Bassam R. Ali

Mutations in the Cilia Gene ARL13B Lead to the Classical Form of Joubert Syndrome

Vincent Cantagrel, Jennifer L. Silhavy, Stephanie Bielas et al. · The American Journal of Human Genetics · 2008 · 395 citations · Full text

Developmental Biology, Mendelian Disorder, Joubert Syndrome +10

SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder

Vincent Cantagrel, Dirk J. Lefeber, Bobby G. Ng et al. · Cell · 2010 · 303 citations · Full text

Is Mutated, Genetics, Glycobiology +3

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

Membrane Targeting of Rab GTPases Is Influenced by the Prenylation Motif

Anita Quintal Gomes, Bassam R. Ali, José S. Ramalho et al. · Molecular Biology of the Cell · 2003 · 153 citations · Full text

Rab Gtpases, Prenylation Motif, Signal Transduction +14

DNA methylation and repressive H3K9 and H3K27 trimethylation in the promoter regions of PD-1, CTLA-4, TIM-3, LAG-3, TIGIT, and PD-L1 genes in human primary breast cancer

Varun Sasidharan Nair, Haytham El Salhat, Rowaida Z. Taha et al. · Clinical Epigenetics · 2018 · 142 citations · Full text