Hande Kaymakcalan (Hande Kaymakçalan)

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 4

Top Topics

Autism Spectrum Disorder

Intellectual Disability

Top Venues

Molecular genetics & genomic medicine

American journal of medical genetics. Part A

Indian journal of pediatrics

This page only lists publications with an associated author ORCID identifier.

Publications

Masoud Edizadeh, Hande Kaymakcalan, Saeed Farajzadeh Valilou, Yavuz Şahin
Eighth case of Li-Campeau syndrome in a Turkish patient caused by a novel pathogenic variant in UBR7 and expanding the phenotype. American journal of medical genetics. Part A (2023)
Weilai Dong, Hande Kaymakcalan, Sheng Chih Jin, Nicholas S Diab, Cansaran Tanıdır, Ali Seyfi Yalim Yalcin, A Gulhan Ercan-Sencicek, Shrikant Mane, Murat Gunel, Richard P Lifton, Kaya Bilguvar, Martina Brueckner
Mutation spectrum of congenital heart disease in a consanguineous Turkish population. Molecular genetics & genomic medicine 10 (6) (2022)
Hande Kaymakcalan, İlyas Kaya, Nagihan Cevher Binici, Emrah Nikerel, Burcu Özbaran, Mehmet Görkem Aksoy, Seda Erbilgin, Gonca Özyurt, Noor Jahan, Didem Çelik, Kanay Yararbaş, Leyla Yalçınkaya, Sezen Köse, Sibel Durak, Adife Gulhan Ercan-Sencicek
Prevalence and clinical/molecular characteristics of PTEN mutations in Turkish children with autism spectrum disorders and macrocephaly. Molecular genetics & genomic medicine 9 (8) (2021)
Hande Kaymakcalan, Peining Li
1q21.1 Deletions and Duplications in 2 Siblings with Psychiatric Problems. Indian journal of pediatrics 86 (11) (2019)