Tsai, Fuu-Jen

Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

Mahajan, A., Spracklen, C. N., Zhang, W., Ng, M. C. Y., Petty, L. E., Kitajima, H., Yu, G. Z., Rüeger, S., Speidel, L., Kim, Y. J., et al. (2022) · Nature Genetics

Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals

Cited by 704

Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

Suzuki, K., Hatzikotoulas, K., Southam, L., Taylor, H. J., Yin, X., Lorenz, K. M., Mandla, R., Huerta-Chagoya, A., Melloni, G. E. M., Kanoni, S., et al. (2024) · Nature

Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals

Cited by 606

Erk Associates with and Primes GSK-3β for Its Inactivation Resulting in Upregulation of β-Catenin

Ding, Q., Xia, W., Liu, J.-C., Yang, J.-Y., Lee, D.-F., Xia, J., Bartholomeusz, G., Li, Y., Pan, Y., Li, Z., et al. (2005) · Molecular Cell

Wnt/β-catenin signaling in development and cancerSignaling Pathways in Disease

Cited by 597

Interleukin gene polymorphisms in age-related macular degeneration

Tsai, Y.-Y., Lin, J.-M., Wan, L., Lin, H.-J., Tsai, Y., Lee, C.-C., Tsai, C.-H., Tsai, F.-J., & Tseng, S.-H. (2008) · Investigative Opthalmology & Visual Science

Retinal Diseases and TreatmentsOcular Diseases and Behçet’s Syndrome

Cited by 69

Dopamine Receptor D2 Gene Polymorphisms Are Associated in Taiwanese Children With Tourette Syndrome

Lee, C.-C., Chou, I.-C., Tsai, C.-H., Wang, T.-R., Li, T.-C., & Tsai, F.-J. (2005) · Pediatric Neurology

Obsessive-Compulsive Spectrum DisordersNeurotransmitter Receptor Influence on Behavior

Cited by 63

Genetic Variation in N-Methyl-D-Aspartate Receptor Subunit NR3A but Not NR3B Influences Susceptibility to Alzheimer’s Disease

Liu, H.-P., Lin, W.-Y., Liu, S.-H., Wang, W.-F., Tsai, C.-H., Wu, B.-T., Wang, C.-K., & Tsai, F.-J. (2009) · Dementia and Geriatric Cognitive Disorders

Alzheimer's disease research and treatmentsDementia and Cognitive Impairment Research

Cited by 29

Low frequency of the CYP21A2 deletion in ethnic Chinese (Taiwanese) patients with 21-hydroxylase deficiency

Lee, H.-H., Lee, Y.-J., Wang, Y.-M., Chao, H.-T., Niu, D.-M., Chao, M.-C., Tsai, F.-J., Lo, F.-S., & Lin, S.-J. (2008) · Molecular Genetics and Metabolism

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 28

Genetic impacts on thermostability of onco-lncRNA HOTAIR during the development and progression of endometriosis

Chang, C. Y.-Y., Tseng, C.-C., Lai, M.-T., Chiang, A.-J., Lo, L.-C., Chen, C.-M., Yen, M.-J., Sun, L., Yang, L., Hwang, T., et al. (2021) · PLOS ONE

Endometriosis Research and TreatmentCancer-related molecular mechanisms research

Cited by 20

Effect of Xanthium Strumarium on HIV-1 5′-LTR Transcriptional Activity and Viral Reactivation in Latently Infected Cells

Chen, C.-J., Chiu, M.-L., Hung, C.-H., Liang, W.-M., Ho, M.-W., Lin, T.-H., Liu, X., Tsang, H., Liao, C.-C., Huang, S.-M., et al. (2021) · Frontiers in Pharmacology

HIV Research and TreatmentHIV/AIDS drug development and treatment

Cited by 5