1
|
Mutations of the BRAF gene in human cancer.
|
Nature
|
2002
|
65.42
|
2
|
Patterns of somatic mutation in human cancer genomes.
|
Nature
|
2007
|
38.41
|
3
|
Lung cancer: intragenic ERBB2 kinase mutations in tumours.
|
Nature
|
2004
|
8.35
|
4
|
Somatic mutations of the protein kinase gene family in human lung cancer.
|
Cancer Res
|
2005
|
7.66
|
5
|
A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapy.
|
Cancer Res
|
2006
|
6.91
|
6
|
A screen of the complete protein kinase gene family identifies diverse patterns of somatic mutations in human breast cancer.
|
Nat Genet
|
2005
|
6.70
|
7
|
Chromosomally unstable mouse tumours have genomic alterations similar to diverse human cancers.
|
Nature
|
2007
|
5.65
|
8
|
Mutation analysis of 24 known cancer genes in the NCI-60 cell line set.
|
Mol Cancer Ther
|
2006
|
4.09
|
9
|
Recurrent KRAS codon 146 mutations in human colorectal cancer.
|
Cancer Biol Ther
|
2006
|
3.56
|
10
|
Sequence analysis of the protein kinase gene family in human testicular germ-cell tumors of adolescents and adults.
|
Genes Chromosomes Cancer
|
2006
|
2.50
|
11
|
Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation.
|
Nat Genet
|
2007
|
2.35
|
12
|
Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus.
|
Nat Genet
|
2006
|
2.08
|
13
|
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
|
14
|
Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardation.
|
Am J Hum Genet
|
2004
|
2.04
|
15
|
X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment.
|
Nat Genet
|
2008
|
1.95
|
16
|
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
|
17
|
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
|
18
|
Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephaly.
|
Am J Hum Genet
|
2007
|
1.26
|
19
|
High throughput DNA sequence variant detection by conformation sensitive capillary electrophoresis and automated peak comparison.
|
Genomics
|
2006
|
1.08
|
20
|
Abacavir hypersensitivity reaction in primary HIV infection.
|
AIDS
|
2006
|
0.80
|
21
|
WORKING TOGETHER TO DELIVER JOINED-UP CARE FOR OUR YOUNG PATIENTS.
|
Prim Dent J
|
2015
|
0.75
|
22
|
Ectodermal Dysplasia: A Clinical Overview for the Dental Practitioner.
|
Dent Update
|
2015
|
0.75
|