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.
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
4.
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
5.
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
6.
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
7.
The recombinational anatomy of a mouse chromosome.
PLoS Genet
; 4(7): e1000119, 2008 Jul 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-18617997
8.
Association of candidate genes with phenotypic traits relevant to anorexia nervosa.
Eur Eat Disord Rev
; 19(6): 487-93, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21780254
9.
Crossover interference underlies sex differences in recombination rates.
Trends Genet
; 23(11): 539-42, 2007 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-17964681
10.
A survey of airway responsiveness in 36 inbred mouse strains facilitates gene mapping studies and identification of quantitative trait loci.
Mol Genet Genomics
; 283(4): 317-26, 2010 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-20143096
11.
Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia.
Nat Commun
; 11(1): 1842, 2020 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-32296054
12.
Characterization of Single Gene Copy Number Variants in Schizophrenia.
Biol Psychiatry
; 87(8): 736-744, 2020 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31767120
13.
Otitis media: a genome-wide linkage scan with evidence of susceptibility loci within the 17q12 and 10q22.3 regions.
BMC Med Genet
; 10: 85, 2009 Sep 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-19728873
14.
Author Correction: Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia.
Nat Commun
; 13(1): 191, 2022 Jan 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-34987162
15.
Exploration of large, rare copy number variants associated with psychiatric and neurodevelopmental disorders in individuals with anorexia nervosa.
Psychiatr Genet
; 27(4): 152-158, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28368970
16.
Defective carbohydrate metabolism in mice homozygous for the tubby mutation.
Physiol Genomics
; 27(2): 131-40, 2006 Oct 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-16849632
17.
Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B alleles.
Nat Commun
; 5: 4757, 2014 Sep 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-25187353
18.
Endogenous retinoids in the pathogenesis of alopecia areata.
J Invest Dermatol
; 133(2): 334-43, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23014334
19.
CGDSNPdb: a database resource for error-checked and imputed mouse SNPs.
Database (Oxford)
; 2010: baq008, 2010 Jul 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-20624716
20.
Patterns of recombination activity on mouse chromosome 11 revealed by high resolution mapping.
PLoS One
; 5(12): e15340, 2010 Dec 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-21170346