Publications
Dark microglia: A new phenotype predominantly associated with pathological states.. Glia. 64(5):826-39.
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2016. Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study.. Lancet. 387(10023):1085-93.
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2016. Behavioural markers for autism in infancy: scores on the Autism Observational Scale for Infants in a prospective study of at-risk siblings.. Infant Behav Dev. 38:107-15.
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2015. Pathway-based association study of multiple candidate genes and multiple traits using structural equation models.. Genet Epidemiol. 39(2):101-13.
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2015. Adolescence: a time of transition for the phenotype of dcc heterozygous mice.. Psychopharmacology (Berl). 231(8):1705-14.
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2014. Advancing research diagnostic criteria for Alzheimer's disease: the IWG-2 criteria.. Lancet Neurol. 13(6):614-29.
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2014. The association between CHRN genetic variants and dizziness at first inhalation of cigarette smoke.. Addict Behav. 39(1):316-20.
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2014. A comparative study of the neuropsychiatric and neurocognitive phenotype in two microdeletion syndromes: velocardiofacial (22q11.2 deletion) and Williams (7q11.23 deletion) syndromes.. Eur Psychiatry. 29(4):203-10.
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2014. The effect of sleep restriction on neurobehavioural functioning in normally developing children and adolescents: insights from the Attention, Behaviour and Sleep Laboratory.. Pathol Biol (Paris). 62(5):319-31.
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2014. Genetic variants and early cigarette smoking and nicotine dependence phenotypes in adolescents.. PLoS One. 9(12):e115716.
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2014. Modeling the phenotypic architecture of autism symptoms from time of diagnosis to age 6.. J Autism Dev Disord. 44(12):3045-55.
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2014. Prenatal maternal stress predicts autism traits in 6½ year-old children: Project Ice Storm.. Psychiatry Res. 219(2):353-60.
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2014. Transcriptional consequences of 16p11.2 deletion and duplication in mouse cortex and multiplex autism families.. Am J Hum Genet. 94(6):870-83.
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2014.