Seyed Hassan Paylakhi

Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma

Mehrnaz Narooie-Nejad, Seyed Hassan Paylakhi, Seyedmehdi Shojaee et al. · Human Molecular Genetics · 2009 · 158 citations

Medicine, Genetics, Ophthalmology +16

LTBP2 mutations cause Weill-Marchesani and Weill-Marchesani-like syndrome and affect disruptions in the extracellular matrix

Ramona Haji‐Seyed‐Javadi, Sahar Jelodari-Mamaghani, Seyed Hassan Paylakhi et al. · Human Mutation · 2012 · 126 citations

Life Sciences, Genetics, Molecular Genetics +14

Variable Expressivity and High Penetrance of CYP1B1 Mutations Associated with Primary Congenital Glaucoma

Fatemeh Suri, Shahin Yazdani, Mehrnaz Narooie-Nejhad et al. · Ophthalmology · 2009 · 51 citations

Medicine, Genetics, Ophthalmology +10

A microRNA signature associated with chondrogenic lineage commitment

Behnaz Bakhshandeh, Masoud Soleimani, Seyed Hassan Paylakhi et al. · Journal of Genetics · 2012 · 50 citations

Life Sciences, Cell Biology, Molecular Biology +13

FOXC1 in human trabecular meshwork cells is involved in regulatory pathway that includes miR-204, MEIS2, and ITGβ1

Seyed Hassan Paylakhi, Hamidreza Moazzeni, Shahin Yazdani et al. · Experimental Eye Research · 2013 · 50 citations

Life Sciences, Cell Biology, Molecular Biology +9