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 *

146 related articles for article (PubMed ID: 25244564)

  • 21. A non-threshold region-specific method for detecting rare variants in complex diseases.
    Hsieh AR; Chen DP; Chattopadhyay AS; Li YJ; Chang CC; Fann CSJ
    PLoS One; 2017; 12(11):e0188566. PubMed ID: 29190701
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Ordered subset analysis for case-control studies.
    Qin X; Hauser ER; Schmidt S
    Genet Epidemiol; 2010 Jul; 34(5):407-17. PubMed ID: 20568256
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A combined association test for rare variants using family and case-control data.
    Lin PL; Tsai WY; Chung RH
    BMC Proc; 2016; 10(Suppl 7):215-219. PubMed ID: 27980639
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Statistical selection strategy for risk and protective rare variants associated with complex traits.
    Kim S; Lee K; Sun H
    J Comput Biol; 2015 Nov; 22(11):1034-43. PubMed ID: 26469994
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Family studies to find rare high risk variants in migraine.
    Hansen RD; Christensen AF; Olesen J
    J Headache Pain; 2017 Dec; 18(1):32. PubMed ID: 28255817
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Family-based association tests for rare variants with censored traits.
    Qi W; Allen AS; Li YJ
    PLoS One; 2019; 14(1):e0210870. PubMed ID: 30682063
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Generalization of Rare Variant Association Tests for Longitudinal Family Studies.
    Chien LC; Hsu FC; Bowden DW; Chiu YF
    Genet Epidemiol; 2016 Feb; 40(2):101-12. PubMed ID: 26783077
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Generalized functional linear models for gene-based case-control association studies.
    Fan R; Wang Y; Mills JL; Carter TC; Lobach I; Wilson AF; Bailey-Wilson JE; Weeks DE; Xiong M
    Genet Epidemiol; 2014 Nov; 38(7):622-637. PubMed ID: 25203683
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Pathway analysis with next-generation sequencing data.
    Zhao J; Zhu Y; Boerwinkle E; Xiong M
    Eur J Hum Genet; 2015 Apr; 23(4):507-15. PubMed ID: 24986826
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Utilizing mutual information for detecting rare and common variants associated with a categorical trait.
    Sun L; Wang C; Hu YQ
    PeerJ; 2016; 4():e2139. PubMed ID: 27350900
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Weighted selective collapsing strategy for detecting rare and common variants in genetic association study.
    Dai Y; Jiang R; Dong J
    BMC Genet; 2012 Feb; 13():7. PubMed ID: 22309429
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Detecting Rare Mutations with Heterogeneous Effects Using a Family-Based Genetic Random Field Method.
    Li M; He Z; Tong X; Witte JS; Lu Q
    Genetics; 2018 Oct; 210(2):463-476. PubMed ID: 30104420
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A unified approach for allele frequency estimation, SNP detection and association studies based on pooled sequencing data using EM algorithms.
    Chen Q; Sun F
    BMC Genomics; 2013; 14 Suppl 1(Suppl 1):S1. PubMed ID: 23369070
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Dynamic Scan Procedure for Detecting Rare-Variant Association Regions in Whole-Genome Sequencing Studies.
    Li Z; Li X; Liu Y; Shen J; Chen H; Zhou H; Morrison AC; Boerwinkle E; Lin X
    Am J Hum Genet; 2019 May; 104(5):802-814. PubMed ID: 30982610
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Identifying rare and common disease associated variants in genomic data using Parkinson's disease as a model.
    Lin YC; Hsieh AR; Hsiao CL; Wu SJ; Wang HM; Lian IeB; Fann CS
    J Biomed Sci; 2014 Aug; 21(1):88. PubMed ID: 25175702
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Empirical power of very rare variants for common traits and disease: results from sanger sequencing 1998 individuals.
    Ladouceur M; Zheng HF; Greenwood CM; Richards JB
    Eur J Hum Genet; 2013 Sep; 21(9):1027-30. PubMed ID: 23321613
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Rare variants analysis by risk-based variable-threshold method.
    Fang H; Hou B; Wang Q; Yang Y
    Comput Biol Chem; 2013 Oct; 46():32-8. PubMed ID: 23764529
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Detecting multiple variants associated with disease based on sequencing data of case-parent trios.
    Wang C; Sun L; Zheng H; Hu YQ
    J Hum Genet; 2016 Oct; 61(10):851-860. PubMed ID: 27278787
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Block-based association tests for rare variants using Kullback-Leibler divergence.
    Zhu D; Hu YQ; Lin S
    J Hum Genet; 2016 Nov; 61(11):965-975. PubMed ID: 27412875
    [TBL] [Abstract][Full Text] [Related]  

  • 40. GENOME-WIDE ASSOCIATION MAPPING AND RARE ALLELES: FROM POPULATION GENOMICS TO PERSONALIZED MEDICINE - Session Introduction.
    DE LA Vega FM; Bustamante CD; Leal SM
    Pac Symp Biocomput; 2011; ():74-5. PubMed ID: 21121034
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.