249 related articles for article (PubMed ID: 19287153)
1. Copy number alterations and copy number variation in cancer: close encounters of the bad kind.
Speleman F; Kumps C; Buysse K; Poppe B; Menten B; De Preter K
Cytogenet Genome Res; 2008; 123(1-4):176-82. PubMed ID: 19287153
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. CNVs and genetic medicine (excitement and consequences of a rediscovery).
Beckmann JS; Sharp AJ; Antonarakis SE
Cytogenet Genome Res; 2008; 123(1-4):7-16. PubMed ID: 19287134
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Mutational and selective effects on copy-number variants in the human genome.
Cooper GM; Nickerson DA; Eichler EE
Nat Genet; 2007 Jul; 39(7 Suppl):S22-9. PubMed ID: 17597777
[TBL] [Abstract][Full Text] [Related]
6. Comparative analysis of copy number variation in primate genomes.
Kehrer-Sawatzki H; Cooper DN
Cytogenet Genome Res; 2008; 123(1-4):288-96. PubMed ID: 19287167
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Chromosome copy number variation and breast cancer risk.
Tchatchou S; Burwinkel B
Cytogenet Genome Res; 2008; 123(1-4):183-7. PubMed ID: 19287154
[TBL] [Abstract][Full Text] [Related]
9. Extending genome-wide association studies to copy-number variation.
McCarroll SA
Hum Mol Genet; 2008 Oct; 17(R2):R135-42. PubMed ID: 18852202
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Germline copy number variation and cancer risk.
Kuiper RP; Ligtenberg MJ; Hoogerbrugge N; Geurts van Kessel A
Curr Opin Genet Dev; 2010 Jun; 20(3):282-9. PubMed ID: 20381334
[TBL] [Abstract][Full Text] [Related]
12. Benign and pathogenic copy number variation on the short arm of chromosome 4.
Hannes F; Vermeesch JR
Cytogenet Genome Res; 2008; 123(1-4):88-93. PubMed ID: 19287142
[TBL] [Abstract][Full Text] [Related]
13. Copy-number variation and association studies of human disease.
McCarroll SA; Altshuler DM
Nat Genet; 2007 Jul; 39(7 Suppl):S37-42. PubMed ID: 17597780
[TBL] [Abstract][Full Text] [Related]
14. Detection and validation of copy number variation in X-linked mental retardation.
Bauters M; Weuts A; Vandewalle J; Nevelsteen J; Marynen P; Van Esch H; Froyen G
Cytogenet Genome Res; 2008; 123(1-4):44-53. PubMed ID: 19287138
[TBL] [Abstract][Full Text] [Related]
15. Copy number variations in chronic pancreatitis.
Chen JM; Masson E; Le Maréchal C; Férec C
Cytogenet Genome Res; 2008; 123(1-4):102-7. PubMed ID: 19287144
[TBL] [Abstract][Full Text] [Related]
16. Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture.
Vissers LE; Bhatt SS; Janssen IM; Xia Z; Lalani SR; Pfundt R; Derwinska K; de Vries BB; Gilissen C; Hoischen A; Nesteruk M; Wisniowiecka-Kowalnik B; Smyk M; Brunner HG; Cheung SW; van Kessel AG; Veltman JA; Stankiewicz P
Hum Mol Genet; 2009 Oct; 18(19):3579-93. PubMed ID: 19578123
[TBL] [Abstract][Full Text] [Related]
17. Somatic mosaicism for copy number variation in differentiated human tissues.
Piotrowski A; Bruder CE; Andersson R; Diaz de Ståhl T; Menzel U; Sandgren J; Poplawski A; von Tell D; Crasto C; Bogdan A; Bartoszewski R; Bebok Z; Krzyzanowski M; Jankowski Z; Partridge EC; Komorowski J; Dumanski JP
Hum Mutat; 2008 Sep; 29(9):1118-24. PubMed ID: 18570184
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. HIV-1/AIDS susceptibility and copy number variation in CCL3L1, a gene encoding a natural ligand for HIV-1 co-receptor CCR5.
Nakajima T; Kaur G; Mehra N; Kimura A
Cytogenet Genome Res; 2008; 123(1-4):156-60. PubMed ID: 19287150
[TBL] [Abstract][Full Text] [Related]
20. Copy number variations and cancer susceptibility.
Shlien A; Malkin D
Curr Opin Oncol; 2010 Jan; 22(1):55-63. PubMed ID: 19952747
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]