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Generation of Human PSC-Derived Kidney Organoids with Patterned Nephron Segments and a De Novo Vascular Network.
Low JH, Li P, Chew EGY, Zhou B, Suzuki K, Zhang T, Lian MM, Liu M, Aizawa E, Rodriguez Esteban C, Yong KSM, Chen Q, Campistol JM, Fang M, Khor CC, Foo JN, Izpisua Belmonte JC, Xia Y. Low JH, et al. Among authors: foo jn. Cell Stem Cell. 2019 Sep 5;25(3):373-387.e9. doi: 10.1016/j.stem.2019.06.009. Epub 2019 Jul 11. Cell Stem Cell. 2019. PMID: 31303547 Free PMC article.
Genome-wide association study of B cell non-Hodgkin lymphoma identifies 3q27 as a susceptibility locus in the Chinese population.
Tan DE, Foo JN, Bei JX, Chang J, Peng R, Zheng X, Wei L, Huang Y, Lim WY, Li J, Cui Q, Chew SH, Ebstein RP, Kuperan P, Lim ST, Tao M, Tan SH, Wong A, Wong GC, Tan SY, Ng SB, Zeng YX, Khor CC, Lin D, Seow AL, Jia WH, Liu J. Tan DE, et al. Among authors: foo jn. Nat Genet. 2013 Jul;45(7):804-7. doi: 10.1038/ng.2666. Epub 2013 Jun 9. Nat Genet. 2013. PMID: 23749188
Coding variants at hexa-allelic amino acid 13 of HLA-DRB1 explain independent SNP associations with follicular lymphoma risk.
Foo JN, Smedby KE, Akers NK, Berglund M, Irwan ID, Jia X, Li Y, Conde L, Darabi H, Bracci PM, Melbye M, Adami HO, Glimelius B, Khor CC, Hjalgrim H, Padyukov L, Humphreys K, Enblad G, Skibola CF, de Bakker PI, Liu J. Foo JN, et al. Am J Hum Genet. 2013 Jul 11;93(1):167-72. doi: 10.1016/j.ajhg.2013.05.020. Epub 2013 Jun 20. Am J Hum Genet. 2013. PMID: 23791106 Free PMC article.
Large-scale genotyping identifies a new locus at 22q13.2 associated with female breast size.
Li J, Foo JN, Schoof N, Varghese JS, Fernandez-Navarro P, Gierach GL, Quek ST, Hartman M, Nord S, Kristensen VN, Pollán M, Figueroa JD, Thompson DJ, Li Y, Khor CC, Humphreys K, Liu J, Czene K, Hall P. Li J, et al. Among authors: foo jn. J Med Genet. 2013 Oct;50(10):666-73. doi: 10.1136/jmedgenet-2013-101708. Epub 2013 Jul 3. J Med Genet. 2013. PMID: 23825393 Free PMC article.
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.
Siddiqi S, Foo JN, Vu A, Azim S, Silver DL, Mansoor A, Tay SK, Abbasi S, Hashmi AH, Janjua J, Khalid S, Tai ES, Yeo GW, Khor CC. Siddiqi S, et al. Among authors: foo jn. PLoS One. 2014 Dec 4;9(12):e113258. doi: 10.1371/journal.pone.0113258. eCollection 2014. PLoS One. 2014. PMID: 25474699 Free PMC article.
Targeted next-generation sequencing to diagnose disorders of HDL cholesterol.
Sadananda SN, Foo JN, Toh MT, Cermakova L, Trigueros-Motos L, Chan T, Liany H, Collins JA, Gerami S, Singaraja RR, Hayden MR, Francis GA, Frohlich J, Khor CC, Brunham LR. Sadananda SN, et al. Among authors: foo jn. J Lipid Res. 2015 Oct;56(10):1993-2001. doi: 10.1194/jlr.P058891. Epub 2015 Aug 8. J Lipid Res. 2015. PMID: 26255038 Free PMC article.
Evaluation of novel Parkinson's disease candidate genes in the Chinese population.
Chew EGY, Liany H, Tan LCS, Au WL, Prakash KM, Annuar AA, Chan AYY, Lim SY, Mok V, Chung SJ, Song K, Liu J, Foo JN, Tan EK. Chew EGY, et al. Among authors: foo jn. Neurobiol Aging. 2019 Feb;74:235.e1-235.e4. doi: 10.1016/j.neurobiolaging.2018.09.013. Epub 2018 Sep 21. Neurobiol Aging. 2019. PMID: 30337193
130 results