Hager Jaouadi

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 12

Top Topics

Dna Methylation

Left Ventricular

Idiopathic Pulmonary Fibrosis

Top Venues

International journal of molecular sciences

Clinical case reports

American journal of respiratory and critical care medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Stephane Zaffran, Lilia Kraoua, Hager Jaouadi
Calcium Handling in Inherited Cardiac Diseases: A Focus on Catecholaminergic Polymorphic Ventricular Tachycardia and Hypertrophic Cardiomyopathy. International journal of molecular sciences 24 (4) (2023)
Stephane Zaffran, Lilia Kraoua, Hager Jaouadi
Calcium Handling in Inherited Cardiac Diseases: A Focus on Catecholaminergic Polymorphic Ventricular Tachycardia and Hypertrophic Cardiomyopathy. International journal of molecular sciences 24 (4) (2023)
Stephane Zaffran, Lilia Kraoua, Hager Jaouadi
Calcium Handling in Inherited Cardiac Diseases: A Focus on Catecholaminergic Polymorphic Ventricular Tachycardia and Hypertrophic Cardiomyopathy. International journal of molecular sciences 24 (4) (2023)
Stephane Zaffran, Lilia Kraoua, Hager Jaouadi
Calcium Handling in Inherited Cardiac Diseases: A Focus on Catecholaminergic Polymorphic Ventricular Tachycardia and Hypertrophic Cardiomyopathy. International journal of molecular sciences 24 (4) (2023)
Stephane Zaffran, Lilia Kraoua, Hager Jaouadi
Calcium Handling in Inherited Cardiac Diseases: A Focus on Catecholaminergic Polymorphic Ventricular Tachycardia and Hypertrophic Cardiomyopathy. International journal of molecular sciences 24 (4) (2023)
David Zhang, Gundula Povysil, Philippe H Kobeissy, Qi Li, Binhan Wang, Mason Amelotte, Hager Jaouadi, Chad A Newton, Toby M Maher, Philip L Molyneaux, Imre Noth, Fernando J Martinez, Ganesh Raghu, Jamie L Todd, Scott M Palmer, Carolina Haefliger, Adam Platt, Slavé Petrovski, Joseph A Garcia, David B Goldstein, Christine Kim Garcia
Rare and Common Variants in KIF15 Contribute to Genetic Risk of Idiopathic Pulmonary Fibrosis. American journal of respiratory and critical care medicine 206 (1) (2022)
Hager Jaouadi, Caroline Ovaert, Chloé Wanert, Aline Cano, Caroline Ovaert, Stephane Zaffran
Dilated-Left Ventricular Non-Compaction Cardiomyopathy in a Pediatric Case with SPEG Compound Heterozygous Variants. International journal of molecular sciences 23 (9) (2022)
Hager Jaouadi, Sonia Chabrak, Saida Lahbib, Sonia Abdelhak, Stephane Zaffran
Identification of two variants in AGRN and RPL3L genes in a patient with catecholaminergic polymorphic ventricular tachycardia suggesting new candidate disease genes and digenic inheritance. Clinical case reports 10 (2) (2022)
Hager Jaouadi, Alexis Theron, Jérôme Hourdain, Hélène Martel, Karine Nguyen, Raja Habachi, Jean-Claude Deharo, Frederic Collart, Jean-François Avierinos, Stephane Zaffran
SCN5A Variants as Genetic Arrhythmias Triggers for Familial Bileaflet Mitral Valve Prolapse. International journal of molecular sciences 23 (22) (2022)
Hager Jaouadi, Yosra Bouyacoub, Sonia Chabrak, Lilia Kraoua, Amira Zaroui, Sahar Elouej, Majdi Nagara, Hamza Dallali, Valérie Delague, Nicolas Levy, Rym Benkhalifa, Rachid Mechmeche, Stéphane Zaffran, Sonia Abdelhak
Multiallelic rare variants support an oligogenic origin of sudden cardiac death in the young. Herz 46 (Suppl 1) (2020)
Hager Jaouadi, Lilia Kraoua, Lilia Chaker, Alexandre Atkinson, Valérie Delague, Nicolas Levy, Rym Benkhalifa, Ridha Mrad, Sonia Abdelhak, Stephane Zaffran
Novel ALPK3 mutation in a Tunisian patient with pediatric cardiomyopathy and facio-thoraco-skeletal features. Journal of human genetics 63 (10) (2018)
Hager Jaouadi, Anissa Zaouak, Khadija Sellami, Olfa Messaoud, Mariem Chargui, Houda Hammami, Meriem Jones, Raja Jouini, Achraf Chadli Debbiche, Karima Chraiet, Sami Fenniche, Ridha Mrad, Mourad Mokni, Hamida Turki, Rym Benkhalifa, Sonia Abdelhak
H syndrome: Clinical, histological and genetic investigation in Tunisian patients. The Journal of dermatology 45 (8) (2018)