Ayşı̇n Bakkaloğlu
Publications by Year
Research Areas
Inflammasome and immune disorders, Renal Diseases and Glomerulopathies, Vasculitis and related conditions, Autoimmune and Inflammatory Disorders Research, Systemic Lupus Erythematosus Research
Most-Cited Works
- → EULAR/PRINTO/PRES criteria for Henoch–Schönlein purpura, childhood polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008. Part II: Final classification criteria(2010)1,398 cited
- → Genetic diagnosis by whole exome capture and massively parallel DNA sequencing(2009)1,333 cited
- → Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness(1999)684 cited
- → Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible(2006)557 cited
- → A new set of criteria for the diagnosis of familial Mediterranean fever in childhood(2009)516 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
- → Patients with Mutations in NPHS2 (Podocin) Do Not Respond to Standard Steroid Treatment of Nephrotic Syndrome(2004)413 cited
- → COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness(2011)394 cited
- → Mutation frequency of Familial Mediterranean Fever and evidence for a high carrier rate in the Turkish population(2001)325 cited
- → Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosis(1998)271 cited