Detalhe da pesquisa
1.
Genetic common variants associated with cerebellar volume and their overlap with mental disorders: a study on 33,265 individuals from the UK-Biobank.
Mol Psychiatry
; 27(4): 2282-2290, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35079123
2.
Autism genetics: opportunities and challenges for clinical translation.
Nat Rev Genet
; 18(6): 362-376, 2017 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28260791
3.
Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders.
Hum Genet
; 133(6): 781-92, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24442360
4.
On genome-wide association studies for family-based designs: an integrative analysis approach combining ascertained family samples with unselected controls.
Am J Hum Genet
; 86(4): 573-80, 2010 Apr 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-20346434
5.
No evidence that common genetic risk variation is shared between schizophrenia and autism.
Am J Med Genet B Neuropsychiatr Genet
; 162B(1): 55-60, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23193033
6.
Investigating Direct and Indirect Genetic Effects in Attention-Deficit/Hyperactivity Disorder Using Parent-Offspring Trios.
Biol Psychiatry
; 93(1): 37-44, 2023 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35933166
7.
Phenotypic effects of genetic variants associated with autism.
Nat Med
; 29(7): 1671-1680, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37365347
8.
Meta-Analyses of Genome-Wide Association Studies for Postpartum Depression.
Am J Psychiatry
; 180(12): 884-895, 2023 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37849304
9.
Investigating regions of shared genetic variation in attention deficit/hyperactivity disorder and major depressive disorder: a GWAS meta-analysis.
Sci Rep
; 11(1): 7353, 2021 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33795730
10.
A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants.
Am J Psychiatry
; 178(1): 77-86, 2021 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33384013
11.
Polygenic risk for schizophrenia and subcortical brain anatomy in the UK Biobank cohort.
Transl Psychiatry
; 10(1): 309, 2020 09 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32908133
12.
Autism symptoms in Attention-Deficit/Hyperactivity Disorder: a familial trait which correlates with conduct, oppositional defiant, language and motor disorders.
J Autism Dev Disord
; 39(2): 197-209, 2009 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18642069
13.
Fine mapping and association studies in a candidate region for autism on chromosome 2q31-q32.
Am J Med Genet B Neuropsychiatr Genet
; 150B(4): 535-44, 2009 Jun 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-18846500
14.
Non-random error in genotype calling procedures: implications for family-based and case-control genome-wide association studies.
Am J Med Genet B Neuropsychiatr Genet
; 147B(8): 1379-86, 2008 Dec 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-18663727
15.
Parent of origin effects in attention/deficit hyperactivity disorder (ADHD): analysis of data from the international multicenter ADHD genetics (IMAGE) program.
Am J Med Genet B Neuropsychiatr Genet
; 147B(8): 1495-500, 2008 Dec 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-18163388
16.
Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder.
Am J Med Genet B Neuropsychiatr Genet
; 147B(8): 1355-8, 2008 Dec 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-18937294
17.
Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.
Am J Med Genet B Neuropsychiatr Genet
; 147B(8): 1369-78, 2008 Dec 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-18951430
18.
Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.
Am J Med Genet B Neuropsychiatr Genet
; 147B(8): 1345-54, 2008 Dec 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-18821565
19.
Variation in the gene coding for the M5 muscarinic receptor (CHRM5) influences cigarette dose but is not associated with dependence to drugs of addiction: evidence from a prospective population based cohort study of young adults.
BMC Genet
; 8: 46, 2007 Jul 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-17608938
20.
Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci.
Eur J Hum Genet
; 24(2): 291-7, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25920553