World's Best Scientists 2026 revealed!
Karen B. Avraham

Karen B. Avraham

D-Index & Metrics

Genetics

D-Index
64
Citations
17128
World Ranking
2773
National Ranking
23

Karen B. Avraham 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 Karen B. Avraham 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: 190 publications — 46th percentile

46% of scientists in this discipline score the same or lower.

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

Karen B. Avraham 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 Karen B. Avraham 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: 64 D-Index — 37th percentile

37% 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

  • Member of the European Molecular Biology Organization (EMBO)
  • Member of the European Molecular Biology Organization (EMBO)

Overview

Karen B. Avraham is affiliated with Tel Aviv University in Israel and focuses their research primarily within the fields of biochemistry, genetics, and molecular biology, as well as neuroscience. Their work spans a range of molecular and cellular topics related to hearing and auditory disorders.

The main subfields of study they contribute to include:

  • Molecular Biology
  • Sensory Systems
  • Genetics
  • Cancer Research
  • Cell Biology

Their research interests cover several key topics such as hearing, cochlea, tinnitus, and genetics; RNA regulation and disease; cancer-related molecular mechanisms; ear surgery and otitis media; vestibular and auditory disorders; RNA and protein synthesis mechanisms; and genomics and rare diseases.

Recent publications by Karen B. Avraham include:

  • Neonatal AAV gene therapy rescues hearing in a mouse model of SYNE4 deafness (2020), published in EMBO Molecular Medicine
  • Mechanical forces drive ordered patterning of hair cells in the mammalian inner ear (2020), published in Nature Communications
  • Genomic analysis of inherited hearing loss in the Palestinian population (2020), published in Proceedings of the National Academy of Sciences
  • Disease-specific ACMG/AMP guidelines improve sequence variant interpretation for hearing loss (2021), published in Genetics in Medicine
  • Auditory Performance in Recovered SARS-COV-2 Patients (2020), published in Otology & Neurotology

Frequent co-authors collaborating with Karen B. Avraham include:

  • Shahar Taiber
  • Zippora Brownstein
  • Amiel A. Dror
  • Mor Bordeynik-Cohen
  • Tal Koffler-Brill

They have published multiple articles in well-known venues such as bioRxiv (Cold Spring Harbor Laboratory), Human Genetics, EMBO Molecular Medicine, Proceedings of the National Academy of Sciences, and Otology & Neurotology, demonstrating an extensive contribution to auditory and genetic research literature.

Karen B. Avraham is recognized as a member of the European Molecular Biology Organization (EMBO), indicating association with a broader scientific community dedicated to molecular biology research.

Best Publications

  • Targeted Disruption of the Mouse Caspase 8 Gene Ablates Cell Death Induction by the TNF Receptors, Fas/Apo1, and DR3 and Is Lethal Prenatally

    Eugene E Varfolomeev;Marcus Schuchmann;Victor Luria;Nuchanard Chiannilkulchai

  • Genome-wide, large-scale production of mutant mice by ENU mutagenesis

    M. H. Hrabe de Angelis;H. Flaswinkel;H. Fuchs;B. Rathkolb

  • GJB2 mutations and degree of hearing loss: a multicenter study.

    Rikkert L. Snoeckx;Patrick L M Huygen;Delphine Feldmann;Sandrine Marlin

  • The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells

    Karen B. Avraham;Tama Hasson;Karen P. Steel;David M. Kingsley

  • Transgenic mice with increased Cu/Zn-superoxide dismutase activity: animal model of dosage effects in Down syndrome.

    Charles J. Epstein;Karen B. Avraham;Michael Lovett;Sandra Smith

  • A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment

    F. J. Del Castillo;M. Rodriguez-Ballesteros;A. Alvarez;T. Hutchin

  • Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans.

    Oz Vahava;Robert Morell;Eric D. Lynch;Sigal Weiss

  • Expert specification of the ACMG/AMP variant interpretation guidelines for genetic hearing loss.

    Andrea M Oza;Andrea M Oza;Marina T DiStefano;Marina T DiStefano;Sarah E Hemphill;Brandon J Cushman

  • Prevalence and Evolutionary Origins of the del(GJB6-D13S1830) Mutation in the DFNB1 Locus in Hearing-Impaired Subjects: a Multicenter Study

    Ignacio Del Castillo;Miguel A. Moreno-Pelayo;Francisco J. Del Castillo;Zippora Brownstein

  • Whole Exome Sequencing and Homozygosity Mapping Identify Mutation in the Cell Polarity Protein GPSM2 as the Cause of Nonsyndromic Hearing Loss DFNB82

    Tom Walsh;Hashem Shahin;Tal Elkan-Miller;Ming K. Lee

  • Role of myosin VI in the differentiation of cochlear hair cells.

    Tim Self;Tama Sobe;Neal G. Copeland;Nancy A. Jenkins

  • Down's syndrome: Abnormal neuromuscular junction in tongue of transgenic mice with elevated levels of human Cu/Zn-superoxide dismutase

    Karen B. Avraham;Michael Schickler;Dan Sapoznikov;Rena Yarom

  • MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss

    Salvatore Melchionda;Nadav Ahituv;Luigi Bisceglia;Tama Sobe

  • Beethoven, a mouse model for dominant, progressive hearing loss DFNA36.

    Sarah Vreugde;Alexandra Erven;Corné J. Kros;Walter Marcotti

  • From flies' eyes to our ears: Mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30

    Tom Walsh;Vanessa Walsh;Sarah Vreugde;Ronna Hertzano

  • Hearing Loss: Mechanisms Revealed by Genetics and Cell Biology

    Amiel A. Dror;Karen B. Avraham

  • Transcription profiling of inner ears from Pou4f3ddl/ddl identifies Gfi1 as a target of the Pou4f3 deafness gene

    Ronna Hertzano;Ronna Hertzano;Mireille Montcouquiol;Sharon Rashi-Elkeles;Rani Elkon

  • The Notch ligand Jagged1 is required for inner ear sensory development

    A. E. Kiernan;N. Ahituv;H. Fuchs;Rudi Balling

  • Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in Middle Eastern families.

    Zippora Brownstein;Lilach M Friedman;Hashem Shahin;Varda Oron-Karni

  • Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22.

    Ingrid Zwaenepoel;Mirna Mustapha;Michel Leibovici;Elisabeth Verpy

Frequent Co-Authors

Mary Claire King
Mary Claire King University of Washington
Tom Walsh
Tom Walsh University of Washington
Mordechai Shohat
Mordechai Shohat Tel Aviv University
Yoram Groner
Yoram Groner Weizmann Institute of Science
Karen P. Steel
Karen P. Steel King's College London
Neal G. Copeland
Neal G. Copeland The University of Texas MD Anderson Cancer Center
Ming K. Lee
Ming K. Lee University of Washington
Nancy A. Jenkins
Nancy A. Jenkins The University of Texas MD Anderson Cancer Center
Thomas B. Friedman
Thomas B. Friedman National Institutes of Health
Heidi L. Rehm
Heidi L. Rehm Brigham and Women's Hospital

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