Mutations in the Cilia Gene ARL13B Lead to the Classical Form of Joubert SyndromeVincent Cantagrel, Joseph G. Gleeson, Stephanie Bielas et al.|The American Journal of Human Genetics|2008Cited by 399
Trafficking defects and loss of ligand binding are the underlying causes of all reported DDR2 missense mutations found in SMED-SL patientsBassam R. Ali, Birgit Leitinger|Human Molecular Genetics|2010Cited by 81
Endoplasmic reticulum quality control of LDLR variants associated with familial hypercholesterolemiaPraseetha Kizhakkedath, Bassam R. Ali|FEBS Open Bio|2019Cited by 52
Pathological Crosstalk Between Oxidized LDL and ER Stress in Human Diseases: A Comprehensive ReviewDivya Saro Varghese, Bassam R. Ali|Frontiers in Cell and Developmental Biology|2021Cited by 45
A novel mutation in DDR2 causing spondylo-meta-epiphyseal dysplasia with short limbs and abnormal calcifications (SMED-SL) results in defective intra-cellular traffickingAdila Al‐Kindi, Bassam R. Ali|BMC Medical Genetics|2014Cited by 33