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Profil bibliographique

Carlos A. Flores

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

24Publications signalées
526Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

interferon and immune responsesSARS-CoV-2 and COVID-19 ResearchCOVID-19 Clinical Research StudiesCOVID-19 and Mental HealthLiver Disease Diagnosis and Treatment

Les publications récentes

Accès ouvert 2025 article OpenAlex

Deleterious variants in the autophagy-related gene RB1CC1/FIP200 impair immunity to SARS-CoV-2

Renée M. van der Sluis, Kennith Brian Castelino, Bao‐cun Zhang, Andreas Ronit et autres

The clinical outcome of SARS-CoV-2 infection spans from asymptomatic viral elimination to lethal COVID-19 pneumonia, which is due to type I interferon (IFN) deficiency in at least 15–20% of cases. We report two unrelated male patients with critical COVID-19 who are heterozygous …

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4 citations Nature Communications
Accès ouvert 2025 article OpenAlex

The seven enigmas of SARS-CoV-2: From the past to the future

Evangelos Andreakos, Lisa M. Arkin, Paul Bastard, Alexandre Bolze et autres

Five years ago, we launched the COVID Human Genetic Effort. Our goal was to explain the clinical variability among SARS-CoV-2-exposed individuals by searching for monogenic inborn errors of immunity (IEI) and their phenocopies. We deciphered the pathogenesis of critical COVID-19 pneumonia and …

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3 citations Journal of Human Immunity
Accès ouvert 2025 report OpenAlex

Causal Effects of Schooling on Memory at Older Ages in Six Low-and-Middle-Income Countries: Nonparametric Evidence with Harmonized Datasets

Vikesh Amin, Jere Richard Behrman, Jason M. Fletcher, Carlos A. Flores et autres

Higher schooling attainment is associated with better cognitive function at older ages, but it remains unclear whether the relationship is causal. We estimate causal effects of schooling on performances on the Consortium to Establish a Registry for Alzheimer’s Disease (CERAD) word-recall (memory) …

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0 citations
Accès ouvert 2024 article OpenAlex

A common form of dominant human IFNAR1 deficiency impairs IFN-α and -ω but not IFN-β-dependent immunity

Fahd A. Al Qureshah, Jérémie Le Pen, Nicole A. de Weerd, Marcela Moncada‐Vélez et autres

Autosomal recessive deficiency of the IFNAR1 or IFNAR2 chain of the human type I IFN receptor abolishes cellular responses to IFN-α, -β, and -ω, underlies severe viral diseases, and is globally very rare, except for IFNAR1 and IFNAR2 deficiency in Western Polynesia …

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14 citations The Journal of Experimental Medicine
Accès ouvert 2024 article OpenAlex

Polygenic risk of idiopathic pulmonary fibrosis and COVID-19 severity

Beatriz Guillén‐Guío, Itahisa Marcelino-Rodríguez, Jose Miguel Lorenzo-Salazar, Olivia C. Leavy et autres

Background: A shared genetic component between coronavirus disease 2019 (COVID-19) and idiopathic pulmonary fibrosis (IPF) has been described based on analyses of individual risk variants. Here we used a whole-genome polygenic risk score (PRS) approach to further evaluate age- and sex-stratified genetic …

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4 citations ERJ Open Research
Accès ouvert 2024 peer-review OpenAlex

Author response: Novel risk loci for COVID-19 hospitalization among admixed American populations

Silvia Diz‐de Almeida, Raquel Cruz, André Ducati Luchessi, Jose Miguel Lorenzo-Salazar et autres

The genetic basis of severe COVID-19 has been thoroughly studied, and many genetic risk factors shared between populations have been identified. However, reduced sample sizes from non-European groups have limited the discovery of population-specific common risk loci. In this second study nested …

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0 citations
Accès ouvert 2024 article OpenAlex

SARS-CoV-2 brainstem encephalitis in human inherited DBR1 deficiency

Yi‐Hao Chan, Vanja Lundberg, Jérémie Le Pen, Jiayi Yuan et autres

Inherited deficiency of the RNA lariat-debranching enzyme 1 (DBR1) is a rare etiology of brainstem viral encephalitis. The cellular basis of disease and the range of viral predisposition are unclear. We report inherited DBR1 deficiency in a 14-year-old boy who suffered from …

us, se, fr, it, Égypte, tr, sa, be, ae, ca, dk, cn (code pays fourni par la source)

21 citations The Journal of Experimental Medicine

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