179 related articles for article (PubMed ID: 23379653)
21.
Lopes BA; Barbosa TC; Souza BKS; Poubel CP; Pombo-de-Oliveira MS; Emerenciano M;
Cancer Prev Res (Phila); 2017 Dec; 10(12):738-744. PubMed ID: 28947432
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. Identification of a novel TP53 cancer susceptibility mutation through whole-genome sequencing of a patient with therapy-related AML.
Link DC; Schuettpelz LG; Shen D; Wang J; Walter MJ; Kulkarni S; Payton JE; Ivanovich J; Goodfellow PJ; Le Beau M; Koboldt DC; Dooling DJ; Fulton RS; Bender RH; Fulton LL; Delehaunty KD; Fronick CC; Appelbaum EL; Schmidt H; Abbott R; O'Laughlin M; Chen K; McLellan MD; Varghese N; Nagarajan R; Heath S; Graubert TA; Ding L; Ley TJ; Zambetti GP; Wilson RK; Mardis ER
JAMA; 2011 Apr; 305(15):1568-76. PubMed ID: 21505135
[TBL] [Abstract][Full Text] [Related]
24. Recurrent somatic mutations and low germline predisposition mutations in Korean ALL patients.
Shin SY; Lee H; Lee ST; Choi JR; Jung CW; Koo HH; Kim SH
Sci Rep; 2021 Apr; 11(1):8893. PubMed ID: 33903686
[TBL] [Abstract][Full Text] [Related]
25. The landscape of somatic mutations in infant MLL-rearranged acute lymphoblastic leukemias.
Andersson AK; Ma J; Wang J; Chen X; Gedman AL; Dang J; Nakitandwe J; Holmfeldt L; Parker M; Easton J; Huether R; Kriwacki R; Rusch M; Wu G; Li Y; Mulder H; Raimondi S; Pounds S; Kang G; Shi L; Becksfort J; Gupta P; Payne-Turner D; Vadodaria B; Boggs K; Yergeau D; Manne J; Song G; Edmonson M; Nagahawatte P; Wei L; Cheng C; Pei D; Sutton R; Venn NC; Chetcuti A; Rush A; Catchpoole D; Heldrup J; Fioretos T; Lu C; Ding L; Pui CH; Shurtleff S; Mullighan CG; Mardis ER; Wilson RK; Gruber TA; Zhang J; Downing JR;
Nat Genet; 2015 Apr; 47(4):330-7. PubMed ID: 25730765
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. Panel-based next-generation sequencing identifies prognostic and actionable genes in childhood acute lymphoblastic leukemia and is suitable for clinical sequencing.
Ishida H; Iguchi A; Aoe M; Takahashi T; Tamefusa K; Kanamitsu K; Fujiwara K; Washio K; Matsubara T; Tsukahara H; Sanada M; Shimada A
Ann Hematol; 2019 Mar; 98(3):657-668. PubMed ID: 30446805
[TBL] [Abstract][Full Text] [Related]
28. Personalized genomic analyses for cancer mutation discovery and interpretation.
Jones S; Anagnostou V; Lytle K; Parpart-Li S; Nesselbush M; Riley DR; Shukla M; Chesnick B; Kadan M; Papp E; Galens KG; Murphy D; Zhang T; Kann L; Sausen M; Angiuoli SV; Diaz LA; Velculescu VE
Sci Transl Med; 2015 Apr; 7(283):283ra53. PubMed ID: 25877891
[TBL] [Abstract][Full Text] [Related]
29. The mutational landscape in pediatric acute lymphoblastic leukemia deciphered by whole genome sequencing.
Lindqvist CM; Nordlund J; Ekman D; Johansson A; Moghadam BT; Raine A; Övernäs E; Dahlberg J; Wahlberg P; Henriksson N; Abrahamsson J; Frost BM; Grandér D; Heyman M; Larsson R; Palle J; Söderhäll S; Forestier E; Lönnerholm G; Syvänen AC; Berglund EC
Hum Mutat; 2015 Jan; 36(1):118-28. PubMed ID: 25355294
[TBL] [Abstract][Full Text] [Related]
30. The silent mutational landscape of infant MLL-AF4 pro-B acute lymphoblastic leukemia.
Dobbins SE; Sherborne AL; Ma YP; Bardini M; Biondi A; Cazzaniga G; Lloyd A; Chubb D; Greaves MF; Houlston RS
Genes Chromosomes Cancer; 2013 Oct; 52(10):954-60. PubMed ID: 23893660
[TBL] [Abstract][Full Text] [Related]
31. Mutation analysis of the HOX paralogous 4-13 genes in children with acute lymphoid malignancies: identification of a novel germline mutation of HOXD4 leading to a partial loss-of-function.
van Scherpenzeel Thim V; Remacle S; Picard J; Cornu G; Gofflot F; Rezsohazy R; Verellen-Dumoulin C
Hum Mutat; 2005 Apr; 25(4):384-95. PubMed ID: 15776434
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Accurate detection of subclonal single nucleotide variants in whole genome amplified and pooled cancer samples using HaloPlex target enrichment.
Berglund EC; Lindqvist CM; Hayat S; Övernäs E; Henriksson N; Nordlund J; Wahlberg P; Forestier E; Lönnerholm G; Syvänen AC
BMC Genomics; 2013 Dec; 14(1):856. PubMed ID: 24314227
[TBL] [Abstract][Full Text] [Related]
34. Clinical relevance of cancer genome sequencing.
Ku CS; Cooper DN; Roukos DH
World J Gastroenterol; 2013 Apr; 19(13):2011-8. PubMed ID: 23599619
[TBL] [Abstract][Full Text] [Related]
35. [Genetic background and treatment of pediatric ALL].
Kato M
Rinsho Ketsueki; 2018; 59(10):2268-2272. PubMed ID: 30305535
[TBL] [Abstract][Full Text] [Related]
36. IL-7 Receptor Mutations and Steroid Resistance in Pediatric T cell Acute Lymphoblastic Leukemia: A Genome Sequencing Study.
Li Y; Buijs-Gladdines JG; Canté-Barrett K; Stubbs AP; Vroegindeweij EM; Smits WK; van Marion R; Dinjens WN; Horstmann M; Kuiper RP; Buijsman RC; Zaman GJ; van der Spek PJ; Pieters R; Meijerink JP
PLoS Med; 2016 Dec; 13(12):e1002200. PubMed ID: 27997540
[TBL] [Abstract][Full Text] [Related]
37. Enrichment of cancer-predisposing germline variants in adult and pediatric patients with acute lymphoblastic leukemia.
Douglas SPM; Lahtinen AK; Koski JR; Leimi L; Keränen MAI; Koskenvuo M; Heckman CA; Jahnukainen K; Pitkänen E; Wartiovaara-Kautto U; Kilpivaara O
Sci Rep; 2022 Jun; 12(1):10670. PubMed ID: 35739278
[TBL] [Abstract][Full Text] [Related]
38. Germline and somatic variant identification using BGISEQ-500 and HiSeq X Ten whole genome sequencing.
Patch AM; Nones K; Kazakoff SH; Newell F; Wood S; Leonard C; Holmes O; Xu Q; Addala V; Creaney J; Robinson BW; Fu S; Geng C; Li T; Zhang W; Liang X; Rao J; Wang J; Tian M; Zhao Y; Teng F; Gou H; Yang B; Jiang H; Mu F; Pearson JV; Waddell N
PLoS One; 2018; 13(1):e0190264. PubMed ID: 29320538
[TBL] [Abstract][Full Text] [Related]
39. Next-generation sequencing using a pre-designed gene panel for the molecular diagnosis of congenital disorders in pediatric patients.
Lim EC; Brett M; Lai AH; Lee SP; Tan ES; Jamuar SS; Ng IS; Tan EC
Hum Genomics; 2015 Dec; 9():33. PubMed ID: 26666243
[TBL] [Abstract][Full Text] [Related]
40. Comprehensive detection of germline variants by MSK-IMPACT, a clinical diagnostic platform for solid tumor molecular oncology and concurrent cancer predisposition testing.
Cheng DT; Prasad M; Chekaluk Y; Benayed R; Sadowska J; Zehir A; Syed A; Wang YE; Somar J; Li Y; Yelskaya Z; Wong D; Robson ME; Offit K; Berger MF; Nafa K; Ladanyi M; Zhang L
BMC Med Genomics; 2017 May; 10(1):33. PubMed ID: 28526081
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
