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Genetics

D-Index
53
Citations
10428
World Ranking
3730
National Ranking
436

Overview

Joy D. A. Delhanty is affiliated with University College London in the United Kingdom. Their research spans multiple intersecting fields related to human health and biology, primarily focusing on medicine and biochemistry, genetics, and molecular biology.

Delhanty's work covers several main topics, including:

  • Prenatal Screening and Diagnostics
  • Epigenetics and DNA Methylation
  • Reproductive Biology and Fertility

The scientist has published research in subfields such as pediatrics, perinatology and child health, molecular biology, and public health, environmental and occupational health. These areas highlight a multidisciplinary approach to understanding early human development and related health conditions.

One of the recent publications by Delhanty is titled Next Generation Sequencing Detects Premeiotic Errors in Human Oocytes, published in 2022 in the International Journal of Molecular Sciences. This paper has been cited 11 times and investigates genetic errors occurring before meiosis in human egg cells, contributing to knowledge in reproductive biology and genetic diagnostics.

Frequent collaborators include:

  • H. Ghevaria
  • Sioban SenGupta
  • Roy Naja
  • Rabi Odia
  • Holly Exeter

The International Journal of Molecular Sciences is a primary venue for Delhanty's research outputs, indicating a focus on molecular-level investigations within biological systems.

Delhanty's interdisciplinary research integrates molecular biology techniques with clinical applications in prenatal and reproductive health, contributing to diagnostics and understanding of epigenetic mechanisms. The scientist's work plays a role in advancing knowledge that intersects laboratory research and practical healthcare concerns.

Best Publications

  • Mutations truncating the EP300 acetylase in human cancers.

    Simon A. Gayther;Sarah J. Batley;Lori Linger;Andy Bannister

  • Biopsy of human preimplantation embryos and sexing by DNA amplification.

    A.H. Handyside;R.J.A. Penketh;R.M.L. Winston;J.K. Pattinson

  • Comprehensive chromosomal analysis of human preimplantation embryos using whole genome amplification and single cell comparative genomic hybridization

    Dagan Wells;Joy D.A. Delhanty

  • Multicolour FISH detects frequent chromosomal mosaicism and chaotic division in normal preimplantation embryos from fertile patients

    J. D. A. Delhanty;Joyce C. Harper;Asangla Ao;Alan H. Handyside

  • Detailed chromosomal and molecular genetic analysis of single cells by whole genome amplification and comparative genomic hybridisation

    Dagan Wells;Jon K. Sherlock;Alan H. Handyside;Joy D. A. Delhanty

  • Mosaicism of autosomes and sex chromosomes in morphologically normal, monospermic preimplantation human embryos.

    Joyce C. Harper;Joyce C. Harper;Edith Coonen;Alan H. Handyside;Robert M. L. Winston

  • Detection of aneuploidy and chromosomal mosaicism in human embryos during preimplantation sex determination by fluorescent in situ hybridisation, (FISH)

    Joy D.A. Delhanty;Darren K. Griffin;Alan H. Handyside;Joyce Harper

  • First clinical application of comparative genomic hybridization and polar body testing for preimplantation genetic diagnosis of aneuploidy.

    Dagan Wells;Dagan Wells;Tomas Escudero;Brynn Levy;Kurt Hirschhorn

  • Infertile couples with Robertsonian translocations: preimplantation genetic analysis of embryos reveals chaotic cleavage divisions

    C. M. Conn;Joyce C. Harper;Robert M. L. Winston;Joy D. A. Delhanty

  • Dual fluorescent in situ hybridisation for simultaneous detection of X and Y chromosome-specific probes for the sexing of human preimplantation embryonic nuclei.

    D. K. Griffin;L. J. Wilton;A. H. Handyside;R. M. L. Winston

  • Preimplantation Genetic Diagnosis of Inherited Cancer: Familial Adenomatous Polyposis Coli

    Asangla Ao;Dagan Wells;Alan H. Handyside;Robert M. L. Winston

  • Preimplantation genetic diagnosis: strategies and surprises.

    Alan H. Handyside;Joy D.A. Delhanty

  • Expression of genes regulating chromosome segregation, the cell cycle and apoptosis during human preimplantation development

    D. Wells;M.G. Bermudez;N. Steuerwald;A.R. Thornhill

  • Fall in implantation rates following ICSI with sperm with high DNA fragmentation

    B.E. Speyer;A.R. Pizzey;M. Ranieri;R. Joshi

  • Regionally clustered APC mutations are associated with a severe phenotype and occur at a high frequency in new mutation cases of adenomatous polyposis coli

    Simon A. Gayther;Dagan Wells;Sioban B. SenGupta;Pamela Chapman

  • Detailed FISH analysis of day 5 human embryos reveals the mechanisms leading to mosaic aneuploidy

    D.D. Daphnis;J.D.A. Delhanty;S. Jerkovic;J. Geyer

  • The UK Northern region genetic register for familial adenomatous polyposis coli: use of age of onset, congenital hypertrophy of the retinal pigment epithelium, and DNA markers in risk calculations.

    J Burn;P Chapman;J Delhanty;C Wood

  • FISH analysis on day 5 post-insemination of human arrested and blastocyst stage embryos

    Pornpimol Ruangvutilert;Joy D. A. Delhanty;Paul Serhal;Mara Simopoulou

  • The why, the how and the when of PGS 2.0: current practices and expert opinions of fertility specialists, molecular biologists, and embryologists.

    Karen Sermon;Antonio Capalbo;Jacques Cohen;Edith Coonen

  • MECHANISMS OF ANEUPLOIDY INDUCTION IN HUMAN OOGENESIS AND EARLY EMBRYOGENESIS

    Joy D A Delhanty

Frequent Co-Authors

Dagan Wells
Dagan Wells John Radcliffe Hospital
Darren K. Griffin
Darren K. Griffin University of Kent
Jude Fitzgibbon
Jude Fitzgibbon Queen Mary University of London
Mary B. Davis
Mary B. Davis University College London
David Hunt
David Hunt University of Edinburgh
John Burn
John Burn Newcastle University
Santiago Munné
Santiago Munné Saint Barnabas Medical Center
Jacques Cohen
Jacques Cohen Reprogenetics
Ian C. Talbot
Ian C. Talbot Leicester Royal Infirmary
Bruce A.J. Ponder
Bruce A.J. Ponder University of Cambridge

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