BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

238 related articles for article (PubMed ID: 26662719)

  • 1. Whole Exome Sequencing Identifies Rare Protein-Coding Variants in Behçet's Disease.
    Ognenovski M; Renauer P; Gensterblum E; Kötter I; Xenitidis T; Henes JC; Casali B; Salvarani C; Direskeneli H; Kaufman KM; Sawalha AH
    Arthritis Rheumatol; 2016 May; 68(5):1272-80. PubMed ID: 26662719
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Deregulated DNA damage response network in Behcet's disease.
    Vlachogiannis NI; Ntouros PA; Pappa M; Verrou KM; Arida A; Souliotis VL; Sfikakis PP
    Clin Immunol; 2023 Jan; 246():109189. PubMed ID: 36400336
    [TBL] [Abstract][Full Text] [Related]  

  • 3. IL10 low-frequency variants in Behçet's disease patients.
    Matos M; Xavier JM; Abrantes P; Sousa I; Rei N; Davatchi F; Shahram F; Jesus G; Barcelos F; Vedes J; Salgado M; Abdollahi BS; Nadji A; Moraes-Fontes MF; Shafiee NM; Ghaderibarmi F; Vaz Patto J; Crespo J; Oliveira SA
    Int J Rheum Dis; 2017 May; 20(5):622-627. PubMed ID: 24708170
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Exome Sequencing of Familial Bipolar Disorder.
    Goes FS; Pirooznia M; Parla JS; Kramer M; Ghiban E; Mavruk S; Chen YC; Monson ET; Willour VL; Karchin R; Flickinger M; Locke AE; Levy SE; Scott LJ; Boehnke M; Stahl E; Moran JL; Hultman CM; Landén M; Purcell SM; Sklar P; Zandi PP; McCombie WR; Potash JB
    JAMA Psychiatry; 2016 Jun; 73(6):590-7. PubMed ID: 27120077
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Replication study confirms the association between UBAC2 and Behçet's disease in two independent Chinese sets of patients and controls.
    Hou S; Shu Q; Jiang Z; Chen Y; Li F; Chen F; Kijlstra A; Yang P
    Arthritis Res Ther; 2012 Mar; 14(2):R70. PubMed ID: 22455605
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Microarray and whole-exome sequencing analysis of familial Behçet's disease patients.
    Okuzaki D; Yoshizaki K; Tanaka T; Hirano T; Fukushima K; Washio T; Nojima H
    Sci Rep; 2016 Jan; 6():19456. PubMed ID: 26785681
    [TBL] [Abstract][Full Text] [Related]  

  • 7. CARD15 polymorphisms in Behçet's disease.
    Ahmad T; Zhang L; Gogus F; Verity D; Wallace G; Madanat W; Fayyad F; James T; Neville M; Kanawati C; Fortune F; Celik A; Stanford M; Jewell DP; Marshall SE
    Scand J Rheumatol; 2005; 34(3):233-7. PubMed ID: 16134731
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Low prevalence of NOD2 SNPs in Behçet's disease suggests protective association in Caucasians.
    Kappen JH; Wallace GR; Stolk L; Rivadeneira F; Uitterlinden AG; van Daele PL; Laman JD; Kuijpers RW; Baarsma GS; Stanford MR; Fortune F; Madanat W; van Hagen PM; van Laar JA
    Rheumatology (Oxford); 2009 Nov; 48(11):1375-7. PubMed ID: 19748964
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Targeted resequencing of candidate genes reveals novel variants associated with severe Behçet's uveitis.
    Kim SJ; Lee S; Park C; Seo JS; Kim JI; Yu HG
    Exp Mol Med; 2013 Oct; 45(10):e49. PubMed ID: 24136464
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A putative functional variant within the UBAC2 gene is associated with increased risk of Behçet's disease.
    Sawalha AH; Hughes T; Nadig A; Yılmaz V; Aksu K; Keser G; Cefle A; Yazıcı A; Ergen A; Alarcón-Riquelme ME; Salvarani C; Casali B; Direskeneli H; Saruhan-Direskeneli G
    Arthritis Rheum; 2011 Nov; 63(11):3607-12. PubMed ID: 21918955
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic Association of a Gain-of-Function IFNGR1 Polymorphism and the Intergenic Region LNCAROD/DKK1 With Behçet's Disease.
    Ortiz Fernández L; Coit P; Yilmaz V; Yentür SP; Alibaz-Oner F; Aksu K; Erken E; Düzgün N; Keser G; Cefle A; Yazici A; Ergen A; Alpsoy E; Salvarani C; Casali B; Kısacık B; Kötter I; Henes J; Çınar M; Schaefer A; Nohutcu RM; Zhernakova A; Wijmenga C; Takeuchi F; Harihara S; Kaburaki T; Messedi M; Song YW; Kaşifoğlu T; Carmona FD; Guthridge JM; James JA; Martin J; González Escribano MF; Saruhan-Direskeneli G; Direskeneli H; Sawalha AH
    Arthritis Rheumatol; 2021 Jul; 73(7):1244-1252. PubMed ID: 33393726
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Spontaneous preterm birth: advances toward the discovery of genetic predisposition.
    Strauss JF; Romero R; Gomez-Lopez N; Haymond-Thornburg H; Modi BP; Teves ME; Pearson LN; York TP; Schenkein HA
    Am J Obstet Gynecol; 2018 Mar; 218(3):294-314.e2. PubMed ID: 29248470
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome.
    Sanna-Cherchi S; Burgess KE; Nees SN; Caridi G; Weng PL; Dagnino M; Bodria M; Carrea A; Allegretta MA; Kim HR; Perry BJ; Gigante M; Clark LN; Kisselev S; Cusi D; Gesualdo L; Allegri L; Scolari F; D'Agati V; Shapiro LS; Pecoraro C; Palomero T; Ghiggeri GM; Gharavi AG
    Kidney Int; 2011 Aug; 80(4):389-96. PubMed ID: 21697813
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Association of NOD1, NOD2, PYDC1 and PYDC2 genes with Behcet's disease susceptibility and clinical manifestations.
    Kocaaga A; Cakmak Genc G; Karakas Celık S; Koca R; Dursun A
    Ophthalmic Genet; 2021 Dec; 42(6):691-697. PubMed ID: 34294014
    [No Abstract]   [Full Text] [Related]  

  • 15. PTPN2 rs1893217 single-nucleotide polymorphism is associated with risk of Behçet's disease in a Chinese Han population.
    Wu Z; Chen H; Sun F; Xu J; Zheng W; Li P; Chen S; Shen M; Zhang W; Li M; You X; Wu Q; Zhang F; Li Y
    Clin Exp Rheumatol; 2014; 32(4 Suppl 84):S20-6. PubMed ID: 24480412
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Ubiquitin Associated and SH3 Domain Containing B (UBASH3B) Gene Association with Behcet's Disease in Iranian Population.
    Shahriyari E; Bonyadi M; Jabbarpoor Bonyadi MH; Soheilian M; Yaseri M; Ebrahimiadib N
    Curr Eye Res; 2019 Feb; 44(2):200-205. PubMed ID: 30289285
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project.
    Auer PL; Nalls M; Meschia JF; Worrall BB; Longstreth WT; Seshadri S; Kooperberg C; Burger KM; Carlson CS; Carty CL; Chen WM; Cupples LA; DeStefano AL; Fornage M; Hardy J; Hsu L; Jackson RD; Jarvik GP; Kim DS; Lakshminarayan K; Lange LA; Manichaikul A; Quinlan AR; Singleton AB; Thornton TA; Nickerson DA; Peters U; Rich SS;
    JAMA Neurol; 2015 Jul; 72(7):781-8. PubMed ID: 25961151
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of Rare Variants in ATP8B4 as a Risk Factor for Systemic Sclerosis by Whole-Exome Sequencing.
    Gao L; Emond MJ; Louie T; Cheadle C; Berger AE; Rafaels N; Vergara C; Kim Y; Taub MA; Ruczinski I; Mathai SC; Rich SS; Nickerson DA; Hummers LK; Bamshad MJ; Hassoun PM; Mathias RA; ; Barnes KC
    Arthritis Rheumatol; 2016 Jan; 68(1):191-200. PubMed ID: 26473621
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Behçet's disease and genetic interactions between HLA-B*51 and variants in genes of autoinflammatory syndromes.
    Burillo-Sanz S; Montes-Cano MA; García-Lozano JR; Olivas-Martínez I; Ortego-Centeno N; García-Hernández FJ; Espinosa G; Graña-Gil G; Sánchez-Bursón J; Juliá MR; Solans R; Blanco R; Barnosi-Marín AC; Gómez de la Torre R; Fanlo P; Rodríguez-Carballeira M; Rodríguez-Rodríguez L; Camps T; Castañeda S; Alegre-Sancho JJ; Martín J; González-Escribano MF
    Sci Rep; 2019 Feb; 9(1):2777. PubMed ID: 30808881
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Behçet's disease risk association fine-mapped on the IL23R-IL12RB2 intergenic region in Koreans.
    Kang EH; Kim S; Park MY; Choi JY; Choi IA; Kim MJ; Ha YJ; Lee EY; Lee YJ; Lee EB; Kang C; Song YW
    Arthritis Res Ther; 2017 Oct; 19(1):227. PubMed ID: 29017598
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.