Salma Ben‐Salem

Mutations in DDHD2, Encoding an Intracellular Phospholipase A1, Cause a Recessive Form of Complex Hereditary Spastic Paraplegia

Janneke Schuurs-Hoeijmakers, Michael T. Geraghty, Erik‐Jan Kamsteeg et al. · The American Journal of Human Genetics · 2012 · 178 citations · Full text

Recessive Form, Signal Transduction, Intracellular Phospholipase A1 +8

Alteration of the serine protease PRSS56 causes angle-closure glaucoma in mice and posterior microphthalmia in humans and mice

K. Saidas Nair, Mounira Hmani‐Aifa, Zain Ali et al. · Nature Genetics · 2011 · 107 citations

Angle-closure Glaucoma, Serine Protease Prss56, Ocular Disease +9

A comprehensive analysis of coregulator recruitment, androgen receptor function and gene expression in prostate cancer

Song Liu, Sangeeta Kumari, Qiang Hu et al. · eLife · 2017 · 76 citations · Full text

A Novel Single-Nucleotide Deletion (c.1020delA) in NSUN2 Causes Intellectual Disability in an Emirati Child

Makanko Komara, Aisha Al‐Shamsi, Salma Ben‐Salem et al. · Journal of Molecular Neuroscience · 2015 · 53 citations

Mendelian Disorder, Emirati Child, Genetic Disorder +7

METTL23, a transcriptional partner of GABPA, is essential for human cognition

Rachel E. Reiff, Bassam R. Ali, Byron Baron et al. · Human Molecular Genetics · 2014 · 50 citations · Full text

Transcriptional Regulation, Systems Biology, Genetic Disorder +15