Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
1
|
Strong association of de novo copy number mutations with autism.
|
Science
|
2007
|
27.84
|
2
|
A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.
|
Science
|
2006
|
27.49
|
3
|
A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis.
|
Am J Hum Genet
|
2004
|
13.71
|
4
|
Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci.
|
Nat Genet
|
2008
|
12.51
|
5
|
TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study.
|
N Engl J Med
|
2007
|
12.24
|
6
|
Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.
|
Nat Genet
|
2010
|
9.90
|
7
|
STAT4 and the risk of rheumatoid arthritis and systemic lupus erythematosus.
|
N Engl J Med
|
2007
|
9.80
|
8
|
Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX.
|
N Engl J Med
|
2008
|
9.61
|
9
|
Two independent alleles at 6q23 associated with risk of rheumatoid arthritis.
|
Nat Genet
|
2007
|
8.74
|
10
|
Common variants at CD40 and other loci confer risk of rheumatoid arthritis.
|
Nat Genet
|
2008
|
7.07
|
11
|
Replication of putative candidate-gene associations with rheumatoid arthritis in >4,000 samples from North America and Sweden: association of susceptibility with PTPN22, CTLA4, and PADI4.
|
Am J Hum Genet
|
2005
|
6.61
|
12
|
Analysis of families in the multiple autoimmune disease genetics consortium (MADGC) collection: the PTPN22 620W allele associates with multiple autoimmune phenotypes.
|
Am J Hum Genet
|
2005
|
5.00
|
13
|
Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study.
|
Nat Genet
|
2009
|
3.65
|
14
|
Genetic variants at CD28, PRDM1 and CD2/CD58 are associated with rheumatoid arthritis risk.
|
Nat Genet
|
2009
|
3.52
|
15
|
REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis.
|
Nat Genet
|
2009
|
3.36
|
16
|
Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis.
|
Nat Genet
|
2010
|
3.15
|
17
|
Regulation of anti-cyclic citrullinated peptide antibodies in rheumatoid arthritis: contrasting effects of HLA-DR3 and the shared epitope alleles.
|
Arthritis Rheum
|
2005
|
2.88
|
18
|
Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus.
|
Nat Genet
|
2010
|
2.61
|
19
|
Data for Genetic Analysis Workshop 16 Problem 1, association analysis of rheumatoid arthritis data.
|
BMC Proc
|
2009
|
2.12
|
20
|
Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.
|
PLoS Genet
|
2011
|
1.92
|
21
|
Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.
|
PLoS Genet
|
2011
|
1.80
|
22
|
Specificity of the STAT4 genetic association for severe disease manifestations of systemic lupus erythematosus.
|
PLoS Genet
|
2008
|
1.80
|
23
|
Several regions in the major histocompatibility complex confer risk for anti-CCP-antibody positive rheumatoid arthritis, independent of the DRB1 locus.
|
Mol Med
|
2008
|
1.69
|
24
|
Plasma carboxypeptidase B downregulates inflammatory responses in autoimmune arthritis.
|
J Clin Invest
|
2011
|
1.63
|
25
|
Circulating immune complexes contain citrullinated fibrinogen in rheumatoid arthritis.
|
Arthritis Res Ther
|
2008
|
1.62
|
26
|
Genome-wide association study of rheumatoid arthritis in Koreans: population-specific loci as well as overlap with European susceptibility loci.
|
Arthritis Rheum
|
2011
|
1.58
|
27
|
Risk alleles for systemic lupus erythematosus in a large case-control collection and associations with clinical subphenotypes.
|
PLoS Genet
|
2011
|
1.57
|
28
|
A pilot study to test the effect of pulsatile insulin infusion on cardiovascular mechanisms that might contribute to attenuation of renal compromise in type 1 diabetes mellitus patients with proteinuria.
|
Metabolism
|
2007
|
1.39
|
29
|
Data for Genetic Analysis Workshop (GAW) 15 Problem 2, genetic causes of rheumatoid arthritis and associated traits.
|
BMC Proc
|
2007
|
1.36
|
30
|
Role for Msh5 in the regulation of Ig class switch recombination.
|
Proc Natl Acad Sci U S A
|
2007
|
1.35
|
31
|
Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency.
|
Nat Genet
|
2010
|
1.32
|
32
|
Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder.
|
Nat Commun
|
2013
|
1.25
|
33
|
Effects of serotonin transporter promoter polymorphisms on serotonin function.
|
Neuropsychopharmacology
|
2004
|
1.21
|
34
|
Association between common variants near the melanocortin 4 receptor gene and severe antipsychotic drug-induced weight gain.
|
Arch Gen Psychiatry
|
2012
|
1.20
|
35
|
Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08.
|
Ann Neurol
|
2012
|
1.19
|
36
|
CSK regulatory polymorphism is associated with systemic lupus erythematosus and influences B-cell signaling and activation.
|
Nat Genet
|
2012
|
1.16
|
37
|
Genome-wide association analysis of anti-TNF drug response in patients with rheumatoid arthritis.
|
Ann Rheum Dis
|
2012
|
1.10
|
38
|
Implications for health and disease in the genetic signature of the Ashkenazi Jewish population.
|
Genome Biol
|
2012
|
1.08
|
39
|
The autoimmunity-associated BLK haplotype exhibits cis-regulatory effects on mRNA and protein expression that are prominently observed in B cells early in development.
|
Hum Mol Genet
|
2012
|
0.97
|
40
|
European population substructure is associated with mucocutaneous manifestations and autoantibody production in systemic lupus erythematosus.
|
Arthritis Rheum
|
2009
|
0.96
|
41
|
High-density SNP mapping of the HLA region identifies multiple independent susceptibility loci associated with selective IgA deficiency.
|
PLoS Genet
|
2012
|
0.94
|
42
|
Genome-wide association study reveals novel genetic determinants of DNA repair capacity in lung cancer.
|
Cancer Res
|
2012
|
0.84
|
43
|
Detection of disease-associated deletions in case-control studies using SNP genotypes with application to rheumatoid arthritis.
|
Hum Genet
|
2009
|
0.83
|
44
|
Risk factors for thromboembolic events in renal failure.
|
Int J Cardiol
|
2005
|
0.83
|
45
|
Locus category based analysis of a large genome-wide association study of rheumatoid arthritis.
|
Hum Mol Genet
|
2010
|
0.82
|
46
|
The serotonin transporter gene and disease modification in psychosis: evidence for systematic differences in allelic directionality at the 5-HTTLPR locus.
|
Schizophr Res
|
2009
|
0.81
|
47
|
Bone morphogenetic protein-focused strategies to induce cytotoxicity in lung cancer cells.
|
Anticancer Res
|
2014
|
0.81
|
48
|
The chromosome 7q region association with rheumatoid arthritis in females in a British population is not replicated in a North American case-control series.
|
Arthritis Rheum
|
2009
|
0.77
|
49
|
Left ventricular mass reduction in type 1 diabetic patients with nephropathy.
|
J Clin Hypertens (Greenwich)
|
2005
|
0.76
|
50
|
Utilization of an abbreviated diabetes impact management scale to assess change in subjective disability during a trial of pulsatile insulin delivery demonstrates benefit.
|
Metabolism
|
2009
|
0.75
|
51
|
A pilot study to assess utility of changes in elements of the Diabetes Impact Management Scale in evaluating diabetic patients for progressive nephropathy.
|
Metabolism
|
2009
|
0.75
|
52
|
Regression of left ventricular hypertrophy in diabetic nephropathy: loss of parasympathetic function predicts response to treatment.
|
J Clin Hypertens (Greenwich)
|
2006
|
0.75
|