Sultan Bahabri

CACP, encoding a secreted proteoglycan, is mutated in camptodactyly-arthropathy-coxa vara-pericarditis syndrome

José Roberto Marcelino, John D. Carpten, Wafaa M. Suwairi et al. · Nature Genetics · 1999 · 322 citations

Cardiomyopathy, Camptodactyly-arthropathy-coxa Vara-pericarditis Syndrome, Medicine +7

Mutation of the matrix metalloproteinase 2 gene (MMP2) causes a multicentric osteolysis and arthritis syndrome

John A. Martignetti, A. Al Aqeel, Wafaa Sewairi et al. · Nature Genetics · 2001 · 311 citations

Bone Disease, Rheumatology, Sclerostin +12

Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasia

Jennifer Hurvitz, Wafaa M. Suwairi, Wim Van Hul et al. · Nature Genetics · 1999 · 277 citations

Autoimmune Disease, Disease Mechanism, Pathogenesis +3

Clinical features of Behçet's disease in children: An international collaborative study of 86 cases

Isabelle Kone‐Paut, Sebahattin Yurdakul, Sultan Bahabri et al. · The Journal of Pediatrics · 1998 · 248 citations

International Collaborative Study, Autoimmune Disease, Immunodeficiencies +3

Divergent cytokine production profile in Behçet's disease. Altered Th1/Th2 cell cytokine pattern.

Syed Raziuddin, Abdullah Al-Dalaan, Sultan Bahabri et al. · PubMed · 1998 · 116 citations