日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Rare case of PLAG1::RUNX1 fusion mimicking classical t(8;21): the value of optical genome mapping in acute myeloid leukemia

PLAG1::RUNX1融合罕见病例模拟经典t(8;21):光学基因组作图在急性髓系白血病中的价值

Assaf, Nada; Alawieh, Shireen; Hammoud, Rawan; Daudignon, Agnès; Luquet, Isabelle; Lambert, Juliette; Terré, Christine

Unravelling a KMT2A::ARHGEF12 fusion within chromoanagenesis in acute myeloid leukemia using Optical Genome Mapping

利用光学基因组图谱揭示急性髓系白血病染色体生成过程中的 KMT2A::ARHGEF12 融合

Klos, Corentine; Roynard, Pauline; Berthon, Céline; Soenen, Valérie; Marceau, Alice; Fournier, Elise; Fenwarth, Laurene; Daudignon, Agnès; Roche, Catherine; Guermouche, Hélène

Combination of t(4;14), del(17p13), del(1p32) and 1q21 gain FISH probes identifies clonal heterogeneity and enhances the detection of adverse cytogenetic profiles in 233 newly diagnosed multiple myeloma

t(4;14)、del(17p13)、del(1p32)和1q21扩增FISH探针的组合可识别克隆异质性,并增强对233例新诊断的多发性骨髓瘤患者不良细胞遗传学特征的检测。

Smol, Thomas; Dufour, Annika; Tricot, Sabine; Wemeau, Mathieu; Stalnikiewicz, Laure; Bernardi, Franck; Terré, Christine; Ducourneau, Benoît; Bisiau, Hervé; Daudignon, Agnès

Chromosomal aberrations and their prognostic value in a series of 174 untreated patients with Waldenström's macroglobulinemia

染色体畸变及其在174例未经治疗的华氏巨球蛋白血症患者中的预后价值

Nguyen-Khac, Florence; Lambert, Jerome; Chapiro, Elise; Grelier, Aurore; Mould, Sarah; Barin, Carole; Daudignon, Agnes; Gachard, Nathalie; Struski, Stéphanie; Henry, Catherine; Penther, Dominique; Mossafa, Hossein; Andrieux, Joris; Eclache, Virginie; Bilhou-Nabera, Chrystèle; Luquet, Isabelle; Terre, Christine; Baranger, Laurence; Mugneret, Francine; Chiesa, Jean; Mozziconacci, Marie-Joelle; Callet-Bauchu, Evelyne; Veronese, Lauren; Blons, Hélène; Owen, Roger; Lejeune, Julie; Chevret, Sylvie; Merle-Beral, Hélène; Leblondon, Véronique