A Bakkaloğlu

Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III

David B. Simon, Ranjit S. Bindra, Traci A. Mansfield et al. · Nature Genetics · 1997 · 870 citations

Life Sciences, Genetics, Molecular Genetics +13

Disease severity in children and adolescents with familial Mediterranean fever: a comparative study to explore environmental effects on a monogenic disease

Seza Özen, Nuray Aktay, Elke Lainka et al. · Annals of the Rheumatic Diseases · 2008 · 116 citations

Life Sciences, Genetics, Pediatrics +14

Diagnostic criteria for polyarteritis nodosa in childhood

Seza Özen, Nesrin Beşbaş, U Saatçi et al. · The Journal of Pediatrics · 1992 · 113 citations

Medicine, Pathology, Pediatrics +5

Implications of certain genetic polymorphisms in scarring in vesicoureteric reflux: Importance of ace polymorphism

Seza Özen, Mehmet Alikasifoglu, U Saatçi et al. · American Journal of Kidney Diseases · 1999 · 74 citations

Life Sciences, Genetics, Urology +7

Molecular basis of hereditary C1q deficiency associated with SLE and IgA nephropathy in a Turkish family

Rezan Topaloğlu, A Bakkaloğlu, J.H. Slingsby et al. · Kidney International · 1996 · 53 citations · Full text

Medicine, Genetics, Nephrology +16