206 related articles for article (PubMed ID: 19287141)
1. Putatively benign copy number variants in subjects with idiopathic autism spectrum disorder and/or intellectual disability.
Qiao Y; Harvard C; Riendeau N; Fawcett C; Liu X; Holden JJ; Lewis ME; Rajcan-Separovic E
Cytogenet Genome Res; 2008; 123(1-4):79-87. PubMed ID: 19287141
[TBL] [Abstract][Full Text] [Related]
2. Copy number variations associated with idiopathic autism identified by whole-genome microarray-based comparative genomic hybridization.
Cho SC; Yim SH; Yoo HK; Kim MY; Jung GY; Shin GW; Kim BN; Hwang JW; Kang JJ; Kim TM; Chung YJ
Psychiatr Genet; 2009 Aug; 19(4):177-85. PubMed ID: 19407672
[TBL] [Abstract][Full Text] [Related]
3. Detection and characterization of copy number variation in autism spectrum disorder.
Marshall CR; Scherer SW
Methods Mol Biol; 2012; 838():115-35. PubMed ID: 22228009
[TBL] [Abstract][Full Text] [Related]
4. Interstitial microduplication of Xp22.31: Causative of intellectual disability or benign copy number variant?
Li F; Shen Y; Köhler U; Sharkey FH; Menon D; Coulleaux L; Malan V; Rio M; McMullan DJ; Cox H; Fagan KA; Gaunt L; Metcalfe K; Heinrich U; Hislop G; Maye U; Sutcliffe M; Wu BL; Thiel BD; Mulchandani S; Conlin LK; Spinner NB; Murphy KM; Batista DA
Eur J Med Genet; 2010; 53(2):93-9. PubMed ID: 20132918
[TBL] [Abstract][Full Text] [Related]
5. Copy-number variants in neurodevelopmental disorders: promises and challenges.
Merikangas AK; Corvin AP; Gallagher L
Trends Genet; 2009 Dec; 25(12):536-44. PubMed ID: 19910074
[TBL] [Abstract][Full Text] [Related]
6. Clinical application of 2.7M Cytogenetics array for CNV detection in subjects with idiopathic autism and/or intellectual disability.
Qiao Y; Tyson C; Hrynchak M; Lopez-Rangel E; Hildebrand J; Martell S; Fawcett C; Kasmara L; Calli K; Harvard C; Liu X; Holden JJ; Lewis SM; Rajcan-Separovic E
Clin Genet; 2013 Feb; 83(2):145-54. PubMed ID: 22369279
[TBL] [Abstract][Full Text] [Related]
7. Copy number variations and clinical cytogenetic diagnosis of constitutional disorders.
Lee C; Iafrate AJ; Brothman AR
Nat Genet; 2007 Jul; 39(7 Suppl):S48-54. PubMed ID: 17597782
[TBL] [Abstract][Full Text] [Related]
8. Detection of pathogenic gene copy number variations in patients with mental retardation by genomewide oligonucleotide array comparative genomic hybridization.
Fan YS; Jayakar P; Zhu H; Barbouth D; Sacharow S; Morales A; Carver V; Benke P; Mundy P; Elsas LJ
Hum Mutat; 2007 Nov; 28(11):1124-32. PubMed ID: 17621639
[TBL] [Abstract][Full Text] [Related]
9. What a difference copy number variation makes.
Kehrer-Sawatzki H
Bioessays; 2007 Apr; 29(4):311-3. PubMed ID: 17373652
[TBL] [Abstract][Full Text] [Related]
10. Array comparative genomic hybridisation of 52 subjects with a Smith-Magenis-like phenotype: identification of dosage sensitive loci also associated with schizophrenia, autism, and developmental delay.
Williams SR; Girirajan S; Tegay D; Nowak N; Hatchwell E; Elsea SH
J Med Genet; 2010 Apr; 47(4):223-9. PubMed ID: 19752160
[TBL] [Abstract][Full Text] [Related]
11. Benign copy number changes in clinical cytogenetic diagnostics by array CGH.
Whitby H; Tsalenko A; Aston E; Tsang P; Mitchell S; Bayrak-Toydemir P; Hopkins C; Peters G; Bailey DK; Bruhn L; Brothman AR
Cytogenet Genome Res; 2008; 123(1-4):94-101. PubMed ID: 19287143
[TBL] [Abstract][Full Text] [Related]
12. Genome arrays for the detection of copy number variations in idiopathic mental retardation, idiopathic generalized epilepsy and neuropsychiatric disorders: lessons for diagnostic workflow and research.
Hochstenbach R; Buizer-Voskamp JE; Vorstman JA; Ophoff RA
Cytogenet Genome Res; 2011; 135(3-4):174-202. PubMed ID: 22056632
[TBL] [Abstract][Full Text] [Related]
13. Recurrent 16p11.2 microdeletions in autism.
Kumar RA; KaraMohamed S; Sudi J; Conrad DF; Brune C; Badner JA; Gilliam TC; Nowak NJ; Cook EH; Dobyns WB; Christian SL
Hum Mol Genet; 2008 Feb; 17(4):628-38. PubMed ID: 18156158
[TBL] [Abstract][Full Text] [Related]
14. Large-scale copy number variants (CNVs) detected in different ethnic human populations.
Takahashi N; Satoh Y; Kodaira M; Katayama H
Cytogenet Genome Res; 2008; 123(1-4):224-33. PubMed ID: 19287159
[TBL] [Abstract][Full Text] [Related]
15. Analysis of copy number variation in the rhesus macaque genome identifies candidate loci for evolutionary and human disease studies.
Lee AS; Gutiérrez-Arcelus M; Perry GH; Vallender EJ; Johnson WE; Miller GM; Korbel JO; Lee C
Hum Mol Genet; 2008 Apr; 17(8):1127-36. PubMed ID: 18180252
[TBL] [Abstract][Full Text] [Related]
16. Emerging themes and new challenges in defining the role of structural variation in human disease.
Sharp AJ
Hum Mutat; 2009 Feb; 30(2):135-44. PubMed ID: 18837009
[TBL] [Abstract][Full Text] [Related]
17. Copy number changes of the microcephalin 1 gene (MCPH1) in patients with autism spectrum disorders.
Ozgen HM; van Daalen E; Bolton PF; Maloney VK; Huang S; Cresswell L; van den Boogaard MJ; Eleveld MJ; van 't Slot R; Hochstenbach R; Beemer FA; Barrow M; Barber JC; Poot M
Clin Genet; 2009 Oct; 76(4):348-56. PubMed ID: 19793310
[TBL] [Abstract][Full Text] [Related]
18. Germline copy number variation in control populations.
Al-Sukhni W; Gallinger S
Cytogenet Genome Res; 2008; 123(1-4):211-23. PubMed ID: 19287158
[TBL] [Abstract][Full Text] [Related]
19. Genotype-phenotype analysis of 18q12.1-q12.2 copy number variation in autism.
Wang P; Carrion P; Qiao Y; Tyson C; Hrynchak M; Calli K; Lopez-Rangel E; Andrieux J; Delobel B; Duban-Bedu B; Thuresson AC; Annerén G; Liu X; Rajcan-Separovic E; Suzanne Lewis ME
Eur J Med Genet; 2013 Aug; 56(8):420-5. PubMed ID: 23727450
[TBL] [Abstract][Full Text] [Related]
20. Comparison of genome-wide array genomic hybridization platforms for the detection of copy number variants in idiopathic mental retardation.
Tucker T; Montpetit A; Chai D; Chan S; Chénier S; Coe BP; Delaney A; Eydoux P; Lam WL; Langlois S; Lemyre E; Marra M; Qian H; Rouleau GA; Vincent D; Michaud JL; Friedman JM
BMC Med Genomics; 2011 Mar; 4():25. PubMed ID: 21439053
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
