Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
1
|
Mutations of the BRAF gene in human cancer.
|
Nature
|
2002
|
65.42
|
2
|
Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing.
|
Nat Genet
|
2008
|
43.63
|
3
|
COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer.
|
Nucleic Acids Res
|
2010
|
25.55
|
4
|
A comprehensive catalogue of somatic mutations from a human cancer genome.
|
Nature
|
2009
|
24.27
|
5
|
A small-cell lung cancer genome with complex signatures of tobacco exposure.
|
Nature
|
2009
|
18.39
|
6
|
Massive genomic rearrangement acquired in a single catastrophic event during cancer development.
|
Cell
|
2011
|
16.72
|
7
|
Systematic sequencing of renal carcinoma reveals inactivation of histone modifying genes.
|
Nature
|
2010
|
14.50
|
8
|
Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma.
|
Nature
|
2011
|
13.30
|
9
|
The patterns and dynamics of genomic instability in metastatic pancreatic cancer.
|
Nature
|
2010
|
12.43
|
10
|
The landscape of cancer genes and mutational processes in breast cancer.
|
Nature
|
2012
|
11.24
|
11
|
Mutational processes molding the genomes of 21 breast cancers.
|
Cell
|
2012
|
11.22
|
12
|
The life history of 21 breast cancers.
|
Cell
|
2012
|
10.59
|
13
|
Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer.
|
Nat Genet
|
2009
|
10.21
|
14
|
COSMIC (the Catalogue of Somatic Mutations in Cancer): a resource to investigate acquired mutations in human cancer.
|
Nucleic Acids Res
|
2009
|
9.59
|
15
|
A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation.
|
Nat Genet
|
2009
|
8.30
|
16
|
Somatic mutations of the protein kinase gene family in human lung cancer.
|
Cancer Res
|
2005
|
7.66
|
17
|
A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapy.
|
Cancer Res
|
2006
|
6.91
|
18
|
Architectures of somatic genomic rearrangement in human cancer amplicons at sequence-level resolution.
|
Genome Res
|
2007
|
6.91
|
19
|
A screen of the complete protein kinase gene family identifies diverse patterns of somatic mutations in human breast cancer.
|
Nat Genet
|
2005
|
6.70
|
20
|
Mutation analysis of 24 known cancer genes in the NCI-60 cell line set.
|
Mol Cancer Ther
|
2006
|
4.09
|
21
|
Data mining using the Catalogue of Somatic Mutations in Cancer BioMart.
|
Database (Oxford)
|
2011
|
2.84
|
22
|
Sequence analysis of the protein kinase gene family in human testicular germ-cell tumors of adolescents and adults.
|
Genes Chromosomes Cancer
|
2006
|
2.50
|
23
|
Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation.
|
Nat Genet
|
2007
|
2.35
|
24
|
Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremor.
|
Am J Hum Genet
|
2007
|
2.07
|
25
|
X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment.
|
Nat Genet
|
2008
|
1.95
|
26
|
Mutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardation.
|
Am J Hum Genet
|
2006
|
1.85
|
27
|
Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a Marfanoid habitus.
|
Am J Hum Genet
|
2007
|
1.73
|
28
|
Whole exome sequencing of adenoid cystic carcinoma.
|
J Clin Invest
|
2013
|
1.58
|
29
|
Frequent mutation of the major cartilage collagen gene COL2A1 in chondrosarcoma.
|
Nat Genet
|
2013
|
1.45
|
30
|
Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephaly.
|
Am J Hum Genet
|
2007
|
1.26
|
31
|
High throughput DNA sequence variant detection by conformation sensitive capillary electrophoresis and automated peak comparison.
|
Genomics
|
2006
|
1.08
|
32
|
Corrigendum: analysis of the genetic phylogeny of multifocal prostate cancer identifies multiple independent clonal expansions in neoplastic and morphologically normal prostate tissue.
|
Nat Genet
|
2015
|
0.79
|
33
|
Polygenic in vivo validation of cancer mutations using transposons.
|
Genome Biol
|
2014
|
0.75
|