399 related articles for article (PubMed ID: 36490288)
1. Efficient identification of trait-associated loss-of-function variants in the UK Biobank cohort by exome-sequencing based genotype imputation.
Yu WY; Yan SS; Zhang SH; Ni JJ; Bin-Li ; Pei YF; Zhang L
Genet Epidemiol; 2023 Mar; 47(2):121-134. PubMed ID: 36490288
[TBL] [Abstract][Full Text] [Related]
2. Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
Barton AR; Sherman MA; Mukamel RE; Loh PR
Nat Genet; 2021 Aug; 53(8):1260-1269. PubMed ID: 34226706
[TBL] [Abstract][Full Text] [Related]
3. Accurate rare variant phasing of whole-genome and whole-exome sequencing data in the UK Biobank.
Hofmeister RJ; Ribeiro DM; Rubinacci S; Delaneau O
Nat Genet; 2023 Jul; 55(7):1243-1249. PubMed ID: 37386248
[TBL] [Abstract][Full Text] [Related]
4. Imputation-powered whole-exome analysis identifies genes associated with kidney function and disease in the UK Biobank.
Wuttke M; König E; Katsara MA; Kirsten H; Farahani SK; Teumer A; Li Y; Lang M; Göcmen B; Pattaro C; Günzel D; Köttgen A; Fuchsberger C
Nat Commun; 2023 Mar; 14(1):1287. PubMed ID: 36890159
[TBL] [Abstract][Full Text] [Related]
5. Evaluation and application of summary statistic imputation to discover new height-associated loci.
Rüeger S; McDaid A; Kutalik Z
PLoS Genet; 2018 May; 14(5):e1007371. PubMed ID: 29782485
[TBL] [Abstract][Full Text] [Related]
6. Imputation of low-coverage sequencing data from 150,119 UK Biobank genomes.
Rubinacci S; Hofmeister RJ; Sousa da Mota B; Delaneau O
Nat Genet; 2023 Jul; 55(7):1088-1090. PubMed ID: 37386250
[TBL] [Abstract][Full Text] [Related]
7. Exome sequencing and analysis of 454,787 UK Biobank participants.
Backman JD; Li AH; Marcketta A; Sun D; Mbatchou J; Kessler MD; Benner C; Liu D; Locke AE; Balasubramanian S; Yadav A; Banerjee N; Gillies CE; Damask A; Liu S; Bai X; Hawes A; Maxwell E; Gurski L; Watanabe K; Kosmicki JA; Rajagopal V; Mighty J; ; ; Jones M; Mitnaul L; Stahl E; Coppola G; Jorgenson E; Habegger L; Salerno WJ; Shuldiner AR; Lotta LA; Overton JD; Cantor MN; Reid JG; Yancopoulos G; Kang HM; Marchini J; Baras A; Abecasis GR; Ferreira MAR
Nature; 2021 Nov; 599(7886):628-634. PubMed ID: 34662886
[TBL] [Abstract][Full Text] [Related]
8. Whole-exome imputation of sequence variants identified two novel alleles associated with adult body height in African Americans.
Du M; Auer PL; Jiao S; Haessler J; Altshuler D; Boerwinkle E; Carlson CS; Carty CL; Chen YD; Curtis K; Franceschini N; Hsu L; Jackson R; Lange LA; Lettre G; Monda KL; ; Nickerson DA; Reiner AP; Rich SS; Rosse SA; Rotter JI; Willer CJ; Wilson JG; North K; Kooperberg C; Heard-Costa N; Peters U
Hum Mol Genet; 2014 Dec; 23(24):6607-15. PubMed ID: 25027330
[TBL] [Abstract][Full Text] [Related]
9. Exome sequencing and characterization of 49,960 individuals in the UK Biobank.
Van Hout CV; Tachmazidou I; Backman JD; Hoffman JD; Liu D; Pandey AK; Gonzaga-Jauregui C; Khalid S; Ye B; Banerjee N; Li AH; O'Dushlaine C; Marcketta A; Staples J; Schurmann C; Hawes A; Maxwell E; Barnard L; Lopez A; Penn J; Habegger L; Blumenfeld AL; Bai X; O'Keeffe S; Yadav A; Praveen K; Jones M; Salerno WJ; Chung WK; Surakka I; Willer CJ; Hveem K; Leader JB; Carey DJ; Ledbetter DH; ; Cardon L; Yancopoulos GD; Economides A; Coppola G; Shuldiner AR; Balasubramanian S; Cantor M; ; Nelson MR; Whittaker J; Reid JG; Marchini J; Overton JD; Scott RA; Abecasis GR; Yerges-Armstrong L; Baras A
Nature; 2020 Oct; 586(7831):749-756. PubMed ID: 33087929
[TBL] [Abstract][Full Text] [Related]
10. A new strategy for enhancing imputation quality of rare variants from next-generation sequencing data via combining SNP and exome chip data.
Kim YJ; Lee J; Kim BJ; ; Park T
BMC Genomics; 2015 Dec; 16():1109. PubMed ID: 26715385
[TBL] [Abstract][Full Text] [Related]
11. Effect of genome-wide genotyping and reference panels on rare variants imputation.
Zheng HF; Ladouceur M; Greenwood CM; Richards JB
J Genet Genomics; 2012 Oct; 39(10):545-50. PubMed ID: 23089364
[TBL] [Abstract][Full Text] [Related]
12. Using off-target data from whole-exome sequencing to improve genotyping accuracy, association analysis and polygenic risk prediction.
Dou J; Wu D; Ding L; Wang K; Jiang M; Chai X; Reilly DF; Tai ES; Liu J; Sim X; Cheng S; Wang C
Brief Bioinform; 2021 May; 22(3):. PubMed ID: 32591784
[TBL] [Abstract][Full Text] [Related]
13. Imputation of genotypes from low density (50,000 markers) to high density (700,000 markers) of cows from research herds in Europe, North America, and Australasia using 2 reference populations.
Pryce JE; Johnston J; Hayes BJ; Sahana G; Weigel KA; McParland S; Spurlock D; Krattenmacher N; Spelman RJ; Wall E; Calus MP
J Dairy Sci; 2014 Mar; 97(3):1799-811. PubMed ID: 24472132
[TBL] [Abstract][Full Text] [Related]
14. A resource-efficient tool for mixed model association analysis of large-scale data.
Jiang L; Zheng Z; Qi T; Kemper KE; Wray NR; Visscher PM; Yang J
Nat Genet; 2019 Dec; 51(12):1749-1755. PubMed ID: 31768069
[TBL] [Abstract][Full Text] [Related]
15. Advancing human genetics research and drug discovery through exome sequencing of the UK Biobank.
Szustakowski JD; Balasubramanian S; Kvikstad E; Khalid S; Bronson PG; Sasson A; Wong E; Liu D; Wade Davis J; Haefliger C; Katrina Loomis A; Mikkilineni R; Noh HJ; Wadhawan S; Bai X; Hawes A; Krasheninina O; Ulloa R; Lopez AE; Smith EN; Waring JF; Whelan CD; Tsai EA; Overton JD; Salerno WJ; Jacob H; Szalma S; Runz H; Hinkle G; Nioi P; Petrovski S; Miller MR; Baras A; Mitnaul LJ; Reid JG;
Nat Genet; 2021 Jul; 53(7):942-948. PubMed ID: 34183854
[TBL] [Abstract][Full Text] [Related]
16. UK Biobank Whole-Exome Sequence Binary Phenome Analysis with Robust Region-Based Rare-Variant Test.
Zhao Z; Bi W; Zhou W; VandeHaar P; Fritsche LG; Lee S
Am J Hum Genet; 2020 Jan; 106(1):3-12. PubMed ID: 31866045
[TBL] [Abstract][Full Text] [Related]
17. Identification of novel rare variants for anxiety: an exome-wide association study in the UK Biobank.
Pan C; Cheng S; Liu L; Chen Y; Meng P; Yang X; Li C; Zhang J; Zhang Z; Zhang H; Cheng B; Wen Y; Jia Y; Zhang F
Prog Neuropsychopharmacol Biol Psychiatry; 2024 Mar; 130():110928. PubMed ID: 38154517
[TBL] [Abstract][Full Text] [Related]
18. Novel genotyping algorithms for rare variants significantly improve the accuracy of Applied Biosystems™ Axiom™ array genotyping calls: Retrospective evaluation of UK Biobank array data.
Mizrahi-Man O; Woehrmann MH; Webster TA; Gollub J; Bivol A; Keeble SM; Aull KH; Mittal A; Roter AH; Wong BA; Schmidt JP
PLoS One; 2022; 17(11):e0277680. PubMed ID: 36395175
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Identification of Rare Loss-of-Function Genetic Variation Regulating Body Fat Distribution.
Koprulu M; Zhao Y; Wheeler E; Dong L; Rocha N; Li C; Griffin JD; Patel S; Van de Streek M; Glastonbury CA; Stewart ID; Day FR; Luan J; Bowker N; Wittemans LBL; Kerrison ND; Cai L; Lucarelli DME; Barroso I; McCarthy MI; Scott RA; Saudek V; Small KS; Wareham NJ; Semple RK; Perry JRB; O'Rahilly S; Lotta LA; Langenberg C; Savage DB
J Clin Endocrinol Metab; 2022 Mar; 107(4):1065-1077. PubMed ID: 34875679
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
