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 *

163 related articles for article (PubMed ID: 19763929)

  • 1. Computing genetic imprinting expressed by haplotypes.
    Cheng Y; Berg A; Wu S; Li Y; Wu R
    Methods Mol Biol; 2009; 573():189-212. PubMed ID: 19763929
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A random model for mapping imprinted quantitative trait loci in a structured pedigree: an implication for mapping canine hip dysplasia.
    Liu T; Todhunter RJ; Wu S; Hou W; Mateescu R; Zhang Z; Burton-Wurster NI; Acland GM; Lust G; Wu R
    Genomics; 2007 Aug; 90(2):276-84. PubMed ID: 17531439
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A statistical model for dissecting genomic imprinting through genetic mapping.
    Cui Y; Cheverud JM; Wu R
    Genetica; 2007 Jul; 130(3):227-39. PubMed ID: 16955328
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A statistical framework for genome-wide scanning and testing of imprinted quantitative trait loci.
    Cui Y
    J Theor Biol; 2007 Jan; 244(1):115-26. PubMed ID: 16959270
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A population-based latent variable approach for association mapping of quantitative trait loci.
    Wang T; Weir B; Zeng ZB
    Ann Hum Genet; 2006 Jul; 70(Pt 4):506-23. PubMed ID: 16759182
    [TBL] [Abstract][Full Text] [Related]  

  • 6. On the use of phylogeny-based tests to detect association between quantitative traits and haplotypes.
    Bardel C; Danjean V; Morange P; Génin E; Darlu P
    Genet Epidemiol; 2009 Dec; 33(8):729-39. PubMed ID: 19399905
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An open-pollinated design for mapping imprinting genes in natural populations.
    Sun L; Zhu X; Bo W; Xu F; Cheng T; Zhang Q; Wu R
    Brief Bioinform; 2015 May; 16(3):449-60. PubMed ID: 24927940
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mapping and exclusion mapping of genomic imprinting effects in mouse F2 families.
    Mantey C; Brockmann GA; Kalm E; Reinsch N
    J Hered; 2005; 96(4):329-38. PubMed ID: 15761081
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A whole genome long-range haplotype (WGLRH) test for detecting imprints of positive selection in human populations.
    Zhang C; Bailey DK; Awad T; Liu G; Xing G; Cao M; Valmeekam V; Retief J; Matsuzaki H; Taub M; Seielstad M; Kennedy GC
    Bioinformatics; 2006 Sep; 22(17):2122-8. PubMed ID: 16845142
    [TBL] [Abstract][Full Text] [Related]  

  • 10. SNP-VISTA: an interactive SNP visualization tool.
    Shah N; Teplitsky MV; Minovitsky S; Pennacchio LA; Hugenholtz P; Hamann B; Dubchak IL
    BMC Bioinformatics; 2005 Dec; 6():292. PubMed ID: 16336665
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Maximum likelihood inference of imprinting and allele-specific expression from EST data.
    Seoighe C; Nembaware V; Scheffler K
    Bioinformatics; 2006 Dec; 22(24):3032-9. PubMed ID: 17038342
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Global survey of genomic imprinting by transcriptome sequencing.
    Babak T; Deveale B; Armour C; Raymond C; Cleary MA; van der Kooy D; Johnson JM; Lim LP
    Curr Biol; 2008 Nov; 18(22):1735-41. PubMed ID: 19026546
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Linkage analysis of affected sib pairs allowing for parent-of-origin effects.
    Wu CC; Shete S; Amos CI
    Ann Hum Genet; 2005 Jan; 69(Pt 1):113-26. PubMed ID: 15638832
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Inferring gene transcriptional modulatory relations: a genetical genomics approach.
    Li H; Lu L; Manly KF; Chesler EJ; Bao L; Wang J; Zhou M; Williams RW; Cui Y
    Hum Mol Genet; 2005 May; 14(9):1119-25. PubMed ID: 15772094
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic linkage and imprinting effects on body mass index in children and young adults.
    Gorlova OY; Amos CI; Wang NW; Shete S; Turner ST; Boerwinkle E
    Eur J Hum Genet; 2003 Jun; 11(6):425-32. PubMed ID: 12774034
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A nonimprinted Prader-Willi Syndrome (PWS)-region gene regulates a different chromosomal domain in trans but the imprinted pws loci do not alter genome-wide mRNA levels.
    Stefan M; Portis T; Longnecker R; Nicholls RD
    Genomics; 2005 May; 85(5):630-40. PubMed ID: 15820315
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genome-wide linkage analysis assessing parent-of-origin effects in the inheritance of birth weight.
    Lindsay RS; Kobes S; Knowler WC; Hanson RL
    Hum Genet; 2002 May; 110(5):503-9. PubMed ID: 12073022
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The parent-of-origin effect of 10q22 in pre-eclamptic females coincides with two regions clustered for genes with down-regulated expression in androgenetic placentas.
    Oudejans CB; Mulders J; Lachmeijer AM; van Dijk M; Könst AA; Westerman BA; van Wijk IJ; Leegwater PA; Kato HD; Matsuda T; Wake N; Dekker GA; Pals G; ten Kate LP; Blankenstein MA
    Mol Hum Reprod; 2004 Aug; 10(8):589-98. PubMed ID: 15208369
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [How about the uncertainty in the haplotypes in the population-based KORA studies?].
    Heid IM; Lamina C; Bongardt F; Fischer G; Klopp N; Huth C; Küchenhoff H; Kronenberg F; Wichmann HE; Illig T
    Gesundheitswesen; 2005 Aug; 67 Suppl 1():S132-6. PubMed ID: 16032531
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Diseases associated with genomic imprinting.
    Wilkins JF; Úbeda F
    Prog Mol Biol Transl Sci; 2011; 101():401-45. PubMed ID: 21507360
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.