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

Sequential Analysis of cfDNA Reveals Clonal Evolution in Patients with Neuroblastoma Receiving ALK-Targeted Therapy

对接受ALK靶向治疗的神经母细胞瘤患者的cfDNA进行序列分析揭示了克隆演变

Bobin, Charles; Iddir, Yasmine; Butterworth, Charlotte; Masliah-Planchon, Julien; Saint-Charles, Alexandra; Bellini, Angela; Bhalshankar, Jaydutt; Pierron, Gaelle; Combaret, Valérie; Attignon, Valéry; André, Nicolas; Corradini, Nadège; Dumont, Benoit; Mansuy, Ludovic; Khanfar, Camille; Klein, Sebastien; Briandet, Claire; Plantaz, Dominique; Millot, Frederic; Thouvenin, Sandrine; Aerts, Isabelle; Ndounga-Diakou, Lee Aymar; Laghouati, Salim; Abbou, Samuel; Jehanno, Nina; Tissot, Hubert; Renault, Shufang; Baulande, Sylvain; Raynal, Virginie; Bozec, Laurence; Bieche, Ivan; Delattre, Olivier; Berlanga, Pablo; Schleiermacher, Gudrun

Frequency and Prognostic Impact of ALK Amplifications and Mutations in the European Neuroblastoma Study Group (SIOPEN) High-Risk Neuroblastoma Trial (HR-NBL1)

欧洲神经母细胞瘤研究组(SIOPEN)高危神经母细胞瘤试验(HR-NBL1)中ALK扩增和突变的频率及预后影响

Bellini, Angela; Pötschger, Ulrike; Bernard, Virginie; Lapouble, Eve; Baulande, Sylvain; Ambros, Peter F; Auger, Nathalie; Beiske, Klaus; Bernkopf, Marie; Betts, David R; Bhalshankar, Jaydutt; Bown, Nick; de Preter, Katleen; Clément, Nathalie; Combaret, Valérie; Font de Mora, Jaime; George, Sally L; Jiménez, Irene; Jeison, Marta; Marques, Barbara; Martinsson, Tommy; Mazzocco, Katia; Morini, Martina; Mühlethaler-Mottet, Annick; Noguera, Rosa; Pierron, Gaelle; Rossing, Maria; Taschner-Mandl, Sabine; Van Roy, Nadine; Vicha, Ales; Chesler, Louis; Balwierz, Walentyna; Castel, Victoria; Elliott, Martin; Kogner, Per; Laureys, Geneviève; Luksch, Roberto; Malis, Josef; Popovic-Beck, Maja; Ash, Shifra; Delattre, Olivier; Valteau-Couanet, Dominique; Tweddle, Deborah A; Ladenstein, Ruth; Schleiermacher, Gudrun

The yield of postmortem genetic testing in sudden death cases with structural findings at autopsy

尸检发现结构异常的猝死病例中,死后基因检测的阳性率

Lahrouchi, Najim; Raju, Hariharan; Lodder, Elisabeth M; Papatheodorou, Stathis; Miles, Chris; Ware, James S; Papadakis, Michael; Tadros, Rafik; Cole, Della; Skinner, Jonathan R; Crawford, Jackie; Love, Donald R; Pua, Chee J; Soh, Bee Y; Bhalshankar, Jaydutt D; Govind, Risha; Tfelt-Hansen, Jacob; Winkel, Bo G; van der Werf, Christian; Wijeyeratne, Yanushi D; Mellor, Greg; Till, Janice; Cohen, Marta; Tome-Esteban, Maria; Sharma, Sanjay; Wilde, Arthur A M; Cook, Stuart A; Sheppard, Mary N; Bezzina, Connie R; Behr, Elijah R

Study of chromatin remodeling genes implicates SMARCA4 as a putative player in oncogenesis in neuroblastoma.

染色质重塑基因的研究表明,SMARCA4 可能是神经母细胞瘤发生过程中的一个潜在因素

Bellini Angela, Bessoltane-Bentahar Nadia, Bhalshankar Jaydutt, Clement Nathalie, Raynal Virginie, Baulande Sylvain, Bernard Virginie, Danzon Adrien, Chicard Mathieu, Colmet-Daage Léo, Pierron Gaelle, Le Roux Laura, Planchon Julien M, Combaret Valérie, Lapouble Eve, Corradini Nadège, Thebaud Estelle, Gambart Marion, Valteau-Couanet Dominique, Michon Jean, Louis-Brennetot Caroline, Janoueix-Lerosey Isabelle, Defachelles Anne-Sophie, Bourdeaut Franck, Delattre Olivier, Schleiermacher Gudrun

Traditional clinical criteria outperform high-sensitivity C-reactive protein for the screening of hepatic nuclear factor 1 alpha maturity-onset diabetes of the young among young Asians with diabetes

在年轻亚洲糖尿病患者中,传统临床标准在筛查肝核因子1α阳性青少年起病型糖尿病方面优于高敏C反应蛋白。

Rama Chandran, Suresh; Bhalshankar, Jaydutt; Farhad Vasanwala, Rashida; Zhao, Yi; Owen, Katharine R; Su-Lyn Gardner, Daphne

Utility of Post-Mortem Genetic Testing in Cases of Sudden Arrhythmic Death Syndrome

死后基因检测在猝死综合征病例中的应用价值

Lahrouchi, Najim; Raju, Hariharan; Lodder, Elisabeth M; Papatheodorou, Efstathios; Ware, James S; Papadakis, Michael; Tadros, Rafik; Cole, Della; Skinner, Jonathan R; Crawford, Jackie; Love, Donald R; Pua, Chee J; Soh, Bee Y; Bhalshankar, Jaydutt D; Govind, Risha; Tfelt-Hansen, Jacob; Winkel, Bo G; van der Werf, Christian; Wijeyeratne, Yanushi D; Mellor, Greg; Till, Jan; Cohen, Marta C; Tome-Esteban, Maria; Sharma, Sanjay; Wilde, Arthur A M; Cook, Stuart A; Bezzina, Connie R; Sheppard, Mary N; Behr, Elijah R

Development of a Comprehensive Sequencing Assay for Inherited Cardiac Condition Genes

开发用于检测遗传性心脏病基因的综合测序方法

Pua, Chee Jian; Bhalshankar, Jaydutt; Miao, Kui; Walsh, Roddy; John, Shibu; Lim, Shi Qi; Chow, Kingsley; Buchan, Rachel; Soh, Bee Yong; Lio, Pei Min; Lim, Jaclyn; Schafer, Sebastian; Lim, Jing Quan; Tan, Patrick; Whiffin, Nicola; Barton, Paul J; Ware, James S; Cook, Stuart A