From: Bibliometric profile of the global scientific research on autism spectrum disorders
No. | Authors | Title | Year | Source title | Number of citations |
---|---|---|---|---|---|
1st | Sebat et al. (2007) | Strong association of de novo copy number mutations with autism | 2007 | Science | 1427 |
2nd | Marshall et al. (2008) | Structural Variation of Chromosomes in Autism Spectrum Disorder | 2008 | American Journal of Human Genetics | 908 |
3rd | Abrahams and Geschwind (2008) | Advances in autism genetics: On the threshold of a new neurobiology | 2008 | Nature Reviews Genetics | 866 |
4th | Pinto et al. (2010) | Functional impact of global rare copy number variation in autism spectrum disorders | 2010 | Nature | 862 |
5th | Weiss et al. (2008) | Association between microdeletion and microduplication at 16p11.2 and autism | 2008 | New England Journal of Medicine | 848 |
6th | Szatmari et al. (2007) | Mapping autism risk loci using genetic linkage and chromosomal rearrangements | 2007 | Nature Genetics | 842 |
7th | Baird et al. (2006) | Prevalence of disorders of the autism spectrum in a population cohort of children in South Thames: the Special Needs and Autism Project (SNAP) | 2006 | Lancet | 826 |
8th | Happé and Frith (2006) | The weak coherence account: Detail-focused cognitive style in autism spectrum disorders | 2006 | Journal of Autism and Developmental Disorders | 757 |
9th | Vargas et al. (2005) | Neuroglial activation and neuroinflammation in the brain of patients with autism | 2005 | Annals of Neurology | 747 |
10th | Dalton et al. (2005) | Gaze fixation and the neural circuitry of face processing in autism | 2005 | Nature Neuroscience | 680 |