Todd E. Druley

6.5k total citations · 3 hit papers
78 papers, 3.0k citations indexed

About

Todd E. Druley is a scholar working on Molecular Biology, Hematology and Cancer Research. According to data from OpenAlex, Todd E. Druley has authored 78 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 26 papers in Hematology and 23 papers in Cancer Research. Recurrent topics in Todd E. Druley's work include Acute Myeloid Leukemia Research (23 papers), Cancer Genomics and Diagnostics (21 papers) and Genomics and Rare Diseases (11 papers). Todd E. Druley is often cited by papers focused on Acute Myeloid Leukemia Research (23 papers), Cancer Genomics and Diagnostics (21 papers) and Genomics and Rare Diseases (11 papers). Todd E. Druley collaborates with scholars based in United States, Canada and United Kingdom. Todd E. Druley's co-authors include Wilfred D. Stein, Andrew L. Young, Susan E. Bates, Thomas Litman, Brenda M. Birmann, Grant A. Challen, Winghing Wong, Igor B. Roninson, Robi D. Mitra and Jamie R. Blundell and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Todd E. Druley

73 papers receiving 2.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

From MDR to MXR: new understanding of multidrug resistance systems, their properties and clinical significance

2001 574 citations Todd E. Druley et al. profile →
Clonal haematopoiesis harbouring AML-associated mutations is ubiquitous in healthy adults

2016 456 citations Andrew L. Young, Brenda M. Birmann et al. profile →
The evolutionary dynamics and fitness landscape of clonal hematopoiesis

2020 254 citations Caroline J. Watson, Winghing Wong et al. Science profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Todd E. Druley United States	26	1.3k	777	773	475	469	78	3.0k
Min Fang United States	34	1.8k 1.4×	1.7k 2.2×	848 1.1×	287 0.6×	517 1.1×	182	4.7k
James F. Beck Germany	36	1.5k 1.1×	950 1.2×	1.2k 1.6×	381 0.8×	276 0.6×	150	3.9k
Seiji Fukuda Japan	41	2.2k 1.7×	851 1.1×	840 1.1×	152 0.3×	418 0.9×	197	5.1k
Sara Teresinha Olalla Saad Brazil	34	1.7k 1.3×	1.6k 2.0×	419 0.5×	388 0.8×	1.4k 2.9×	298	4.5k
Luíz Gonzaga Tone Brazil	30	1.9k 1.4×	425 0.5×	639 0.8×	358 0.8×	650 1.4×	226	3.6k
Mark J. Koury United States	40	1.9k 1.4×	2.1k 2.7×	532 0.7×	305 0.6×	1.2k 2.6×	123	5.5k
Jean‐Pierre Bourquin Switzerland	34	2.0k 1.5×	1.3k 1.7×	889 1.2×	357 0.8×	280 0.6×	129	3.9k
Markus Y. Mapara United States	35	2.5k 1.9×	1.5k 1.9×	1.8k 2.4×	145 0.3×	548 1.2×	174	5.0k
Astrid Gruber Sweden	34	1.8k 1.4×	643 0.8×	927 1.2×	116 0.2×	230 0.5×	99	3.5k
Kajsa Paulsson Sweden	33	1.0k 0.8×	1.1k 1.4×	409 0.5×	466 1.0×	265 0.6×	88	2.8k

Countries citing papers authored by Todd E. Druley

Since Specialization

Citations

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

Fields of papers citing papers by Todd E. Druley

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Todd E. Druley. 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 Todd E. Druley. The network helps show where Todd E. Druley may publish in the future.

Co-authorship network of co-authors of Todd E. Druley

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Berko, Esther R., Arlene Naranjo, Samantha N. McNulty, et al.. (2025). Frequency and Clinical Significance of Clonal and Subclonal Driver Mutations in High-Risk Neuroblastoma at Diagnosis: A Children's Oncology Group Study. Journal of Clinical Oncology. 43(14). 1673–1684. 1 indexed citations

Sciambi, Adam, Daniel Mendoza, Kathryn Thompson, et al.. (2024). Single-Cell Multi-Omic Analysis of AML MRD Reveals Differences in Clonal Architecture between Relapse and Non-Relapse Cases. Blood. 144(Supplement 1). 1568–1568.

Thompson, Kathryn, Benjamin S. Geller, Indira Krishnan, et al.. (2024). A Multiomic, Single-Cell Measurable Residual Disease (scMRD) Assay for Simultaneous Assessment of DNA Mutations and Surface Immunophenotypes in Acute Myeloid Leukemia. Blood. 144(Supplement 1). 6168–6168.

Gillis, Nancy, Eric Padron, Tao Wang, et al.. (2023). Pilot Study of Donor-Engrafted Clonal Hematopoiesis Evolution and Clinical Outcomes in Allogeneic Hematopoietic Cell Transplantation Recipients Using a National Registry. Transplantation and Cellular Therapy. 29(10). 640.e1–640.e8. 4 indexed citations

Friedman, Danielle Novetsky, Chaya S. Moskowitz, Kimberly L. Turner, et al.. (2023). Clonal hematopoiesis in survivors of childhood cancer. Blood Advances. 7(15). 4102–4106. 13 indexed citations

Friedman, Danielle Novetsky, Chaya S. Moskowitz, Kimberly L. Turner, et al.. (2023). Clonal hematopoiesis in survivors of childhood cancer.. Journal of Clinical Oncology. 41(16_suppl). 10014–10014. 1 indexed citations

Wong, Winghing, Sima Bhatt, Kathryn Trinkaus, et al.. (2020). Engraftment of rare, pathogenic donor hematopoietic mutations in unrelated hematopoietic stem cell transplantation. Science Translational Medicine. 12(526). 36 indexed citations

Barwe, Sonali P., et al.. (2020). Strong concordance between RNA structural and single nucleotide variants identified via next generation sequencing techniques in primary pediatric leukemia and patient-derived xenograft samples. Genomics & Informatics. 18(1). e6–e6. 2 indexed citations

Watson, Caroline J., Winghing Wong, Andrew L. Young, et al.. (2020). The evolutionary dynamics and fitness landscape of clonal hematopoiesis. Science. 367(6485). 1449–1454. 254 indexed citations breakdown →

10.

Crowgey, Erin L., Nitin Mahajan, Winghing Wong, et al.. (2020). Error-corrected sequencing strategies enable comprehensive detection of leukemic mutations relevant for diagnosis and minimal residual disease monitoring. BMC Medical Genomics. 13(1). 32–32. 14 indexed citations

11.

Ramos, Enrique, et al.. (2018). Age-specific changes in genome-wide methylation enrich for Foxa2 and estrogen receptor alpha binding sites. PLoS ONE. 13(9). e0203147–e0203147. 3 indexed citations

12.

Young, Andrew L., et al.. (2017). Utility of Detecting Rare Clonal Hematopoiesis for Predicting Leukemic Transformation in Healthy Individuals. Blood. 130. 304–304. 1 indexed citations

13.

Wong, Winghing, et al.. (2017). Error-Corrected Sequencing of Cord Bloods Identifies Pediatric AML-Associated Clonal Hematopoiesis. Blood. 130. 2687–2687. 3 indexed citations

14.

Johnson, Kimberly, Kazi Ahsan, Qianxi Feng, et al.. (2017). Pediatric cancer risk in association with birth defects: A systematic review. PLoS ONE. 12(7). e0181246–e0181246. 35 indexed citations

15.

Lee, Joseph H., Rong Cheng, Lawrence S. Honig, et al.. (2014). Genome wide association and linkage analyses identified three loci—4q25, 17q23.2, and 10q11.21—associated with variation in leukocyte telomere length: the Long Life Family Study. Frontiers in Genetics. 4. 310–310. 50 indexed citations

16.

Horani, Amjad, Todd E. Druley, Maimoona A. Zariwala, et al.. (2012). Whole-Exome Capture and Sequencing Identifies HEATR2 Mutation as a Cause of Primary Ciliary Dyskinesia. The American Journal of Human Genetics. 91(4). 685–693. 111 indexed citations

17.

Chatterjee, Rajshekhar, Enrique Ramos, Daniel R. Martin, et al.. (2012). Traditional and targeted exome sequencing reveals common, rare and novel functional deleterious variants in RET-signaling complex in a cohort of living US patients with urinary tract malformations. Human Genetics. 131(11). 1725–1738. 54 indexed citations

18.

Haller, Gabe, Todd E. Druley, Francesco Vallania, et al.. (2011). Rare missense variants in CHRNB4 are associated with reduced risk of nicotine dependence. Human Molecular Genetics. 21(3). 647–655. 43 indexed citations

19.

Druley, Todd E., Francesco Vallania, Daniel Wegner, et al.. (2009). Quantification of rare allelic variants from pooled genomic DNA. Nature Methods. 6(4). 263–265. 125 indexed citations

20.

Druley, Todd E., Robert J. Hayashi, David B. Mansur, et al.. (2008). Early outcomes after allogeneic hematopoietic SCT in pediatric patients with hematologic malignancies following single fraction TBI. Bone Marrow Transplantation. 43(4). 307–314. 9 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.

Explore authors with similar magnitude of impact