Harika Alpay

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

Mutations in the chloride-bicarbonate exchanger gene <i>AE1</i> cause autosomal dominant but not autosomal recessive distal renal tubular acidosis

Fiona E. Karet, Á. Z. Györy, Robert J. Unwin et al. · Proceedings of the National Academy of Sciences · 1998 · 274 citations · Full text

Medicine, Genetics, Molecular Genetics +15

Clinical and metabolic features of urolithiasis and microlithiasis in children

Harika Alpay, Ahmet Ozen, İbrahim Gökçe · Pediatric Nephrology · 2009 · 143 citations

Medicine, Pediatrics, Urology +12

Etiology and outcome of acute kidney injury in children

Ali Düzova, Ayşı̇n Bakkaloğlu, Mukaddes Kalyoncu et al. · Pediatric Nephrology · 2010 · 133 citations

Medicine, Nephrology, Pediatrics +11

Childhood vasculitides in Turkey: a nationwide survey

Seza Özen, Ayşı̇n Bakkaloğlu, Ruhan Düşünsel et al. · Clinical Rheumatology · 2006 · 104 citations

Medicine, Child Health, Pediatrics +14