Diagnostic Yield and Clinical Impact of Germline Sequencing in Children with CNS and Extracranial Solid Tumors—a Nationwide, Prospective Swedish Study
Bianca Tesi,Kristina Lagerstedt Robinson,Frida Abel,Teresita Diaz de Stahl,Sara Orrsjoe,Anna Poluha, Maria Hellberg,Sandra Wessman,Sofie Samuelsson,Tony Frisk,Hartmut Vogt, Karin Henning,Magnus Sabel,Torben Ek,Niklas Pal,Per Nyman,Geraldine Giraud,Joakim Wille,Cornelis Jan Pronk,Ulrika Noren-Nystroem,Magnus Borssen,Maria Fili,Gustav Stalhammar,Nikolas Herold,Giorgio Tettamanti,Carolina Maya-Gonzalez,Linda Arvidsson,Anna Rosen,Katja Ekholm,Ekaterina Kuchinskaya,Anna-Lotta Hallbeck,Margareta Nordling, Pia Palmebaeck,Per Kogner,Gunilla Kanter Smoler, Paeivi Laehteenmaeki, Susanne Fransso,Tommy Martinsson, Alia Shamik,Fredrik Mertens,Richard Rosenquist,Valtteri Wirta,Emma Tham,Pernilla Grillner,Johanna Sandgren,Gustaf Ljungman,David Gisselsson,Fulya Taylan,Ann Nordgren LANCET REGIONAL HEALTH-EUROPE（2024）
Key words
Childhood cancer predisposition,Whole-genome sequencing,Germline variants,Somatic mutations
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