Browsing by Author Foo, Jia Nee


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Showing results 13 to 27 of 27 < previous 
Issue DateTitleAuthor(s)
2021Modulation of instagram number of followings by avoidance in close relationships in young adults under a gene x environment perspectiveBonassi, Andrea; Carollo, Alessandro; Cataldo, Ilaria; Gabrieli, Giulio; Tandiono, Moses; Foo, Jia Nee; Lepri, Bruno; Esposito, Gianluca
2018No association of DNM3 with age of onset in Asian Parkinson's diseaseFoo, Jia Nee; Tan, Louis C.; Au, Wing-Lok; Prakash, Kumar-M.; Liu, Jianjun; Tan, Eng-King
2019A novel homozygous frameshift variant in XYLT2 causes spondyloocular syndrome in a consanguineous Pakistani familyKausar, Mehran; Chew, Elaine Guo Yan; Ullah, Hazrat; Anees, Mariam; Khor, Chiea Chuen; Foo, Jia Nee; Makitie, Outi; Siddiqi, Saima
2018Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis ImperfectaKausar, Mehran; Saima Siddiqi; Muhammad Yaqoob; Sajid Mansoor; Makitie, Outi; Asif Mir; Khor, Chiea Chuen; Foo, Jia Nee; Anees, Mariam
2021Novel optineurin frameshift insertion in a family with frontotemporal dementia and parkinsonism without amyotrophic lateral sclerosisDominguez, 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.
2020Oxytocin receptor gene and parental bonding modulate prefrontal responses to cries : a NIRS studyCataldo, Ilaria; Neoh, Michelle Jin-Yee; Chew, Wei Fang; Foo, Jia Nee; Lepri, Bruno; Esposito, Gianluca
2020Oxytocin receptor gene polymorphisms and early parental bonding interact in shaping Instagram social behaviorBonassi, Andrea; Cataldo, Ilaria; Gabrieli, Giulio; Foo, Jia Nee; Lepri, Bruno; Esposito, Gianluca
2020P.677 Serotonin transporter gene polymorphisms and confidence in adult relationships affect the number of followed people on InstagramBonassi, A.; Cataldo, I.; Gabrieli, Giulio; Foo, Jia Nee; Lepri, B.; Esposito, Gianluca
 2020Phenotypic bases of NOTCH2NLC GGC expansion positive neuronal intranuclear inclusion disease in a Southeast Asian cohortChen, 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.
2019Polycystic kidney disease : new knowledge and future promisesFoo, Jia Nee; Xia, Yun
2021Recalled parental bonding interacts with oxytocin receptor gene polymorphism in modulating anxiety and avoidance in adult relationshipsCataldo, Ilaria; Bonassi, Andrea; Lepri, Bruno; Foo, Jia Nee; Setoh, Peipei; Esposito, Gianluca
2019A recurrent missense mutation in the EDAR gene causes severe autosomal recessive hypohidrotic ectodermal dysplasia in two consanguineous Kashmiri familiesSadia; Foo, Jia Nee; Khor, Chiea Chuen; Jelani, Musharraf; Ali, Ghazanfar
2021The relation between oxytocin receptor gene polymorphisms, adult attachment and Instagram sociability : an exploratory analysisCarollo, Alessandro; Bonassi, Andrea; Cataldo, Ilaria; Gabrieli, Giulio; Tandiono, Moses; Foo, Jia Nee; Lepri, Bruno; Esposito, Gianluca
2018Systematic evaluation of CRISPR-Cas systems reveals design principles for genome editing in human cellsWang, Yuanming; Liu, Ivy Kaiwen; Sutrisnoh, Norfala-Aliah; Srinivasan, Harini; Zhang, Junyi; Li, Jia; Zhang, Fan; Lalith, Charles Richard John; Xing, Heyun; Shanmugam, Raghuvaran; Foo, Jia Nee; Yeo, Hwee Ting; Ooi, Kean Hean; Bleckwehl, Tore; Par, Rachel Yi Yun; Lee, Shi Mun; Ismail, Nur Nadiah; Sanwari, Nur Aidah; Lee, Vanessa Si Ting; Lew, Jan; Tan, Meng How
2018Targeted exome sequencing reveals homozygous TREM2 R47C mutation presenting with behavioral variant frontotemporal dementia without bone involvementNg, 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