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Items: 1 to 20 of 106

1.

Developmental timing of mutations revealed by whole-genome sequencing of twins with acute lymphoblastic leukemia.

Ma Y, Dobbins SE, Sherborne AL, Chubb D, Galbiati M, Cazzaniga G, Micalizzi C, Tearle R, Lloyd AL, Hain R, Greaves M, Houlston RS.

Proc Natl Acad Sci U S A. 2013 Apr 30;110(18):7429-33. doi: 10.1073/pnas.1221099110. Epub 2013 Apr 8.

2.

Acquisition of genome-wide copy number alterations in monozygotic twins with acute lymphoblastic leukemia.

Bateman CM, Colman SM, Chaplin T, Young BD, Eden TO, Bhakta M, Gratias EJ, van Wering ER, Cazzaniga G, Harrison CJ, Hain R, Ancliff P, Ford AM, Kearney L, Greaves M.

Blood. 2010 Apr 29;115(17):3553-8. doi: 10.1182/blood-2009-10-251413. Epub 2010 Jan 8.

3.

Pre-natal, clonal origin of t(1;11)(p32;q23) acute lymphoblastic leukemia in monozygotic twins.

Kotecha RS, Murch A, Kees U, Cole CH.

Leuk Res. 2012 Jan;36(1):46-50. doi: 10.1016/j.leukres.2011.03.014. Epub 2011 Apr 6.

PMID:
21474181
4.

Developmental origins and impact of BCR-ABL1 fusion and IKZF1 deletions in monozygotic twins with Ph+ acute lymphoblastic leukemia.

Cazzaniga G, van Delft FW, Lo Nigro L, Ford AM, Score J, Iacobucci I, Mirabile E, Taj M, Colman SM, Biondi A, Greaves M.

Blood. 2011 Nov 17;118(20):5559-64. doi: 10.1182/blood-2011-07-366542. Epub 2011 Sep 29.

5.

Evolutionary trajectories of hyperdiploid ALL in monozygotic twins.

Bateman CM, Alpar D, Ford AM, Colman SM, Wren D, Morgan M, Kearney L, Greaves M.

Leukemia. 2015 Jan;29(1):58-65. doi: 10.1038/leu.2014.177. Epub 2014 Jun 4.

PMID:
24897505
6.

Monoclonal origin of concordant T-cell malignancy in identical twins.

Ford AM, Pombo-de-Oliveira MS, McCarthy KP, MacLean JM, Carrico KC, Vincent RF, Greaves M.

Blood. 1997 Jan 1;89(1):281-5.

7.

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. doi: 10.1002/humu.22719.

8.

Concordant childhood acute lymphoblastic leukemia in monozygotic twins.

Chin YM, Wan Ariffin A, Lin HP, Chan YS.

Med J Malaysia. 1996 Mar;51(1):145-8.

9.

Darwin and evolutionary tales in leukemia. The Ham-Wasserman Lecture.

Greaves M.

Hematology Am Soc Hematol Educ Program. 2009:3-12. doi: 10.1182/asheducation-2009.1.3.

PMID:
20008176
10.

Identification of somatic and germline mutations using whole exome sequencing of congenital acute lymphoblastic leukemia.

Chang VY, Basso G, Sakamoto KM, Nelson SF.

BMC Cancer. 2013 Feb 4;13:55. doi: 10.1186/1471-2407-13-55.

11.

Fetal origins of the TEL-AML1 fusion gene in identical twins with leukemia.

Ford AM, Bennett CA, Price CM, Bruin MC, Van Wering ER, Greaves M.

Proc Natl Acad Sci U S A. 1998 Apr 14;95(8):4584-8.

12.

Clonal evolution of acute leukemia genomes.

Jan M, Majeti R.

Oncogene. 2013 Jan 10;32(2):135-40. doi: 10.1038/onc.2012.48. Epub 2012 Feb 20. Review.

13.

Aging as accelerated accumulation of somatic variants: whole-genome sequencing of centenarian and middle-aged monozygotic twin pairs.

Ye K, Beekman M, Lameijer EW, Zhang Y, Moed MH, van den Akker EB, Deelen J, Houwing-Duistermaat JJ, Kremer D, Anvar SY, Laros JF, Jones D, Raine K, Blackburne B, Potluri S, Long Q, Guryev V, van der Breggen R, Westendorp RG, 't Hoen PA, den Dunnen J, van Ommen GJ, Willemsen G, Pitts SJ, Cox DR, Ning Z, Boomsma DI, Slagboom PE.

Twin Res Hum Genet. 2013 Dec;16(6):1026-32. doi: 10.1017/thg.2013.73. Epub 2013 Nov 4.

PMID:
24182360
14.

Joint genotype inference with germline and somatic mutations.

Bareke E, Saillour V, Spinella JF, Vidal R, Healy J, Sinnett D, Csűrös M.

BMC Bioinformatics. 2013;14 Suppl 5:S3. doi: 10.1186/1471-2105-14-S5-S3. Epub 2013 Apr 10.

15.

Protracted and variable latency of acute lymphoblastic leukemia after TEL-AML1 gene fusion in utero.

Wiemels JL, Ford AM, Van Wering ER, Postma A, Greaves M.

Blood. 1999 Aug 1;94(3):1057-62.

16.

Prenatal origin of hyperdiploid acute lymphoblastic leukemia in identical twins.

Maia AT, van der Velden VH, Harrison CJ, Szczepanski T, Williams MD, Griffiths MJ, van Dongen JJ, Greaves MF.

Leukemia. 2003 Nov;17(11):2202-6.

PMID:
12931229
17.

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 23;15:539. doi: 10.1186/s12885-015-1549-6.

18.

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. doi: 10.1016/j.leukres.2015.06.005. Epub 2015 Jun 14.

PMID:
26189108
19.

Relapsed childhood high hyperdiploid acute lymphoblastic leukemia: presence of preleukemic ancestral clones and the secondary nature of microdeletions and RTK-RAS mutations.

Davidsson J, Paulsson K, Lindgren D, Lilljebjörn H, Chaplin T, Forestier E, Andersen MK, Nordgren A, Rosenquist R, Fioretos T, Young BD, Johansson B.

Leukemia. 2010 May;24(5):924-31. doi: 10.1038/leu.2010.39. Epub 2010 Mar 18.

PMID:
20237506
20.

Pediatric T-cell lymphoblastic leukemia evolves into relapse by clonal selection, acquisition of mutations and promoter hypomethylation.

Kunz JB, Rausch T, Bandapalli OR, Eilers J, Pechanska P, Schuessele S, Assenov Y, Stütz AM, Kirschner-Schwabe R, Hof J, Eckert C, von Stackelberg A, Schrappe M, Stanulla M, Koehler R, Avigad S, Elitzur S, Handgretinger R, Benes V, Weischenfeldt J, Korbel JO, Muckenthaler MU, Kulozik AE.

Haematologica. 2015 Nov;100(11):1442-50. doi: 10.3324/haematol.2015.129692. Epub 2015 Aug 20.

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