World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
68
Citations
15773
World Ranking
2437
National Ranking
1097

Wendy H. Raskind 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 Wendy H. Raskind 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: 181 publications — 43rd percentile

43% of scientists in this discipline score the same or lower.

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

Wendy H. Raskind 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 Wendy H. Raskind 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: 68 D-Index — 45th percentile

45% of scientists in this discipline score the same or lower.

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

Overview

Wendy H. Raskind is affiliated with the University of Washington in the United States and conducts research primarily in the fields of Neuroscience and Biochemistry, Genetics and Molecular Biology. Their work intersects several subfields, including Neurology, Molecular Biology, Immunology, Cellular and Molecular Neuroscience, and Genetics.

The main topics addressed in their research include:

  • Neuroinflammation and Neurodegeneration Mechanisms
  • Inflammation biomarkers and pathways
  • Genetic Neurodegenerative Diseases
  • Neurological Disease Mechanisms and Treatments
  • Mitochondrial Function and Pathology
  • Genetics and Neurodevelopmental Disorders
  • RNA Research and Splicing

Raskind has authored several recent papers with a focus on neurodegenerative and immune processes related to neurological diseases. Key publications include:

  • Defects in lysosomal function and lipid metabolism in human microglia harboring a TREM2 loss of function mutation, 2023, Acta Neuropathologica
  • Triggering Receptor Expressed on Myeloid Cell 2 R47H Exacerbates Immune Response in Alzheimer's Disease Brain, 2020, Frontiers in Immunology
  • Novel TREM2 splicing isoform that lacks the V-set immunoglobulin domain is abundant in the human brain, 2021, Journal of Leukocyte Biology
  • Heterozygous STUB1 missense variants cause ataxia, cognitive decline, and STUB1 mislocalization, 2020, Neurology Genetics
  • Mutations in protein kinase Cγ promote spinocerebellar ataxia type 14 by impairing kinase autoinhibition, 2022, Science Signaling

Frequent coauthors collaborating with Raskind include:

  • Olena Korvatska
  • Kostantin Kiianitsa
  • Mark Matsushita
  • Michael O. Dorschner
  • Thomas D. Bird

Their research has been published in several prominent venues, with multiple contributions to:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • Neurology Genetics
  • Alzheimer's & Dementia
  • Acta Neuropathologica
  • Frontiers in Immunology

Best Publications

  • A p53-Dependent Mouse Spindle Checkpoint

    Shawn M. Cross;Carissa A. Sanchez;Catherine A. Morgan;Melana K. Schimke

  • Mutation of a Putative Mitochondrial Iron Transporter Gene ( ABC7 ) in X-Linked Sideroblastic Anemia and Ataxia (XLSA/A)

    Rando Allikmets;Rando Allikmets;Rando Allikmets;Wendy H Raskind;Wendy H Raskind;Wendy H Raskind;Amy Hutchinson;Amy Hutchinson;Amy Hutchinson;Nichole D Schueck;Nichole D Schueck;Nichole D Schueck

  • In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of pathogenesis

    Joëlle Michaud;Feng Wu;Motomi Osato;Gregory M. Cottles

  • Actionable, Pathogenic Incidental Findings in 1,000 Participants’ Exomes

    Michael O. Dorschner;Laura M. Amendola;Emily H. Turner;Peggy D. Robertson

  • Actionable exomic incidental findings in 6503 participants: challenges of variant classification

    Laura M. Amendola;Michael O. Dorschner;Peggy D. Robertson;Joseph S. Salama

  • Writing problems in developmental dyslexia: under-recognized and under-treated.

    Virginia W. Berninger;Kathleen H. Nielsen;Robert D. Abbott;Ellen Wijsman

  • Clonal development, stem-cell differentiation, and clinical remissions in acute nonlymphocytic leukemia

    Philip J. Fialkow;Jack W. Singer;Wendy H. Raskind;John W. Adamson

  • Relative Burden of Large CNVs on a Range of Neurodevelopmental Phenotypes

    Santhosh Girirajan;Zoran Brkanac;Bradley P. Coe;Carl Baker

  • Evidence for a Multistep Pathogenesis of a Myelodysplastic Syndrome

    Wendy H. Raskind;Wendy H. Raskind;Nagendra Tirumali;Nagendra Tirumali;Robert Jacobson;Robert Jacobson;Jack Singer;Jack Singer

  • Missense Mutations in the Regulatory Domain of PKCγ: A New Mechanism for Dominant Nonepisodic Cerebellar Ataxia

    Dong Hui Chen;Zoran Brkanac;Christophe L M J Verlinde;Xiao Jian Tan

  • X-linked thrombocytopenia with thalassemia from a mutation in the amino finger of GATA-1 affecting DNA binding rather than FOG-1 interaction

    Channing Yu;Kathy K. Niakan;Mark Matsushita;George Stamatoyannopoulos

  • Temperature-sensitive mutations in the III-IV cytoplasmic loop region of the skeletal muscle sodium channel gene in paramyotonia congenita.

    Andrea I. McClatchey;Peter Van den Bergh;Margaret A. Pericak-Vance;Wendy Raskind

  • Mutations in the EXT1 and EXT2 Genes in Hereditary Multiple Exostoses

    W. Wuyts;W. van Hul;K. de Boulle;J.J. Hendrickx

  • Expression of the gene defect in X-linked agammaglobulinemia.

    Mary Ellen Conley;Persymphonie Brown;Allan R. Pickard;Rebecca H. Buckley

  • A clinic-based study of the LRRK2 gene in Parkinson disease yields new mutations

    C. P. Zabetian;A. Samii;A. D. Mosley;J. W. Roberts

  • Gender differences in severity of writing and reading disabilities

    Virginia W. Berninger;Kathleen H. Nielsen;Robert D. Abbott;Ellen Wijsman

  • Hereditary Spastic Paraplegia Advances in Genetic Research

    J. K. Fink;T. Heiman-Patterson;T. Bird;F. Cambi

  • Complete deletion of the proteolipid protein gene (PLP) in a family with X-linked Pelizaeus-Merzbacher disease.

    Wendy H. Raskind;Charles A. Williams;Lynn D. Hudson;Thomas D. Bird

  • Modeling Phonological Core Deficits Within a Working Memory Architecture in Children and Adults With Developmental Dyslexia.

    Virginia W. Berninger;Robert D. Abbott;Jennifer Thomson;Richard Wagner

  • Loss of heterozygosity in chondrosarcomas for markers linked to hereditary multiple exostoses loci on chromosomes 8 and 11.

    W H Raskind;E U Conrad;H Chansky;M Matsushita

Frequent Co-Authors

Thomas D. Bird
Thomas D. Bird University of Washington
Ellen M. Wijsman
Ellen M. Wijsman University of Washington
Virginia W. Berninger
Virginia W. Berninger University of Washington
Jack W. Singer
Jack W. Singer University of Washington
Deborah A. Nickerson
Deborah A. Nickerson University of Washington
Michael O. Dorschner
Michael O. Dorschner University of Washington
Robert D. Abbott
Robert D. Abbott University of Washington
Raphael Bernier
Raphael Bernier University of Washington
Peter H. Byers
Peter H. Byers University of Washington
Evan E. Eichler
Evan E. Eichler University of Washington

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