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Current Opinion in Genetics & Development|September 3, 2019
Polycystic kidney disease: new knowledge and future promisesJia Nee Foo, Yun XiaHuman Genetics|March 26, 2013
Next-generation sequencing diagnostics for neurological diseases/disorders: from a clinical perspectiveJia Nee Foo, Jianjun Liu, Eng-King TanNature Reviews. Neurology|August 1, 2012
Whole-genome and whole-exome sequencing in neurological diseasesJia-Nee Foo, Jian-Jun Liu, Eng-King TanFrontiers in Cellular Neuroscience|September 20, 2024
Synaptic Vesicle Glycoprotein 2C: a role in Parkinson's diseaseChu Hua Chang, Kah Leong Lim, Jia Nee FooAnnals of Neurology|March 10, 2026
Predominance of Ferroptotic Cell Death Mechanisms in Substantia Nigra Neurodegeneration in Parkinson's DiseaseYue Jing Heng, Anusha Jayaraman, Richard Reynolds, et al.The Journal of Gene Medicine|July 17, 2019
A recurrent missense mutation in the EDAR gene causes severe autosomal recessive hypohidrotic ectodermal dysplasia in two consanguineous Kashmiri familiesSadia, Jia Nee Foo, Chiea Chuen Khor, et al.BMC Proceedings|December 19, 2014
Combined linkage and family-based association analysis improves candidate gene detection in Genetic Analysis Workshop 18 simulation dataYi Li, Jia Nee Foo, Herty Liany, et al.Brain Sciences|April 30, 2021
Recalled Parental Bonding Interacts with Oxytocin Receptor Gene Polymorphism in Modulating Anxiety and Avoidance in Adult RelationshipsIlaria Cataldo, Andrea Bonassi, Bruno Lepri, et al.Clinical Biochemistry|January 23, 2013
Association of single nucleotide polymorphism rs6903956 on chromosome 6p24.1 with coronary artery disease and lipid levels in different ethnic groups of the Singaporean populationNaeimeh Tayebi, Tingjing Ke, Jia Nee Foo, et al.Journal of Biomolecular Structure & Dynamics|June 22, 2023
Structural and functional insights into a novel homozygous missense pathogenic variant in <i>CUL7</i> identified in consanguineous Pakistani familyAyesha Zaka, Maha Yousaf, Shaheen Shahzad, et al.Pageof 161