Detalhe da pesquisa
1.
Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia.
Mol Psychiatry
; 28(1): 475-482, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36380236
2.
The impact of educational attainment, intelligence and intellectual disability on schizophrenia: a Swedish population-based register and genetic study.
Mol Psychiatry
; 27(5): 2439-2447, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35379910
3.
Elevated common variant genetic risk for tourette syndrome in a densely-affected pedigree.
Mol Psychiatry
; 26(12): 7522-7529, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34526668
4.
Correction: Common-variant associations with fragile X syndrome.
Mol Psychiatry
; 25(12): 3450, 2020 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-31548576
5.
Association test using Copy Number Profile Curves (CONCUR) enhances power in rare copy number variant analysis.
PLoS Comput Biol
; 16(5): e1007797, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32365089
6.
Common-variant associations with fragile X syndrome.
Mol Psychiatry
; 24(3): 338-344, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30531935
7.
A randomized approach to speed up the analysis of large-scale read-count data in the application of CNV detection.
BMC Bioinformatics
; 19(1): 74, 2018 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29490610
8.
A New Method for Detecting Associations with Rare Copy-Number Variants.
PLoS Genet
; 11(10): e1005403, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26431523
9.
Implication of LRRC4C and DPP6 in neurodevelopmental disorders.
Am J Med Genet A
; 173(2): 395-406, 2017 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-27759917
10.
Allele-specific copy-number discovery from whole-genome and whole-exome sequencing.
Nucleic Acids Res
; 43(14): e90, 2015 Aug 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-25883151
11.
CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1.
Hum Mol Genet
; 23(6): 1669-76, 2014 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24163246
12.
An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis.
Hum Mol Genet
; 23(12): 3316-26, 2014 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24474471
13.
One CNV Discordance in NRXN1 Observed Upon Genome-wide Screening in 38 Pairs of Adult Healthy Monozygotic Twins.
Twin Res Hum Genet
; 19(2): 97-103, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26899349
14.
Improving detection of copy-number variation by simultaneous bias correction and read-depth segmentation.
Nucleic Acids Res
; 41(3): 1519-32, 2013 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23275535
15.
DeepGWAS: Enhance GWAS Signals for Neuropsychiatric Disorders via Deep Neural Network.
Res Sq
; 2023 Feb 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-36824788
16.
Increased Prevalence of Rare Copy Number Variants in Treatment-Resistant Psychosis.
Schizophr Bull
; 49(4): 881-892, 2023 07 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36454006
17.
Leveraging Base Pair Mammalian Constraint to Understand Genetic Variation and Human Disease.
bioRxiv
; 2023 Mar 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36945512
18.
Leveraging base-pair mammalian constraint to understand genetic variation and human disease.
Science
; 380(6643): eabn2937, 2023 04 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-37104612
19.
Genome-wide association mapping of loci for antipsychotic-induced extrapyramidal symptoms in mice.
Mamm Genome
; 23(5-6): 322-35, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22207321
20.
A customized and versatile high-density genotyping array for the mouse.
Nat Methods
; 6(9): 663-6, 2009 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-19668205