293 related articles for article (PubMed ID: 21956041)
1. Implications of gene copy-number variation in health and diseases.
Almal SH; Padh H
J Hum Genet; 2012 Jan; 57(1):6-13. PubMed ID: 21956041
[TBL] [Abstract][Full Text] [Related]
2. Detection of copy number variation using SNP genotyping.
Cooper GM; Mefford HC
Methods Mol Biol; 2011; 767():243-52. PubMed ID: 21822880
[TBL] [Abstract][Full Text] [Related]
3. Pharmacogenetics: technologies to detect copy number variations.
Dhawan D; Padh H
Curr Opin Mol Ther; 2009 Dec; 11(6):670-80. PubMed ID: 20072944
[TBL] [Abstract][Full Text] [Related]
4. Genomic copy number variations: A breakthrough in our knowledge on schizophrenia etiology?
Hosak L; Silhan P; Hosakova J
Neuro Endocrinol Lett; 2012; 33(2):183-90. PubMed ID: 22592199
[TBL] [Abstract][Full Text] [Related]
5. The clinical context of copy number variation in the human genome.
Lee C; Scherer SW
Expert Rev Mol Med; 2010 Mar; 12():e8. PubMed ID: 20211047
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. [DNA polymorphisms].
Suehiro Y; Furuya T; Sasaki K; Hinota Y
Rinsho Byori; 2013 Nov; 61(11):1001-7. PubMed ID: 24450105
[TBL] [Abstract][Full Text] [Related]
8. Copy number variation in Fayoumi and Leghorn chickens analyzed using array comparative genomic hybridization.
Abernathy J; Li X; Jia X; Chou W; Lamont SJ; Crooijmans R; Zhou H
Anim Genet; 2014 Jun; 45(3):400-11. PubMed ID: 24628374
[TBL] [Abstract][Full Text] [Related]
9. Analysis of copy number variants in the cattle genome.
Kijas JW; Barendse W; Barris W; Harrison B; McCulloch R; McWilliam S; Whan V
Gene; 2011 Aug; 482(1-2):73-7. PubMed ID: 21620936
[TBL] [Abstract][Full Text] [Related]
10. Structural variation in the human genome and its role in disease.
Stankiewicz P; Lupski JR
Annu Rev Med; 2010; 61():437-55. PubMed ID: 20059347
[TBL] [Abstract][Full Text] [Related]
11. Copy-number variations, noncoding sequences, and human phenotypes.
Klopocki E; Mundlos S
Annu Rev Genomics Hum Genet; 2011; 12():53-72. PubMed ID: 21756107
[TBL] [Abstract][Full Text] [Related]
12. Genome-wide copy number profiling on high-density bacterial artificial chromosomes, single-nucleotide polymorphisms, and oligonucleotide microarrays: a platform comparison based on statistical power analysis.
Hehir-Kwa JY; Egmont-Petersen M; Janssen IM; Smeets D; van Kessel AG; Veltman JA
DNA Res; 2007 Feb; 14(1):1-11. PubMed ID: 17363414
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Structural variants: changing the landscape of chromosomes and design of disease studies.
Feuk L; Marshall CR; Wintle RF; Scherer SW
Hum Mol Genet; 2006 Apr; 15 Spec No 1():R57-66. PubMed ID: 16651370
[TBL] [Abstract][Full Text] [Related]
15. Copy number variation and psychiatric disease risk.
Levy RJ; Xu B; Gogos JA; Karayiorgou M
Methods Mol Biol; 2012; 838():97-113. PubMed ID: 22228008
[TBL] [Abstract][Full Text] [Related]
16. The discovery of human genetic variations and their use as disease markers: past, present and future.
Ku CS; Loy EY; Salim A; Pawitan Y; Chia KS
J Hum Genet; 2010 Jul; 55(7):403-15. PubMed ID: 20485443
[TBL] [Abstract][Full Text] [Related]
17. Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree.
Lesch KP; Selch S; Renner TJ; Jacob C; Nguyen TT; Hahn T; Romanos M; Walitza S; Shoichet S; Dempfle A; Heine M; Boreatti-Hümmer A; Romanos J; Gross-Lesch S; Zerlaut H; Wultsch T; Heinzel S; Fassnacht M; Fallgatter A; Allolio B; Schäfer H; Warnke A; Reif A; Ropers HH; Ullmann R
Mol Psychiatry; 2011 May; 16(5):491-503. PubMed ID: 20308990
[TBL] [Abstract][Full Text] [Related]
18. Comparative genomic hybridization to detect variation in the copy number of large DNA segments.
Holcomb IN; Trask BJ
Cold Spring Harb Protoc; 2011 Nov; 2011(11):1323-33. PubMed ID: 22046040
[TBL] [Abstract][Full Text] [Related]
19. The impact of human copy number variation on a new era of genetic testing.
Choy KW; Setlur SR; Lee C; Lau TK
BJOG; 2010 Mar; 117(4):391-8. PubMed ID: 20105165
[TBL] [Abstract][Full Text] [Related]
20. Copy number variants, diseases and gene expression.
Henrichsen CN; Chaignat E; Reymond A
Hum Mol Genet; 2009 Apr; 18(R1):R1-8. PubMed ID: 19297395
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]