GWAS reveal novel IgA nephropathy risk loci

gan Foo, Jia Nee, Liu, Jianjun, Yu, Xue-Qing
Cyhoeddwyd yn Oncotarget (2015)

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

gan Li, Yi, Foo, Jia Nee, Liany, Herty, Low, Hui-Qi, Liu, Jianjun
Cyhoeddwyd 2014

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

gan Cataldo, Ilaria, Bonassi, Andrea, Lepri, Bruno, Foo, Jia Nee, Setoh, Peipei, Esposito, Gianluca
Cyhoeddwyd yn Brain Sci (2021)

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

gan Cataldo, Ilaria, Neoh, Michelle Jin-Yee, Chew, Wei Fang, Foo, Jia Nee, Lepri, Bruno, Esposito, Gianluca
Cyhoeddwyd yn Sci Rep (2020)

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

gan Bonassi, Andrea, Carollo, Alessandro, Cataldo, Ilaria, Gabrieli, Giulio, Tandiono, Moses, Foo, Jia Nee, Lepri, Bruno, Esposito, Gianluca
Cyhoeddwyd yn Int J Environ Res Public Health (2021)

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

gan Kausar, Mehran, Siddiqi, Saima, Yaqoob, Muhammad, Mansoor, Sajid, Makitie, Outi, Mir, Asif, Khor, Chiea Chuen, Foo, Jia Nee, Anees, Mariam
Cyhoeddwyd yn J Biomed Sci (2018)

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

gan Kausar, Mehran, Chew, Elaine Guo Yan, Ullah, Hazrat, Anees, Mariam, Khor, Chiea Chuen, Foo, Jia Nee, Makitie, Outi, Siddiqi, Saima
Cyhoeddwyd yn Front Genet (2019)

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

gan Kausar, Mehran, Siddiqi, Saima, Yaqoob, Muhammad, Mansoor, Sajid, Makitie, Outi, Mir, Asif, Khor, Chiea Chuen, Foo, Jia Nee, Anees, Mariam
Cyhoeddwyd yn J Biomed Sci (2019)

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

gan Ajmal, Muhammad, Mir, Asif, Wahid, Sughra, Khor, Chiea Chuen, Foo, Jia Nee, Siddiqi, Saima, Kauser, Mehran, Malik, Salman Akbar, Nasir, Muhammad
Cyhoeddwyd yn BMC Med Genet (2017)

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

gan Deng, Xiao, Xiao, Bin, Allen, John Carson, Ng, Ebonne, Foo, Jia Nee, Lo, Yew-Long, Tan, Louis C S, Tan, Eng-King
Cyhoeddwyd yn J Med Genet (2019)

Apolipoprotein C3 Gene Variants in Nonalcoholic Fatty Liver Disease

gan Petersen, Kitt Falk, Dufour, Sylvie, Hariri, Ali, Nelson-Williams, Carol, Foo, Jia Nee, Zhang, Xian-Man, Dziura, James, Lifton, Richard P., Shulman, Gerald I.
Cyhoeddwyd 2010

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

gan 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.
Cyhoeddwyd yn Front Neurol (2021)

Rare independent mutations in renal salt handling genes contribute to blood pressure variation

gan Ji, Weizhen, Foo, Jia Nee, O'Roak, Brian J., Zhao, Hongyu, Larson, Martin G., Simon, David B., Newton-Cheh, Christopher, State, Matthew W., Levy, Daniel, Lifton, Richard P.
Cyhoeddwyd 2008

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

gan 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
Cyhoeddwyd 2011

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

gan 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
Cyhoeddwyd 2012

A comprehensive evaluation of the role of genetic variation in follicular lymphoma survival

gan Baecklund, Fredrik, Foo, Jia-Nee, Bracci, Paige, Darabi, Hatef, Karlsson, Robert, Hjalgrim, Henrik, Rosenquist, Richard, Adami, Hans-Olov, Glimelius, Bengt, Melbye, Mads, Conde, Lucia, Liu, Jianjun, Humphreys, Keith, Skibola, Christine F, Smedby, Karin E
Cyhoeddwyd yn BMC Med Genet (2014)

A Novel Splice-Site Mutation in ALS2 Establishes the Diagnosis of Juvenile Amyotrophic Lateral Sclerosis in a Family with Early Onset Anarthria and Generalized Dystonias

gan Siddiqi, Saima, Foo, Jia Nee, Vu, Anthony, Azim, Saad, Silver, David L., Mansoor, Atika, Tay, Stacey Kiat Hong, Abbasi, Sumiya, Hashmi, Asraf Hussain, Janjua, Jamal, Khalid, Sumbal, Tai, E. Shyong, Yeo, Gene W., Khor, Chiea Chuen
Cyhoeddwyd yn PLoS One (2014)

Novel Optineurin Frameshift Insertion in a Family With Frontotemporal Dementia and Parkinsonism Without Amyotrophic Lateral Sclerosis

gan Dominguez, Jacqueline, Yu, Jeryl Tan, Tan, Yi Jayne, Ng, Arlene, De Guzman, Ma Fe, Natividad, Boots, Daroy, Ma Luisa, Cano, Jemellee, Yu, Justine, Lian, Michelle M., Zeng, Li, Lim, Weng Khong, Foo, Jia Nee, Ng, Adeline S. L.
Cyhoeddwyd yn Front Neurol (2021)

Genetic Variants in ER Cofactor Genes and Endometrial Cancer Risk

gan Li, Yuqing, Low, Hui-Qi, Foo, Jia Nee, Darabi, Hatef, Einarsdόttir, Kristjana, Humphreys, Keith, Spurdle, Amanda, Easton, Douglas F., Thompson, Deborah J., Dunning, Alison M., Pharoah, Paul D. P., Czene, Kamila, Chia, Kee Seng, Hall, Per, Liu, Jianjun
Cyhoeddwyd 2012

Targeted next-generation sequencing to diagnose disorders of HDL cholesterol

gan Sadananda, Singh N., Foo, Jia Nee, Toh, Meng Tiak, Cermakova, Lubomira, Trigueros-Motos, Laia, Chan, Teddy, Liany, Herty, Collins, Jennifer A., Gerami, Sima, Singaraja, Roshni R., Hayden, Michael R., Francis, Gordon A., Frohlich, Jiri, Khor, Chiea Chuen, Brunham, Liam R.
Cyhoeddwyd yn J Lipid Res (2015)