LRRK2 variant associated with Alzheimer's disease

بواسطة Zhao, Y., Ho, P., Yih, Y., Chen, C., Lee, W.L., Tan, E.K.
منشور في 2014

Glucocerebrosidase mutations and risk of Parkinson disease in Chinese patients [2]

بواسطة Tan E.-K., Tong J., Fook-Chong S., Yih Y., Wong M.-C., Pavanni R., Zhao Y.
منشور في 2018

CALHM1 variant is not associated with Alzheimer's disease among Asians

بواسطة Tan, E.K., Ho, P., Cheng, S.Y., Yih, Y., Li, H.H., Fook-Chong, S., Lee, W.L., Zhao, Y.
منشور في 2014

Alpha synuclein promoter and risk of Parkinson's disease: Microsatellite and allelic size variability

بواسطة Tan E.-K., Tan C., Shen H., Chai A., Lum S.-Y., Teoh M.-L., Yih Y., Wong M.-C., Zhao Y.
منشور في 2018

Essential tremor linked TENM4 mutation found in healthy Chinese individuals

بواسطة Chao Y.X., Lin Ng E.Y., Tio M., Kumar P., Tan L., Au W.L., Yih Y., Tan E.K.
منشور في 2018

DRD3 variant and risk of essential tremor

بواسطة Tan E.-K., Prakash K.M., Fook-Chong S., Yih Y., Chua E., Lum S.Y., Wong M.C., Pavanni R., Zhao Y.
منشور في 2018

Monoamine oxidase B polymorphism, cigarette smoking and risk of Parkinson's disease: A study in an Asian population

بواسطة Tan E.K., Chai A., Lum S.Y., Shen H., Tan C., Teoh M.L., Yih Y., Wong M.C., Zhao Y.
منشور في 2018

Restless legs symptoms in thyroid disorders

بواسطة Tan E.K., Ho S.C., Eng P., Loh L.M., Koh L., Lum S.Y., Teoh M.L., Yih Y., Khoo D.
منشور في 2018

Evaluation of somnolence in Parkinson's disease: Comparison with age- and sex-matched controls

بواسطة Tan E.-K., Lum S.Y., Fook-Chong S.M.C., Teoh M.L., Yih Y., Tan L., Tan A., Wong M.C.
منشور في 2018

Genetic analysis of DJ-1 in a cohort Parkinson's disease patients of different ethnicity

بواسطة Tan E.-K., Tan C., Zhao Y., Yew K., Shen H., Chandran V.R., Teoh M.-L., Yih Y., Pavanni R., Wong M.-C.
منشور في 2018

LRRK2 R1628P increases risk of Parkinson's disease: Replication evidence

بواسطة Tan, E.K., Tan, L.C., Lim, H.Q., Li, R., Tang, M., Yih, Y., Pavanni, R., Prakash, K.M., Fook-Chong, S., Zhao, Y.
منشور في 2014

Exploring an interaction of adenosine A2A receptor variability with coffee and tea intake in Parkinson's disease

بواسطة Tan, E.K., Lu, Z.Y., Fook-Chong, S.M.C., Tan, E., Shen, H., Chua, E., Yih, Y., Teo, Y.Y., Zhao, Y.
منشور في 2014

Genetic analysis of Nurr1 haplotypes in Parkinson's disease

بواسطة Tan E.-K., Chung H., Zhao Y., Shen H., Chandran V.R., Tan C., Teoh M.-L., Yih Y., Pavanni R., Wong M.-C.
منشور في 2018

Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease

بواسطة Skipper L., Li Y., Bonnard C., Pavanni R., Yih Y., Chua E., Sung W.-K., Tan L., Wong M.-C., Tan E.-K., Liu J.
منشور في 2018

Mitochondrial complex I polymorphism and cigarette smoking in Parkinson's disease

بواسطة Tan E.K., Chai A., Zhao Y., Lum S.Y., Fook-Chong S.M.C., Teoh M.L., Yih Y., Pavanni R., Wong M.C.
منشور في 2018

Lingo1 variant increases risk of familial essential tremor

بواسطة Tan, E.-K., Teo, Y.-Y., Prakash, K.-M., Li, R., Lim, H.-Q., Angeles, D., Tan, L.-C., Au, W.-L., Yih, Y., Zhao, Y.
منشور في 2014

Nurr1 mutational screen in Parkinson's disease

بواسطة Tan E.-K., Chung H., Chandran V.R., Tan C., Shen H., Yew K., Pavanni R., Puvan K.-A., Wong M.-C., Teoh M.-L., Yih Y., Zhao Y.
منشور في 2018

Dopamine D2 receptor taqIA and TaqIB polymorphisms in Parkinson's disease

بواسطة Tan E.-K., Tan Y., Chai A., Tan C., Shen H., Lum S.Y., Fook-Cheong S.M.C., Teoh M.-L., Yih Y., Wong M.-C., Zhao Y.
منشور في 2018

Analysis of PINK1 in Asian patients with familial parkinsonism [1]

بواسطة Tan E.-K., Yew K., Chua E., Shen H., Jamora R.D., Lee E., Puong K.Y., Zhao Y., Pavanni R., Wong M.C., Puvan K., Yih Y., Tan L.C.S.
منشور في 2018

Alpha-synuclein haplotypes implicated in risk of Parkinson's disease

بواسطة Tan E.-K., Chai A., Teo Y.Y., Zhao Y., Tan C., Shen H., Chandran V.R., Teoh M.L., Yih Y., Pavanni R., Wong M.C., Puvan K., Lo Y.L., Yap E.
منشور في 2018