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Cancer risk and tumour spectrum in 172 patients with a germline SUFU pathogenic variation: a collaborative study of the SIOPE Host Genome Working Group.
Guerrini-Rousseau, Léa; Masliah-Planchon, Julien; Waszak, Sebastian M; Alhopuro, Pia; Benusiglio, Patrick R; Bourdeaut, Franck; Brecht, Ines B; Del Baldo, Giada; Dhanda, Sandeep Kumar; Garrè, Maria Luisa; Gidding, Corrie E M; Hirsch, Steffen; Hoarau, Pauline; Jorgensen, Mette; Kratz, Christian; Lafay-Cousin, Lucie; Mastronuzzi, Angela; Pastorino, Lorenza; Pfister, Stefan M; Schroeder, Christopher; Smith, Miriam Jane; Vahteristo, Pia; Vibert, Roseline; Vilain, Catheline; Waespe, Nicolas; Winship, Ingrid M; Evans, D Gareth; Brugieres, Laurence.
Afiliação
  • Guerrini-Rousseau L; Department of Children and Adolescents Oncology, Gustave Roussy, Villejuif, France lea.guerrini-rousseau@gustaveroussy.fr.
  • Masliah-Planchon J; Team "Genomics and Oncogenesis of pediatric Brain Tumors"-Paris Saclay University, INSERM U981, VILLEJUIF, France.
  • Waszak SM; INSERM U830, Laboratory of Translational Research in Pediatric Oncology, SIREDO Pediatric Oncology Center, Institute Curie, Paris, France.
  • Alhopuro P; Centre for Molecular Medicine Norway (NCMM), Nordic EMBL Partnership, University of Oslo and Oslo University Hospital, Oslo, Norway.
  • Benusiglio PR; Department of Pediatric Research, Oslo University Hospital, Oslo, Norway.
  • Bourdeaut F; Department of Medical and Clinical Genetics, University of Helsinki, Helsinki, Finland.
  • Brecht IB; Département de Génétique et Institut Universitaire de Cancérologie, Sorbonne University Faculty of Medicine Pitié-Salpêtrière Campus, Paris, France.
  • Del Baldo G; INSERM U830, Laboratory of Translational Research in Pediatric Oncology, SIREDO Pediatric Oncology Center, Institute Curie, Paris, France.
  • Dhanda SK; Department of Pediatric Oncology and Hematology, University Hospitals Tubingen, Tubingen, Germany.
  • Garrè ML; Department of Hematology/Oncology, Cell Therapy, Gene Therapy and Hemopoietic Transplant, IRCCS, Bambino Gesu Pediatric Hospital, Roma, Italy.
  • Gidding CEM; Department of Oncology, St Jude Children's Research Hospital, Memphis, Tennessee, USA.
  • Hirsch S; Neuro-Oncology Unit, Department of Neurochirurgia, IRCCS Istituto Giannina Gaslini, Genova, Italy.
  • Hoarau P; Neuro-Oncology Department, Princess Maxima Center for Pediatric Oncology, Utrecht, The Netherlands.
  • Jorgensen M; Institute of Human Genetics, University Hospital Heidelberg, Heidelberg, Germany.
  • Kratz C; Hopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg Health Center, Heidelberg, Germany.
  • Lafay-Cousin L; Department of Children and Adolescents Oncology, Gustave Roussy, Villejuif, France.
  • Mastronuzzi A; Oncology, Great Ormond Street Hospital For Children NHS Foundation Trust, London, UK.
  • Pastorino L; Paediatric Haematology and Oncology, Hannover Medical School, Hannover, Germany.
  • Pfister SM; Section of Pediatric Hematology Oncology and Bone Marrow Transplantation, Alberta Children's Hospital and Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Schroeder C; Pediatric Hematology/Oncology and Stem Cells Transplatation, Bambino Gesu Pediatric Hospital, Roma, Italy.
  • Smith MJ; Department of Oncology, Biology and Genetics, University of Genoa, Genoa, Italy.
  • Vahteristo P; Genetics of Rare Cancers, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
  • Vibert R; Hopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg Health Center, Heidelberg, Germany.
  • Vilain C; Division of Pediatric Neurooncology, DKFZ, Heidelberg, Germany.
  • Waespe N; Department of Pediatric Oncology, Hematology and Immunology, University Hospital Heidelberg, Heidelberg, Germany.
  • Winship IM; Institute of Medical Genetics and Applied Genomics, University of Tubingen Institute of Human Genetics, Tubingen, Germany.
  • Evans DG; Division of Evolution, Infection and Genomics, The University of Manchester, Manchester, UK.
  • Brugieres L; Department of Medical and Clinical Genetics, University of Helsinki, Helsinki, Finland.
J Med Genet ; 2022 Jun 29.
Article em En | MEDLINE | ID: mdl-35768194
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Risk_factors_studies Idioma: En Revista: J Med Genet Ano de publicação: 2022 Tipo de documento: Article País de afiliação: França
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Risk_factors_studies Idioma: En Revista: J Med Genet Ano de publicação: 2022 Tipo de documento: Article País de afiliação: França