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 *

190 related articles for article (PubMed ID: 35193936)

  • 1. Functional noncoding SNPs in human endothelial cells fine-map vascular trait associations.
    Toropainen A; Stolze LK; Örd T; Whalen MB; Torrell PM; Link VM; Kaikkonen MU; Romanoski CE
    Genome Res; 2022 Mar; 32(3):409-424. PubMed ID: 35193936
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Systems Genetics in Human Endothelial Cells Identifies Non-coding Variants Modifying Enhancers, Expression, and Complex Disease Traits.
    Stolze LK; Conklin AC; Whalen MB; López Rodríguez M; Õunap K; Selvarajan I; Toropainen A; Örd T; Li J; Eshghi A; Solomon AE; Fang Y; Kaikkonen MU; Romanoski CE
    Am J Hum Genet; 2020 Jun; 106(6):748-763. PubMed ID: 32442411
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic regulatory signatures underlying islet gene expression and type 2 diabetes.
    Varshney A; Scott LJ; Welch RP; Erdos MR; Chines PS; Narisu N; Albanus RD; Orchard P; Wolford BN; Kursawe R; Vadlamudi S; Cannon ME; Didion JP; Hensley J; Kirilusha A; ; Bonnycastle LL; Taylor DL; Watanabe R; Mohlke KL; Boehnke M; Collins FS; Parker SC; Stitzel ML
    Proc Natl Acad Sci U S A; 2017 Feb; 114(9):2301-2306. PubMed ID: 28193859
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic variant at coronary artery disease and ischemic stroke locus 1p32.2 regulates endothelial responses to hemodynamics.
    Krause MD; Huang RT; Wu D; Shentu TP; Harrison DL; Whalen MB; Stolze LK; Di Rienzo A; Moskowitz IP; Civelek M; Romanoski CE; Fang Y
    Proc Natl Acad Sci U S A; 2018 Nov; 115(48):E11349-E11358. PubMed ID: 30429326
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Integrative analysis of liver-specific non-coding regulatory SNPs associated with the risk of coronary artery disease.
    Selvarajan I; Toropainen A; Garske KM; López Rodríguez M; Ko A; Miao Z; Kaminska D; Õunap K; Örd T; Ravindran A; Liu OH; Moreau PR; Jawahar Deen A; Männistö V; Pan C; Levonen AL; Lusis AJ; Heikkinen S; Romanoski CE; Pihlajamäki J; Pajukanta P; Kaikkonen MU
    Am J Hum Genet; 2021 Mar; 108(3):411-430. PubMed ID: 33626337
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Blood cell traits' GWAS loci colocalization with variation in PU.1 genomic occupancy prioritizes causal noncoding regulatory variants.
    Jeong R; Bulyk ML
    Cell Genom; 2023 Jul; 3(7):100327. PubMed ID: 37492098
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Epigenomes of Human Hearts Reveal New Genetic Variants Relevant for Cardiac Disease and Phenotype.
    Tan WLW; Anene-Nzelu CG; Wong E; Lee CJM; Tan HS; Tang SJ; Perrin A; Wu KX; Zheng W; Ashburn RJ; Pan B; Lee MY; Autio MI; Morley MP; Tam WL; Cheung C; Margulies KB; Chen L; Cappola TP; Loh M; Chambers J; Prabhakar S; Foo RSY;
    Circ Res; 2020 Aug; 127(6):761-777. PubMed ID: 32529949
    [TBL] [Abstract][Full Text] [Related]  

  • 8. High-throughput functional dissection of noncoding SNPs with biased allelic enhancer activity for insulin resistance-relevant phenotypes.
    Duan YY; Chen XF; Zhu RJ; Jia YY; Huang XT; Zhang M; Yang N; Dong SS; Zeng M; Feng Z; Zhu DL; Wu H; Jiang F; Shi W; Hu WX; Ke X; Chen H; Liu Y; Jing RH; Guo Y; Li M; Yang TL
    Am J Hum Genet; 2023 Aug; 110(8):1266-1288. PubMed ID: 37506691
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A non-coding genetic variant associated with abdominal aortic aneurysm alters ERG gene regulation.
    Marsman J; Gimenez G; Day RC; Horsfield JA; Jones GT
    Hum Mol Genet; 2020 Mar; 29(4):554-565. PubMed ID: 31691800
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Human-genome single nucleotide polymorphisms affecting transcription factor binding and their role in pathogenesis.
    Antontseva EV; Degtyareva AO; Korbolina EE; Damarov IS; Merkulova TI
    Vavilovskii Zhurnal Genet Selektsii; 2023 Oct; 27(6):662-675. PubMed ID: 37965371
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Regulatory SNPs: Altered Transcription Factor Binding Sites Implicated in Complex Traits and Diseases.
    Degtyareva AO; Antontseva EV; Merkulova TI
    Int J Mol Sci; 2021 Jun; 22(12):. PubMed ID: 34208629
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Functional genomics elucidates regulatory mechanisms of Parkinson's disease-associated variants.
    Chen R; Liu J; Li S; Li X; Huo Y; Yao YG; Xiao X; Li M; Luo XJ
    BMC Med; 2022 Feb; 20(1):68. PubMed ID: 35168626
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Cell-type-specific effects of genetic variation on chromatin accessibility during human neuronal differentiation.
    Liang D; Elwell AL; Aygün N; Krupa O; Wolter JM; Kyere FA; Lafferty MJ; Cheek KE; Courtney KP; Yusupova M; Garrett ME; Ashley-Koch A; Crawford GE; Love MI; de la Torre-Ubieta L; Geschwind DH; Stein JL
    Nat Neurosci; 2021 Jul; 24(7):941-953. PubMed ID: 34017130
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Functional genomic analysis delineates regulatory mechanisms of GWAS-identified bipolar disorder risk variants.
    Chen R; Yang Z; Liu J; Cai X; Huo Y; Zhang Z; Li M; Chang H; Luo XJ
    Genome Med; 2022 May; 14(1):53. PubMed ID: 35590387
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Allele-specific enhancers mediate associations between LCAT and ABCA1 polymorphisms and HDL metabolism.
    Howard AD; Wang X; Prasad M; Sahu AD; Aniba R; Miller M; Hannenhalli S; Chang YC
    PLoS One; 2019; 14(4):e0215911. PubMed ID: 31039173
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Single Nucleotide Polymorphisms at a Distance from Aryl Hydrocarbon Receptor (AHR) Binding Sites Influence AHR Ligand-Dependent Gene Expression.
    Neavin DR; Lee JH; Liu D; Ye Z; Li H; Wang L; Ordog T; Weinshilboum RM
    Drug Metab Dispos; 2019 Sep; 47(9):983-994. PubMed ID: 31292129
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Single-Nucleotide Polymorphisms Sequencing Identifies Candidate Functional Variants at Prostate Cancer Risk Loci.
    Zhang P; Tillmans LS; Thibodeau SN; Wang L
    Genes (Basel); 2019 Jul; 10(7):. PubMed ID: 31323811
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Trans-Ancestral Fine-Mapping and Epigenetic Annotation as Tools to Delineate Functionally Relevant Risk Alleles at
    Vyse TJ; Cunninghame Graham DS
    Int J Mol Sci; 2020 Nov; 21(21):. PubMed ID: 33182226
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.