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

by Amina Kamar, Athar Khalil, Georges Nemer, Georges Nemer
Published 2021-01-01

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

by Athar Khalil, Amina Kamar, Georges Nemer, Georges Nemer
Published 2020-05-01

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

by Athar Khalil, Samer Bou Karroum, Rana Barake, Gabriel Dunya, Samer Abou-Rizk, Amina Kamar, Georges Nemer, Marc Bassim
Published 2020-01-01

Two heterozygous mutations in NFATC1 in a patient with Tricuspid Atresia.

by Zahi Abdul-Sater, Amin Yehya, Jean Beresian, Elie Salem, Amina Kamar, Serine Baydoun, Kamel Shibbani, Ayman Soubra, Fadi Bitar, Georges Nemer
Published 2012-01-01

A Novel Role for CSRP1 in a Lebanese Family with Congenital Cardiac Defects

by Amina Kamar, Akl C. Fahed, Akl C. Fahed, Akl C. Fahed, Kamel Shibbani, Nehme El-Hachem, Salim Bou-Slaiman, Mariam Arabi, Mazen Kurban, Mazen Kurban, Mazen Kurban, Jonathan G. Seidman, Christine E. Seidman, Christine E. Seidman, Rachid Haidar, Elias Baydoun, Georges Nemer, Fadi Bitar
Published 2017-12-01