134 related articles for article (PubMed ID: 20564784)
1. Challenges in the identification and use of rare disease-associated predisposition variants.
Carvajal-Carmona LG
Curr Opin Genet Dev; 2010 Jun; 20(3):277-81. PubMed ID: 20564784
[TBL] [Abstract][Full Text] [Related]
2. On rare-variant analysis in population-based designs: decomposing the likelihood to two informative components.
Won S; Kim Y; Lange C
Hum Hered; 2013; 76(2):76-85. PubMed ID: 24434864
[TBL] [Abstract][Full Text] [Related]
3. An evaluation of statistical approaches to rare variant analysis in genetic association studies.
Morris AP; Zeggini E
Genet Epidemiol; 2010 Feb; 34(2):188-93. PubMed ID: 19810025
[TBL] [Abstract][Full Text] [Related]
4. Genetic variants in association studies--review of strengths and weaknesses in study design and current knowledge of impact on cancer risk.
Andersson U; McKean-Cowdin R; Hjalmars U; Malmer B
Acta Oncol; 2009; 48(7):948-54. PubMed ID: 19863254
[TBL] [Abstract][Full Text] [Related]
5. A Fast Association Test for Identifying Pathogenic Variants Involved in Rare Diseases.
Greene D; ; Richardson S; Turro E
Am J Hum Genet; 2017 Jul; 101(1):104-114. PubMed ID: 28669401
[TBL] [Abstract][Full Text] [Related]
6. Uncovering the roles of rare variants in common disease through whole-genome sequencing.
Cirulli ET; Goldstein DB
Nat Rev Genet; 2010 Jun; 11(6):415-25. PubMed ID: 20479773
[TBL] [Abstract][Full Text] [Related]
7. Do common variants play a role in risk for autism? Evidence and theoretical musings.
Devlin B; Melhem N; Roeder K
Brain Res; 2011 Mar; 1380():78-84. PubMed ID: 21078308
[TBL] [Abstract][Full Text] [Related]
8. Genetic dissection of intermediate phenotypes as a way to discover novel cancer susceptibility alleles.
Carvajal-Carmona LG
Curr Opin Genet Dev; 2010 Jun; 20(3):308-14. PubMed ID: 20456939
[TBL] [Abstract][Full Text] [Related]
9. How important are rare variants in common disease?
Saint Pierre A; Génin E
Brief Funct Genomics; 2014 Sep; 13(5):353-61. PubMed ID: 25005607
[TBL] [Abstract][Full Text] [Related]
10. Using gene genealogies to detect rare variants associated with complex traits.
Burkett KM; McNeney B; Graham J; Greenwood CM
Hum Hered; 2014; 78(3-4):117-30. PubMed ID: 25138120
[TBL] [Abstract][Full Text] [Related]
11. Genetic Modifiers and Rare Mendelian Disease.
Rahit KMTH; Tarailo-Graovac M
Genes (Basel); 2020 Feb; 11(3):. PubMed ID: 32106447
[TBL] [Abstract][Full Text] [Related]
12. A genome-wide analysis in cluster headache points to neprilysin and PACAP receptor gene variants.
Bacchelli E; Cainazzo MM; Cameli C; Guerzoni S; Martinelli A; Zoli M; Maestrini E; Pini LA
J Headache Pain; 2016 Dec; 17(1):114. PubMed ID: 27957625
[TBL] [Abstract][Full Text] [Related]
13. Association Analysis and Meta-Analysis of Multi-Allelic Variants for Large-Scale Sequence Data.
Jiang Y; Chen S; Wang X; Liu M; Iacono WG; Hewitt JK; Hokanson JE; Krauter K; Laakso M; Li KW; Lutz SM; McGue M; Pandit A; Zajac GJM; Boehnke M; Abecasis GR; Vrieze SI; Jiang B; Zhan X; Liu DJ
Genes (Basel); 2020 May; 11(5):. PubMed ID: 32466134
[TBL] [Abstract][Full Text] [Related]
14. Rare variants and cardiovascular disease.
Wain LV
Brief Funct Genomics; 2014 Sep; 13(5):384-91. PubMed ID: 24771349
[TBL] [Abstract][Full Text] [Related]
15. Rare genetic variants and the risk of cancer.
Bodmer W; Tomlinson I
Curr Opin Genet Dev; 2010 Jun; 20(3):262-7. PubMed ID: 20554195
[TBL] [Abstract][Full Text] [Related]
16. Poisson Approximation-Based Score Test for Detecting Association of Rare Variants.
Fang H; Zhang H; Yang Y
Ann Hum Genet; 2016 Jul; 80(4):221-34. PubMed ID: 27346734
[TBL] [Abstract][Full Text] [Related]
17. Second-generation Irish genome-wide association study for amyotrophic lateral sclerosis.
McLaughlin RL; Kenna KP; Vajda A; Bede P; Elamin M; Cronin S; Donaghy CG; Bradley DG; Hardiman O
Neurobiol Aging; 2015 Feb; 36(2):1221.e7-13. PubMed ID: 25442119
[TBL] [Abstract][Full Text] [Related]
18. Association Tests for Rare Variants.
Nicolae DL
Annu Rev Genomics Hum Genet; 2016 Aug; 17():117-30. PubMed ID: 27147090
[TBL] [Abstract][Full Text] [Related]
19. Genome-wide association studies.
Yang TH; Kon M; DeLisi C
Methods Mol Biol; 2013; 939():233-51. PubMed ID: 23192550
[TBL] [Abstract][Full Text] [Related]
20. Functional and Structural Consequence of Rare Exonic Single Nucleotide Polymorphisms: One Story, Two Tales.
Gu W; Gurguis CI; Zhou JJ; Zhu Y; Ko EA; Ko JH; Wang T; Zhou T
Genome Biol Evol; 2015 Oct; 7(10):2929-40. PubMed ID: 26454016
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
