BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

488 related articles for article (PubMed ID: 34475392)

  • 1. Genome-wide sequencing-based identification of methylation quantitative trait loci and their role in schizophrenia risk.
    Perzel Mandell KA; Eagles NJ; Wilton R; Price AJ; Semick SA; Collado-Torres L; Ulrich WS; Tao R; Han S; Szalay AS; Hyde TM; Kleinman JE; Weinberger DR; Jaffe AE
    Nat Commun; 2021 Sep; 12(1):5251. PubMed ID: 34475392
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Characterization of cross-tissue genetic-epigenetic effects and their patterns in schizophrenia.
    Lin D; Chen J; Perrone-Bizzozero N; Bustillo JR; Du Y; Calhoun VD; Liu J
    Genome Med; 2018 Feb; 10(1):13. PubMed ID: 29482655
    [TBL] [Abstract][Full Text] [Related]  

  • 3. An integrated genetic-epigenetic analysis of schizophrenia: evidence for co-localization of genetic associations and differential DNA methylation.
    Hannon E; Dempster E; Viana J; Burrage J; Smith AR; Macdonald R; St Clair D; Mustard C; Breen G; Therman S; Kaprio J; Toulopoulou T; Hulshoff Pol HE; Bohlken MM; Kahn RS; Nenadic I; Hultman CM; Murray RM; Collier DA; Bass N; Gurling H; McQuillin A; Schalkwyk L; Mill J
    Genome Biol; 2016 Aug; 17(1):176. PubMed ID: 27572077
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mapping DNA methylation across development, genotype and schizophrenia in the human frontal cortex.
    Jaffe AE; Gao Y; Deep-Soboslay A; Tao R; Hyde TM; Weinberger DR; Kleinman JE
    Nat Neurosci; 2016 Jan; 19(1):40-7. PubMed ID: 26619358
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Schizophrenia risk variants influence multiple classes of transcripts of sorting nexin 19 (SNX19).
    Ma L; Semick SA; Chen Q; Li C; Tao R; Price AJ; Shin JH; Jia Y; ; Brandon NJ; Cross AJ; Hyde TM; Kleinman JE; Jaffe AE; Weinberger DR; Straub RE
    Mol Psychiatry; 2020 Apr; 25(4):831-843. PubMed ID: 30635639
    [TBL] [Abstract][Full Text] [Related]  

  • 7. DNA methylation mapping identifies gene regulatory effects in patients with systemic lupus erythematosus.
    Imgenberg-Kreuz J; Carlsson Almlöf J; Leonard D; Alexsson A; Nordmark G; Eloranta ML; Rantapää-Dahlqvist S; Bengtsson AA; Jönsen A; Padyukov L; Gunnarsson I; Svenungsson E; Sjöwall C; Rönnblom L; Syvänen AC; Sandling JK
    Ann Rheum Dis; 2018 May; 77(5):736-743. PubMed ID: 29437559
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases.
    Ahsan M; Ek WE; Rask-Andersen M; Karlsson T; Lind-Thomsen A; Enroth S; Gyllensten U; Johansson Å
    PLoS Genet; 2017 Sep; 13(9):e1007005. PubMed ID: 28915241
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Identification of schizophrenia-associated loci by combining DNA methylation and gene expression data from whole blood.
    van Eijk KR; de Jong S; Strengman E; Buizer-Voskamp JE; Kahn RS; Boks MP; Horvath S; Ophoff RA
    Eur J Hum Genet; 2015 Aug; 23(8):1106-10. PubMed ID: 25424713
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Multi-omics analysis identifies CpGs near G6PC2 mediating the effects of genetic variants on fasting glucose.
    Chung RH; Chiu YF; Wang WC; Hwu CM; Hung YJ; Lee IT; Chuang LM; Quertermous T; Rotter JI; Chen YI; Chang IS; Hsiung CA
    Diabetologia; 2021 Jul; 64(7):1613-1625. PubMed ID: 33842983
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Epigenome-wide scans identify differentially methylated regions for age and age-related phenotypes in a healthy ageing population.
    Bell JT; Tsai PC; Yang TP; Pidsley R; Nisbet J; Glass D; Mangino M; Zhai G; Zhang F; Valdes A; Shin SY; Dempster EL; Murray RM; Grundberg E; Hedman AK; Nica A; Small KS; ; Dermitzakis ET; McCarthy MI; Mill J; Spector TD; Deloukas P
    PLoS Genet; 2012; 8(4):e1002629. PubMed ID: 22532803
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. A Genome-Wide mQTL Analysis in Human Adipose Tissue Identifies Genetic Variants Associated with DNA Methylation, Gene Expression and Metabolic Traits.
    Volkov P; Olsson AH; Gillberg L; Jørgensen SW; Brøns C; Eriksson KF; Groop L; Jansson PA; Nilsson E; Rönn T; Vaag A; Ling C
    PLoS One; 2016; 11(6):e0157776. PubMed ID: 27322064
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genome-wide associations between genetic and epigenetic variation influence mRNA expression and insulin secretion in human pancreatic islets.
    Olsson AH; Volkov P; Bacos K; Dayeh T; Hall E; Nilsson EA; Ladenvall C; Rönn T; Ling C
    PLoS Genet; 2014 Nov; 10(11):e1004735. PubMed ID: 25375650
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Deep learning predicts DNA methylation regulatory variants in the human brain and elucidates the genetics of psychiatric disorders.
    Zhou J; Chen Q; Braun PR; Perzel Mandell KA; Jaffe AE; Tan HY; Hyde TM; Kleinman JE; Potash JB; Shinozaki G; Weinberger DR; Han S
    Proc Natl Acad Sci U S A; 2022 Aug; 119(34):e2206069119. PubMed ID: 35969790
    [TBL] [Abstract][Full Text] [Related]  

  • 17. GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.
    Rentería ME; Coolen MW; Statham AL; Choi RS; Qu W; Campbell MJ; Smith S; Henders AK; Montgomery GW; Clark SJ; Martin NG; Medland SE
    Twin Res Hum Genet; 2013 Aug; 16(4):767-81. PubMed ID: 23725790
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Methylation QTLs in the developing brain and their enrichment in schizophrenia risk loci.
    Hannon E; Spiers H; Viana J; Pidsley R; Burrage J; Murphy TM; Troakes C; Turecki G; O'Donovan MC; Schalkwyk LC; Bray NJ; Mill J
    Nat Neurosci; 2016 Jan; 19(1):48-54. PubMed ID: 26619357
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genome-wide identification of splicing QTLs in the human brain and their enrichment among schizophrenia-associated loci.
    Takata A; Matsumoto N; Kato T
    Nat Commun; 2017 Feb; 8():14519. PubMed ID: 28240266
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Characterizing the genetic basis of methylome diversity in histologically normal human lung tissue.
    Shi J; Marconett CN; Duan J; Hyland PL; Li P; Wang Z; Wheeler W; Zhou B; Campan M; Lee DS; Huang J; Zhou W; Triche T; Amundadottir L; Warner A; Hutchinson A; Chen PH; Chung BS; Pesatori AC; Consonni D; Bertazzi PA; Bergen AW; Freedman M; Siegmund KD; Berman BP; Borok Z; Chatterjee N; Tucker MA; Caporaso NE; Chanock SJ; Laird-Offringa IA; Landi MT
    Nat Commun; 2014 Feb; 5():3365. PubMed ID: 24572595
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 25.