BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

198 related articles for article (PubMed ID: 36810956)

  • 21. Glioma risk associated with extent of estimated European genetic ancestry in African Americans and Hispanics.
    Ostrom QT; Egan KM; Nabors LB; Gerke T; Thompson RC; Olson JJ; LaRocca R; Chowdhary S; Eckel-Passow JE; Armstrong G; Wiencke JK; Bernstein JL; Claus EB; Il'yasova D; Johansen C; Lachance DH; Lai RK; Merrell RT; Olson SH; Sadetzki S; Schildkraut JM; Shete S; Houlston RS; Jenkins RB; Wrensch MR; Melin B; Amos CI; Huse JT; Barnholtz-Sloan JS; Bondy ML
    Int J Cancer; 2020 Feb; 146(3):739-748. PubMed ID: 30963577
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Association of CDKN2A/CDKN2B with inflammatory bowel disease in Koreans.
    Lee HS; Lee SB; Kim BM; Hong M; Jung S; Hong J; Baek J; Han B; Oh SH; Kim KM; Park SH; Yang SK; Ye BD; Song K
    J Gastroenterol Hepatol; 2018 Apr; 33(4):887-893. PubMed ID: 29063720
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Local genetic ancestry in CDKN2B-AS1 is associated with primary open-angle glaucoma in an African American cohort extracted from de-identified electronic health records.
    Restrepo NA; Laper SM; Farber-Eger E; Crawford DC
    BMC Med Genomics; 2018 Sep; 11(Suppl 3):70. PubMed ID: 30255811
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Ancestry and frequency of genetic variants in the general population are confounders in the characterization of germline variants linked to cancer.
    Bobyn A; Zarrei M; Zhu Y; Hoffman M; Brenner D; Resnick AC; Scherer SW; Gallo M
    BMC Med Genet; 2020 May; 21(1):92. PubMed ID: 32375678
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Genome-wide association study of glioma and meta-analysis.
    Rajaraman P; Melin BS; Wang Z; McKean-Cowdin R; Michaud DS; Wang SS; Bondy M; Houlston R; Jenkins RB; Wrensch M; Yeager M; Ahlbom A; Albanes D; Andersson U; Freeman LE; Buring JE; Butler MA; Braganza M; Carreon T; Feychting M; Fleming SJ; Gapstur SM; Gaziano JM; Giles GG; Hallmans G; Henriksson R; Hoffman-Bolton J; Inskip PD; Johansen C; Kitahara CM; Lathrop M; Liu C; Le Marchand L; Linet MS; Lonn S; Peters U; Purdue MP; Rothman N; Ruder AM; Sanson M; Sesso HD; Severi G; Shu XO; Simon M; Stampfer M; Stevens VL; Visvanathan K; White E; Wolk A; Zeleniuch-Jacquotte A; Zheng W; Decker P; Enciso-Mora V; Fridley B; Gao YT; Kosel M; Lachance DH; Lau C; Rice T; Swerdlow A; Wiemels JL; Wiencke JK; Shete S; Xiang YB; Xiao Y; Hoover RN; Fraumeni JF; Chatterjee N; Hartge P; Chanock SJ
    Hum Genet; 2012 Dec; 131(12):1877-88. PubMed ID: 22886559
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Utilizing the Dog Genome in the Search for Novel Candidate Genes Involved in Glioma Development-Genome Wide Association Mapping followed by Targeted Massive Parallel Sequencing Identifies a Strongly Associated Locus.
    Truvé K; Dickinson P; Xiong A; York D; Jayashankar K; Pielberg G; Koltookian M; Murén E; Fuxelius HH; Weishaupt H; Swartling FJ; Andersson G; Hedhammar Å; Bongcam-Rudloff E; Forsberg-Nilsson K; Bannasch D; Lindblad-Toh K
    PLoS Genet; 2016 May; 12(5):e1006000. PubMed ID: 27171399
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Polymorphisms in the long non-coding RNA CDKN2B-AS1 may contribute to higher systolic blood pressure levels in hypertensive patients.
    Bayoglu B; Yuksel H; Cakmak HA; Dirican A; Cengiz M
    Clin Biochem; 2016 Jul; 49(10-11):821-7. PubMed ID: 26944720
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Chromosome 9p21 primary open-angle glaucoma susceptibility locus: a review.
    Ng SK; Casson RJ; Burdon KP; Craig JE
    Clin Exp Ophthalmol; 2014; 42(1):25-32. PubMed ID: 24112133
    [TBL] [Abstract][Full Text] [Related]  

  • 29. DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma.
    Burdon KP; Awadalla MS; Mitchell P; Wang JJ; White A; Keane MC; Souzeau E; Graham SL; Goldberg I; Healey PR; Landers J; Mills RAD; Best S; Hewitt AW; Sharma S; Craig JE
    Ophthalmic Genet; 2018 Apr; 39(2):221-227. PubMed ID: 29265947
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Meta-Analysis of Genome-Wide Association Studies Identifies Genetic Risk Factors for Stroke in African Americans.
    Carty CL; Keene KL; Cheng YC; Meschia JF; Chen WM; Nalls M; Bis JC; Kittner SJ; Rich SS; Tajuddin S; Zonderman AB; Evans MK; Langefeld CD; Gottesman R; Mosley TH; Shahar E; Woo D; Yaffe K; Liu Y; Sale MM; Dichgans M; Malik R; Longstreth WT; Mitchell BD; Psaty BM; Kooperberg C; Reiner A; Worrall BB; Fornage M;
    Stroke; 2015 Aug; 46(8):2063-8. PubMed ID: 26089329
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genomic predictors of combat stress vulnerability and resilience in U.S. Marines: A genome-wide association study across multiple ancestries implicates PRTFDC1 as a potential PTSD gene.
    Nievergelt CM; Maihofer AX; Mustapic M; Yurgil KA; Schork NJ; Miller MW; Logue MW; Geyer MA; Risbrough VB; O'Connor DT; Baker DG
    Psychoneuroendocrinology; 2015 Jan; 51():459-71. PubMed ID: 25456346
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Genome-wide admixture and association analysis identifies African ancestry-specific risk loci of eosinophilic esophagitis in African Americans.
    Gautam Y; Caldwell J; Kottyan L; Chehade M; Dellon ES; Rothenberg ME; Mersha TB;
    J Allergy Clin Immunol; 2023 May; 151(5):1337-1350. PubMed ID: 36400179
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A variant on chromosome 2p13.3 is associated with atopic dermatitis in Chinese Han population.
    Cai XY; Zheng XD; Fang L; Zhou FS; Sheng YJ; Wu YY; Yu CX; Zhu J; Xiao FL
    Gene; 2017 Sep; 628():281-285. PubMed ID: 28739399
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Investigation of CAV1/CAV2 rs4236601 and CDKN2B-AS1 rs2157719 in primary open-angle glaucoma patients from Brazil.
    Nunes HF; Ananina G; Costa VP; Zanchin NIT; de Vasconcellos JPC; de Melo MB
    Ophthalmic Genet; 2018 Apr; 39(2):194-199. PubMed ID: 29111846
    [TBL] [Abstract][Full Text] [Related]  

  • 35. New findings in the roles of Cyclin-dependent Kinase inhibitors 2B Antisense RNA 1 (
    Yuan W; Zhang W; Zhang W; Ruan ZB; Zhu L; Liu Y; Mi YY; Zhang LF
    Bioengineered; 2020 Dec; 11(1):1084-1098. PubMed ID: 33054494
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Asian-specific 3'UTR variant in CDKN2B associated with risk of pituitary adenoma.
    Youn BJ; Cheong HS; Namgoong S; Kim LH; Baek IK; Kim JH; Yoon SJ; Kim EH; Kim SH; Chang JH; Kim SH; Shin HD
    Mol Biol Rep; 2022 Nov; 49(11):10339-10346. PubMed ID: 36097105
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Genome-wide association study across pediatric central nervous system tumors implicates shared predisposition and points to 1q25.2 (PAPPA2) and 11p12 (LRRC4C) as novel candidate susceptibility loci.
    Foss-Skiftesvik J; Hagen CM; Mathiasen R; Adamsen D; Bækvad-Hansen M; Børglum AD; Nordentoft M; Werge T; Christiansen M; Schmiegelow K; Juhler M; Mortensen PB; Hougaard DM; Bybjerg-Grauholm J
    Childs Nerv Syst; 2021 Mar; 37(3):819-830. PubMed ID: 33226468
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome.
    Lahrouchi N; Tadros R; Crotti L; Mizusawa Y; Postema PG; Beekman L; Walsh R; Hasegawa K; Barc J; Ernsting M; Turkowski KL; Mazzanti A; Beckmann BM; Shimamoto K; Diamant UB; Wijeyeratne YD; Kucho Y; Robyns T; Ishikawa T; Arbelo E; Christiansen M; Winbo A; Jabbari R; Lubitz SA; Steinfurt J; Rudic B; Loeys B; Shoemaker MB; Weeke PE; Pfeiffer R; Davies B; Andorin A; Hofman N; Dagradi F; Pedrazzini M; Tester DJ; Bos JM; Sarquella-Brugada G; Campuzano Ó; Platonov PG; Stallmeyer B; Zumhagen S; Nannenberg EA; Veldink JH; van den Berg LH; Al-Chalabi A; Shaw CE; Shaw PJ; Morrison KE; Andersen PM; Müller-Nurasyid M; Cusi D; Barlassina C; Galan P; Lathrop M; Munter M; Werge T; Ribasés M; Aung T; Khor CC; Ozaki M; Lichtner P; Meitinger T; van Tintelen JP; Hoedemaekers Y; Denjoy I; Leenhardt A; Napolitano C; Shimizu W; Schott JJ; Gourraud JB; Makiyama T; Ohno S; Itoh H; Krahn AD; Antzelevitch C; Roden DM; Saenen J; Borggrefe M; Odening KE; Ellinor PT; Tfelt-Hansen J; Skinner JR; van den Berg MP; Olesen MS; Brugada J; Brugada R; Makita N; Breckpot J; Yoshinaga M; Behr ER; Rydberg A; Aiba T; Kääb S; Priori SG; Guicheney P; Tan HL; Newton-Cheh C; Ackerman MJ; Schwartz PJ; Schulze-Bahr E; Probst V; Horie M; Wilde AA; Tanck MWT; Bezzina CR
    Circulation; 2020 Jul; 142(4):324-338. PubMed ID: 32429735
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genome-wide association study identifies TNFSF15 associated with childhood asthma.
    Kim KW; Kim DY; Yoon D; Kim KK; Jang H; Schoettler N; Kim EG; Kim MN; Hong JY; Lee JK; Kim S; Ober C; Gee HY; Sohn MH
    Allergy; 2022 Jan; 77(1):218-229. PubMed ID: 34022066
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors.
    Melin BS; Barnholtz-Sloan JS; Wrensch MR; Johansen C; Il'yasova D; Kinnersley B; Ostrom QT; Labreche K; Chen Y; Armstrong G; Liu Y; Eckel-Passow JE; Decker PA; Labussière M; Idbaih A; Hoang-Xuan K; Di Stefano AL; Mokhtari K; Delattre JY; Broderick P; Galan P; Gousias K; Schramm J; Schoemaker MJ; Fleming SJ; Herms S; Heilmann S; Nöthen MM; Wichmann HE; Schreiber S; Swerdlow A; Lathrop M; Simon M; Sanson M; Andersson U; Rajaraman P; Chanock S; Linet M; Wang Z; Yeager M; ; Wiencke JK; Hansen H; McCoy L; Rice T; Kosel ML; Sicotte H; Amos CI; Bernstein JL; Davis F; Lachance D; Lau C; Merrell RT; Shildkraut J; Ali-Osman F; Sadetzki S; Scheurer M; Shete S; Lai RK; Claus EB; Olson SH; Jenkins RB; Houlston RS; Bondy ML
    Nat Genet; 2017 May; 49(5):789-794. PubMed ID: 28346443
    [TBL] [Abstract][Full Text] [Related]  

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