Michael Christopher Wendl
#57,641
Most Influential Person Now
American mathematician and biomedical engineer
Michael Christopher Wendl's AcademicInfluence.com Rankings
Michael Christopher Wendlengineering Degrees
Engineering
#3208
World Rank
#4248
Historical Rank
#948
USA Rank
Biomedical Engineering
#814
World Rank
#826
Historical Rank
#59
USA Rank
Michael Christopher Wendlmathematics Degrees
Mathematics
#5429
World Rank
#7640
Historical Rank
#1782
USA Rank
Applied Mathematics
#304
World Rank
#329
Historical Rank
#73
USA Rank
Measure Theory
#2789
World Rank
#3327
Historical Rank
#806
USA Rank
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Engineering Mathematics
Michael Christopher Wendl's Degrees
- Bachelors Mathematics Stanford University
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Why Is Michael Christopher Wendl Influential?
(Suggest an Edit or Addition)According to Wikipedia, Michael Christopher Wendl is a mathematician and biomedical engineer who has worked on DNA sequencing theory, covering and matching problems in probability, theoretical fluid mechanics, and co-wrote Phred. He was a scientist on the Human Genome Project and has done bioinformatics and biostatistics work in cancer. Wendl is of ethnic German heritage and is the son of the aerospace engineer Michael J. Wendl.
Michael Christopher Wendl's Published Works
Published Works
- Initial sequencing and analysis of the human genome. (2001) (15222)
- Base-calling of automated sequencer traces using phred. I. Accuracy assessment. (1998) (7790)
- An integrated map of genetic variation from 1,092 human genomes (2012) (7565)
- Integrated Genomic Analyses of Ovarian Carcinoma (2011) (6411)
- Comprehensive genomic characterization defines human glioblastoma genes and core pathways (2008) (5775)
- Initial sequencing and comparative analysis of the mouse genome. (2002) (4609)
- Comprehensive molecular profiling of lung adenocarcinoma (2014) (4095)
- Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia. (2013) (3821)
- Mutational landscape and significance across 12 major cancer types (2013) (3589)
- Somatic mutations affect key pathways in lung adenocarcinoma (2008) (2640)
- Initial sequence of the chimpanzee genome and comparison with the human genome (2005) (2222)
- Clonal evolution in relapsed acute myeloid leukemia revealed by whole genome sequencing (2011) (1935)
- BreakDancer: An algorithm for high resolution mapping of genomic structural variation (2009) (1381)
- Comprehensive Characterization of Cancer Driver Genes and Mutations (2018) (1360)
- Genome Remodeling in a Basal-like Breast Cancer Metastasis and Xenograft (2010) (1171)
- Cancer Exome Analysis Reveals a T Cell Dependent Mechanism of Cancer Immunoediting (2012) (1076)
- Age-related cancer mutations associated with clonal hematopoietic expansion (2014) (1053)
- Whole Genome Analysis Informs Breast Cancer Response to Aromatase Inhibition (2012) (998)
- MuSiC: Identifying mutational significance in cancer genomes (2012) (593)
- Pathogenic Germline Variants in 10,389 Adult Cancers (2018) (501)
- MSIsensor: microsatellite instability detection using paired tumor-normal sequence data (2014) (459)
- The DNA sequence of human chromosome 7 (2003) (425)
- Patterns of somatic structural variation in human cancer genomes (2020) (377)
- Comprehensive Characterization of Cancer Driver Genes and Mutations (2018) (340)
- Driver Fusions and Their Implications in the Development and Treatment of Human Cancers (2018) (332)
- Integrated Analysis of Germline and Somatic Variants in Ovarian Cancer (2014) (259)
- Perspective on Oncogenic Processes at the End of the Beginning of Cancer Genomics (2018) (234)
- The Human Tumor Atlas Network: Charting Tumor Transitions across Space and Time at Single-Cell Resolution (2020) (234)
- Patterns and functional implications of rare germline variants across 12 cancer types (2015) (222)
- Comprehensive molecular characterization of mitochondrial genomes in human cancers (2017) (197)
- Background mutations in parental cells account for most of the genetic heterogeneity of induced pluripotent stem cells. (2012) (195)
- Expanding the computational toolbox for mining cancer genomes (2014) (181)
- Optimizing cancer genome sequencing and analysis. (2015) (179)
- Proteogenomic and metabolomic characterization of human glioblastoma. (2021) (176)
- Analysis of next-generation genomic data in cancer: accomplishments and challenges. (2010) (157)
- Systematic Analysis of Splice-Site-Creating Mutations in Cancer (2018) (156)
- Protein-structure-guided discovery of functional mutations across 19 cancer types (2016) (118)
- Proteogenomic insights into the biology and treatment of HPV-negative head and neck squamous cell carcinoma. (2021) (118)
- Characteristics of de novo structural changes in the human genome (2015) (113)
- Proteogenomic integration reveals therapeutic targets in breast cancer xenografts (2017) (108)
- Erratum: Initial sequencing and analysis of the human genome: International Human Genome Sequencing Consortium (Nature (2001) 409 (860-921)) (2001) (106)
- H-index: however ranked, citations need context (2007) (103)
- Generation and annotation of the DNA sequences of human chromosomes 2 and 4 (2005) (98)
- Tumor Evolution in Two Patients with Basal-like Breast Cancer: A Retrospective Genomics Study of Multiple Metastases (2016) (92)
- PathScan: a tool for discerning mutational significance in groups of putative cancer genes (2011) (87)
- PolyScan: an automatic indel and SNP detection approach to the analysis of human resequencing data. (2007) (80)
- Clonal Architectures and Driver Mutations in Metastatic Melanomas (2014) (72)
- Advances for studying clonal evolution in cancer. (2013) (70)
- Divergent viral presentation among human tumors and adjacent normal tissues (2016) (58)
- Codon usage patterns in Nematoda: analysis based on over 25 million codons in thirty-two species (2006) (55)
- Systematic Discovery of Complex Indels in Human Cancers (2015) (50)
- Sex differences in oncogenic mutational processes (2019) (41)
- Co-evolution of tumor and immune cells during progression of multiple myeloma (2021) (38)
- General solution for the Couette flow profile. (1999) (35)
- Comprehensive characterization of 536 patient-derived xenograft models prioritizes candidates for targeted treatment (2021) (33)
- Aspects of coverage in medical DNA sequencing (2008) (33)
- Automated sequence preprocessing in a large-scale sequencing environment. (1998) (31)
- Coverage theories for metagenomic DNA sequencing based on a generalization of Stevens’ theorem (2012) (31)
- Generalized gap model for bacterial artificial chromosome clone fingerprint mapping and shotgun sequencing. (2002) (29)
- Collision probability between sets of random variables (2003) (25)
- Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples (2020) (22)
- MITI minimum information guidelines for highly multiplexed tissue images (2021) (22)
- Modeling of jet-induced geyser formation in a reduced gravity environment (1991) (20)
- Extension of Lander-Waterman theory for sequencing filtered DNA libraries (2005) (20)
- Spatially restricted drivers and transitional cell populations cooperate with the microenvironment in untreated and chemo-resistant pancreatic cancer (2022) (20)
- A General Coverage Theory for Shotgun DNA Sequencing (2006) (19)
- Theories and applications for sequencing randomly selected clones. (2001) (18)
- Gap statistics for whole genome shotgun DNA sequencing projects (2004) (18)
- Discovery of driver non-coding splice-site-creating mutations in cancer (2020) (17)
- GenomeVIP: a cloud platform for genomic variant discovery and interpretation (2017) (17)
- Moving pan-cancer studies from basic research toward the clinic (2021) (16)
- Computational modeling of the pressurization process in a NASP vehicle propellant tank experimental simulation (1991) (15)
- Integrative omics analyses broaden treatment targets in human cancer (2018) (14)
- Occupancy Modeling of Coverage Distribution for Whole Genome Shotgun Dna Sequencing (2006) (14)
- Open-source answer to bibliography problem (2003) (14)
- The theory of discovering rare variants via DNA sequencing (2009) (13)
- Consortium, G.P A map of human genome variation from population-scale sequencing. Nature 467, 1061-1073 (2010) (13)
- Protein-structure-guided discovery of functional mutations across 19 cancer types (2016) (13)
- Conservation of copy number profiles during engraftment and passaging of patient-derived cancer xenografts (2021) (12)
- Design and implementation of a generalized laboratory data model (2007) (12)
- MSIsensor-ct: microsatellite instability detection using cfDNA sequencing data (2021) (12)
- Statistical aspects of discerning indel-type structural variation via DNA sequence alignment (2009) (11)
- Pseudonymous fame. (2016) (10)
- Probabilistic Assessment of Clone Overlaps in DNA Fingerprint Mapping via a Priori Models (2005) (10)
- Spatial drivers and pre-cancer populations collaborate with the microenvironment in untreated and chemo-resistant pancreatic cancer (2021) (9)
- Spatially interacting phosphorylation sites and mutations in cancer (2021) (9)
- Integrated transcriptomic–genomic tool Texomer profiles cancer tissues (2019) (8)
- Regulated Phosphosignaling Associated with Breast Cancer Subtypes and Druggability* (2019) (8)
- Correction: Tumor Evolution in Two Patients with Basal-like Breast Cancer: A Retrospective Genomics Study of Multiple Metastases (2017) (7)
- Corrigendum: Proteogenomic integration reveals therapeutic targets in breast cancer xenografts (2017) (6)
- Automated processing of raw DNA sequence data (2001) (5)
- Mass conservation and the accuracy of non–staggered grid incompressible flow schemes (2003) (4)
- BreakPoint Surveyor: a pipeline for structural variant visualization (2017) (4)
- Regulated Phosphosignaling Associated with Breast Cancer Subtypes and Druggability. (2019) (3)
- PDXNet portal: patient-derived Xenograft model, data, workflow and tool discovery (2022) (3)
- Random Covering of Multiple One-Dimensional Domains with an Application to DNA Sequencing (2008) (3)
- Differences that matter in cancer genomics (2013) (3)
- Histopathologic and proteogenomic heterogeneity reveals features of clear cell renal cell carcinoma aggressiveness. (2022) (3)
- Bioweapons could kill more in one strike than guns (2005) (2)
- A method for obtaining benchmark Navier-Stokes solutions (1999) (2)
- Author Correction: Conservation of copy number profiles during engraftment and passaging of patient-derived cancer xenografts (2021) (2)
- Algebraic correction methods for computational assessment of clone overlaps in DNA fingerprint mapping (2007) (2)
- NIH SenNet Consortium to map senescent cells throughout the human lifespan to understand physiological health. (2022) (2)
- Sequencing an Acute Myeloid Leukemia (AML) Genome with “Next Generation” Technologies. (2007) (1)
- Comprehensive Characterization of the Multiple Myeloma Immune Microenvironment Using Integrated scRNA-seq, CyTOF, and CITE-seq Analysis (2022) (1)
- Author Correction: Pan-cancer analysis of whole genomes (2023) (1)
- Abstract 61: Sequence and structure-guided approach to identify functional mutations in G-protein coupled receptors (2015) (1)
- Mathematical analysis of coaxial disk cellular shear loading devices (2001) (1)
- AeQTL: eQTL analysis using region-based aggregation of rare genomic variants (2020) (1)
- Viscous Dissipation in Finite Thin-Gap Couette Devices (2002) (1)
- Erratum: Differences that matter in cancer genomics (2013) (1)
- Author Correction: The evolutionary history of 2,658 cancers (2023) (0)
- Couette Flow Profiles for Two Nonclassical Taylor-Couette Cells (2000) (0)
- Integrated transcriptomic–genomic tool Texomer profiles cancer tissues (2019) (0)
- Abstract 419: Reproducibility assessment of mutations calls in exome- and whole-genome sequencing using consensus calling from TCGA and ICGC (2018) (0)
- Driver Fusions and Their I mplications in the Development and Treatment of Human Cancers Graphical (2018) (0)
- Abstract B11: The MuSiC2 system for discovery and visualization of coding and noncoding cancer drivers (2018) (0)
- Class Notes for ME 371) (2005) (0)
- Residual dilation and the accuracy of non-staggered grid incompressible flow schemes (1999) (0)
- Units: Don't tamper with SI-unit consistency (2017) (0)
- Author Correction: Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples (2020) (0)
- Myeloma Cell Associated Therapeutic Protein Discovery Using Single Cell RNA-Seq Data (2020) (0)
- Abstract LB-239: Mutational and clonal analyses across TCGA cancer types using the MuSiC suite of tools. (2013) (0)
- Coverage theories for metagenomic DNA sequencing based on a generalization of Stevens’ theorem (2012) (0)
- Abstract 2362: Comprehensive portrait of canonical and non-canonical splicing in cancer (2018) (0)
- Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis (2017) (0)
- Author Correction: Patterns of somatic structural variation in human cancer genomes (2020) (0)
- The question of forbidden knowledge. (2005) (0)
- Technology takes on deadlines for fetal human rights (2009) (0)
- Uncovering Clonal and Subclonal Druggable Targets in Multiple Myeloma Using Omic Data (2016) (0)
- Abstract 2357: Utilizing biological and protein structure-guided features to improve driver mutation discovery (2018) (0)
- Abstract 1306: Density-based mutation clustering in 3D space (2018) (0)
- Abstract LB-423: Whole genome comparisons of pre- and post- aromatase inhibitor treatment in estrogen receptor positive breast cancer (2012) (0)
- Author Correction: Comprehensive characterization of 536 patient-derived xenograft models prioritizes candidates for targeted treatment (2022) (0)
- Abstract 1929: Pan-Cancer analysis of the effects of splice-altering variants on mRNA splicing and stability (2015) (0)
- Abstract 1932: Pollock: Fishing for cell states (2022) (0)
- Integrative omics analyses broaden treatment targets in human cancer (2018) (0)
- Author Correction: Inferring structural variant cancer cell fraction (2022) (0)
- Abstract 1939: Discovery and proteogenomic investigation of genetic variants in human cancers (2015) (0)
- Abstract 845: Pan-cancer proteogenomic signatures associated with HRD, MSI, APOBEC, and smoking (2022) (0)
- THE MOUSE GENOME SEQUENCING PROJECT: AN OVERVIEW (2005) (0)
- Epigenetic and transcriptomic characterization reveals progression markers and essential pathways in clear cell renal cell carcinoma (2023) (0)
- Abstract 4106: Curating protein complexes from multiple resources and validate their co-regulations at RNA/protein level in pan-cancer (2022) (0)
- Single-Cell Discovery and Multiomic Characterization of Therapeutic Targets in Multiple Myeloma (2023) (0)
- Pollock: fishing for cell states (2022) (0)
- Author Correction: Comprehensive characterization of 536 patient-derived xenograft models prioritizes candidates for targeted treatment (2022) (0)
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