1
|
Identification of in vivo expressed vaccine candidate antigens from Staphylococcus aureus.
|
Proc Natl Acad Sci U S A
|
2002
|
1.75
|
2
|
Loss-of-function variant in DNASE1L3 causes a familial form of systemic lupus erythematosus.
|
Nat Genet
|
2011
|
1.57
|
3
|
Molecular characterization of retinitis pigmentosa in Saudi Arabia.
|
Mol Vis
|
2009
|
1.18
|
4
|
Mutations in C2orf37, encoding a nucleolar protein, cause hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome.
|
Am J Hum Genet
|
2008
|
1.05
|
5
|
Molecular signatures mostly associated with NK cells are predictive of relapse free survival in breast cancer patients.
|
J Transl Med
|
2013
|
1.03
|
6
|
A study of the role of the Myocyte-specific Enhancer Factor-2A gene in coronary artery disease.
|
Atherosclerosis
|
2009
|
0.90
|
7
|
Haplotypes encompassing the KIAA0391 and PSMA6 gene cluster confer a genetic link for myocardial infarction and coronary artery disease.
|
Ann Hum Genet
|
2009
|
0.79
|
8
|
Expression biomarkers for clinical efficacy and outcome prediction in cancer.
|
Pharmacogenomics
|
2006
|
0.77
|
9
|
Characterization of H5N1 influenza A virus that caused the first highly pathogenic avian influenza outbreak in Saudi Arabia.
|
J Infect Dev Ctries
|
2015
|
0.75
|