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 |