The interaction between serotonin transporter allelic variation and maternal care modulates instagram sociability in a sample of Singaporean users

by Bonassi, Andrea, Cataldo, Ilaria, Gabrieli, Giulio, Tandiono, Moses, Foo, Jia Nee, Lepri, Bruno, Esposito, Gianluca
Published 2022

The relation between oxytocin receptor gene polymorphisms, adult attachment and Instagram sociability : an exploratory analysis

by Carollo, Alessandro, Bonassi, Andrea, Cataldo, Ilaria, Gabrieli, Giulio, Tandiono, Moses, Foo, Jia Nee, Lepri, Bruno, Esposito, Gianluca
Published 2021

Modulation of instagram number of followings by avoidance in close relationships in young adults under a gene x environment perspective

by Bonassi, Andrea, Carollo, Alessandro, Cataldo, Ilaria, Gabrieli, Giulio, Tandiono, Moses, Foo, Jia Nee, Lepri, Bruno, Esposito, Gianluca
Published 2021

Functional characterisation of SV2C and its variants as a Parkinson’s Disease-associated gene

by Chang, Chu-Hua, Chew, Elaine Guo Yan, Tandiono, Moses, Zhang, Tian, Gong, Ximing, Xia, Yun, Foo, Jia Nee
Published 2023

Gene-environment interactions in face categorization: oxytocin receptor genotype x childcare experience shortens reaction time

by Neoh, Michelle Jin Yee, Setoh, Peipei, Bizzego, Andrea, Tandiono, Moses, Foo, Jia Nee, Lee, Albert, Bornstein, Marc H., Esposito, Gianluca
Published 2022

Case report: expanding the phenotype of ARHGEF17 mutations from increased intracranial aneurysm risk to a neurodevelopmental disease

by Ravindran, Ethiraj, Ullah, Noor, Mani, Shyamala, Chew, Elaine Guo Yan, Tandiono, Moses, Foo, Jia Nee, Khor, Chiea Chuen, Kaindl, Angela M., Siddiqi, Saima
Published 2023

High diagnostic utility incorporating a targeted neurodegeneration gene panel with MRI brain diagnostic algorithms in patients with young-onset cognitive impairment with leukodystr...

by Chen, Zhiyong, Tan, Yi Jayne, Lian, Michelle Mulan, Tandiono, Moses, Foo, Jia Nee, Lim, Weng Khong, Kandiah, Nagaendran, Tan, Eng-King, Ng, Adeline S. L.
Published 2021

Targeted exome sequencing reveals homozygous TREM2 R47C mutation presenting with behavioral variant frontotemporal dementia without bone involvement

by Ng, Adeline S. L., Tan, Yi Jayne, Yi, Zhao, Tandiono, Moses, Chew, Elaine, Dominguez, Jacqueline, Macas, Mabel, Ng, Ebonne, Hameed, Shahul, Ting, Simon, Tan, Eng King, Foo, Jia Nee, Kandiah, Nagaendran
Published 2019

Association analysis of PSAP variants in Parkinson's disease patients

by Chao, Yin Xia, Lee, Bernett, Ng, Ebonne Yulin, Lian, Michelle Mulan, Chew, Elaine Guo Yan, Tandiono, Moses, Li, Zheng, Khor, Chiea Chuen, Kumar, Prakash, Tan, Louis C. S., Foo, Jia Nee, Tan, Eng-King
Published 2021