Michael D. McLellan

114.1k total citations · 7 hit papers
35 papers, 11.7k citations indexed

About

Michael D. McLellan is a scholar working on Molecular Biology, Cancer Research and Hematology. According to data from OpenAlex, Michael D. McLellan has authored 35 papers receiving a total of 11.7k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 18 papers in Cancer Research and 6 papers in Hematology. Recurrent topics in Michael D. McLellan's work include Cancer Genomics and Diagnostics (14 papers), Acute Myeloid Leukemia Research (6 papers) and Epigenetics and DNA Methylation (6 papers). Michael D. McLellan is often cited by papers focused on Cancer Genomics and Diagnostics (14 papers), Acute Myeloid Leukemia Research (6 papers) and Epigenetics and DNA Methylation (6 papers). Michael D. McLellan collaborates with scholars based in United States, Canada and Spain. Michael D. McLellan's co-authors include Li Ding, Richard K. Wilson, Qunyuan Zhang, Elaine R. Mardis, Christopher A. Miller, David E. Larson, Daniel C. Koboldt, Michael C. Wendl, Dong Shen and Ling Lin and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nature Medicine.

In The Last Decade

Michael D. McLellan

35 papers receiving 11.6k citations

Hit Papers

5 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.

Mutational landscape and significance across 12 major cancer types

2013 3.1k citations Cyriac Kandoth, Michael D. McLellan et al. Nature profile →
VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing

2012 3.1k citations Daniel C. Koboldt, Qunyuan Zhang et al. Genome Research profile →
Age-related mutations associated with clonal hematopoietic expansion and malignancies

2014 1.2k citations Mingchao Xie, Charles Lu et al. Nature Medicine profile →
BreakDancer: an algorithm for high-resolution mapping of genomic structural variation

2009 997 citations Ken Chen, John W. Wallis et al. Nature Methods profile →
VarScan: variant detection in massively parallel sequencing of individual and pooled samples

2009 917 citations Daniel C. Koboldt, Ken Chen et al. Bioinformatics profile →
Pan-cancer network analysis identifies combinations of rare somatic mutations across pathways and protein complexes

2014 588 citations Mark D.M. Leiserson, Fabio Vandin et al. Nature Genetics profile →
MSIsensor: microsatellite instability detection using paired tumor-normal sequence data

2013 462 citations Beifang Niu, Kai Ye et al. Bioinformatics profile →

Peers

Countries citing papers authored by Michael D. McLellan

Since Specialization

Citations

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

Fields of papers citing papers by Michael D. McLellan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michael D. McLellan

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Gut microbiome-mediated nutrients alter opportunistic bacterial growth in peritonitis 2025 ·American Journal of Physiology-Gastrointestinal and Liver Physiology ·Kale S. Bongers, (unknown), Larisa Yeomans, (unknown), (unknown), Nicole R. Falkowski, Roderick A. McDonald, (unknown), Jennifer M. Baker, Michael D. McLellan, Lemnuel V. Aragones, (unknown), Benjamin H. Singer, Robert P. Dickson, Kathleen A. Stringer	1
2	HPV transcript expression affects cervical cancer response to chemoradiation 2021 ·JCI Insight ·(unknown), Matthew Inkman, (unknown), Naoshad Muhammad, (unknown), Christopher A. Miller, Michael D. McLellan, Michael A. Goldstein, Stephanie Markovina, Perry W. Grigsby, Jin Zhang, Julie K. Schwarz	14
3	Preliminary Results Of A Phase Ib Clinical Trial Of A Neoantigen Dna Vaccine For Pancreatic Cancer 2020 ·HPB ·Darren R. Cullinan, Michael D. McLellan, (unknown), Tammi L. Vickery, Nicole Myers, Mark Sturmoski, Marianna B. Ruzinova, Jasreet Hundal, C. Ryan Miller, (unknown), Robert D. Schreiber, (unknown), S. Peter Goedegebuure, William G. Hawkins, William E. Gillanders	3
4	Protein-structure-guided discovery of functional mutations across 19 cancer types 2016 ·Nature Genetics ·Beifang Niu, Adam Scott, Sohini Sengupta, Matthew H. Bailey, Prag Batra, Jie Ning, Matthew A. Wyczalkowski, Wen-Wei Liang, Qunyuan Zhang, Michael D. McLellan, Sam Q. Sun, Piyush Tripathi, (unknown), Kai Ye, R. Jay Mashl, John Wallis, Michael C. Wendl, Feng Chen, Li Ding	87
5	Systematic discovery of complex insertions and deletions in human cancers 2015 ·Nature Medicine ·Kai Ye, Jiayin Wang, Reyka G. Jayasinghe, Eric-Wubbo Lameijer, Joshua F. McMichael, Jie Ning, Michael D. McLellan, Mingchao Xie, Song Cao, Venkata Yellapantula, Kuan‐lin Huang, Adam Scott, Steven M. Foltz, Beifang Niu, Kimberly J. Johnson, Matthijs Moed, P. Eline Slagboom, Feng Chen, Michael C. Wendl, Li Ding	66
6	Clonal evolution revealed by whole genome sequencing in a case of primary myelofibrosis transformed to secondary acute myeloid leukemia 2014 ·Leukemia ·Elizabeth K. Engle, D. Fisher, Chris Miller, Michael D. McLellan, Robert S. Fulton, (unknown), Richard K. Wilson, T J Ley, Stephen T. Oh	32
7	Pan-cancer network analysis identifies combinations of rare somatic mutations across pathways and protein complexes breakdown → 2014 ·Nature Genetics ·Mark D.M. Leiserson, Fabio Vandin, Hsin-Ta Wu, Jason R. Dobson, (unknown), Jacob Thomas, Alexandra Papoutsaki, Younhun Kim, Beifang Niu, Michael D. McLellan, Michael S. Lawrence, Abel González-Pérez, David Tamborero, Yu‐Wei Cheng, Gregory Ryslik, Núria López-Bigas, Gad Getz, Li Ding, Benjamin J. Raphael	588
8	Age-related mutations associated with clonal hematopoietic expansion and malignancies breakdown → 2014 ·Nature Medicine ·Mingchao Xie, Charles Lu, Jiayin Wang, Michael D. McLellan, Kimberly Johnson, Michael C. Wendl, Joshua F. McMichael, Heather K. Schmidt, Venkata Yellapantula, Christopher A. Miller, Bradley A. Ozenberger, John S. Welch, Daniel C. Link, Matthew J. Walter, Elaine R. Mardis, John F. DiPersio, Feng Chen, Richard K. Wilson, Timothy J. Ley, Li Ding	1204
9	Mutational landscape and significance across 12 major cancer types breakdown → 2013 ·Nature ·Cyriac Kandoth, Michael D. McLellan, Fabio Vandin, Kai Ye, Beifang Niu, Charles Lu, Mingchao Xie, Qunyuan Zhang, Joshua F. McMichael, Matthew A. Wyczalkowski, Mark D.M. Leiserson, Christopher A. Miller, John S. Welch, Matthew J. Walter, Michael C. Wendl, Timothy J. Ley, Richard K. Wilson, Benjamin J. Raphael, Li Ding	3134
10	Identification of a pan-cancer oncogenic microRNA superfamily anchored by a central core seed motif 2013 ·Nature Communications ·Mark P. Hamilton, Kimal Rajapakshe, Sean M. Hartig, Boris Reva, Michael D. McLellan, Cyriac Kandoth, Jun Li, Travis Zack, Preethi H. Gunaratne, David A. Wheeler, Cristian Coarfa, Sean E. McGuire	91
11	VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing breakdown → 2012 ·Genome Research ·Daniel C. Koboldt, Qunyuan Zhang, David E. Larson, Dong Shen, Michael D. McLellan, Ling Lin, Christopher A. Miller, Elaine R. Mardis, Li Ding, Richard K. Wilson	3093
12	Somatic neurofibromatosis type 1 (NF1) inactivation characterizes NF1-associated pilocytic astrocytoma 2012 ·Genome Research ·David H. Gutmann, Michael D. McLellan, Ibrahim Hussain, John W. Wallis, Lucinda Fulton, Robert S. Fulton, Vincent Magrini, Ryan Demeter, Todd Wylie, Cyriac Kandoth, Jeffrey R. Leonard, Abhijit Guha, Christopher A. Miller, Jun Li, Elaine R. Mardis	90
13	Recurrent DNMT3A mutations in patients with myelodysplastic syndromes 2011 ·Leukemia ·Matthew J. Walter, Li Ding, Dong Shen, Jieya Shao, (unknown), Michael D. McLellan, Robert S. Fulton, H Schmidt, Joelle Kalicki-Veizer, Michele O’Laughlin, Cyriac Kandoth, Jack Baty, Peter Westervelt, John F. DiPersio, Elaine R. Mardis, Richard K. Wilson, T J Ley, Timothy A. Graubert	392
14	VarScan: variant detection in massively parallel sequencing of individual and pooled samples breakdown → 2009 ·Bioinformatics ·Daniel C. Koboldt, Ken Chen, Todd Wylie, David E. Larson, Michael D. McLellan, Elaine R. Mardis, George M. Weinstock, Richard K. Wilson, Li Ding	917
15	BreakDancer: an algorithm for high-resolution mapping of genomic structural variation breakdown → 2009 ·Nature Methods ·Ken Chen, John W. Wallis, Michael D. McLellan, David E. Larson, Joelle Kalicki, Craig Pohl, Sean McGrath, Michael C. Wendl, Qunyuan Zhang, Devin P. Locke, Xiaoqi Shi, Robert S. Fulton, Timothy J. Ley, Richard K. Wilson, Li Ding, Elaine R. Mardis	997
16	PolyScan: An automatic indel and SNP detection approach to the analysis of human resequencing data 2007 ·Genome Research ·Ken Chen, Michael D. McLellan, Li Ding, Michael C. Wendl, Yumi Kasai, Richard K. Wilson, Elaine R. Mardis	62
17	Mutational Analysis of EGFR and Related Signaling Pathway Genes in Lung Adenocarcinomas Identifies a Novel Somatic Kinase Domain Mutation in FGFR4 2007 ·PLoS ONE ·Jenifer L. Marks, Michael D. McLellan, Maureen F. Zakowski, Alex Lash, Yumi Kasai, Stephen Broderick, Inderpal S. Sarkaria, DuyKhanh Pham, Bhuvanesh Singh, Tracie L. Miner, Ginger Fewell, Lucinda Fulton, Elaine R. Mardis, Richard K. Wilson, Mark G. Kris, Valerie W. Rusch, Harold Varmus, William Pao	74
18	Low Frequency of Telomerase RNA Mutations Among Children With Aplastic Anemia or Myelodysplastic Syndrome 2006 ·Journal of Pediatric Hematology/Oncology ·Joshua J. Field, Philip J. Mason, Ping An, Yumi Kasai, Michael D. McLellan, Sara R. Jaeger, Yvonne Barnes, Allison A. King, Monica Bessler, David B. Wilson	18
19	ReducedPU.1expression causes myeloid progenitor expansion and increased leukemia penetrance in mice expressing PML-RARα 2005 ·Proceedings of the National Academy of Sciences ·Matthew J. Walter, John S. Park, Rhonda E. Ries, Steven Lau, Michael D. McLellan, Sara R. Jaeger, Richard K. Wilson, Elaine R. Mardis, Timothy J. Ley	70
20	Mutational Profiling in the Human Genome 2003 ·Cold Spring Harbor Symposia on Quantitative Biology ·Rebecca K. Wilson, Timothy J. Ley, F. Sessions Cole, Jeffrey Milbrandt, Sandra W. Clifton, Lucinda Fulton, Ginger Fewell, Patrick Minx, Hui Sun, Michael D. McLellan, Craig Pohl, Elaine R. Mardis	8

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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