PubRank

Sheila A Fisher

Author PubWeight™ 110.51‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. Nat Genet 2008 30.20
2 Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. Nat Genet 2007 13.74
3 Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants. Nat Genet 2007 12.62
4 Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk. Hum Mol Genet 2005 6.36
5 The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease. Gastroenterology 2002 4.20
6 Age-related macular degeneration is associated with an unstable ARMS2 (LOC387715) mRNA. Nat Genet 2008 4.16
7 Common variants at five new loci associated with early-onset inflammatory bowel disease. Nat Genet 2009 3.82
8 A nonsynonymous SNP in ATG16L1 predisposes to ileal Crohn's disease and is independent of CARD15 and IBD5. Gastroenterology 2007 3.37
9 IL23R variation determines susceptibility but not disease phenotype in inflammatory bowel disease. Gastroenterology 2007 2.97
10 Stem cell treatment for acute myocardial infarction. Cochrane Database Syst Rev 2012 2.78
11 Investigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship. Gastroenterology 2008 2.17
12 Association of DLG5 R30Q variant with inflammatory bowel disease. Eur J Hum Genet 2005 1.84
13 Relationship between p53 codon 72 polymorphism and susceptibility to sunburn and skin cancer. J Invest Dermatol 2002 1.66
14 Inflammatory bowel disease susceptibility loci defined by genome scan meta-analysis of 1952 affected relative pairs. Hum Mol Genet 2004 1.66
15 Association of R602W in a protein tyrosine phosphatase gene with a high risk of rheumatoid arthritis in a British population: evidence for an early onset/disease severity effect. Arthritis Rheum 2005 1.59
16 Genetic evidence for interaction of the 5q31 cytokine locus and the CARD15 gene in Crohn disease. Am J Hum Genet 2003 1.32
17 Meta-analysis of genome-wide scans for hypertension and blood pressure in Caucasians shows evidence of susceptibility regions on chromosomes 2 and 3. Hum Mol Genet 2004 1.29
18 Genetic variation in myosin IXB is associated with ulcerative colitis. Gastroenterology 2006 1.29
19 Log odds of carrying an Ancestral Mutation in BRCA1 or BRCA2 for a Defined personal and family history in an Ashkenazi Jewish woman (LAMBDA). Breast Cancer Res 2003 1.25
20 Independent and population-specific association of risk variants at the IRGM locus with Crohn's disease. Hum Mol Genet 2010 1.21
21 The -174G allele of the interleukin-6 gene confers susceptibility to systemic arthritis in children: a multicenter study using simplex and multiplex juvenile idiopathic arthritis families. Arthritis Rheum 2003 1.20
22 Associations of allelic variants of the multidrug resistance gene (ABCB1 or MDR1) and inflammatory bowel disease and their effects on disease behavior: a case-control and meta-analysis study. Inflamm Bowel Dis 2006 1.11
23 Long-term effects of autologous bone marrow stem cell treatment in acute myocardial infarction: factors that may influence outcomes. PLoS One 2012 1.05
24 Oral or parenteral iron supplementation to reduce deferral, iron deficiency and/or anaemia in blood donors. Cochrane Database Syst Rev 2014 0.99
25 Meta-analysis of genome-wide linkage studies across autoimmune diseases. Eur J Hum Genet 2008 0.92
26 Mutation, selection, and evolution of the Crohn disease susceptibility gene CARD15. Hum Mutat 2006 0.88
27 Germline mutation in ATR in autosomal- dominant oropharyngeal cancer syndrome. Am J Hum Genet 2012 0.88
28 Meta-analysis of genome-wide linkage studies for multiple sclerosis, using an extended GSMA method. Eur J Hum Genet 2007 0.87
29 Variance components linkage analysis for adjusted systolic blood pressure in the Framingham Heart Study. BMC Genet 2003 0.83
30 Diverse effects of the CARD15 and IBD5 loci on clinical phenotype in 630 patients with Crohn's disease. Eur J Gastroenterol Hepatol 2008 0.83
31 Data acquisition for meta-analysis of genome-wide linkage studies using the genome search meta-analysis method. Hum Hered 2007 0.83
32 Investigation of association of the DLG5 gene with phenotypes of inflammatory bowel disease in the British population. Int J Colorectal Dis 2006 0.83
33 Combined evidence from three large British Association studies rejects TUCAN/CARD8 as an IBD susceptibility gene. Gastroenterology 2007 0.82
34 A systematic review of factors associated with the deferral of donors failing to meet low haemoglobin thresholds. Transfus Med 2013 0.82
35 Searching for genotype-phenotype structure: using hierarchical log-linear models in Crohn disease. Am J Hum Genet 2009 0.78
36 Identification, evolution, and association study of a novel promoter and first exon of the human NOD2 (CARD15) gene. Genomics 2007 0.76
37 A decision theory approach to fitness for purpose in analytical measurement. Analyst 2002 0.75
38 Current evidence of the efficacy of cell-based therapies in heart failure. Circ J 2015 0.75