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About
Michael S Lawrence
Author PubWeight™ 262.31
‹?›
Top papers
Rank
Title
Journal
Year
PubWeight™
‹?›
1
The landscape of somatic copy-number alteration across human cancers.
Nature
2010
31.88
2
Somatic mutations affect key pathways in lung adenocarcinoma.
Nature
2008
30.02
3
Initial genome sequencing and analysis of multiple myeloma.
Nature
2011
17.28
4
The mutational landscape of head and neck squamous cell carcinoma.
Science
2011
16.88
5
Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples.
Nat Biotechnol
2013
16.13
6
The genomic complexity of primary human prostate cancer.
Nature
2011
14.06
7
A landscape of driver mutations in melanoma.
Cell
2012
12.61
8
Mapping the hallmarks of lung adenocarcinoma with massively parallel sequencing.
Cell
2012
11.69
9
SF3B1 and other novel cancer genes in chronic lymphocytic leukemia.
N Engl J Med
2011
11.07
10
Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer.
Nat Genet
2012
9.93
11
Evolution and impact of subclonal mutations in chronic lymphocytic leukemia.
Cell
2013
9.24
12
Melanoma genome sequencing reveals frequent PREX2 mutations.
Nature
2012
7.77
13
Sequence analysis of mutations and translocations across breast cancer subtypes.
Nature
2012
7.76
14
Pan-cancer patterns of somatic copy number alteration.
Nat Genet
2013
7.73
15
Punctuated evolution of prostate cancer genomes.
Cell
2013
7.23
16
Discovery and prioritization of somatic mutations in diffuse large B-cell lymphoma (DLBCL) by whole-exome sequencing.
Proc Natl Acad Sci U S A
2012
7.14
17
Comprehensive, Integrative Genomic Analysis of Diffuse Lower-Grade Gliomas.
N Engl J Med
2015
5.71
18
Medulloblastoma exome sequencing uncovers subtype-specific somatic mutations.
Nature
2012
5.23
19
Mutations in the DDR2 kinase gene identify a novel therapeutic target in squamous cell lung cancer.
Cancer Discov
2011
4.80
20
The genetic landscape of high-risk neuroblastoma.
Nat Genet
2013
4.71
21
An APOBEC cytidine deaminase mutagenesis pattern is widespread in human cancers.
Nat Genet
2013
4.69
22
Exome and whole-genome sequencing of esophageal adenocarcinoma identifies recurrent driver events and mutational complexity.
Nat Genet
2013
4.48
23
Comprehensive identification of mutational cancer driver genes across 12 tumor types.
Sci Rep
2013
3.92
24
Functional analysis of receptor tyrosine kinase mutations in lung cancer identifies oncogenic extracellular domain mutations of ERBB2.
Proc Natl Acad Sci U S A
2012
3.06
25
A remarkably simple genome underlies highly malignant pediatric rhabdoid cancers.
J Clin Invest
2012
2.42
26
Experimental discovery of sRNAs in Vibrio cholerae by direct cloning, 5S/tRNA depletion and parallel sequencing.
Nucleic Acids Res
2009
2.25
27
Somatic rearrangements across cancer reveal classes of samples with distinct patterns of DNA breakage and rearrangement-induced hypermutability.
Genome Res
2012
1.82
28
Somatic mutation of CDKN1B in small intestine neuroendocrine tumors.
Nat Genet
2013
1.56
29
Oncotator: cancer variant annotation tool.
Hum Mutat
2015
1.52
30
Paired-end sequencing of Fosmid libraries by Illumina.
Genome Res
2012
1.52
31
Comprehensive analysis of cancer-associated somatic mutations in class I HLA genes.
Nat Biotechnol
2015
1.47
32
Identification of driver genes in hepatocellular carcinoma by exome sequencing.
Hepatology
2013
1.41
33
Integrative and comparative genomic analysis of lung squamous cell carcinomas in East Asian patients.
J Clin Oncol
2013
1.40
34
Genomic analysis of diffuse pediatric low-grade gliomas identifies recurrent oncogenic truncating rearrangements in the transcription factor MYBL1.
Proc Natl Acad Sci U S A
2013
1.33
35
Genomic Correlates of Immune-Cell Infiltrates in Colorectal Carcinoma.
Cell Rep
2016
0.96
36
Sporadic hemangioblastomas are characterized by cryptic VHL inactivation.
Acta Neuropathol Commun
2014
0.84
37
Colon cancer-derived oncogenic EGFR G724S mutant identified by whole genome sequence analysis is dependent on asymmetric dimerization and sensitive to cetuximab.
Mol Cancer
2014
0.80