Detalhe da pesquisa
1.
A framework for an evidence-based gene list relevant to autism spectrum disorder.
Nat Rev Genet
; 21(6): 367-376, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32317787
2.
Startle responses in Duchenne muscular dystrophy: a novel biomarker of brain dystrophin deficiency.
Brain
; 146(1): 252-265, 2023 01 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35136951
3.
Trajectories of autistic social traits in childhood and adolescence and disordered eating behaviours at age 14 years: A UK general population cohort study.
J Child Psychol Psychiatry
; 62(1): 75-85, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32361997
4.
Experiences of social interaction in young women with Turner syndrome: A qualitative study.
Child Care Health Dev
; 46(1): 46-55, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31322282
5.
Structural connectivity of the amygdala in young adults with autism spectrum disorder.
Hum Brain Mapp
; 39(3): 1270-1282, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29265723
6.
The development of autistic social traits across childhood and adolescence in males and females.
J Child Psychol Psychiatry
; 59(11): 1143-1151, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29672866
7.
Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplications.
Am J Med Genet B Neuropsychiatr Genet
; 177(4): 397-405, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29603867
8.
Cognitive, behavioral, and neural consequences of sex chromosome aneuploidy.
J Neurosci Res
; 95(1-2): 311-319, 2017 01 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27870409
9.
Evaluating social (pragmatic) communication disorder.
J Child Psychol Psychiatry
; 58(10): 1166-1175, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28741680
10.
Common polymorphism in the oxytocin receptor gene (OXTR) is associated with human social recognition skills.
Proc Natl Acad Sci U S A
; 111(5): 1987-92, 2014 Feb 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-24367110
11.
Neurodevelopmental, emotional, and behavioural problems in Duchenne muscular dystrophy in relation to underlying dystrophin gene mutations.
Dev Med Child Neurol
; 58(1): 77-84, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26365034
12.
A randomised controlled trial of PEGASUS, a psychoeducational programme for young people with high-functioning autism spectrum disorder.
J Child Psychol Psychiatry
; 56(4): 468-76, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25132516
13.
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.
PLoS Genet
; 8(2): e1002521, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22346768
14.
Xlr3b is a new imprinted candidate for X-linked parent-of-origin effects on cognitive function in mice.
Nat Genet
; 37(6): 625-9, 2005 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-15908950
15.
The effect of pre-treatment and process conditions on the gas barrier properties of fibrillated cellulose films and coatings: A review.
Carbohydr Polym
; 337: 122085, 2024 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38710579
16.
Rare neurodevelopmental conditions and parents' mental health - how and when does genetic diagnosis matter?
Orphanet J Rare Dis
; 19(1): 70, 2024 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38360654
17.
Detecting Autism Spectrum Disorder and Attention Deficit Hyperactivity Disorder Using Multimodal Time-Frequency Analysis with Machine Learning Using the Electroretinogram from Two Flash Strengths.
J Autism Dev Disord
; 2024 Feb 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-38393437
18.
Utility of the 3Di short version in the identification and diagnosis of autism in children at the Kenyan coast.
Front Psychiatry
; 15: 1234929, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38487576
19.
Practising psychiatry in Sri Lanka: challenges and opportunities.
BJPsych Int
; 20(1): 1, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-36812010
20.
The benefits of digitisation of psychiatric care facilities.
BJPsych Int
; 20(3): 53, 2023 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-37531243