BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 26936114)

  • 1. A Distinct Class of Chromoanagenesis Events Characterized by Focal Copy Number Gains.
    Masset H; Hestand MS; Van Esch H; Kleinfinger P; Plaisancié J; Afenjar A; Molignier R; Schluth-Bolard C; Sanlaville D; Vermeesch JR
    Hum Mutat; 2016 Jul; 37(7):661-8. PubMed ID: 26936114
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangements.
    Liu P; Erez A; Nagamani SC; Dhar SU; Kołodziejska KE; Dharmadhikari AV; Cooper ML; Wiszniewska J; Zhang F; Withers MA; Bacino CA; Campos-Acevedo LD; Delgado MR; Freedenberg D; Garnica A; Grebe TA; Hernández-Almaguer D; Immken L; Lalani SR; McLean SD; Northrup H; Scaglia F; Strathearn L; Trapane P; Kang SH; Patel A; Cheung SW; Hastings PJ; Stankiewicz P; Lupski JR; Bi W
    Cell; 2011 Sep; 146(6):889-903. PubMed ID: 21925314
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mechanisms for Complex Chromosomal Insertions.
    Gu S; Szafranski P; Akdemir ZC; Yuan B; Cooper ML; Magriñá MA; Bacino CA; Lalani SR; Breman AM; Smith JL; Patel A; Song RH; Bi W; Cheung SW; Carvalho CM; Stankiewicz P; Lupski JR
    PLoS Genet; 2016 Nov; 12(11):e1006446. PubMed ID: 27880765
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genomic Chaos (Multiple Copy Number Variations and Structural Reorganization) Detected in Two Prenatal Cases.
    Lloveras E; Canellas A; Plaja A; Barranco L; Fernández D; Mendez B; Piqué M; de la Iglesia C; Palau N; Costa M; Herrero M; Yeste D; Auge M; Puig L; Pérez C
    Cytogenet Genome Res; 2021; 161(5):236-242. PubMed ID: 34274931
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Flanking complex copy number variants in the same family formed through unequal crossing-over during meiosis.
    Pettersson M; Eisfeldt J; Syk Lundberg E; Lundin J; Lindstrand A
    Mutat Res; 2018 Nov; 812():1-4. PubMed ID: 30384002
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Replicative and non-replicative mechanisms in the formation of clustered CNVs are indicated by whole genome characterization.
    Nazaryan-Petersen L; Eisfeldt J; Pettersson M; Lundin J; Nilsson D; Wincent J; Lieden A; Lovmar L; Ottosson J; Gacic J; Mäkitie O; Nordgren A; Vezzi F; Wirta V; Käller M; Hjortshøj TD; Jespersgaard C; Houssari R; Pignata L; Bak M; Tommerup N; Lundberg ES; Tümer Z; Lindstrand A
    PLoS Genet; 2018 Nov; 14(11):e1007780. PubMed ID: 30419018
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Catastrophic cellular events leading to complex chromosomal rearrangements in the germline.
    Fukami M; Shima H; Suzuki E; Ogata T; Matsubara K; Kamimaki T
    Clin Genet; 2017 May; 91(5):653-660. PubMed ID: 27888607
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Long-read sequence analysis for clustered genomic copy number aberrations revealed architectures of intricately intertwined rearrangements.
    Tamura T; Yamamoto Shimojima K; Okamoto N; Yagasaki H; Morioka I; Kanno H; Minakuchi Y; Toyoda A; Yamamoto T
    Am J Med Genet A; 2023 Jan; 191(1):112-119. PubMed ID: 36282026
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Two Patients with Complex Rearrangements Suggestive of Germline Chromoanagenesis.
    Arya P; Hodge JC; Matlock PA; Vance GH; Breman AM
    Cytogenet Genome Res; 2020; 160(11-12):671-679. PubMed ID: 33535208
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Deciphering the complexity of simple chromosomal insertions by genome sequencing.
    Dong Z; Chau MHK; Zhang Y; Dai P; Zhu X; Leung TY; Kong X; Kwok YK; Stankiewicz P; Cheung SW; Choy KW
    Hum Genet; 2021 Feb; 140(2):361-380. PubMed ID: 32728808
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Complex Chromosomal Rearrangements in B-Cell Lymphoma: Evidence of Chromoanagenesis? A Case Report.
    Ortega V; Chaubey A; Mendiola C; Ehman W; Vadlamudi K; Dupont B; Velagaleti G
    Neoplasia; 2016 Apr; 18(4):223-8. PubMed ID: 27108385
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Chromoanagenesis and cancer: mechanisms and consequences of localized, complex chromosomal rearrangements.
    Holland AJ; Cleveland DW
    Nat Med; 2012 Nov; 18(11):1630-8. PubMed ID: 23135524
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Unbalanced translocations arise from diverse mutational mechanisms including chromothripsis.
    Weckselblatt B; Hermetz KE; Rudd MK
    Genome Res; 2015 Jul; 25(7):937-47. PubMed ID: 26070663
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Int22h-1/int22h-2-mediated Xq28 rearrangements: intellectual disability associated with duplications and in utero male lethality with deletions.
    El-Hattab AW; Fang P; Jin W; Hughes JR; Gibson JB; Patel GS; Grange DK; Manwaring LP; Patel A; Stankiewicz P; Cheung SW
    J Med Genet; 2011 Dec; 48(12):840-50. PubMed ID: 21984752
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses.
    Villela D; Mazzonetto PC; Migliavacca MP; Perrone E; Guida G; Milanezi MFG; Jorge AAL; Ribeiro-Bicudo LA; Kok F; Campagnari F; de Rosso-Giuliani L; da Costa SS; Vianna-Morgante AM; Pearson PL; Krepischi ACV; Rosenberg C
    Am J Med Genet A; 2021 Aug; 185(8):2335-2344. PubMed ID: 33988290
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome.
    Collins RL; Brand H; Redin CE; Hanscom C; Antolik C; Stone MR; Glessner JT; Mason T; Pregno G; Dorrani N; Mandrile G; Giachino D; Perrin D; Walsh C; Cipicchio M; Costello M; Stortchevoi A; An JY; Currall BB; Seabra CM; Ragavendran A; Margolin L; Martinez-Agosto JA; Lucente D; Levy B; Sanders SJ; Wapner RJ; Quintero-Rivera F; Kloosterman W; Talkowski ME
    Genome Biol; 2017 Mar; 18(1):36. PubMed ID: 28260531
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Chromoanagenesis: cataclysms behind complex chromosomal rearrangements.
    Pellestor F
    Mol Cytogenet; 2019; 12():6. PubMed ID: 30805029
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genomic Characterization of Chromosomal Insertions: Insights into the Mechanisms Underlying Chromothripsis.
    Kato T; Ouchi Y; Inagaki H; Makita Y; Mizuno S; Kajita M; Ikeda T; Takeuchi K; Kurahashi H
    Cytogenet Genome Res; 2017; 153(1):1-9. PubMed ID: 29073611
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Breakpoint profiling of 64 cancer genomes reveals numerous complex rearrangements spawned by homology-independent mechanisms.
    Malhotra A; Lindberg M; Faust GG; Leibowitz ML; Clark RA; Layer RM; Quinlan AR; Hall IM
    Genome Res; 2013 May; 23(5):762-76. PubMed ID: 23410887
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Chromothripsis and focal copy number alterations determine poor outcome in malignant melanoma.
    Hirsch D; Kemmerling R; Davis S; Camps J; Meltzer PS; Ried T; Gaiser T
    Cancer Res; 2013 Mar; 73(5):1454-60. PubMed ID: 23271725
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.