Michael C. Wendl

85.0k total citations · 6 hit papers
55 papers, 14.0k citations indexed

About

Michael C. Wendl is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Michael C. Wendl has authored 55 papers receiving a total of 14.0k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 18 papers in Cancer Research and 12 papers in Genetics. Recurrent topics in Michael C. Wendl's work include Genomics and Phylogenetic Studies (23 papers), Cancer Genomics and Diagnostics (18 papers) and RNA and protein synthesis mechanisms (11 papers). Michael C. Wendl is often cited by papers focused on Genomics and Phylogenetic Studies (23 papers), Cancer Genomics and Diagnostics (18 papers) and RNA and protein synthesis mechanisms (11 papers). Michael C. Wendl collaborates with scholars based in United States, Canada and Australia. Michael C. Wendl's co-authors include LaDeana Hillier, Brent Ewing, Phil Green, Li Ding, Richard K. Wilson, Michael D. McLellan, Qunyuan Zhang, Mingchao Xie, Timothy J. Ley and Charles Lu and has published in prestigious journals such as Nature, Nature Medicine and Nature Communications.

In The Last Decade

Michael C. Wendl

53 papers receiving 13.7k 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.

Base-Calling of Automated Sequencer Traces UsingPhred. I. Accuracy Assessment

1998 5.7k citations Michael C. Wendl et al. Genome Research profile →
Mutational landscape and significance across 12 major cancer types

2013 3.1k citations Cyriac Kandoth, Michael D. McLellan et al. Nature profile →
Age-related mutations associated with clonal hematopoietic expansion and malignancies

2014 1.2k citations Mingchao Xie, Charles Lu et al. 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 →
Cancer exome analysis reveals a T-cell-dependent mechanism of cancer immunoediting

2012 932 citations Daniel C. Koboldt, Michael C. Wendl et al. Nature profile →
MSIsensor: microsatellite instability detection using paired tumor-normal sequence data

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

Peers

Countries citing papers authored by Michael C. Wendl

Since Specialization

Citations

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

Fields of papers citing papers by Michael C. Wendl

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michael C. Wendl

This figure shows the co-authorship network connecting the top 25 collaborators of Michael C. Wendl. A scholar is included among the top collaborators of Michael C. Wendl 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 C. Wendl. Michael C. Wendl 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	Pollock: fishing for cell states 2022 ·Bioinformatics Advances ·Erik Storrs, Daniel Cui Zhou, Michael C. Wendl, Matthew A. Wyczalkowski, Alla Karpova, Liang-Bo Wang, Yize Li, Austin N. Southard-Smith, Reyka G. Jayasinghe, Lijun Yao, Ruiyang Liu, Yige Wu, Nadezhda V. Terekhanova, Houxiang Zhu, John M. Herndon, (unknown), Feng Chen, William E. Gillanders, Ryan C. Fields, Li Ding	2
2	Moving pan-cancer studies from basic research toward the clinic 2021 ·Nature Cancer ·Feng Chen, Michael C. Wendl, Matthew A. Wyczalkowski, Matthew H. Bailey, Yize Li, Li Ding	57
3	Spatially interacting phosphorylation sites and mutations in cancer 2021 ·Nature Communications ·Kuan‐lin Huang, Adam Scott, Daniel Cui Zhou, Liang-Bo Wang, Amila Weerasinghe, (unknown), Ruiyang Liu, Yige Wu, Michael C. Wendl, Matthew A. Wyczalkowski, Jessika Baral, Sohini Sengupta, Chin‐Wen Lai, Kelly V. Ruggles, Samuel Payne, Benjamin J. Raphael, David Fenyö, Ken Chen, Gordon B. Mills, Li Ding	13
4	Discovery of driver non-coding splice-site-creating mutations in cancer 2020 ·Nature Communications ·Song Cao, Daniel Cui Zhou, Clara Oh, Reyka G. Jayasinghe, Yanyan Zhao, Christopher J. Yoon, Matthew A. Wyczalkowski, Matthew H. Bailey, (unknown), Qingsong Gao, Andrew F. Malone, Sheila M. Reynolds, Ilya Shmulevich, Michael C. Wendl, Feng Chen, Li Ding	19
5	Integrated transcriptomic–genomic tool Texomer profiles cancer tissues 2019 ·Nature Methods ·Fang Wang, Shaojun Zhang, Tae-Beom Kim, (unknown), Ramiz Iqbal, Zixing Wang, Vakul Mohanty, Kanishka Sircar, José A. Karam, Michael C. Wendl, Funda Meric‐Bernstam, John N. Weinstein, Li Ding, Gordon B. Mills, Ken Chen	6
6	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
7	Divergent viral presentation among human tumors and adjacent normal tissues 2016 ·Scientific Reports ·Song Cao, Michael C. Wendl, Matthew A. Wyczalkowski, Kristine M. Wylie, Kai Ye, Reyka G. Jayasinghe, Mingchao Xie, Song Wu, Beifang Niu, Robert L. Grubb, Kimberly Johnson, Hiram A. Gay, Ken Chen, Janet S. Rader, John F. DiPersio, Feng Chen, Li Ding	51
8	Expanding the computational toolbox for mining cancer genomes 2014 ·Nature Reviews Genetics ·Li Ding, Michael C. Wendl, Joshua F. McMichael, Benjamin J. Raphael	129
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	MuSiC: Identifying mutational significance in cancer genomes 2012 ·Genome Research ·Nathan D. Dees, Qunyuan Zhang, Cyriac Kandoth, Michael C. Wendl, William Schierding, Daniel C. Koboldt, Thomas B. Mooney, (unknown), David J. Dooling, Elaine R. Mardis, Richard K. Wilson, Li Ding	420
11	Coverage theories for metagenomic DNA sequencing based on a generalization of Stevens’ theorem 2012 ·Journal of Mathematical Biology ·Michael C. Wendl, Karthik Kota, George M. Weinstock, Makedonka Mitreva	20
12	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
13	The theory of discovering rare variants via DNA sequencing 2009 ·BMC Genomics ·Michael C. Wendl, Richard K. Wilson	11
14	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
15	Design and implementation of a generalized laboratory data model 2007 ·BMC Bioinformatics ·Michael C. Wendl, Scott M. Smith, Craig Pohl, David J. Dooling, Asif Chinwalla, Kevin Crouse, (unknown), (unknown), Lynn K. Carmichael, (unknown), (unknown), Elaine R. Mardis, LaDeana W. Hillier, Richard K. Wilson	8
16	Algebraic correction methods for computational assessment of clone overlaps in DNA fingerprint mapping 2007 ·BMC Bioinformatics ·Michael C. Wendl	3
17	Generalized Gap Model for Bacterial Artificial Chromosome Clone Fingerprint Mapping and Shotgun Sequencing 2002 ·Genome Research ·Michael C. Wendl, R Waterston	20
18	Automated processing of raw DNA sequence data 2001 ·IEEE Engineering in Medicine and Biology Magazine ·Michael C. Wendl, Ian Korf, Asif Chinwalla, LaDeana W. Hillier	2
19	General solution for the Couette flow profile 1999 ·Physical review. E, Statistical physics, plasmas, fluids, and related interdisciplinary topics ·Michael C. Wendl	23
20	a Pressure-Based Finite-Volume Time-Stepping Algorithm for the Numerical Simulation of Incompressible Flows 1994 ·PhDT ·Michael C. Wendl	0

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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