The evolutionary impact of childhood cancer on the human gene pool
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DOI: 10.1038/s41467-024-45975-9
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- Jeremy Schwartzentruber & Andrey Korshunov & Xiao-Yang Liu & David T. W. Jones & Elke Pfaff & Karine Jacob & Dominik Sturm & Adam M. Fontebasso & Dong-Anh Khuong Quang & Martje Tönjes & Volker Hovesta, 2012. "Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma," Nature, Nature, vol. 482(7384), pages 226-231, February.
- Xiaotu Ma & Yu Liu & Yanling Liu & Ludmil B. Alexandrov & Michael N. Edmonson & Charles Gawad & Xin Zhou & Yongjin Li & Michael C. Rusch & John Easton & Robert Huether & Veronica Gonzalez-Pena & Mark , 2018. "Pan-cancer genome and transcriptome analyses of 1,699 paediatric leukaemias and solid tumours," Nature, Nature, vol. 555(7696), pages 371-376, March.
- Isabella Versteege & Nicolas Sévenet & Julian Lange & Marie-Françoise Rousseau-Merck & Peter Ambros & Rupert Handgretinger & Alain Aurias & Olivier Delattre, 1998. "Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer," Nature, Nature, vol. 394(6689), pages 203-206, July.
- Konrad J. Karczewski & Laurent C. Francioli & Grace Tiao & Beryl B. Cummings & Jessica Alföldi & Qingbo Wang & Ryan L. Collins & Kristen M. Laricchia & Andrea Ganna & Daniel P. Birnbaum & Laura D. Gau, 2020. "The mutational constraint spectrum quantified from variation in 141,456 humans," Nature, Nature, vol. 581(7809), pages 434-443, May.
- Nazneen Rahman, 2014. "Correction: Corrigendum: Realizing the promise of cancer predisposition genes," Nature, Nature, vol. 510(7503), pages 176-176, June.
- Sebastian M. Waszak & Giles W, Robinson & Brian L. Gudenas & Kyle S. Smith & Antoine Forget & Marija Kojic & Jesus Garcia-Lopez & Jennifer Hadley & Kayla V. Hamilton & Emilie Indersie & Ivo Buchhalter, 2020. "Germline Elongator mutations in Sonic Hedgehog medulloblastoma," Nature, Nature, vol. 580(7803), pages 396-401, April.
- Zhi-Yan Han & Wilfrid Richer & Paul Fréneaux & Céline Chauvin & Carlo Lucchesi & Delphine Guillemot & Camille Grison & Delphine Lequin & Gaelle Pierron & Julien Masliah-Planchon & André Nicolas & Domi, 2016. "The occurrence of intracranial rhabdoid tumours in mice depends on temporal control of Smarcb1 inactivation," Nature Communications, Nature, vol. 7(1), pages 1-11, April.
- Jeremie Vitte & Fuying Gao & Giovanni Coppola & Alexander R. Judkins & Marco Giovannini, 2017. "Timing of Smarcb1 and Nf2 inactivation determines schwannoma versus rhabdoid tumor development," Nature Communications, Nature, vol. 8(1), pages 1-13, December.
- Nazneen Rahman, 2014. "Realizing the promise of cancer predisposition genes," Nature, Nature, vol. 505(7483), pages 302-308, January.
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