scholarly journals Genetic association studies in pre-eclampsia: systematic meta-analyses and field synopsis

2012 ◽  
Vol 41 (6) ◽  
pp. 1764-1775 ◽  
Author(s):  
Eleonora Staines-Urias ◽  
María C Paez ◽  
Pat Doyle ◽  
Frank Dudbridge ◽  
Norma C Serrano ◽  
...  
2018 ◽  
Author(s):  
Olena Ohlei ◽  
Valerija Dobricic ◽  
Katja Lohmann ◽  
Christine Klein ◽  
Christina Lill ◽  
...  

AbstractBackground and objectivesDystonia is a genetically complex disease with both monogenic and polygenic causes. For the latter, numerous genetic associations studies have been performed with largely inconsistent results. The aim of this study was to perform a field synopsis including systematic meta-analyses of genetic association studies in isolated dystoniaMethodsFor the field synopsis we systematically screened and scrutinized the published literature using NCBI’s PubMed database. For genetic variants with sufficient information in at least two independent datasets, random-effects meta-analyses were performed, including meta-analyses stratified by ethnic descent and dystonia subtypes.ResultsA total of 3,575 articles were identified and scrutinized resulting in the inclusion of 42 independent publications allowing 134 meta-analyses on 45 variants across 17 genes. While our meta-analyses pinpointed several significant association signals with variants in TOR1A, DRD1, and ARSG, no single variant displayed compelling association with dystonia in the available data.ConclusionsOur study provides an up-to-date summary of the status of dystonia genetic association studies. Additional large-scale studies are needed to better understand the genetic causes of isolated dystonia.


2011 ◽  
Vol 103 (16) ◽  
pp. 1227-1235 ◽  
Author(s):  
F. Chatzinasiou ◽  
C. M. Lill ◽  
K. Kypreou ◽  
I. Stefanaki ◽  
V. Nicolaou ◽  
...  

2010 ◽  
Vol 25 (11) ◽  
pp. 765-775 ◽  
Author(s):  
Stefania Boccia ◽  
Emma De Feo ◽  
Paola Gallì ◽  
Francesco Gianfagna ◽  
Rosarita Amore ◽  
...  

2012 ◽  
Vol 104 (19) ◽  
pp. 1433-1457 ◽  
Author(s):  
E. Theodoratou ◽  
Z. Montazeri ◽  
S. Hawken ◽  
G. C. Allum ◽  
J. Gong ◽  
...  

2015 ◽  
Vol 135 (4) ◽  
pp. 1074-1079 ◽  
Author(s):  
Kyriaki Antonopoulou ◽  
Irene Stefanaki ◽  
Christina M. Lill ◽  
Foteini Chatzinasiou ◽  
Katerina P. Kypreou ◽  
...  

BMC Genetics ◽  
2015 ◽  
Vol 16 (1) ◽  
Author(s):  
Zahra N. Sohani ◽  
David Meyre ◽  
Russell J. de Souza ◽  
Philip G. Joseph ◽  
Mandark Gandhi ◽  
...  

Author(s):  
Pantelis G Bagos ◽  
Georgios K Nikolopoulos

We propose here a simple and robust approach for meta-analysis of molecular association studies. Making use of the binary structure of the data, and by treating the genotypes as independent variables in a logistic regression, we apply a simple and commonly used methodology that performs satisfactorily, being at the same time very flexible. We present simple tests for detecting heterogeneity and we describe a random effects extension of the method in order to allow for between studies heterogeneity. We derive also simple tests for assessing the most plausible genetic model of inheritance, and its between-studies heterogeneity as well as adjusting for covariates. The methodology introduced here is easily extended in cases with polytomous or continuous outcomes as well as in cases with more than two alleles. We apply the methodology in several published meta-analyses of genetic association studies with very encouraging results. The main advantages of the proposed methodology is its flexibility and the ease of use, while at the same time covers almost every aspect of a meta-analysis providing overall estimates without the need of multiple comparisons. We anticipate that this simple method would be used in the future in meta-analyses of genetic association studies. A STATA command performing all the available computations is available at http://bioinformatics.biol.uoa.gr/~pbagos/metagen/.


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