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 *

330 related articles for article (PubMed ID: 29405991)

  • 41. Characterization of complex chromosomal rearrangements by targeted capture and next-generation sequencing.
    Sobreira NL; Gnanakkan V; Walsh M; Marosy B; Wohler E; Thomas G; Hoover-Fong JE; Hamosh A; Wheelan SJ; Valle D
    Genome Res; 2011 Oct; 21(10):1720-7. PubMed ID: 21890680
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Structural rearrangements as a recurrent pathogenic mechanism for SETBP1 haploinsufficiency.
    Alesi V; Genovese S; Roberti MC; Sallicandro E; Di Tommaso S; Loddo S; Orlando V; Pompili D; Calacci C; Mei V; Pisaneschi E; Faggiano MV; Morgia A; Mammì C; Astrea G; Battini R; Priolo M; Dentici ML; Milone R; Novelli A
    Hum Genomics; 2024 Mar; 18(1):29. PubMed ID: 38520002
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Next generation mapping reveals novel large genomic rearrangements in prostate cancer.
    Jaratlerdsiri W; Chan EKF; Petersen DC; Yang C; Croucher PI; Bornman MSR; Sheth P; Hayes VM
    Oncotarget; 2017 Apr; 8(14):23588-23602. PubMed ID: 28423598
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Cryptic breakpoint identified by whole-genome mate-pair sequencing in a rare paternally inherited complex chromosomal rearrangement.
    Aristidou C; Theodosiou A; Ketoni A; Bak M; Mehrjouy MM; Tommerup N; Sismani C
    Mol Cytogenet; 2018; 11():34. PubMed ID: 29930709
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Reconstructing cancer karyotypes from short read data: the half empty and half full glass.
    Eitan R; Shamir R
    BMC Bioinformatics; 2017 Nov; 18(1):488. PubMed ID: 29141589
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Theragnostic chromosomal rearrangements in treatment-naive pancreatic ductal adenocarcinomas obtained via endoscopic ultrasound.
    Murphy SJ; Levy MJ; Smadbeck JB; Karagouga G; McCune AF; Harris FR; Udell JB; Johnson SH; Kerr SE; Cheville JC; Kipp BR; Vasmatzis G; Gleeson FC
    J Cell Mol Med; 2021 Apr; 25(8):4110-4123. PubMed ID: 33704908
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Genomic Investigation of Balanced Chromosomal Rearrangements in Patients with Abnormal Phenotypes.
    Simioni M; Artiguenave F; Meyer V; Sgardioli IC; Viguetti-Campos NL; Lopes Monlleó I; Maciel-Guerra AT; Steiner CE; Gil-da-Silva-Lopes VL
    Mol Syndromol; 2017 Jun; 8(4):187-194. PubMed ID: 28690484
    [TBL] [Abstract][Full Text] [Related]  

  • 48. A Complex Genomic Rearrangement Resulting in Loss of Function of
    Orlando V; Di Tommaso S; Alesi V; Loddo S; Genovese S; Catino G; Martucci L; Roberti MC; Trivisano M; Dentici ML; Specchio N; Dallapiccola B; Ferretti A; Novelli A
    Int J Mol Sci; 2022 Oct; 23(21):. PubMed ID: 36361691
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases.
    Lu X; Shaw CA; Patel A; Li J; Cooper ML; Wells WR; Sullivan CM; Sahoo T; Yatsenko SA; Bacino CA; Stankiewicz P; Ou Z; Chinault AC; Beaudet AL; Lupski JR; Cheung SW; Ward PA
    PLoS One; 2007 Mar; 2(3):e327. PubMed ID: 17389918
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Design of large-insert jumping libraries for structural variant detection using Illumina sequencing.
    Hanscom C; Talkowski M
    Curr Protoc Hum Genet; 2014 Jan; 80():7.22.1-7.22.9. PubMed ID: 24789519
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Assessing genome-wide copy number aberrations and copy-neutral loss-of-heterozygosity as best practice: An evidence-based review from the Cancer Genomics Consortium working group for plasma cell disorders.
    Pugh TJ; Fink JM; Lu X; Mathew S; Murata-Collins J; Willem P; Fang M;
    Cancer Genet; 2018 Dec; 228-229():184-196. PubMed ID: 30393007
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Detection of variations and identifying genomic breakpoints for large deletions in the LDLR by Ion Torrent semiconductor sequencing.
    Faiz F; Allcock RJ; Hooper AJ; van Bockxmeer FM
    Atherosclerosis; 2013 Oct; 230(2):249-55. PubMed ID: 24075752
    [TBL] [Abstract][Full Text] [Related]  

  • 53. SVachra: a tool to identify genomic structural variation in mate pair sequencing data containing inward and outward facing reads.
    Hampton OA; English AC; Wang M; Salerno WJ; Liu Y; Muzny DM; Han Y; Wheeler DA; Worley KC; Lupski JR; Gibbs RA
    BMC Genomics; 2017 Oct; 18(Suppl 6):691. PubMed ID: 28984202
    [TBL] [Abstract][Full Text] [Related]  

  • 54. DELLY: structural variant discovery by integrated paired-end and split-read analysis.
    Rausch T; Zichner T; Schlattl A; Stütz AM; Benes V; Korbel JO
    Bioinformatics; 2012 Sep; 28(18):i333-i339. PubMed ID: 22962449
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Detection of recurrent rearrangement breakpoints from copy number data.
    Ritz A; Paris PL; Ittmann MM; Collins C; Raphael BJ
    BMC Bioinformatics; 2011 Apr; 12():114. PubMed ID: 21510904
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Optical genome mapping in acute myeloid leukemia: a multicenter evaluation.
    Levy B; Baughn LB; Akkari Y; Chartrand S; LaBarge B; Claxton D; Lennon PA; Cujar C; Kolhe R; Kroeger K; Pitel B; Sahajpal N; Sathanoori M; Vlad G; Zhang L; Fang M; Kanagal-Shamanna R; Broach JR
    Blood Adv; 2023 Apr; 7(7):1297-1307. PubMed ID: 36417763
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Whole genome paired-end sequencing elucidates functional and phenotypic consequences of balanced chromosomal rearrangement in patients with developmental disorders.
    Schluth-Bolard C; Diguet F; Chatron N; Rollat-Farnier PA; Bardel C; Afenjar A; Amblard F; Amiel J; Blesson S; Callier P; Capri Y; Collignon P; Cordier MP; Coubes C; Demeer B; Chaussenot A; Demurger F; Devillard F; Doco-Fenzy M; Dupont C; Dupont JM; Dupuis-Girod S; Faivre L; Gilbert-Dussardier B; Guerrot AM; Houlier M; Isidor B; Jaillard S; Joly-Hélas G; Kremer V; Lacombe D; Le Caignec C; Lebbar A; Lebrun M; Lesca G; Lespinasse J; Levy J; Malan V; Mathieu-Dramard M; Masson J; Masurel-Paulet A; Mignot C; Missirian C; Morice-Picard F; Moutton S; Nadeau G; Pebrel-Richard C; Odent S; Paquis-Flucklinger V; Pasquier L; Philip N; Plutino M; Pons L; Portnoï MF; Prieur F; Puechberty J; Putoux A; Rio M; Rooryck-Thambo C; Rossi M; Sarret C; Satre V; Siffroi JP; Till M; Touraine R; Toutain A; Toutain J; Valence S; Verloes A; Whalen S; Edery P; Tabet AC; Sanlaville D
    J Med Genet; 2019 Aug; 56(8):526-535. PubMed ID: 30923172
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Genome-wide sequencing for the identification of rearrangements associated with Tourette syndrome and obsessive-compulsive disorder.
    Hooper SD; Johansson AC; Tellgren-Roth C; Stattin EL; Dahl N; Cavelier L; Feuk L
    BMC Med Genet; 2012 Dec; 13():123. PubMed ID: 23253088
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Resolving Breakpoints of Chromosomal Rearrangements at the Nucleotide Level Using Sanger Sequencing.
    Nalbandian K; Piña-Aguilar RE; Morton CC
    Curr Protoc Hum Genet; 2020 Dec; 108(1):e107. PubMed ID: 33369263
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Whole-genome sequencing identifies new genetic alterations in meningiomas.
    Tang M; Wei H; Han L; Deng J; Wang Y; Yang M; Tang Y; Guo G; Zhou L; Tong A
    Oncotarget; 2017 Mar; 8(10):17070-17080. PubMed ID: 28177878
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.