World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

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

Ying-Hui Fu publication distribution in Genetics in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Genetics in 2026. The highlighted bar marks where Ying-Hui Fu sits on this spectrum.

45–54 publications: 6 scientists 55–64 publications: 10 scientists 65–74 publications: 35 scientists 75–84 publications: 84 scientists 85–94 publications: 102 scientists 95–104 publications: 151 scientists 105–114 publications: 175 scientists 115–124 publications: 203 scientists 125–134 publications: 217 scientists 135–144 publications: 205 scientists 145–154 publications: 193 scientists 155–164 publications: 188 scientists 165–174 publications: 170 scientists 175–184 publications: 178 scientists 185–194 publications: 164 scientists 195–204 publications: 173 scientists 205–214 publications: 159 scientists 215–224 publications: 134 scientists 225–234 publications: 143 scientists 235–244 publications: 105 scientists 245–254 publications: 114 scientists 255–264 publications: 92 scientists 265–274 publications: 88 scientists 275–284 publications: 87 scientists 285–294 publications: 80 scientists 295–304 publications: 62 scientists 305–314 publications: 75 scientists 315–324 publications: 67 scientists 325–334 publications: 60 scientists 335–344 publications: 52 scientists 345–354 publications: 40 scientists 355–364 publications: 48 scientists 365–374 publications: 47 scientists 375–384 publications: 46 scientists 385–394 publications: 31 scientists 395–404 publications: 27 scientists 405–414 publications: 40 scientists 415–424 publications: 30 scientists 425–434 publications: 43 scientists 435–444 publications: 29 scientists 445–454 publications: 14 scientists 455–464 publications: 28 scientists 465–474 publications: 21 scientists 475–484 publications: 21 scientists 485–494 publications: 22 scientists 495–504 publications: 17 scientists 505–514 publications: 12 scientists 515–524 publications: 11 scientists 525–534 publications: 8 scientists 535–544 publications: 8 scientists 545–554 publications: 14 scientists 555–564 publications: 4 scientists 565–574 publications: 11 scientists 575–584 publications: 5 scientists 585–594 publications: 11 scientists 595–604 publications: 12 scientists 605–614 publications: 7 scientists 615–624 publications: 6 scientists 625–634 publications: 10 scientists 635–644 publications: 9 scientists 645–654 publications: 10 scientists 655–664 publications: 6 scientists 665–674 publications: 6 scientists 675–684 publications: 6 scientists 685–694 publications: 4 scientists 695–702 publications: 6 scientists 703+ publications: 100 scientists
45 publications 703+

This scientist: 165 publications — 36th percentile

36% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 703 publications or more.

Ying-Hui Fu D-index placement in Genetics in 2026

The chart shows the D-index (discipline H-index) distribution of Genetics scientists ranked by Research.com in 2026. The highlighted bar marks where Ying-Hui Fu sits on this spectrum.

40–41 D-Index: 24 scientists 42–43 D-Index: 52 scientists 44–45 D-Index: 84 scientists 46–47 D-Index: 112 scientists 48–49 D-Index: 118 scientists 50–51 D-Index: 141 scientists 52–53 D-Index: 143 scientists 54–55 D-Index: 145 scientists 56–57 D-Index: 179 scientists 58–59 D-Index: 162 scientists 60–61 D-Index: 175 scientists 62–63 D-Index: 191 scientists 64–65 D-Index: 172 scientists 66–67 D-Index: 184 scientists 68–69 D-Index: 164 scientists 70–71 D-Index: 158 scientists 72–73 D-Index: 150 scientists 74–75 D-Index: 136 scientists 76–77 D-Index: 127 scientists 78–79 D-Index: 127 scientists 80–81 D-Index: 111 scientists 82–83 D-Index: 110 scientists 84–85 D-Index: 110 scientists 86–87 D-Index: 84 scientists 88–89 D-Index: 102 scientists 90–91 D-Index: 66 scientists 92–93 D-Index: 72 scientists 94–95 D-Index: 70 scientists 96–97 D-Index: 54 scientists 98–99 D-Index: 60 scientists 100–101 D-Index: 49 scientists 102–103 D-Index: 55 scientists 104–105 D-Index: 45 scientists 106–107 D-Index: 42 scientists 108–109 D-Index: 28 scientists 110–111 D-Index: 39 scientists 112–113 D-Index: 25 scientists 114–115 D-Index: 31 scientists 116–117 D-Index: 29 scientists 118–119 D-Index: 34 scientists 120–121 D-Index: 29 scientists 122–123 D-Index: 29 scientists 124–125 D-Index: 18 scientists 126–127 D-Index: 27 scientists 128–129 D-Index: 22 scientists 130–131 D-Index: 16 scientists 132–133 D-Index: 11 scientists 134–135 D-Index: 17 scientists 136–137 D-Index: 12 scientists 138–139 D-Index: 21 scientists 140–141 D-Index: 4 scientists 142–143 D-Index: 9 scientists 144–145 D-Index: 14 scientists 146–147 D-Index: 6 scientists 148–149 D-Index: 10 scientists 150–151 D-Index: 7 scientists 152–153 D-Index: 9 scientists 154–155 D-Index: 8 scientists 156–157 D-Index: 8 scientists 158–159 D-Index: 9 scientists 160+ D-Index: 96 scientists
40 D-Index 160+

This scientist: 73 D-Index — 54th percentile

54% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 160 D-Index or more.

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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