103 related articles for article (PubMed ID: 21615327)
1. The relative importance of common and rare genetic variants in the development of hypertriglyceridemia.
Evans D; Aberle J; Beil FU
Expert Rev Cardiovasc Ther; 2011 May; 9(5):637-44. PubMed ID: 21615327
[TBL] [Abstract][Full Text] [Related]
2. The genetic basis of complex traits: rare variants or "common gene, common disease"?
Iyengar SK; Elston RC
Methods Mol Biol; 2007; 376():71-84. PubMed ID: 17984539
[TBL] [Abstract][Full Text] [Related]
3. Strategies for identifying the genetic basis of dyslipidemia: genome-wide association studies vs. the resequencing of extremes.
Khor CC; Goh DL
Curr Opin Lipidol; 2010 Apr; 21(2):123-7. PubMed ID: 20125008
[TBL] [Abstract][Full Text] [Related]
4. Rare-variant genome-wide association studies: a new frontier in genetic analysis of complex traits.
Wagner MJ
Pharmacogenomics; 2013 Mar; 14(4):413-24. PubMed ID: 23438888
[TBL] [Abstract][Full Text] [Related]
5. Genetic association studies of complex traits: design and analysis issues.
Newton-Cheh C; Hirschhorn JN
Mutat Res; 2005 Jun; 573(1-2):54-69. PubMed ID: 15829237
[TBL] [Abstract][Full Text] [Related]
6. Genome-wide association studies for detecting cancer susceptibility.
Hosking FJ; Dobbins SE; Houlston RS
Br Med Bull; 2011; 97():27-46. PubMed ID: 21247937
[TBL] [Abstract][Full Text] [Related]
7. How many genes underlie the occurrence of common complex diseases in the population?
Yang Q; Khoury MJ; Friedman J; Little J; Flanders WD
Int J Epidemiol; 2005 Oct; 34(5):1129-37. PubMed ID: 16043441
[TBL] [Abstract][Full Text] [Related]
8. The common variants/multiple disease hypothesis of common complex genetic disorders.
Becker KG
Med Hypotheses; 2004; 62(2):309-17. PubMed ID: 14962646
[TBL] [Abstract][Full Text] [Related]
9. Rare and low-frequency variants in human common diseases and other complex traits.
Lettre G
J Med Genet; 2014 Nov; 51(11):705-14. PubMed ID: 25185437
[TBL] [Abstract][Full Text] [Related]
10. Evidence-based psychiatric genetics, AKA the false dichotomy between common and rare variant hypotheses.
Visscher PM; Goddard ME; Derks EM; Wray NR
Mol Psychiatry; 2012 May; 17(5):474-85. PubMed ID: 21670730
[TBL] [Abstract][Full Text] [Related]
11. How important are rare variants in common disease?
Saint Pierre A; GĂ©nin E
Brief Funct Genomics; 2014 Sep; 13(5):353-61. PubMed ID: 25005607
[TBL] [Abstract][Full Text] [Related]
12. New technologies provide insights into genetic basis of psychiatric disorders and explain their co-morbidity.
Rudan I
Psychiatr Danub; 2010 Jun; 22(2):190-2. PubMed ID: 20562745
[TBL] [Abstract][Full Text] [Related]
13. Future nutrigenetics: in search of the missing genetic variation.
Mariman EC
J Nutrigenet Nutrigenomics; 2009; 2(4-5):257-62. PubMed ID: 20453519
[TBL] [Abstract][Full Text] [Related]
14. Haplotypes produced from rare variants in the promoter and coding regions of angiotensinogen contribute to variation in angiotensinogen levels.
Zhu X; Fejerman L; Luke A; Adeyemo A; Cooper RS
Hum Mol Genet; 2005 Mar; 14(5):639-43. PubMed ID: 15649942
[TBL] [Abstract][Full Text] [Related]
15. Health-related disparities: influence of environmental factors.
Olden K; White SL
Med Clin North Am; 2005 Jul; 89(4):721-38. PubMed ID: 15925646
[TBL] [Abstract][Full Text] [Related]
16. The power of genome-wide association studies of complex disease genes: statistical limitations of indirect approaches using SNP markers.
Ohashi J; Tokunaga K
J Hum Genet; 2001; 46(8):478-82. PubMed ID: 11501946
[TBL] [Abstract][Full Text] [Related]
17. Recent developments in genome and exome-wide analyses of plasma lipids.
Lange LA; Willer CJ; Rich SS
Curr Opin Lipidol; 2015 Apr; 26(2):96-102. PubMed ID: 25692345
[TBL] [Abstract][Full Text] [Related]
18. A remark on rare variants.
Oexle K
J Hum Genet; 2010 Apr; 55(4):219-26. PubMed ID: 20203695
[TBL] [Abstract][Full Text] [Related]
19. Next generation sequencing and rare genetic variants: from human population studies to medical genetics.
Matullo G; Di Gaetano C; Guarrera S
Environ Mol Mutagen; 2013 Aug; 54(7):518-32. PubMed ID: 23922201
[TBL] [Abstract][Full Text] [Related]
20. Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia.
Johansen CT; Wang J; Lanktree MB; Cao H; McIntyre AD; Ban MR; Martins RA; Kennedy BA; Hassell RG; Visser ME; Schwartz SM; Voight BF; Elosua R; Salomaa V; O'Donnell CJ; Dallinga-Thie GM; Anand SS; Yusuf S; Huff MW; Kathiresan S; Hegele RA
Nat Genet; 2010 Aug; 42(8):684-7. PubMed ID: 20657596
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]