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1
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Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia.
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Science
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2008
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20.68
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2
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Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing.
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Proc Natl Acad Sci U S A
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2010
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5.60
|
|
3
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Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing.
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Proc Natl Acad Sci U S A
|
2011
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3.99
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4
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A public gene trap resource for mouse functional genomics.
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Nat Genet
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2004
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3.96
|
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5
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A high-resolution enhancer atlas of the developing telencephalon.
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Cell
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2013
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2.34
|
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6
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Fine tuning of craniofacial morphology by distant-acting enhancers.
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Science
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2013
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2.16
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7
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ColoSeq provides comprehensive lynch and polyposis syndrome mutational analysis using massively parallel sequencing.
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J Mol Diagn
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2012
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1.99
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8
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Perioperative stroke in infants undergoing open heart operations for congenital heart disease.
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Ann Thorac Surg
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2009
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1.82
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9
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Patient characteristics are important determinants of neurodevelopmental outcome at one year of age after neonatal and infant cardiac surgery.
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J Thorac Cardiovasc Surg
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2007
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1.71
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10
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Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families.
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Eur J Hum Genet
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2009
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1.67
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11
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Neurodevelopmental outcomes after staged palliation for hypoplastic left heart syndrome.
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Pediatrics
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2008
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1.55
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12
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Genome-wide association study of plasma lipoprotein(a) levels identifies multiple genes on chromosome 6q.
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J Lipid Res
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2009
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1.34
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13
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Polymorphisms of the IL1-receptor antagonist gene (IL1RN) are associated with multiple markers of systemic inflammation.
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Arterioscler Thromb Vasc Biol
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2008
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1.32
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14
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Genomic duplication and overexpression of TJP2/ZO-2 leads to altered expression of apoptosis genes in progressive nonsyndromic hearing loss DFNA51.
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Am J Hum Genet
|
2010
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1.31
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15
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Apolipoprotein E genotype modifies the risk of behavior problems after infant cardiac surgery.
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Pediatrics
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2009
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1.30
|
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16
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Is cardiac diagnosis a predictor of neurodevelopmental outcome after cardiac surgery in infancy?
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J Thorac Cardiovasc Surg
|
2010
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1.24
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17
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Predictors of impaired neurodevelopmental outcomes at one year of age after infant cardiac surgery.
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Eur J Cardiothorac Surg
|
2009
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1.17
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18
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Formation of chimeric genes by copy-number variation as a mutational mechanism in schizophrenia.
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Am J Hum Genet
|
2013
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1.10
|
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19
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Genetic factors are important determinants of neurodevelopmental outcome after repair of tetralogy of Fallot.
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J Thorac Cardiovasc Surg
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2008
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1.10
|
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20
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A common VLDLR polymorphism interacts with APOE genotype in the prediction of carotid artery disease risk.
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J Lipid Res
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2007
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0.99
|
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21
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Targeted capture and sequencing for detection of mutations causing early onset epileptic encephalopathy.
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Epilepsia
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2013
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0.96
|
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22
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TagSNP evaluation for the association of 42 inflammation loci and vascular disease: evidence of IL6, FGB, ALOX5, NFKBIA, and IL4R loci effects.
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Hum Genet
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2006
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0.95
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23
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Genetic variation in LPAL2, LPA, and PLG predicts plasma lipoprotein(a) level and carotid artery disease risk.
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Stroke
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2010
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0.92
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24
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Congenital heart defects in patients with deletions upstream of SOX9.
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Hum Mutat
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2013
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0.87
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25
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Comparison of tagging single-nucleotide polymorphism methods in association analyses.
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BMC Proc
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2007
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0.84
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