Author details

Full Name

Cordelia Langford

Affiliation

ORCID

Career Start Year

1992

Papers

109

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
34387545	Patterns of within-host genetic diversity in SARS-CoV-2.	Elife	2021
33650490	Genomic epidemiology of COVID-19 in care homes in the east of England.	Elife	2021
27236921	Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children.	Am J Hum Genet	2016
26551672	Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.	Nat Genet	2015
25056318	5' isomiR variation is of functional and evolutionary importance.	Nucleic Acids Research	2014
23871474	A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation.	Biol Psychiatry	2014
24510098	Selective nuclear export of specific classes of mRNA from mammalian nuclei is promoted by GANP.	Nucleic Acids Res	2014
24509480	Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.	Nat Genet	2014
25003214	The correlation between reading and mathematics ability at age twelve has a substantial genetic component.	Nat Commun	2014
23202125	Large-scale association analysis identifies new risk loci for coronary artery disease.	Nat Genet	2013
23912340	Epigenetic regulation of COL15A1 in smooth muscle cell replicative aging and atherosclerosis.	Hum Mol Genet	2013
24076602	Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.	Nat Genet	2013
23974872	Genome-wide association analysis identifies 13 new risk loci for schizophrenia.	Nat Genet	2013
23131088	The future role of genetic screening to detect newborns at risk of childhood-onset hearing loss.	Int J Audiol	2013
23291585	Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis.	Nat Genet	2013
23143594	Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity.	Nat Genet	2012
22306652	Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke.	Nat Genet	2012
22885922	Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes.	Nat Genet	2012
22961001	Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus.	Nat Genet	2012
22761904	Genome-wide screening for genetic alterations in esophageal cancer by aCGH identifies 11q13 amplification oncogenes associated with nodal metastasis.	PLoS One	2012
22446964	Genetics of gene expression in primary immune cells identifies cell type-specific master regulators and roles of HLA alleles.	Nat Genet	2012
23143596	High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis.	Nat Genet	2012
22057235	Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease.	Nat Genet	2011
21044948	Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.	Hum Mol Genet	2011
21186350	Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes.	Nat Genet	2011
22200769	Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry.	Nat Genet	2011
21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Nature	2011
21827714	Identification of candidate genes linking systemic inflammation to atherosclerosis; results of a human in vivo LPS infusion study.	BMC Med Genomics	2011
20140202	Genomic approaches uncover increasing complexities in the regulatory landscape at the human SCL (TAL1) locus.	PLoS ONE	2010
20953190	A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.	Nat Genet	2010
20808788	Complex exon-intron marking by histone modifications is not determined solely by nucleosome distribution.	PLoS One	2010
20833976	Transcription profiling in human platelets reveals LRRFIP1 as a novel protein regulating platelet function.	Blood	2010
20081834	FRT-seq: amplification-free, strand-specific transcriptome sequencing.	Nat Methods	2010
20164239	Distinct patterns of 1p and 19q alterations identify subtypes of human gliomas that have different prognoses.	Neuro Oncol	2010
19924136	Molecular analysis of tumor-promoting CD8+ T cells in two-stage cutaneous chemical carcinogenesis.		2010
20453838	Genome-wide association study identifies five new breast cancer susceptibility loci.	Nat Genet	2010
20360734	Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls.	Nature	2010
19915572	Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.	Nat Genet	2009
19363478	An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice.	Nat Genet	2009
19544422	CARM1 is required in embryonic stem cells to maintain pluripotency and resist differentiation.	Stem Cells	2009
19401398	Functional diversity for REST (NRSF) is defined by in vivo binding affinity hierarchies at the DNA sequence level.	Genome Res	2009
19544311	Neonates harbour highly active gammadelta T cells with selective impairments in preterm infants.	European Journal of Immunology	2009
19672776	Genome-wide microarray-based comparative genomic hybridization analysis of lymphoplasmacytic lymphomas reveals heterogeneous aberrations.	Leuk Lymphoma	2009
19337847	Influence of genetic background on tumor karyotypes: evidence for breed-associated cytogenetic aberrations in canine appendicular osteosarcoma.	Chromosome Res	2009
19333554	'Putting our heads together': insights into genomic conservation between human and canine intracranial tumors.	Journal of Neuro-Oncology	2009
19228925	A HaemAtlas: characterizing gene expression in differentiated human blood cells.	Blood	2009
19505295	Tissue-specific variation in DNA methylation levels along human chromosome 1.	Epigenetics Chromatin	2009
19845972	Genomic and epigenetic evidence for oxytocin receptor deficiency in autism.	BMC Med	2009
19941159	Microarray-based cytogenetic profiling reveals recurrent and subtype-associated genomic copy number aberrations in feline sarcomas.	Chromosome Res	2009
19959666	Adventitious changes in long-range gene expression caused by polymorphic structural variation and promoter competition.	Proceedings of the National Academy of Sciences of the United States of America	2009