BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

156 related articles for article (PubMed ID: 20718041)

  • 1. On the genome-wide analysis of copy number variants in family-based designs: methods for combining family-based and population-based information for testing dichotomous or quantitative traits, or completely ascertained samples.
    Murphy A; Won S; Rogers A; Chu JH; Raby BA; Lange C
    Genet Epidemiol; 2010 Sep; 34(6):582-90. PubMed ID: 20718041
    [TBL] [Abstract][Full Text] [Related]  

  • 2. On the analysis of copy-number variations in genome-wide association studies: a translation of the family-based association test.
    Ionita-Laza I; Perry GH; Raby BA; Klanderman B; Lee C; Laird NM; Weiss ST; Lange C
    Genet Epidemiol; 2008 Apr; 32(3):273-84. PubMed ID: 18228561
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Screening and replication using the same data set: testing strategies for family-based studies in which all probands are affected.
    Murphy A; Weiss ST; Lange C
    PLoS Genet; 2008 Sep; 4(9):e1000197. PubMed ID: 18802462
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A general framework for robust and efficient association analysis in family-based designs: quantitative and dichotomous phenotypes.
    Won S; Lange C
    Stat Med; 2013 Nov; 32(25):4482-98. PubMed ID: 23740776
    [TBL] [Abstract][Full Text] [Related]  

  • 5. On the association analysis of CNV data: a fast and robust family-based association method.
    Liu M; Moon S; Wang L; Kim S; Kim YJ; Hwang MY; Kim YJ; Elston RC; Kim BJ; Won S
    BMC Bioinformatics; 2017 Apr; 18(1):217. PubMed ID: 28420343
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Two-stage testing strategies for genome-wide association studies in family-based designs.
    Murphy A; T Weiss S; Lange C
    Methods Mol Biol; 2010; 620():485-96. PubMed ID: 20652517
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genome-wide copy number variation (CNV) detection in Nelore cattle reveals highly frequent variants in genome regions harboring QTLs affecting production traits.
    da Silva JM; Giachetto PF; da Silva LO; Cintra LC; Paiva SR; Yamagishi ME; Caetano AR
    BMC Genomics; 2016 Jun; 17():454. PubMed ID: 27297173
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genome-wide CNV analysis reveals variants associated with growth traits in Bos indicus.
    Zhou Y; Utsunomiya YT; Xu L; Hay el HA; Bickhart DM; Alexandre PA; Rosen BD; Schroeder SG; Carvalheiro R; de Rezende Neves HH; Sonstegard TS; Van Tassell CP; Ferraz JB; Fukumasu H; Garcia JF; Liu GE
    BMC Genomics; 2016 Jun; 17():419. PubMed ID: 27245577
    [TBL] [Abstract][Full Text] [Related]  

  • 9. On the analysis of genome-wide association studies in family-based designs: a universal, robust analysis approach and an application to four genome-wide association studies.
    Won S; Wilk JB; Mathias RA; O'Donnell CJ; Silverman EK; Barnes K; O'Connor GT; Weiss ST; Lange C
    PLoS Genet; 2009 Nov; 5(11):e1000741. PubMed ID: 19956679
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Rare variant analysis for family-based design.
    De G; Yip WK; Ionita-Laza I; Laird N
    PLoS One; 2013; 8(1):e48495. PubMed ID: 23341868
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Rare CNVs in Suicide Attempt include Schizophrenia-Associated Loci and Neurodevelopmental Genes: A Pilot Genome-Wide and Family-Based Study.
    Sokolowski M; Wasserman J; Wasserman D
    PLoS One; 2016; 11(12):e0168531. PubMed ID: 28030616
    [TBL] [Abstract][Full Text] [Related]  

  • 12. CNV Association of Diverse Clinical Phenotypes from eMERGE reveals novel disease biology underlying cardiovascular disease.
    Glessner JT; Li J; Desai A; Palmer M; Kim D; Lucas AM; Chang X; Connolly JJ; Almoguera B; Harley JB; Jarvik GP; Ritchie MD; Sleiman PMA; Roden DM; Crosslin D; Hakonarson H
    Int J Cardiol; 2020 Jan; 298():107-113. PubMed ID: 31447229
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A Statistical Method for Identifying Trait-Associated Copy Number Variants.
    Jeng J; Wu Q; Li H
    Hum Hered; 2015; 79(3-4):147-56. PubMed ID: 26201700
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Family-based bivariate association tests for quantitative traits.
    Zhang L; Bonham AJ; Li J; Pei YF; Chen J; Papasian CJ; Deng HW
    PLoS One; 2009 Dec; 4(12):e8133. PubMed ID: 19956578
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Detecting Population-Differentiation Copy Number Variants in Human Population Tree by Sparse Group Selection.
    Zhang H; Roe D; Kuang R
    IEEE/ACM Trans Comput Biol Bioinform; 2019; 16(2):538-549. PubMed ID: 29990238
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Copy number variation genotyping using family information.
    Chu JH; Rogers A; Ionita-Laza I; Darvishi K; Mills RE; Lee C; Raby BA
    BMC Bioinformatics; 2013 May; 14():157. PubMed ID: 23656838
    [TBL] [Abstract][Full Text] [Related]  

  • 17. An omnibus test for family-based association studies with multiple SNPs and multiple phenotypes.
    Lasky-Su J; Murphy A; McQueen MB; Weiss S; Lange C
    Eur J Hum Genet; 2010 Jun; 18(6):720-5. PubMed ID: 20087406
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Evaluation of population stratification adjustment using genome-wide or exonic variants.
    Chen Y; Peloso GM; Liu CT; DeStefano AL; Dupuis J
    Genet Epidemiol; 2020 Oct; 44(7):702-716. PubMed ID: 32608112
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Maximizing the Power of Genome-Wide Association Studies: A Novel Class of Powerful Family-Based Association Tests.
    Won S; Bertram L; Becker D; Tanzi RE; Lange C
    Stat Biosci; 2009 Nov; 1(2):125-143. PubMed ID: 22582089
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Parsing the effects of individual SNPs in candidate genes with family data.
    Hoffmann TJ; Lange C; Vansteelandt S; Raby BA; DeMeo DL; Silverman EK; Weiss ST; Laird NM
    Hum Hered; 2010; 69(2):91-103. PubMed ID: 19996607
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.