BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

507 related articles for article (PubMed ID: 28099038)

  • 1. An Exome Sequencing Study to Assess the Role of Rare Genetic Variation in Pulmonary Fibrosis.
    Petrovski S; Todd JL; Durheim MT; Wang Q; Chien JW; Kelly FL; Frankel C; Mebane CM; Ren Z; Bridgers J; Urban TJ; Malone CD; Finlen Copeland A; Brinkley C; Allen AS; O'Riordan T; McHutchison JG; Palmer SM; Goldstein DB
    Am J Respir Crit Care Med; 2017 Jul; 196(1):82-93. PubMed ID: 28099038
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Analysis of protein-altering variants in telomerase genes and their association with MUC5B common variant status in patients with idiopathic pulmonary fibrosis: a candidate gene sequencing study.
    Dressen A; Abbas AR; Cabanski C; Reeder J; Ramalingam TR; Neighbors M; Bhangale TR; Brauer MJ; Hunkapiller J; Reeder J; Mukhyala K; Cuenco K; Tom J; Cowgill A; Vogel J; Forrest WF; Collard HR; Wolters PJ; Kropski JA; Lancaster LH; Blackwell TS; Arron JR; Yaspan BL
    Lancet Respir Med; 2018 Aug; 6(8):603-614. PubMed ID: 29891356
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening.
    Stuart BD; Choi J; Zaidi S; Xing C; Holohan B; Chen R; Choi M; Dharwadkar P; Torres F; Girod CE; Weissler J; Fitzgerald J; Kershaw C; Klesney-Tait J; Mageto Y; Shay JW; Ji W; Bilguvar K; Mane S; Lifton RP; Garcia CK
    Nat Genet; 2015 May; 47(5):512-7. PubMed ID: 25848748
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Rare and Common Variants in
    Zhang D; Povysil G; Kobeissy PH; Li Q; Wang B; Amelotte M; Jaouadi H; Newton CA; Maher TM; Molyneaux PL; Noth I; Martinez FJ; Raghu G; Todd JL; Palmer SM; Haefliger C; Platt A; Petrovski S; Garcia JA; Goldstein DB; Garcia CK
    Am J Respir Crit Care Med; 2022 Jul; 206(1):56-69. PubMed ID: 35417304
    [No Abstract]   [Full Text] [Related]  

  • 5. Idiopathic Pulmonary Fibrosis Is Associated with Common Genetic Variants and Limited Rare Variants.
    Peljto AL; Blumhagen RZ; Walts AD; Cardwell J; Powers J; Corte TJ; Dickinson JL; Glaspole I; Moodley YP; Vasakova MK; Bendstrup E; Davidsen JR; Borie R; Crestani B; Dieude P; Bonella F; Costabel U; Gudmundsson G; Donnelly SC; Egan J; Henry MT; Keane MP; Kennedy MP; McCarthy C; McElroy AN; Olaniyi JA; O'Reilly KMA; Richeldi L; Leone PM; Poletti V; Puppo F; Tomassetti S; Luzzi V; Kokturk N; Mogulkoc N; Fiddler CA; Hirani N; Jenkins RG; Maher TM; Molyneaux PL; Parfrey H; Braybrooke R; Blackwell TS; Jackson PD; Nathan SD; Porteous MK; Brown KK; Christie JD; Collard HR; Eickelberg O; Foster EE; Gibson KF; Glassberg M; Kass DJ; Kropski JA; Lederer D; Linderholm AL; Loyd J; Mathai SK; Montesi SB; Noth I; Oldham JM; Palmisciano AJ; Reichner CA; Rojas M; Roman J; Schluger N; Shea BS; Swigris JJ; Wolters PJ; Zhang Y; Prele CMA; Enghelmayer JI; Otaola M; Ryerson CJ; Salinas M; Sterclova M; Gebremariam TH; Myllärniemi M; Carbone RG; Furusawa H; Hirose M; Inoue Y; Miyazaki Y; Ohta K; Ohta S; Okamoto T; Kim DS; Pardo A; Selman M; Aranda AU; Park MS; Park JS; Song JW; Molina-Molina M; Planas-Cerezales L; Westergren-Thorsson G; Smith AV; Manichaikul AW; Kim JS; Rich SS; Oelsner EC; Barr RG; Rotter JI; Dupuis J; O'Connor G; Vasan RS; Cho MH; Silverman EK; Schwarz MI; Steele MP; Lee JS; Yang IV; Fingerlin TE; Schwartz DA
    Am J Respir Crit Care Med; 2023 May; 207(9):1194-1202. PubMed ID: 36602845
    [No Abstract]   [Full Text] [Related]  

  • 6. Resequencing Study Confirms That Host Defense and Cell Senescence Gene Variants Contribute to the Risk of Idiopathic Pulmonary Fibrosis.
    Moore C; Blumhagen RZ; Yang IV; Walts A; Powers J; Walker T; Bishop M; Russell P; Vestal B; Cardwell J; Markin CR; Mathai SK; Schwarz MI; Steele MP; Lee J; Brown KK; Loyd JE; Crapo JD; Silverman EK; Cho MH; James JA; Guthridge JM; Cogan JD; Kropski JA; Swigris JJ; Bair C; Kim DS; Ji W; Kim H; Song JW; Maier LA; Pacheco KA; Hirani N; Poon AS; Li F; Jenkins RG; Braybrooke R; Saini G; Maher TM; Molyneaux PL; Saunders P; Zhang Y; Gibson KF; Kass DJ; Rojas M; Sembrat J; Wolters PJ; Collard HR; Sundy JS; O'Riordan T; Strek ME; Noth I; Ma SF; Porteous MK; Kreider ME; Patel NB; Inoue Y; Hirose M; Arai T; Akagawa S; Eickelberg O; Fernandez IE; Behr J; Mogulkoc N; Corte TJ; Glaspole I; Tomassetti S; Ravaglia C; Poletti V; Crestani B; Borie R; Kannengiesser C; Parfrey H; Fiddler C; Rassl D; Molina-Molina M; Machahua C; Worboys AM; Gudmundsson G; Isaksson HJ; Lederer DJ; Podolanczuk AJ; Montesi SB; Bendstrup E; Danchel V; Selman M; Pardo A; Henry MT; Keane MP; Doran P; Vašáková M; Sterclova M; Ryerson CJ; Wilcox PG; Okamoto T; Furusawa H; Miyazaki Y; Laurent G; Baltic S; Prele C; Moodley Y; Shea BS; Ohta K; Suzukawa M; Narumoto O; Nathan SD; Venuto DC; Woldehanna ML; Kokturk N; de Andrade JA; Luckhardt T; Kulkarni T; Bonella F; Donnelly SC; McElroy A; Armstong ME; Aranda A; Carbone RG; Puppo F; Beckman KB; Nickerson DA; Fingerlin TE; Schwartz DA
    Am J Respir Crit Care Med; 2019 Jul; 200(2):199-208. PubMed ID: 31034279
    [No Abstract]   [Full Text] [Related]  

  • 7. Pulmonary fibrosis in the era of stratified medicine.
    Mathai SK; Newton CA; Schwartz DA; Garcia CK
    Thorax; 2016 Dec; 71(12):1154-1160. PubMed ID: 27799632
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A Rare Missense Variant in Telomerase Reverse Transcriptase is Associated with Idiopathic Pulmonary Fibrosis in a Chinese Han Family.
    Zheng CM; Zhan X; Yang YH; Jiang T; Ye Q; Lu Y
    Chin Med J (Engl); 2018 Sep; 131(18):2205-2209. PubMed ID: 30203795
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study.
    Noth I; Zhang Y; Ma SF; Flores C; Barber M; Huang Y; Broderick SM; Wade MS; Hysi P; Scuirba J; Richards TJ; Juan-Guardela BM; Vij R; Han MK; Martinez FJ; Kossen K; Seiwert SD; Christie JD; Nicolae D; Kaminski N; Garcia JGN
    Lancet Respir Med; 2013 Jun; 1(4):309-317. PubMed ID: 24429156
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Heterozygous RTEL1 mutations are associated with familial pulmonary fibrosis.
    Kannengiesser C; Borie R; Ménard C; Réocreux M; Nitschké P; Gazal S; Mal H; Taillé C; Cadranel J; Nunes H; Valeyre D; Cordier JF; Callebaut I; Boileau C; Cottin V; Grandchamp B; Revy P; Crestani B
    Eur Respir J; 2015 Aug; 46(2):474-85. PubMed ID: 26022962
    [TBL] [Abstract][Full Text] [Related]  

  • 11. From organ to cell: Multi-level telomere length assessment in patients with idiopathic pulmonary fibrosis.
    van Batenburg AA; Kazemier KM; van Oosterhout MFM; van der Vis JJ; van Es HW; Grutters JC; Goldschmeding R; van Moorsel CHM
    PLoS One; 2020; 15(1):e0226785. PubMed ID: 31910222
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Lung Transplant Outcomes in Patients With Pulmonary Fibrosis With Telomere-Related Gene Variants.
    Swaminathan AC; Neely ML; Frankel CW; Kelly FL; Petrovski S; Durheim MT; Bush E; Snyder L; Goldstein DB; Todd JL; Palmer SM
    Chest; 2019 Sep; 156(3):477-485. PubMed ID: 30978332
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Shared genetic predisposition in rheumatoid arthritis-interstitial lung disease and familial pulmonary fibrosis.
    Juge PA; Borie R; Kannengiesser C; Gazal S; Revy P; Wemeau-Stervinou L; Debray MP; Ottaviani S; Marchand-Adam S; Nathan N; Thabut G; Richez C; Nunes H; Callebaut I; Justet A; Leulliot N; Bonnefond A; Salgado D; Richette P; Desvignes JP; Lioté H; Froguel P; Allanore Y; Sand O; Dromer C; Flipo RM; Clément A; Béroud C; Sibilia J; Coustet B; Cottin V; Boissier MC; Wallaert B; Schaeverbeke T; Dastot le Moal F; Frazier A; Ménard C; Soubrier M; Saidenberg N; Valeyre D; Amselem S; ; Boileau C; Crestani B; Dieudé P
    Eur Respir J; 2017 May; 49(5):. PubMed ID: 28495692
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Rare variants in RTEL1 are associated with familial interstitial pneumonia.
    Cogan JD; Kropski JA; Zhao M; Mitchell DB; Rives L; Markin C; Garnett ET; Montgomery KH; Mason WR; McKean DF; Powers J; Murphy E; Olson LM; Choi L; Cheng DS; Blue EM; Young LR; Lancaster LH; Steele MP; Brown KK; Schwarz MI; Fingerlin TE; Schwartz DA; Lawson WE; Loyd JE; Zhao Z; Phillips JA; Blackwell TS
    Am J Respir Crit Care Med; 2015 Mar; 191(6):646-55. PubMed ID: 25607374
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Telomere-related lung fibrosis is diagnostically heterogeneous but uniformly progressive.
    Newton CA; Batra K; Torrealba J; Kozlitina J; Glazer CS; Aravena C; Meyer K; Raghu G; Collard HR; Garcia CK
    Eur Respir J; 2016 Dec; 48(6):1710-1720. PubMed ID: 27540018
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Whole-exome sequencing identifies susceptibility genes and pathways for idiopathic pulmonary fibrosis in the Chinese population.
    Fang C; Huang H; Feng Y; Zhang Q; Wang N; Jing X; Guo J; Ferianc M; Xu Z
    Sci Rep; 2021 Jan; 11(1):1443. PubMed ID: 33446833
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A Newfoundland cohort of familial and sporadic idiopathic pulmonary fibrosis patients: clinical and genetic features.
    Fernandez BA; Fox G; Bhatia R; Sala E; Noble B; Denic N; Fernandez D; Duguid N; Dohey A; Kamel F; Edwards L; Mahoney K; Stuckless S; Parfrey PS; Woods MO
    Respir Res; 2012 Aug; 13(1):64. PubMed ID: 22853774
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The genetic basis of idiopathic pulmonary fibrosis.
    Kropski JA; Blackwell TS; Loyd JE
    Eur Respir J; 2015 Jun; 45(6):1717-27. PubMed ID: 25837031
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Desmoplakin Variants Are Associated with Idiopathic Pulmonary Fibrosis.
    Mathai SK; Pedersen BS; Smith K; Russell P; Schwarz MI; Brown KK; Steele MP; Loyd JE; Crapo JD; Silverman EK; Nickerson D; Fingerlin TE; Yang IV; Schwartz DA
    Am J Respir Crit Care Med; 2016 May; 193(10):1151-60. PubMed ID: 26669357
    [TBL] [Abstract][Full Text] [Related]  

  • 20. MMP19 Variants in Familial and Sporadic Idiopathic Pulmonary Fibrosis.
    Fan Y; Zheng C; Ma R; Wang J; Yang S; Ye Q
    Lung; 2023 Dec; 201(6):571-580. PubMed ID: 37971547
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 26.