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 *

129 related articles for article (PubMed ID: 24522295)

  • 41. EVI5 is a risk gene for multiple sclerosis.
    Hoppenbrouwers IA; Aulchenko YS; Ebers GC; Ramagopalan SV; Oostra BA; van Duijn CM; Hintzen RQ
    Genes Immun; 2008 Jun; 9(4):334-7. PubMed ID: 18401352
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Estimating the heritability of colorectal cancer.
    Jiao S; Peters U; Berndt S; Brenner H; Butterbach K; Caan BJ; Carlson CS; Chan AT; Chang-Claude J; Chanock S; Curtis KR; Duggan D; Gong J; Harrison TA; Hayes RB; Henderson BE; Hoffmeister M; Kolonel LN; Le Marchand L; Potter JD; Rudolph A; Schoen RE; Seminara D; Slattery ML; White E; Hsu L
    Hum Mol Genet; 2014 Jul; 23(14):3898-905. PubMed ID: 24562164
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Regulation of inflammation in diabetes: From genetics to epigenomics evidence.
    Diedisheim M; Carcarino E; Vandiedonck C; Roussel R; Gautier JF; Venteclef N
    Mol Metab; 2020 Nov; 41():101041. PubMed ID: 32603690
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Genetic burden of common variants in progressive and bout-onset multiple sclerosis.
    Sorosina M; Brambilla P; Clarelli F; Barizzone N; Lupoli S; Guaschino C; Osiceanu AM; Moiola L; Ghezzi A; Coniglio G; Patti F; Mancardi G; Manunta P; Glorioso N; Guerini FR; Bergamaschi R; Perla F; ; ; Martinelli V; Cusi D; Leone M; Comi G; D'Alfonso S; Martinelli-Boneschi F
    Mult Scler; 2014 Jun; 20(7):802-11. PubMed ID: 24277324
    [TBL] [Abstract][Full Text] [Related]  

  • 45. LincSNP 3.0: an updated database for linking functional variants to human long non-coding RNAs, circular RNAs and their regulatory elements.
    Gao Y; Li X; Shang S; Guo S; Wang P; Sun D; Gan J; Sun J; Zhang Y; Wang J; Wang X; Li X; Zhang Y; Ning S
    Nucleic Acids Res; 2021 Jan; 49(D1):D1244-D1250. PubMed ID: 33219661
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Next-generation sequencing identifies contribution of both class I and II HLA genes on susceptibility of multiple sclerosis in Japanese.
    Ogawa K; Okuno T; Hosomichi K; Hosokawa A; Hirata J; Suzuki K; Sakaue S; Kinoshita M; Asano Y; Miyamoto K; Inoue I; Kusunoki S; Okada Y; Mochizuki H
    J Neuroinflammation; 2019 Aug; 16(1):162. PubMed ID: 31382992
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Disease-Associated Single-Nucleotide Polymorphisms From Noncoding Regions in Juvenile Idiopathic Arthritis Are Located Within or Adjacent to Functional Genomic Elements of Human Neutrophils and CD4+ T Cells.
    Jiang K; Zhu L; Buck MJ; Chen Y; Carrier B; Liu T; Jarvis JN
    Arthritis Rheumatol; 2015 Jul; 67(7):1966-77. PubMed ID: 25833190
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Targeted resequencing of regulatory regions at schizophrenia risk loci: Role of rare functional variants at chromatin repressive states.
    González-Peñas J; Amigo J; Santomé L; Sobrino B; Brenlla J; Agra S; Paz E; Páramo M; Carracedo Á; Arrojo M; Costas J
    Schizophr Res; 2016 Jul; 174(1-3):10-16. PubMed ID: 27066855
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Many inflammatory bowel disease risk loci include regions that regulate gene expression in immune cells and the intestinal epithelium.
    Mokry M; Middendorp S; Wiegerinck CL; Witte M; Teunissen H; Meddens CA; Cuppen E; Clevers H; Nieuwenhuis EE
    Gastroenterology; 2014 Apr; 146(4):1040-7. PubMed ID: 24333384
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Prostate cancer risk-associated variants reported from genome-wide association studies: meta-analysis and their contribution to genetic Variation.
    Kim ST; Cheng Y; Hsu FC; Jin T; Kader AK; Zheng SL; Isaacs WB; Xu J; Sun J
    Prostate; 2010 Dec; 70(16):1729-38. PubMed ID: 20564319
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Fine-Mapping of Common Genetic Variants Associated with Colorectal Tumor Risk Identified Potential Functional Variants.
    Du M; Jiao S; Bien SA; Gala M; Abecasis G; Bezieau S; Brenner H; Butterbach K; Caan BJ; Carlson CS; Casey G; Chang-Claude J; Conti DV; Curtis KR; Duggan D; Gallinger S; Haile RW; Harrison TA; Hayes RB; Hoffmeister M; Hopper JL; Hudson TJ; Jenkins MA; Küry S; Le Marchand L; Leal SM; Newcomb PA; Nickerson DA; Potter JD; Schoen RE; Schumacher FR; Seminara D; Slattery ML; Hsu L; Chan AT; White E; Berndt SI; Peters U
    PLoS One; 2016; 11(7):e0157521. PubMed ID: 27379672
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Independent replication of STAT3 association with multiple sclerosis risk in a large German case-control sample.
    Lill CM; Schjeide BM; Akkad DA; Blaschke P; Winkelmann A; Gerdes LA; Hoffjan S; Luessi F; Dörner T; Li SC; Steinhagen-Thiessen E; Lindenberger U; Chan A; Hartung HP; Aktas O; Lohse P; Kümpfel T; Kubisch C; Epplen JT; Zettl UK; Bertram L; Zipp F
    Neurogenetics; 2012 Feb; 13(1):83-6. PubMed ID: 22095036
    [TBL] [Abstract][Full Text] [Related]  

  • 53. [New gene map for multiple sclerosis].
    Harbo HF; Lorentzen AR; Lie BA; Celius EG; Spurkland A
    Tidsskr Nor Laegeforen; 2011 Nov; 131(21):2126-30. PubMed ID: 22048209
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Function of multiple sclerosis-protective HLA class I alleles revealed by genome-wide protein-quantitative trait loci mapping of interferon signalling.
    Lundtoft C; Pucholt P; Imgenberg-Kreuz J; Carlsson-Almlöf J; Eloranta ML; Syvänen AC; Nordmark G; Sandling JK; Kockum I; Olsson T; Rönnblom L; Hagberg N
    PLoS Genet; 2020 Oct; 16(10):e1009199. PubMed ID: 33104735
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Perspectives on the use of multiple sclerosis risk genes for prediction.
    Jafari N; Broer L; van Duijn CM; Janssens AC; Hintzen RQ
    PLoS One; 2011; 6(12):e26493. PubMed ID: 22164203
    [TBL] [Abstract][Full Text] [Related]  

  • 56. MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis.
    ; Lill CM; Schjeide BM; Graetz C; Ban M; Alcina A; Ortiz MA; Pérez J; Damotte V; Booth D; Lopez de Lapuente A; Broer L; Schilling M; Akkad DA; Aktas O; Alloza I; Antigüedad A; Arroyo R; Blaschke P; Buttmann M; Chan A; Compston A; Cournu-Rebeix I; Dörner T; Epplen JT; Fernández Ó; Gerdes LA; Guillot-Noël L; Hartung HP; Hoffjan S; Izquierdo G; Kemppinen A; Kroner A; Kubisch C; Kümpfel T; Li SC; Lindenberger U; Lohse P; Lubetzki C; Luessi F; Malhotra S; Mescheriakova J; Montalban X; Papeix C; Paredes LF; Rieckmann P; Steinhagen-Thiessen E; Winkelmann A; Zettl UK; Hintzen R; Vandenbroeck K; Stewart G; Fontaine B; Comabella M; Urcelay E; Matesanz F; Sawcer S; Bertram L; Zipp F
    Brain; 2013 Jun; 136(Pt 6):1778-82. PubMed ID: 23739915
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Replication analysis of variants associated with multiple sclerosis risk.
    Dashti M; Ateyah K; Alroughani R; Al-Temaimi R
    Sci Rep; 2020 Apr; 10(1):7327. PubMed ID: 32355262
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Genome-wide association studies in multiple sclerosis: lessons and future prospects.
    Kemppinen A; Sawcer S; Compston A
    Brief Funct Genomics; 2011 Mar; 10(2):61-70. PubMed ID: 21310812
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Susceptibility variants in the CD58 gene locus point to a role of microRNA-548ac in the pathogenesis of multiple sclerosis.
    Hecker M; Fitzner B; Blaschke J; Blaschke P; Zettl UK
    Mutat Res Rev Mutat Res; 2015; 763():161-7. PubMed ID: 25795118
    [TBL] [Abstract][Full Text] [Related]  

  • 60. ZFAT gene variant association with multiple sclerosis in the Arabian Gulf population: A genetic basis for gender-associated susceptibility.
    Bourguiba-Hachemi S; Ashkanani TK; Kadhem FJ; Almawi WY; Alroughani R; Fathallah MD
    Mol Med Rep; 2016 Oct; 14(4):3543-50. PubMed ID: 27572828
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.