Browsing by Author Foo, Jia Nee
Showing results 2 to 21 of 27
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| Issue Date | Title | Author(s) | |
|---|---|---|---|
 | 2017 | Array-based sequencing of filaggrin gene for comprehensive detection of disease-associated variants | Wong, Colin C. X. F.; Denil, Simon L. I. J.; McLean, W. H. Irwin; Smith, Frances J. D.; Common, John E. A.; Tang, Mark B. Y.; Foo, Jia Nee; Chen, Huijia; Tay, Angeline Su Ling; Haines, Rebecca L.; Sandilands, Aileen; Lane, E. Birgitte; Liu, Jianjun |
| 2021 | Association analysis of PSAP variants in Parkinson's disease patients | 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 |
| 2018 | Evaluation of novel Parkinson's disease candidate genes in the Chinese population | Chew, Elaine Guo Yan; Liany, Herty; Tan, Louis C. S.; Au, Wing-Lok; Prakash, Kumar-M.; Azlina Ahmad Annuar; Chan, Anne Y. Y.; Lim, Shen-Yang; Mok, Vincent; Chung, Sun Ju; Song, Kyuyoung; Liu, Jianjun; Foo, Jia Nee; Tan, Eng-King |
| 2016 | Genome-wide association study of Parkinson’s disease in East Asians | Foo, Jia Nee; Tan, Louis C.; Irwan, Ishak D.; Au, Wing-Lok; Low, Hui Qi; Prakash, Kumar-M.; Azlina Ahmad-Annuar; Bei, Jinxin; Chan, Anne Y. Y.; Chen, Chiung Mei; Chen, Yi-Chun; Chung, Sun Ju; Deng, Hao; Lim, Shen-Yang; Mok, Vincent; Pang, Hao; Pei, Zhong; Peng, Rong; Shang, Hui-Fang; Song, Kyuyoung; Tan, Ai Huey; Wu, Yih-Ru; Aung, Tin; Cheng, Ching-Yu; Chew, Fook Tim; Chew, Soo-Hong; Chong, Siow-Ann; Ebstein, Richard P.; Lee, Jimmy; Saw, Seang-Mei; Seow, Adeline; Subramaniam, Mythily; Tai, E-Shyong; Vithana, Eranga N.; Wong, Tien-Yin; Heng, Khai Koon; Meah, Wee-Yang; Khor, Chiea Chuen; Liu, Hong; Zheng, Furen; Liu, Jianjun; Tan, Eng-King |
| 2021 | High diagnostic utility incorporating a targeted neurodegeneration gene panel with MRI brain diagnostic algorithms in patients with young-onset cognitive impairment with leukodystrophy | 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. |
| 2017 | 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 | Ajmal, Muhammad; Mir, Asif; Wahid, Sughra; Khor, Chiea Chuen; Foo, Jia Nee; Siddiqi, Saima; Kauser, Mehran; Malik, Salman Akbar; Nasir, Muhammad |
| 2021 | Identification of a novel homozygous missense (c.443A>T:p.N148I) mutation in BBS2 in a Kashmiri family with Bardet-Biedl syndrome | Ali, Ghazanfar; Sadia; Foo, Jia Nee; Nasir, Abdul; Chang, Chu-Hua; Chew, Elaine GuoYan; Latif, Zahid; Azeem, Zahid; Ain-Ul-Batool, Syeda; Kazmi, Syed Akif Raza; Awan, Naheed Bashir; Khan, Abdul Hameed; Fazal-Ur-Rehman; Khalid, Madiha; Wali, Abdul; Sarwar, Samina; Akhtar, Wasim; Ahmed Abbasi, Ansar; Nisar, Rameez |
| 2018 | Identifying genes in Parkinson’s disease : state of the art | Chew, Elaine Guo Yan; Foo, Jia Nee; Tan, Eng-King |
| 2019 | ITPKB and ZNF184 are associated with Parkinson’s disease risk in East Asians | Chew, Elaine Guo Yan; Tan, Louis C. S.; Au, Wing-Lok; Prakash, Kumar-M.; Liu, Jianjun; Foo, Jia Nee; Tan, Eng-King |
| 2016 | Large 3‐Mb deletions at 22q11.2 locus in Parkinson's disease and schizophrenia | Foo, Jia Nee; Lee, Jimmy; Tan, Louis C.; Liu, Jianjun; Tan, Eng-King |
| 2019 | Large-scale whole-genome sequencing of three diverse Asian populations in Singapore | Wu, Degang; Dou, Jinzhuang; Chai, Xiaoran; Bellis, Claire; Wilm, Andreas; Shih, Chih Chuan; Soon, Wendy Wei Jia; Bertin, Nicolas; Lin, Clarabelle Bitong; Khor, Chiea Chuen; DeGiorgio, Michael; Cheng, Shanshan; Bao, Li; Karnani, Neerja; Hwang, William Ying Khee; Davila, Sonia; Tan, Patrick; Shabbir, Asim; Moh, Angela; Tan, Eng-King; Foo, Jia Nee; Goh, Liuh Ling; Leong, Khai Pang; Foo, Roger Sik Yin; Lam, Carolyn Su Ping; Richards, Arthur Mark; Cheng, Ching-Yu; Aung, Tin; Wong, Tien Yin; Ng, Huck Hui; Liu, Jianjun; Wang, Chaolong |
| 2021 | Modulation of instagram number of followings by avoidance in close relationships in young adults under a gene x environment perspective | Bonassi, Andrea; Carollo, Alessandro; Cataldo, Ilaria; Gabrieli, Giulio; Tandiono, Moses; Foo, Jia Nee; Lepri, Bruno; Esposito, Gianluca |
| 2018 | No association of DNM3 with age of onset in Asian Parkinson's disease | Foo, Jia Nee; Tan, Louis C.; Au, Wing-Lok; Prakash, Kumar-M.; Liu, Jianjun; Tan, Eng-King |
| 2019 | A novel homozygous frameshift variant in XYLT2 causes spondyloocular syndrome in a consanguineous Pakistani family | Kausar, Mehran; Chew, Elaine Guo Yan; Ullah, Hazrat; Anees, Mariam; Khor, Chiea Chuen; Foo, Jia Nee; Makitie, Outi; Siddiqi, Saima |
| 2018 | Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta | Kausar, Mehran; Saima Siddiqi; Muhammad Yaqoob; Sajid Mansoor; Makitie, Outi; Asif Mir; Khor, Chiea Chuen; Foo, Jia Nee; Anees, Mariam |
| 2021 | Novel optineurin frameshift insertion in a family with frontotemporal dementia and parkinsonism without amyotrophic lateral sclerosis | Dominguez, Jacqueline; Yu, Jeryl Tan; Tan, Jayne Yi; Ng, Arlene; De Guzman, Ma Fe; Natividad, Boots; Daroy, Ma Luisa; Cano, Jemellee; Yu, Justine; Lian, Michelle Mulan; Zeng, Li; Lim, Weng Khong; Foo, Jia Nee; Ng, Adeline S. L. |
| 2020 | Oxytocin receptor gene and parental bonding modulate prefrontal responses to cries : a NIRS study | Cataldo, Ilaria; Neoh, Michelle Jin-Yee; Chew, Wei Fang; Foo, Jia Nee; Lepri, Bruno; Esposito, Gianluca |
| 2020 | Oxytocin receptor gene polymorphisms and early parental bonding interact in shaping Instagram social behavior | Bonassi, Andrea; Cataldo, Ilaria; Gabrieli, Giulio; Foo, Jia Nee; Lepri, Bruno; Esposito, Gianluca |
| 2020 | P.677 Serotonin transporter gene polymorphisms and confidence in adult relationships affect the number of followed people on Instagram | Bonassi, A.; Cataldo, I.; Gabrieli, Giulio; Foo, Jia Nee; Lepri, B.; Esposito, Gianluca |
| 2020 | Phenotypic bases of NOTCH2NLC GGC expansion positive neuronal intranuclear inclusion disease in a Southeast Asian cohort | Chen, Zhiyong; Xu, Zheyu; Cheng, Qianhui; Tan, Jayne Yi; Ong, Helen L.; Zhao, Yi; Lim, Weng Khong; Teo, Jing Xian; Foo, Jia Nee; Lee, Hwei Yee; Tan, Jeanne M. M.; Hang, Liting; Yu, Wai-Yung; Ting, Simon K. S.; Tan, Eng-King; Lim, Tchoyoson C. C.; Ng, Adeline S. L. |