GWAS reveal novel IgA nephropathy risk loci

por Foo, Jia Nee, Liu, Jianjun, Yu, Xue-Qing
Publicado 2015

Combined linkage and family-based association analysis improves candidate gene detection in Genetic Analysis Workshop 18 simulation data

por Li, Yi, Foo, Jia Nee, Liany, Herty, Low, Hui-Qi, Liu, Jianjun
Publicado 2014

Recalled Parental Bonding Interacts with Oxytocin Receptor Gene Polymorphism in Modulating Anxiety and Avoidance in Adult Relationships

por Cataldo, Ilaria, Bonassi, Andrea, Lepri, Bruno, Foo, Jia Nee, Setoh, Peipei, Esposito, Gianluca
Publicado 2021

The Interaction between Serotonin Transporter Allelic Variation and Maternal Care Modulates Instagram Sociability in a Sample of Singaporean Users

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

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

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

Modulation of Instagram Number of Followings by Avoidance in Close Relationships in Young Adults under a Gene x Environment Perspective

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

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

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

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

por Kausar, Mehran, Siddiqi, Saima, Yaqoob, Muhammad, Mansoor, Sajid, Makitie, Outi, Mir, Asif, Khor, Chiea Chuen, Foo, Jia Nee, Anees, Mariam
Publicado 2018

A Novel Homozygous Frameshift Variant in XYLT2 Causes Spondyloocular Syndrome in a Consanguineous Pakistani Family

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

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

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

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

por Naito, Tatsuhiko, Satake, Wataru, Ogawa, Kotaro, Suzuki, Ken, Hirata, Jun, Foo, Jia Nee, Tan, Eng‐King, Toda, Tatsushi, Okada, Yukinori
Publicado 2021

Gene–Environment Interactions in Face Categorization: Oxytocin Receptor Genotype x Childcare Experience Shortens Reaction Time

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

por Ajmal, Muhammad, Mir, Asif, Wahid, Sughra, Khor, Chiea Chuen, Foo, Jia Nee, Siddiqi, Saima, Kauser, Mehran, Malik, Salman Akbar, Nasir, Muhammad
Publicado 2017

Parkinson’s disease GWAS-linked Park16 carriers show greater motor progression

por Deng, Xiao, Xiao, Bin, Allen, John Carson, Ng, Ebonne, Foo, Jia Nee, Lo, Yew-Long, Tan, Louis C S, Tan, Eng-King
Publicado 2019

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

por Ravindran, Ethiraj, Ullah, Noor, Mani, Shyamala, Chew, Elaine Guo Yan, Tandiono, Moses, Foo, Jia Nee, Khor, Chiea Chuen, Kaindl, Angela M., Siddiqi, Saima
Publicado 2022

High Diagnostic Utility Incorporating a Targeted Neurodegeneration Gene Panel With MRI Brain Diagnostic Algorithms in Patients With Young-Onset Cognitive Impairment With Leukodystr...

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

RIC3 variants are not associated with Parkinson’s disease in large European, Latin American, or East Asian cohorts

por Brolin, Kajsa, Bandres-Ciga, Sara, Leonard, Hampton, Makarious, Mary B., Blauwendraat, Cornelis, Mata, Ignacio F, Foo, Jia Nee, Pihlstrøm, Lasse, Swanberg, Maria, Gan-Or, Ziv, Tan, Manuela MX
Publicado 2022

A Comprehensive Association Analysis of Homocysteine Metabolic Pathway Genes in Singaporean Chinese with Ischemic Stroke

por Low, Hui-Qi, Chen, Christopher P. L. H., Kasiman, Katherine, Thalamuthu, Anbupalam, Ng, Seok-Shin, Foo, Jia-Nee, Chang, Hui-Meng, Wong, Meng-Cheong, Tai, E-Shyong, Liu, Jianjun
Publicado 2011

A meta-analysis of genome-wide association studies of follicular lymphoma

por Skibola, Christine F, Conde, Lucia, Foo, Jia-Nee, Riby, Jacques, Humphreys, Keith, Sillé, Fenna CM, Darabi, Hatef, Sanchez, Sylvia, Hjalgrim, Henrik, Liu, Jianjun, Bracci, Paige M, Smedby, Karin E
Publicado 2012

A 3D Fiber‐Hydrogel Based Non‐Viral Gene Delivery Platform Reveals that microRNAs Promote Axon Regeneration and Enhance Functional Recovery Following Spinal Cord Injury

por Zhang, Na, Lin, Junquan, Lin, Vincent Po Hen, Milbreta, Ulla, Chin, Jiah Shin, Chew, Elaine Guo Yan, Lian, Michelle Mulan, Foo, Jia Nee, Zhang, Kunyu, Wu, Wutian, Chew, Sing Yian
Publicado 2021