Inaam El‐Rassy

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

S. Azar, A. Fahed, G. Nemer, 2016, Molecular genetics & genomic medicine.

GATA5 mutation homozygosity linked to a double outlet right ventricle phenotype in a Lebanese patient

I. El-rassi, A. Fahed, M. Nemer, 2015, Molecular genetics & genomic medicine.

A novel nonsense mutation in NPHS1: is aortic stenosis associated with congenital nephropathy?

A. Fahed, Z. Kambris, G. Nemer, 2015, Journal of Genetics.

A novel nonsense mutation in NPHS1: is aortic stenosis associated with congenital nephropathy?

A. Fahed, Z. Kambris, G. Nemer, 2015, Journal of Genetics.

A novel TRAF3IP2 variant causing familial scarring alopecia with mixed features of discoid lupus erythematosus and folliculitis decalvans

N. El-Hachem, A. Khalil, Y. Shimomura, 2020, Clinical genetics.

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

G. Nemer, Sara Al-Ghadban, F. Bitar, 2008, American journal of medical genetics. Part A.