Search details
1.
A framework for an evidence-based gene list relevant to autism spectrum disorder.
Nat Rev Genet
; 21(6): 367-376, 2020 06.
Article
in English
| MEDLINE | ID: mdl-32317787
2.
Early development and epilepsy in tuberous sclerosis complex: A prospective longitudinal study.
Dev Med Child Neurol
; 66(5): 635-643, 2024 May.
Article
in English
| MEDLINE | ID: mdl-37885138
3.
Epilepsy severity mediates association between mutation type and ADHD symptoms in tuberous sclerosis complex.
Epilepsia
; 64(3): e30-e35, 2023 03.
Article
in English
| MEDLINE | ID: mdl-36633094
4.
Alpha oscillatory activity during attentional control in children with Autism Spectrum Disorder (ASD), Attention-Deficit/Hyperactivity Disorder (ADHD), and ASD+ADHD.
J Child Psychol Psychiatry
; 63(7): 745-761, 2022 07.
Article
in English
| MEDLINE | ID: mdl-34477232
5.
Perinatal adversities in tuberous sclerosis complex: Determinants and neurodevelopmental outcomes.
Dev Med Child Neurol
; 64(10): 1237-1245, 2022 10.
Article
in English
| MEDLINE | ID: mdl-35366331
6.
Autism spectrum disorder and obstetric optimality: a twin study and meta-analysis of sibling studies.
J Child Psychol Psychiatry
; 62(11): 1353-1362, 2021 11.
Article
in English
| MEDLINE | ID: mdl-34590310
7.
Sex-chromosome dosage effects on gene expression in humans.
Proc Natl Acad Sci U S A
; 115(28): 7398-7403, 2018 07 10.
Article
in English
| MEDLINE | ID: mdl-29946024
8.
Guidance for identification and treatment of individuals with attention deficit/hyperactivity disorder and autism spectrum disorder based upon expert consensus.
BMC Med
; 18(1): 146, 2020 05 25.
Article
in English
| MEDLINE | ID: mdl-32448170
9.
Synaptic, transcriptional and chromatin genes disrupted in autism.
Nature
; 515(7526): 209-15, 2014 Nov 13.
Article
in English
| MEDLINE | ID: mdl-25363760
10.
Long-term cognitive outcomes in tuberous sclerosis complex.
Dev Med Child Neurol
; 62(3): 322-329, 2020 03.
Article
in English
| MEDLINE | ID: mdl-31538337
11.
Good social skills despite poor theory of mind: exploring compensation in autism spectrum disorder.
J Child Psychol Psychiatry
; 60(1): 102-110, 2019 01.
Article
in English
| MEDLINE | ID: mdl-29582425
12.
Commando care for individuals living with severe mental illness: Equally Well goes beyond metabolic health alone.
Aust N Z J Psychiatry
; : 48674241240601, 2024 Apr 01.
Article
in English
| MEDLINE | ID: mdl-38561868
13.
Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment.
PLoS Genet
; 11(3): e1004925, 2015 Mar.
Article
in English
| MEDLINE | ID: mdl-25781923
14.
In search of biomarkers for autism: scientific, social and ethical challenges.
Nat Rev Neurosci
; 12(10): 603-12, 2011 09 20.
Article
in English
| MEDLINE | ID: mdl-21931335
15.
Immune signatures and disorder-specific patterns in a cross-disorder gene expression analysis.
Br J Psychiatry
; 209(3): 202-8, 2016 09.
Article
in English
| MEDLINE | ID: mdl-27151072
16.
Heritability of autism spectrum disorders: a meta-analysis of twin studies.
J Child Psychol Psychiatry
; 57(5): 585-95, 2016 May.
Article
in English
| MEDLINE | ID: mdl-26709141
17.
Response time variability under slow and fast-incentive conditions in children with ASD, ADHD and ASD+ADHD.
J Child Psychol Psychiatry
; 57(12): 1414-1423, 2016 12.
Article
in English
| MEDLINE | ID: mdl-27465225
18.
Diagnosing autism spectrum disorder in community settings using the Development and Well-Being Assessment: validation in a UK population-based twin sample.
J Child Psychol Psychiatry
; 57(2): 161-70, 2016 Feb.
Article
in English
| MEDLINE | ID: mdl-26174111
19.
Functional impact of global rare copy number variation in autism spectrum disorders.
Nature
; 466(7304): 368-72, 2010 Jul 15.
Article
in English
| MEDLINE | ID: mdl-20531469
20.
Rare deletions at the neurexin 3 locus in autism spectrum disorder.
Am J Hum Genet
; 90(1): 133-41, 2012 Jan 13.
Article
in English
| MEDLINE | ID: mdl-22209245