Publication: 3129

Publication: 3129

Clinical and molecular relevance of genetic variants in the non-coding transcriptome of patients with cytogenetically normal acute myeloid leukemia.

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Citation:: Haematologica vol 107 (5) 1034-1044

Year:: 2022
Type:: Manuscript
Funding:: NCTN
Endpoint:: Secondary-not-in-original
Analysis:: Primary
Data Sharing:: No-Data-Sharing
Status:: Presented/Published
Citation Status:: pub

Note:

Methodological:: No
Biospecimen:: Yes
SDC:: No
Book Volume:: 11

Parents:: 2784
Children:: None

Program:: TRP
Primary Committee:: Leuk Corr Sci
Sec. Committees:

Pharmas:
Grants:: U10CA180821, U10CA180882, , U24CA196171, U10CA180833, U10CA180850, U10CA180861, U10CA180866, U10CA180867, P50CA140158, P30CA16058, R35CA197734, G-509200-004

Corr. Author:
Authors:: Dimitrios Papaioannou Hatice G Ozer Deedra Nicolet Amog P Urs Tobias Herold Krzysztof Mrózek Aarif M N Batcha Klaus H Metzeler Ayse S Yilmaz Stefano Volinia Marius Bill Jessica Kohlschmidt Maciej Pietrzak Christopher J Walker Andrew J Carroll Jan Braess Bayard L Powell Ann-Kathrin Eisfeld Geoffrey L Uy Eunice S Wang Jonathan E Kolitz Richard M Stone Wolfgang Hiddemann John C Byrd Clara D Bloomfield Ramiro Garzon

Networks:: CT063, IL040, LAPS-AL002, LAPS-MA036, LAPS-MO011, LAPS-NY158, LAPS-OH007, NC002, NORTHWELL, OH070

Study
Multiple Studies, or Legacy Studies in Alliance Study:: CALGB-20202
Phases:: N/A

Keywords:: Adult, Cytosine, Humans, Leukemia, Myeloid, Acute, Middle Aged, Mutation, Prognosis, RNA, Long Noncoding, Thymidine, Transcriptome