Lista de obras -

A global ocean atlas of eukaryotic genes.

artículo científico publicado en 2018

A loss-of-function IFNAR1 allele in Polynesia underlies severe viral diseases in homozygotes

artículo científico publicado en 2022

Accessing the genomic information of unculturable oceanic picoeukaryotes by combining multiple single cells.

artículo científico publicado en 2017

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

artículo científico publicado en 2020

Common homozygosity for predicted loss-of-function variants reveals both redundant and advantageous effects of dispensable human genes

scientific article published on 02 June 2020

Correction: Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome

artículo científico publicado en 2020

Detection of homozygous and hemizygous complete or partial exon deletions by whole-exome sequencing

artículo científico publicado en 2021

Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome

artículo científico publicado en 2020

Herpes simplex encephalitis in a patient with a distinctive form of inherited IFNAR1 deficiency

scientific article published on 22 September 2020

Homozygosity for TYK2 P1104A underlies tuberculosis in about 1% of patients in a cohort of European ancestry

scientific article published on 08 May 2019

Human IFN-γ immunity to mycobacteria is governed by both IL-12 and IL-23

artículo científico publicado en 2018

Human T-bet Governs Innate and Innate-like Adaptive IFN-γ Immunity against Mycobacteria

scientific article published on 03 December 2020

Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

scientific article published on 24 September 2020

Inherited IFNAR1 deficiency in otherwise healthy patients with adverse reaction to measles and yellow fever live vaccines

artículo científico publicado en 2019

Inherited human IFNγ deficiency underlies mycobacterial disease

artículo científico publicado en 2020

Single-cell genomics of multiple uncultured stramenopiles reveals underestimated functional diversity across oceans

artículo científico publicado en 2018

Survey of the green picoalga Bathycoccus genomes in the global ocean

artículo científico publicado en 2016

The immunopathological landscape of human pre-TCRα deficiency: From rare to common variants

artículo científico publicado en 2024

X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19

scholarly article by Takaki Asano published in 2021

Lista de obras de

A global ocean atlas of eukaryotic genes.

A loss-of-function IFNAR1 allele in Polynesia underlies severe viral diseases in homozygotes

Accessing the genomic information of unculturable oceanic picoeukaryotes by combining multiple single cells.

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

Common homozygosity for predicted loss-of-function variants reveals both redundant and advantageous effects of dispensable human genes

Correction: Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome

Detection of homozygous and hemizygous complete or partial exon deletions by whole-exome sequencing

Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome

Herpes simplex encephalitis in a patient with a distinctive form of inherited IFNAR1 deficiency

Homozygosity for TYK2 P1104A underlies tuberculosis in about 1% of patients in a cohort of European ancestry

Human IFN-γ immunity to mycobacteria is governed by both IL-12 and IL-23

Human T-bet Governs Innate and Innate-like Adaptive IFN-γ Immunity against Mycobacteria

Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

Inherited IFNAR1 deficiency in otherwise healthy patients with adverse reaction to measles and yellow fever live vaccines

Inherited human IFNγ deficiency underlies mycobacterial disease

Single-cell genomics of multiple uncultured stramenopiles reveals underestimated functional diversity across oceans

Survey of the green picoalga Bathycoccus genomes in the global ocean

The immunopathological landscape of human pre-TCRα deficiency: From rare to common variants

X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19