These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

196 related articles for article (PubMed ID: 28844485)

  • 1. Unified Sequence-Based Association Tests Allowing for Multiple Functional Annotations and Meta-analysis of Noncoding Variation in Metabochip Data.
    He Z; Xu B; Lee S; Ionita-Laza I
    Am J Hum Genet; 2017 Sep; 101(3):340-352. PubMed ID: 28844485
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Incorporating Non-Coding Annotations into Rare Variant Analysis.
    Richardson TG; Campbell C; Timpson NJ; Gaunt TR
    PLoS One; 2016; 11(4):e0154181. PubMed ID: 27128317
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale.
    Li X; Li Z; Zhou H; Gaynor SM; Liu Y; Chen H; Sun R; Dey R; Arnett DK; Aslibekyan S; Ballantyne CM; Bielak LF; Blangero J; Boerwinkle E; Bowden DW; Broome JG; Conomos MP; Correa A; Cupples LA; Curran JE; Freedman BI; Guo X; Hindy G; Irvin MR; Kardia SLR; Kathiresan S; Khan AT; Kooperberg CL; Laurie CC; Liu XS; Mahaney MC; Manichaikul AW; Martin LW; Mathias RA; McGarvey ST; Mitchell BD; Montasser ME; Moore JE; Morrison AC; O'Connell JR; Palmer ND; Pampana A; Peralta JM; Peyser PA; Psaty BM; Redline S; Rice KM; Rich SS; Smith JA; Tiwari HK; Tsai MY; Vasan RS; Wang FF; Weeks DE; Weng Z; Wilson JG; Yanek LR; ; ; Neale BM; Sunyaev SR; Abecasis GR; Rotter JI; Willer CJ; Peloso GM; Natarajan P; Lin X
    Nat Genet; 2020 Sep; 52(9):969-983. PubMed ID: 32839606
    [TBL] [Abstract][Full Text] [Related]  

  • 4. FunSPU: A versatile and adaptive multiple functional annotation-based association test of whole-genome sequencing data.
    Ma Y; Wei P
    PLoS Genet; 2019 Apr; 15(4):e1008081. PubMed ID: 31034468
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Integrating comprehensive functional annotations to boost power and accuracy in gene-based association analysis.
    Quick C; Wen X; Abecasis G; Boehnke M; Kang HM
    PLoS Genet; 2020 Dec; 16(12):e1009060. PubMed ID: 33320851
    [TBL] [Abstract][Full Text] [Related]  

  • 6. In Silico Functional Annotation of Genomic Variation.
    Butkiewicz M; Bush WS
    Curr Protoc Hum Genet; 2016 Jan; 88():6.15.1-6.15.17. PubMed ID: 26724722
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Incorporating Functional Annotations for Fine-Mapping Causal Variants in a Bayesian Framework Using Summary Statistics.
    Chen W; McDonnell SK; Thibodeau SN; Tillmans LS; Schaid DJ
    Genetics; 2016 Nov; 204(3):933-958. PubMed ID: 27655946
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Functional annotation signatures of disease susceptibility loci improve SNP association analysis.
    Iversen ES; Lipton G; Clyde MA; Monteiro AN
    BMC Genomics; 2014 May; 15(1):398. PubMed ID: 24886216
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Leveraging functional genomic annotations and genome coverage to improve polygenic prediction of complex traits within and between ancestries.
    Zheng Z; Liu S; Sidorenko J; Wang Y; Lin T; Yengo L; Turley P; Ani A; Wang R; Nolte IM; Snieder H; ; Yang J; Wray NR; Goddard ME; Visscher PM; Zeng J
    Nat Genet; 2024 May; 56(5):767-777. PubMed ID: 38689000
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Weighting sequence variants based on their annotation increases the power of genome-wide association studies in dairy cattle.
    Cai Z; Guldbrandtsen B; Lund MS; Sahana G
    Genet Sel Evol; 2019 May; 51(1):20. PubMed ID: 31077144
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Methods for meta-analysis of multiple traits using GWAS summary statistics.
    Ray D; Boehnke M
    Genet Epidemiol; 2018 Mar; 42(2):134-145. PubMed ID: 29226385
    [TBL] [Abstract][Full Text] [Related]  

  • 12. PALM: a powerful and adaptive latent model for prioritizing risk variants with functional annotations.
    Yu X; Xiao J; Cai M; Jiao Y; Wan X; Liu J; Yang C
    Bioinformatics; 2023 Feb; 39(2):. PubMed ID: 36744920
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A spectral approach integrating functional genomic annotations for coding and noncoding variants.
    Ionita-Laza I; McCallum K; Xu B; Buxbaum JD
    Nat Genet; 2016 Feb; 48(2):214-20. PubMed ID: 26727659
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identifying and exploiting trait-relevant tissues with multiple functional annotations in genome-wide association studies.
    Hao X; Zeng P; Zhang S; Zhou X
    PLoS Genet; 2018 Jan; 14(1):e1007186. PubMed ID: 29377896
    [TBL] [Abstract][Full Text] [Related]  

  • 15. iFunMed: Integrative functional mediation analysis of GWAS and eQTL studies.
    Rojo C; Zhang Q; Keleş S
    Genet Epidemiol; 2019 Oct; 43(7):742-760. PubMed ID: 31328826
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A multi-dimensional integrative scoring framework for predicting functional variants in the human genome.
    Li X; Yung G; Zhou H; Sun R; Li Z; Hou K; Zhang MJ; Liu Y; Arapoglou T; Wang C; Ionita-Laza I; Lin X
    Am J Hum Genet; 2022 Mar; 109(3):446-456. PubMed ID: 35216679
    [TBL] [Abstract][Full Text] [Related]  

  • 17. General framework for meta-analysis of rare variants in sequencing association studies.
    Lee S; Teslovich TM; Boehnke M; Lin X
    Am J Hum Genet; 2013 Jul; 93(1):42-53. PubMed ID: 23768515
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Annotation of functional variation in personal genomes using RegulomeDB.
    Boyle AP; Hong EL; Hariharan M; Cheng Y; Schaub MA; Kasowski M; Karczewski KJ; Park J; Hitz BC; Weng S; Cherry JM; Snyder M
    Genome Res; 2012 Sep; 22(9):1790-7. PubMed ID: 22955989
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The eigen higher criticism and eigen Berk-Jones tests for multiple trait association studies based on GWAS summary statistics.
    Liu W; Xu Y; Wang A; Huang T; Liu Z
    Genet Epidemiol; 2022 Mar; 46(2):89-104. PubMed ID: 35192735
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies.
    Li Z; Li X; Zhou H; Gaynor SM; Selvaraj MS; Arapoglou T; Quick C; Liu Y; Chen H; Sun R; Dey R; Arnett DK; Auer PL; Bielak LF; Bis JC; Blackwell TW; Blangero J; Boerwinkle E; Bowden DW; Brody JA; Cade BE; Conomos MP; Correa A; Cupples LA; Curran JE; de Vries PS; Duggirala R; Franceschini N; Freedman BI; Göring HHH; Guo X; Kalyani RR; Kooperberg C; Kral BG; Lange LA; Lin BM; Manichaikul A; Manning AK; Martin LW; Mathias RA; Meigs JB; Mitchell BD; Montasser ME; Morrison AC; Naseri T; O'Connell JR; Palmer ND; Peyser PA; Psaty BM; Raffield LM; Redline S; Reiner AP; Reupena MS; Rice KM; Rich SS; Smith JA; Taylor KD; Taub MA; Vasan RS; Weeks DE; Wilson JG; Yanek LR; Zhao W; ; ; Rotter JI; Willer CJ; Natarajan P; Peloso GM; Lin X
    Nat Methods; 2022 Dec; 19(12):1599-1611. PubMed ID: 36303018
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.