Exome sequencing in Asian populations identifies low-frequency and rare coding variation influencing Parkinson’s disease risk

Elaine G.Y. Chew, Zhehao Liu, Zheng Li, Sun Ju Chung, Michelle M. Lian, Moses Tandiono, Yue Jing Heng, Ebonne Y. Ng, Louis C.S. Tan, Wee Ling Chng, Tiak Ju Tan, Esther K.L. Peh, Ying Swan Ho, Xiao Yin Chen, Erin Y.T. Lim, Chu Hua Chang, Jonavan J. Leong, Ting Xuan Peh, Ling Ling Chan, Yinxia ChaoWing Lok Au, Kumar M. Prakash, Jia Lun Lim, Yi Wen Tay, Vincent Mok, Anne Y.Y. Chan, Juei Jueng Lin, Beom S. Jeon, Kyuyoung Song, Clement C. Tham, Chi Pui Pang, Jeeyun Ahn, Kyu Hyung Park, Janey L. Wiggs, Tin Aung, Ai Huey Tan, Azlina Ahmad Annuar, Mary B. Makarious, Cornelis Blauwendraat, Mike A. Nalls, Laurie A. Robak, Roy N. Alcalay, Ziv Gan-Or, Richard Reynolds, Shen Yang Lim, Yun Xia, Chiea Chuen Khor*, Eng King Tan*, Zhenxun Wang*, Jia Nee Foo*

*Corresponding author for this work

Research output: Contribution to journalLetterpeer-review

2 Citations (Scopus)

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Biochemistry, Genetics and Molecular Biology

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