Longitudinal copy number, whole exome and targeted deep sequencing of 'good risk' IGHV-mutated CLL patients with progressive disease-Reference-Cited by-同舟云学术

Longitudinal copy number, whole exome and targeted deep sequencing of 'good risk' IGHV-mutated CLL patients with progressive disease

Published:2016-02-05 Issue:6 Volume:30 Page:1301-1310
ISSN:0887-6924
Container-title:Leukemia
language:en
Short-container-title:Leukemia

Author:

Rose-Zerilli M J J,Gibson J,Wang J,Tapper W,Davis Z,Parker H,Larrayoz M,McCarthy H,Walewska R,Forster J,Gardiner A,Steele A J,Chelala C,Ennis S,Collins A,Oakes C C,Oscier D G,Strefford J C

Publisher

Springer Science and Business Media LLC

Subject

Oncology,Cancer Research,Hematology

Link

http://www.nature.com/articles/leu201610.pdf

Reference52 articles.

1. Pflug N, Bahlo J, Shanafelt TD, Eichhorst BF, Bergmann MA, Elter T et al. Development of a comprehensive prognostic index for patients with chronic lymphocytic leukemia. Blood 2014; 124: 49–62.

2. Skowronska A, Austen B, Powell JE, Weston V, Oscier DG, Dyer MJ et al. ATM germline heterozygosity does not play a role in chronic lymphocytic leukemia initiation but influences rapid disease progression through loss of the remaining ATM allele. Haematologica 2012; 97: 142–146.

3. Clifford R, Louis T, Robbe P, Ackroyd S, Burns A, Timbs AT et al. SAMHD1 is mutated recurrently in chronic lymphocytic leukemia and is involved in response to DNA damage. Blood 2014; 123: 1021–1031.

4. Rossi D, Khiabanian H, Spina V, Ciardullo C, Bruscaggin A, Famà R et al. Clinical impact of small TP53 mutated subclones in chronic lymphocytic leukemia. Blood 2014; 123: 2139–2147.

5. Lionetti M, Fabris S, Cutrona G, Agnelli L, Ciardullo C, Matis S et al. High-throughput sequencing for the identification of NOTCH1 mutations in early stage chronic lymphocytic leukaemia: biological and clinical implications. Br J Haematol 2014; 165: 629–639.

Cited by 36 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. HATCHet2: clone- and haplotype-specific copy number inference from bulk tumor sequencing data;Genome Biology;2024-05-21

2. IκBε deficiency accelerates disease development in chronic lymphocytic leukemia;Leukemia;2024-04-04

3. Integrative NGS testing reveals clonal dynamics of adverse genomic defects contributing to a natural progression in treatment‐naïve CLL patients;British Journal of Haematology;2023-12-07

4. HATCHet2: clone- and haplotype-specific copy number inference from bulk tumor sequencing data;2023-07-15

5. Whole-genome sequencing of chronic lymphocytic leukemia identifies subgroups with distinct biological and clinical features;Nature Genetics;2022-11