Andrew Menzies

Author PubWeight™ 330.86‹?›

Top papers

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