World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
47
Citations
7623
World Ranking
4129
National Ranking
19

G. Jane Farrar 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 G. Jane Farrar 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: 142 publications — 26th percentile

26% of scientists in this discipline score the same or lower.

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

G. Jane Farrar 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 G. Jane Farrar 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: 47 D-Index — 6th percentile

6% of scientists in this discipline score the same or lower.

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

Overview

G. Jane Farrar is affiliated with Trinity College Dublin in Ireland and is an active researcher in the fields of biochemistry, genetics, and molecular biology, with additional work in medicine. Their research portfolio includes 61 publications in biochemistry, genetics, and molecular biology, and 16 in medicine, reflecting a strong interdisciplinary focus. The scientist's subfields of study emphasize molecular biology, genetics, and ophthalmology, alongside sensory systems and cell biology.

The main topics of Farrar's research focus on retinal development and disorders, retinal diseases and treatments, CRISPR and genetic engineering, RNA regulation and disease, genomics and rare diseases, virus-based gene therapy research, and advanced biosensing and bioanalysis techniques.

Recent publications by Farrar include:

  • Modeling and Rescue of RP2 Retinitis Pigmentosa Using iPSC-Derived Retinal Organoids (2020, Stem Cell Reports)
  • Next-Generation Sequencing Applications for Inherited Retinal Diseases (2021, International Journal of Molecular Sciences)
  • Findings from a Genotyping Study of over 1000 People with Inherited Retinal Disorders in Ireland (2020, Genes)
  • Whole genome sequencing and in vitro splice assays reveal genetic causes for inherited retinal diseases (2021, npj Genomic Medicine)
  • Usher syndrome type IV: clinically and molecularly confirmed by novel ARSG variants (2022, Human Genetics)

Farrar frequently publishes in a variety of scientific journals. The most common venues include:

  • International Journal of Molecular Sciences
  • bioRxiv (Cold Spring Harbor Laboratory)
  • Genes
  • Frontiers in Neuroscience
  • Scientific Reports

Throughout their career, Farrar has collaborated closely with several co-authors, including:

  • Paul F. Kenna
  • Naomi Chadderton
  • Arpad Palfi
  • Adrian Dockery
  • Laura Whelan

Best Publications

  • Retinopathy induced in mice by targeted disruption of the rhodopsin gene

    Humphries Mm;Rancourt D;Farrar Gj;Kenna P;Kenna P

  • NLRP3 has a protective role in age-related macular degeneration through the induction of IL-18 by drusen components

    Sarah L. Doyle;Matthew Campbell;Ema Ozaki;Robert G. Salomon

  • Autosomal dominant retinitis pigmentosa (ADRP): Localization of an ADRP gene to the long arm of chromosome 3

    Peter McWilliam;G.Jane Farrar;Paul Kenna;Daniel G. Bradley

  • On the genetics of retinitis pigmentosa and on mutation-independent approaches to therapeutic intervention

    G. Jane Farrar;Paul F. Kenna;Peter Humphries

  • On the molecular genetics of retinitis pigmentosa

    P Humphries;P Kenna;GJ Farrar

  • Effective delivery of large genes to the retina by dual AAV vectors

    Ivana Trapani;Pasqualina Colella;Andrea Sommella;Carolina Iodice

  • RNA interference-mediated suppression and replacement of human rhodopsin in vivo.

    Mary O’Reilly;Arpad Palfi;Naomi Chadderton;Sophia Millington-Ward

  • Retinal cells integrate into the outer nuclear layer and differentiate into mature photoreceptors after subretinal transplantation into adult mice.

    Udo Bartsch;Wasi Oriyakhel;Paul F. Kenna;Stephan Linke

  • Altered retinal microRNA expression profile in a mouse model of retinitis pigmentosa.

    Carol J Loscher;Karsten Hokamp;Paul F Kenna;Alasdair C Ivens

  • Improved retinal function in a mouse model of dominant retinitis pigmentosa following AAV-delivered gene therapy.

    Naomi Chadderton;Sophia Millington-Ward;Arpad Palfi;Mary O'Reilly

  • Suppression and Replacement Gene Therapy for Autosomal Dominant Disease in a Murine Model of Dominant Retinitis Pigmentosa

    Sophia Millington-Ward;Naomi Chadderton;Mary O'Reilly;Arpad Palfi

  • A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement

    Sara J. Bowne;Marian M. Humphries;Lori S. Sullivan;Paul F. Kenna;Paul F. Kenna

  • Autosomal dominant retinitis pigmentosa: linkage to rhodopsin and evidence for genetic heterogeneity

    G. Jane Farrar;Peter McWilliam;Daniel G. Bradley;Paul Kenna

  • CHD5 Is Required for Neurogenesis and Has a Dual Role in Facilitating Gene Expression and Polycomb Gene Repression

    Chris M. Egan;Ulrika Nyman;Julie Skotte;Gundula Streubel

  • Retinitis Pigmentosa and Progressive Sensorineural Hearing Loss Caused by a C12258A Mutation in the Mitochondrial MTTS2 Gene

    Fiona C. Mansergh;Sophia Millington-Ward;Avril Kennan;Anna-Sophia Kiang

  • Modeling and Rescue of RP2 Retinitis Pigmentosa Using iPSC-Derived Retinal Organoids.

    Amelia Lane;Katarina Jovanovic;Ciara Shortall;Daniele Ottaviani

  • A NOVEL MUTATION WITHIN THE RHODOPSIN GENE (THR-94-ILE) CAUSING AUTOSOMAL DOMINANT CONGENITAL STATIONARY NIGHT BLINDNESS

    Najma al-Jandal;G. Jane Farrar;Anna-Sophia Kiang;Marian M. Humphries

  • Toward a Gene Therapy for Dominant Disease: Validation of an RNA Interference-Based Mutation-Independent Approach

    Anna-Sophia Kiang;Arpad Palfi;Marius Ader;Paul F. Kenna

  • Autosomal dominant retinitis pigmentosa: localization of a disease gene (RP6) to the short arm of chromosome 6.

    G.Jane Farrar;Siobhán A. Jordan;Paul Kenna;Marian M. Humphries

  • On the molecular pathology of neurodegeneration in IMPDH1-based retinitis pigmentosa

    Aileen Aherne;Avril Kennan;Paul F. Kenna;Niamh McNally

Frequent Co-Authors

Paul F. Kenna
Paul F. Kenna Trinity College Dublin
Peter Humphries
Peter Humphries Trinity College Dublin
Frans P.M. Cremers
Frans P.M. Cremers Radboud University
Karsten Hokamp
Karsten Hokamp Trinity College Dublin
Caroline C W Klaver
Caroline C W Klaver Erasmus University Rotterdam
Stephen P. Daiger
Stephen P. Daiger The University of Texas Health Science Center at Houston
Alison J. Hardcastle
Alison J. Hardcastle University College London
Christian Gilissen
Christian Gilissen Radboud University
Daniel G. Bradley
Daniel G. Bradley Trinity College Dublin
Uwe Wolfrum
Uwe Wolfrum Johannes Gutenberg University of Mainz

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