Michael Dean

75.0k total citations · 17 hit papers
385 papers, 41.2k citations indexed

About

Michael Dean is a scholar working on Molecular Biology, Oncology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Michael Dean has authored 385 papers receiving a total of 41.2k indexed citations (citations by other indexed papers that have themselves been cited), including 196 papers in Molecular Biology, 121 papers in Oncology and 58 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Michael Dean's work include Drug Transport and Resistance Mechanisms (69 papers), Cystic Fibrosis Research Advances (42 papers) and Cholesterol and Lipid Metabolism (30 papers). Michael Dean is often cited by papers focused on Drug Transport and Resistance Mechanisms (69 papers), Cystic Fibrosis Research Advances (42 papers) and Cholesterol and Lipid Metabolism (30 papers). Michael Dean collaborates with scholars based in United States, United Kingdom and China. Michael Dean's co-authors include Susan E. Bates, Rando Allikmets, Tito Fojo, Andrey Rzhetsky, Bert Gold, Stephen J. O’Brien, Tarmo Annilo, David Goldman, Giovanna Chimini and Yannick Hamon and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Michael Dean

376 papers receiving 40.1k citations

Hit Papers

The BDNF val66met Polymor... 1984 2026 1998 2012 2003 2005 1989 1996 2001 1000 2.0k 3.0k

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Michael Dean 18.0k 12.7k 5.3k 5.1k 4.6k 385 41.2k
Simon C. Watkins 28.3k 1.6× 5.8k 0.5× 5.9k 1.1× 4.9k 1.0× 12.9k 2.8× 788 59.2k
Richard A. Lempicki 36.6k 2.0× 5.1k 0.4× 2.9k 0.6× 4.5k 0.9× 8.5k 1.8× 130 60.5k
Beth Levine 38.4k 2.1× 3.9k 0.3× 4.0k 0.8× 2.1k 0.4× 9.4k 2.0× 187 83.7k
Nicoletta Sacchi 26.0k 1.4× 5.4k 0.4× 3.8k 0.7× 2.0k 0.4× 7.6k 1.6× 150 50.8k
Brad T. Sherman 37.7k 2.1× 5.1k 0.4× 2.9k 0.6× 4.8k 0.9× 7.0k 1.5× 43 59.6k
Claudio Franceschi 23.8k 1.3× 3.7k 0.3× 2.5k 0.5× 1.7k 0.3× 11.6k 2.5× 816 62.5k
Noboru Mizushima 42.9k 2.4× 3.1k 0.2× 4.5k 0.8× 2.0k 0.4× 8.9k 1.9× 272 94.2k
Randal J. Kaufman 42.0k 2.3× 3.8k 0.3× 10.3k 2.0× 2.1k 0.4× 9.1k 2.0× 466 82.2k
James M. Wilson 37.1k 2.1× 8.6k 0.7× 5.1k 1.0× 5.1k 1.0× 6.8k 1.5× 900 64.0k
Antonio Giordano 19.5k 1.1× 13.8k 1.1× 2.6k 0.5× 4.1k 0.8× 2.4k 0.5× 874 36.6k

Countries citing papers authored by Michael Dean

Since Specialization
Citations

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

Fields of papers citing papers by Michael Dean

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michael Dean

This figure shows the co-authorship network connecting the top 25 collaborators of Michael Dean. A scholar is included among the top collaborators of Michael Dean 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 Michael Dean. Michael Dean 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.
Nelson, Chase W., Meredith Yeager, Zigui Chen, et al.. (2025). Whole‐genome sequencing of 1,083 HPV45 cases and controls identifies genetic variants associated with glandular cervical lesions. International Journal of Cancer. 157(6). 1130–1141.
2.
Karyadi, Danielle M., Bogdanova Ti, Caitlin M. Milder, et al.. (2025). Distinctive molecular features of radiation-induced thyroid cancers. Science Advances. 11(34). eadw7680–eadw7680.
3.
Xie, Yi, Hyo‐Jung Lee, Laurie Burdett, et al.. (2024). Analysis of the progression of cervical cancer in a low-and-middle-income country: From pre-malignancy to invasive disease. SHILAP Revista de lepidopterología. 19. 200299–200299. 1 indexed citations
4.
Lee, Yeh Chen, et al.. (2024). Use of cell-free DNA from ascites to identify variants and tumour evolution in a cohort of patients with advanced ovarian cancer.. Journal of Clinical Oncology. 42(16_suppl). 5547–5547.
5.
Dean, Michael, Christopher T. Eberlin, Charles Wang, et al.. (2024). Association Between Chondrolabral Junction Breakdown and Conversion to Total Hip Arthroplasty After Hip Arthroscopy for Symptomatic Labral Tears: Minimum 8-Year Follow-up. The American Journal of Sports Medicine. 52(5). 1153–1164. 5 indexed citations
7.
Dean, Michael, Donghyuk Lee, Amber N. Hurson, et al.. (2023). Nitrated Polycyclic Aromatic Hydrocarbon (Nitro-PAH) Signatures and Somatic Mutations in Diesel Exhaust-Exposed Bladder Tumors. Cancer Epidemiology Biomarkers & Prevention. 32(6). 840–847. 2 indexed citations
8.
Xie, Yi, Darawalee Wangsa, Kerstin Heselmeyer‐Haddad, et al.. (2023). Extrachromosomal Amplification of Human Papillomavirus Episomes Is a Mechanism of Cervical Carcinogenesis. Cancer Research. 83(11). 1768–1781. 16 indexed citations
9.
Lei, Haoyun, E. Michael Gertz, Alejandro A. Schäffer, et al.. (2021). Tumor heterogeneity assessed by sequencing and fluorescence in situ hybridization (FISH) data. Bioinformatics. 37(24). 4704–4711. 9 indexed citations
10.
Koutros, Stella, Lee E. Moore, Michael L. Nickerson, et al.. (2021). Targeted Deep Sequencing of Bladder Tumors Reveals Novel Associations between Cancer Gene Mutations and Mutational Signatures with Major Risk Factors. Clinical Cancer Research. 27(13). 3725–3733. 11 indexed citations
11.
Wu, Liang, Miaomiao Jiang, Yun‐Fan Sun, et al.. (2021). scDPN for High-Throughput Single-Cell CNV Detection to Uncover Clonal Evolution During HCC Recurrence. Genomics Proteomics & Bioinformatics. 19(3). 346–357. 2 indexed citations
12.
Lou, Hong, Joseph F. Boland, Weiyin Zhou, et al.. (2020). The D2 and D3 Sublineages of Human Papilloma Virus 16–Positive Cervical Cancer in Guatemala Differ in Integration Rate and Age of Diagnosis. Cancer Research. 80(18). 3803–3809. 8 indexed citations
13.
Zhou, Weiyin, Lynn R. Goldin, Mingyi Wang, et al.. (2018). Combined somatic mutation and copy number analysis in the survival of familial CLL. British Journal of Haematology. 181(5). 604–613.
14.
Nickerson, Michael L., Garrett M. Dancik, Kate M. Im, et al.. (2014). Concurrent Alterations in TERT , KDM6A , and the BRCA Pathway in Bladder Cancer. Clinical Cancer Research. 20(18). 4935–4948. 87 indexed citations
15.
Silverman, Robert H., Jaydip Das Gupta, Vincent C. Lombardi, et al.. (2011). Partial Retraction. Science. 334(6053). 176–176. 16 indexed citations
16.
Kirchhoff, Tomas, Zhang-qun Chen, Bert Gold, et al.. (2009). The 6q22.33 Locus and Breast Cancer Susceptibility. Cancer Epidemiology Biomarkers & Prevention. 18(9). 2468–2475. 15 indexed citations
17.
Bullard, Janine, Susan E. Wert, Jeffrey A. Whitsett, Michael Dean, & Lawrence M. Nogee. (2005). ABCA3 Mutations Associated with Pediatric Interstitial Lung Disease. American Journal of Respiratory and Critical Care Medicine. 172(8). 1026–1031. 214 indexed citations
18.
Simonelli, Francesca, Francesco Testa, Giuseppe de Crecchio, et al.. (2000). New ABCR mutations and clinical phenotype in Italian patients with Stargardt disease.. PubMed. 41(3). 892–7. 69 indexed citations
19.
Will, Katrin, Jochen Reiss, Michael Dean, et al.. (1993). CFTR transcripts are undetectable in lymphocytes and respiratory epithelial cells of a CF patient homozygous for the nonsense mutation R553X.. Journal of Medical Genetics. 30(10). 833–837. 14 indexed citations
20.
White, Marga Belle, et al.. (1990). A frame-shift mutation in the cystic fibrosis gene. Nature. 344(6267). 665–667. 92 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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