Author

K. Puvan

Observed names: K Puvan, Kathi‐avelu Puvan

Institutions: Singapore General Hospital, National Neuroscience Institute

Observed institutions: Mayo Clinic, SingHealth, Singapore General Hospital, National Neuroscience Institute, Genome Institute of Singapore

OpenAlex ID: A5113638699

The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients

2005 · E.K. Tan, H. Shen, et al. · Neuroscience Letters · 155

PINK1 mutations in sporadic early‐onset Parkinson's disease

2006 · Eng‐King Tan, Kenneth Yew, et al. · Movement Disorders · 105

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

2004 · E. K. Tan, A. Chai, et al. · Neurology · 81

Analysis of LRRK2 functional domains in nondominant Parkinson disease

2005 · L. Skipper, H. Shen, et al. · Neurology · 75

Differential expression of splice variant and wild-type parkin in sporadic Parkinson's disease

2005 · E. K. Tan, H. Shen, et al. · Neurogenetics · 38

Impaired transcriptional upregulation of Parkin promoter variant under oxidative stress and proteasomal inhibition: clinical association

2005 · E. K. Tan, K. Y. Puong, et al. · Human Genetics · 30

Nurr1 mutational screen in Parkinson's disease

2004 · Eng‐King Tan, Henry Chung, et al. · Movement Disorders · 19

Analysis of PINK1 in Asian patients with familial parkinsonism

2005 · EK Tan, K Yew, et al. · Clinical Genetics · 14

A case of sarcoidosis presenting as cranial polyneuritis.

1989 · S H Lim, K Puvan, et al. · PubMed · 4

Syringomyelia with Arnold Chiari I malformation: a report of four cases.

1989 · S H Lim, M C Wong, et al. · PubMed · 2

Intramedullary spinal cord metastasis.

1989 · S H Lim, K Puvan · PubMed · 1

Works count: 11

Citation count: 524

H-index: 8

I10-index: 8