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 *

87 related articles for article (PubMed ID: 19661241)

  • 21. JEasyTFM: an open-source software package for the analysis of large 2D TFM data within ImageJ.
    Carl P; Rondé P
    Bioinform Adv; 2023; 3(1):vbad156. PubMed ID: 37928344
    [TBL] [Abstract][Full Text] [Related]  

  • 22. ViSiElse: an innovative R-package to visualize raw behavioral data over time.
    Garnier EM; Fouret N; Descoins M
    PeerJ; 2020; 8():e8341. PubMed ID: 32117603
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Analysis of the caudate nucleus transcriptome in individuals with schizophrenia highlights effects of antipsychotics and new risk genes.
    Benjamin KJM; Chen Q; Jaffe AE; Stolz JM; Collado-Torres L; Huuki-Myers LA; Burke EE; Arora R; Feltrin AS; Barbosa AR; Radulescu E; Pergola G; Shin JH; Ulrich WS; Deep-Soboslay A; Tao R; ; Hyde TM; Kleinman JE; Erwin JA; Weinberger DR; Paquola ACM
    Nat Neurosci; 2022 Nov; 25(11):1559-1568. PubMed ID: 36319771
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Systematic Analysis of Molecular Characterization and Clinical Relevance of Liquid-Liquid Phase Separation Regulators in Digestive System Neoplasms.
    Zhang Y; Li J; Feng D; Peng X; Wang B; Han T; Zhang Y
    Front Cell Dev Biol; 2021; 9():820174. PubMed ID: 35252219
    [No Abstract]   [Full Text] [Related]  

  • 25. Identification of tissue-specific and common methylation quantitative trait loci in healthy individuals using MAGAR.
    Scherer M; Gasparoni G; Rahmouni S; Shashkova T; Arnoux M; Louis E; Nostaeva A; Avalos D; Dermitzakis ET; Aulchenko YS; Lengauer T; Lyons PA; Georges M; Walter J
    Epigenetics Chromatin; 2021 Sep; 14(1):44. PubMed ID: 34530905
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes.
    Feliciano P; Zhou X; Astrovskaya I; Turner TN; Wang T; Brueggeman L; Barnard R; Hsieh A; Snyder LG; Muzny DM; Sabo A; ; Gibbs RA; Eichler EE; O'Roak BJ; Michaelson JJ; Volfovsky N; Shen Y; Chung WK
    NPJ Genom Med; 2019; 4():19. PubMed ID: 31452935
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Pathway analysis of transcriptomic data shows immunometabolic effects of vitamin D.
    Muñoz Garcia A; Kutmon M; Eijssen L; Hewison M; Evelo CT; Coort SL
    J Mol Endocrinol; 2018 Feb; 60(2):95-108. PubMed ID: 29233860
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A user guide to the Brassica 60K Illumina Infinium™ SNP genotyping array.
    Mason AS; Higgins EE; Snowdon RJ; Batley J; Stein A; Werner C; Parkin IA
    Theor Appl Genet; 2017 Apr; 130(4):621-633. PubMed ID: 28220206
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A new model calling procedure for Illumina BeadArray data.
    Li G
    BMC Genet; 2016 Jun; 17(1):90. PubMed ID: 27343118
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA.
    Turner TN; Hormozdiari F; Duyzend MH; McClymont SA; Hook PW; Iossifov I; Raja A; Baker C; Hoekzema K; Stessman HA; Zody MC; Nelson BJ; Huddleston J; Sandstrom R; Smith JD; Hanna D; Swanson JM; Faustman EM; Bamshad MJ; Stamatoyannopoulos J; Nickerson DA; McCallion AS; Darnell R; Eichler EE
    Am J Hum Genet; 2016 Jan; 98(1):58-74. PubMed ID: 26749308
    [TBL] [Abstract][Full Text] [Related]  

  • 31. argyle: An R Package for Analysis of Illumina Genotyping Arrays.
    Morgan AP
    G3 (Bethesda); 2015 Dec; 6(2):281-6. PubMed ID: 26684930
    [TBL] [Abstract][Full Text] [Related]  

  • 32. M(3)-S: a genotype calling method incorporating information from samples with known genotypes.
    Li G; Zhao H
    BMC Bioinformatics; 2015 Dec; 16():403. PubMed ID: 26634345
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Transcriptional Impact of Rare and Private Copy Number Variants in Hypoplastic Left Heart Syndrome.
    Glidewell SC; Miyamoto SD; Grossfeld PD; Clouthier DE; Coldren CD; Stearman RS; Geraci MW
    Clin Transl Sci; 2015 Dec; 8(6):682-9. PubMed ID: 26534787
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Comparative genomic and genetic analysis of glioblastoma-derived brain tumor-initiating cells and their parent tumors.
    Davis B; Shen Y; Poon CC; Luchman HA; Stechishin OD; Pontifex CS; Wu W; Kelly JJ; Blough MD;
    Neuro Oncol; 2016 Mar; 18(3):350-60. PubMed ID: 26245525
    [TBL] [Abstract][Full Text] [Related]  

  • 35. affy2sv: an R package to pre-process Affymetrix CytoScan HD and 750K arrays for SNP, CNV, inversion and mosaicism calling.
    Hernandez-Ferrer C; Quintela Garcia I; Danielski K; Carracedo Á; Pérez-Jurado LA; González JR
    BMC Bioinformatics; 2015 May; 16():167. PubMed ID: 25991004
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Excess of rare, inherited truncating mutations in autism.
    Krumm N; Turner TN; Baker C; Vives L; Mohajeri K; Witherspoon K; Raja A; Coe BP; Stessman HA; He ZX; Leal SM; Bernier R; Eichler EE
    Nat Genet; 2015 Jun; 47(6):582-8. PubMed ID: 25961944
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Endometriosis is associated with rare copy number variants.
    Chettier R; Ward K; Albertsen HM
    PLoS One; 2014; 9(8):e103968. PubMed ID: 25083881
    [TBL] [Abstract][Full Text] [Related]  

  • 38. KRLMM: an adaptive genotype calling method for common and low frequency variants.
    Liu R; Dai Z; Yeager M; Irizarry RA; Ritchie ME
    BMC Bioinformatics; 2014 May; 15():158. PubMed ID: 24886250
    [TBL] [Abstract][Full Text] [Related]  

  • 39. illuminaio: An open source IDAT parsing tool for Illumina microarrays.
    Smith ML; Baggerly KA; Bengtsson H; Ritchie ME; Hansen KD
    F1000Res; 2013; 2():264. PubMed ID: 24701342
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The 5p12 breast cancer susceptibility locus affects MRPS30 expression in estrogen-receptor positive tumors.
    Quigley DA; Fiorito E; Nord S; Van Loo P; Alnæs GG; Fleischer T; Tost J; Moen Vollan HK; Tramm T; Overgaard J; Bukholm IR; Hurtado A; Balmain A; Børresen-Dale AL; Kristensen V
    Mol Oncol; 2014 Mar; 8(2):273-84. PubMed ID: 24388359
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.