PubRank

Cordelia Langford

Author PubWeight™ 156.72‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. Nature 2011 13.23
2 Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. Nat Genet 2012 11.09
3 The zebrafish reference genome sequence and its relationship to the human genome. Nature 2013 8.52
4 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. Nat Genet 2010 8.48
5 A novel CpG island set identifies tissue-specific methylation at developmental gene loci. PLoS Biol 2008 7.95
6 Genome-wide association study identifies five new breast cancer susceptibility loci. Nat Genet 2010 7.62
7 Large-scale association analysis identifies new risk loci for coronary artery disease. Nat Genet 2012 7.59
8 Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Nat Genet 2013 7.44
9 The DNA sequence of the human X chromosome. Nature 2005 6.97
10 Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease. Nat Genet 2011 6.36
11 Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. Nat Genet 2011 5.56
12 Accurate and reliable high-throughput detection of copy number variation in the human genome. Genome Res 2006 5.50
13 Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. Nat Genet 2013 4.62
14 Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region. Nat Genet 2009 4.61
15 High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis. Nat Genet 2012 4.46
16 Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes. Nat Genet 2010 4.42
17 Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. Nat Genet 2014 4.13
18 Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. Nat Genet 2012 4.13
19 Genetics of gene expression in primary immune cells identifies cell type-specific master regulators and roles of HLA alleles. Nat Genet 2012 3.77
20 Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke. Nat Genet 2012 3.40
21 Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. Hum Mol Genet 2010 3.34
22 Whole-genome microarrays of fission yeast: characteristics, accuracy, reproducibility, and processing of array data. BMC Genomics 2003 3.30
23 An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice. Nat Genet 2009 3.05
24 Binding sites for metabolic disease related transcription factors inferred at base pair resolution by chromatin immunoprecipitation and genomic microarrays. Hum Mol Genet 2005 2.56
25 Exon array CGH: detection of copy-number changes at the resolution of individual exons in the human genome. Am J Hum Genet 2005 1.78
26 Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus. Nat Genet 2012 1.52
27 Distinct cytokine-driven responses of activated blood gammadelta T cells: insights into unconventional T cell pleiotropy. J Immunol 2007 1.42
28 Spreading of mammalian DNA-damage response factors studied by ChIP-chip at damaged telomeres. EMBO J 2007 1.38
29 Adventitious changes in long-range gene expression caused by polymorphic structural variation and promoter competition. Proc Natl Acad Sci U S A 2009 1.35
30 Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry. Nat Genet 2011 1.30
31 Neonates harbour highly active gammadelta T cells with selective impairments in preterm infants. Eur J Immunol 2009 1.23
32 Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the alpha-thalassemia myelodysplasia syndrome (ATMDS). Nat Genet 2003 1.17
33 Transcription profiling in human platelets reveals LRRFIP1 as a novel protein regulating platelet function. Blood 2010 1.16
34 Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis. Nat Genet 2013 1.15
35 Complex exon-intron marking by histone modifications is not determined solely by nucleosome distribution. PLoS One 2010 1.09
36 Generation of a genomic tiling array of the human major histocompatibility complex (MHC) and its application for DNA methylation analysis. BMC Med Genomics 2008 1.04
37 Genomic approaches uncover increasing complexities in the regulatory landscape at the human SCL (TAL1) locus. PLoS One 2010 0.99
38 Genome-wide screening for genetic alterations in esophageal cancer by aCGH identifies 11q13 amplification oncogenes associated with nodal metastasis. PLoS One 2012 0.99
39 Selective nuclear export of specific classes of mRNA from mammalian nuclei is promoted by GANP. Nucleic Acids Res 2014 0.89
40 A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation. Biol Psychiatry 2013 0.87
41 The future role of genetic screening to detect newborns at risk of childhood-onset hearing loss. Int J Audiol 2012 0.83
42 DNA copy number alterations and expression of relevant genes in mouse thymic lymphomas induced by gamma-irradiation and N-methyl-N-nitrosourea. Cancer Genet Cytogenet 2006 0.82
43 Definition of a minimal region of deletion of chromosome 7 in uterine leiomyomas by tiling-path microarray CGH and mutation analysis of known genes in this region. Genes Chromosomes Cancer 2007 0.78
44 Improving the power to detect differentially expressed genes in comparative microarray experiments by including information from self-self hybridizations. Comput Biol Chem 2007 0.76