Laurent Argiro

Inserm — France

Medicine · Health Sciences

23h-index2.0kcitations56works9.02yr avg
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Research Topics

Research on Leishmaniasis Studies(22), Parasites and Host Interactions(18), Trypanosoma species research and implications(15), Congenital heart defects research(7), Hepatitis C virus research(6)

Publications56 total

Gastruloids are competent to specify both cardiac and skeletal muscle lineages
Nature Communications·2024· 13 citedOpen Access
TAK1 operates at the primary cilium in non-canonical TGFB/BMP signaling to control heart development
2024· 5 citedOpen Access
Cardiopharyngeal Mesoderm specification into cardiac and skeletal muscle lineages in gastruloids
2023· 1 citedOpen Access
Gastruloids as an in vitro model of Cardiopharyngeal Mesoderm specification into skeletal and cardiac muscle lineages
Archives of Cardiovascular Diseases Supplements·2023· 1 cited
Hox-dependent coordination of mouse cardiac progenitor cell patterning and differentiation
eLife·2020· 58 citedOpen Access
Author response: Hox-dependent coordination of mouse cardiac progenitor cell patterning and differentiation
2020· 2 citedOpen Access
<i>Hox</i> -dependent coordination of cardiac progenitor cell patterning and differentiation
2020· 2 citedOpen Access
A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide with<i>RAF1</i>S259Y neomutation
Genetics Research·2019· 5 citedOpen Access
&lt;i&gt;Hox&lt;/i&gt;-Dependent Coordination of Cardiac Cell Patterning and Differentiation
SSRN Electronic Journal·2019· 1 citedOpen Access
Low plasma haptoglobin is a risk factor for life-threatening childhood severe malarial anemia and not an exclusive consequence of hemolysis
Scientific Reports·2018· 15 citedOpen Access
Exome Sequencing Identifies Two Variants of the Alkylglycerol Monooxygenase Gene as a Cause of Relapses in Visceral Leishmaniasis in Children, in Sudan
The Journal of Infectious Diseases·2017· 14 citedOpen Access
A Functional IL22 Polymorphism (rs2227473) Is Associated with Predisposition to Childhood Cerebral Malaria
Scientific Reports·2017· 18 citedOpen Access
Exome sequencing identifies two variants of the alkylglycerol monooxygenase gene (AGMO) as a cause of relapses in visceral leishmaniasis in children, in Sudan.
HAL (Le Centre pour la Communication Scientifique Directe)·2017
Exome sequencing identifies a mutation associated with hepatocellular carcinoma development in hepatitis C virus infected individuals
Journal of Hepatology·2017
The <i>IL17F</i> and <i>IL17RA</i> Genetic Variants Increase Risk of Cerebral Malaria in Two African Populations
Infection and Immunity·2015· 18 citedOpen Access
<i>IL2RA</i> Genetic Variants Reduce IL-2–Dependent Responses and Aggravate Human Cutaneous Leishmaniasis
The Journal of Immunology·2015· 24 citedOpen Access
Potential Use of Interleukin-10 Blockade as a Therapeutic Strategy in Human Cutaneous Leishmaniasis
Journal of Immunology Research·2015· 25 citedOpen Access
Cutaneous Leishmaniasis Dependent Responses and Aggravate Human - Genetic Variants Reduce IL-2 IL2RA
2015
IL‐22 and IL‐22 binding protein (IL‐22BP) regulate fibrosis and cirrhosis in hepatitis C virus and schistosome infections
Hepatology·2014· 75 citedOpen Access
Impact of common risk factors of fibrosis progression in chronic hepatitis C
Gut·2014· 98 cited
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Frequent Co-authors

Alain Dessein(27), Hélia Dessein(19), Christophe Chevillard(12), Sandrine Marquet(11), Sandrine Henri(8), Laurent Abel(8), Fabienne Lescroart(8), Stéphane Zaffran(8), Sandrine Cabantous(6), Marc Bourlière(6), Virmondes Rodrigues(6), Adil Mergani(6), Jean‐Pierre Desvignes(6), Christophe Béroud(6), Audrey Romano(5), Bourèma Kouriba(5), Bruno Bucheton(5), Sayda El‐Safi(5), Philippe Halfon(5), Alain Bourgois(5)