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 *

197 related articles for article (PubMed ID: 23418889)

  • 41. Biological characterization of expression quantitative trait loci (eQTLs) showing tissue-specific opposite directional effects.
    Mizuno A; Okada Y
    Eur J Hum Genet; 2019 Nov; 27(11):1745-1756. PubMed ID: 31296926
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Molecular genetic aetiology of general cognitive function is enriched in evolutionarily conserved regions.
    Hill WD; Davies G; Harris SE; Hagenaars SP; ; Liewald DC; Penke L; Gale CR; Deary IJ
    Transl Psychiatry; 2016 Dec; 6(12):e980. PubMed ID: 27959336
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Integration of VDR genome wide binding and GWAS genetic variation data reveals co-occurrence of VDR and NF-κB binding that is linked to immune phenotypes.
    Singh PK; van den Berg PR; Long MD; Vreugdenhil A; Grieshober L; Ochs-Balcom HM; Wang J; Delcambre S; Heikkinen S; Carlberg C; Campbell MJ; Sucheston-Campbell LE
    BMC Genomics; 2017 Feb; 18(1):132. PubMed ID: 28166722
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Limits on the reproducibility of marker associations with southern leaf blight resistance in the maize nested association mapping population.
    Bian Y; Yang Q; Balint-Kurti PJ; Wisser RJ; Holland JB
    BMC Genomics; 2014 Dec; 15(1):1068. PubMed ID: 25475173
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Secondary analyses for genome-wide association studies using expression quantitative trait loci.
    Ngwa JS; Yanek LR; Kammers K; Kanchan K; Taub MA; Scharpf RB; Faraday N; Becker LC; Mathias RA; Ruczinski I
    Genet Epidemiol; 2022 Apr; 46(3-4):170-181. PubMed ID: 35312098
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Multiple Functional Variants at 13q14 Risk Locus for Osteoporosis Regulate RANKL Expression Through Long-Range Super-Enhancer.
    Zhu DL; Chen XF; Hu WX; Dong SS; Lu BJ; Rong Y; Chen YX; Chen H; Thynn HN; Wang NN; Guo Y; Yang TL
    J Bone Miner Res; 2018 Jul; 33(7):1335-1346. PubMed ID: 29528523
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Physiology and Endocrinology Symposium: How single nucleotide polymorphism chips will advance our knowledge of factors controlling puberty and aid in selecting replacement beef females.
    Snelling WM; Cushman RA; Fortes MR; Reverter A; Bennett GL; Keele JW; Kuehn LA; McDaneld TG; Thallman RM; Thomas MG
    J Anim Sci; 2012 Apr; 90(4):1152-65. PubMed ID: 22038989
    [TBL] [Abstract][Full Text] [Related]  

  • 48. GenoWAP: GWAS signal prioritization through integrated analysis of genomic functional annotation.
    Lu Q; Yao X; Hu Y; Zhao H
    Bioinformatics; 2016 Feb; 32(4):542-8. PubMed ID: 26504140
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Using chromatin marks to interpret and localize genetic associations to complex human traits and diseases.
    Trynka G; Raychaudhuri S
    Curr Opin Genet Dev; 2013 Dec; 23(6):635-41. PubMed ID: 24287333
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Accuracy of prediction of simulated polygenic phenotypes and their underlying quantitative trait loci genotypes using real or imputed whole-genome markers in cattle.
    Hassani S; Saatchi M; Fernando RL; Garrick DJ
    Genet Sel Evol; 2015 Dec; 47():99. PubMed ID: 26698091
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Integrating functional data to prioritize causal variants in statistical fine-mapping studies.
    Kichaev G; Yang WY; Lindstrom S; Hormozdiari F; Eskin E; Price AL; Kraft P; Pasaniuc B
    PLoS Genet; 2014 Oct; 10(10):e1004722. PubMed ID: 25357204
    [TBL] [Abstract][Full Text] [Related]  

  • 52. 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]  

  • 53. In-silico analysis of inflammatory bowel disease (IBD) GWAS loci to novel connections.
    Mesbah-Uddin M; Elango R; Banaganapalli B; Shaik NA; Al-Abbasi FA
    PLoS One; 2015; 10(3):e0119420. PubMed ID: 25786114
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Genomic partitioning of inbreeding depression in humans.
    Yengo L; Yang J; Keller MC; Goddard ME; Wray NR; Visscher PM
    Am J Hum Genet; 2021 Aug; 108(8):1488-1501. PubMed ID: 34214457
    [TBL] [Abstract][Full Text] [Related]  

  • 55. JEPEG: a summary statistics based tool for gene-level joint testing of functional variants.
    Lee D; Williamson VS; Bigdeli TB; Riley BP; Fanous AH; Vladimirov VI; Bacanu SA
    Bioinformatics; 2015 Apr; 31(8):1176-82. PubMed ID: 25505091
    [TBL] [Abstract][Full Text] [Related]  

  • 56. LSMM: a statistical approach to integrating functional annotations with genome-wide association studies.
    Ming J; Dai M; Cai M; Wan X; Liu J; Yang C
    Bioinformatics; 2018 Aug; 34(16):2788-2796. PubMed ID: 29608640
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Identification of breast cancer associated variants that modulate transcription factor binding.
    Liu Y; Walavalkar NM; Dozmorov MG; Rich SS; Civelek M; Guertin MJ
    PLoS Genet; 2017 Sep; 13(9):e1006761. PubMed ID: 28957321
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Selecting Closely-Linked SNPs Based on Local Epistatic Effects for Haplotype Construction Improves Power of Association Mapping.
    Liu F; Schmidt RH; Reif JC; Jiang Y
    G3 (Bethesda); 2019 Dec; 9(12):4115-4126. PubMed ID: 31604824
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Prioritizing sequence variants in conserved non-coding elements in the chicken genome using chCADD.
    Groß C; Bortoluzzi C; de Ridder D; Megens HJ; Groenen MAM; Reinders M; Bosse M
    PLoS Genet; 2020 Sep; 16(9):e1009027. PubMed ID: 32966296
    [TBL] [Abstract][Full Text] [Related]  

  • 60. A genome-wide survey for SNPs altering microRNA seed sites identifies functional candidates in GWAS.
    Richardson K; Lai CQ; Parnell LD; Lee YC; Ordovas JM
    BMC Genomics; 2011 Oct; 12():504. PubMed ID: 21995669
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.