World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
50
Citations
10419
World Ranking
3919
National Ranking
1690

Robert J. Morell 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 Robert J. Morell 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: 90 publications — 4th percentile

4% of scientists in this discipline score the same or lower.

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

Robert J. Morell 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 Robert J. Morell 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: 50 D-Index — 11th percentile

11% of scientists in this discipline score the same or lower.

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

Overview

Robert J. Morell is affiliated with the National Institutes of Health in the United States. Their research spans multiple fields within biomedical science, focusing primarily on molecular biology, sensory systems, and neuroscience. Their work integrates biochemistry, genetics, molecular biology, and medicine.

The scientist's main fields of study include:

  • Biochemistry, Genetics and Molecular Biology
  • Neuroscience
  • Medicine

Morell's research also extends into subfields such as molecular biology, sensory systems, cognitive neuroscience, cell biology, and rheumatology.

  • Molecular Biology
  • Sensory Systems
  • Cognitive Neuroscience
  • Cell Biology
  • Rheumatology

The topics addressed in their scientific work cover diverse areas, particularly focused on hearing and cochlear function, as well as genetics and associated conditions. These include:

  • Hearing, Cochlea, Tinnitus, Genetics
  • Hearing Loss and Rehabilitation
  • Cancer-related molecular mechanisms research
  • Bone and Dental Protein Studies
  • Dental development and anomalies
  • Single-cell and spatial transcriptomics
  • Cellular transport and secretion

Morell has published extensively, with a record of papers appearing frequently in venues such as:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • Frontiers in Molecular Neuroscience
  • Clinical Genetics
  • Scientific Reports
  • Genes

Recent papers authored or co-authored by Morell illustrate their research interests:

  • Single-Cell RNA-Sequencing From Mouse Incisor Reveals Dental Epithelial Cell-Type Specific Genes, 2020, Frontiers in Cell and Developmental Biology
  • TGF-β uncouples glycolysis and inflammation in macrophages and controls survival during sepsis, 2023, Science Signaling
  • Characterizing Adult Cochlear Supporting Cell Transcriptional Diversity Using Single-Cell RNA-Seq: Validation in the Adult Mouse and Translational Implications for the Adult Human Cochlea, 2020, Frontiers in Molecular Neuroscience
  • Characterization of rare spindle and root cell transcriptional profiles in the stria vascularis of the adult mouse cochlea, 2020, Scientific Reports
  • Single-Cell RNA-Seq of Cisplatin-Treated Adult Stria Vascularis Identifies Cell Type-Specific Regulatory Networks and Novel Therapeutic Gene Targets, 2021, Frontiers in Molecular Neuroscience

Collaboration is a significant aspect of Morell's work, with frequent co-authors including:

  • Michael Hoa
  • Shoujun Gu
  • Rafal T. Olszewski
  • Thomas B. Friedman
  • Daniel Martı́n

Best Publications

  • Mutations in the Connexin 26 Gene (GJB2) among Ashkenazi Jews with Nonsyndromic Recessive Deafness

    Morell Rj;Kim Hj;Hood Lj;Goforth L

  • Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23

    Julie M. Bork;Linda M. Peters;Saima Riazuddin;Saima Riazuddin;Steve L. Bernstein

  • Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29.

    Edward R Wilcox;Quianna L Burton;Sadaf Naz;Saima Riazuddin;Saima Riazuddin

  • Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene

    Frank J. Probst;Robert A. Fridell;Yehoash Raphael;Thomas L. Saunders

  • Association of Unconventional Myosin MYO15 Mutations with Human Nonsyndromic Deafness DFNB3

    Aihui Wang;Yong Liang;Robert A. Fridell;Frank J. Probst

  • Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F.

    Zubair M. Ahmed;Saima Riazuddin;Steve L. Bernstein;Zahoor Ahmed

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

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

  • A dysbiotic microbiome triggers T H 17 cells to mediate oral mucosal immunopathology in mice and humans.

    Nicolas Dutzan;Nicolas Dutzan;Tetsuhiro Kajikawa;Loreto Abusleme;Loreto Abusleme;Teresa Greenwell-Wild

  • CDH23 Mutation and Phenotype Heterogeneity: A Profile of 107 Diverse Families with Usher Syndrome and Nonsyndromic Deafness

    L.M. Astuto;J.M. Bork;M.D. Weston;J.W. Askew

  • Mutations in the γ-Actin Gene (ACTG1) Are Associated with Dominant Progressive Deafness (DFNA20/26)

    M. Zhu;T. Yang;S. Wei;A.T. DeWan

  • Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease

    Emma M. Jenkinson;Atteeq U. Rehman;Tom Walsh;Jill Clayton-Smith

  • Targeted Capture and Next-Generation Sequencing Identifies C9orf75, Encoding Taperin, as the Mutated Gene in Nonsyndromic Deafness DFNB79

    Atteeq Ur Rehman;Atteeq Ur Rehman;Robert J. Morell;Inna A. Belyantseva;Shahid Y. Khan

  • Single-cell RNA-Seq resolves cellular complexity in sensory organs from the neonatal inner ear

    Joseph C. Burns;Michael C. Kelly;Michael Hoa;Robert J. Morell

  • Mutations of MYO6 Are Associated with Recessive Deafness, DFNB37

    Zubair M. Ahmed;Robert J. Morell;Saima Riazuddin;Andrea Gropman

  • Modification of Human Hearing Loss by Plasma-Membrane Calcium Pump PMCA2

    Julie M. Schultz;Yandan Yang;Ariel J. Caride;Adelaida G. Filoteo

  • Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probands.

    Arti Pandya;Kathleen S. Arnos;Xia J. Xia;Katherine O. Welch

  • Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locus.

    Sadaf Naz;Chantal M. Giguere;David C. Kohrman;Kristina L. Mitchem

  • Spatiotemporal pattern and isoforms of cadherin 23 in wild type and waltzer mice during inner ear hair cell development.

    Ayala Lagziel;Zubair M. Ahmed;Julie M. Schultz;Robert J. Morell

  • Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28

    Linda M. Peters;David W. Anderson;Andrew J. Griffith;Kenneth M. Grundfast

  • Loss-of-Function Mutations of ILDR1 Cause Autosomal-Recessive Hearing Impairment DFNB42

    Guntram Borck;Atteeq Ur Rehman;Atteeq Ur Rehman;Kwanghyuk Lee;Hans Martin Pogoda

Frequent Co-Authors

Thomas B. Friedman
Thomas B. Friedman National Institutes of Health
Sheikh Riazuddin
Sheikh Riazuddin University of Health Sciences Lahore
Saima Riazuddin
Saima Riazuddin University of Maryland, Baltimore
Andrew J. Griffith
Andrew J. Griffith National Institutes of Health
Zubair M. Ahmed
Zubair M. Ahmed University of Maryland, Baltimore
Shaheen N. Khan
Shaheen N. Khan University of the Punjab
Inna A. Belyantseva
Inna A. Belyantseva National Institutes of Health
Suzanne M. Leal
Suzanne M. Leal Columbia University Medical Center
Wasim Ahmad
Wasim Ahmad Quaid-i-Azam University
Richard J.H. Smith
Richard J.H. Smith University of Iowa

If you think any of the details on this page are incorrect, let us know.

Report an issue

We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:

Related Online Degrees & Career Pathways

Genetics opens doors to a wide range of healthcare careers, many of which require advanced education and specialized skills. Professionals seeking to deepen their understanding of genetics or transition into healthcare roles can explore several affordable online degree options tailored to different career pathways.

For those interested in direct patient care at an advanced level, affordable online fnp programs can lead to a rewarding career as a Family Nurse Practitioner. Nursing is another foundation for those intrigued by genetics, and there are many most affordable nursing programs available online for entry-level or advancing nurses.

Nurses aiming to move into leadership or research roles related to genetics may consider msn to dnp programs online, which provide advanced clinical and academic expertise. RNs looking to expand their professional horizon or specialize further can benefit from rn to bsn cheapest programs, offering greater flexibility and affordability.

By leveraging these online degree pathways, students and working professionals can integrate genetics into diverse careers while managing costs and career advancement.

Best Scientists Citing Robert J. Morell

Trending Scientists

Recently Published Articles