Polycystic kidney disease : new knowledge and future promises

by Foo, Jia Nee, Xia, Yun
Published 2020

Identifying genes in Parkinson’s disease : state of the art

by Chew, Elaine Guo Yan, Foo, Jia Nee, Tan, Eng-King
Published 2020

A recurrent missense mutation in the EDAR gene causes severe autosomal recessive hypohidrotic ectodermal dysplasia in two consanguineous Kashmiri families

by Sadia, Foo, Jia Nee, Khor, Chiea Chuen, Jelani, Musharraf, Ali, Ghazanfar
Published 2021

Large 3‐Mb deletions at 22q11.2 locus in Parkinson's disease and schizophrenia

by Foo, Jia Nee, Lee, Jimmy, Tan, Louis C., Liu, Jianjun, Tan, Eng-King
Published 2020

Oxytocin receptor gene polymorphisms and early parental bonding interact in shaping Instagram social behavior

by Bonassi, Andrea, Cataldo, Ilaria, Gabrieli, Giulio, Foo, Jia Nee, Lepri, Bruno, Esposito, Gianluca
Published 2020

P.677 Serotonin transporter gene polymorphisms and confidence in adult relationships affect the number of followed people on Instagram

by Bonassi, A., Cataldo, I., Gabrieli, Giulio, Foo, Jia Nee, Lepri, B., Esposito, Gianluca
Published 2021

Recalled parental bonding interacts with oxytocin receptor gene polymorphism in modulating anxiety and avoidance in adult relationships

by Cataldo, Ilaria, Bonassi, Andrea, Lepri, Bruno, Foo, Jia Nee, Setoh, Peipei, Esposito, Gianluca
Published 2021

Structural and functional insights into a novel homozygous missense pathogenic variant in CUL7 identified in consanguineous Pakistani family

by Zaka, Ayesha, Yousaf, Maha, Shahzad, Shaheen, Rao, Hadi Zahid, Foo, Jia Nee, Siddiqi, Saima
Published 2023

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

Oxytocin receptor gene and parental bonding modulate prefrontal responses to cries : a NIRS study

by Cataldo, Ilaria, Neoh, Michelle Jin-Yee, Chew, Wei Fang, Foo, Jia Nee, Lepri, Bruno, Esposito, Gianluca
Published 2020

No association of DNM3 with age of onset in Asian Parkinson's disease

by Foo, Jia Nee, Tan, Louis C., Au, Wing-Lok, Prakash, Kumar-M., Liu, Jianjun, Tan, Eng-King
Published 2020

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

A novel homozygous frameshift variant in XYLT2 causes spondyloocular syndrome in a consanguineous Pakistani family

by Kausar, Mehran, Chew, Elaine Guo Yan, Ullah, Hazrat, Anees, Mariam, Khor, Chiea Chuen, Foo, Jia Nee, Makitie, Outi, Siddiqi, Saima
Published 2019

Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta

by Kausar, Mehran, Saima Siddiqi, Muhammad Yaqoob, Sajid Mansoor, Makitie, Outi, Asif Mir, Khor, Chiea Chuen, Foo, Jia Nee, Anees, Mariam
Published 2019

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

Trans-Ethnic Fine-Mapping of the Major Histocompatibility Complex Region Linked to Parkinson's Disease

by Naito, Tatsuhiko, Satake, Wataru, Ogawa, Kotaro, Suzuki, Ken, Hirata, Jun, Foo, Jia Nee, Tan, Eng-King, Toda, Tatsushi, Okada, Yukinori
Published 2022

Identification and in silico characterization of a novel p.P208PfsX1 mutation in V-ATPase a3 subunit associated with autosomal recessive osteopetrosis in a Pakistani family

by Ajmal, Muhammad, Mir, Asif, Wahid, Sughra, Khor, Chiea Chuen, Foo, Jia Nee, Siddiqi, Saima, Kauser, Mehran, Malik, Salman Akbar, Nasir, Muhammad
Published 2018

ITPKB and ZNF184 are associated with Parkinson’s disease risk in East Asians

by Chew, Elaine Guo Yan, Tan, Louis C. S., Au, Wing-Lok, Prakash, Kumar-M., Liu, Jianjun, Foo, Jia Nee, Tan, Eng-King
Published 2020