Genetic analysis of reelin gene (RELN) SNPs: No association with autism spectrum disorder in the Indian population
- 1 August 2008
- journal article
- research article
- Published by Elsevier in Neuroscience Letters
- Vol. 441 (1) , 56-60
- https://doi.org/10.1016/j.neulet.2008.06.022
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- Glutamate Receptor 6 Gene (GluR6 or GRIK2) Polymorphisms in the Indian Population: A Genetic Association Study on Autism Spectrum DisorderCellular and Molecular Neurobiology, 2007
- Investigation of potential gene–gene interactions between apoe and reln contributing to autism riskPsychiatric Genetics, 2007
- Reelin gene polymorphisms in the Indian population: A possible paternal 5′UTR‐CGG‐repeat‐allele effect on autismAmerican Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, 2006
- Pervasive Developmental Disorders in Preschool Children: Confirmation of High PrevalenceAmerican Journal of Psychiatry, 2005
- Haploview: analysis and visualization of LD and haplotype mapsBioinformatics, 2004
- Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA networkAmerican Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, 2004
- Analysis of reelin as a candidate gene for autismMolecular Psychiatry, 2003
- Pedigree disequilibrium tests for multilocus haplotypesGenetic Epidemiology, 2003
- A protein related to extracellular matrix proteins deleted in the mouse mutant reelerNature, 1995
- Autism as a strongly genetic disorder: evidence from a British twin studyPsychological Medicine, 1995