Gavin R. Oliver

1.9k total citations
31 papers, 496 citations indexed

About

Gavin R. Oliver is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Gavin R. Oliver has authored 31 papers receiving a total of 496 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 16 papers in Genetics and 9 papers in Cancer Research. Recurrent topics in Gavin R. Oliver's work include Genomics and Rare Diseases (8 papers), Cancer Genomics and Diagnostics (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Gavin R. Oliver is often cited by papers focused on Genomics and Rare Diseases (8 papers), Cancer Genomics and Diagnostics (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Gavin R. Oliver collaborates with scholars based in United States, United Kingdom and Belgium. Gavin R. Oliver's co-authors include Eric W. Klee, Steven N. Hart, Margot A. Cousin, Deirdre O’Shea, Grant W. Hennig, Pieter Vanden Berghe, Garrett Jenkinson, Nick J. Spencer, Terence K. Smith and Patrick R. Blackburn and has published in prestigious journals such as Journal of Biological Chemistry, Bioinformatics and Gastroenterology.

In The Last Decade

Gavin R. Oliver

30 papers receiving 489 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Gavin R. Oliver United States	13	316	127	107	53	52	31	496
Donatella Montanaro Italy	10	191 0.6×	55 0.4×	72 0.7×	35 0.7×	22 0.4×	15	336
Katrina L. Scarff Australia	7	146 0.5×	50 0.4×	54 0.5×	30 0.6×	15 0.3×	9	312
David Crawford United States	12	210 0.7×	44 0.3×	29 0.3×	73 1.4×	60 1.2×	22	418
Céline Villenet France	14	176 0.6×	58 0.5×	51 0.5×	9 0.2×	73 1.4×	31	472
Puneet Seth United States	7	232 0.7×	86 0.7×	72 0.7×	9 0.2×	8 0.2×	11	618
E Emison United States	3	400 1.3×	172 1.4×	76 0.7×	16 0.3×	19 0.4×	5	681
Sika Ristevski Australia	11	359 1.1×	135 1.1×	38 0.4×	8 0.2×	18 0.3×	15	541
Julia T. Tanassi Denmark	10	186 0.6×	23 0.2×	46 0.4×	20 0.4×	24 0.5×	15	414
Juha Ollila Finland	11	416 1.3×	238 1.9×	33 0.3×	10 0.2×	16 0.3×	15	800
Soo Hyun Seo South Korea	14	241 0.8×	81 0.6×	81 0.8×	6 0.1×	35 0.7×	45	496

Countries citing papers authored by Gavin R. Oliver

Since Specialization

Citations

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

Fields of papers citing papers by Gavin R. Oliver

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gavin R. Oliver. 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 Gavin R. Oliver. The network helps show where Gavin R. Oliver may publish in the future.

Co-authorship network of co-authors of Gavin R. Oliver

This figure shows the co-authorship network connecting the top 25 collaborators of Gavin R. Oliver. A scholar is included among the top collaborators of Gavin R. Oliver 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 Gavin R. Oliver. Gavin R. Oliver is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Gnanaolivu, Rohan, Gavin R. Oliver, Garrett Jenkinson, et al.. (2025). A clinical knowledge graph-based framework to prioritize candidate genes for facilitating diagnosis of Mendelian diseases and rare genetic conditions. BMC Bioinformatics. 26(1). 82–82.

Khanna, Cheryl L., James B. Smadbeck, Sarah H. Johnson, et al.. (2024). Complex balanced intrachromosomal rearrangement involving PITX2 identified as a cause of Axenfeld‐Rieger Syndrome. American Journal of Medical Genetics Part A. 194(5). e63542–e63542. 2 indexed citations

Fadra, Numrah, Laura Schultz‐Rogers, Pritha Chanana, et al.. (2024). Identification of skewed X chromosome inactivation using exome and transcriptome sequencing in patients with suspected rare genetic disease. BMC Genomics. 25(1). 371–371. 1 indexed citations

Jenkinson, Garrett, Asha Nair, Jesse S. Voss, et al.. (2021). SeekFusion - A Clinically Validated Fusion Transcript Detection Pipeline for PCR-Based Next-Generation Sequencing of RNA. Frontiers in Genetics. 12. 739054–739054. 11 indexed citations

Morales‐Rosado, Joel A., Erica L. Macke, Margot A. Cousin, et al.. (2020). Interpretation challenges of novel dual‐class missense and splice‐impacting variant in POLR3A‐related late‐onset hereditary spastic ataxia. Molecular Genetics & Genomic Medicine. 8(9). e1341–e1341. 6 indexed citations

Jenkinson, Garrett, et al.. (2020). LeafCutterMD: an algorithm for outlier splicing detection in rare diseases. Bioinformatics. 36(17). 4609–4615. 31 indexed citations

Oliver, Gavin R., Garrett Jenkinson, & Eric W. Klee. (2020). Computational Detection of Known Pathogenic Gene Fusions in a Normal Tissue Database and Implications for Genetic Disease Research. Frontiers in Genetics. 11. 173–173. 7 indexed citations

Zepeda‐Mendoza, Cinthya, Margot A. Cousin, Garrett Jenkinson, et al.. (2019). An intragenic duplication of TRPS1 leading to abnormal transcripts and causing trichorhinophalangeal syndrome type I. Molecular Case Studies. 5(6). a004655–a004655. 6 indexed citations

Cousin, Margot A., Matthew J. Smith, Ashley N. Sigafoos, et al.. (2018). Utility of DNA, RNA, Protein, and Functional Approaches to Solve Cryptic Immunodeficiencies. Journal of Clinical Immunology. 38(3). 307–319. 21 indexed citations

10.

Boczek, Nicole J., Katharina Hopp, Daniel Kraft, et al.. (2018). Characterization of three ciliopathy pedigrees expands the phenotype associated with biallelic C2CD3 variants. European Journal of Human Genetics. 26(12). 1797–1809. 17 indexed citations

11.

Zimmermann, Michael T., Raúl Urrutia, Margot A. Cousin, Gavin R. Oliver, & Eric W. Klee. (2018). Assessing Human Genetic Variations in Glucose Transporter SLC2A10 and Their Role in Altering Structural and Functional Properties. Frontiers in Genetics. 9. 276–276. 10 indexed citations

12.

Davila, Jaime, Jason S. Starr, Steven Attia, et al.. (2017). Comprehensive Genomic Profiling of a Rare Thyroid Follicular Dendritic Cell Sarcoma. Rare Tumors. 9(2). 50–53. 10 indexed citations

13.

Zimmermann, Michael T., Raúl Urrutia, Gavin R. Oliver, et al.. (2017). Molecular modeling and molecular dynamic simulation of the effects of variants in the TGFBR2 kinase domain as a paradigm for interpretation of variants obtained by next generation sequencing. PLoS ONE. 12(2). e0170822–e0170822. 19 indexed citations

14.

Blackburn, Patrick R., Alexander Tischer, Michael T. Zimmermann, et al.. (2017). A Novel Kleefstra Syndrome-associated Variant That Affects the Conserved TPLX Motif within the Ankyrin Repeat of EHMT1 Leads to Abnormal Protein Folding. Journal of Biological Chemistry. 292(9). 3866–3876. 12 indexed citations

15.

Tibes, Raoul, Aref Al‐Kali, Gavin R. Oliver, et al.. (2015). The Hedgehog pathway as targetable vulnerability with 5-azacytidine in myelodysplastic syndrome and acute myeloid leukemia. Journal of Hematology & Oncology. 8(1). 114–114. 49 indexed citations

16.

Plebani, Roberto, Gavin R. Oliver, Marco Trerotola, et al.. (2012). Long-range Transcriptome Sequencing Reveals Cancer Cell Growth Regulatory Chimeric mRNA. Neoplasia. 14(11). 1087–49. 17 indexed citations

17.

Allen, Wendy L., Puthen V. Jithesh, Gavin R. Oliver, et al.. (2010). The Colorectal cancer disease-specific transcriptome may facilitate the discovery of more biologically and clinically relevant information. BMC Cancer. 10(1). 687–687. 7 indexed citations

18.

Grigoriadis, Anita, Gavin R. Oliver, Howard Kendrick, et al.. (2009). Identification of differentially expressed sense and antisense transcript pairs in breast epithelial tissues. BMC Genomics. 10(1). 324–324. 26 indexed citations

19.

Oliver, Gavin R., Vadim Farztdinov, Richard D. Kennedy, et al.. (2008). Generation of a non-small cell lung cancer transcriptome microarray. BMC Medical Genomics. 1(1). 20–20. 18 indexed citations

20.

Smith, Terence K., Gavin R. Oliver, Grant W. Hennig, et al.. (2003). A smooth muscle tone-dependent stretch-activated migrating motor pattern in isolated guinea-pig distal colon. The Journal of Physiology. 551(3). 955–969. 43 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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