James Dalton

13.0k total citations · 3 hit papers
44 papers, 5.2k citations indexed

About

James Dalton is a scholar working on Genetics, Molecular Biology and Oncology. According to data from OpenAlex, James Dalton has authored 44 papers receiving a total of 5.2k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 17 papers in Molecular Biology and 9 papers in Oncology. Recurrent topics in James Dalton's work include Glioma Diagnosis and Treatment (16 papers), Acute Lymphoblastic Leukemia research (8 papers) and Cancer Genomics and Diagnostics (7 papers). James Dalton is often cited by papers focused on Glioma Diagnosis and Treatment (16 papers), Acute Lymphoblastic Leukemia research (8 papers) and Cancer Genomics and Diagnostics (7 papers). James Dalton collaborates with scholars based in United States, United Kingdom and Canada. James Dalton's co-authors include Anthony V. Seaber, William E. Garrett, Dean C. Taylor, Amar Gajjar, Xiaoping Su, Richard J. Gilbertson, Michael D. Taylor, David W. Ellison, Christine Fuller and James R. Downing and has published in prestigious journals such as Nature, Journal of Clinical Oncology and Genes & Development.

In The Last Decade

James Dalton

42 papers receiving 5.1k citations

Hit Papers

Genome-wide analysis of genetic alterations i... 1990 2026 2002 2014 2007 2005 1990 400 800 1.2k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
James Dalton United States 27 2.3k 1.9k 870 797 733 44 5.2k
Federica Benvenuto Italy 31 1.6k 0.7× 3.0k 1.6× 148 0.2× 859 1.1× 859 1.2× 64 6.1k
Feng‐Chun Yang United States 39 2.8k 1.2× 764 0.4× 115 0.1× 686 0.9× 1.2k 1.7× 131 5.6k
Volker Eckstein Germany 37 2.2k 0.9× 2.9k 1.5× 121 0.1× 1.3k 1.6× 1.4k 1.9× 121 6.4k
Toshihide Iwashita Japan 36 3.5k 1.5× 859 0.5× 135 0.2× 1.3k 1.6× 1.7k 2.4× 106 7.3k
Luciano Neder Brazil 33 2.0k 0.9× 1.1k 0.6× 157 0.2× 508 0.6× 78 0.1× 128 4.1k
Tatyana V. Michurina United States 18 1.6k 0.7× 1.4k 0.7× 115 0.1× 825 1.0× 1.2k 1.6× 32 4.3k
Alexander Medvinsky United Kingdom 34 3.7k 1.6× 582 0.3× 231 0.3× 523 0.7× 1.9k 2.5× 66 6.6k
Sandra Pinho United States 24 2.4k 1.0× 1.6k 0.9× 115 0.1× 890 1.1× 2.9k 3.9× 53 6.2k
Lies H. Hoefsloot Netherlands 45 3.7k 1.6× 1.1k 0.6× 160 0.2× 511 0.6× 253 0.3× 136 6.6k
William E. Janssen United States 27 1.1k 0.5× 1.2k 0.6× 158 0.2× 1.3k 1.7× 759 1.0× 84 3.7k

Countries citing papers authored by James Dalton

Since Specialization
Citations

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

Fields of papers citing papers by James Dalton

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of James Dalton

This figure shows the co-authorship network connecting the top 25 collaborators of James Dalton. A scholar is included among the top collaborators of James Dalton 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 James Dalton. James Dalton 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.
Flasch, Diane A., Xiaolong Chen, Bensheng Ju, et al.. (2022). Somatic LINE-1 promoter acquisition drives oncogenic FOXR2 activation in pediatric brain tumor. Acta Neuropathologica. 143(5). 605–607. 4 indexed citations
2.
Keenan, Camille, Julie H. Harreld, John T. Lucas, et al.. (2020). Infratentorial C11orf95-fused gliomas share histologic, immunophenotypic, and molecular characteristics of supratentorial RELA-fused ependymoma. Acta Neuropathologica. 140(6). 963–965. 10 indexed citations
3.
Ozawa, Tatsuya, Sonali Arora, Frank Szulzewsky, et al.. (2018). A De Novo Mouse Model of C11orf95-RELA Fusion-Driven Ependymoma Identifies Driver Functions in Addition to NF-κB. Cell Reports. 23(13). 3787–3797. 37 indexed citations
4.
Xu, Ke, Liang Ding, Ti‐Cheng Chang, et al.. (2018). Structure and evolution of double minutes in diagnosis and relapse brain tumors. Acta Neuropathologica. 137(1). 123–137. 59 indexed citations
5.
Harreld, Julie H., Scott N. Hwang, Ibrahim Qaddoumi, et al.. (2016). Relative ADC and Location Differ between Posterior Fossa Pilocytic Astrocytomas with and without Gangliocytic Differentiation. American Journal of Neuroradiology. 37(12). 2370–2375. 4 indexed citations
6.
Wu, Gang, Raymond L. Barnhill, Seungjae Lee, et al.. (2016). The landscape of fusion transcripts in spitzoid melanoma and biologically indeterminate spitzoid tumors by RNA sequencing. Modern Pathology. 29(4). 359–369. 56 indexed citations
7.
Gupta, Kirti, Wilda Orisme, Julie H. Harreld, et al.. (2014). Posterior fossa and spinal gangliogliomas form two distinct clinicopathologic and molecular subgroups. Acta Neuropathologica Communications. 2(1). 18–18. 43 indexed citations
8.
9.
Bahrami, Armita, et al.. (2012). PLAG1 Alteration in Carcinoma Ex Pleomorphic Adenoma: Immunohistochemical and Fluorescence In Situ Hybridization Studies of 22 Cases. Head and Neck Pathology. 6(3). 328–335. 72 indexed citations
10.
Bahrami, Armita, James Dalton, Jeffrey F. Krane, & Christopher D.�M. Fletcher. (2011). A subset of cutaneous and soft tissue mixed tumors are genetically linked to their salivary gland counterpart. Genes Chromosomes and Cancer. 51(2). 140–148. 81 indexed citations
11.
Ellison, David W., Mehmet Koçak, James Dalton, et al.. (2010). Definition of Disease-Risk Stratification Groups in Childhood Medulloblastoma Using Combined Clinical, Pathologic, and Molecular Variables. Journal of Clinical Oncology. 29(11). 1400–1407. 203 indexed citations
12.
Forshew, Tim, Ruth Tatevossian, Andrew Lawson, et al.. (2009). Activation of the ERK/MAPK pathway: a signature genetic defect in posterior fossa pilocytic astrocytomas. The Journal of Pathology. 218(2). 172–181. 218 indexed citations
13.
Fernández-L, Africa, Paul A. Northcott, James Dalton, et al.. (2009). YAP1 is amplified and up-regulated in hedgehog-associated medulloblastomas and mediates Sonic hedgehog-driven neural precursor proliferation. Genes & Development. 23(23). 2729–2741. 314 indexed citations
14.
Mullighan, Charles G., Salil Goorha, Ina Radtke, et al.. (2007). Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia. Nature. 446(7137). 758–764. 1237 indexed citations breakdown →
15.
Taylor, Michael D., Helen Poppleton, Christine Fuller, et al.. (2005). Radial glia cells are candidate stem cells of ependymoma. Cancer Cell. 8(4). 323–335. 579 indexed citations breakdown →
16.
Fouladi, Maryam, Kathleen J. Helton, James Dalton, et al.. (2003). Clear cell ependymoma: A clinicopathologic and radiographic analysis of 10 patients. Cancer. 98(10). 2232–2244. 65 indexed citations
17.
Subramaniyam, Shivakumar, Susan Mathew, James Dalton, Mammen Chandy, & Alok Srivastava. (2002). A Complex Karyotype Involving Chromosomes 3, 6, 11, 12, and 22 in Adult Acute Lymphoblastic Leukemia. Leukemia & lymphoma. 43(8). 1673–1677. 3 indexed citations
18.
Mathew, S, et al.. (2001). Multicolor spectral karyotyping identifies novel translocations in childhood acute lymphoblastic leukemia. Leukemia. 15(3). 468–472. 28 indexed citations
19.
Sallay, Peter I., Robert A. Pedowitz, William J. Mallon, et al.. (1997). Reliability and reproducibility of radiographic interpretation of proximal humeral fracture pathoanatomy. Journal of Shoulder and Elbow Surgery. 6(1). 60–69. 48 indexed citations
20.
Qumsiyeh, Mazin Β., James Dalton, Patricia Gordon, R. Sid Wilroy, & Avirachan T. Tharapel. (1992). Deletion of chromosome 15pter→q11.2 due to t(Y;15) in a boy with Prader‐Willi syndrome. American Journal of Medical Genetics. 42(1). 109–111. 7 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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