Pınar Ata

9PUBLICATIONS
56CO-AUTHORS
Infant and child healthNeonatologyEpigenetics (incl. genome methylation and epigenomics)Predictive and prognostic markersDevelopmental genetics (incl. sex determination)
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Publications (9)

|Mar 04, 2026
Clinical course of proteinuria due to cubilin variants: a large multicenter pediatric cohort.

Neslihan Cicek, Ceren Alavanda, Ayse Seda Pınarbası

|Dec 20, 2025
Predictors of kidney survival in children with autosomal recessive polycystic kidney disease.

Neslihan Çiçek, İbrahim Gökçe, Ceren Alavanda

|Nov 14, 2025
Benign proximal tubular albuminuria due to AMN mutation: A challenging presentation of Imerslund-Gräsbeck syndrome.

Serim Pul, Serçin Güven, Neslihan Çiçek

|Jan 06, 2025
Multigene Panel Testing Reveals Novel Variants in Hereditary Spherocytosis Patients in Türkiye

Ömer Doğru, Ceren Alavanda, Şenol Demir

|Dec 19, 2024
Clinical and Molecular Genetic Characteristics of Patients with Hereditary Hypophosphatemia.

Mehmet Eltan, Ceren Alavanda, Zehra Yavas Abali

|Sep 16, 2022
Clinical and genetic characterization of children with cubilin variants.

Neslihan Cicek, Harika Alpay, Sercin Guven

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Frequent Collaborators

6 joint publications

Ceren Alavanda

5 joint publications

Ibrahim Gokce

5 joint publications

Sercin Guven

4 joint publications

Serim Pul