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Author Details

Anna Rautanen
2004
49
29
PMIDPaper TitleJournal TitlePublished Year
36245764Longitudinal Evaluation of Visual Function Impairments in Early and Intermediate Age-Related Macular Degeneration Patients.Ophthalmol Sci2022
35396580Mapping genomic loci implicates genes and synaptic biology in schizophrenia.Nature2022
32645954Large-Scale Production of Human iPSC-Derived Macrophages for Drug Screening.Int J Mol Sci2020
31517041The ferroportin Q248H mutation protects from anemia, but not malaria or bacteremia.Science advances2019
29588414Genetic variation in is associated with bacteremia secondary to diverse pathogens in African children.Proceedings of the National Academy of Sciences of the United States of America2018
29523850Risk of nontyphoidal Salmonella bacteraemia in African children is modified by STAT4.Nat Commun2018
28492228Association between a common immunoglobulin heavy chain allele and rheumatic heart disease risk in Oceania.Nat Commun2017
28345042Human genetic and metabolite variation reveals that methylthioadenosine is a prognostic biomarker and an inflammatory regulator in sepsis.Sci Adv2017
27639821Genetic Factors of the Disease Course after Sepsis: A Genome-Wide Study for 28Day Mortality.eBioMedicine2016
27236921Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children.Am J Hum Genet2016
26744416Environmental Correlation Analysis for Genes Associated with Protection against Malaria.Molecular Biology and Evolution2016
26917434Genomic landscape of the individual host response and outcomes in sepsis: a prospective cohort study.Lancet Respir Med2016
26077084Response to Schöneweck et al.: Common genomic variation in the FER gene: useful to stratify patients with sepsis due to pneumonia?Intensive Care Medicine2015
25886387Rare variants in MYD88, IRAK4 and IKBKG and susceptibility to invasive pneumococcal disease: a population-based case-control study.PLoS ONE2015
25533491Genome-wide association study of survival from sepsis due to pneumonia: an observational cohort study.Lancet Respir Med2015
25969530Variants in the Mannose-binding Lectin Gene MBL2 do not Associate With Sepsis Susceptibility or Survival in a Large European Cohort.Clin Infect Dis2015
26312835Genetic variants associated with non-typhoidal Salmonella bacteraemia in African children.Lancet2015
25003214The correlation between reading and mathematics ability at age twelve has a substantial genetic component.Nat Commun2014
23997235IFITM3 and susceptibility to respiratory viral infections in the community.J Infect Dis2014
23871474A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation.Biol Psychiatry2014
24813206RNA and imidazoquinolines are sensed by distinct TLR7/8 ectodomain sites resulting in functionally disparate signaling events.Journal of Immunology2014
23291585Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis.Nat Genet2013
23974872Genome-wide association analysis identifies 13 new risk loci for schizophrenia.Nat Genet2013
22961001Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus.Nat Genet2012
22306652Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke.Nat Genet2012
21833088Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.Nature2011
21044948Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.Hum Mol Genet2011
20946152Factor V Leiden as a risk factor for preterm birth--a population-based nested case-control study.J Thromb Haemost2011
21477816Glucocorticoid receptor gene haplotype predicts increased risk of hospital admission for depressive disorders in the Helsinki birth cohort study.J Psychiatr Res2011
21186350Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes.Nat Genet2011
20966070Two human MYD88 variants, S34Y and R98C, interfere with MyD88-IRAK4-myddosome assembly.Journal of Biological Chemistry2011
19828176Factor V Leiden as risk factor for unexplained stillbirth--a population-based nested case-control study.Thromb Res2010
19798075NFKBIZ polymorphisms and susceptibility to pneumococcal disease in European and African populations.Genes and Immunity2010
20953190A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.Nat Genet2010
21171993Common NFKBIL2 polymorphisms and susceptibility to pneumococcal disease: a genetic association study.Critical Care2010
20843814A naturally occurring variant in human TLR9, P99L, is associated with loss of CpG oligonucleotide responsiveness.Journal of Biological Chemistry2010
20484391CISH and susceptibility to infectious diseases.New England Journal of Medicine2010
20617178Leprosy and the adaptation of human toll-like receptor 1.PLoS Pathog2010
20164415MyD88 adaptor-like D96N is a naturally occurring loss-of-function variant of TIRAP.Journal of Immunology2010
20078874Mannose-binding lectin genotypes: lack of association with susceptibility to thoracic empyema.BMC Medical Genetics2010
19915572Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.Nat Genet2009
19110300Blood group AB and factor V Leiden as risk factors for pre-eclampsia: a population-based nested case-control study.Thromb Res2009
16765424An unfavorable combination of Factor V Leiden with age, weight, and blood group causes high risk of pregnancy-associated venous thrombosis: a population-based nested case-control study.Thromb Res2007
16940157Analysis of the mouse and human acyl-CoA thioesterase (ACOT) gene clusters shows that convergent, functional evolution results in a reduced number of human peroxisomal ACOTs.FASEB Journal2006
16895953Associations of body size at birth with late-life cortisol concentrations and glucose tolerance are modified by haplotypes of the glucocorticoid receptor gene.J Clin Endocrinol Metab2006
16388838Thrombophilia: a new potential risk factor for cervical insufficiency.Thrombosis Research2006
16150567Gene mapping with pooled samples on three genotyping platforms.Mol Cell Probes2005
15073379Characterization of a common susceptibility locus for asthma-related traits.Science2004
15531537The effects of the ACE gene insertion/deletion polymorphism on glucose tolerance and insulin secretion in elderly people are modified by birth weight.J Clin Endocrinol Metab2004
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Folkhalsan Research Center, University of Helsinki
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