PubRank

Sarah O'Meara

Author PubWeight™ 191.07‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing. Nat Genet 2008 43.63
2 Patterns of somatic mutation in human cancer genomes. Nature 2007 38.41
3 A small-cell lung cancer genome with complex signatures of tobacco exposure. Nature 2009 18.39
4 Systematic sequencing of renal carcinoma reveals inactivation of histone modifying genes. Nature 2010 14.50
5 Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer. Nat Genet 2009 10.21
6 Lung cancer: intragenic ERBB2 kinase mutations in tumours. Nature 2004 8.35
7 A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation. Nat Genet 2009 8.30
8 Somatic mutations of the protein kinase gene family in human lung cancer. Cancer Res 2005 7.66
9 A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapy. Cancer Res 2006 6.91
10 A screen of the complete protein kinase gene family identifies diverse patterns of somatic mutations in human breast cancer. Nat Genet 2005 6.70
11 Clinical and biological implications of driver mutations in myelodysplastic syndromes. Blood 2013 6.50
12 Mutation analysis of 24 known cancer genes in the NCI-60 cell line set. Mol Cancer Ther 2006 4.09
13 Recurrent KRAS codon 146 mutations in human colorectal cancer. Cancer Biol Ther 2006 3.56
14 Sequence analysis of the protein kinase gene family in human testicular germ-cell tumors of adolescents and adults. Genes Chromosomes Cancer 2006 2.50
15 Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation. Nat Genet 2007 2.35
16 Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus. Nat Genet 2006 2.08
17 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
18 Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardation. Am J Hum Genet 2004 2.04
19 X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment. Nat Genet 2008 1.95
20 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
21 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
22 Whole exome sequencing of adenoid cystic carcinoma. J Clin Invest 2013 1.58
23 The genetic heterogeneity and mutational burden of engineered melanomas in zebrafish models. Genome Biol 2013 1.54
24 Frequent mutation of the major cartilage collagen gene COL2A1 in chondrosarcoma. Nat Genet 2013 1.45
25 Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephaly. Am J Hum Genet 2007 1.26
26 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
27 Polygenic in vivo validation of cancer mutations using transposons. Genome Biol 2014 0.75
28 At the very heart of progress. Nature 2015 0.75
29 China's plan to cut coal and boost green growth. Nature 2020 0.75
30 The engineer making energy storage more efficient. Nature 2020 0.75