Hande Kaymakçalan
5PUBLICATIONS
23CO-AUTHORS
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Publications (5)
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|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
1 joint publications
Ce Zhang
1 joint publications
Aybike S Bulut
1 joint publications
Joelly Cortes
1 joint publications
Iris Q Cheng
1 joint publications
Octavian Henegariu
1 joint publications
Sayoko Nishimura
