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The first Malay database toward the ethnic-specific target molecular variation.
Halim-Fikri H, Etemad A, Abdul Latif AZ, Merican AF, Baig AA, Annuar AA, Ismail E, Salahshourifar I, Liza-Sharmini AT, Ramli M, Shah MI, Johan MF, Hassan NN, Abdul-Aziz NM, Mohd Noor NH, Nur-Shafawati AR, Hassan R, Bahar R, Zain RB, Yusoff SM, Yusoff S, Tan SG, Thong MK, Wan-Isa H, Abdullah WZ, Mohamed Z, Abdul Latiff Z, Zilfalil BA; members of the Malaysian Node of the Human Variome Project. Halim-Fikri H, et al. Among authors: annuar aa. BMC Res Notes. 2015 Apr 30;8:176. doi: 10.1186/s13104-015-1123-y. BMC Res Notes. 2015. PMID: 25925844 Free PMC article.
Identification of Risk Loci for Parkinson Disease in Asians and Comparison of Risk Between Asians and Europeans: A Genome-Wide Association Study.
Foo JN, Chew EGY, Chung SJ, Peng R, Blauwendraat C, Nalls MA, Mok KY, Satake W, Toda T, Chao Y, Tan LCS, Tandiono M, Lian MM, Ng EY, Prakash KM, Au WL, Meah WY, Mok SQ, Annuar AA, Chan AYY, Chen L, Chen Y, Jeon BS, Jiang L, Lim JL, Lin JJ, Liu C, Mao C, Mok V, Pei Z, Shang HF, Shi CH, Song K, Tan AH, Wu YR, Xu YM, Xu R, Yan Y, Yang J, Zhang B, Koh WP, Lim SY, Khor CC, Liu J, Tan EK. Foo JN, et al. Among authors: annuar aa. JAMA Neurol. 2020 Jun 1;77(6):746-754. doi: 10.1001/jamaneurol.2020.0428. JAMA Neurol. 2020. PMID: 32310270 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: annuar aa. 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
Understanding monogenic Parkinson's disease at a global scale.
Junker J, Lange LM, Vollstedt EJ, Roopnarain K, Doquenia MLM, Annuar AA, Avenali M, Bardien S, Bahr N, Ellis M, Galandra C, Gasser T, Heutink P, Illarionova A, Kanana Y, Keller Sarmiento IJ, Kumar KR, Lim SY, Madoev H, Mata IF, Mencacci NE, Nalls MA, Padmanabhan S, Shambetova C, Solle J, Tan AH, Trinh J, Valente EM, Singleton A, Blauwendraat C, Lohmann K, Fang ZH, Klein C; Global Parkinson’s Genetics Program (GP2). Junker J, et al. Among authors: annuar aa. medRxiv [Preprint]. 2024 Apr 9:2024.03.12.24304154. doi: 10.1101/2024.03.12.24304154. medRxiv. 2024. PMID: 38529492 Free PMC article. Preprint.
Loss-of-function SMPD1 gene variant in Progressive Supranuclear Palsy-Richardson Syndrome patients of Chinese ancestry.
Lim SY, Tan AH, Foo JN, Tan YJ, Chew EG, Annuar AA, Closas AMD, Pajo A, Lim JL, Tay YW, Nadhirah A, Hor JW, Toh TS, Lit LC, Zulkefli J, Ngim SJ, Lim WK, Morris HR, Tan EK, Ng AS. Lim SY, et al. Among authors: annuar aa. J Mov Disord. 2024 Jan 31. doi: 10.14802/jmd.24009. Online ahead of print. J Mov Disord. 2024. PMID: 38291878 Free article.
Karyotype patterns, clinical features, and parental ages of three predominant live born autosomal trisomies of Northeast Malaysia.
Ankathil R, Zakaria WNA, Rostenberghe HV, Ibrahim NR, Ramli N, Ismail SM, Mohd Nawi NA, Mat Zin NMZ, Ramli N, Abu Bakar Z, Rasudin NFS, Chia BH, Mohd Adam NA, Mohd Yunus N, Annuar AA, Sulong S, Alwi Z. Ankathil R, et al. Among authors: annuar aa. Malays J Pathol. 2022 Aug;44(2):235-244. Malays J Pathol. 2022. PMID: 36043586 Free article.
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