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The Annals of Otology, Rhinology, and Laryngology|May 16, 2017
Self-extubation Laryngeal Injuries at an Academic Tertiary Care Center: A Retrospective Pilot StudyJason E Cohn, Andrew Touati, Mark Lentner, et al.
Dermatology Online Journal|February 22, 2023
An unexpected case of non-uremic calciphylaxis in a patient with multiple risk factorsShannon Nugent, Fred Karaisz, Maisa Elbadawi, et al.
Orphanet Journal of Rare Diseases|December 7, 2017
A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndromeLeila Youssefian, Andrew Touati, Amir Hossein Saeidian, et al.
Experimental Dermatology|April 30, 2020
The matriptase-prostasin proteolytic cascade in dermatologic diseasesAndrew Touati, Amir Hossein Saeidian, Leila Youssefian, et al.
BMC Medical Genetics|May 27, 2018
The genetic basis of hyaline fibromatosis syndrome in patients from a consanguineous background: a case seriesLeila Youssefian, Hassan Vahidnezhad, Andrew Touati, et al.
Scientific Reports|August 9, 2016
Regulation of proinflammatory genes by the circulating microRNA hsa-miR-939Marguerite K McDonald, Sujay Ramanathan, Andrew Touati, et al.
Human Mutation|July 18, 2018
Next generation sequencing identifies double homozygous mutations in two distinct genes (EXPH5 and COL17A1) in a patient with concomitant simplex and junctional epidermolysis bullosaHassan Vahidnezhad, Leila Youssefian, Amir Hossein Saeidian, et al.
Human Mutation|December 23, 2018
Autosomal recessive congenital ichthyosis: Genomic landscape and phenotypic spectrum in a cohort of 125 consanguineous familiesLeila Youssefian, Hassan Vahidnezhad, Amir Hossein Saeidian, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|November 16, 2017
Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathyHassan Vahidnezhad, Leila Youssefian, Amir Hossein Saeidian, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Genetic heterogeneity of heritable ectopic mineralization disorders in a large international cohortAmir Hossein Saeidian, Leila Youssefian, Jianhe Huang, et al.
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