Ali Kemal Topaloglu

5PUBLICATIONS
21CO-AUTHORS
Infant and child healthGene expression (incl. microarray and other genome-wide approaches)HaematologyCrystallographyChild and adolescent development
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Publications (5)

|Jan 16, 2026
Targeting Hypercalciuria in SLC34A1-Related Disorders: Impact of Oral Phosphate Therapy and Novel Genetic Insights in Pediatric Case Series.

Ihsan Turan, Muge Atar, Mehmet Eltan

|Dec 31, 2021
Review of human genetic and clinical studies directly relevant to GnRH signalling.

Stephanie B Seminara, A Kemal Topaloglu

|Apr 14, 2021
Experience with the targeted next-generation sequencing in the diagnosis of hereditary hypophosphatemic rickets.

Ihsan Turan, Sevcan Erdem, Leman Damla Kotan

|Jan 26, 2021
Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism.

Leman Damla Kotan, Gaetan Ternier, Aydilek Dagdeviren Cakir

|Mar 27, 2020
Gender Identity and Assignment Recommendations in Disorders of Sex Development Patients: 20 Years’ Experience and Challenges

Fatih Gürbüz, Murat Alkan, Gonca Çelik

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Frequent Collaborators

3 joint publications

İlker Ünal

3 joint publications

Bilgin Yüksel

2 joint publications

Fatih Gürbüz

2 joint publications

Ihsan Turan