Ramona Haji‐Seyed‐Javadi

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 · 125 citations

EZH2 has a non-catalytic and PRC2-independent role in stabilizing DDB2 to promote nucleotide excision repair

Allyson E. Koyen, Matthew Z. Madden, Dongkyoo Park et al. · Oncogene · 2020 · 52 citations · Full text

Chromatin, Genome Instability, Prc2-independent Role +9

The second mutation of SYCE1 gene associated with autosomal recessive nonobstructive azoospermia

Mahdieh Pashaei, Mohammad Masoud Rahimi Bidgoli, Davood Zare‐Abdollahi et al. · Journal of Assisted Reproduction and Genetics · 2020 · 51 citations · Full text

Developmental Biology, Genetic Disorder, Genetics +4

Contribution of the latent transforming growth factor-β binding protein 2 gene to etiology of primary open angle glaucoma and pseudoexfoliation syndrome.

Sahar Jelodari-Mamaghani, Ramona Haji‐Seyed‐Javadi, Fatemeh Suri et al. · PubMed · 2013 · 41 citations · Full text

SAMHD1 deacetylation by SIRT1 promotes DNA end resection by facilitating DNA binding at double-strand breaks

Priya Kapoor-Vazirani, Sandip Kumar Rath, Xu Liu et al. · Nature Communications · 2022 · 25 citations · Full text