PubRank

Alex S Nord

Author PubWeight™ 60.29‹?›

Top papers

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