| Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
|
1
|
Risk alleles for multiple sclerosis identified by a genomewide study.
|
N Engl J Med
|
2007
|
17.06
|
|
2
|
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
|
Nature
|
2011
|
13.23
|
|
3
|
Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis.
|
Nat Genet
|
2007
|
5.09
|
|
4
|
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.
|
Nat Genet
|
2013
|
4.62
|
|
5
|
Mapping multiple sclerosis susceptibility to the HLA-DR locus in African Americans.
|
Am J Hum Genet
|
2003
|
2.71
|
|
6
|
A high-density screen for linkage in multiple sclerosis.
|
Am J Hum Genet
|
2005
|
2.50
|
|
7
|
Gene copy number regulates the production of the human chemokine CCL3-L1.
|
Eur J Immunol
|
2002
|
2.24
|
|
8
|
A second major histocompatibility complex susceptibility locus for multiple sclerosis.
|
Ann Neurol
|
2007
|
1.99
|
|
9
|
An application of Random Forests to a genome-wide association dataset: methodological considerations & new findings.
|
BMC Genet
|
2010
|
1.96
|
|
10
|
Clustering of inflammatory bowel disease with immune mediated diseases among members of a northern california-managed care organization.
|
Am J Gastroenterol
|
2007
|
1.78
|
|
11
|
118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects.
|
BMC Med Genet
|
2009
|
1.74
|
|
12
|
Genome-wide pharmacogenomic analysis of the response to interferon beta therapy in multiple sclerosis.
|
Arch Neurol
|
2008
|
1.59
|
|
13
|
Fine-mapping the genetic association of the major histocompatibility complex in multiple sclerosis: HLA and non-HLA effects.
|
PLoS Genet
|
2013
|
1.55
|
|
14
|
The R620W polymorphism of the protein tyrosine phosphatase PTPN22 is not associated with multiple sclerosis.
|
Am J Hum Genet
|
2005
|
1.26
|
|
15
|
Novel childhood ALL susceptibility locus BMI1-PIP4K2A is specifically associated with the hyperdiploid subtype.
|
Blood
|
2013
|
1.25
|
|
16
|
Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis.
|
Nat Genet
|
2010
|
1.16
|
|
17
|
Uncoupling the roles of HLA-DRB1 and HLA-DRB5 genes in multiple sclerosis.
|
J Immunol
|
2008
|
1.13
|
|
18
|
Genetic analysis of multiple sclerosis in Europeans.
|
J Neuroimmunol
|
2003
|
1.12
|
|
19
|
Association of the truncating splice site mutation in BTNL2 with multiple sclerosis is secondary to HLA-DRB1*15.
|
Hum Mol Genet
|
2005
|
1.10
|
|
20
|
Associations between single nucleotide polymorphisms in iron-related genes and iron status in multiethnic populations.
|
PLoS One
|
2012
|
1.03
|
|
21
|
Unraveling multiple MHC gene associations with systemic lupus erythematosus: model choice indicates a role for HLA alleles and non-HLA genes in Europeans.
|
Am J Hum Genet
|
2012
|
1.02
|
|
22
|
Genome-wide association study identifies genetic loci associated with iron deficiency.
|
PLoS One
|
2011
|
1.01
|
|
23
|
Multiple susceptibility loci for multiple sclerosis.
|
Hum Mol Genet
|
2002
|
1.01
|
|
24
|
CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosis.
|
Hum Mol Genet
|
2010
|
1.01
|
|
25
|
Genetic variants in the folate pathway and risk of childhood acute lymphoblastic leukemia.
|
Cancer Causes Control
|
2011
|
1.00
|
|
26
|
Searching for additional disease loci in a genomic region.
|
Adv Genet
|
2008
|
1.00
|
|
27
|
Complex gene-gene interactions in multiple sclerosis: a multifactorial approach reveals associations with inflammatory genes.
|
Neurogenetics
|
2006
|
0.97
|
|
28
|
Genetic variants in ARID5B and CEBPE are childhood ALL susceptibility loci in Hispanics.
|
Cancer Causes Control
|
2013
|
0.97
|
|
29
|
Association of polymorphisms in the apolipoprotein E region with susceptibility to and progression of multiple sclerosis.
|
Am J Hum Genet
|
2002
|
0.96
|
|
30
|
Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA-CLEC16A-SOCS1 gene complex.
|
Hum Mol Genet
|
2011
|
0.95
|
|
31
|
Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12,566 individuals.
|
Hum Mol Genet
|
2010
|
0.93
|
|
32
|
Variation within DNA repair pathway genes and risk of multiple sclerosis.
|
Am J Epidemiol
|
2010
|
0.93
|
|
33
|
The HLA locus and multiple sclerosis in Spain. Role in disease susceptibility, clinical course and response to interferon-beta.
|
J Neuroimmunol
|
2002
|
0.93
|
|
34
|
Genomic ancestry and somatic alterations correlate with age at diagnosis in Hispanic children with B-cell acute lymphoblastic leukemia.
|
Am J Hematol
|
2014
|
0.92
|
|
35
|
CYP1A1/2 haplotypes and lung cancer and assessment of confounding by population stratification.
|
Cancer Res
|
2009
|
0.90
|
|
36
|
Comparison of statistical methods for estimating genetic admixture in a lung cancer study of African Americans and Latinos.
|
Am J Epidemiol
|
2008
|
0.89
|
|
37
|
Variation in xenobiotic transport and metabolism genes, household chemical exposures, and risk of childhood acute lymphoblastic leukemia.
|
Cancer Causes Control
|
2012
|
0.88
|
|
38
|
GATA3 risk alleles are associated with ancestral components in Hispanic children with ALL.
|
Blood
|
2013
|
0.87
|
|
39
|
Male microchimerism in peripheral blood leukocytes from women with multiple sclerosis.
|
Chimerism
|
2011
|
0.86
|
|
40
|
Socioeconomic status and lung cancer: unraveling the contribution of genetic admixture.
|
Am J Public Health
|
2013
|
0.86
|
|
41
|
Investigation of seven proposed regions of linkage in multiple sclerosis: an American and French collaborative study.
|
Neurogenetics
|
2003
|
0.85
|
|
42
|
Genetic polymorphisms in adaptive immunity genes and childhood acute lymphoblastic leukemia.
|
Cancer Epidemiol Biomarkers Prev
|
2010
|
0.85
|
|
43
|
HLA-DP genetic variation, proxies for early life immune modulation and childhood acute lymphoblastic leukemia risk.
|
Blood
|
2012
|
0.83
|
|
44
|
Haplotypes of DNA repair and cell cycle control genes, X-ray exposure, and risk of childhood acute lymphoblastic leukemia.
|
Cancer Causes Control
|
2011
|
0.83
|
|
45
|
Association between celiac disease and iron deficiency in Caucasians, but not non-Caucasians.
|
Clin Gastroenterol Hepatol
|
2013
|
0.83
|
|
46
|
Fetal growth and body size genes and risk of childhood acute lymphoblastic leukemia.
|
Cancer Causes Control
|
2012
|
0.80
|
|
47
|
Causal Effect of Genetic Variants Associated With Body Mass Index on Multiple Sclerosis Susceptibility.
|
Am J Epidemiol
|
2017
|
0.77
|
|
48
|
Association of genetic variation in IKZF1, ARID5B, and CEBPE and surrogates for early-life infections with the risk of acute lymphoblastic leukemia in Hispanic children.
|
Cancer Causes Control
|
2015
|
0.77
|
|
49
|
Smoking and risk of multiple sclerosis: evidence of modification by NAT1 variants.
|
Epidemiology
|
2014
|
0.77
|
|
50
|
SNP association mapping across the extended major histocompatibility complex and risk of B-cell precursor acute lymphoblastic leukemia in children.
|
PLoS One
|
2013
|
0.77
|
|
51
|
Analysis of maternal-offspring HLA compatibility, parent-of-origin effects, and noninherited maternal antigen effects for HLA-DRB1 in systemic lupus erythematosus.
|
Arthritis Rheum
|
2010
|
0.75
|
|
52
|
Chromosome 7q21-22 and multiple sclerosis.
|
J Neuroimmunol
|
2004
|
0.75
|
|
53
|
Evidence for a complex interaction between HLA-DRB1 and environmental factors in MS.
|
Neurology
|
2008
|
0.75
|