data sharing: a new type of capital]

[The ownership of genetic data: from data to information]