Inaam El‐Rassy

<scp>GATA</scp>5 mutation homozygosity linked to a double outlet right ventricle phenotype in a Lebanese patient

Kameel Kassab, Hadla Hariri, Lara Gharibeh et al. · Molecular Genetics & Genomic Medicine · 2015 · 27 citations · Full text

Medicine, Cardiology, Genetics +15

Variable expressivity and co‐occurrence of <i>LDLR</i> and <i>LDLRAP1</i> mutations in familial hypercholesterolemia: failure of the dominant and recessive dichotomy

Akl C. Fahed, Ruby Ibrahim Khalaf, Rony H. Salloum et al. · Molecular Genetics & Genomic Medicine · 2016 · 19 citations · Full text

Medicine, Genetics, Molecular Genetics +13

A novel <scp> <i>TRAF3IP2</i> </scp> variant causing familial scarring alopecia with mixed features of discoid lupus erythematosus and folliculitis decalvans

Georges Nemer, Nehmé El-Hachem, Edward Eid et al. · Clinical Genetics · 2020 · 19 citations

Life Sciences, Dermatology, Genetics +17

Absence of <i>NOTCH2</i> and <i>Hey2</i> mutations in a familial Alagille syndrome case with a novel frameshift mutation in <i>JAG1</i>

Inaam El‐Rassy, Jad Bou‐Abdallah, Sara Al‐Ghadban et al. · American Journal of Medical Genetics Part A · 2008 · 11 citations

Life Sciences, Genetics, Molecular Genetics +10