Helen J. Eyre

5.1k total citations
63 papers, 3.8k citations indexed

About

Helen J. Eyre is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Helen J. Eyre has authored 63 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Molecular Biology, 25 papers in Genetics and 9 papers in Plant Science. Recurrent topics in Helen J. Eyre's work include Genomic variations and chromosomal abnormalities (16 papers), Genetics and Neurodevelopmental Disorders (14 papers) and Genomics and Chromatin Dynamics (9 papers). Helen J. Eyre is often cited by papers focused on Genomic variations and chromosomal abnormalities (16 papers), Genetics and Neurodevelopmental Disorders (14 papers) and Genomics and Chromatin Dynamics (9 papers). Helen J. Eyre collaborates with scholars based in Australia, United States and United Kingdom. Helen J. Eyre's co-authors include Grant R. Sutherland, David F. Callen, Elizabeth Baker, Eric Haan, Robert I. Richards, Mai H. Tran, Daniel H. Wreschner, Michael A. McGuckin, Joanna Crawford and Lynne Hobson and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Helen J. Eyre

63 papers receiving 3.7k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Helen J. Eyre Australia 33 2.3k 1.5k 483 475 426 63 3.8k
Roger V. Lebo United States 25 2.2k 1.0× 2.3k 1.5× 515 1.1× 243 0.5× 361 0.8× 70 5.0k
R S Sparkes United States 37 2.9k 1.3× 2.1k 1.4× 344 0.7× 476 1.0× 374 0.9× 142 5.1k
Glen A. Evans United States 36 2.3k 1.0× 861 0.6× 808 1.7× 246 0.5× 353 0.8× 80 4.0k
Rudolf Jaenisch United States 22 3.9k 1.7× 2.0k 1.3× 719 1.5× 237 0.5× 479 1.1× 27 5.8k
T. Mohandas United States 37 3.1k 1.4× 2.3k 1.5× 1.1k 2.3× 512 1.1× 427 1.0× 98 5.9k
Giuseppe Borsani Italy 37 3.1k 1.4× 1.2k 0.8× 485 1.0× 248 0.5× 307 0.7× 90 4.7k
Elizabeth Baker Australia 44 3.4k 1.5× 2.9k 1.9× 1.3k 2.7× 435 0.9× 629 1.5× 116 6.7k
Sohaila Rastan United Kingdom 27 3.0k 1.3× 2.2k 1.5× 450 0.9× 363 0.8× 156 0.4× 45 4.1k
Chih‐Lin Hsieh United States 33 3.6k 1.6× 988 0.7× 321 0.7× 212 0.4× 333 0.8× 77 4.2k
Heidemarie Neitzel Germany 30 2.5k 1.1× 1.5k 1.0× 357 0.7× 605 1.3× 549 1.3× 95 4.0k

Countries citing papers authored by Helen J. Eyre

Since Specialization
Citations

This map shows the geographic impact of Helen J. Eyre's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Helen J. Eyre with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Helen J. Eyre more than expected).

Fields of papers citing papers by Helen J. Eyre

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Helen J. Eyre. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Helen J. Eyre. The network helps show where Helen J. Eyre may publish in the future.

Co-authorship network of co-authors of Helen J. Eyre

This figure shows the co-authorship network connecting the top 25 collaborators of Helen J. Eyre. A scholar is included among the top collaborators of Helen J. Eyre based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Helen J. Eyre. Helen J. Eyre is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
McMahon, Jacinta M., Ingrid E. Scheffer, Jillian Nicholl, et al.. (2010). Detection of microchromosomal aberrations in refractory epilepsy: a pilot study. Epileptic Disorders. 12(3). 192–198. 14 indexed citations
2.
Heron, Sarah E., Ingrid E. Scheffer, Bronwyn E. Grinton, et al.. (2010). Familial neonatal seizures with intellectual disability caused by a microduplication of chromosome 2q24.3. Epilepsia. 51(9). 1865–1869. 24 indexed citations
3.
Cappello, Jean, Marjorie Coggan, Juleen A. Cavanaugh, et al.. (2008). Deletion of Glu155 causes a deficiency of glutathione transferase Omega 1-1 but does not alter sensitivity to arsenic trioxide and other cytotoxic drugs. The International Journal of Biochemistry & Cell Biology. 40(11). 2553–2559. 22 indexed citations
4.
Ingley, Evan, Peta A. Tilbrook, Martin Thompson, et al.. (2004). HLS5, a Novel RBCC (Ring Finger, B Box, Coiled-coil) Family Member Isolated from a Hemopoietic Lineage Switch, Is a Candidate Tumor Suppressor. Journal of Biological Chemistry. 279(9). 8181–8189. 24 indexed citations
5.
Bhalla, Kavita, Hilary A. Phillips, Joanna Crawford, et al.. (2004). The de novo chromosome 16 translocations of two patients with abnormal phenotypes (mental retardation and epilepsy) disrupt the A2BP1 gene. Journal of Human Genetics. 49(6). 308–311. 121 indexed citations
6.
Whitbread, Astrid K., Natasha Tetlow, Helen J. Eyre, Grant R. Sutherland, & Philip G. Board. (2003). Characterization of the human Omega class glutathione transferase genes and associated polymorphisms. Pharmacogenetics. 13(3). 131–144. 144 indexed citations
7.
Bouillet, Philippe, David C.S. Huang, Graham C. Webb, et al.. (2001). Gene structure, alternative splicing, and chromosomal localization of pro-apoptotic Bcl-2 relative Bim. Mammalian Genome. 12(2). 163–168. 127 indexed citations
8.
Zamostiano, Rachel, Albert Pinhasov, E. Gelber, et al.. (2001). Cloning and Characterization of the Human Activity-dependent Neuroprotective Protein. Journal of Biological Chemistry. 276(1). 708–714. 192 indexed citations
9.
Hulett, Mark D., Eloisa Pagler, J. Hornby, et al.. (2001). Isolation, Tissue Distribution, and Chromosomal Localization of a Novel Testis-Specific Human Four-Transmembrane Gene Related to CD20 and FcϵRI-β. Biochemical and Biophysical Research Communications. 280(1). 374–379. 14 indexed citations
10.
Shimizu, Yoshio, Shin‐ichiro Honda, Katsumi Yotsumoto, et al.. (2001). Fcα/µ receptor is a single gene-family member closely related to polymeric immunoglobulin receptor encoded on Chromosome 1. Immunogenetics. 53(8). 709–711. 29 indexed citations
11.
Shibuya, Akira, Norihisa Sakamoto, Yoshio Shimizu, et al.. (2000). Fcα/μ receptor mediates endocytosis of IgM-coated microbes. Nature Immunology. 1(5). 441–446. 300 indexed citations
12.
Liu, Marjorie, Rachel M.C. Parker, Helen J. Eyre, et al.. (1999). GPR56, a Novel Secretin-like Human G-Protein-Coupled Receptor Gene. Genomics. 55(3). 296–305. 76 indexed citations
13.
Liu, Xifu, Elizabeth Baker, Helen J. Eyre, Grant R. Sutherland, & Mingdong Zhou. (1999). γ-Heregulin: a fusion gene of DOC-4 and neuregulin-1 derived from a chromosome translocation. Oncogene. 18(50). 7110–7114. 25 indexed citations
14.
Kuss, Bryone J., Geraldine M. O’Neill, Helen J. Eyre, et al.. (1998). ARA,a Novel ABC Transporter, Is Located at 16p13.1, Is Deleted in inv(16) Leukemias, and Is Shown To Be Expressed in Primitive Hematopoietic Precursors. Genomics. 51(3). 455–458. 14 indexed citations
15.
Robert, Stanley, et al.. (1998). The Identification and Localization of a Human Gene with Sequence Similarity toPolycomblikeofDrosophila melanogaster. Genomics. 48(3). 381–383. 41 indexed citations
16.
Tymms, Martin J., Annie Ng, Ross S. Thomas, et al.. (1997). A novel epithelial-expressed ETS gene, ELF3: human and murine cDNA sequences, murine genomic organization, human mapping to 1q32.2 and expression in tissues and cancer. Oncogene. 15(20). 2449–2462. 127 indexed citations
17.
Yu, Sui, Marie Mangelsdorf, D. Hewett, et al.. (1997). Human Chromosomal Fragile Site FRA16B Is an Amplified AT-Rich Minisatellite Repeat. Cell. 88(3). 367–374. 155 indexed citations
18.
Kuss, Bryone J., Helen J. Eyre, Sharon Lane, et al.. (1994). Deletion of gene for multidrug resistance in acute myeloid leukaemia with inversion in chromosome 16: prognostic implications. The Lancet. 343(8912). 1531–1534. 88 indexed citations
19.
Callen, David F., Norman A. Doggett, Raymond L. Stallings, et al.. (1992). High-resolution cytogenetic-based physical map of human chromosome 16. Genomics. 13(4). 1178–1185. 44 indexed citations
20.
Callen, David F., et al.. (1992). Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes. American Journal of Medical Genetics. 43(4). 709–715. 109 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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