Richard W Francis
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Explore the profile of Richard W Francis including associated specialties, affiliations and a list of published articles.
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26
Citations
770
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Recent Articles
11.
Yip B, Leonard H, Stock S, Stoltenberg C, Francis R, Gissler M, et al.
Int J Epidemiol
. 2016 Dec;
46(2):429-439.
PMID: 28017932
Background: The positive association between caesarean section (CS) and autism spectrum disorder (ASD) may be attributed to preterm delivery. However, due to lack of statistical power, no previous study thoroughly...
12.
Reference genotype and exome data from an Australian Aboriginal population for health-based research
Tang D, Anderson D, Francis R, Syn G, Jamieson S, Lassmann T, et al.
Sci Data
. 2016 Apr;
3:160023.
PMID: 27070114
Genetic analyses, including genome-wide association studies and whole exome sequencing (WES), provide powerful tools for the analysis of complex and rare genetic diseases. To date there are no reference data...
13.
Carter K, Francis R, Carter K, Francis R, Bresnahan M, Gissler M, et al.
Int J Epidemiol
. 2015 Oct;
45(2):408-416.
PMID: 26452388
Background: Research studies exploring the determinants of disease require sufficient statistical power to detect meaningful effects. Sample size is often increased through centralized pooling of disparately located datasets, though ethical,...
14.
Anderson D, Cordell H, Fakiola M, Francis R, Syn G, Scaman E, et al.
PLoS One
. 2015 Mar;
10(3):e0119333.
PMID: 25760438
A body mass index (BMI) >22kg/m2 is a risk factor for type 2 diabetes (T2D) in Aboriginal Australians. To identify loci associated with BMI and T2D we undertook a genome-wide...
15.
Gaye A, Marcon Y, Isaeva J, Laflamme P, Turner A, Jones E, et al.
Int J Epidemiol
. 2014 Sep;
43(6):1929-44.
PMID: 25261970
Background: Research in modern biomedicine and social science requires sample sizes so large that they can often only be achieved through a pooled co-analysis of data from several studies. But...
16.
Francis R
Int J Genomics
. 2014 Feb;
2013:594528.
PMID: 24524070
The Gene Ontology (GO) provides a resource for consistent annotation of genes and gene products that is extensively used by numerous large public repositories. The GO is constructed of three...
17.
Rye M, Scaman E, Thornton R, Vijayasekaran S, Coates H, Francis R, et al.
BMC Med Genet
. 2014 Feb;
15:18.
PMID: 24499112
Background: Otitis media (OM) is a common childhood disease characterised by middle ear effusion and inflammation. Susceptibility to recurrent acute OM and chronic OM with effusion is 40-70% heritable. Linkage...
18.
Schendel D, Bresnahan M, Carter K, Francis R, Gissler M, Gronborg T, et al.
J Autism Dev Disord
. 2013 Apr;
43(11):2650-63.
PMID: 23563868
The International Collaboration for Autism Registry Epidemiology (iCARE) is the first multinational research consortium (Australia, Denmark, Finland, Israel, Norway, Sweden, USA) to promote research in autism geographical and temporal heterogeneity,...
19.
Rye M, Wiertsema S, Scaman E, Thornton R, Francis R, Vijayasekaran S, et al.
Infect Genet Evol
. 2013 Mar;
16:411-8.
PMID: 23538334
Otitis media (OM) is a common disease in early childhood characterised by inflammation of the middle ear. Susceptibility to recurrent acute OM (rAOM; ≥3 episodes AOM in 6 months) and...
20.
Francis R, Thompson-Wicking K, Carter K, Anderson D, Kees U, Beesley A
PLoS One
. 2012 Jul;
7(6):e39987.
PMID: 22761941
The hallmarks of many haematological malignancies and solid tumours are chromosomal translocations, which may lead to gene fusions. Recently, next-generation sequencing techniques at the transcriptome level (RNA-Seq) have been used...