The genetics of autism spectrum disorders and related neuropsychiatric disorders in childhood.
By P. Lichtenstein, E. Carlström, M. Råstam, C. Gillberg, H. Anckarsäter. American Journal of Psychiatry, 2010
761 citations recorded by the source corpus.
Subfields: Cognitive Neuroscience, Genetics, Psychiatry and Mental health
View Paper: https://www.semanticscholar.org/paper/1ff13fd46798a120376a3afbdec4f5ce608c8cfe
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Cognitive Neuroscience
- Catherine Lord
- Daniel H. Geschwind
- Marion Leboyer
- Pauline Chaste
- Edwin H. Cook Jr.
- Eric Fombonne
- Stephen V. Faraone
- Michael Rutter
In Genetics
- Catherine Lord
- Eric Fombonne
- Edwin H. Cook Jr.
- Brian J. O'Roak
- Shrikant M. Mane
- Michael Rutter
- Daniel H. Geschwind
- F. Happé
In Psychiatry and Mental health
Citations in the corpus
- Autism risk factors: genes, environment, and gene-environment interactions (2012, background): “One study showed that monozygotic twins had higher concordance rates than dizygotic twins for ASDs, attention deficit hyperactivity disorder (ADHD), developmental coordination disorder, and tic disorder with differences in cross-disorder effects between monozygotic and dizygotic twins, raising the q”
- Heritability of autism spectrum disorders: a meta‐analysis of twin studies (2015, background): “…are in line with the results from the largest extended family population study (Sandin et al., 2014), (showing no effects of shared environment) as well as results from the only random population twin study, which did not need to rely on fixed threshold correction (Lichtenstein et al., 2010).”
- Genetics of attention deficit hyperactivity disorder (2018, background): “Studies of community samples of youth, from the United States of America [46], the United Kingdom [47], and Sweden [11, 48] show that”
- THE FAMILIAL RISK OF AUTISM (2014, neutral): “Age at ASD diagnosis 13 (4-22) 13 (4-22) 13 (4-23) 13 (4-22) 11 (4-21) 10 (4-25)”
- Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. (2011, background): “A genetic contribution is well established from twin studies (Bailey et al., 1995; Lichtenstein et al., 2010; Liu et al., 2001).”