Works by Ahmad-Annuar, Azlina


Results: 44
    1

    LRRK2 N551K and R1398H variants are protective in Malays and Chinese in Malaysia: A case–control association study for Parkinson's disease.

    Published in:
    Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 11, p. N.PAG, doi. 10.1002/mgg3.604
    By:
    • Gopalai, Aroma Agape;
    • Lim, Jia Lun;
    • Li, Hui‐Hua;
    • Zhao, Yi;
    • Lim, Thien Thien;
    • Eow, Gaik B.;
    • Puvanarajah, Santhi;
    • Viswanathan, Shanthi;
    • Norlinah, Mohamed Ibrahim;
    • Abdul Aziz, Zariah;
    • Lim, Soo Kun;
    • Tan, Chong Tin;
    • Tan, Ai Huey;
    • Lim, Shen‐Yang;
    • Tan, Eng‐King;
    • Ahmad Annuar, Azlina
    Publication type:
    Article
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    Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson's Disease Project.

    Published in:
    PLoS ONE, 2023, v. 18, n. 10, p. 1, doi. 10.1371/journal.pone.0292180
    By:
    • Vollstedt, Eva-Juliane;
    • Madoev, Harutyun;
    • Aasly, Anna;
    • Ahmad-Annuar, Azlina;
    • Al-Mubarak, Bashayer;
    • Alcalay, Roy N.;
    • Alvarez, Victoria;
    • Amorin, Ignacio;
    • Annesi, Grazia;
    • Arkadir, David;
    • Bardien, Soraya;
    • Barker, Roger A.;
    • Barkhuizen, Melinda;
    • Basak, A. Nazli;
    • Bonifati, Vincenzo;
    • Boon, Agnita;
    • Brighina, Laura;
    • Brockmann, Kathrin;
    • Carmine Belin, Andrea;
    • Carr, Jonathan
    Publication type:
    Article
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    Using global team science to identify genetic parkinson's disease worldwide.

    Published in:
    2019
    By:
    • Vollstedt, Eva‐Juliane;
    • Kasten, Meike;
    • Klein, Christine;
    • Aasly, Jan;
    • Adler, Charles;
    • Ahmad‐Annuar, Azlina;
    • Albanese, Alberto;
    • Alcalay, Roy N.;
    • Al‐Mubarak, Bashayer;
    • Alvarez, Victoria;
    • Andree‐Muñoz, Brennie;
    • Annesi, Grazia;
    • Appel‐Cresswell, Silke;
    • Arkadir, David;
    • Armasu, Sebastian;
    • Barber, Thomas R.;
    • Bardien, Soraya;
    • Barkhuizen, Melinda;
    • Barrett, Matthew J.;
    • Başak, A. Nazlı
    Publication type:
    Editorial
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    Underrepresented Populations in Parkinson's Genetics Research: Current Landscape and Future Directions.

    Published in:
    Movement Disorders, 2022, v. 37, n. 8, p. 1593, doi. 10.1002/mds.29126
    By:
    • Schumacher‐Schuh, Artur Francisco;
    • Bieger, Andrei;
    • Okunoye, Olaitan;
    • Mok, Kin Ying;
    • Lim, Shen‐Yang;
    • Bardien, Soraya;
    • Ahmad‐Annuar, Azlina;
    • Santos‐Lobato, Bruno Lopes;
    • Strelow, Matheus Zschornack;
    • Salama, Mohamed;
    • Rao, Shilpa C.;
    • Zewde, Yared Zenebe;
    • Dindayal, Saiesha;
    • Azar, Jihan;
    • Prashanth, Lingappa Kukkle;
    • Rajan, Roopa;
    • Noyce, Alastair J.;
    • Okubadejo, Njideka;
    • Rizig, Mie;
    • Lesage, Suzanne
    Publication type:
    Article
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    Identification of the genomic mutation in Epha4<sup> rb-2J/rb-2J</sup> mice.

    Published in:
    Genome, 2016, v. 59, n. 7, p. 439, doi. 10.1139/gen-2015-0142
    By:
    • Mohd-Zin, Siti W.;
    • Abdullah, Nor-Linda;
    • Abdullah, Aminah;
    • Greene, Nicholas D.E.;
    • Cheah, Pike-See;
    • Ling, King-Hwa;
    • Yusof, Hadri;
    • Marwan, Ahmed I.;
    • Williams, Sarah M.;
    • York, Kerri T.;
    • Ahmad-Annuar, Azlina;
    • Abdul-Aziz, Noraishah M.;
    • Cristescu, M.E.
    Publication type:
    Article
    16

    Clinical Phenotype of LRRK2 R1441C in 2 Chinese Sisters.

    Published in:
    Neurodegenerative Diseases, 2020, v. 20, n. 1, p. 39, doi. 10.1159/000508131
    By:
    • Lim, Shen-Yang;
    • Lim, Jia Lun;
    • Ahmad-Annuar, Azlina;
    • Lohmann, Katja;
    • Tan, Ai Huey;
    • Lim, Kai Bin;
    • Tay, Yi Wen;
    • Shing, Yee Lee;
    • Muthusamy, Kalai Arasu;
    • Bauer, Peter;
    • Rolfs, Arndt;
    • Klein, Christine
    Publication type:
    Article
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    Association study of MCCC1/LAMP3 and DGKQ variants with Parkinson's disease in patients of Malay ancestry.

    Published in:
    Neurological Sciences, 2021, v. 42, n. 10, p. 4203, doi. 10.1007/s10072-021-05056-x
    By:
    • Lim, Jia Lun;
    • Ng, Ebonne Yulin;
    • Lim, Shen-Yang;
    • Tan, Ai Huey;
    • Abdul-Aziz, Zariah;
    • Ibrahim, Khairul Azmi;
    • Gopalai, Aroma Agape;
    • Tay, Yi Wen;
    • Vijayanathan, Yuganthini;
    • Toh, Tzi Shin;
    • Lim, Soo Kun;
    • Bee, Ping-Chong;
    • Puvanarajah, Santhi Datuk;
    • Viswanathan, Shanthi;
    • Looi, Irene;
    • Lim, Thien Thien;
    • Eow, Gaik Bee;
    • Cheah, Wee Kooi;
    • Tan, Eng-King;
    • Ahmad-Annuar, Azlina
    Publication type:
    Article
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    PARK16 is associated with PD in the Malaysian population.

    Published in:
    American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 839, doi. 10.1002/ajmg.b.32454
    By:
    • Gopalai, Aroma Agape;
    • Ahmad‐Annuar, Azlina;
    • Li, Hui‐Hua;
    • Zhao, Yi;
    • Lim, Shen‐Yang;
    • Tan, Ai Huey;
    • Lim, Thien Thein;
    • Eow, Gaik Bee;
    • Santhi, Puvanarajah;
    • Shanthi, Viswanathan;
    • Norlinah, Mohamed Ibrahim;
    • Aziz, Zariah Abdul;
    • Lim, Soo Kun;
    • Tan, Chong Tin;
    • Tan, Eng‐King
    Publication type:
    Article
    25

    Cranial neural tube defect after trimethoprim exposure.

    Published in:
    BMC Research Notes, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13104-018-3593-1
    By:
    • Abdullah, Nor Linda;
    • Gunasekaran, Renuka;
    • Mohd-Zin, Siti Waheeda;
    • Lim, Bee-Hui;
    • Maniam, Pramila;
    • Mohd-Salleh, Anis Shuhada;
    • Thong, Meow-Keong;
    • Chik, Zamri;
    • Nordin, Noreena;
    • Omar, Zaliha;
    • Engkasan, Julia Patrick;
    • Ganesan, Dharmendra;
    • Aiezzah, Zakaria Nurul;
    • Ahmad-Annuar, Azlina;
    • Abdul-Aziz, Noraishah Mydin
    Publication type:
    Article
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    Genome-wide association study of Parkinson's disease in East Asians.

    Published in:
    Human Molecular Genetics, 2017, v. 26, n. 1, p. 226, doi. 10.1093/hmg/ddw379
    By:
    • Jia Nee Foo;
    • Tan, Louis C.;
    • Irwan, Ishak D.;
    • Wing-Lok Au;
    • Hui Qi Low;
    • Prakash, Kumar-M.;
    • Ahmad-Annuar, Azlina;
    • Jinxin Bei;
    • Chan, Anne Y. Y.;
    • Chiung Mei Chen;
    • Yi-Chun Chen;
    • Sun Ju Chung;
    • Hao Deng;
    • Shen-Yang Lim;
    • Mok, Vincent;
    • Hao Pang;
    • Zhong Pei;
    • Rong Peng;
    • Hui-Fang Shang;
    • Kyuyoung Song
    Publication type:
    Article
    33

    Analysis of non-synonymous-coding variants of Parkinson's disease-related pathogenic and susceptibility genes in East Asian populations.

    Published in:
    Human Molecular Genetics, 2014, v. 23, n. 14, p. 3891, doi. 10.1093/hmg/ddu086
    By:
    • Foo, Jia Nee;
    • Tan, Louis C.;
    • Liany, Herty;
    • Koh, Tat Hung;
    • Irwan, Ishak D.;
    • Ng, Yen Yek;
    • Ahmad-Annuar, Azlina;
    • Au, Wing-Lok;
    • Aung, Tin;
    • Chan, Anne Y.Y.;
    • Chong, Siow-Ann;
    • Chung, Sun Ju;
    • Jung, Yusun;
    • Khor, Chiea Chuen;
    • Kim, Juyeon;
    • Lee, Jimmy;
    • Lim, Shen-Yang;
    • Mok, Vincent;
    • Prakash, Kumar-M.;
    • Song, Kyuyoung
    Publication type:
    Article
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    Glucocerebrosidase (GBA) gene variants in a multi-ethnic Asian cohort with Parkinson's disease: mutational spectrum and clinical features.

    Published in:
    Journal of Neural Transmission, 2022, v. 129, n. 1, p. 37, doi. 10.1007/s00702-021-02421-0
    By:
    • Lim, Jia Lun;
    • Lohmann, Katja;
    • Tan, Ai Huey;
    • Tay, Yi Wen;
    • Ibrahim, Khairul Azmi;
    • Abdul Aziz, Zariah;
    • Mawardi, Ahmad Shahir;
    • Puvanarajah, Santhi Datuk;
    • Lim, Thien Thien;
    • Looi, Irene;
    • Ooi, Joshua Chin Ern;
    • Chia, Yuen Kang;
    • Muthusamy, Kalai Arasu;
    • Bauer, Peter;
    • Rolfs, Arndt;
    • Klein, Christine;
    • Ahmad-Annuar, Azlina;
    • Lim, Shen-Yang
    Publication type:
    Article
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    Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian family.

    Published in:
    Neurogenetics, 2019, v. 20, n. 3, p. 117, doi. 10.1007/s10048-019-00576-3
    By:
    • Tey, Shelisa;
    • Shahrizaila, Nortina;
    • Drew, Alexander P.;
    • Samulong, Sarimah;
    • Goh, Khean-Jin;
    • Battaloglu, Esra;
    • Atkinson, Derek;
    • Parman, Yesim;
    • Jordanova, Albena;
    • Chung, Ki Wha;
    • Choi, Byung-Ok;
    • Li, Yi-Chung;
    • Auer-Grumbach, Michaela;
    • Nicholson, Garth A.;
    • Kennerson, Marina L.;
    • Ahmad-Annuar, Azlina
    Publication type:
    Article
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    Clinical and functional evidence for the pathogenicity of the LRRK2 p.Arg1067Gln variant.

    Published in:
    NPJ Parkinson's Disease, 2025, v. 11, n. 1, p. 1, doi. 10.1038/s41531-025-00884-6
    By:
    • Lim, Shen-Yang;
    • Toh, Tzi Shin;
    • Hor, Jia Wei;
    • Lim, Jia Lun;
    • Lit, Lei Cheng;
    • Ahmad-Annuar, Azlina;
    • Tay, Yi Wen;
    • Foo, Jia Nee;
    • Ng, Ebonne Yulin;
    • Muthusamy, Kalai Arasu;
    • Mohamed Ibrahim, Norlinah;
    • Ibrahim, Khairul Azmi;
    • Tan, Louis Chew Seng;
    • Zulkefli, Jannah;
    • Khairul Anuar, Anis Nadhirah;
    • Black, Kirsten;
    • Lis, Pawel;
    • Xie, Fei;
    • Cen, Zhidong;
    • Lim, Kai Shi
    Publication type:
    Article
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    LRRK2 G2385R and R1628P Mutations Are Associated with an Increased Risk of Parkinson's Disease in the Malaysian Population.

    Published in:
    BioMed Research International, 2014, v. 2014, p. 1, doi. 10.1155/2014/867321
    By:
    • Gopalai, Aroma Agape;
    • Shen-Yang Lim;
    • Jing Yi Chua;
    • Shelisa Tey;
    • Thien Thien Lim;
    • Ibrahim, Norlinah Mohamed;
    • Ai Huey Tan;
    • Gaik Bee Eow;
    • Aziz, Zariah Abdul;
    • Puvanarajah, Santhi Datuk;
    • Viswanathan, Shanthi;
    • Looi, Irene;
    • Soo Kun Lim;
    • Li Ping Tan;
    • Yip Boon Chong;
    • Chong Tin Tan;
    • Yi Zhao;
    • E. K. Tan;
    • Ahmad-Annuar, Azlina
    Publication type:
    Article
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