428 related articles for article (PubMed ID: 30849219)
1. Methods for the Analysis and Interpretation for Rare Variants Associated with Complex Traits.
Weissenkampen JD; Jiang Y; Eckert S; Jiang B; Li B; Liu DJ
Curr Protoc Hum Genet; 2019 Apr; 101(1):e83. PubMed ID: 30849219
[TBL] [Abstract][Full Text] [Related]
2. Imputation-based assessment of next generation rare exome variant arrays.
Martin AR; Tse G; Bustamante CD; Kenny EE
Pac Symp Biocomput; 2014; ():241-52. PubMed ID: 24297551
[TBL] [Abstract][Full Text] [Related]
3. Unique roles of rare variants in the genetics of complex diseases in humans.
Momozawa Y; Mizukami K
J Hum Genet; 2021 Jan; 66(1):11-23. PubMed ID: 32948841
[TBL] [Abstract][Full Text] [Related]
4. Genomic Analysis in the Age of Human Genome Sequencing.
Lappalainen T; Scott AJ; Brandt M; Hall IM
Cell; 2019 Mar; 177(1):70-84. PubMed ID: 30901550
[TBL] [Abstract][Full Text] [Related]
5. Molecular genetic studies of complex phenotypes.
Marian AJ
Transl Res; 2012 Feb; 159(2):64-79. PubMed ID: 22243791
[TBL] [Abstract][Full Text] [Related]
6. Accurate Imputation of Untyped Variants from Deep Sequencing Data.
Torkamaneh D; Belzile F
Methods Mol Biol; 2021; 2243():271-281. PubMed ID: 33606262
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Analysis and Annotation of Whole-Genome or Whole-Exome Sequencing Derived Variants for Clinical Diagnosis.
Worthey EA
Curr Protoc Hum Genet; 2017 Oct; 95():9.24.1-9.24.28. PubMed ID: 29044471
[TBL] [Abstract][Full Text] [Related]
9. In search of low-frequency and rare variants affecting complex traits.
Panoutsopoulou K; Tachmazidou I; Zeggini E
Hum Mol Genet; 2013 Oct; 22(R1):R16-21. PubMed ID: 23922232
[TBL] [Abstract][Full Text] [Related]
10. Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use.
Brazel DM; Jiang Y; Hughey JM; Turcot V; Zhan X; Gong J; Batini C; Weissenkampen JD; Liu M; ; ; Barnes DR; Bertelsen S; Chou YL; Erzurumluoglu AM; Faul JD; Haessler J; Hammerschlag AR; Hsu C; Kapoor M; Lai D; Le N; de Leeuw CA; Loukola A; Mangino M; Melbourne CA; Pistis G; Qaiser B; Rohde R; Shao Y; Stringham H; Wetherill L; Zhao W; Agrawal A; Bierut L; Chen C; Eaton CB; Goate A; Haiman C; Heath A; Iacono WG; Martin NG; Polderman TJ; Reiner A; Rice J; Schlessinger D; Scholte HS; Smith JA; Tardif JC; Tindle HA; van der Leij AR; Boehnke M; Chang-Claude J; Cucca F; David SP; Foroud T; Howson JMM; Kardia SLR; Kooperberg C; Laakso M; Lettre G; Madden P; McGue M; North K; Posthuma D; Spector T; Stram D; Tobin MD; Weir DR; Kaprio J; Abecasis GR; Liu DJ; Vrieze S
Biol Psychiatry; 2019 Jun; 85(11):946-955. PubMed ID: 30679032
[TBL] [Abstract][Full Text] [Related]
11. PLINK: Key Functions for Data Analysis.
Slifer SH
Curr Protoc Hum Genet; 2018 Apr; 97(1):e59. PubMed ID: 30040203
[TBL] [Abstract][Full Text] [Related]
12. Estimation of regional polygenicity from GWAS provides insights into the genetic architecture of complex traits.
Johnson R; Burch KS; Hou K; Paciuc M; Pasaniuc B; Sankararaman S
PLoS Comput Biol; 2021 Oct; 17(10):e1009483. PubMed ID: 34673766
[TBL] [Abstract][Full Text] [Related]
13. Identification of putative causal loci in whole-genome sequencing data via knockoff statistics.
He Z; Liu L; Wang C; Le Guen Y; Lee J; Gogarten S; Lu F; Montgomery S; Tang H; Silverman EK; Cho MH; Greicius M; Ionita-Laza I
Nat Commun; 2021 May; 12(1):3152. PubMed ID: 34035245
[TBL] [Abstract][Full Text] [Related]
14. Efficient and flexible Integration of variant characteristics in rare variant association studies using integrated nested Laplace approximation.
Susak H; Serra-Saurina L; Demidov G; Rabionet R; Domènech L; Bosio M; Muyas F; Estivill X; Escaramís G; Ossowski S
PLoS Comput Biol; 2021 Feb; 17(2):e1007784. PubMed ID: 33606672
[TBL] [Abstract][Full Text] [Related]
15. Biobank-scale inference of ancestral recombination graphs enables genealogical analysis of complex traits.
Zhang BC; Biddanda A; Gunnarsson ÁF; Cooper F; Palamara PF
Nat Genet; 2023 May; 55(5):768-776. PubMed ID: 37127670
[TBL] [Abstract][Full Text] [Related]
16. Identifying rare variants associated with complex traits via sequencing.
Li B; Liu DJ; Leal SM
Curr Protoc Hum Genet; 2013 Jul; Chapter 1():Unit 1.26. PubMed ID: 23853079
[TBL] [Abstract][Full Text] [Related]
17. Phenome-Wide Association Studies as a Tool to Advance Precision Medicine.
Denny JC; Bastarache L; Roden DM
Annu Rev Genomics Hum Genet; 2016 Aug; 17():353-73. PubMed ID: 27147087
[TBL] [Abstract][Full Text] [Related]
18. Quantifying the mapping precision of genome-wide association studies using whole-genome sequencing data.
Wu Y; Zheng Z; Visscher PM; Yang J
Genome Biol; 2017 May; 18(1):86. PubMed ID: 28506277
[TBL] [Abstract][Full Text] [Related]
19. Investigation of rare and low-frequency variants using high-throughput sequencing with pooled DNA samples.
Wang J; Skoog T; Einarsdottir E; Kaartokallio T; Laivuori H; Grauers A; Gerdhem P; Hytönen M; Lohi H; Kere J; Jiao H
Sci Rep; 2016 Sep; 6():33256. PubMed ID: 27633116
[TBL] [Abstract][Full Text] [Related]
20. Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia.
Harold D; Connolly S; Riley BP; Kendler KS; McCarthy SE; McCombie WR; Richards A; Owen MJ; O'Donovan MC; Walters J; ; ; Donohoe G; Gill M; Corvin A; Morris DW
Am J Med Genet B Neuropsychiatr Genet; 2019 Apr; 180(3):223-231. PubMed ID: 30801977
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
