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 *

180 related articles for article (PubMed ID: 28512778)

  • 1. CAGI4 Crohn's exome challenge: Marker SNP versus exome variant models for assigning risk of Crohn disease.
    Pal LR; Kundu K; Yin Y; Moult J
    Hum Mutat; 2017 Sep; 38(9):1225-1234. PubMed ID: 28512778
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Working toward precision medicine: Predicting phenotypes from exomes in the Critical Assessment of Genome Interpretation (CAGI) challenges.
    Daneshjou R; Wang Y; Bromberg Y; Bovo S; Martelli PL; Babbi G; Lena PD; Casadio R; Edwards M; Gifford D; Jones DT; Sundaram L; Bhat RR; Li X; Pal LR; Kundu K; Yin Y; Moult J; Jiang Y; Pejaver V; Pagel KA; Li B; Mooney SD; Radivojac P; Shah S; Carraro M; Gasparini A; Leonardi E; Giollo M; Ferrari C; Tosatto SCE; Bachar E; Azaria JR; Ofran Y; Unger R; Niroula A; Vihinen M; Chang B; Wang MH; Franke A; Petersen BS; Pirooznia M; Zandi P; McCombie R; Potash JB; Altman RB; Klein TE; Hoskins RA; Repo S; Brenner SE; Morgan AA
    Hum Mutat; 2017 Sep; 38(9):1182-1192. PubMed ID: 28634997
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Crohn disease risk prediction-Best practices and pitfalls with exome data.
    Giollo M; Jones DT; Carraro M; Leonardi E; Ferrari C; Tosatto SCE
    Hum Mutat; 2017 Sep; 38(9):1193-1200. PubMed ID: 28087895
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identifying Crohn's disease signal from variome analysis.
    Wang Y; Miller M; Astrakhan Y; Petersen BS; Schreiber S; Franke A; Bromberg Y
    Genome Med; 2019 Sep; 11(1):59. PubMed ID: 31564248
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Performance of risk prediction for inflammatory bowel disease based on genotyping platform and genomic risk score method.
    Chen GB; Lee SH; Montgomery GW; Wray NR; Visscher PM; Gearry RB; Lawrance IC; Andrews JM; Bampton P; Mahy G; Bell S; Walsh A; Connor S; Sparrow M; Bowdler LM; Simms LA; Krishnaprasad K; ; Radford-Smith GL; Moser G
    BMC Med Genet; 2017 Aug; 18(1):94. PubMed ID: 28851283
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Multivariate genome-wide association study models to improve prediction of Crohn's disease risk and identification of potential novel variants.
    Garza-Hernandez D; Estrada K; Trevino V
    Comput Biol Med; 2022 Jun; 145():105398. PubMed ID: 35306380
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Improved risk prediction for Crohn's disease with a multi-locus approach.
    Kang J; Kugathasan S; Georges M; Zhao H; Cho JH;
    Hum Mol Genet; 2011 Jun; 20(12):2435-42. PubMed ID: 21427131
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The Unsolved Link of Genetic Markers and Crohn's Disease Progression: A North American Cohort Experience.
    O'Donnell S; Borowski K; Espin-Garcia O; Milgrom R; Kabakchiev B; Stempak J; Panikkath D; Eksteen B; Xu W; Steinhart AH; Kaplan GG; McGovern DPB; Silverberg MS
    Inflamm Bowel Dis; 2019 Aug; 25(9):1541-1549. PubMed ID: 30801121
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Detecting identity by descent and homozygosity mapping in whole-exome sequencing data.
    Zhuang Z; Gusev A; Cho J; Pe'er I
    PLoS One; 2012; 7(10):e47618. PubMed ID: 23071825
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Inferring Crohn's disease association from exome sequences by integrating biological knowledge.
    Jeong CS; Kim D
    BMC Med Genomics; 2016 Aug; 9 Suppl 1(Suppl 1):35. PubMed ID: 27535358
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Exome sequence analysis identifies rare coding variants associated with a machine learning-based marker for coronary artery disease.
    Petrazzini BO; Forrest IS; Rocheleau G; Vy HMT; Márquez-Luna C; Duffy Á; Chen R; Park JK; Gibson K; Goonewardena SN; Malick WA; Rosenson RS; Jordan DM; Do R
    Nat Genet; 2024 Jul; 56(7):1412-1419. PubMed ID: 38862854
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Predicting venous thromboembolism risk from exomes in the Critical Assessment of Genome Interpretation (CAGI) challenges.
    McInnes G; Daneshjou R; Katsonis P; Lichtarge O; Srinivasan R; Rana S; Radivojac P; Mooney SD; Pagel KA; Stamboulian M; Jiang Y; Capriotti E; Wang Y; Bromberg Y; Bovo S; Savojardo C; Martelli PL; Casadio R; Pal LR; Moult J; Brenner SE; Altman R
    Hum Mutat; 2019 Sep; 40(9):1314-1320. PubMed ID: 31140652
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic Complexity of Crohn's Disease in Two Large Ashkenazi Jewish Families.
    Levine AP; Pontikos N; Schiff ER; Jostins L; Speed D; ; Lovat LB; Barrett JC; Grasberger H; Plagnol V; Segal AW
    Gastroenterology; 2016 Oct; 151(4):698-709. PubMed ID: 27373512
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Whole genome and exome sequencing of monozygotic twins discordant for Crohn's disease.
    Petersen BS; Spehlmann ME; Raedler A; Stade B; Thomsen I; Rabionet R; Rosenstiel P; Schreiber S; Franke A
    BMC Genomics; 2014 Jul; 15(1):564. PubMed ID: 24996980
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data.
    Romagnoni A; Jégou S; Van Steen K; Wainrib G; Hugot JP;
    Sci Rep; 2019 Jul; 9(1):10351. PubMed ID: 31316157
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Determination of disease phenotypes and pathogenic variants from exome sequence data in the CAGI 4 gene panel challenge.
    Kundu K; Pal LR; Yin Y; Moult J
    Hum Mutat; 2017 Sep; 38(9):1201-1216. PubMed ID: 28497567
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations.
    Yang SK; Hong M; Zhao W; Jung Y; Baek J; Tayebi N; Kim KM; Ye BD; Kim KJ; Park SH; Lee I; Lee EJ; Kim WH; Cheon JH; Kim YH; Jang BI; Kim HS; Choi JH; Koo JS; Lee JH; Jung SA; Lee YJ; Jang JY; Shin HD; Kang D; Youn HS; Liu J; Song K
    Gut; 2014 Jan; 63(1):80-7. PubMed ID: 23850713
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Exome sequencing identifies DLG1 as a novel gene for potential susceptibility to Crohn's disease in a Chinese family study.
    Xu S; Zhou F; Tao J; Song L; Ng SC; Wang X; Chen L; Yi F; Ran Z; Zhou R; Xia B
    PLoS One; 2014; 9(6):e99807. PubMed ID: 24937328
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The role of genetics in Crohn's disease: how could it influence future therapies?
    Geremia A; Satsangi J
    Expert Rev Gastroenterol Hepatol; 2018 Nov; 12(11):1075-1077. PubMed ID: 30124365
    [No Abstract]   [Full Text] [Related]  

  • 20. Identification of risk loci for Crohn's disease phenotypes using a genome-wide association study.
    Alonso A; Domènech E; Julià A; Panés J; García-Sánchez V; Mateu PN; Gutiérrez A; Gomollón F; Mendoza JL; Garcia-Planella E; Barreiro-de Acosta M; Muñoz F; Vera M; Saro C; Esteve M; Andreu M; Chaparro M; Manyé J; Cabré E; López-Lasanta M; Tortosa R; Gelpí JL; García-Montero AC; Bertranpetit J; Absher D; Myers RM; Marsal S; Gisbert JP
    Gastroenterology; 2015 Apr; 148(4):794-805. PubMed ID: 25557950
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.