Matthew Schwede

959 total citations
22 papers, 398 citations indexed

About

Matthew Schwede is a scholar working on Molecular Biology, Cancer Research and Hematology. According to data from OpenAlex, Matthew Schwede has authored 22 papers receiving a total of 398 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Cancer Research and 7 papers in Hematology. Recurrent topics in Matthew Schwede's work include Acute Myeloid Leukemia Research (7 papers), Cancer Genomics and Diagnostics (7 papers) and Respiratory Support and Mechanisms (3 papers). Matthew Schwede is often cited by papers focused on Acute Myeloid Leukemia Research (7 papers), Cancer Genomics and Diagnostics (7 papers) and Respiratory Support and Mechanisms (3 papers). Matthew Schwede collaborates with scholars based in United States, Canada and Switzerland. Matthew Schwede's co-authors include Aedín C. Culhane, Tan A. Ince, Terri Woo, Eric M. Morrow, David W. Kindelberger, Bin Wang, Rulla M. Tamimi, J. Chuck Harrell, Sandro Santagata and Stuart J. Schnitt and has published in prestigious journals such as Journal of Clinical Investigation, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Matthew Schwede

21 papers receiving 392 citations

Peers

Matthew Schwede
Laura Feeney United Kingdom
Andrew Gray Australia
Elizabeth Ormondroyd United Kingdom
Eddie Myers Ireland
Elisa J. Cops Australia
Matthew Schwede
Citations per year, relative to Matthew Schwede Matthew Schwede (= 1×) peers Alfredo Löhr

Countries citing papers authored by Matthew Schwede

Since Specialization
Citations

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

Fields of papers citing papers by Matthew Schwede

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matthew Schwede

This figure shows the co-authorship network connecting the top 25 collaborators of Matthew Schwede. A scholar is included among the top collaborators of Matthew Schwede 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 Matthew Schwede. Matthew Schwede 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.
Schwede, Matthew, Katharina Jahn, Jack Kuipers, et al.. (2024). Mutation order in acute myeloid leukemia identifies uncommon patterns of evolution and illuminates phenotypic heterogeneity. Leukemia. 38(7). 1501–1510. 10 indexed citations
2.
Schwede, Matthew, et al.. (2024). Web-Based Scaffolds: The Feasibility of a Constructivist Approach to Oncology Fellow Learning. JMIR Cancer. 10. e52501–e52501. 1 indexed citations
3.
Gunaratne, Ruwan, Matthew S. Alkaitis, Matthew Schwede, et al.. (2024). Circulating Tumor DNA (ctDNA) Enables Superior and Universal Measurable Residual Disease (MRD) Monitoring in Acute Myeloid Leukemia (AML) Highly Predictive of Relapse Free and Overall Survival. Blood. 144(Supplement 1). 2955–2955. 1 indexed citations
4.
Nilforoshan, Hamed, Matthew Schwede, Jiaxuan You, et al.. (2023). Graph-based clinical recommender: Predicting specialists procedure orders using graph representation learning. Journal of Biomedical Informatics. 143. 104407–104407. 3 indexed citations
5.
Gunaratne, Ruwan, Matthew Schwede, Matthew S. Alkaitis, et al.. (2023). Development of Circulating Tumor DNA (ctDNA) for Molecular Measurable Residual Disease (MRD) in Acute Myeloid Leukemia (AML). Blood. 142(Supplement 1). 4307–4307. 1 indexed citations
6.
Schwede, Matthew, et al.. (2023). Acute Myeloid Leukemia with Inv(3) or t(3;3): A Clinical and Cytogenetic Characterization of 40 Patients. Blood. 142(Supplement 1). 4231–4231. 1 indexed citations
9.
Wilfong, Erin M., Roxanne H. Croze, Xiaohui Fang, et al.. (2020). Proinflammatory cytokines and ARDS pulmonary edema fluid induce CD40 on human mesenchymal stromal cells—A potential mechanism for immune modulation. PLoS ONE. 15(10). e0240319–e0240319. 6 indexed citations
10.
Richardson, Andrea L., Bin Wang, Tan A. Ince, et al.. (2020). Taxonomy of breast cancer based on normal cell phenotype predicts outcome. UNC Libraries.
11.
Schwede, Matthew, Levi Waldron, Samuel C. Mok, et al.. (2019). The Impact of Stroma Admixture on Molecular Subtypes and Prognostic Gene Signatures in Serous Ovarian Cancer. Cancer Epidemiology Biomarkers & Prevention. 29(2). 509–519. 24 indexed citations
12.
Schwede, Matthew, Shailender Nagpal, Michael J. Gandal, et al.. (2018). Strong correlation of downregulated genes related to synaptic transmission and mitochondria in post-mortem autism cerebral cortex. Journal of Neurodevelopmental Disorders. 10(1). 18–18. 41 indexed citations
13.
Schwede, Matthew, Erin M. Wilfong, Rachel L. Zemans, et al.. (2018). Effects of bone marrow-derived mesenchymal stromal cells on gene expression in human alveolar type II cells exposed to TNF-α, IL-1β, and IFN-γ. Physiological Reports. 6(16). e13831–e13831. 6 indexed citations
14.
Daniel, Michelle, Claire Williams, Kelly T. Macdonald, et al.. (2015). Preparing for Clerkships: Learning to Deliver Specialty-Specific Oral Presentations. SHILAP Revista de lepidopterología. 1 indexed citations
15.
Santagata, Sandro, Bin Wang, Terri Woo, et al.. (2014). Taxonomy of breast cancer based on normal cell phenotype predicts outcome. Journal of Clinical Investigation. 124(2). 859–870. 141 indexed citations
16.
Pescosolido, Matthew F., Matthew Schwede, Ashley J. Harrison, et al.. (2014). Expansion of the clinical phenotype associated with mutations in activity-dependent neuroprotective protein. Journal of Medical Genetics. 51(9). 587–589. 21 indexed citations
17.
Schwede, Matthew, Dimitrios Spentzos, Stefan Bentink, et al.. (2013). Stem Cell-Like Gene Expression in Ovarian Cancer Predicts Type II Subtype and Prognosis. PLoS ONE. 8(3). e57799–e57799. 30 indexed citations
18.
Pescosolido, Matthew F., et al.. (2013). An unbalanced translocation involving loss of 10q26.2 and gain of 11q25 in a pedigree with autism spectrum disorder and cerebellar juvenile pilocytic astrocytoma. American Journal of Medical Genetics Part A. 161(4). 787–791. 22 indexed citations
19.
Merritt, Melissa A., Stefan Bentink, Matthew Schwede, et al.. (2013). Gene Expression Signature of Normal Cell-of-Origin Predicts Ovarian Tumor Outcomes. PLoS ONE. 8(11). e80314–e80314. 36 indexed citations
20.
Drolet, Brian C., Matthew Schwede, Kenneth D. Bishop, & Staci A. Fischer. (2013). Compliance and Falsification of Duty Hours: Reports From Residents and Program Directors. Journal of Graduate Medical Education. 5(3). 368–373. 33 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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