|
1
|
Frequent pathway mutations of splicing machinery in myelodysplasia.
|
Nature
|
2011
|
11.44
|
|
2
|
Integrated molecular analysis of clear-cell renal cell carcinoma.
|
Nat Genet
|
2013
|
4.61
|
|
3
|
Somatic Mutations and Clonal Hematopoiesis in Aplastic Anemia.
|
N Engl J Med
|
2015
|
3.42
|
|
4
|
Recurrent mutations in multiple components of the cohesin complex in myeloid neoplasms.
|
Nat Genet
|
2013
|
2.14
|
|
5
|
Somatic SETBP1 mutations in myeloid malignancies.
|
Nat Genet
|
2013
|
2.12
|
|
6
|
Variant ALDH2 is associated with accelerated progression of bone marrow failure in Japanese Fanconi anemia patients.
|
Blood
|
2013
|
1.79
|
|
7
|
Exome sequencing identifies secondary mutations of SETBP1 and JAK3 in juvenile myelomonocytic leukemia.
|
Nat Genet
|
2013
|
1.71
|
|
8
|
ACTN1 mutations cause congenital macrothrombocytopenia.
|
Am J Hum Genet
|
2013
|
1.49
|
|
9
|
The landscape of somatic mutations in Down syndrome-related myeloid disorders.
|
Nat Genet
|
2013
|
1.31
|
|
10
|
BCOR and BCORL1 mutations in myelodysplastic syndromes and related disorders.
|
Blood
|
2013
|
1.16
|
|
11
|
ClipCrop: a tool for detecting structural variations with single-base resolution using soft-clipping information.
|
BMC Bioinformatics
|
2011
|
1.15
|
|
12
|
Deep sequencing reveals stepwise mutation acquisition in paroxysmal nocturnal hemoglobinuria.
|
J Clin Invest
|
2014
|
1.09
|
|
13
|
Integrated quantitative analysis of the phosphoproteome and transcriptome in tamoxifen-resistant breast cancer.
|
J Biol Chem
|
2010
|
0.98
|
|
14
|
Loss of function mutations in RPL27 and RPS27 identified by whole-exome sequencing in Diamond-Blackfan anaemia.
|
Br J Haematol
|
2014
|
0.88
|
|
15
|
Clonal leukemic evolution in myelodysplastic syndromes with TET2 and IDH1/2 mutations.
|
Haematologica
|
2013
|
0.87
|
|
16
|
Tracing the development of acute myeloid leukemia in CBL syndrome.
|
Blood
|
2014
|
0.78
|
|
17
|
Erratum: Whole-genome mutational landscape and characterization of noncoding and structural mutations in liver cancer.
|
Nat Genet
|
2016
|
0.77
|
|
18
|
Identification of a homozygous JAK3 V674A mutation caused by acquired uniparental disomy in a relapsed early T-cell precursor ALL patient.
|
Int J Hematol
|
2014
|
0.76
|
|
19
|
Clonal selection in xenografted TAM recapitulates the evolutionary process of myeloid leukemia in Down syndrome.
|
Blood
|
2013
|
0.76
|
|
20
|
Aggressive transformation of anaplastic large cell lymphoma with increased number of ALK-translocated chromosomes.
|
Int J Hematol
|
2014
|
0.75
|
|
21
|
OVarCall: Bayesian Mutation Calling Method Utilizing Overlapping Paired-End Reads.
|
IEEE Trans Nanobioscience
|
2017
|
0.75
|
|
22
|
Correction: Integrated Multiregional Analysis Proposing a New Model of Colorectal Cancer Evolution.
|
PLoS Genet
|
2017
|
0.75
|
|
23
|
A novel adaptive penalized logistic regression for uncovering biomarker associated with anti-cancer drug sensitivity.
|
IEEE/ACM Trans Comput Biol Bioinform
|
2016
|
0.75
|