Elizabeth Spiteri

5.1k total citations · 1 hit paper
28 papers, 2.9k citations indexed

About

Elizabeth Spiteri is a scholar working on Genetics, Molecular Biology and Ocean Engineering. According to data from OpenAlex, Elizabeth Spiteri has authored 28 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 11 papers in Molecular Biology and 7 papers in Ocean Engineering. Recurrent topics in Elizabeth Spiteri's work include Genomic variations and chromosomal abnormalities (8 papers), Enhanced Oil Recovery Techniques (7 papers) and Congenital heart defects research (6 papers). Elizabeth Spiteri is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Enhanced Oil Recovery Techniques (7 papers) and Congenital heart defects research (6 papers). Elizabeth Spiteri collaborates with scholars based in United States, United Kingdom and Netherlands. Elizabeth Spiteri's co-authors include Franklin M. Orr, Rubén Juanes, Martin J. Blunt, Ruben Juanes, Daniel H. Geschwind, Simon E. Fisher, Sonja C. Vernes, Matthias Groszer, Jérôme Nicod and Kay E. Davies and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Blood and Neurology.

In The Last Decade

Elizabeth Spiteri

28 papers receiving 2.8k citations

Hit Papers

Impact of relative permeability hysteresis on geological ... 2006 2026 2012 2019 2006 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elizabeth Spiteri United States 19 1.1k 995 837 614 527 28 2.9k
Ichirô KIMURA Japan 24 97 0.1× 78 0.1× 411 0.5× 84 0.1× 80 0.2× 194 2.0k
Qingsong Tang China 17 21 0.0× 52 0.1× 1.1k 1.3× 120 0.2× 70 0.1× 53 2.0k
Robert F. Mueller United Kingdom 21 47 0.0× 22 0.0× 859 1.0× 16 0.0× 479 0.9× 37 1.7k
Matthew Kirkham United Kingdom 22 120 0.1× 256 0.3× 2.4k 2.9× 20 0.0× 214 0.4× 40 3.9k
Adrian Wolny Germany 8 27 0.0× 53 0.1× 811 1.0× 78 0.1× 73 0.1× 11 2.0k
Stuart Berg United States 4 26 0.0× 52 0.1× 752 0.9× 71 0.1× 90 0.2× 5 1.9k
Sihan Liu China 21 41 0.0× 20 0.0× 243 0.3× 130 0.2× 31 0.1× 118 1.2k
Yalan Zhang China 17 35 0.0× 12 0.0× 354 0.4× 107 0.2× 78 0.1× 81 1.3k
Hao Ding China 21 59 0.1× 54 0.1× 295 0.4× 7 0.0× 54 0.1× 123 1.5k
Gustavo A. Gomez United States 18 17 0.0× 68 0.1× 765 0.9× 83 0.1× 77 0.1× 30 1.1k

Countries citing papers authored by Elizabeth Spiteri

Since Specialization
Citations

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

Fields of papers citing papers by Elizabeth Spiteri

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Elizabeth Spiteri. 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 Elizabeth Spiteri. The network helps show where Elizabeth Spiteri may publish in the future.

Co-authorship network of co-authors of Elizabeth Spiteri

This figure shows the co-authorship network connecting the top 25 collaborators of Elizabeth Spiteri. A scholar is included among the top collaborators of Elizabeth Spiteri 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 Elizabeth Spiteri. Elizabeth Spiteri 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.
Church, Alanna J., Yassmine Akkari, Kristin K. Deeb, et al.. (2024). Section E6.7-6.12 of the American College of Medical Genetics and Genomics (ACMG) Technical Laboratory Standards: Cytogenomic studies of acquired chromosomal abnormalities in solid tumors. Genetics in Medicine. 26(4). 101070–101070. 2 indexed citations
2.
Wigby, Kristen, Deanna Brockman, Gregory Costain, et al.. (2024). Evidence review and considerations for use of first line genome sequencing to diagnose rare genetic disorders. npj Genomic Medicine. 9(1). 15–15. 8 indexed citations
3.
Jobanputra, Vaidehi, Brock E. Schroeder, Heidi L. Rehm, et al.. (2024). Advancing access to genome sequencing for rare genetic disorders: recent progress and call to action. npj Genomic Medicine. 9(1). 23–23. 7 indexed citations
4.
Khanna, Vishesh, Rong Lü, Jyoti Kumar, et al.. (2023). The clinical, molecular, and prognostic features of the 2022 WHO and ICC classification systems for myelodysplastic neoplasms. Leukemia Research. 136. 107433–107433. 5 indexed citations
5.
Lindström, S., Stuart A. Scott, Elizabeth Spiteri, et al.. (2023). Two epilepsy‐associated variants in KCNA2 (KV1.2) at position H310 oppositely affect channel functional expression. The Journal of Physiology. 601(23). 5367–5389. 6 indexed citations
6.
Taylor‐Harding, Barbie, Paul‐Joseph Aspuria, Hasmik Agadjanian, et al.. (2014). Cyclin E1 and RTK/RAS signaling drive CDK inhibitor resistance via activation of E2F and ETS. Oncotarget. 6(2). 696–714. 88 indexed citations
7.
Paquette, Ronald, John Nicoll, Meenal Chalukya, et al.. (2011). Frequent EVI1 translocations in myeloid blast crisis CML that evolves through tyrosine kinase inhibitors. Cancer Genetics. 204(7). 392–397. 28 indexed citations
8.
Vernes, Sonja C., Peter L. Oliver, Elizabeth Spiteri, et al.. (2011). Foxp2 Regulates Gene Networks Implicated in Neurite Outgrowth in the Developing Brain. PLoS Genetics. 7(7). e1002145–e1002145. 205 indexed citations
9.
Miller, Julie E., et al.. (2008). Birdsong Decreases Protein Levels of FoxP2, a Molecule Required for Human Speech. Journal of Neurophysiology. 100(4). 2015–2025. 70 indexed citations
10.
Spiteri, Elizabeth, Robert J. Sims, Adriana Arita, et al.. (2007). FANCI is a second monoubiquitinated member of the Fanconi anemia pathway. Nature Structural & Molecular Biology. 14(6). 564–567. 223 indexed citations
11.
Spiteri, Elizabeth, Geneviève Konopka, Giovanni Coppola, et al.. (2007). Identification of the Transcriptional Targets of FOXP2, a Gene Linked to Speech and Language, in Developing Human Brain. The American Journal of Human Genetics. 81(6). 1144–1157. 211 indexed citations
12.
Vernes, Sonja C., Elizabeth Spiteri, Jérôme Nicod, et al.. (2007). High-Throughput Analysis of Promoter Occupancy Reveals Direct Neural Targets of FOXP2, a Gene Mutated in Speech and Language Disorders. The American Journal of Human Genetics. 81(6). 1232–1250. 194 indexed citations
13.
Oliveira, João Ricardo Mendes de, M.J. Sobrido, Elizabeth Spiteri, et al.. (2007). Analysis of Candidate Genes at the IBGC1 Locus Associated with Idiopathic Basal Ganglia Calcification (“Fahr” Disease’). Journal of Molecular Neuroscience. 33(2). 151–154. 20 indexed citations
14.
Juanes, Rubén, Elizabeth Spiteri, Franklin M. Orr, & Martin J. Blunt. (2006). Impact of relative permeability hysteresis on geological CO2 storage. Water Resources Research. 42(12). 773 indexed citations breakdown →
15.
Spiteri, Elizabeth & Ruben Juanes. (2005). Impact of relative permeability hysteresis on the numerical simulation of WAG injection. Journal of Petroleum Science and Engineering. 50(2). 115–139. 116 indexed citations
16.
Spiteri, Elizabeth & Ruben Juanes. (2004). Impact of Relative Permeability Hysteresis on the Numerical Simulation of WAG Injection. SPE Annual Technical Conference and Exhibition. 134 indexed citations
17.
Spiteri, Elizabeth, Melanie Babcock, Catherine D. Kashork, et al.. (2003). Frequent translocations occur between low copy repeats on chromosome 22q11.2 (LCR22s) and telomeric bands of partner chromosomes. Human Molecular Genetics. 12(15). 1823–1837. 43 indexed citations
18.
Edelmann, Lisa, Elizabeth Spiteri, Raj K. Pandita, et al.. (2001). Two Functional Copies of the DGCR6 Gene Are Present on Human Chromosome 22q11 Due to a Duplication of an Ancestral Locus. Genome Research. 11(2). 208–217. 5 indexed citations
19.
Edelmann, Lisa, Elizabeth Spiteri, Venkat Pulijaal, et al.. (2001). AT-Rich Palindromes Mediate the Constitutional t(11;22) Translocation. The American Journal of Human Genetics. 68(1). 1–13. 144 indexed citations
20.
Edelmann, Lisa, Elizabeth Spiteri, Rosalie Goldberg, et al.. (1999). A Common Breakpoint on 11q23 in Carriers of the Constitutional t(11;22) Translocation. The American Journal of Human Genetics. 65(6). 1608–1616. 46 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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