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D-Index & Metrics

Genetics

D-Index
73
Citations
36085
World Ranking
2002
National Ranking
912

Research.com Recognitions

  • 2018 - Member of the National Academy of Sciences

Overview

Ying-Hui Fu is a researcher affiliated with the University of California, San Francisco in the United States. Their work primarily focuses on neuroscience, with a significant emphasis on circadian rhythm and melatonin, sleep and wakefulness research, and sleep-related disorders. Their research also spans mitochondrial function and pathology, genetic neurodegenerative diseases, RNA research and splicing, and neuroscience and neuropharmacology research.

The scientist has published extensively, with notable recurring venues including the Proceedings of the National Academy of Sciences, Journal of Clinical Investigation, Movement Disorders, Current Opinion in Neurobiology, and SLEEP. Their published works contribute to advancing knowledge in experimental and cognitive psychology, endocrine and autonomic systems, molecular biology, cellular and molecular neuroscience, and cognitive neuroscience.

Some recent papers include:

  • Human circadian variations, 2021, Journal of Clinical Investigation
  • Mutations in Metabotropic Glutamate Receptor 1 Contribute to Natural Short Sleep Trait, 2020, Current Biology
  • Adaptive Long-Read Sequencing Reveals GGC Repeat Expansion in ZFHX3 Associated with Spinocerebellar Ataxia Type 4, 2024, Movement Disorders
  • Microglia are involved in the protection of memories formed during sleep deprivation, 2021, Neurobiology of Sleep and Circadian Rhythms
  • Familial natural short sleep mutations reduce Alzheimer pathology in mice, 2022, iScience

Frequent co-authors who have collaborated with Ying-Hui Fu include:

  • Louis J. Ptáček
  • Thomas McMahon
  • Nicholas W. Gentry
  • Liza Ashbrook
  • John M. Webb

Their research covers a range of topics related to circadian biology and sleep, including the mechanisms underlying natural short sleep traits, the effects of sleep deprivation on memory and neurobiology, and the genetic basis of sleep-related neurodegenerative disorders.

Ying-Hui Fu was recognized as a Member of the National Academy of Sciences in 2018, reflecting their contributions to their scientific field.

Best Publications

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

    Annemiske J.M.H. Verkerk;Maura Pieretti;James S. Sutcliffe;Ying-Hui Fu

  • Candidate gene for the chromosome 1 familial Alzheimer's disease locus

    Ephrat Levy-Lahad;Wilma Wasco;Parvoneh Poorkaj;Donna M. Romano

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

    Ying-Hui Fu;Derek P.A. Kuhl;Antonio Pizzuti;Maura Pieretti

  • Positional Cloning of the Werner's Syndrome Gene

    Chang En Yu;Junko Oshima;Ying Hui Fu;Ellen M. Wijsman

  • An unstable triplet repeat in a gene related to myotonic muscular dystrophy.

    Y. H. Fu;A. Pizzuti;R. G. Fenwick;J. King

  • An hPer2 Phosphorylation Site Mutation in Familial Advanced Sleep Phase Syndrome

    Kong L. Toh;Christopher R. Jones;Yan He;Erik J. Eide

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

    Maura Pieretti;Fuping Zhang;Ying-Hui Fu;Stephen T. Warren

  • Bone dysplasia sclerosteosis results from loss of the SOST gene product, a novel cystine knot-containing protein

    Mary E. Brunkow;Jessica C. Gardner;Jeff Van Ness;Bryan W. Paeper

  • Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome

    Nikki M. Plaster;Rabi Tawil;Martin Tristani-Firouzi;Sonia Canún

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

    Ying Xu;Quasar S. Padiath;Robert E. Shapiro;Christopher R. Jones

  • Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)

    Martin Tristani-Firouzi;Judy L. Jensen;Matthew R. Donaldson;Valeria Sansone

  • Sex increases the efficacy of natural selection in experimental yeast populations

    Matthew R. Goddard;Matthew R. Goddard;H. Charles J. Godfray;Austin Burt

  • Triplet Repeat Mutations in Human Disease

    C. T. Caskey;A. Pizzuti;Ying-Hui Fu;R. G. Fenwick

  • Lamin B1 duplications cause autosomal dominant leukodystrophy

    Quasar S Padiath;Kazumasa Saigoh;Kazumasa Saigoh;Raphael Schiffmann;Hideaki Asahara

  • Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia New diagnostic criteria

    M. K. Bruno;M. Hallett;K. Gwinn-Hardy;B. Sorensen

  • Modeling of a Human Circadian Mutation Yields Insights into Clock Regulation by PER2

    Y. Xu;K. L. Toh;C. R. Jones;Ji-Yeon Shin

  • Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophy.

    Fu Yh;Friedman Dl;Richards S;Pearlman Ja

  • The transcriptional repressor DEC2 regulates sleep length in mammals.

    Ying He;Christopher R. Jones;Nobuhiro Fujiki;Ying Xu

  • Electrocardiographic Features in Andersen-Tawil Syndrome Patients With KCNJ2 Mutations: Characteristic T-U–Wave Patterns Predict the KCNJ2 Genotype

    Li Zhang;Li Zhang;D. Woodrow Benson;Martin Tristani-Firouzi;Louis J. Ptacek

  • Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's Syndrome

    N Plaster;R Tawil;M Tristani-Firouzi;S Canun

Frequent Co-Authors

Louis J. Ptáček
Louis J. Ptáček University of California, San Francisco
George A. Marzluf
George A. Marzluf The Ohio State University
Gerard D. Schellenberg
Gerard D. Schellenberg University of Pennsylvania
Junko Oshima
Junko Oshima University of Washington
Antonio Pizzuti
Antonio Pizzuti Sapienza University of Rome
Len A. Pennacchio
Len A. Pennacchio Lawrence Berkeley National Laboratory
Rabi Tawil
Rabi Tawil University of Rochester Medical Center
Tetsuo Ashizawa
Tetsuo Ashizawa Houston Methodist
David L. Nelson
David L. Nelson Baylor College of Medicine
Stephen T. Warren
Stephen T. Warren Emory University

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