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Page 1
Wilms tumor primary cultures capture phenotypic heterogeneity and facilitate preclinical screening.
Götz L, Wegert J, Paikari A, Appenzeller S, Bausenwein S, Vokuhl C, Treger TD, Drost J, Linderkamp C, Schneider DT, Ernestus K, Warman SW, Fuchs J, Welter N, Graf N, Behjati S, Furtwängler R, Gessler M. Götz L, et al. Among authors: behjati s. Transl Oncol. 2024 Dec 30;52:102263. doi: 10.1016/j.tranon.2024.102263. Online ahead of print. Transl Oncol. 2024. PMID: 39740515 Free article.
Predisposition footprints in the somatic genome of Wilms tumours.
Treger TD, Wegert J, Wenger A, Coorens THH, Al-Saadi R, Kemps PG, Kennedy J, Parks C, Anderson ND, Hodder A, Letunovska A, Jung H, Ogbonnah T, Trinh MK, Lee-Six H, Morcrette G, van den Heuvel-Eibrink MM, Drost J, van Boxtel R, Bertrums EJM, Goemans BF, Antoniou E, Reinhardt D, Streitenberger H, Ziegler B, Bartram J, Hutchinson JC, Vujanic GM, Vokuhl C, Chowdhury T, Furtwängler R, Graf N, Pritchard-Jones K, Gessler M, Behjati S. Treger TD, et al. Among authors: behjati s. Cancer Discov. 2024 Dec 12. doi: 10.1158/2159-8290.CD-24-0878. Online ahead of print. Cancer Discov. 2024. PMID: 39665570
HOX gene expression in the developing human spine.
Lawrence JEG, Roberts K, Tuck E, Li T, Mamanova L, Balogh P, Usher I, Piapi A, Mazin P, Anderson ND, Bolt L, Richardson L, Prigmore E, He X, Barker RA, Flanagan A, Young MD, Teichmann SA, Bayraktar O, Behjati S. Lawrence JEG, et al. Among authors: behjati s. Nat Commun. 2024 Nov 20;15(1):10023. doi: 10.1038/s41467-024-54187-0. Nat Commun. 2024. PMID: 39567486 Free PMC article.
A diagnosis of Noonan syndrome through routine whole genome sequencing in a child with an intracranial nongerminomatous germ cell tumor.
Mahmood S, Leiter SM, Phyu P, Craven C, Horan G, Gains J, Briggs M, Blanco E, Behjati S, Watkins J, Tadross JA, Roberts T, Trotman J, Tarpey P, Armstrong R, Murray MJ. Mahmood S, et al. Among authors: behjati s. Pediatr Blood Cancer. 2024 Dec;71(12):e31368. doi: 10.1002/pbc.31368. Epub 2024 Oct 8. Pediatr Blood Cancer. 2024. PMID: 39380176 No abstract available.
Multifocal, multiphenotypic tumours arising from an MTOR mutation acquired in early embryogenesis.
Pacyna CN, Anandapadamanaban M, Loudon KW, Hay IM, Perisic O, Li R, Byrne M, Allen L, Roberts K, Hooks Y, Warren AY, Stewart GD, Clatworthy MR, Teichmann SA, Behjati S, Campbell PJ, Williams RL, Mitchell TJ. Pacyna CN, et al. Among authors: behjati s. Oncogene. 2024 Oct;43(44):3268-3276. doi: 10.1038/s41388-024-03137-7. Epub 2024 Sep 13. Oncogene. 2024. PMID: 39271965 Free PMC article.
Benefits for children with suspected cancer from routine whole-genome sequencing.
Hodder A, Leiter SM, Kennedy J, Addy D, Ahmed M, Ajithkumar T, Allinson K, Ancliff P, Bailey S, Barnard G, Burke GAA, Burns C, Cano-Flanagan J, Chalker J, Coleman N, Cheng D, Clinch Y, Dryden C, Ghorashian S, Griffin B, Horan G, Hubank M, May P, McDerra J, Nagrecha R, Nicholson J, O'Connor D, Pavasovic V, Quaegebeur A, Rao A, Roberts T, Samarasinghe S, Stasevich I, Tadross JA, Trayers C, Trotman J, Vora A, Watkins J, Chitty LS, Bowdin S, Armstrong R, Murray MJ, Hook CE, Tarpey P, Vedi A, Bartram J, Behjati S. Hodder A, et al. Among authors: behjati s. Nat Med. 2024 Jul;30(7):1905-1912. doi: 10.1038/s41591-024-03056-w. Epub 2024 Jul 2. Nat Med. 2024. PMID: 38956197 Free PMC article.
179 results