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Author Details

Jenefer M Blackwell
1979
254
66
PMIDPaper TitleJournal TitlePublished Year
32830257A Genome-wide Association Study Identifies SERPINB10, CRLF3, STX7, LAMP3, IFNG-AS1, and KRT80 As Risk Loci Contributing to Cutaneous Leishmaniasis in Brazil.Clin Infect Dis2021
33693626Common and Rare Genetic Variants That Could Contribute to Severe Otitis Media in an Australian Aboriginal Population.Clin Infect Dis2021
32614452Anti-Interleukin-10 Unleashes Transcriptional Response to Leishmanial Antigens in Visceral Leishmaniasis Patients.Journal of Infectious Diseases2021
32614431Zika Virus Changes Methylation of Genes Involved in Immune Response and Neural Development in Brazilian Babies Born With Congenital Microcephaly.J Infect Dis2021
33324576Genetics, Transcriptomics and Meta-Taxonomics in Visceral Leishmaniasis.Frontiers in Cellular and Infection Microbiology2020
32350262Reference exome data for Australian Aboriginal populations to support health-based research.Sci Data2020
32055998Human genetics of leishmania infections.Human Genetics2020
33303739A flexible computational pipeline for research analyses of unsolved clinical exome cases.NPJ Genom Med2020
33087711Reference exome data for a Northern Brazilian population.Sci Data2020
31415630Transketolase and vitamin B1 influence on ROS-dependent neutrophil extracellular traps (NETs) formation.PLoS ONE2019
31754101Personalised analytics for rare disease diagnostics.Nat Commun2019
30403401HLA-DR Class II expression on myeloid and lymphoid cells in relation to HLA-DRB1 as a genetic risk factor for visceral leishmaniasis.Immunology2019
31490933Meta-taxonomic analysis of prokaryotic and eukaryotic gut flora in stool samples from visceral leishmaniasis cases and endemic controls in Bihar State India.PLoS Neglected Tropical Diseases2019
30917114Determinants for progression from asymptomatic infection to symptomatic visceral leishmaniasis: A cohort study.PLoS Neglected Tropical Diseases2019
31419223Transcriptional blood signatures for active and amphotericin B treated visceral leishmaniasis in India.PLoS Neglected Tropical Diseases2019
29846382An in silico pipeline to filter the Toxoplasma gondii proteome for proteins that could traffic to the host cell nucleus and influence host cell epigenetic regulation.Memorias do Instituto Oswaldo Cruz2018
30026549Arylsulphatase A Pseudodeficiency (ARSA-PD), hypertension and chronic renal disease in Aboriginal Australians.Sci Rep2018
30055328Epigenetic dysregulation of host gene expression in Toxoplasma infection with specific reference to dopamine and amyloid pathways.Infection, Genetics and Evolution2018
29507109Epitope-Binding Characteristics for Risk versus Protective DRB1 Alleles for Visceral Leishmaniasis.Journal of Immunology2018
28119029Analysis of expression of FLI1 and MMP1 in American cutaneous leishmaniasis caused by Leishmania braziliensis infection.Infection, Genetics and Evolution2017
28904337Toxoplasma Modulates Signature Pathways of Human Epilepsy, Neurodegeneration & Cancer.Sci Rep2017
28848712Evades Nramp1 (Slc11a1)- and NADPH Oxidase-Mediated Killing in Macrophages and Exhibits Nramp1-Dependent Virulence Gene Expression.Frontiers in Cellular and Infection Microbiology2017
28370072Expression profiling of Sudanese visceral leishmaniasis patients pre- and post-treatment with sodium stibogluconate.Parasite Immunology2017
29029143Genome-Wide Analysis of Genetic Risk Factors for Rheumatic Heart Disease in Aboriginal Australians Provides Support for Pathogenic Molecular Mimicry.Journal of Infectious Diseases2017
28606698Comparative analyses of whole genome sequences of Leishmania infantum isolates from humans and dogs in northeastern Brazil.International Journal for Parasitology2017
29312892Infection Is Associated with Mitochondrial Dysfunction .Frontiers in Cellular and Infection Microbiology2017
28054334Comprehensive candidate gene analysis for symptomatic or asymptomatic outcomes of Leishmania infantum infection in Brazil.Ann Hum Genet2017
27070114Reference genotype and exome data from an Australian Aboriginal population for health-based research.Sci Data2016
27155051Fine mapping under linkage peaks for symptomatic or asymptomatic outcomes of Leishmania infantum infection in Brazil.Infect Genet Evol2016
27236921Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children.Am J Hum Genet2016
27287197The rare and undiagnosed diseases diagnostic service - application of massively parallel sequencing in a state-wide clinical service.Orphanet J Rare Dis2016
26829382The -308 bp TNF gene polymorphism influences tumor necrosis factor expression in leprosy patients in Bahia State, Brazil.Infection, Genetics and Evolution2016
26937418Candidate gene analysis supports a role for polymorphisms at TCF7L2 as risk factors for type 2 diabetes in Sudan.Journal of Diabetes and Metabolic Disorders2015
25928883Genome-wide association study of IgG1 responses to the choline-binding protein PspC of Streptococcus pneumoniae.Genes and Immunity2015
25562121Wound healing genes and susceptibility to cutaneous leishmaniasis in Brazil: role of COL1A1.Infection, Genetics and Evolution2015
25760438First genome-wide association study in an Australian aboriginal population provides insights into genetic risk factors for body mass index and type 2 diabetes.PLoS One2015
25208829Genome-wide association study of vitamin D levels in children: replication in the Western Australian Pregnancy Cohort (Raine) study.Genes and Immunity2014
25466928Insights into the possible role of IFNG and IFNGR1 in Kala-azar and Post Kala-azar Dermal Leishmaniasis in Sudanese patients.BMC Infectious Diseases2014
24499112Genetic and functional evidence for a locus controlling otitis media at chromosome 10q26.3.BMC Medical Genetics2014
24863979Host genetic factors in American cutaneous leishmaniasis: a critical appraisal of studies conducted in an endemic area of Brazil.Memorias do Instituto Oswaldo Cruz2014
24676663Examining ERBB2 as a candidate gene for susceptibility to leprosy (Hansen's disease) in Brazil.Memorias do Instituto Oswaldo Cruz2014
25033443Comparison of methods to account for relatedness in genome-wide association studies with family-based data.PLoS Genet2014
25003214The correlation between reading and mathematics ability at age twelve has a substantial genetic component.Nat Commun2014
23538334Genetic and functional evidence for a role for SLC11A1 in susceptibility to otitis media in early childhood in a Western Australian population.Infection, Genetics and Evolution2013
23937595A genome-wide search for type 2 diabetes susceptibility genes in an extended Arab family.Ann Hum Genet2013
23974872Genome-wide association analysis identifies 13 new risk loci for schizophrenia.Nat Genet2013
23100559Association of a NOD2 gene polymorphism and T-helper 17 cells with presumed ocular toxoplasmosis.Journal of Infectious Diseases2013
23291585Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis.Nat Genet2013
22252840Genetic susceptibility to otitis media in childhood.Laryngoscope2012
22554650Wound healing genes and susceptibility to cutaneous leishmaniasis in Brazil.Infection, Genetics and Evolution2012
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