BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

641 related articles for article (PubMed ID: 26201965)

  • 1. Whole-exome sequencing of a rare case of familial childhood acute lymphoblastic leukemia reveals putative predisposing mutations in Fanconi anemia genes.
    Spinella JF; Healy J; Saillour V; Richer C; Cassart P; Ouimet M; Sinnett D
    BMC Cancer; 2015 Jul; 15():539. PubMed ID: 26201965
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Rare allelic forms of PRDM9 associated with childhood leukemogenesis.
    Hussin J; Sinnett D; Casals F; Idaghdour Y; Bruat V; Saillour V; Healy J; Grenier JC; de Malliard T; Busche S; Spinella JF; Larivière M; Gibson G; Andersson A; Holmfeldt L; Ma J; Wei L; Zhang J; Andelfinger G; Downing JR; Mullighan CG; Awadalla P
    Genome Res; 2013 Mar; 23(3):419-30. PubMed ID: 23222848
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Next-generation-sequencing-based risk stratification and identification of new genes involved in structural and sequence variations in near haploid lymphoblastic leukemia.
    Chen C; Bartenhagen C; Gombert M; Okpanyi V; Binder V; Röttgers S; Bradtke J; Teigler-Schlegel A; Harbott J; Ginzel S; Thiele R; Fischer U; Dugas M; Hu J; Borkhardt A
    Genes Chromosomes Cancer; 2013 Jun; 52(6):564-79. PubMed ID: 23508829
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Allelic variants of PRDM9 associated with high hyperdiploid childhood acute lymphoblastic leukaemia.
    Woodward EL; Olsson ML; Johansson B; Paulsson K
    Br J Haematol; 2014 Sep; 166(6):947-9. PubMed ID: 24754746
    [No Abstract]   [Full Text] [Related]  

  • 5. Molecular defects identified by whole exome sequencing in a child with Fanconi anemia.
    Zheng Z; Geng J; Yao RE; Li C; Ying D; Shen Y; Ying L; Yu Y; Fu Q
    Gene; 2013 Nov; 530(2):295-300. PubMed ID: 23973728
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Next-generation-sequencing of recurrent childhood high hyperdiploid acute lymphoblastic leukemia reveals mutations typically associated with high risk patients.
    Chen C; Bartenhagen C; Gombert M; Okpanyi V; Binder V; Röttgers S; Bradtke J; Teigler-Schlegel A; Harbott J; Ginzel S; Thiele R; Husemann P; Krell PF; Borkhardt A; Dugas M; Hu J; Fischer U
    Leuk Res; 2015 Sep; 39(9):990-1001. PubMed ID: 26189108
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Germline genetic variation in ETV6 and risk of childhood acute lymphoblastic leukaemia: a systematic genetic study.
    Moriyama T; Metzger ML; Wu G; Nishii R; Qian M; Devidas M; Yang W; Cheng C; Cao X; Quinn E; Raimondi S; Gastier-Foster JM; Raetz E; Larsen E; Martin PL; Bowman WP; Winick N; Komada Y; Wang S; Edmonson M; Xu H; Mardis E; Fulton R; Pui CH; Mullighan C; Evans WE; Zhang J; Hunger SP; Relling MV; Nichols KE; Loh ML; Yang JJ
    Lancet Oncol; 2015 Dec; 16(16):1659-66. PubMed ID: 26522332
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The genomic landscape of high hyperdiploid childhood acute lymphoblastic leukemia.
    Paulsson K; Lilljebjörn H; Biloglav A; Olsson L; Rissler M; Castor A; Barbany G; Fogelstrand L; Nordgren A; Sjögren H; Fioretos T; Johansson B
    Nat Genet; 2015 Jun; 47(6):672-6. PubMed ID: 25961940
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutations of the SLX4 gene in Fanconi anemia.
    Kim Y; Lach FP; Desetty R; Hanenberg H; Auerbach AD; Smogorzewska A
    Nat Genet; 2011 Feb; 43(2):142-6. PubMed ID: 21240275
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Analysis of the novel fanconi anemia gene SLX4/FANCP in familial breast cancer cases.
    Bakker JL; van Mil SE; Crossan G; Sabbaghian N; De Leeneer K; Poppe B; Adank M; Gille H; Verheul H; Meijers-Heijboer H; de Winter JP; Claes K; Tischkowitz M; Waisfisz Q
    Hum Mutat; 2013 Jan; 34(1):70-3. PubMed ID: 22911665
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A novel somatic mutation in ACD induces telomere lengthening and apoptosis resistance in leukemia cells.
    Spinella JF; Cassart P; Garnier N; Rousseau P; Drullion C; Richer C; Ouimet M; Saillour V; Healy J; Autexier C; Sinnett D
    BMC Cancer; 2015 Sep; 15():621. PubMed ID: 26345285
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Evaluation of Fanconi Anemia genes in familial breast cancer predisposition.
    Seal S; Barfoot R; Jayatilake H; Smith P; Renwick A; Bascombe L; McGuffog L; Evans DG; Eccles D; Easton DF; Stratton MR; Rahman N;
    Cancer Res; 2003 Dec; 63(24):8596-9. PubMed ID: 14695169
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Whole exome sequencing unveils a frameshift mutation in CNGB3 for cone dystrophy: A case report of an Indian family.
    Gupta S; Chaurasia A; Pathak E; Mishra R; Chaudhry VN; Chaudhry P; Mukherjee A; Mutsuddi M
    Medicine (Baltimore); 2017 Jul; 96(30):e7490. PubMed ID: 28746191
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Concordant B-cell precursor acute lymphoblastic leukemia in non-twinned siblings.
    Pombo-de-Oliveira MS; Emerenciano M; Winn AP; Costa I; Mansur MB; Ford AM
    Blood Cells Mol Dis; 2015 Jan; 54(1):110-5. PubMed ID: 25150625
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Paternal or Maternal Uniparental Disomy of Chromosome 16 Resulting in Homozygosity of a Mutant Allele Causes Fanconi Anemia.
    Donovan FX; Kimble DC; Kim Y; Lach FP; Harper U; Kamat A; Jones M; Sanborn EM; Tryon R; Wagner JE; MacMillan ML; Ostrander EA; Auerbach AD; Smogorzewska A; Chandrasekharappa SC
    Hum Mutat; 2016 May; 37(5):465-8. PubMed ID: 26841305
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Whole-exome sequencing of pediatric acute lymphoblastic leukemia.
    Lilljebjörn H; Rissler M; Lassen C; Heldrup J; Behrendtz M; Mitelman F; Johansson B; Fioretos T
    Leukemia; 2012 Jul; 26(7):1602-7. PubMed ID: 22094584
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Detection of a new heterozygous germline ETV6 mutation in a case with hyperdiploid acute lymphoblastic leukemia.
    Duployez N; Abou Chahla W; Lejeune S; Marceau-Renaut A; Letizia G; Boyer T; Geffroy S; Peyrouze P; Grardel N; Nelken B; Michel G; Bertrand Y; Preudhomme C
    Eur J Haematol; 2018 Jan; 100(1):104-107. PubMed ID: 29034503
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Whole exome sequencing reveals uncommon mutations in the recently identified Fanconi anemia gene SLX4/FANCP.
    Schuster B; Knies K; Stoepker C; Velleuer E; Friedl R; Gottwald-Mühlhauser B; de Winter JP; Schindler D
    Hum Mutat; 2013 Jan; 34(1):93-6. PubMed ID: 23033263
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Spectrum of sequence variations in the FANCA gene: an International Fanconi Anemia Registry (IFAR) study.
    Levran O; Diotti R; Pujara K; Batish SD; Hanenberg H; Auerbach AD
    Hum Mutat; 2005 Feb; 25(2):142-9. PubMed ID: 15643609
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Exome sequencing analysis reveals variants in primary immunodeficiency genes in patients with very early onset inflammatory bowel disease.
    Kelsen JR; Dawany N; Moran CJ; Petersen BS; Sarmady M; Sasson A; Pauly-Hubbard H; Martinez A; Maurer K; Soong J; Rappaport E; Franke A; Keller A; Winter HS; Mamula P; Piccoli D; Artis D; Sonnenberg GF; Daly M; Sullivan KE; Baldassano RN; Devoto M
    Gastroenterology; 2015 Nov; 149(6):1415-24. PubMed ID: 26193622
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 33.