Polycystic kidney disease : new knowledge and future promises by Foo, Jia Nee, Xia, Yun

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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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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Case report: expanding the phenotype of ARHGEF17 mutations from increased intracranial aneurysm risk to a neurodevelopmental disease by Ravindran, Ethiraj, Ullah, Noor, Mani, Shyamala, Chew, Elaine Guo Yan, Tandiono, Moses, Foo, Jia Nee, Khor, Chiea Chuen, Kaindl, Angela M., Siddiqi, Saima

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High diagnostic utility incorporating a targeted neurodegeneration gene panel with MRI brain diagnostic algorithms in patients with young-onset cognitive impairment with leukodystr... by 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.

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

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Targeted exome sequencing reveals homozygous TREM2 R47C mutation presenting with behavioral variant frontotemporal dementia without bone involvement by Ng, 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

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A 3D fiber-hydrogel based non-viral gene delivery platform reveals that microRNAs promote axon regeneration and enhance functional recovery following spinal cord injury by 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

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Association analysis of PSAP variants in Parkinson's disease patients by 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

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