Fu, Ying-Hui

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

Verkerk, A. J. M. H., Pieretti, M., Sutcliffe, J. S., Fu, Y.-H., Kuhl, D. P. A., Pizzuti, A., Reiner, O., Richards, S., Victoria, M. F., Zhang, F., et al. (1991) · Cell

Genetics and Neurodevelopmental DisordersGenomic variations and chromosomal abnormalities

Cited by 3,481

Candidate gene for the chromosome 1 familial Alzheimer’s disease locus

Levy-Lahad, E., Wasco, W., Poorkaj, P., Romano, D. M., Oshima, J., Pettingell, W. H., Yu, C.-E., Jondro, P. D., Schmidt, S. D., Wang, K., et al. (1995) · Science

Alzheimer's disease research and treatmentsDementia and Cognitive Impairment Research

Cited by 2,577

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

Fu, Y.-H., Kuhl, D. P. A., Pizzuti, A., Pieretti, M., Sutcliffe, J. S., Richards, S., Verkert, A. J. M. H., Holden, J. J. A., Fenwick, R. G., Warren, S. T., et al. (1991) · Cell

Genetics and Neurodevelopmental DisordersGenetic Neurodegenerative Diseases

Cited by 2,080

Absence of expression of the FMR-1 gene in fragile X syndrome

Pieretti, M., Zhang, F., Fu, Y.-H., Warren, S. T., Oostra, B. A., Caskey, C. T., & Nelson, D. L. (1991) · Cell

Genetics and Neurodevelopmental DisordersGenetic Neurodegenerative Diseases

Cited by 1,476

An h Per2 Phosphorylation Site Mutation in Familial Advanced Sleep Phase Syndrome

Toh, K. L., Jones, C. R., He, Y., Eide, E. J., Hinz, W. A., Virshup, D. M., Ptáček, L. J., & Fu, Y.-H. (2001) · Science

Circadian rhythm and melatoninSleep and Wakefulness Research

Cited by 1,460

Bone Dysplasia Sclerosteosis Results from Loss of the SOST Gene Product, a Novel Cystine Knot–Containing Protein

Brunkow, M. E., Gardner, J. C., Van Ness, J., Paeper, B. W., Kovacevich, B. R., Proll, S., Skonier, J. E., Zhao, L., Sabo, P. J., Fu, Y.-H., et al. (2001) · The American Journal of Human Genetics

Bone Metabolism and DiseasesDermatological and Skeletal Disorders

Cited by 1,011

Functional consequences of a CKIδ mutation causing familial advanced sleep phase syndrome

Xu, Y., Padiath, Q. S., Shapiro, R. E., Jones, C. R., Wu, S. C., Saigoh, N., Saigoh, K., Ptáček, L. J., & Fu, Y.-H. (2005) · Nature

Circadian rhythm and melatoninSleep and Wakefulness Research

Cited by 861

A PERIOD3 variant causes a circadian phenotype and is associated with a seasonal mood trait

Zhang, L., Hirano, A., Hsu, P.-K., Jones, C. R., Sakai, N., Okuro, M., McMahon, T., Yamazaki, M., Xu, Y., Saigoh, N., et al. (2016) · Proceedings of the National Academy of Sciences

Circadian rhythm and melatoninSleep and Wakefulness Research

Cited by 169

Genetics of the human circadian clock and sleep homeostat

Ashbrook, L. H., Krystal, A. D., Fu, Y.-H., & Ptáček, L. J. (2020) · Neuropsychopharmacology

Circadian rhythm and melatoninSleep and Wakefulness Research

Cited by 123

MicroRNA-23a promotes myelination in the central nervous system

Lin, S.-T., Huang, Y., Zhang, L., Heng, M. Y., Ptáček, L. J., & Fu, Y.-H. (2013) · Proceedings of the National Academy of Sciences

Neurogenesis and neuroplasticity mechanismsMicroRNA in disease regulation

Cited by 117

Lamin B1 mediates cell-autonomous neuropathology in a leukodystrophy mouse model

Heng, M. Y., Lin, S.-T., Verret, L., Huang, Y., Kamiya, S., Padiath, Q. S., Tong, Y., Palop, J. J., Huang, E. J., Ptácχek, L. J., et al. (2013) · Journal of Clinical Investigation

Nuclear Structure and FunctionHereditary Neurological Disorders

Cited by 78

Regulation of Myelination in the Central Nervous System by Nuclear Lamin B1 and Non-coding RNAs

Lin, S.-T., Heng, M. Y., Ptáček, L. J., & Fu, Y.-H. (2014) · Translational Neurodegeneration

Neurogenesis and neuroplasticity mechanismsNuclear Structure and Function

Cited by 40

Genetics of Human Sleep Behavioral Phenotypes

Hsu, P.-K., Ptáček, L. J., & Fu, Y.-H. (2015) · Methods in Enzymology

Sleep and Wakefulness ResearchCircadian rhythm and melatonin

Cited by 29

Intragenic probe used for diagnostics in fragile X families

Verkerk, A. J. M. H., De Vries, B. B. A., Niermeijer, M. F., Fu, Y., Nelson, D. L., Warren, S. T., Majoor‐Krakauer, D. F., Halley, D. J. J., & Oostra, B. A. (1992) · American Journal of Medical Genetics

Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases

Cited by 17