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 *

164 related articles for article (PubMed ID: 38601445)

  • 1. A cross-trait study of lung cancer and its related respiratory diseases based on large-scale exome sequencing population.
    Jiang Y; Li H; Li Z; Du S; Zhang R; Zhao Y; Christiani DC; Shen S; Chen F
    Transl Lung Cancer Res; 2024 Mar; 13(3):512-525. PubMed ID: 38601445
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Shared genetic aetiology of respiratory diseases: a genome-wide multitraits association analysis.
    Chen Z; Gao N; Wang X; Chen X; Zeng Y; Li C; Yang X; Cai Q; Wang X
    BMJ Open Respir Res; 2024 Jun; 11(1):. PubMed ID: 38834332
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Exome Array Analysis Identifies a Common Variant in IL27 Associated with Chronic Obstructive Pulmonary Disease.
    Hobbs BD; Parker MM; Chen H; Lao T; Hardin M; Qiao D; Hawrylkiewicz I; Sliwinski P; Yim JJ; Kim WJ; Kim DK; Castaldi PJ; Hersh CP; Morrow J; Celli BR; Pinto-Plata VM; Criner GJ; Marchetti N; Bueno R; Agustí A; Make BJ; Crapo JD; Calverley PM; Donner CF; Lomas DA; Wouters EF; Vestbo J; Paré PD; Levy RD; Rennard SI; Zhou X; Laird NM; Lin X; Beaty TH; Silverman EK; Cho MH; ; ; ;
    Am J Respir Crit Care Med; 2016 Jul; 194(1):48-57. PubMed ID: 26771213
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic overlap analysis of endometriosis and asthma identifies shared loci implicating sex hormones and thyroid signalling pathways.
    Adewuyi EO; Mehta D; ; ; Nyholt DR
    Hum Reprod; 2022 Jan; 37(2):366-383. PubMed ID: 35472084
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Integrated gene-based and pathway analyses using UK Biobank data identify novel genes for chronic respiratory diseases.
    Wang L; Fang R; Zhu M; Qin N; Wang Y; Fan J; Sun Q; Ji M; Fan X; Xie J; Ma H; Dai J
    Gene; 2021 Jan; 767():145287. PubMed ID: 33181258
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A Large-Scale Exome-Wide Association Study Identifies Novel Germline Mutations in Lung Cancer.
    Shen S; Li Z; Jiang Y; Duan W; Li H; Du S; Esteller M; Shen H; Hu Z; Zhao Y; Christiani DC; Chen F
    Am J Respir Crit Care Med; 2023 Aug; 208(3):280-289. PubMed ID: 37167549
    [No Abstract]   [Full Text] [Related]  

  • 7. A systematic analysis of protein-altering exonic variants in chronic obstructive pulmonary disease.
    Moll M; Jackson VE; Yu B; Grove ML; London SJ; Gharib SA; Bartz TM; Sitlani CM; Dupuis J; O'Connor GT; Xu H; Cassano PA; Patchen BK; Kim WJ; Park J; Kim KH; Han B; Barr RG; Manichaikul A; Nguyen JN; Rich SS; Lahousse L; Terzikhan N; Brusselle G; Sakornsakolpat P; Liu J; Benway CJ; Hall IP; Tobin MD; Wain LV; Silverman EK; Cho MH; Hobbs BD
    Am J Physiol Lung Cell Mol Physiol; 2021 Jul; 321(1):L130-L143. PubMed ID: 33909500
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Extreme Trait Whole-Genome Sequencing Identifies PTPRO as a Novel Candidate Gene in Emphysema with Severe Airflow Obstruction.
    Radder JE; Zhang Y; Gregory AD; Yu S; Kelly NJ; Leader JK; Kaminski N; Sciurba FC; Shapiro SD
    Am J Respir Crit Care Med; 2017 Jul; 196(2):159-171. PubMed ID: 28199135
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Exploring the Common Genetic Underpinnings of Chronic Pulmonary Disease and Esophageal Carcinoma Susceptibility.
    Zhang D; Zhou Y; Lu T; Li J; Zhu L; Li S; Li Y; Duan X
    J Cancer; 2024; 15(11):3406-3417. PubMed ID: 38817868
    [No Abstract]   [Full Text] [Related]  

  • 10. Focused Analysis of Exome Sequencing Data for Rare Germline Mutations in Familial and Sporadic Lung Cancer.
    Liu Y; Kheradmand F; Davis CF; Scheurer ME; Wheeler D; Tsavachidis S; Armstrong G; Simpson C; Mandal D; Kupert E; Anderson M; You M; Xiong D; Pikielny C; Schwartz AG; Bailey-Wilson J; Gaba C; De Andrade M; Yang P; Pinney SM; ; Amos CI; Spitz MR
    J Thorac Oncol; 2016 Jan; 11(1):52-61. PubMed ID: 26762739
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Efficient identification of trait-associated loss-of-function variants in the UK Biobank cohort by exome-sequencing based genotype imputation.
    Yu WY; Yan SS; Zhang SH; Ni JJ; Bin-Li ; Pei YF; Zhang L
    Genet Epidemiol; 2023 Mar; 47(2):121-134. PubMed ID: 36490288
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Targeted high-throughput sequencing of candidate genes for chronic obstructive pulmonary disease.
    Matsson H; Söderhäll C; Einarsdottir E; Lamontagne M; Gudmundsson S; Backman H; Lindberg A; Rönmark E; Kere J; Sin D; Postma DS; Bossé Y; Lundbäck B; Klar J
    BMC Pulm Med; 2016 Nov; 16(1):146. PubMed ID: 27835950
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Common and Rare Variants Genetic Association Analysis of Cigarettes per Day Among Ever-Smokers in Chronic Obstructive Pulmonary Disease Cases and Controls.
    Lutz SM; Frederiksen B; Begum F; McDonald MN; Cho MH; Hobbs BD; Parker MM; DeMeo DL; Hersh CP; Ehringer MA; Young K; Jiang L; Foreman MG; Kinney GL; Make BJ; Lomas DA; Bakke P; Gulsvik A; Crapo JD; Silverman EK; Beaty TH; Hokanson JE;
    Nicotine Tob Res; 2019 May; 21(6):714-722. PubMed ID: 29767774
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank.
    Wain LV; Shrine N; Miller S; Jackson VE; Ntalla I; Soler Artigas M; Billington CK; Kheirallah AK; Allen R; Cook JP; Probert K; Obeidat M; Bossé Y; Hao K; Postma DS; Paré PD; Ramasamy A; ; Mägi R; Mihailov E; Reinmaa E; Melén E; O'Connell J; Frangou E; Delaneau O; ; Freeman C; Petkova D; McCarthy M; Sayers I; Deloukas P; Hubbard R; Pavord I; Hansell AL; Thomson NC; Zeggini E; Morris AP; Marchini J; Strachan DP; Tobin MD; Hall IP
    Lancet Respir Med; 2015 Oct; 3(10):769-81. PubMed ID: 26423011
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Evidence that the pituitary gland connects type 2 diabetes mellitus and schizophrenia based on large-scale trans-ethnic genetic analyses.
    Cai L; Sun Y; Liu Y; Chen W; He L; Wei DQ
    J Transl Med; 2022 Nov; 20(1):501. PubMed ID: 36329495
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A genome wide association study for lung function in the Korean population using an exome array.
    Lee KS; Kim KH; Oh YM; Han B; Kim WJ
    Korean J Intern Med; 2021 Mar; 36(Suppl 1):S142-S150. PubMed ID: 32336055
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Exome sequencing and analysis of 454,787 UK Biobank participants.
    Backman JD; Li AH; Marcketta A; Sun D; Mbatchou J; Kessler MD; Benner C; Liu D; Locke AE; Balasubramanian S; Yadav A; Banerjee N; Gillies CE; Damask A; Liu S; Bai X; Hawes A; Maxwell E; Gurski L; Watanabe K; Kosmicki JA; Rajagopal V; Mighty J; ; ; Jones M; Mitnaul L; Stahl E; Coppola G; Jorgenson E; Habegger L; Salerno WJ; Shuldiner AR; Lotta LA; Overton JD; Cantor MN; Reid JG; Yancopoulos G; Kang HM; Marchini J; Baras A; Abecasis GR; Ferreira MAR
    Nature; 2021 Nov; 599(7886):628-634. PubMed ID: 34662886
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mortality and Morbidity Effects of Long-Term Exposure to Low-Level PM
    Brunekreef B; Strak M; Chen J; Andersen ZJ; Atkinson R; Bauwelinck M; Bellander T; Boutron MC; Brandt J; Carey I; Cesaroni G; Forastiere F; Fecht D; Gulliver J; Hertel O; Hoffmann B; de Hoogh K; Houthuijs D; Hvidtfeldt U; Janssen N; Jorgensen J; Katsouyanni K; Ketzel M; Klompmaker J; Hjertager Krog N; Liu S; Ljungman P; Mehta A; Nagel G; Oftedal B; Pershagen G; Peters A; Raaschou-Nielsen O; Renzi M; Rodopoulou S; Samoli E; Schwarze P; Sigsgaard T; Stafoggia M; Vienneau D; Weinmayr G; Wolf K; Hoek G
    Res Rep Health Eff Inst; 2021 Sep; 2021(208):1-127. PubMed ID: 36106702
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Whole-Genome Sequencing in Severe Chronic Obstructive Pulmonary Disease.
    Prokopenko D; Sakornsakolpat P; Fier HL; Qiao D; Parker MM; McDonald MN; Manichaikul A; Rich SS; Barr RG; Williams CJ; Brantly ML; Lange C; Beaty TH; Crapo JD; Silverman EK; Cho MH
    Am J Respir Cell Mol Biol; 2018 Nov; 59(5):614-622. PubMed ID: 29949718
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.