Research Topics
Genomes and Genes
| Manuel A R FerreiraSummaryAffiliation: Queensland Institute of Medical Research Country: Australia Publications
| Collaborators
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Detail Information
Publications
A multivariate test of associationManuel A R Ferreira
Department of Psychiatry, Massachusetts General Hospital, Boston, USA
Bioinformatics 25:132-3. 2009..We describe a test of association that can be efficiently applied to large population-based designs. AVAILABILITY: A C++ implementation can be obtained from the authors...
Identification of IL6R and chromosome 11q13.5 as risk loci for asthmaManuel A R Ferreira
The Queensland Institute of Medical Research, Brisbane, QLD, Australia
Lancet 378:1006-14. 2011..We aimed to identify novel genetic variants affecting asthma risk, since these might provide novel insights into molecular mechanisms underlying the disease...
Sequence variants in three loci influence monocyte counts and erythrocyte volumeManuel A R Ferreira
Queensland Institute of Medical Research QIMR, Brisbane, QLD 4029, Australia
Am J Hum Genet 85:745-9. 2009..001, 9.9x10(-5), and 7x10(-5), respectively). The identification of these QTL provides new opportunities for furthering our understanding of the mechanisms regulating hemopoietic cell fate...
Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in AustraliaManuel A R Ferreira
Queensland Institute of Medical Research, Brisbane, QLD, Australia
Eur J Hum Genet 19:458-64. 2011..In conclusion, we confirm the association between asthma risk and variants in ORMDL3 and identify a novel risk variant in IL1RL1. Follow-up of the 17q21 deletion in larger cohorts is warranted...
Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune controlManuel A R Ferreira
Queensland Institute of Medical Research, Brisbane, QLD, Australia
Am J Hum Genet 86:88-92. 2010....
Common variants in the trichohyalin gene are associated with straight hair in EuropeansSarah E Medland
Queensland Institute of Medical Research, Brisbane 4029, Australia
Am J Hum Genet 85:750-5. 2009..5x10(-31)). These variants are at their highest frequency in Northern Europeans, paralleling the distribution of the straight-hair EDAR variant in Asian populations...
Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traitsRita P S Middelberg
Genetic Epidemiology Unit, Queensland Institute of Medical Research, Brisbane, Australia
BMC Med Genet 12:123. 2011....
A simple method to localise pleiotropic susceptibility loci using univariate linkage analyses of correlated traitsManuel A R Ferreira
Queensland Institute of Medical Research, Royal Brisbane Hospital, Brisbane, Australia
Eur J Hum Genet 14:953-62. 2006..We illustrate the utility of our approach with a genome scan of three asthma traits measured in families with a twin proband...
Assumption-free estimation of heritability from genome-wide identity-by-descent sharing between full siblingsPeter M Visscher
Genetic Epidemiology Group, Queensland Institute of Medical Research, Brisbane, Australia
PLoS Genet 2:e41. 2006....
LPAR1 and ITGA4 regulate peripheral blood monocyte countsNarelle Maugeri
Queensland Institute of Medical Research, Brisbane, Australia
Hum Mutat 32:873-6. 2011..Further studies that investigate the downstream mechanism involved and the impact on immune function are warranted...
Common variants in TMPRSS6 are associated with iron status and erythrocyte volumeBeben Benyamin
Queensland Institute of Medical Research, Brisbane, Queensland, Australia
Nat Genet 41:1173-5. 2009..1 x 10(-10)). We also find suggestive evidence of association with blood hemoglobin levels (combined P = 5.3 x 10(-7)). These findings demonstrate the involvement of TMPRSS6 in control of iron homeostasis and in normal erythropoiesis...
Robust estimation of experimentwise P values applied to a genome scan of multiple asthma traits identifies a new region of significant linkage on chromosome 20q13Manuel A R Ferreira
Queensland Institute of Medical Research, Brisbane, Australia
Am J Hum Genet 77:1075-85. 2005....
GENOVA: gene overlap analysis of GWAS resultsClara S Tang
Queensland Institute of Medical Research, Brisbane, Australia
Stat Appl Genet Mol Biol 11:Article 6. 2012..A weaker association was observed for BMI (1.09-fold, P = 0.008) and WHR (1.09-fold, P = 0.014). GENOVA is implemented in C++ and is freely available at https://genepi.qimr.edu.au/staff/manuelF/genova/main.html...
Multivariate genomewide linkage scan of neurocognitive traits and ADHD symptoms: suggestive linkage to 3q13Alysa E Doyle
Pediatric Psychopharmacology Unit, Massachusetts General Hospital, Boston, Massachusetts, USA
Am J Med Genet B Neuropsychiatr Genet 147:1399-411. 2008..Overall, these data support the utility of neurocognitive traits as ADHD endophenotypes, but also highlight their limited genetic overlap with the disorder...
Sex-limited genome-wide linkage scan for body mass index in an unselected sample of 933 Australian twin familiesBelinda K Cornes
Genetic Epidemiology, Queensland Institute of Medical Research, Post Office Royal Brisbane Hospital, QLD, Australia
Twin Res Hum Genet 8:616-32. 2005....
A genomewide association study of response to lithium for prevention of recurrence in bipolar disorderRoy H Perlis
Department of Psychiatry, Massachusetts General Hospital, Boston, MA, USA
Am J Psychiatry 166:718-25. 2009....
Genomewide significant linkage to migrainous headache on chromosome 5q21Dale R Nyholt
Queensland Institute of Medical Research, Brisbane, Australia
Am J Hum Genet 77:500-12. 2005..These results will prove to be invaluable in the design and analysis of future linkage and linkage disequilibrium studies of migraine...
Practical aspects of imputation-driven meta-analysis of genome-wide association studiesPaul I W de Bakker
Division of Genetics, Department of Medicine, Brigham and Women s Hospital, Harvard Medical School Partners Healthcare Systems Center for Genetics and Genomics, Boston, MA 02115, USA
Hum Mol Genet 17:R122-8. 2008..As many groups are forming collaborations to engage in these efforts, this review collects a series of guidelines, practical detail and learned experiences from a variety of individuals who have contributed to the subject...
PLINK: a tool set for whole-genome association and population-based linkage analysesShaun Purcell
Center for Human Genetic Research, Massachusetts General Hospital, Boston, MA 02114, USA
Am J Hum Genet 81:559-75. 2007..Analysis of the patterns of segmental sharing has the potential to map disease loci that contain multiple rare variants in a population-based linkage analysis...
Cytokine expression in allergic inflammation: systematic review of in vivo challenge studiesManuel A R Ferreira
Queensland Institute of Medical Research, P O Royal Brisbane Hospital, Brisbane 4029, Australia
Mediators Inflamm 12:259-67. 2003..Allergic inflammatory responses are driven by cells of the immune system that rely on cytokines to regulate the activity of other immune and structural cells...
Association between microdeletion and microduplication at 16p11.2 and autismLauren A Weiss
Autism Consortium, Boston, USA
N Engl J Med 358:667-75. 2008..Autism spectrum disorder is a heritable developmental disorder in which chromosomal abnormalities are thought to play a role...
Linkage analysis: principles and methods for the analysis of human quantitative traitsManuel A R Ferreira
Queensland Institute of Medical Research, Royal Brisbane Hospital, Brisbane, Australia
Twin Res 7:513-30. 2004..The type-I error rate and power of these methods are discussed. Finally, rough guidelines are provided to help guide the choice of linkage statistics...
A gene-based test of association using canonical correlation analysisClara S Tang
Queensland Institute of Medical Research, Brisbane, QLD 4029, Australia
Bioinformatics 28:845-50. 2012..Application to a GWAS of leukocyte levels identified SAFB and a histone gene cluster as novel putative loci harboring multiple independent variants regulating lymphocyte and neutrophil counts...
Ascertainment through family history of disease often decreases the power of family-based association studiesManuel A R Ferreira
Center for Human Genetic Research, Massachusetts General Hospital, Harvard Medical School, 185 Cambridge St, Boston, MA 02114, USA
Behav Genet 37:631-6. 2007..Our analytic approach to estimate the asymptotic power of the TDT is implemented online at http://pngu.mgh.harvard.edu/ ~purcell/gpc/...
Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorderManuel A R Ferreira
Department of Psychiatry, Massachusetts General Hospital, Boston, Massachusetts 02114, USA
Nat Genet 40:1056-8. 2008..0 x 10(-8), rs1006737). Our results suggest that ion channelopathies may be involved in the pathogenesis of bipolar disorder...
Inflammation in allergic asthma: initiating events, immunological response and risk factorsManuel A R Ferreira
Queensland Institute of Medical Research, Brisbane, Queensland, Australia
Respirology 9:16-24. 2004..Finally, it integrates these concepts in a theoretical causal model for atopic asthma...
