Gavin Chapman

3.7k total citations
44 papers, 2.4k citations indexed

About

Gavin Chapman is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Gavin Chapman has authored 44 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 10 papers in Genetics and 6 papers in Epidemiology. Recurrent topics in Gavin Chapman's work include Congenital heart defects research (14 papers), Developmental Biology and Gene Regulation (14 papers) and Pluripotent Stem Cells Research (7 papers). Gavin Chapman is often cited by papers focused on Congenital heart defects research (14 papers), Developmental Biology and Gene Regulation (14 papers) and Pluripotent Stem Cells Research (7 papers). Gavin Chapman collaborates with scholars based in Australia, United Kingdom and United States. Gavin Chapman's co-authors include Urban Lendahl, Sally L. Dunwoodie, Duncan B. Sparrow, Emil M. Hansson, Peter D. Rathjen, Elisabeth Kremmer, Camilla Dahlqvist, Julie-Anne Lake, Joy Rathjen and Michael D. Bettess and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

Gavin Chapman

42 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gavin Chapman Australia 25 1.8k 382 268 247 243 44 2.4k
Evgenia Pak United States 23 2.4k 1.3× 445 1.2× 217 0.8× 158 0.6× 129 0.5× 42 3.3k
Melissa C. Colbert United States 26 1.8k 1.0× 296 0.8× 206 0.8× 287 1.2× 214 0.9× 33 2.8k
Kumi Kawai Japan 22 1.0k 0.6× 218 0.6× 240 0.9× 175 0.7× 179 0.7× 36 1.8k
Lynn Sanford United States 20 2.0k 1.1× 460 1.2× 319 1.2× 141 0.6× 161 0.7× 37 2.8k
Michelle Wei United States 11 1.2k 0.7× 349 0.9× 251 0.9× 129 0.5× 186 0.8× 17 1.9k
Mary Shago Canada 21 1.4k 0.8× 613 1.6× 250 0.9× 225 0.9× 83 0.3× 57 2.3k
Atsushi Otani Japan 40 2.2k 1.2× 160 0.4× 163 0.6× 273 1.1× 110 0.5× 87 4.7k
Deborah Lang United States 21 1.3k 0.7× 242 0.6× 305 1.1× 159 0.6× 150 0.6× 37 2.0k
Koichi Miyake Japan 26 1.2k 0.7× 379 1.0× 182 0.7× 144 0.6× 150 0.6× 73 2.1k
Mordechai Shohat Israel 26 1.7k 0.9× 540 1.4× 139 0.5× 129 0.5× 121 0.5× 83 2.9k

Countries citing papers authored by Gavin Chapman

Since Specialization
Citations

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

Fields of papers citing papers by Gavin Chapman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gavin Chapman

This figure shows the co-authorship network connecting the top 25 collaborators of Gavin Chapman. A scholar is included among the top collaborators of Gavin Chapman 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 Chapman. Gavin Chapman 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.
Thibaut, L, Debjani Das, David S. Winlaw, et al.. (2024). Benchmarking of variant pathogenicity prediction methods using a population genetics approach. Bioinformatics Advances. 5(1). vbaf227–vbaf227.
2.
Enriquez, Annabelle, Robert D. Steiner, David T. Humphreys, et al.. (2022). Myhre syndrome is caused by dominant-negative dysregulation of SMAD4 and other co-factors. Differentiation. 128. 1–12. 5 indexed citations
3.
Ward, Alexander, Vaibhao Janbandhu, Gavin Chapman, Sally L. Dunwoodie, & Richard P. Harvey. (2022). An image analysis protocol using CellProfiler for automated quantification of post-ischemic cardiac parameters. STAR Protocols. 3(1). 101097–101097. 9 indexed citations
4.
Janbandhu, Vaibhao, Ella MMA Martin, Gavin Chapman, Sally L. Dunwoodie, & Richard P. Harvey. (2021). Quantitative 3D analysis and visualization of cardiac fibrosis by microcomputed tomography. STAR Protocols. 3(1). 101055–101055. 3 indexed citations
5.
Ip, Eddie, Gavin Chapman, David S. Winlaw, Sally L. Dunwoodie, & Eleni Giannoulatou. (2019). VPOT: A Customizable Variant Prioritization Ordering Tool for Annotated Variants. Genomics Proteomics & Bioinformatics. 17(5). 540–545. 9 indexed citations
6.
Moreau, Julie, Scott Kesteven, Ella MMA Martin, et al.. (2019). Gene-environment interaction impacts on heart development and embryo survival. Development. 146(4). 49 indexed citations
7.
Szot, Justin O., Nick Pachter, Anne Slavotinek, et al.. (2019). Functional characterization of a novel PBX1 de novo missense variant identified in a patient with syndromic congenital heart disease. Human Molecular Genetics. 29(7). 1068–1082. 26 indexed citations
8.
Dorward, David A., Christopher D. Lucas, Mary K. Doherty, et al.. (2017). Novel role for endogenous mitochondrial formylated peptide-driven formyl peptide receptor 1 signalling in acute respiratory distress syndrome. Thorax. 72(10). 928–936. 66 indexed citations
9.
Bouveret, Romaric, Ashley J. Waardenberg, Nicole Schönrock, et al.. (2015). NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targets. eLife. 4. 58 indexed citations
10.
Dorward, David A., Christopher D. Lucas, Gavin Chapman, et al.. (2015). The Role of Formylated Peptides and Formyl Peptide Receptor 1 in Governing Neutrophil Function during Acute Inflammation. American Journal Of Pathology. 185(5). 1172–1184. 200 indexed citations
11.
James, Alexander C., et al.. (2014). Notch4 reveals a novel mechanism regulating Notch signal transduction. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1843(7). 1272–1284. 41 indexed citations
12.
O׳Reilly, Victoria C., Hongjun Shi, Bogdan E. Chapman, et al.. (2014). Gene–environment interaction demonstrates the vulnerability of the embryonic heart. Developmental Biology. 391(1). 99–110. 12 indexed citations
13.
Newman, Morgan, Giuseppe Verdile, Seyyed Hani Moussavi Nik, et al.. (2013). Differential, dominant activation and inhibition of Notch signalling and APP cleavage by truncations of PSEN1 in human disease. Human Molecular Genetics. 23(3). 602–617. 40 indexed citations
14.
Sparrow, Duncan B., Gavin Chapman, & Sally L. Dunwoodie. (2011). The mouse notches up another success: understanding the causes of human vertebral malformation. Mammalian Genome. 22(7-8). 362–376. 22 indexed citations
15.
Artap, Stanley T, Jost I. Preis, Diane Fatkin, et al.. (2010). Loss of Cited2 causes congenital heart disease by perturbing left–right patterning of the body axis. Human Molecular Genetics. 20(6). 1097–1110. 49 indexed citations
16.
Chapman, Gavin, Duncan B. Sparrow, Elisabeth Kremmer, & Sally L. Dunwoodie. (2010). Notch inhibition by the ligand Delta-Like 3 defines the mechanism of abnormal vertebral segmentation in spondylocostal dysostosis. Human Molecular Genetics. 20(5). 905–916. 136 indexed citations
17.
Chapman, Gavin & Sally L. Dunwoodie. (2008). Role of Delta-Like-3 in Mammalian Somitogenesis and Vertebral Column Formation. Advances in experimental medicine and biology. 638. 95–112. 2 indexed citations
18.
Hansson, Emil M., Ana I. Teixeira, Maria Gustafsson, et al.. (2006). Recording Notch Signaling in Real Time. Developmental Neuroscience. 28(1-2). 118–127. 38 indexed citations
19.
Sparrow, Duncan B., Gavin Chapman, Merridee A. Wouters, et al.. (2005). Mutation of the LUNATIC FRINGE Gene in Humans Causes Spondylocostal Dysostosis with a Severe Vertebral Phenotype. The American Journal of Human Genetics. 78(1). 28–37. 182 indexed citations
20.
Chapman, Gavin, et al.. (1997). The Mouse Homeobox Gene,Gbx2:Genomic Organization and Expression in Pluripotent Cellsin Vitroandin Vivo. Genomics. 46(2). 223–233. 37 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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