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

Single cell transcriptional evolution of myeloid leukemia of Down syndrome

唐氏综合征髓系白血病的单细胞转录演变

Trinh, Mi K; Schuschel, Konstantin; Issa, Hasan; Thomas, Rebecca; Parks, Conor; Oszlanczi, Agnes; Ogbonnah, Toochi; Zhou, Di; Mamanova, Lira; Prigmore, Elena; Robertson, Emilia R; Hodder, Angus; Wenger, Anna; Anderson, Nathaniel D; Whitfield, Holly J; Treger, Taryn D; Gonçalves-Dias, José; Straathof, Karin; O'Connor, David; Young, Matthew D; Jardine, Laura; Adams, Stuart; Klusmann, Jan-Henning; Bartram, Jack; Behjati, Sam

Improving the diagnosis of renal tumours of young people through integrated molecular analysis

通过综合分子分析提高青少年肾脏肿瘤的诊断率

Leiter, Sarah M; Guobadia, Aisosa O; Fleming, Ben; Ajithkumar, Thankamma V; Armitage, James N; Burke, G A Amos; Burns, Charlotte M; Coleman, Nicholas; Hatcher, Helen; Horan, Gail; Long, Anna-May; McDonald, Sarah; Mitchell, Thomas J; Nicholson, James C; Roberts, Thomas; Stewart, Grant D; Tadross, John A; Tarpey, Patrick S; Trayers, Claire; Trotman, Jamie; Watkins, James A; Warren, Anne Y; Vujanic, Gordan M; Armstrong, Ruth; Behjati, Sam; Hook, C Elizabeth; Murray, Matthew J

Predisposition Footprints in the Somatic Genome of Wilms Tumors

肾母细胞瘤体细胞基因组中的易感性足迹

Treger, Taryn D; Wegert, Jenny; Wenger, Anna; Coorens, Tim H H; Al-Saadi, Reem; Kemps, Paul G; Kennedy, Jonathan; Parks, Conor; Anderson, Nathaniel D; Hodder, Angus; Letunovska, Aleksandra; Jung, Hyunchul; Ogbonnah, Toochi; Trinh, Mi K; Lee-Six, Henry; Morcrette, Guillaume; van den Heuvel-Eibrink, Marry M; Drost, Jarno; van Boxtel, Ruben; Bertrums, Eline J M; Goemans, Bianca F; Antoniou, Evangelia; Reinhardt, Dirk; Streitenberger, Heike; Ziegler, Barbara; Bartram, Jack; Hutchinson, John C; Vujanic, Gordan M; Vokuhl, Christian; Chowdhury, Tanzina; Furtwängler, Rhoikos; Graf, Norbert; Pritchard-Jones, Kathy; Gessler, Manfred; Behjati, Sam

A non-canonical lymphoblast in refractory childhood T-cell leukaemia

难治性儿童T细胞白血病中的非典型淋巴母细胞

Lim, Bram S J; Whitfield, Holly J; Trinh, Mi K; Bloye, Gianna; Thomas, Rebecca; Anderson, Nathaniel D; Wenger, Anna; Hodder, Angus; Treger, Taryn D; Lee-Six, Henry; Coorens, Tim H H; Parks, Conor; Ogbonnah, Toochi; Pölönen, Petri; Mullighan, Charles G; Teachey, David T; Xu, Jason; Tan, Kai; Hagleitner, Melanie; Kester, Lennart; van Leeuwen, Frank N; Beattie, Gordon; Mansour, Marc R; Williams, Owen; Bartram, Jack; Adams, Stuart; Jardine, Laura; Behjati, Sam; O'Connor, David

High resolution clonal architecture of hypomutated Wilms tumours.

低突变型 Wilms 肿瘤的高分辨率克隆结构

Lee-Six Henry, Treger Taryn D, Dave Manas, Coorens Tim Hh, Anderson Nathaniel D, Tiersma Yvonne, Derakhshan Sepide, de Haan Sanne, van den Heuvel-Eibrink Marry M, Wang Yichen, Wenger Anna, Al-Saadi Reem, Lawford Alice, Letunovska Aleksandra, Wegert Jenny, Parks Conor, Morcrette Guillaume, Gessler Manfred, Vujanic Gordan, Chowdhury Tanzina, J O'Sullivan Maureen, de Krijger Ronald R, Stratton Michael R, Pritchard-Jones Kathy, Hutchinson J Ciaran, Drost Jarno, Behjati Sam

Distinct pathways for genetic and epigenetic predisposition in familial and bilateral Wilms tumor

家族性和双侧肾母细胞瘤的遗传和表观遗传易感性存在不同的途径

Wegert, Jenny; Appenzeller, Silke; Treger, Taryn D; Streitenberger, Heike; Ziegler, Barbara; Bausenwein, Sabrina; Vokuhl, Christian; Parks, Conor; Jüttner, Eva; Gramlich, Susanne; Ernestus, Karen; Warman, Steven W; Fuchs, Jörg; Hubertus, Jochen; von Schweinitz, Dietrich; Fröhlich, Birgit; Jorch, Norbert; Knöfler, Ralf; Friedrich, Carsten; Corbacioglu, Selim; Frühwald, Michael C; Pekrun, Arnulf; Schneider, Dominik T; Faber, Jörg; Stursberg, Jana; Metzler, Markus; Welter, Nils; Pritchard-Jones, Kathy; Graf, Norbert; Furtwängler, Rhoikos; Behjati, Sam; Gessler, Manfred

Lingual hamartoma-like lipoblastoma: the diagnostic value of routine whole-genome sequencing

舌部错构瘤样脂肪母细胞瘤:常规全基因组测序的诊断价值

Kan, Sheng-Yuan; Ferro, Ashley; Watkins, James A; Behjati, Sam; Murray, Matthew J; Coleman, Nicholas; Roberts, Thomas; Cross, Justin; Trotman, Jamie; Tarpey, Patrick; Hook, C Elizabeth; Cameron, Malcolm; Tadross, John A

Wilms tumor primary cultures capture phenotypic heterogeneity and facilitate preclinical screening.

Wilms肿瘤原代培养物能够捕捉表型异质性,并有助于临床前筛选

Götz Lisa, Wegert Jenny, Paikari Alireza, Appenzeller Silke, Bausenwein Sabrina, Vokuhl Christian, Treger Taryn D, Drost Jarno, Linderkamp Christin, Schneider Dominik T, Ernestus Karen, Warman Steven W, Fuchs Jörg, Welter Nils, Graf Norbert, Behjati Sam, Furtwängler Rhoikos, Gessler Manfred

Advancing sarcoma diagnostics with expanded DNA methylation-based classification

利用扩展的基于DNA甲基化的分类推进肉瘤诊断

Jäger, Natalie; Reuss, David E; Sill, Martin; Schrimpf, Daniel; Suwala, Abigail K; Sievers, Philipp; Banan, Rouzbeh; Hinz, Felix; Rahmanzade, Ramin; Bogumil, Henry; Aras, Kaan Fuat; Patel, Areeba; Korshunov, Andrey; Bewerunge-Hudler, Melanie; Cleven, Arjen Hg; Esteller, Manel; Glimm, Hanno; Hartmann, Wolfgang; Kreutzfeld, Simon; Heilig, Christoph; Milde, Till; Petersen, Iver; Vokuhl, Christian M; Wick, Wolfgang; Witt, Olaf; Kervarrec, Thibault; Miele, Evelina; Serrano, Jonathan; Frank, Stephan; Kashofer, Karl; Leer, Anne Mc; Pfaff, Elke; Pages, Melanie; Tauziede-Espariat, Arnault; Toberer, Ferdinand; Boldt, Henning B; Martinek, Petr; Brandner, Sebastian; Euzebio, Mayara; Siegfried, Aurore; Chalker, Jane; Harter, Patrik; Appay, Romain; Dietmaier, Wolfgang; Hasselblatt, Martin; Flucke, Uta E; Hiemcke-Jiwa, Laura S; Solomon, David; Frydrychowicz, Clara; Varlet, Pascale; Goeppert, Benjamin; Nathrath, Michaela; Blattmann, Claudia; Sparber-Sauer, Monika; Kolb, August; Mittelbronn, Michel; Mentzel, Thomas; Leisz, Sandra; Harder, Anja; Acker, Till; Pratt, Drew; Wardelmann, Eva; Benhamida, Jamal; Ladanyi, Mark; Jurmeister, Philipp; Foulkes, William; Ajuyah, Pamela; Ziegler, David Z; Hench, Jürgen; Nederkoorn, Maikel Jl; Versleijen-Jonkers, Yvonne Mh; Mechtersheimer, Gunhild; Krieg, Sandro; Gessler, Manfred; Baumhoer, Daniel; Behjati, Sam; Bertero, Luca; Griwank, Klaus; Schadendorf, Dirk; Hogendoorn, Pancras Cw; Emile, Jean-Francois; Kemps, Paul G; Jarosch, Armin; Ronellenfitsch, Michael W; Idler, Toni Su; Aust, Daniela; Herold, Sylvia; Pablik, Jessica; Al-Hussaini, Maysa; Abdullaev, Zied; Yeung, Maximus; Wachtel, Marco; Brack, Eva; Kommoss, Felix Kf; Miettinen, Markku; Aldape, Ken; Flanagan, Adrienne Mh; Dirksen, Uta; Pajtler, Kristian; Grünewald, Thomas Gp; Lipka, Daniel; Fröhling, Stefan; Koelsche, Christian; Snuderl, Matija; Capper, David; Pfister, Stefan M; Jones, David Tw; Sahm, Felix; von Deimling, Andreas

Benefits for children with suspected cancer from routine whole-genome sequencing

常规全基因组测序对疑似癌症儿童的益处

Hodder, Angus; Leiter, Sarah M; Kennedy, Jonathan; Addy, Dilys; Ahmed, Munaza; Ajithkumar, Thankamma; Allinson, Kieren; Ancliff, Phil; Bailey, Shivani; Barnard, Gemma; Burke, G A Amos; Burns, Charlotte; Cano-Flanagan, Julian; Chalker, Jane; Coleman, Nicholas; Cheng, Danny; Clinch, Yasmin; Dryden, Caryl; Ghorashian, Sara; Griffin, Blanche; Horan, Gail; Hubank, Michael; May, Phillippa; McDerra, Joanna; Nagrecha, Rajvi; Nicholson, James; O'Connor, David; Pavasovic, Vesna; Quaegebeur, Annelies; Rao, Anupama; Roberts, Thomas; Samarasinghe, Sujith; Stasevich, Iryna; Tadross, John A; Trayers, Claire; Trotman, Jamie; Vora, Ajay; Watkins, James; Chitty, Lyn S; Bowdin, Sarah; Armstrong, Ruth; Murray, Matthew J; Hook, Catherine E; Tarpey, Patrick; Vedi, Aditi; Bartram, Jack; Behjati, Sam