BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

184 related articles for article (PubMed ID: 30146008)

  • 21. Convergence of evidence from a methylome-wide CpG-SNP association study and GWAS of major depressive disorder.
    Aberg KA; Shabalin AA; Chan RF; Zhao M; Kumar G; van Grootheest G; Clark SL; Xie LY; Milaneschi Y; Penninx BWJH; van den Oord EJCG
    Transl Psychiatry; 2018 Aug; 8(1):162. PubMed ID: 30135428
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Novel DNA methylation loci and genes showing pleiotropic association with Alzheimer's dementia: a network Mendelian randomization analysis.
    Liu D; Wang Y; Jing H; Meng Q; Yang J
    Epigenetics; 2022; 17(7):746-758. PubMed ID: 34461811
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Association of variants in PTPN22, CTLA-4, IL2-RA, and INS genes with type 1 diabetes in Emiratis.
    Sharma C; R Ali B; Osman W; Afandi B; Aburawi EH; Beshyah SA; Al-Mahayri Z; Al-Rifai RH; Al Yafei Z; ElGhazali G; Alkaabi J
    Ann Hum Genet; 2021 Mar; 85(2):48-57. PubMed ID: 32970831
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Role of DNA methylation at the placental RTL1 gene locus in type 1 diabetes.
    Belot MP; Nadéri K; Mille C; Boëlle PY; Benachi A; Bougnères P; Fradin D
    Pediatr Diabetes; 2017 May; 18(3):178-187. PubMed ID: 27174469
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Functional relevance for type 1 diabetes mellitus-associated genetic variants by using integrative analyses.
    Qiu YH; Deng FY; Tang ZX; Jiang ZH; Lei SF
    Hum Immunol; 2015 Oct; 76(10):753-8. PubMed ID: 26429317
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Investigation of the vitamin D receptor gene (VDR) and its interaction with protein tyrosine phosphatase, non-receptor type 2 gene (PTPN2) on risk of islet autoimmunity and type 1 diabetes: the Diabetes Autoimmunity Study in the Young (DAISY).
    Frederiksen B; Liu E; Romanos J; Steck AK; Yin X; Kroehl M; Fingerlin TE; Erlich H; Eisenbarth GS; Rewers M; Norris JM
    J Steroid Biochem Mol Biol; 2013 Jan; 133():51-7. PubMed ID: 22960018
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Deep molecular phenotypes link complex disorders and physiological insult to CpG methylation.
    Zaghlool SB; Mook-Kanamori DO; Kader S; Stephan N; Halama A; Engelke R; Sarwath H; Al-Dous EK; Mohamoud YA; Roemisch-Margl W; Adamski J; Kastenmüller G; Friedrich N; Visconti A; Tsai PC; Spector T; Bell JT; Falchi M; Wahl A; Waldenberger M; Peters A; Gieger C; Pezer M; Lauc G; Graumann J; Malek JA; Suhre K
    Hum Mol Genet; 2018 Mar; 27(6):1106-1121. PubMed ID: 29325019
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Epigenome-wide association study of seizures in childhood and adolescence.
    Caramaschi D; Hatcher C; Mulder RH; Felix JF; Cecil CAM; Relton CL; Walton E
    Clin Epigenetics; 2020 Jan; 12(1):8. PubMed ID: 31915053
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Epigenome-wide association study of whole blood gene expression in Framingham Heart Study participants provides molecular insight into the potential role of CHRNA5 in cigarette smoking-related lung diseases.
    Yao C; Joehanes R; Wilson R; Tanaka T; Ferrucci L; Kretschmer A; Prokisch H; Schramm K; Gieger C; Peters A; Waldenberger M; Marzi C; Herder C; Levy D
    Clin Epigenetics; 2021 Mar; 13(1):60. PubMed ID: 33752734
    [TBL] [Abstract][Full Text] [Related]  

  • 30. High density methylation QTL analysis in human blood via next-generation sequencing of the methylated genomic DNA fraction.
    McClay JL; Shabalin AA; Dozmorov MG; Adkins DE; Kumar G; Nerella S; Clark SL; Bergen SE; ; Hultman CM; Magnusson PK; Sullivan PF; Aberg KA; van den Oord EJ
    Genome Biol; 2015 Dec; 16():291. PubMed ID: 26699738
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genetic contribution to variation in DNA methylation at maternal smoking-sensitive loci in exposed neonates.
    Gonseth S; de Smith AJ; Roy R; Zhou M; Lee ST; Shao X; Ohja J; Wrensch MR; Walsh KM; Metayer C; Wiemels JL
    Epigenetics; 2016 Sep; 11(9):664-673. PubMed ID: 27403598
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Genome-wide identification of DNA methylation QTLs in whole blood highlights pathways for cardiovascular disease.
    Huan T; Joehanes R; Song C; Peng F; Guo Y; Mendelson M; Yao C; Liu C; Ma J; Richard M; Agha G; Guan W; Almli LM; Conneely KN; Keefe J; Hwang SJ; Johnson AD; Fornage M; Liang L; Levy D
    Nat Commun; 2019 Sep; 10(1):4267. PubMed ID: 31537805
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Systematic identification of genetic influences on methylation across the human life course.
    Gaunt TR; Shihab HA; Hemani G; Min JL; Woodward G; Lyttleton O; Zheng J; Duggirala A; McArdle WL; Ho K; Ring SM; Evans DM; Davey Smith G; Relton CL
    Genome Biol; 2016 Mar; 17():61. PubMed ID: 27036880
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Genetic control of individual differences in gene-specific methylation in human brain.
    Zhang D; Cheng L; Badner JA; Chen C; Chen Q; Luo W; Craig DW; Redman M; Gershon ES; Liu C
    Am J Hum Genet; 2010 Mar; 86(3):411-9. PubMed ID: 20215007
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Genome-wide DNA methylation study in human placenta identifies novel loci associated with maternal smoking during pregnancy.
    Morales E; Vilahur N; Salas LA; Motta V; Fernandez MF; Murcia M; Llop S; Tardon A; Fernandez-Tardon G; Santa-Marina L; Gallastegui M; Bollati V; Estivill X; Olea N; Sunyer J; Bustamante M
    Int J Epidemiol; 2016 Oct; 45(5):1644-1655. PubMed ID: 27591263
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Insights into non-autoimmune type 1 diabetes with 13 novel loci in low polygenic risk score patients.
    Qu J; Qu HQ; Bradfield JP; Glessner JT; Chang X; Tian L; March M; Connolly JJ; Roizen JD; Sleiman PMA; Hakonarson H
    Sci Rep; 2021 Aug; 11(1):16013. PubMed ID: 34362956
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Genetic and epigenetic factors in etiology of diabetes mellitus type 1.
    Stankov K; Benc D; Draskovic D
    Pediatrics; 2013 Dec; 132(6):1112-22. PubMed ID: 24190679
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A polymorphism in PTPN2 gene is associated with an earlier onset of type 1 diabetes.
    Espino-Paisan L; de la Calle H; Fernández-Arquero M; Figueredo MA; de la Concha EG; Urcelay E; Santiago JL
    Immunogenetics; 2011 Apr; 63(4):255-8. PubMed ID: 21246196
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Shared and distinct genetic variants in type 1 diabetes and celiac disease.
    Smyth DJ; Plagnol V; Walker NM; Cooper JD; Downes K; Yang JH; Howson JM; Stevens H; McManus R; Wijmenga C; Heap GA; Dubois PC; Clayton DG; Hunt KA; van Heel DA; Todd JA
    N Engl J Med; 2008 Dec; 359(26):2767-77. PubMed ID: 19073967
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Polymorphisms involving gain or loss of CpG sites are significantly enriched in trait-associated SNPs.
    Zhou D; Li Z; Yu D; Wan L; Zhu Y; Lai M; Zhang D
    Oncotarget; 2015 Nov; 6(37):39995-40004. PubMed ID: 26503467
    [TBL] [Abstract][Full Text] [Related]  

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