World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
65
Citations
14527
World Ranking
2707
National Ranking
94

Overview

Elizabeth Baker is affiliated with Pathwest Laboratory Medicine in Australia and specializes in the field of Medicine with a focus on Obstetrics and Gynecology, Rheumatology, and Public Health, Environmental and Occupational Health. Their research primarily addresses maternal and perinatal health interventions, pelvic floor disorders treatments, and pregnancy-related medical research.

Their publication record includes works in several reputable scientific journals, such as the American Journal of Obstetrics & Gynecology MFM, American Journal of Obstetrics and Gynecology, European Journal of Obstetrics & Gynecology and Reproductive Biology, and Nutrients.

Baker's recent papers include:

  • Traction vs no traction in Foley catheter use for induction of labor: a systematic review and meta-analysis of randomized trials, 2022, American Journal of Obstetrics & Gynecology MFM
  • Infectious morbidity associated with early amniotomy during labor induction, 2021, American Journal of Obstetrics and Gynecology
  • Infectious morbidity associated with early amniotomy during labor induction, 2025, European Journal of Obstetrics & Gynecology and Reproductive Biology
  • Effects of Greek Yogurt Supplementation and Exercise on Markers of Bone Turnover and Inflammation in Older Adult Exercisers: An 8-Week Pilot Intervention Trial, 2025, Nutrients

Their collaborations extend to frequent co-authors including Corina N. Schoen, Ravneet Thind, Gabriele Saccone, Vincenzo Berghella, and Lauren C. Orr, reflecting a network of specialists active in similar research areas.

Elizabeth Baker's contributions span topics centered on:

  • Maternal and Perinatal Health Interventions
  • Pelvic floor disorders treatments
  • Pregnancy-related medical research

Best Publications

  • Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n.

    EJ Kremer;M Pritchard;M Lynch;S Yu

  • Fragile X genotype characterized by an unstable region of DNA

    S. Yu;M. Pritchard;E. Kremer;M. Lynch

  • CD30 antigen, a marker for Hodgkin's lymphoma, is a receptor whose ligand defines an emerging family of cytokines with homology to TNF

    Craig A. Smith;Hans Juergen Gruss;Terri Davis;Dirk Anderson

  • Molecular characterization of murine and human OX40/OX40 ligand systems: identification of a human OX40 ligand as the HTLV-1-regulated protein gp34.

    P.R. Baum;R.B. Gayle rd;F. Ramsdell;S. Srinivasan

  • Molecular and biological characterization of a ligand for CD27 defines a new family of cytokines with homology to tumor necrosis factor

    Raymond G. Goodwin;Mark R. Alderson;Craig A. Smith;Richard J. Armitage

  • Molecular and biological characterization of human 4-1BB and its ligand.

    Mark R. Alderson;Craig A. Smith;Teresa W. Tough;Terri Davis-Smith

  • bcl-w, a novel member of the bcl-2 family, promotes cell survival.

    Leonie Gibson;Shaun P. Holmgreen;David C.S. Huang;Ora Bernard

  • The CD39 lymphoid cell activation antigen. Molecular cloning and structural characterization.

    C R Maliszewski;G J Delespesse;M A Schoenborn;R J Armitage

  • Common chromosomal fragile site FRA16D sequence: identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells

    Karin Ried;Merran Finnis;Lynne Hobson;Marie Mangelsdorf

  • Myeloid DAP12-associating lectin (MDL)-1 is a cell surface receptor involved in the activation of myeloid cells

    Alexander B. H. Bakker;Elizabeth Baker;Grant R. Sutherland;Joseph H. Phillips

  • Fragile X syndrome without CCG amplification has an FMR1 deletion.

    Gedeon Ak;Baker E;Robinson H;Partington Mw

  • Localization of the human multiple drug resistance gene, MDR1, to 7q21.1.

    D F Callen;E Baker;R N Simmers;R Seshadri

  • Cloning, chromosomal mapping and characterization of the human metal-regulatory transcription factor MTF-1.

    Enrico Brugnera;Oleg Georgiev;Freddy Radtke;Rainer Heuchel

  • Fragile sites still breaking

    Grant R Sutherland;Elizabeth Baker;Elizabeth Baker;Robert I Richards;Robert I Richards

  • Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2

    C. Jones;L. Penny;T. Mattina;S. Yu

  • Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeat

    Sui Yu;Marie Mangelsdorf;Duncan Hewett;Lynne Hobson

  • Genomic organization, exact localization, and tissue expression of the human CD26 (dipeptidyl peptidase IV) gene.

    Catherine A. Abbott;Geoffrey W. McCaughan;Elizabeth Baker;Grant R. Sutherland

  • The mouse CD69 gene. Structure, expression, and mapping to the NK gene complex.

    Steven F. Ziegler;Steven D. Levin;Lisabeth Johnson;Neal G. Copeland

  • Structure and chromosomal localization of the human renal kallikrein gene.

    B A Evans;Z X Yun;J A Close;G W Tregear

  • Cloning of the sulphamidase gene and identification of mutations in Sanfilippo A syndrome

    H. S. Scott;L. Blanch;Xiao-Hui Guo;C. Freeman

Frequent Co-Authors

Grant R. Sutherland
Grant R. Sutherland University of Adelaide
David F. Callen
David F. Callen University of Adelaide
Robert I. Richards
Robert I. Richards University of Adelaide
John C. Mulley
John C. Mulley Bangor University
Eric Haan
Eric Haan University of Adelaide
Eric J. Kremer
Eric J. Kremer University of Montpellier
Jozef Gecz
Jozef Gecz University of Adelaide
John J. Hopwood
John J. Hopwood University of Adelaide
Peter R. Schofield
Peter R. Schofield Neuroscience Research Australia
Nancy A. Jenkins
Nancy A. Jenkins The University of Texas MD Anderson Cancer Center

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