Luke St Heaps

630 total citations
22 papers, 379 citations indexed

About

Luke St Heaps is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Luke St Heaps has authored 22 papers receiving a total of 379 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 12 papers in Genetics and 5 papers in Plant Science. Recurrent topics in Luke St Heaps's work include Genomic variations and chromosomal abnormalities (9 papers), Chromosomal and Genetic Variations (5 papers) and Genetic Syndromes and Imprinting (4 papers). Luke St Heaps is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Chromosomal and Genetic Variations (5 papers) and Genetic Syndromes and Imprinting (4 papers). Luke St Heaps collaborates with scholars based in Australia, United States and Germany. Luke St Heaps's co-authors include Gregory B. Peters, Greg B. Peters, Art Daniel, Robyn V. Jamieson, John Grigg, Patrick Tam, Arabella Smith, Frank A. Billson, Nicole Chia and David J. Amor and has published in prestigious journals such as Cancer Research, Oncogene and International Journal of Molecular Sciences.

In The Last Decade

Luke St Heaps

22 papers receiving 353 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Luke St Heaps Australia 10 214 188 53 38 38 22 379
Anthony Raizis New Zealand 9 434 2.0× 136 0.7× 84 1.6× 22 0.6× 20 0.5× 18 550
Annemieke H. van der Hout Netherlands 8 227 1.1× 223 1.2× 25 0.5× 29 0.8× 13 0.3× 13 451
Anna Sowińska‐Seidler Poland 13 254 1.2× 237 1.3× 74 1.4× 21 0.6× 23 0.6× 38 409
Nora Wasserman United States 5 228 1.1× 150 0.8× 37 0.7× 17 0.4× 14 0.4× 6 479
K. Okui Japan 13 318 1.5× 119 0.6× 18 0.3× 12 0.3× 28 0.7× 18 447
Pauline A.M. Roest Netherlands 8 281 1.3× 111 0.6× 41 0.8× 25 0.7× 9 0.2× 8 461
Eddy N. de Boer Netherlands 8 213 1.0× 202 1.1× 32 0.6× 20 0.5× 7 0.2× 17 425
Anna Newlin United States 12 147 0.7× 210 1.1× 96 1.8× 13 0.3× 16 0.4× 17 425
E. Natt Germany 10 314 1.5× 84 0.4× 17 0.3× 19 0.5× 19 0.5× 13 510
L.A. Menlove Belgium 2 177 0.8× 165 0.9× 22 0.4× 43 1.1× 29 0.8× 2 342

Countries citing papers authored by Luke St Heaps

Since Specialization
Citations

This map shows the geographic impact of Luke St Heaps'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 Luke St Heaps with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Luke St Heaps more than expected).

Fields of papers citing papers by Luke St Heaps

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Luke St Heaps. 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 Luke St Heaps. The network helps show where Luke St Heaps may publish in the future.

Co-authorship network of co-authors of Luke St Heaps

This figure shows the co-authorship network connecting the top 25 collaborators of Luke St Heaps. A scholar is included among the top collaborators of Luke St Heaps 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 Luke St Heaps. Luke St Heaps 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.
Wright, Dale, Artur Darmanian, Luke St Heaps, et al.. (2023). Saliva DNA: An alternative biospecimen for single nucleotide polymorphism chromosomal microarray analysis in autism. American Journal of Medical Genetics Part A. 191(12). 2913–2920. 1 indexed citations
2.
Bennetts, Bruce, Artur Darmanian, Luke Jones, et al.. (2023). SNP chromosome microarray genotyping for detection of uniparental disomy in the clinical diagnostic laboratory. Pathology. 55(6). 818–826. 1 indexed citations
3.
Nash, Benjamin M., Alan Ma, Gladys Ho, et al.. (2022). Whole Genome Sequencing, Focused Assays and Functional Studies Increasing Understanding in Cryptic Inherited Retinal Dystrophies. International Journal of Molecular Sciences. 23(7). 3905–3905. 7 indexed citations
4.
Khan, Tayyaba, Luke St Heaps, Mark Dexter, et al.. (2021). FISH analysis of brain smears obtained at intraoperative diagnosis – An accurate and fast method to detect 1p/19q-codeletion in gliomas. Journal of Clinical Neuroscience. 92. 115–119. 1 indexed citations
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Pangon, Laurent, Marc Giry-Laterrière, Nicola Currey, et al.. (2015). JRK is a positive regulator of β-catenin transcriptional activity commonly overexpressed in colon, breast and ovarian cancer. Oncogene. 35(22). 2834–2841. 21 indexed citations
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Heaps, Luke St, Maree Flaherty, Frank A. Billson, et al.. (2008). Chromosomal Rearrangements and Novel Genes in Disorders of Eye Development, Cataract and Glaucoma. Twin Research and Human Genetics. 11(4). 412–421. 13 indexed citations
9.
Nolen, Leisha D., David J. Amor, Ashley Haywood, et al.. (2006). Deletion at 14q22‐23 indicates a contiguous gene syndrome comprising anophthalmia, pituitary hypoplasia, and ear anomalies. American Journal of Medical Genetics Part A. 140A(16). 1711–1718. 71 indexed citations
10.
Byrne, Jennifer A., Rosemary L. Balleine, Marlena S. Fejzo, et al.. (2005). Tumor protein D52 (TPD52) is overexpressed and a gene amplification target in ovarian cancer. International Journal of Cancer. 117(6). 1049–1054. 75 indexed citations
11.
Neas, Katherine, Janine Smith, Nicole Chia, et al.. (2005). Three patients with terminal deletions within the subtelomeric region of chromosome 9q. American Journal of Medical Genetics Part A. 132A(4). 425–430. 24 indexed citations
12.
Maclean, Kenneth N., James E. Smith, Luke St Heaps, et al.. (2005). Axenfeld-Rieger malformation and distinctive facial features: Clues to a recognizable 6p25 microdeletion syndrome. American Journal of Medical Genetics Part A. 132A(4). 381–385. 60 indexed citations
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Smith, Arabella, Luke St Heaps, & Lisa Robson. (2002). Apparently unrelated cytogenetic abnormalities among 462 probands referred for the detection of del(22q) by FISH. American Journal of Medical Genetics. 113(4). 346–350. 6 indexed citations
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Smith, Arabella, Lisa Robson, Luke St Heaps, et al.. (2001). Routine fluorescence in situ hybridization with the MLL probe does not reliably detect two separate signals on one chromosome 11 in patients with trisomy 11. Cancer Genetics and Cytogenetics. 129(2). 173–176. 1 indexed citations
18.
Sharma, Praveen, et al.. (2001). Complex variant t(4;11) characterized by fluorescence in situ hybridization in infant acute lymphoblastic leukemia. Cancer Genetics and Cytogenetics. 127(2). 177–180. 4 indexed citations
19.
Smith, Arabella, et al.. (2001). Abnormal dicentric chromosome with co-amplification of sequences from chromosomes 11 and 19. Cancer Genetics and Cytogenetics. 130(1). 29–32. 4 indexed citations
20.
Smith, Arabella, Anna Jauch, Luke St Heaps, Lisa Robson, & Brian P. Kearney. (2000). Unbalanced translocation t(15;22) in ‘severe’ Prader–Willi syndrome. Annales de Génétique. 43(3-4). 125–130. 10 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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