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1
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Risk alleles for multiple sclerosis identified by a genomewide study.
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N Engl J Med
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2007
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17.06
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2
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The DNA sequence of the human X chromosome.
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Nature
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2005
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6.97
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|
3
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A high-density screen for linkage in multiple sclerosis.
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Am J Hum Genet
|
2005
|
2.50
|
|
4
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SNPselector: a web tool for selecting SNPs for genetic association studies.
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Bioinformatics
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2005
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2.14
|
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5
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Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9p.
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Am J Hum Genet
|
2009
|
2.14
|
|
6
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A second major histocompatibility complex susceptibility locus for multiple sclerosis.
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Ann Neurol
|
2007
|
1.99
|
|
7
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Integrated genomic analyses identify ERRFI1 and TACC3 as glioblastoma-targeted genes.
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Oncotarget
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2010
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1.88
|
|
8
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Definition and characterization of a region of 1p36.3 consistently deleted in neuroblastoma.
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Oncogene
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2005
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1.86
|
|
9
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A stress response pathway regulates DNA damage through β2-adrenoreceptors and β-arrestin-1.
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Nature
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2011
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1.64
|
|
10
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Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease.
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Am J Hum Genet
|
2007
|
1.55
|
|
11
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A candidate gene for congenital bilateral isolated ptosis identified by molecular analysis of a de novo balanced translocation.
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Hum Genet
|
2002
|
1.41
|
|
12
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GATA2 is associated with familial early-onset coronary artery disease.
|
PLoS Genet
|
2006
|
1.32
|
|
13
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Replication of TCF4 through association and linkage studies in late-onset Fuchs endothelial corneal dystrophy.
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PLoS One
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2011
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1.30
|
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14
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Enhancing linkage analysis of complex disorders: an evaluation of high-density genotyping.
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Hum Mol Genet
|
2004
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1.29
|
|
15
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Comprehensive genetic analysis of the platelet activating factor acetylhydrolase (PLA2G7) gene and cardiovascular disease in case-control and family datasets.
|
Hum Mol Genet
|
2008
|
1.21
|
|
16
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Neuropeptide Y gene polymorphisms confer risk of early-onset atherosclerosis.
|
PLoS Genet
|
2009
|
1.20
|
|
17
|
Fine structure mapping of CIAS1: identification of an ancestral haplotype and a common FCAS mutation, L353P.
|
Hum Genet
|
2002
|
1.07
|
|
18
|
Genetic effects in the leukotriene biosynthesis pathway and association with atherosclerosis.
|
Hum Genet
|
2009
|
1.04
|
|
19
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Clinical, radiological, and genetic similarities between patients with Chiari Type I and Type 0 malformations.
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J Neurosurg Pediatr
|
2012
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1.04
|
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20
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Alternative splicing in multiple sclerosis and other autoimmune diseases.
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RNA Biol
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2010
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1.02
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21
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Genetic and functional association of FAM5C with myocardial infarction.
|
BMC Med Genet
|
2008
|
0.96
|
|
22
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Aging-related atherosclerosis is exacerbated by arterial expression of tumor necrosis factor receptor-1: evidence from mouse models and human association studies.
|
Hum Mol Genet
|
2010
|
0.92
|
|
23
|
Fine mapping of a linkage peak with integration of lipid traits identifies novel coronary artery disease genes on chromosome 5.
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BMC Genet
|
2012
|
0.92
|
|
24
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Association of mtDNA haplogroup F with healthy longevity in the female Chuang population, China.
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Exp Gerontol
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2011
|
0.91
|
|
25
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Comprehensive DNA copy number profiling of meningioma using a chromosome 1 tiling path microarray identifies novel candidate tumor suppressor loci.
|
Cancer Res
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2005
|
0.91
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|
26
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Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease.
|
Hum Genet
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2011
|
0.91
|
|
27
|
The kinetics of urinary fumonisin B1 excretion in humans consuming maize-based diets.
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Mol Nutr Food Res
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2012
|
0.90
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28
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HDMX regulates p53 activity and confers chemoresistance to 3-bis(2-chloroethyl)-1-nitrosourea.
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Neuro Oncol
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2010
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0.89
|
|
29
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SNPs in Multi-species Conserved Sequences (MCS) as useful markers in association studies: a practical approach.
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BMC Genomics
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2007
|
0.89
|
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30
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The S1103Y cardiac sodium channel variant is associated with implantable cardioverter-defibrillator events in blacks with heart failure and reduced ejection fraction.
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Circ Cardiovasc Genet
|
2011
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0.89
|
|
31
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Gene-smoking interactions in multiple Rho-GTPase pathway genes in an early-onset coronary artery disease cohort.
|
Hum Genet
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2013
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0.88
|
|
32
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Distinct patterns of 1p and 19q alterations identify subtypes of human gliomas that have different prognoses.
|
Neuro Oncol
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2010
|
0.86
|
|
33
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Genome-wide linkage analysis of quantitative biomarker traits of osteoarthritis in a large, multigenerational extended family.
|
Arthritis Rheum
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2010
|
0.85
|
|
34
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Genetic evaluation and application of posterior cranial fossa traits as endophenotypes for Chiari type I malformation.
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Ann Hum Genet
|
2013
|
0.85
|
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35
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Epigenetic regulation of COL15A1 in smooth muscle cell replicative aging and atherosclerosis.
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Hum Mol Genet
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2013
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0.84
|
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36
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Urinary fumonisin B1 and estimated fumonisin intake in women from high- and low-exposure communities in Guatemala.
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Mol Nutr Food Res
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2013
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0.83
|
|
37
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Stratified whole genome linkage analysis of Chiari type I malformation implicates known Klippel-Feil syndrome genes as putative disease candidates.
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PLoS One
|
2013
|
0.81
|
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38
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Mapping and characterization of the amplicon near APOA2 in 1q23 in human sarcomas by FISH and array CGH.
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Mol Cancer
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2005
|
0.81
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39
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Association of Roadway Proximity with Fasting Plasma Glucose and Metabolic Risk Factors for Cardiovascular Disease in a Cross-Sectional Study of Cardiac Catheterization Patients.
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Environ Health Perspect
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2015
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0.81
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40
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Cleavage and polyadenylation specificity factor 1 (CPSF1) regulates alternative splicing of interleukin 7 receptor (IL7R) exon 6.
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RNA
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2012
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0.81
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41
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Using circulating tumor cells to inform on prostate cancer biology and clinical utility.
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Crit Rev Clin Lab Sci
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2015
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0.80
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42
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A general integrative genomic feature transcription factor binding site prediction method applied to analysis of USF1 binding in cardiovascular disease.
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Hum Genomics
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2009
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0.80
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43
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Transcriptome profiling of genes involved in neural tube closure during human embryonic development using long serial analysis of gene expression (long-SAGE).
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Birth Defects Res A Clin Mol Teratol
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2012
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0.80
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44
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Interactions between social/ behavioral factors and ADRB2 genotypes may be associated with health at advanced ages in China.
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BMC Geriatr
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2013
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0.79
|
|
45
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Refinement of 2q and 7p loci in a large multiplex NTD family.
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Birth Defects Res A Clin Mol Teratol
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2008
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0.79
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46
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Missing genetic risk in neural tube defects: can exome sequencing yield an insight?
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Birth Defects Res A Clin Mol Teratol
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2014
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0.79
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|
47
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Genome-wide linkage analysis of cardiovascular disease biomarkers in a large, multigenerational family.
|
PLoS One
|
2013
|
0.78
|
|
48
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A blood spot method for detecting fumonisin-induced changes in putative sphingolipid biomarkers in LM/Bc mice and humans.
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Food Addit Contam Part A Chem Anal Control Expo Risk Assess
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2015
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0.78
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49
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Detailed assessment of chromosome 22 aberrations in sporadic pheochromocytoma using array-CGH.
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Int J Cancer
|
2006
|
0.78
|
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50
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Linkage and association with type 1 diabetes on chromosome 1q42.
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Diabetes
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2002
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0.77
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51
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Organization of the MASP2 locus and its expression profile in mouse and rat.
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Mamm Genome
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2004
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0.76
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52
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Genetic association analyses of nitric oxide synthase genes and neural tube defects vary by phenotype.
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Birth Defects Res B Dev Reprod Toxicol
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2013
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0.75
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