Irman Forghani
8PUBLICATIONS
11CO-AUTHORS
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Publications (8)
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|Feb 13, 2024
EFEMP1 haploinsufficiency causes a Marfan-like hereditary connective tissue disorder.Irman Forghani, Steven H Lang, Matthew J Rodier
|Mar 03, 2023
Prevalence of cardiovascular manifestations in patients with hypermobile Ehlers-Danlos syndrome at the University of Miami.Jariselle M Pietri-Toro, Olivia K Gardner, Jessica D Leuchter
|Mar 04, 2022
A novel pathogenic variant at the C-terminal propeptide cleavage site of COL1A1, causing osteogenesis imperfecta with intrafamilial variability.Steven H Lang, Ryan A Gallo, Irman Forghani
|Jun 21, 2021
Application of the ACMG/NSGC genetic referral guidelines for hereditary renal cell carcinoma at the University of Miami, from 2014 to 2017.Jessica D Leuchter, Priyen M Patel, Kayla M Fourzali
|Jan 11, 2021
First reported adult patient with retinal dystrophy and leukodystrophy caused by a novel ACBD5 variant: A case report and review of literature.Michelle Bartlett, Nima Nasiri, Rena Pressman
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Frequent Collaborators
1 joint publications
Neda Ghiam
1 joint publications
Kathleen S Hruska
1 joint publications
J William Harbour
1 joint publications
Steven H Lang
1 joint publications
Ryan A Gallo
1 joint publications
Guney Bademci
1 joint publications
Mustafa Tekin
1 joint publications
Hisham F Bahmad
1 joint publications
Ghassan Ghssein
1 joint publications
Marwan Bahmad