Ahmet Nayır
Istanbul University-Cerrahpaşa(TR)Istanbul University(TR)Beykent University(TR)
Publications by Year
Research Areas
Pediatric Urology and Nephrology Studies, Renal Diseases and Glomerulopathies, Kidney Stones and Urolithiasis Treatments, Ion Transport and Channel Regulation, Urological Disorders and Treatments
Most-Cited Works
- → Genetic diagnosis by whole exome capture and massively parallel DNA sequencing(2009)1,333 cited
- → Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III(1997)863 cited
- → Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness(1999)684 cited
- → Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing(2000)415 cited
- → Exome Capture Reveals ZNF423 and CEP164 Mutations, Linking Renal Ciliopathies to DNA Damage Response Signaling(2012)391 cited
- → Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosis(1998)271 cited