267 related articles for article (PubMed ID: 23591402)
1. The genome-wide landscape of copy number variations in the MUSGEN study provides evidence for a founder effect in the isolated Finnish population.
Kanduri C; Ukkola-Vuoti L; Oikkonen J; Buck G; Blancher C; Raijas P; Karma K; Lähdesmäki H; Järvelä I
Eur J Hum Genet; 2013 Dec; 21(12):1411-6. PubMed ID: 23591402
[TBL] [Abstract][Full Text] [Related]
2. Inter- and intra-breed genome-wide copy number diversity in a large cohort of European equine breeds.
Solé M; Ablondi M; Binzer-Panchal A; Velie BD; Hollfelder N; Buys N; Ducro BJ; François L; Janssens S; Schurink A; Viklund Å; Eriksson S; Isaksson A; Kultima H; Mikko S; Lindgren G
BMC Genomics; 2019 Oct; 20(1):759. PubMed ID: 31640551
[TBL] [Abstract][Full Text] [Related]
3. Copy number variations in East-Asian population and their evolutionary and functional implications.
Yim SH; Kim TM; Hu HJ; Kim JH; Kim BJ; Lee JY; Han BG; Shin SH; Jung SH; Chung YJ
Hum Mol Genet; 2010 Mar; 19(6):1001-8. PubMed ID: 20026555
[TBL] [Abstract][Full Text] [Related]
4. Genome-wide copy number variation analysis in extended families and unrelated individuals characterized for musical aptitude and creativity in music.
Ukkola-Vuoti L; Kanduri C; Oikkonen J; Buck G; Blancher C; Raijas P; Karma K; Lähdesmäki H; Järvelä I
PLoS One; 2013; 8(2):e56356. PubMed ID: 23460800
[TBL] [Abstract][Full Text] [Related]
5. A comprehensive survey of copy number variation in 18 diverse pig populations and identification of candidate copy number variable genes associated with complex traits.
Chen C; Qiao R; Wei R; Guo Y; Ai H; Ma J; Ren J; Huang L
BMC Genomics; 2012 Dec; 13():733. PubMed ID: 23270433
[TBL] [Abstract][Full Text] [Related]
6. Functional and population genetic features of copy number variations in two dairy cattle populations.
Lee YL; Bosse M; Mullaart E; Groenen MAM; Veerkamp RF; Bouwman AC
BMC Genomics; 2020 Jan; 21(1):89. PubMed ID: 31992181
[TBL] [Abstract][Full Text] [Related]
7. A Genome Wide Study of Copy Number Variation Associated with Nasopharyngeal Carcinoma in Malaysian Chinese Identifies CNVs at 11q14.3 and 6p21.3 as Candidate Loci.
Low JS; Chin YM; Mushiroda T; Kubo M; Govindasamy GK; Pua KC; Yap YY; Yap LF; Subramaniam SK; Ong CA; Tan TY; Khoo AS; ; Ng CC
PLoS One; 2016; 11(1):e0145774. PubMed ID: 26730743
[TBL] [Abstract][Full Text] [Related]
8. Analysis of copy number variations in the sheep genome using 50K SNP BeadChip array.
Liu J; Zhang L; Xu L; Ren H; Lu J; Zhang X; Zhang S; Zhou X; Wei C; Zhao F; Du L
BMC Genomics; 2013 Apr; 14():229. PubMed ID: 23565757
[TBL] [Abstract][Full Text] [Related]
9. Copy number variations in the genome of the Qatari population.
Fakhro KA; Yousri NA; Rodriguez-Flores JL; Robay A; Staudt MR; Agosto-Perez F; Salit J; Malek JA; Suhre K; Jayyousi A; Zirie M; Stadler D; Mezey JG; Crystal RG
BMC Genomics; 2015 Oct; 16():834. PubMed ID: 26490036
[TBL] [Abstract][Full Text] [Related]
10. Genome-wide detection of CNV regions and their potential association with growth and fatness traits in Duroc pigs.
Qiu Y; Ding R; Zhuang Z; Wu J; Yang M; Zhou S; Ye Y; Geng Q; Xu Z; Huang S; Cai G; Wu Z; Yang J
BMC Genomics; 2021 May; 22(1):332. PubMed ID: 33964879
[TBL] [Abstract][Full Text] [Related]
11. Copy number variation in human genomes from three major ethno-linguistic groups in Africa.
Nyangiri OA; Noyes H; Mulindwa J; Ilboudo H; Kabore JW; Ahouty B; Koffi M; Asina OF; Mumba D; Ofon E; Simo G; Kimuda MP; Enyaru J; Alibu VP; Kamoto K; Chisi J; Simuunza M; Camara M; Sidibe I; MacLeod A; Bucheton B; Hall N; Hertz-Fowler C; Matovu E;
BMC Genomics; 2020 Apr; 21(1):289. PubMed ID: 32272904
[TBL] [Abstract][Full Text] [Related]
12. Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysis.
Jarick I; Vogel CI; Scherag S; Schäfer H; Hebebrand J; Hinney A; Scherag A
Hum Mol Genet; 2011 Feb; 20(4):840-52. PubMed ID: 21131291
[TBL] [Abstract][Full Text] [Related]
13. Identification of copy number variation hotspots in human populations.
Fu W; Zhang F; Wang Y; Gu X; Jin L
Am J Hum Genet; 2010 Oct; 87(4):494-504. PubMed ID: 20920665
[TBL] [Abstract][Full Text] [Related]
14. Copy number variation associates with mortality in long-lived individuals: a genome-wide assessment.
Nygaard M; Debrabant B; Tan Q; Deelen J; Andersen-Ranberg K; de Craen AJ; Beekman M; Jeune B; Slagboom PE; Christensen K; Christiansen L
Aging Cell; 2016 Feb; 15(1):49-55. PubMed ID: 26446717
[TBL] [Abstract][Full Text] [Related]
15. Global patterns of large copy number variations in the human genome reveal complexity in chromosome organization.
Veerappa AM; Suresh RV; Vishweswaraiah S; Lingaiah K; Murthy M; Manjegowda DS; Padakannaya P; Ramachandra NB
Genet Res (Camb); 2015 Sep; 97():e18. PubMed ID: 26390810
[TBL] [Abstract][Full Text] [Related]
16. Genome wide copy number variations using Porcine 60K SNP Beadchip in Landlly pigs.
Panda S; Kumar A; Gaur GK; Ahmad SF; Chauhan A; Mehrotra A; Dutt T
Anim Biotechnol; 2023 Nov; 34(6):1891-1899. PubMed ID: 35369845
[TBL] [Abstract][Full Text] [Related]
17. CNV analysis in the Lithuanian population.
Urnikyte A; Domarkiene I; Stoma S; Ambrozaityte L; Uktveryte I; Meskiene R; Kasiulevičius V; Burokiene N; Kučinskas V
BMC Genet; 2016 May; 17(1):64. PubMed ID: 27142071
[TBL] [Abstract][Full Text] [Related]
18. Genome-wide elucidation of CNV regions and their association with production and reproduction traits in composite Vrindavani cattle.
Ahmad SF; Singh A; Panda S; Malla WA; Kumar A; Dutt T
Gene; 2022 Jul; 830():146510. PubMed ID: 35447249
[TBL] [Abstract][Full Text] [Related]
19. Identification of copy number variation in Tibetan sheep using whole genome resequencing reveals evidence of genomic selection.
Shi H; Li T; Su M; Wang H; Li Q; Lang X; Ma Y
BMC Genomics; 2023 Sep; 24(1):555. PubMed ID: 37726692
[TBL] [Abstract][Full Text] [Related]
20. Genome-wide association study between CNVs and milk production traits in Valle del Belice sheep.
Di Gerlando R; Sutera AM; Mastrangelo S; Tolone M; Portolano B; Sottile G; Bagnato A; Strillacci MG; Sardina MT
PLoS One; 2019; 14(4):e0215204. PubMed ID: 31013280
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]