Hande Kaymakcalan Celebiler

6PUBLICATIONS
41CO-AUTHORS
Neurology and neuromuscular diseasesHaematological tumoursDevelopmental genetics (incl. sex determination)Gene mappingInfant and child health
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Publications (6)

|Oct 15, 2026
Diagnostic timing in cerebral creatine deficiency syndromes: neurodevelopmental and genetic characterization of a multicenter cohort.

|Jan 01, 2025
Dysregulation of mTOR signalling is a converging mechanism in lissencephaly.

Ce Zhang, Dan Liang, A Gulhan Ercan-Sencicek

|Feb 09, 2023
Eighth case of Li-Campeau syndrome in a Turkish patient caused by a novel pathogenic variant in UBR7 and expanding the phenotype.

Masoud Edizadeh, Hande Kaymakcalan, Saeed Farajzadeh Valilou

|Apr 28, 2022
Mutation spectrum of congenital heart disease in a consanguineous Turkish population.

Weilai Dong, Hande Kaymakcalan, Sheng Chih Jin

|Jul 16, 2021
Prevalence and clinical/molecular characteristics of PTEN mutations in Turkish children with autism spectrum disorders and macrocephaly.

Hande Kaymakcalan, İlyas Kaya, Nagihan Cevher Binici

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Frequent Collaborators

2 joint publications

A Gulhan Ercan-Sencicek

1 joint publications

Seda Erbilgin

1 joint publications

Sheng Chih Jin

1 joint publications

Saeed Farajzadeh Valilou