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Hande Kaymakçalan

5PUBLICATIONS

23CO-AUTHORS

Haematological tumoursDevelopmental genetics (incl. sex determination)Gene mappingInfant and child health

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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

|Jul 05, 2019

1q21.1 Deletions and Duplications in 2 Siblings with Psychiatric Problems.

Hande Kaymakçalan, Peining Li

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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

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

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