Channel: National Taiwan University

This collection includes bioRxiv and medRxiv papers from authors at National Taiwan University.

587 Articles

The LRRK2 p.A419V variant associates with risk of Parkinson disease in the East Asian population and an evaluation on age of onset

Lim, K. S., Perinan, M. T., Chew, E. G. Y., Lee, P. S., Akcimen, F., Lim, J. L., Koretsky, M. J., Funayama, M., Yoshino, H., Hattori, N., Kaiyrzhanov, R., Houlden, H., Isayan, M., Tay, Y. W., Toh, T. S., Lit, L.-C., Khairul Anuar, A. N., Ding, H. X., Screven, L., Mohamed Ibrahim, N., Lin, C.-H., Kim, H.-J., Lee, J.-Y., Chung, S. J., Foo, J. N., Tan, E.-K., Lim, S.-Y., Tan, A. H., Bandres Ciga, S., Ahmad-Annuar, A., Global Parkinson's Genetics Program (GP2)

10.1101/2025.08.28.25333987 — Posted: 2025-09-02

Utilization of Arabidopsis E3 ubiquitin decoys high-throughput yeast screen platform to dissect the ubiquitin-mediated circadian clock regulation

Tu, Y.-T., Chen, C.-A., Gendron, J., Lee, C.-M.

10.1101/2025.08.31.673341 — Posted: 2025-09-01

Source-specific exposure and burden of disease attributable to volatile organic compounds (VOCs) in China's residences

Liu, N., Huang, C.-S., Yin, Y., Dai, X., Pei, J., Liu, J., Zhao, Z., Zhang, Y., Larson, T., Seto, E., Austin, E.

10.1101/2025.08.25.25333590 — Posted: 2025-08-28

Prediction and Screening for Asymptomatic Carotid Artery Stenosis in Post-Radiotherapy Nasopharyngeal Carcinoma Patients

Lin, C.-Y., Kuo, P.-H., Wu, S.-Y., Chen, C.-N., Ko, J.-Y.

10.1101/2025.08.19.25334024 — Posted: 2025-08-24

Spatiotemporal Dynamics of fMRI Signal Changes Induced by High Concentration Normobaric Oxygen Inhalation

Su, Y.-S., Wu, C.-T., Goh, J. O. S., Sanes, J. N., Chao, Z. C.

10.1101/2025.07.29.667573 — Posted: 2025-08-05

Population-Specific Polygenic Risk Scores Developed for the Han Chinese

Chen, H.-H., Chen, C.-H., Hou, M.-C., Fu, Y.-C., Li, L.-H., Chou, C.-Y., Yeh, E.-C., Tsai, M.-F., Chen, C.-h., Yang, H.-C., Huang, Y.-T., Liu, Y.-M., Wei, C.-y., Su, J.-P., Lin, W.-J., Wang, E. H. F., Chiang, C.-L., Jiang, J.-K., Lee, I.-H., Liang, K.-H., Chen, W.-S., Tsai, H.-C., Lin, S.-Y., Chang, F.-P., Ho, H.-L., Yeh, Y.-C., Tseng, W.-C., Lin, M.-H., Chang, H.-T., Tseng, L.-M., Liang, W.-Y., Chen, P. C.-H., Hsieh, Y.-C., Chen, Y.-M., Hsiao, T.-H., Lin, C., Chen, Y.-J., Chen, I.-C., Mao, C.-L., Chang, S.-J., Chang, Y.-L., Liao, Y., Lai, C.-H., Lee, W.-J., Tung, H., Yen, T.-T., Yen, H.-C., C

10.1101/2024.10.14.24315279 — Posted: 2025-08-03

CNV-Finder: Streamlining Copy Number Variation Discovery

Kuznetsov, N., Daida, K., Makarious, M. B., Al-Mubarak, B., Atterling Brolin, K., Malik, L., Kouam, C., Baker, B., Real, R., Step, K., Lange, L. M., Wu, L., Ostrozovicova, M., Andersh, K. M., Kung, P.-J., Mecheri, Y., Tay, Y.-W., Soundous Malek, B., Al Tassan, N., Teresa Perinan, M., Hong, S., Koretsky, M. J., Sargeant, L., Levine, K., Blauwendraat, C., Billingsley, K. J., Bandres-Ciga, S., Leonard, H. L., Bardien, S., Morris, H. R., Singleton, A. B., Nalls, M. A., Vitale, D., The Global Parkinson's Genetics Program

10.1101/2024.11.22.624040 — Posted: 2025-07-26

Multi-ancestry polygenic risk scores for the prediction of type 2 diabetes and complications in diverse ancestries.

Huerta-Chagoya, A., Kim, J., Mandla, R., Lu, Y., Suzuki, K., Petty, L. E., Ng, H. K., Choi, J., Lee, S., Rout, M., Lin, K., Adair, L. S., Adeyemo, A., Ahsan, H., Akiyama, M., An, P., Anand, S. S., Becker, D. M., Bertoni, A. G., Bian, Z., Bielak, L. F., Blangero, J., Boehnke, M., Bottinger, E. P., Bowden, D. W., Bragg, F., Brody, J. A., Buchanan, T. A., Cade, B. E., Chai, J.-F., Chambers, J. C., Chandak, G. R., Chang, L.-C., Chang, K.-M., Chee, M.-L., Chen, C.-H., Chen, Y.-T., Chen, Z., Chen, Y.-D. I., Chen, J., Chen, G., Chen, S.-H., Chen, W.-M., Cheng, C.-Y., Cho, Y. S., Choi, H. S., Chuang

10.1101/2025.07.21.25331778 — Posted: 2025-07-23

Massively Parallel Polyribosome Profiling Reveals Translation Defects of Human Disease-Relevant UTR Mutations

Li, W.-P., Su, J.-Y., Chang, Y.-C., Wang, Y.-L., Chiang, H.-L., Huang, A.-C., Hsieh, Y.-T., Chiang, Y.-H., Ko, Y.-L., Chiang, B.-J., Yang, C.-H., Huang, Y.-T., Lin, C.-L.

10.1101/2024.04.11.589132 — Posted: 2025-07-21

Rare but Relevant: Assessing Variants in Dystonia-linked Genes in Parkinson's Disease

Lange, L. M., Fang, Z.-H., Screven, L., Tan, A. H., Alcalay, R. N., Amouri, R., Bovenzi, R., Fenn, M., Frost, J. L. I., Jankovic, J., Jasaityte, S., Jaunmuktane, Z., Jeon, B., Keller Sarmiento, I. J., Krueger, R., Kuhlenbaeumer, G., Lin, C.-H., Pavelka, L., Perinan, M. T. M., Ben Sassi, S., Schirinzi, T., Shin, J. H., Shulman, J. M., Tay, Y. W., Uitti, R., Warner, T., Wszolek, Z. K., Wu, L., Wu, R.-M., Zeuner, K. E., Blauwendraat, C., Singleton, A., Mencacci, N. E., Morris, H., Lim, S.-Y., Lohmann, K., Klein, C., the Global Parkinson's Genetics Program (GP2)

10.1101/2025.07.10.25330831 — Posted: 2025-07-11

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