Thalidomide-Revisited: Are COVID-19 Patients Going to Be the Latest Victims of Yet Another Theoretical Drug-Repurposing?

por Khalil, Athar, Kamar, Amina, Nemer, Georges
Publicado 2020

The Lebanese COVID-19 Cohort; A Challenge for the ABO Blood Group System

por Khalil, Athar, Feghali, Rita, Hassoun, Mahmoud
Publicado 2020

The Digenic Causality in Familial Hypercholesterolemia: Revising the Genotype–Phenotype Correlations of the Disease

por Kamar, Amina, Khalil, Athar, Nemer, Georges
Publicado 2021

Mutational signatures in GATA3 transcription factor and its DNA binding domain that stimulate breast cancer and HDR syndrome

por El-Assaad, Atlal, Dawy, Zaher, Khalil, Athar, Nemer, Georges
Publicado 2021

Questioning the sex-specific differences in the association of smoking on the survival rate of hospitalized COVID-19 patients

por Khalil, Athar, Dhingra, Radhika, Al-Mulki, Jida, Hassoun, Mahmoud, Alexis, Neil
Publicado 2021

Epigenetic Suppression of the T-box Subfamily 2 (TBX2) in Human Non-Small Cell Lung Cancer

por Nehme, Eliana, Rahal, Zahraa, Sinjab, Ansam, Khalil, Athar, Chami, Hassan, Nemer, Georges, Kadara, Humam
Publicado 2019

A HAND to TBX5 Explains the Link Between Thalidomide and Cardiac Diseases

por Khalil, Athar, Tanos, Rachel, El-Hachem, Nehmé, Kurban, Mazen, Bouvagnet, Patrice, Bitar, Fadi, Nemer, Georges
Publicado 2017

Weekly Nowcasting of New COVID-19 Cases Using Past Viral Load Measurements

por Khalil, Athar, Al Handawi, Khalil, Mohsen, Zeina, Abdel Nour, Afif, Feghali, Rita, Chamseddine, Ibrahim, Kokkolaras, Michael
Publicado 2022

A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations

por Khalil, Athar, Al-Haddad, Christiane, Hariri, Hadla, Shibbani, Kamel, Bitar, Fadi, Kurban, Mazen, Nemer, Georges, Arabi, Mariam
Publicado 2017

Post-lingual non-syndromic hearing loss phenotype: a polygenic case with 2 biallelic mutations in MYO15A and MITF

por Khalil, Athar, Karroum, Samer Bou, Barake, Rana, Dunya, Gabriel, Abou-Rizk, Samer, Kamar, Amina, Nemer, Georges, Bassim, Marc
Publicado 2020

Transcriptomic Alterations in Lung Adenocarcinoma Unveil New Mechanisms Targeted by the TBX2 Subfamily of Tumor Suppressor Genes

por Khalil, Athar, Dekmak, Batoul, Boulos, Fouad, Kantrowitz, Jake, Spira, Avrum, Fujimoto, Junya, Kadara, Humam, El-Hachem, Nehme, Nemer, Georges
Publicado 2018

TBX2 subfamily suppression in lung cancer pathogenesis: a high-potential marker for early detection

por Khalil, Athar A., Sivakumar, Smruthy, Lucas, Frances Anthony San, McDowell, Tina, Lang, Wenhua, Tabata, Kazuhiro, Fujimoto, Junya, Yatabe, Yasushi, Spira, Avrum, Scheet, Paul, Nemer, Georges, Kadara, Humam
Publicado 2017

Non-familial cardiomyopathies in Lebanon: exome sequencing results for five idiopathic cases

por Refaat, Marwan M., Hassanieh, Sylvana, Ballout, Jad A., Zakka, Patrick, Hotait, Mostafa, Khalil, Athar, Bitar, Fadi, Arabi, Mariam, Arnaout, Samir, Skouri, Hadi, Abchee, Antoine, Abi-Saleh, Bernard, Khoury, Maurice, Massouras, Andreas, Nemer, Georges
Publicado 2019

Founder Mutation in N Terminus of Cardiac Troponin I Causes Malignant Hypertrophic Cardiomyopathy

por Fahed, Akl C., Nemer, Georges, Bitar, Fadi F., Arnaout, Samir, Abchee, Antoine B., Batrawi, Manal, Khalil, Athar, Abou Hassan, Ossama K., DePalma, Steven R., McDonough, Barbara, Arabi, Mariam T., Ware, James S., Seidman, Jonathan G., Seidman, Christine E.
Publicado 2020