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 *

109 related articles for article (PubMed ID: 30346245)

  • 1. Interpretation of the noncoding genome in medicine.
    Iulio JD
    Per Med; 2018 Nov; 15(6):453-455. PubMed ID: 30346245
    [No Abstract]   [Full Text] [Related]  

  • 2. Genome Sequencing and RNA-Motif Analysis Reveal Novel Damaging Noncoding Mutations in Human Tumors.
    Singh B; Trincado JL; Tatlow PJ; Piccolo SR; Eyras E
    Mol Cancer Res; 2018 Jul; 16(7):1112-1124. PubMed ID: 29592900
    [TBL] [Abstract][Full Text] [Related]  

  • 3. CRISPR Screens to Discover Functional Noncoding Elements.
    Wright JB; Sanjana NE
    Trends Genet; 2016 Sep; 32(9):526-529. PubMed ID: 27423542
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Widely distributed noncoding purifying selection in the human genome.
    Asthana S; Noble WS; Kryukov G; Grant CE; Sunyaev S; Stamatoyannopoulos JA
    Proc Natl Acad Sci U S A; 2007 Jul; 104(30):12410-5. PubMed ID: 17640883
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Conserved tissue expression signatures of intronic noncoding RNAs transcribed from human and mouse loci.
    Louro R; El-Jundi T; Nakaya HI; Reis EM; Verjovski-Almeida S
    Genomics; 2008 Jul; 92(1):18-25. PubMed ID: 18495418
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Statement on bioinformatics and capturing the benefits of genome sequencing for society.
    Capps B; Chadwick R; Joly Y; Lysaght T; Mills C; Mulvihill JJ; Zwart H
    Hum Genomics; 2019 May; 13(1):24. PubMed ID: 31142362
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Human genome variation in health and in neuropsychiatric disorders.
    Buretić-Tomljanović A; Tomljanović D
    Psychiatr Danub; 2009 Dec; 21(4):562-9. PubMed ID: 19935494
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Systematic analysis of cis-nested gene pairs in the human genome].
    Tuju CL; Lü GT; Zeng CQ
    Yi Chuan; 2010 Sep; 32(9):914-20. PubMed ID: 20870612
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The Case of "Missing Causal Genes" and the Practice of Medicine: A Sherlock Holmes Approach of Deductive Reasoning.
    Marian AJ
    Circ Res; 2016 Jun; 119(1):21-4. PubMed ID: 27340268
    [No Abstract]   [Full Text] [Related]  

  • 10. Portals for Exploring Noncoding Variants in Pediatric Cancer.
    Creighton CJ
    Trends Genet; 2021 Apr; 37(4):297-298. PubMed ID: 33494957
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The Kipoi repository accelerates community exchange and reuse of predictive models for genomics.
    Avsec Ž; Kreuzhuber R; Israeli J; Xu N; Cheng J; Shrikumar A; Banerjee A; Kim DS; Beier T; Urban L; Kundaje A; Stegle O; Gagneur J
    Nat Biotechnol; 2019 Jun; 37(6):592-600. PubMed ID: 31138913
    [No Abstract]   [Full Text] [Related]  

  • 12. A complete human genome sequence is close: how scientists filled in the gaps.
    Reardon S
    Nature; 2021 Jun; 594(7862):158-159. PubMed ID: 34089035
    [No Abstract]   [Full Text] [Related]  

  • 13. Gene expression and adaptive noncoding changes during human evolution.
    Babbitt CC; Haygood R; Nielsen WJ; Wray GA
    BMC Genomics; 2017 Jun; 18(1):435. PubMed ID: 28583075
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Long intronic noncoding RNA transcription: expression noise or expression choice?
    Louro R; Smirnova AS; Verjovski-Almeida S
    Genomics; 2009 Apr; 93(4):291-8. PubMed ID: 19071207
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genomics: Encyclopaedia of humble DNA.
    Greally JM
    Nature; 2007 Jun; 447(7146):782-3. PubMed ID: 17568731
    [No Abstract]   [Full Text] [Related]  

  • 16. Whole-exome/genome sequencing and genomics.
    Grody WW; Thompson BH; Hudgins L
    Pediatrics; 2013 Dec; 132(Suppl 3):S211-5. PubMed ID: 24298129
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Brain evolution and uniqueness in the human genome.
    Amadio JP; Walsh CA
    Cell; 2006 Sep; 126(6):1033-5. PubMed ID: 16990130
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genome sequencing identifies a non-coding variant in the MCDR1 locus as a cause of macular dystrophy.
    Ellingford JM; Sergouniotis PI; Jenkins E; Black GC
    Clin Exp Ophthalmol; 2017 Apr; 45(3):297-299. PubMed ID: 27551809
    [No Abstract]   [Full Text] [Related]  

  • 19. Characterization of noncoding regulatory DNA in the human genome.
    Elkon R; Agami R
    Nat Biotechnol; 2017 Aug; 35(8):732-746. PubMed ID: 28787426
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Disease-Associated Single-Nucleotide Polymorphisms From Noncoding Regions in Juvenile Idiopathic Arthritis Are Located Within or Adjacent to Functional Genomic Elements of Human Neutrophils and CD4+ T Cells.
    Jiang K; Zhu L; Buck MJ; Chen Y; Carrier B; Liu T; Jarvis JN
    Arthritis Rheumatol; 2015 Jul; 67(7):1966-77. PubMed ID: 25833190
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.