703 related articles for article (PubMed ID: 18288195)
1. Genotype, haplotype and copy-number variation in worldwide human populations.
Jakobsson M; Scholz SW; Scheet P; Gibbs JR; VanLiere JM; Fung HC; Szpiech ZA; Degnan JH; Wang K; Guerreiro R; Bras JM; Schymick JC; Hernandez DG; Traynor BJ; Simon-Sanchez J; Matarin M; Britton A; van de Leemput J; Rafferty I; Bucan M; Cann HM; Hardy JA; Rosenberg NA; Singleton AB
Nature; 2008 Feb; 451(7181):998-1003. PubMed ID: 18288195
[TBL] [Abstract][Full Text] [Related]
2. Integrated detection and population-genetic analysis of SNPs and copy number variation.
McCarroll SA; Kuruvilla FG; Korn JM; Cawley S; Nemesh J; Wysoker A; Shapero MH; de Bakker PI; Maller JB; Kirby A; Elliott AL; Parkin M; Hubbell E; Webster T; Mei R; Veitch J; Collins PJ; Handsaker R; Lincoln S; Nizzari M; Blume J; Jones KW; Rava R; Daly MJ; Gabriel SB; Altshuler D
Nat Genet; 2008 Oct; 40(10):1166-74. PubMed ID: 18776908
[TBL] [Abstract][Full Text] [Related]
3. A worldwide survey of haplotype variation and linkage disequilibrium in the human genome.
Conrad DF; Jakobsson M; Coop G; Wen X; Wall JD; Rosenberg NA; Pritchard JK
Nat Genet; 2006 Nov; 38(11):1251-60. PubMed ID: 17057719
[TBL] [Abstract][Full Text] [Related]
4. MOCSphaser: a haplotype inference tool from a mixture of copy number variation and single nucleotide polymorphism data.
Kato M; Nakamura Y; Tsunoda T
Bioinformatics; 2008 Jul; 24(14):1645-6. PubMed ID: 18492685
[TBL] [Abstract][Full Text] [Related]
5. Inference of haplotypic phase and missing genotypes in polyploid organisms and variable copy number genomic regions.
Su SY; White J; Balding DJ; Coin LJ
BMC Bioinformatics; 2008 Dec; 9():513. PubMed ID: 19046436
[TBL] [Abstract][Full Text] [Related]
6. DNA sequence variation in a 3.7-kb noncoding sequence 5' of the CYP1A2 gene: implications for human population history and natural selection.
Wooding SP; Watkins WS; Bamshad MJ; Dunn DM; Weiss RB; Jorde LB
Am J Hum Genet; 2002 Sep; 71(3):528-42. PubMed ID: 12181774
[TBL] [Abstract][Full Text] [Related]
7. Global variation in copy number in the human genome.
Redon R; Ishikawa S; Fitch KR; Feuk L; Perry GH; Andrews TD; Fiegler H; Shapero MH; Carson AR; Chen W; Cho EK; Dallaire S; Freeman JL; González JR; Gratacòs M; Huang J; Kalaitzopoulos D; Komura D; MacDonald JR; Marshall CR; Mei R; Montgomery L; Nishimura K; Okamura K; Shen F; Somerville MJ; Tchinda J; Valsesia A; Woodwark C; Yang F; Zhang J; Zerjal T; Zhang J; Armengol L; Conrad DF; Estivill X; Tyler-Smith C; Carter NP; Aburatani H; Lee C; Jones KW; Scherer SW; Hurles ME
Nature; 2006 Nov; 444(7118):444-54. PubMed ID: 17122850
[TBL] [Abstract][Full Text] [Related]
8. Population-genetic nature of copy number variations in the human genome.
Kato M; Kawaguchi T; Ishikawa S; Umeda T; Nakamichi R; Shapero MH; Jones KW; Nakamura Y; Aburatani H; Tsunoda T
Hum Mol Genet; 2010 Mar; 19(5):761-73. PubMed ID: 19966329
[TBL] [Abstract][Full Text] [Related]
9. Human loci involved in drug biotransformation: worldwide genetic variation, population structure, and pharmacogenetic implications.
Maisano Delser P; Fuselli S
Hum Genet; 2013 May; 132(5):563-77. PubMed ID: 23354977
[TBL] [Abstract][Full Text] [Related]
10. An Evolutionary Perspective on the Impact of Genomic Copy Number Variation on Human Health.
Saitou M; Gokcumen O
J Mol Evol; 2020 Jan; 88(1):104-119. PubMed ID: 31522275
[TBL] [Abstract][Full Text] [Related]
11. Characterisation of SNP haplotype structure in chemokine and chemokine receptor genes using CEPH pedigrees and statistical estimation.
Clark VJ; Dean M
Hum Genomics; 2004 Mar; 1(3):195-207. PubMed ID: 15588479
[TBL] [Abstract][Full Text] [Related]
12. Geographic and haplotype structure of candidate type 2 diabetes susceptibility variants at the calpain-10 locus.
Fullerton SM; Bartoszewicz A; Ybazeta G; Horikawa Y; Bell GI; Kidd KK; Cox NJ; Hudson RR; Di Rienzo A
Am J Hum Genet; 2002 May; 70(5):1096-106. PubMed ID: 11891618
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Population structure, migration, and diversifying selection in the Netherlands.
Abdellaoui A; Hottenga JJ; de Knijff P; Nivard MG; Xiao X; Scheet P; Brooks A; Ehli EA; Hu Y; Davies GE; Hudziak JJ; Sullivan PF; van Beijsterveldt T; Willemsen G; de Geus EJ; Penninx BW; Boomsma DI
Eur J Hum Genet; 2013 Nov; 21(11):1277-85. PubMed ID: 23531865
[TBL] [Abstract][Full Text] [Related]
15. Population analysis of large copy number variants and hotspots of human genetic disease.
Itsara A; Cooper GM; Baker C; Girirajan S; Li J; Absher D; Krauss RM; Myers RM; Ridker PM; Chasman DI; Mefford H; Ying P; Nickerson DA; Eichler EE
Am J Hum Genet; 2009 Feb; 84(2):148-61. PubMed ID: 19166990
[TBL] [Abstract][Full Text] [Related]
16. Singapore Genome Variation Project: a haplotype map of three Southeast Asian populations.
Teo YY; Sim X; Ong RT; Tan AK; Chen J; Tantoso E; Small KS; Ku CS; Lee EJ; Seielstad M; Chia KS
Genome Res; 2009 Nov; 19(11):2154-62. PubMed ID: 19700652
[TBL] [Abstract][Full Text] [Related]
17. SNP and haplotype variation in the human genome.
Salisbury BA; Pungliya M; Choi JY; Jiang R; Sun XJ; Stephens JC
Mutat Res; 2003 May; 526(1-2):53-61. PubMed ID: 12714183
[TBL] [Abstract][Full Text] [Related]
18. A genomic portrait of haplotype diversity and signatures of selection in indigenous southern African populations.
Chimusa ER; Meintjies A; Tchanga M; Mulder N; Seoighe C; Soodyall H; Ramesar R
PLoS Genet; 2015 Mar; 11(3):e1005052. PubMed ID: 25811879
[TBL] [Abstract][Full Text] [Related]
19. PKLR- GBA region shows almost complete linkage disequilibrium over 70 kb in a set of worldwide populations.
Mateu E; Pérez-Lezaun A; Martínez-Arias R; Andrés A; Vallés M; Bertranpetit J; Calafell F
Hum Genet; 2002 Jun; 110(6):532-44. PubMed ID: 12107439
[TBL] [Abstract][Full Text] [Related]
20. A whole genome long-range haplotype (WGLRH) test for detecting imprints of positive selection in human populations.
Zhang C; Bailey DK; Awad T; Liu G; Xing G; Cao M; Valmeekam V; Retief J; Matsuzaki H; Taub M; Seielstad M; Kennedy GC
Bioinformatics; 2006 Sep; 22(17):2122-8. PubMed ID: 16845142
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
