ArticleLeukemia2016
Multiplexed targeted sequencing of recurrent fusion genes in acute leukaemia.
Abstract readLetter
In one paragraph
Article in Leukemia, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.
0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.1field-weighted citation impact, top 21% of its field
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
19 citing papers in PubMed, 40 citations in OpenAlex.
- Machine learning identifies the independent role of dysplasia in the prediction of response to chemotherapy in AML.Leukemia · 2022Trial
- An improved assay for detection of theranostic gene translocations and MET exon 14 skipping in thoracic oncology.Laboratory investigation; a journal of technical methods and pathology · 2021Trial
- Comprehensive mutational profiling and clinical outcome of adult acute myeloid leukemia patients with NUP98 rearrangement.Leukemia · 2026Article
- Assessment of measurable residual disease in ovarian tissue collected for fertility preservation in patients in remission from acute myeloid leukaemia: A pilot study.British journal of haematology · 2026Article
- Rare case of PLAG1::RUNX1 fusion mimicking classical t(8;21): the value of optical genome mapping in acute myeloid leukemia.Molecular cytogenetics · 2025Article
- Myeloid Neoplasms With Erythroid Predominance and Excess Blasts in Young Adults Exhibit Distinct Genetic Profiles.European journal of haematology · 2025Article
- Detection of Cancer-Associated Gene Fusion by Ligation-Dependent RT-PCR.Methods in molecular biology (Clifton, N.J.) · 2025Article
- Characteristics and Prognosis of "Acute Promyelocytic Leukemia-like" Nucleophosmin-1-Mutated Acute Myeloid Leukemia in a Retrospective Patient Cohort.Biomedicines · 2024Article
- Concurrent CDX2 cis-deregulation and UBTF::ATXN7L3 fusion define a novel high-risk subtype of B-cell ALL.Blood · 2022Article
- Detection of sarcoma fusions by a next-generation sequencing based-ligation-dependent multiplex RT-PCR assay.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2022Article
- Clinico-biological features of T-cell acute lymphoblastic leukemia with fusion proteins.Blood cancer journal · 2022Article
- Challenging conventional karyotyping by next-generation karyotyping in 281 intensively treated patients with AML.Blood advances · 2021Article
- Article
- Association Analysis of TP53 rs1042522, MDM2 rs2279744, rs3730485, MDM4 rs4245739 Variants and Acute Myeloid Leukemia Susceptibility, Risk Stratification Scores, and Clinical Features: An Exploratory Study.Journal of clinical medicine · 2020Article
- Article
- Efficacy of Tyrosine Kinase Inhibitor Therapy in a Chemotherapy-refractory B-cell Precursor Acute Lymphoblastic Leukemia WithHemaSphere · 2019Article
- Ligation-dependent RT-PCR: a new specific and low-cost technique to detect ALK, ROS, and RET rearrangements in lung adenocarcinoma.Laboratory investigation; a journal of technical methods and pathology · 2018Article
- NUP214-ABL1 fusion defines a rare subtype of B-cell precursor acute lymphoblastic leukemia that could benefit from tyrosine kinase inhibitors.Haematologica · 2016Article
- Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
28 authors at 8 institutions in 1 country.
P RuminyInserm U918, Centre Henri Becquerel, Institute for Research and Innovation in Biomedicine, University of Rouen, Rouen, France.
V MarchandInserm U918, Centre Henri Becquerel, Institute for Research and Innovation in Biomedicine, University of Rouen, Rouen, France.
N BuchbinderPaediatric Oncology and Haematology Unit, Charles Nicolle Rouen University Hospital, Rouen, France.
T LarsonInserm U918, Centre Henri Becquerel, Institute for Research and Innovation in Biomedicine, University of Rouen, Rouen, France.
B JolyInserm U918, Centre Henri Becquerel, Institute for Research and Innovation in Biomedicine, University of Rouen, Rouen, France.
D PentherInserm U918, Centre Henri Becquerel, Institute for Research and Innovation in Biomedicine, University of Rouen, Rouen, France.
E LemasleDepartment of Haematology, Centre Henri Becquerel, Rouen, France.
S LepretreInserm U918, Centre Henri Becquerel, Institute for Research and Innovation in Biomedicine, University of Rouen, Rouen, France.
E AngotDepartment of Pathology, Charles Nicolle Rouen University Hospital, Rouen, France.
S MareschalInserm U918, Centre Henri Becquerel, Institute for Research and Innovation in Biomedicine, University of Rouen, Rouen, France.
P-J ViaillyInserm U918, Centre Henri Becquerel, Institute for Research and Innovation in Biomedicine, University of Rouen, Rouen, France.
S DuboisInserm U918, Centre Henri Becquerel, Institute for Research and Innovation in Biomedicine, University of Rouen, Rouen, France.
F ClatotDepartment of Oncology, Centre Henri Becquerel, Rouen, France.
M ViennotInserm U918, Centre Henri Becquerel, Institute for Research and Innovation in Biomedicine, University of Rouen, Rouen, France.
E BohersInserm U918, Centre Henri Becquerel, Institute for Research and Innovation in Biomedicine, University of Rouen, Rouen, France.
D RizzoInserm U918, Centre Henri Becquerel, Institute for Research and Innovation in Biomedicine, University of Rouen, Rouen, France.
M CornicDepartment of Pathology, Centre Henri Becquerel, Rouen, France.
P BertrandInserm U918, Centre Henri Becquerel, Institute for Research and Innovation in Biomedicine, University of Rouen, Rouen, France.
C GirodPaediatric Oncology and Haematology Unit, Charles Nicolle Rouen University Hospital, Rouen, France.
V CamusDepartment of Haematology, Centre Henri Becquerel, Rouen, France.
P EtancelinInserm U918, Centre Henri Becquerel, Institute for Research and Innovation in Biomedicine, University of Rouen, Rouen, France.
G BuchonnetHaematology Unit, Charles Nicolle University Hospital, Rouen, France.
P SchneiderPaediatric Oncology and Haematology Unit, Charles Nicolle Rouen University Hospital, Rouen, France.
J-M PicquenotInserm U918, Centre Henri Becquerel, Institute for Research and Innovation in Biomedicine, University of Rouen, Rouen, France.
J-P VannierPaediatric Oncology and Haematology Unit, Charles Nicolle Rouen University Hospital, Rouen, France.
C BastardInserm U918, Centre Henri Becquerel, Institute for Research and Innovation in Biomedicine, University of Rouen, Rouen, France.
H TillyInserm U918, Centre Henri Becquerel, Institute for Research and Innovation in Biomedicine, University of Rouen, Rouen, France.
F JardinInserm U918, Centre Henri Becquerel, Institute for Research and Innovation in Biomedicine, University of Rouen, Rouen, France.
Université de Rouen Normandie · FRBiotherapy of Genetic Diseases, Inflammatory Disorders and Cancers · FRInserm · FRCentre Henri BecquerelInstitute for Research and Innovation in Biomedicine · FRHôpital Charles-Nicolle · FRCentre Hospitalier Universitaire de Rouen · FRCentre Virchow-Villermé · FR
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Indexed as
Biological AssayAcute DiseaseBase SequenceChromosomes, Human, Pair 15Chromosomes, Human, Pair 17Chromosomes, Human, Pair 21Cytogenetic AnalysisHigh-Throughput Nucleotide SequencingHumansLeukemiaMolecular Sequence DataOligonucleotide ProbesOncogene Proteins, FusionRetrospective StudiesReverse Transcriptase Polymerase Chain ReactionTranslocation, GeneticOligonucleotide ProbesOncogene Proteins, Fusion
Identifiers
What OpenQuestion holds
Textmetadata
Read underepoch 390
Registered trials
None linked
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.