370 related articles for article (PubMed ID: 21587107)
1. Genetic predisposition in degenerative lumbar scoliosis due to the copy number variation.
Shin JH; Ha KY; Jung SH; Chung YJ
Spine (Phila Pa 1976); 2011 Oct; 36(21):1782-93. PubMed ID: 21587107
[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. Large scale copy number variation (CNV) at 14q12 is associated with the presence of genomic abnormalities in neoplasia.
Braude I; Vukovic B; Prasad M; Marrano P; Turley S; Barber D; Zielenska M; Squire JA
BMC Genomics; 2006 Jun; 7():138. PubMed ID: 16756668
[TBL] [Abstract][Full Text] [Related]
4. Clinical significance of rare copy number variations in epilepsy: a case-control survey using microarray-based comparative genomic hybridization.
Striano P; Coppola A; Paravidino R; Malacarne M; Gimelli S; Robbiano A; Traverso M; Pezzella M; Belcastro V; Bianchi A; Elia M; Falace A; Gazzerro E; Ferlazzo E; Freri E; Galasso R; Gobbi G; Molinatto C; Cavani S; Zuffardi O; Striano S; Ferrero GB; Silengo M; Cavaliere ML; Benelli M; Magi A; Piccione M; Dagna Bricarelli F; Coviello DA; Fichera M; Minetti C; Zara F
Arch Neurol; 2012 Mar; 69(3):322-30. PubMed ID: 22083797
[TBL] [Abstract][Full Text] [Related]
5. Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer.
Kloth JN; Oosting J; van Wezel T; Szuhai K; Knijnenburg J; Gorter A; Kenter GG; Fleuren GJ; Jordanova ES
BMC Genomics; 2007 Feb; 8():53. PubMed ID: 17311676
[TBL] [Abstract][Full Text] [Related]
6. Copy number gain at 8q12.1-q22.1 is associated with a malignant tumor phenotype in salivary gland myoepitheliomas.
Vékony H; Röser K; Löning T; Ylstra B; Meijer GA; van Wieringen WN; van de Wiel MA; Carvalho B; Kok K; Leemans CR; van der Waal I; Bloemena E
Genes Chromosomes Cancer; 2009 Feb; 48(2):202-12. PubMed ID: 19009612
[TBL] [Abstract][Full Text] [Related]
7. A genome-wide analysis of loss of heterozygosity and chromosomal copy number variation in Proteus syndrome using high-density SNP microarrays.
Yilmaz A; Hamel N; Schwartz CE; Houlston RS; Harper JI; Foulkes WD
J Hum Genet; 2010 Sep; 55(9):627-30. PubMed ID: 20555334
[TBL] [Abstract][Full Text] [Related]
8. Identification of novel gastric cancer-associated CNVs by integrated analysis of microarray.
Park CH; Rha SY; Jeung HC; Kang SH; Ki DH; Lee WS; Noh SH; Chung HC
J Surg Oncol; 2010 Oct; 102(5):454-61. PubMed ID: 20872948
[TBL] [Abstract][Full Text] [Related]
9. Genomic changes in chromosomes 10, 16, and X in malignant peripheral nerve sheath tumors identify a high-risk patient group.
Brekke HR; Ribeiro FR; Kolberg M; Agesen TH; Lind GE; Eknaes M; Hall KS; Bjerkehagen B; van den Berg E; Teixeira MR; Mandahl N; Smeland S; Mertens F; Skotheim RI; Lothe RA
J Clin Oncol; 2010 Mar; 28(9):1573-82. PubMed ID: 20159821
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Genetic aberrations in prostate carcinoma detected by comparative genomic hybridization and microsatellite analysis: association with progression and angiogenesis.
Strohmeyer DM; Berger AP; Moore DH; Bartsch G; Klocker H; Carroll PR; Loening SA; Jensen RH
Prostate; 2004 Apr; 59(1):43-58. PubMed ID: 14991865
[TBL] [Abstract][Full Text] [Related]
12. A homozygous deletion of a normal variation locus in a patient with hearing loss from non-consanguineous parents.
Knijnenburg J; Oberstein SA; Frei K; Lucas T; Gijsbers AC; Ruivenkamp CA; Tanke HJ; Szuhai K
J Med Genet; 2009 Jun; 46(6):412-7. PubMed ID: 19246478
[TBL] [Abstract][Full Text] [Related]
13. Genome-wide analysis of DNA copy number alterations and gene expression in gastric cancer.
Tsukamoto Y; Uchida T; Karnan S; Noguchi T; Nguyen LT; Tanigawa M; Takeuchi I; Matsuura K; Hijiya N; Nakada C; Kishida T; Kawahara K; Ito H; Murakami K; Fujioka T; Seto M; Moriyama M
J Pathol; 2008 Dec; 216(4):471-82. PubMed ID: 18798223
[TBL] [Abstract][Full Text] [Related]
14. Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays.
Komura D; Shen F; Ishikawa S; Fitch KR; Chen W; Zhang J; Liu G; Ihara S; Nakamura H; Hurles ME; Lee C; Scherer SW; Jones KW; Shapero MH; Huang J; Aburatani H
Genome Res; 2006 Dec; 16(12):1575-84. PubMed ID: 17122084
[TBL] [Abstract][Full Text] [Related]
15. Array-based comparative genomic hybridization of mapped BAC DNA clones to screen for chromosome 14 copy number abnormalities in meningiomas.
Espinosa AB; Mackintosh C; Maíllo A; Gutierrez L; Sousa P; Merino M; Ortiz J; de Alava E; Orfao A; Tabernero MD
Eur J Hum Genet; 2008 Dec; 16(12):1450-8. PubMed ID: 18628790
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Identification of gene copy number variations in patients with mental retardation using array-CGH: Novel syndromes in a large French series.
Jaillard S; Drunat S; Bendavid C; Aboura A; Etcheverry A; Journel H; Delahaye A; Pasquier L; Bonneau D; Toutain A; Burglen L; Guichet A; Pipiras E; Gilbert-Dussardier B; Benzacken B; Martin-Coignard D; Henry C; David A; Lucas J; Mosser J; David V; Odent S; Verloes A; Dubourg C
Eur J Med Genet; 2010; 53(2):66-75. PubMed ID: 19878743
[TBL] [Abstract][Full Text] [Related]
18. High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays.
Pinkel D; Segraves R; Sudar D; Clark S; Poole I; Kowbel D; Collins C; Kuo WL; Chen C; Zhai Y; Dairkee SH; Ljung BM; Gray JW; Albertson DG
Nat Genet; 1998 Oct; 20(2):207-11. PubMed ID: 9771718
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Genomic copy number of a carcinogenic single nucleotide polymorphism at 8q24 in non-risk allele colorectal cancer associated with insulin growth factor 2 receptor expression.
Takahashi Y; Mimori K; Yamamoto K; Watanabe M; Tanaka J; Kudo SE; Sugihara K; Hase K; Mochizuki H; Kusunoki M; Yamada K; Shimada Y; Moriya Y; Mori M
J Gastroenterol Hepatol; 2012 Apr; 27 Suppl 3():95-9. PubMed ID: 22486879
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]