부산대학교 도서관

Blackburn PR; Department of Pathology, St. Jude Children's Research Hospital, Memphis, TN, USA.; Ebstein F; Institute of Medical Biochemistry and Molecular Biology, University Medicine Greifswald, Greifswald, Germany.; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du Thorax, Nantes, France.; Hsieh TC; Institute of Genomic Statistics and Bioinformatics, University of Bonn, Bonn, Germany.; Motta M; Molecular Genetics and Functional Genomics, Ospedale Pediatrico Bambino Gesù, IRCCS, Rome, Italy.; Radio FC; Molecular Genetics and Functional Genomics, Ospedale Pediatrico Bambino Gesù, IRCCS, Rome, Italy.; Herkert JC; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.; Rinne T; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.; Thiffault I; Center for Pediatric Genomic Medicine, Children's Mercy Hospital, Kansas City, MO, USA.; Department of Pathology and Laboratory Medicine, Children's Mercy Hospitals, Kansas City, MO, USA.; Rapp M; Department of Pediatrics-Clinical Genetics and Metabolism, Children's Hospital Colorado, Aurora, CO, USA.; Alders M; Amsterdam University Medical Center, University of Amsterdam, Department of Clinical Genetics, Amsterdam, The Netherlands.; Maas S; Amsterdam University Medical Center, University of Amsterdam, Department of Clinical Genetics, Amsterdam, The Netherlands.; Gerard B; Unité de Biologie et de Génétique Moléculaire, Center Hospitalier Universitaire de Strasbourg, Strasbourg, France.; Smol T; Univ Lille, CHU Lille, RADEME Team, Institut de Génétique Médicale, Lille, France.; Vincent-Delorme C; Department of Clinical Genetics, Hôpital Jeanne de Flandre, CHU Lille, Lille, France.; Cogné B; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du Thorax, Nantes, France.; Nantes Université, CHU de Nantes, Service de Génétique Médicale, Nantes, France.; Isidor B; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du Thorax, Nantes, France.; Nantes Université, CHU de Nantes, Service de Génétique Médicale, Nantes, France.; Vincent M; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du Thorax, Nantes, France.; Nantes Université, CHU de Nantes, Service de Génétique Médicale, Nantes, France.; Bachmann-Gagescu R; Institute of Medical Genetics, University of Zurich, Schlieren, Switzerland.; Department of Molecular Life Sciences, University of Zurich, Zurich, Switzerland.; Rauch A; Institute of Medical Genetics, University of Zurich, Schlieren, Switzerland.; Joset P; Medical Genetics, Institute of Medical Genetics and Pathology, University Hospital Basel, Basel, Switzerland.; Ferrero GB; Department of Clinical and Biological Sciences, San Luigi Gonzaga University Hospital, University of Torino, Turin, Italy.; Ciolfi A; Molecular Genetics and Functional Genomics, Ospedale Pediatrico Bambino Gesù, IRCCS, Rome, Italy.; Husson T; Department of Research, Center Hospitalier du Rouvray, Rouen, France.; Normandie Univ, UNIROUEN, Inserm U1245 and CHU Rouen, Department of Genetics and Reference Center for Developmental Disorders, Rouen, France.; Guerrot AM; Normandie Univ, UNIROUEN, Inserm U1245 and CHU Rouen, Department of Genetics and Reference Center for Developmental Disorders, Rouen, France.; Bacino C; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Macmurdo C; Division of Medical Genetics, Department of Internal Medicine, Baylor Scott and White Medical Center, Temple, TX, USA.; Thompson SS; Division of Medical Genetics, Department of Internal Medicine, Baylor Scott and White Medical Center, Temple, TX, USA.; Rosenfeld JA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Baylor Genetics, Houston, TX, USA.; Faivre L; Centre de Génétique et Centre de Référence Anomalies du Développement et Syndromes Malformatifs, FHU TRANSLAD CHU, Dijon, France.; INSERM UMR1231, équipe GAD, Université de Bourgogne-Franche Comté, Dijon, France.; Mau-Them FT; INSERM UMR1231, équipe GAD, Université de Bourgogne-Franche Comté, Dijon, France.; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; Deb W; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du Thorax, Nantes, France.; Nantes Université, CHU de Nantes, Service de Génétique Médicale, Nantes, France.; Vignard V; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du Thorax, Nantes, France.; Nantes Université, CHU de Nantes, Service de Génétique Médicale, Nantes, France.; Agrawal PB; Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston, MA, USA.; Division of Neonatology, Department of Pediatrics, University of Miami Miller School of Medicine and Holtz Children's Hospital, Jackson Health System, Miami, FL, USA.; Madden JA; Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston, MA, USA.; Division of Neonatology, Department of Pediatrics, University of Miami Miller School of Medicine and Holtz Children's Hospital, Jackson Health System, Miami, FL, USA.; Goldenberg A; Normandie Univ, UNIROUEN, Inserm U1245 and CHU Rouen, Department of Genetics and Reference Center for Developmental Disorders, Rouen, France.; Lecoquierre F; Normandie Univ, UNIROUEN, Inserm U1245 and CHU Rouen, Department of Genetics and Reference Center for Developmental Disorders, Rouen, France.; Zech M; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany.; Institute of Human Genetics, School of Medicine, Technical University of Munich, Munich, Germany.; Institute for Advanced Study, Technical University of Munich, Garching, Germany.; Prokisch H; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany.; Institute of Human Genetics, School of Medicine, Technical University of Munich, Munich, Germany.; Institute for Advanced Study, Technical University of Munich, Garching, Germany.; Necpál J; Department of Neurology, Zvolen Hospital, Zvolen, Slovakia.; Department of Neurology, Faculty of Medicine, Comenius University, Bratislava, Slovakia.; Jech R; Department of Neurology, Charles University, First Faculty of Medicine and General University Hospital, Prague, Czech Republic.; Winkelmann J; Institute of Neurogenomics, Helmholtz Zentrum Muenchen, Neuherberg, Germany.; Neurogenetics, Technische Universitaet Muenchen, Munich, Germany.; Institute of Human Genetics, Klinikum rechts der Isar der TUM, Munich, Germany.; Munich Cluster for Systems Neurology (SyNergy), Munich, Germany.; Koprušáková MT; Jessenius Faculty of Medicine in Martin, Comenius University Bratislava, Martin, Slovakia.; Konstantopoulou V; Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.; Younce JR; Department of Neurology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.; Shinawi M; Division of Genetics and Genomic Medicine, St. Louis Children's Hospital, St. Louis, MO, USA.; Department of Neurology, Washington University School of Medicine, St. Louis, MO, USA.; Mighton C; Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, Canada.; Genomics Health Services and Policy Research Program, Li Ka Shing Knowledge Institute, St. Michael's Hospital, Unity Health Toronto, Toronto, Canada.; Fung C; The Fred A. Litwin Family Centre in Genetic Medicine, University Health Network and Sinai Health System, Toronto, Canada.; Department of Molecular Genetics, University of Toronto, Toronto, Canada.; Morel CF; The Fred A. Litwin Family Centre in Genetic Medicine, University Health Network and Sinai Health System, Toronto, Canada.; Department of Medicine, University of Toronto, Toronto, Canada.; Lerner-Ellis J; Pathology and Laboratory Medicine, Mount Sinai Hospital, Sinai Health, Toronto, Canada.; Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Canada.; Lunenfeld-Tanenbaum Research Institute, Sinai Health, Toronto, Canada.; DiTroia S; Center for Mendelian Genomics, Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Barth M; Department of Biochemistry and Genetics, University Hospital of Angers, Angers, France.; Mitovasc Unit, UMR CNRS 6015-INSERM 1083, Angers, France.; Bonneau D; Department of Biochemistry and Genetics, University Hospital of Angers, Angers, France.; Krapels I; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.; Department of Clinical Genetics and School for Oncology and Developmental Biology, Maastricht UMC, Maastricht, The Netherlands.; Stegmann APA; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.; Department of Clinical Genetics and School for Oncology and Developmental Biology, Maastricht UMC, Maastricht, The Netherlands.; van der Schoot V; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.; Department of Clinical Genetics and School for Oncology and Developmental Biology, Maastricht UMC, Maastricht, The Netherlands.; Brunet T; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, Munich, Germany.; Dr. v. Hauner Children's Hospital, Department of Pediatric Neurology and Developmental Medicine, LMU-University of Munich, Munich, Germany.; Bußmann C; Department of Neuropediatrics, ATOS Klinik Heidelberg, Heidelberg, Germany.; Mignot C; Département de Génétique, AP-HP-Sorbonne Université, Hôpital Trousseau & Groupe Hospitalier Pitié-Salpêtrière, Paris, France.; Zampino G; Center for Rare Diseases and Birth Defects, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.; Dipartimento di Scienze Della Vita e Sanità Pubblica, Università Cattolica del Sacro Cuore, Rome, Italy.; Wortmann SB; University Children's Hospital, Paracelsus Medical University (PMU), Salzburg, Austria.; Mayr JA; University Children's Hospital, Paracelsus Medical University (PMU), Salzburg, Austria.; Feichtinger RG; University Children's Hospital, Paracelsus Medical University (PMU), Salzburg, Austria.; Courtin T; Center for Molecular and Chromosomal Genetics, AP-HP-Sorbonne University, Pitié-Salpêtrière Hospital, Paris, France.; Ravelli C; Department of Pediatric Neurology and Neurogenetic Referral Center, AP-HP-Sorbonne Université, Armand Trousseau Hospital, Paris, France.; Keren B; Département de Génétique, AP-HP-Sorbonne Université, Hôpital Trousseau & Groupe Hospitalier Pitié-Salpêtrière, Paris, France.; Ziegler A; Mitovasc Unit, UMR CNRS 6015-INSERM 1083, Angers, France.; Department of Biochemistry and Genetics, Angers University Hospital and UMR CNRS, Angers, France.; Hasadsri L; Division of Laboratory Genetics and Genomics, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.; Pichurin PN; Department of Clinical Genomics, Mayo Clinic, Rochester, MN, USA.; Klee EW; Department of Clinical Genomics, Mayo Clinic, Rochester, MN, USA.; Department of Quantitative Health Sciences Research, Mayo Clinic, Rochester, MN, USA.; Center for Individualized Medicine, Mayo Clinic, Rochester, MN, USA.; Grand K; Department of Pediatrics, Guerin Children's at Cedars-Sinai Medical Center, Los Angeles, CA, USA.; Sanchez-Lara PA; Department of Pediatrics, Guerin Children's at Cedars-Sinai Medical Center, Los Angeles, CA, USA.; Krüger E; Institute of Medical Biochemistry and Molecular Biology, University Medicine Greifswald, Greifswald, Germany.; Bézieau S; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du Thorax, Nantes, France.; Nantes Université, CHU de Nantes, Service de Génétique Médicale, Nantes, France.; Klinkhammer H; Institute of Genomic Statistics and Bioinformatics, University of Bonn, Bonn, Germany.; Institute of Medical Biometry, Informatics and Epidemiology, University of Bonn, Bonn, Germany.; Krawitz PM; Institute of Genomic Statistics and Bioinformatics, University of Bonn, Bonn, Germany.; Eichler EE; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.; Howard Hughes Medical Institute, University of Washington, Seattle, WA, USA.; Tartaglia M; Molecular Genetics and Functional Genomics, Ospedale Pediatrico Bambino Gesù, IRCCS, Rome, Italy.; Küry S; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du Thorax, Nantes, France.; Nantes Université, CHU de Nantes, Service de Génétique Médicale, Nantes, France.; Wang T; Department of Medical Genetics, Center for Medical Genetics, School of Basic Medical Sciences, Peking University, Beijing, China.; Neuroscience Research Institute, Peking University, Beijing, China.; Key Laboratory for Neuroscience, Ministry of Education of China & National Health Commission of China, Beijing, China.; Autism Research Center, Peking University Health Science Center, Beijing, China.

Publisher: Wiley-Liss Country of Publication: United States NLM ID: 7707449 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1531-8249 (Electronic) Linking ISSN: 03645134 NLM ISO Abbreviation: Ann Neurol Subsets: MEDLINE

Seng E; Department of Neurology, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.; Lampl C; Department of Neurology, Konventhospital Barmherzige Brüder Linz, Linz, Austria.; Viktrup L; Eli Lilly and Company, Indianapolis, IN, USA. viktrup_lars@lilly.com.; Lilly Neuroscience, Lilly Corporate Center, DC 1745, 75/4, Indianapolis, IN, 46285, USA. viktrup_lars@lilly.com.; Lenderking WR; Evidera, 500 Totten Pond Road, Wilmington, NC, 28401, USA.; Karn H; Evidera, 500 Totten Pond Road, Wilmington, NC, 28401, USA.; Hoyt M; Eli Lilly and Company, Indianapolis, IN, USA.; Kim G; Eli Lilly and Company, Indianapolis, IN, USA.; Ruff D; Eli Lilly and Company, Indianapolis, IN, USA.; Ossipov MH; Evidera, 500 Totten Pond Road, Wilmington, NC, 28401, USA.; Vincent M; Eli Lilly and Company, Indianapolis, IN, USA.; School of Medicine, Federal University of Rio de Janeiro (UFRJ), Rio de Janeiro, 21044-020, RJ, Brazil.

Publisher: Adis Country of Publication: New Zealand NLM ID: 101634491 Publication Model: Print-Electronic Cited Medium: Print ISSN: 2193-8237 (Print) NLM ISO Abbreviation: Pain Ther

Davril J; Faculté d'odontologie de Lorraine, Centre d'essais et de certification, Vandœuvre-lès-Nancy, Université de Lorraine, France; Laboratoire d'étude des Microstructures et de Mécanique des Matériaux (LEM3), UMR CNRS 7239, Metz, Université de Lorraine, France. Electronic address: jeanne.davril@univ-lorraine.fr.; Hocquel R; Faculté d'odontologie de Lorraine, Centre d'essais et de certification, Vandœuvre-lès-Nancy, Université de Lorraine, France.; Vincent M; Faculté d'odontologie de Lorraine, Centre d'essais et de certification, Vandœuvre-lès-Nancy, Université de Lorraine, France; Laboratoire d'étude des Microstructures et de Mécanique des Matériaux (LEM3), UMR CNRS 7239, Metz, Université de Lorraine, France.; Balthazard R; Faculté d'odontologie de Lorraine, Centre d'essais et de certification, Vandœuvre-lès-Nancy, Université de Lorraine, France; Institut Jean Lamour (IJL), UMR CNRS 7198, Nancy, Université de Lorraine, France.; Claude S; Coltene Micro-Mega S.A, Besançon, France.; Mortier E; Faculté d'odontologie de Lorraine, Centre d'essais et de certification, Vandœuvre-lès-Nancy, Université de Lorraine, France; Institut Jean Lamour (IJL), UMR CNRS 7198, Nancy, Université de Lorraine, France.; Baldit A; Laboratoire d'étude des Microstructures et de Mécanique des Matériaux (LEM3), UMR CNRS 7239, Metz, Université de Lorraine, France.; Rahouadj R; Faculté d'odontologie de Lorraine, Centre d'essais et de certification, Vandœuvre-lès-Nancy, Université de Lorraine, France; Laboratoire d'étude des Microstructures et de Mécanique des Matériaux (LEM3), UMR CNRS 7239, Metz, Université de Lorraine, France.

Publisher: Elsevier Country of Publication: Netherlands NLM ID: 101322406 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1878-0180 (Electronic) Linking ISSN: 18780180 NLM ISO Abbreviation: J Mech Behav Biomed Mater Subsets: MEDLINE

Jury J; Service de Génétique médicale, Nantes Université, CHU de Nantes, Nantes, France.; Benoist JF; Laboratoire de Biochimie Métabolique, Hôpital Necker-Enfants-Malades, APHP, Paris, France.; CEA, INRAE, DMTS, SPI, MetaboHUB-IDF, Université Paris-Saclay, Gif-sur-Yvette, France.; Joubert M; Unité de Fœtopathologie et Génétique, CHU de Nantes, Nantes, France.; Quelin C; Service de Génétique Clinique, CLAD Ouest, CHU Rennes, Hôpital Sud, Rennes, France.; Besnard T; Service de Génétique médicale, Nantes Université, CHU de Nantes, Nantes, France.; l'institut du thorax, Nantes Université, CHU de Nantes, CNRS, INSERM, Nantes, France.; Conrad S; Service de Génétique médicale, Nantes Université, CHU de Nantes, Nantes, France.; Le Vaillant C; Service de Gynécologie et Obstétrique, CHU Nantes, Nantes, France.; Bézieau S; Service de Génétique médicale, Nantes Université, CHU de Nantes, Nantes, France.; l'institut du thorax, Nantes Université, CHU de Nantes, CNRS, INSERM, Nantes, France.; Isidor B; Service de Génétique médicale, Nantes Université, CHU de Nantes, Nantes, France.; l'institut du thorax, Nantes Université, CHU de Nantes, CNRS, INSERM, Nantes, France.; Attié-Bitach T; Imagine Institute, INSERM UMR1163, Paris, France.; Service de Médecine Génomique des Maladies Rares, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Faculté de Médecine, Université de Paris Cité, Paris, France.; Laboratoire SeqOIA (PFMG 2025), Paris, France.; Cogné B; Service de Génétique médicale, Nantes Université, CHU de Nantes, Nantes, France.; l'institut du thorax, Nantes Université, CHU de Nantes, CNRS, INSERM, Nantes, France.; Laboratoire SeqOIA (PFMG 2025), Paris, France.; Vincent M; Service de Génétique médicale, Nantes Université, CHU de Nantes, Nantes, France.; l'institut du thorax, Nantes Université, CHU de Nantes, CNRS, INSERM, Nantes, France.

Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE

Orti R; Laboratory of Cognitive Science and Immersive Virtual Reality, CS-IVR, Department of Psychology, University of Campania L. Vanvitelli, Viale Ellittico, 31, 81100, Caserta, Italy.; Coello Y; UMR 9193, SCALab, Sciences Cognitives et Sciences Affectives, Université de Lille, 59000, Lille, France.; Ruotolo F; Laboratory of Cognitive Science and Immersive Virtual Reality, CS-IVR, Department of Psychology, University of Campania L. Vanvitelli, Viale Ellittico, 31, 81100, Caserta, Italy.; Vincent M; UMR 9193, SCALab, Sciences Cognitives et Sciences Affectives, Université de Lille, 59000, Lille, France.; Bartolo A; UMR 9193, SCALab, Sciences Cognitives et Sciences Affectives, Université de Lille, 59000, Lille, France.; Iachini T; Laboratory of Cognitive Science and Immersive Virtual Reality, CS-IVR, Department of Psychology, University of Campania L. Vanvitelli, Viale Ellittico, 31, 81100, Caserta, Italy.; Ruggiero G; Laboratory of Cognitive Science and Immersive Virtual Reality, CS-IVR, Department of Psychology, University of Campania L. Vanvitelli, Viale Ellittico, 31, 81100, Caserta, Italy. gennaro.ruggiero@unicampania.it.

Publisher: Kluwer Academic/Plenum Publishers Country of Publication: United States NLM ID: 8903034 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1573-6792 (Electronic) Linking ISSN: 08960267 NLM ISO Abbreviation: Brain Topogr Subsets: MEDLINE

Jones C; Heroes in Mind, Advocacy and Research Consortium (HiMARC), Faculty of Rehabilitation Medicine, University of Alberta, Edmonton, AB T6G 2R3, Canada.; Alberta Health Services, Edmonton, AB T5J 3E4, Canada.; Vincent M; Heroes in Mind, Advocacy and Research Consortium (HiMARC), Faculty of Rehabilitation Medicine, University of Alberta, Edmonton, AB T6G 2R3, Canada.; O'Greysik E; Heroes in Mind, Advocacy and Research Consortium (HiMARC), Faculty of Rehabilitation Medicine, University of Alberta, Edmonton, AB T6G 2R3, Canada.; Alberta Health Services, Edmonton, AB T5J 3E4, Canada.; Faculty of Nursing, MacEwan University, Edmonton, AB T5J 2P2, Canada.; Bright K; Heroes in Mind, Advocacy and Research Consortium (HiMARC), Faculty of Rehabilitation Medicine, University of Alberta, Edmonton, AB T6G 2R3, Canada.; Alberta Health Services, Edmonton, AB T5J 3E4, Canada.; Faculty of Nursing, University of Calgary, Calgary, AB T2N 4V8, Canada.; School of Nursing and Midwifery, Faculty of Health, Community and Education, Mount Royal University, Calgary, AB T3E 6K6, Canada.; Spencer S; Heroes in Mind, Advocacy and Research Consortium (HiMARC), Faculty of Rehabilitation Medicine, University of Alberta, Edmonton, AB T6G 2R3, Canada.; Beck A; Heroes in Mind, Advocacy and Research Consortium (HiMARC), Faculty of Rehabilitation Medicine, University of Alberta, Edmonton, AB T6G 2R3, Canada.; Faculty of Nursing, University of Calgary, Calgary, AB T2N 4V8, Canada.; School of Nursing and Midwifery, Faculty of Health, Community and Education, Mount Royal University, Calgary, AB T3E 6K6, Canada.; Gross DP; Department of Physical Therapy, Faculty of Rehabilitation Medicine, University of Alberta, Edmonton, AB T6G 2G4, Canada.; Brémault-Phillips S; Heroes in Mind, Advocacy and Research Consortium (HiMARC), Faculty of Rehabilitation Medicine, University of Alberta, Edmonton, AB T6G 2R3, Canada.; Department of Occupational Therapy, Faculty of Rehabilitation Medicine, University of Alberta, Edmonton, AB T6G 2G4, Canada.

Publisher: SAGE Publishing Country of Publication: United States NLM ID: 8910581 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1705-7051 (Electronic) Linking ISSN: 08445621 NLM ISO Abbreviation: Can J Nurs Res Subsets: MEDLINE

Thomas H; Laboratoire de Génétique, CHRU de Nancy, Vandœuvre-lès-Nancy, France.; Service de Génétique Clinique, CHRU de Nancy, Nancy, France.; Alix T; Laboratoire de Génétique, CHRU de Nancy, Vandœuvre-lès-Nancy, France.; INSERM NGERE U1256, Université de Lorraine, Vandœuvre-lès-Nancy, France.; Renard É; INSERM NGERE U1256, Université de Lorraine, Vandœuvre-lès-Nancy, France.; Endocrinologie pédiatrique, CHRU de Nancy, Vandœuvre-lès-Nancy, France.; Renaud M; Service de Génétique Clinique, CHRU de Nancy, Nancy, France.; INSERM NGERE U1256, Université de Lorraine, Vandœuvre-lès-Nancy, France.; Service de Neurologie, CHRU de Nancy, Nancy, France.; Wourms J; Service de Génétique Clinique, CHRU de Nancy, Nancy, France.; Zuily S; Médecine Vasculaire, CHRU de Nancy, Vandœuvre-lès-Nancy, France.; UMR_S 916 DCAC, INSERM, Vandœuvre-lès-Nancy, France.; Leheup B; INSERM NGERE U1256, Université de Lorraine, Vandœuvre-lès-Nancy, France.; Geneviève D; Centre de référence anomalies du développement et syndromes malformatifs, Département de Génétique Medicale, Maladies Rares et Médecine Personnalisée, Hôpital Arnaud de Villeneuve, CHU de Montpellier, Montpellier, France.; Inserm U1183, Université Montpellier 1, Faculté de Médecine Montpellier-Nîmes, Montpellier, France.; Dreumont N; INSERM NGERE U1256, Université de Lorraine, Vandœuvre-lès-Nancy, France.; Schmitt E; Neuroradiologie, CHRU de Nancy, Vandœuvre-lès-Nancy, France.; Bronner M; Laboratoire de Génétique, CHRU de Nancy, Vandœuvre-lès-Nancy, France.; Muller M; Laboratoire de Génétique, CHRU de Nancy, Vandœuvre-lès-Nancy, France.; Divoux M; Laboratoire de Génétique, CHRU de Nancy, Vandœuvre-lès-Nancy, France.; INSERM NGERE U1256, Université de Lorraine, Vandœuvre-lès-Nancy, France.; Wandzel M; Laboratoire de Génétique, CHRU de Nancy, Vandœuvre-lès-Nancy, France.; Ravel JM; Laboratoire de Génétique, CHRU de Nancy, Vandœuvre-lès-Nancy, France.; INSERM NGERE U1256, Université de Lorraine, Vandœuvre-lès-Nancy, France.; Dexheimer M; Laboratoire de Génétique, CHRU de Nancy, Vandœuvre-lès-Nancy, France.; Becker A; Laboratoire de Génétique, CHRU de Nancy, Vandœuvre-lès-Nancy, France.; Roth V; Laboratoire de Génétique, CHRU de Nancy, Vandœuvre-lès-Nancy, France.; Willems M; Centre de référence anomalies du développement et syndromes malformatifs, Département de Génétique Medicale, Maladies Rares et Médecine Personnalisée, Hôpital Arnaud de Villeneuve, CHU de Montpellier, Montpellier, France.; Coubes C; Centre de référence anomalies du développement et syndromes malformatifs, Département de Génétique Medicale, Maladies Rares et Médecine Personnalisée, Hôpital Arnaud de Villeneuve, CHU de Montpellier, Montpellier, France.; Vieville G; Département de Génétique et Procréation, Hôpital Couple Enfant, CHU Grenoble Alpes, Grenoble, France.; Devillard F; Département de Génétique et Procréation, Hôpital Couple Enfant, CHU Grenoble Alpes, Grenoble, France.; Schaefer É; Service de Génétique médicale, Institut de Génétique Médicale d'Alsace, CHU de Strasbourg, Strasbourg, France.; Baer S; Service de Génétique médicale, Institut de Génétique Médicale d'Alsace, CHU de Strasbourg, Strasbourg, France.; Piton A; Service de Génétique médicale, Institut de Génétique Médicale d'Alsace, CHU de Strasbourg, Strasbourg, France.; Gérard B; Service de Génétique médicale, Institut de Génétique Médicale d'Alsace, CHU de Strasbourg, Strasbourg, France.; Vincent M; Service de Génétique Médicale, Centre Hospitalier Universitaire de Nantes, Nantes, France.; CNRS, INSERM, Institut du thorax, Nantes Université, Nantes, France.; Nizon M; Service de Génétique Médicale, Centre Hospitalier Universitaire de Nantes, Nantes, France.; CNRS, INSERM, Institut du thorax, Nantes Université, Nantes, France.; Cogné B; Service de Génétique Médicale, Centre Hospitalier Universitaire de Nantes, Nantes, France.; CNRS, INSERM, Institut du thorax, Nantes Université, Nantes, France.; Ruaud L; Département de Génétique, Hôpital Robert Debré, APHP Nord, Paris, France.; Couque N; Département de Génétique, Hôpital Robert Debré, APHP Nord, Paris, France.; Putoux A; Service de Génétique, Hospices Civils de Lyon, Groupe Hospitalier Est, Bron, France.; CNRS UMR5310, INSERM U1217, Institut NeuroMyoGene PNMG, Université Claude Bernard Lyon 1, Lyon, France.; Edery P; Service de Génétique, Hospices Civils de Lyon, Groupe Hospitalier Est, Bron, France.; CNRS UMR5310, INSERM U1217, Institut NeuroMyoGene PNMG, Université Claude Bernard Lyon 1, Lyon, France.; Lesca G; Service de Génétique, Hospices Civils de Lyon, Groupe Hospitalier Est, Bron, France.; CNRS UMR5310, INSERM U1217, Institut NeuroMyoGene PNMG, Université Claude Bernard Lyon 1, Lyon, France.; Chatron N; Service de Génétique, Hospices Civils de Lyon, Groupe Hospitalier Est, Bron, France.; CNRS UMR5310, INSERM U1217, Institut NeuroMyoGene PNMG, Université Claude Bernard Lyon 1, Lyon, France.; Till M; Service de Génétique, Hospices Civils de Lyon, Groupe Hospitalier Est, Bron, France.; CNRS UMR5310, INSERM U1217, Institut NeuroMyoGene PNMG, Université Claude Bernard Lyon 1, Lyon, France.; Faivre L; Centre de référence anomalies du développement et syndromes malformatifs et Centre de référence Déficiences Intellectuelles de causes rares, FHU TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; UMR1231 GAD, Inserm, Université Bourgogne Franche-Comté, Dijon, France.; Tran-Mau-Them F; UMR1231 GAD, Inserm, Université Bourgogne Franche-Comté, Dijon, France.; Unité Fonctionnelle Innovation en Diagnostic génomique des maladies rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; Alessandri JL; Service de génétique médicale, CHU de La Réunion, Hôpital Félix Guyon, Bellepierre, Saint-Denis, Réunion.; Lebrun M; Département de Génétique, Centre Hospitalier Universitaire de Saint-Etienne, Saint-Etienne, France.; Quélin C; Département de génétique moléculaire et génomique, CHU Rennes, Rennes, France.; Odent S; Département de génétique moléculaire et génomique, CHU Rennes, Rennes, France.; Dubourg C; Département de génétique moléculaire et génomique, CHU Rennes, Rennes, France.; David V; Département de génétique moléculaire et génomique, CHU Rennes, Rennes, France.; Faoucher M; Département de génétique moléculaire et génomique, CHU Rennes, Rennes, France.; Mignot C; Département de Génétique, Groupe Hospitalier Pitié-Salpêtrière, APHP Sorbonne Université, Paris, France.; Keren B; Département de Génétique, Groupe Hospitalier Pitié-Salpêtrière, APHP Sorbonne Université, Paris, France.; Pisan É; Département de Génétique, Groupe Hospitalier Pitié-Salpêtrière, APHP Sorbonne Université, Paris, France.; Afenjar A; Département de Génétique, Groupe Hospitalier Pitié-Salpêtrière, APHP Sorbonne Université, Paris, France.; Julia S; Département de Génétique médicale, CHU Toulouse, Toulouse, France.; Bieth É; Département de Génétique médicale, CHU Toulouse, Toulouse, France.; Banneau G; Département de Génétique médicale, CHU Toulouse, Toulouse, France.; Goldenberg A; Department of Genetics and Reference Center for Developmental Disorders, CHU de Rouen, Rouen, France.; Inserm U1245, Université de Rouen Normandie, Rouen, France.; Husson T; Inserm U1245, Université de Rouen Normandie, Rouen, France.; Department of Psychiatry, CHU de Rouen, Rouen, France.; Department of Research, Centre hospitalier du Rouvray, Sotteville-Lès-Rouen, France.; Campion D; Inserm U1245, Université de Rouen Normandie, Rouen, France.; Department of Psychiatry, CHU de Rouen, Rouen, France.; Department of Research, Centre hospitalier du Rouvray, Sotteville-Lès-Rouen, France.; Lecoquierre F; Department of Genetics and Reference Center for Developmental Disorders, CHU de Rouen, Rouen, France.; Inserm U1245, Université de Rouen Normandie, Rouen, France.; Nicolas G; Department of Genetics and Reference Center for Developmental Disorders, CHU de Rouen, Rouen, France.; Inserm U1245, Université de Rouen Normandie, Rouen, France.; Charbonnier C; Inserm U1245, Université de Rouen Normandie, Rouen, France.; Department of Biotatistics, CHU de Rouen, Rouen, France.; De Saint Martin A; Centre de Référence des épilepsies Rares, Hopitaux universitaires de Strasbourg, Strasbourg, France.; Naudion S; Service de Génétique Médicale, Centre Hospitalier Universitaire de Bordeaux, Groupe hospitalier Pellegrin, Bordeaux, France.; Degoutin M; Service de Génétique Médicale, Centre Hospitalier Universitaire de Bordeaux, Groupe hospitalier Pellegrin, Bordeaux, France.; Rondeau S; Centre de référence des maladies osseuses constitutionnelles, Necker-Enfants Malades Hospitals, Paris, France.; INSERM UMR 1163, Imagine Institute, Paris, France.; Michot C; Centre de référence des maladies osseuses constitutionnelles, Necker-Enfants Malades Hospitals, Paris, France.; INSERM UMR 1163, Imagine Institute, Paris, France.; Cormier-Daire V; Centre de référence des maladies osseuses constitutionnelles, Necker-Enfants Malades Hospitals, Paris, France.; INSERM UMR 1163, Imagine Institute, Paris, France.; Oussalah A; INSERM NGERE U1256, Université de Lorraine, Vandœuvre-lès-Nancy, France.; Department of Molecular Medicine, Division of Biochemistry, Molecular Biology, and Nutrition, CHRU de Nancy, Nancy, France.; Pourié C; INSERM NGERE U1256, Université de Lorraine, Vandœuvre-lès-Nancy, France.; Lambert L; Service de Génétique Clinique, CHRU de Nancy, Nancy, France.; INSERM NGERE U1256, Université de Lorraine, Vandœuvre-lès-Nancy, France.; Bonnet C; Laboratoire de Génétique, CHRU de Nancy, Vandœuvre-lès-Nancy, France ce.bonnet@chru-nancy.fr.; INSERM NGERE U1256, Université de Lorraine, Vandœuvre-lès-Nancy, France.

Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Electronic Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE

Jensen M; Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA.; Bioinformatics and Genomics Graduate program, Pennsylvania State University, University Park, PA 16802, USA.; Smolen C; Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA.; Bioinformatics and Genomics Graduate program, Pennsylvania State University, University Park, PA 16802, USA.; Tyryshkina A; Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA.; Pizzo L; Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA.; Banerjee D; Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA.; Oetjens M; Autism & Developmental Medicine Institute, Geisinger, Lewisburg, PA 17837, USA.; Shimelis H; Autism & Developmental Medicine Institute, Geisinger, Lewisburg, PA 17837, USA.; Taylor CM; Autism & Developmental Medicine Institute, Geisinger, Lewisburg, PA 17837, USA.; Pounraja VK; Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA.; Bioinformatics and Genomics Graduate program, Pennsylvania State University, University Park, PA 16802, USA.; Song H; Department of Statistics, Pennsylvania State University, University Park, PA 16802, USA.; Rohan L; Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA.; Huber E; Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA.; El Khattabi L; Institut Cochin, Inserm U1016, CNRS UMR8104, Université Paris Cité, CARPEM, Paris, France.; van de Laar I; Department of Clinical Genetics, Erasmus MC, Univ. Medical Center Rotterdam, Rotterdam, The Netherlands.; Tadros R; Department of Clinical Genetics, Erasmus MC, Univ. Medical Center Rotterdam, Rotterdam, The Netherlands.; Bezzina C; Department of Clinical Genetics, Erasmus MC, Univ. Medical Center Rotterdam, Rotterdam, The Netherlands.; van Slegtenhorst M; Department of Clinical Genetics, Erasmus MC, Univ. Medical Center Rotterdam, Rotterdam, The Netherlands.; Kammeraad J; Department of Clinical Genetics, Erasmus MC, Univ. Medical Center Rotterdam, Rotterdam, The Netherlands.; Prontera P; Medical Genetics Unit, Hospital Santa Maria della Misericordia, Perugia, Italy.; Caberg JH; Centre Hospitalier Universitaire de Liège. Domaine Universitaire du Sart Tilman, Liège, Belgium.; Fraser H; Division of Evolution and Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.; Banka S; Division of Evolution and Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.; Manchester Centre for Genomic Medicine, St. Mary's Hospital, Central Manchester University Hospitals, NHS Foundation Trust Manchester Academic Health Sciences Centre, Manchester, UK.; Van Dijck A; Department of Medical Genetics, University and University Hospital Antwerp, Antwerp, Belgium.; Schwartz C; Greenwood Genetic Center, Greenwood, SC 29646, USA.; Voorhoeve E; Department of Clinical Genetics, Amsterdam UMC, Amsterdam, The Netherlands.; Callier P; Center for Rare Diseases and Reference Developmental Anomalies and Malformation Syndromes, CHU Dijon, Dijon, France.; Mosca-Boidron AL; Center for Rare Diseases and Reference Developmental Anomalies and Malformation Syndromes, CHU Dijon, Dijon, France.; Marle N; Center for Rare Diseases and Reference Developmental Anomalies and Malformation Syndromes, CHU Dijon, Dijon, France.; Lefebvre M; Laboratoire de Genetique Chromosomique et Moleculaire, CHU Dijon, France.; Pope K; Bruce Lefroy Centre, Murdoch Children's Research Institute, Melbourne, Australia.; Snell P; Bruce Lefroy Centre, Murdoch Children's Research Institute, Melbourne, Australia.; Boys A; Bruce Lefroy Centre, Murdoch Children's Research Institute, Melbourne, Australia.; Lockhart PJ; Bruce Lefroy Centre, Murdoch Children's Research Institute, Melbourne, Australia.; Department of Paediatrics, University of Melbourne, Melbourne, Australia.; Ashfaq M; Department of Pediatrics, McGovern Medical School, University of Texas Health Science Center, Houston, TX 77030, USA.; McCready E; Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, Canada.; Nowacyzk M; Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, Canada.; Castiglia L; Research Unit of Rare Diseases and Neurodevelopmental Disorders, Oasi Research Institute-IRCCS, Troina, Italy.; Galesi O; Research Unit of Rare Diseases and Neurodevelopmental Disorders, Oasi Research Institute-IRCCS, Troina, Italy.; Avola E; Research Unit of Rare Diseases and Neurodevelopmental Disorders, Oasi Research Institute-IRCCS, Troina, Italy.; Mattina T; Research Unit of Rare Diseases and Neurodevelopmental Disorders, Oasi Research Institute-IRCCS, Troina, Italy.; Fichera M; Research Unit of Rare Diseases and Neurodevelopmental Disorders, Oasi Research Institute-IRCCS, Troina, Italy.; Section of Clinical Biochemistry and Medical Genetics, Department of Biomedical and Biotechnological Sciences, University of Catania School of Medicine, Catania, Italy.; Bruccheri MG; Research Unit of Rare Diseases and Neurodevelopmental Disorders, Oasi Research Institute-IRCCS, Troina, Italy.; Mandarà GML; Medical Genetics, ASP Ragusa, Ragusa, Italy.; Mari F; Laboratory of Clinical Molecular Genetics and Cytogenetics, IRCCS San Raffaele Scientific Institute, Milan, Italy.; Privitera F; Laboratory of Clinical Molecular Genetics and Cytogenetics, IRCCS San Raffaele Scientific Institute, Milan, Italy.; Longo I; Laboratory of Clinical Molecular Genetics and Cytogenetics, IRCCS San Raffaele Scientific Institute, Milan, Italy.; Curró A; Laboratory of Clinical Molecular Genetics and Cytogenetics, IRCCS San Raffaele Scientific Institute, Milan, Italy.; Renieri A; Laboratory of Clinical Molecular Genetics and Cytogenetics, IRCCS San Raffaele Scientific Institute, Milan, Italy.; Keren B; Département de Génétique, Hôpital Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris, Sorbonne Université, 75019 Paris, France.; Charles P; Département de Génétique, Hôpital Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris, Sorbonne Université, 75019 Paris, France.; Cuinat S; CHU Nantes, Medical Genetics Department, Nantes, France.; Nizon M; CHU Nantes, Medical Genetics Department, Nantes, France.; Pichon O; CHU Nantes, Medical Genetics Department, Nantes, France.; Bénéteau C; CHU Nantes, Medical Genetics Department, Nantes, France.; Stoeva R; CHU Nantes, Medical Genetics Department, Nantes, France.; Martin-Coignard D; Service de Cytogenetique, CHU de Le Mans, Le Mans, France.; Blesson S; Department of Genetics, Bretonneau University Hospital, Tours, France.; Le Caignec C; CHU Toulouse, Department of Medical Genetics, Toulouse, France.; Toulouse Neuro Imaging, Center, Inserm, UPS, Université de Toulouse, Toulouse, France.; Mercier S; Department of Genetics, Bretonneau University Hospital, Tours, France.; Vincent M; Department of Genetics, Bretonneau University Hospital, Tours, France.; Martin C; Autism & Developmental Medicine Institute, Geisinger, Lewisburg, PA 17837, USA.; Mannik K; Institute of Genomics, University of Tartu, Estonia.; Health2030 Genome Center, Fondation Campus Biotech, Geneva, Switzerland.; Reymond A; Center for Integrative Genomics, Faculty of Biology and Medicine, University of Lausanne, Switzerland.; Faivre L; Center for Rare Diseases and Reference Developmental Anomalies and Malformation Syndromes, CHU Dijon, Dijon, France.; Laboratoire de Genetique Chromosomique et Moleculaire, CHU Dijon, France.; Sistermans E; Department of Clinical Genetics, Amsterdam UMC, Amsterdam, The Netherlands.; Kooy RF; Department of Medical Genetics, University and University Hospital Antwerp, Antwerp, Belgium.; Amor DJ; Department of Clinical Genetics, Amsterdam UMC, Amsterdam, The Netherlands.; Romano C; Research Unit of Rare Diseases and Neurodevelopmental Disorders, Oasi Research Institute-IRCCS, Troina, Italy.; Section of Clinical Biochemistry and Medical Genetics, Department of Biomedical and Biotechnological Sciences, University of Catania School of Medicine, Catania, Italy.; Andrieux J; Institut de Genetique Medicale, Hopital Jeanne de Flandre, CHRU de Lille, Lille, France.; Girirajan S; Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA.; Bioinformatics and Genomics Graduate program, Pennsylvania State University, University Park, PA 16802, USA.; Department of Anthropology, Pennsylvania State University, University Park, PA 16802, USA.

Country of Publication: United States NLM ID: 101767986 Publication Model: Electronic Cited Medium: Internet NLM ISO Abbreviation: medRxiv Subsets: PubMed not MEDLINE

Piccirillo MC; Clinical Trials Unit, Istituto Nazionalei Tumori Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Fondazione G. Pascale, Napoli, Italy.; Chu Q; Cross Cancer Institute, Edmonton, Alberta, Canada.; Bradbury P; University Health Network, Toronto, Ontario, Canada.; Tu W; Canadian Cancer Trials Group, Kingston, Ontario, Canada.; Coschi CH; Canadian Cancer Trials Group, Kingston, Ontario, Canada.; Grosso F; Mesothelioma Unit (FG) & Department of Integrated Activities Research and Innovation (FU), SS. Antonio e Biagio C. Arrigo Hospital, Alessandria, Italy.; Florescu M; Centre Hospitalier de l'Université de Montréal (CHUM), Montreal, Quebec, Canada.; Mencoboni M; Oncology Unit ASL 3, Villa Scassi Hospital, Genova, Italy.; Goffin JR; Juravinski Cancer Centre, Ontario, Canada.; Pagano M; Medical Oncology, Comprehensive Cancer Centre, AUSL Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) of Reggio Emilia, Reggio Emilia, Italy.; Ciardiello F; Oncology and Hematology Unit, University of Campania 'Luigi Vanvitelli,' Naples, Italy.; Cecere FL; Oncology Unit, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Istituti Fisioterapici Ospitalieri (IFO) Istituto Regina Elena, Rome, Italy.; Vincent M; London Regional Cancer Program, London, Ontario, Canada.; Ferrara R; Thoracic Oncology Unit, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Istituto Nazionale Tumori, Milano, Italy.; Dawe DE; Department of Medical Oncology and Hematology, CancerCare Manitoba, Winnipeg, Canada.; Hao D; Tom Baker Cancer Centre and Cumming School of Medicine, Calgary, Alberta, Canada.; Lee CW; British Columbia Cancer Agency, Surrey, British Columbia, Canada.; Morabito A; Thoracic Oncology Unit, Istituto Nazionale Tumori Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Fondazione G. Pascale, Napoli, Italy.; Gridelli C; Oncology Unit, S. Giuseppe Moscati Hospital, Avellino, Italy.; Cavanna L; Oncology and Hematology Department, USL Piacenza, Gugliemimo da Saliceto Hospital, Piacenza, Italy.; Iqbal M; Allan Blair Cancer Centre, Regina, Saskatchewan, Canada.; Blais N; Centre Hospitalier de l'Université de Montréal (CHUM), Montreal, Quebec, Canada.; Leighl NB; University Health Network, Toronto, Ontario, Canada.; Wheatley-Price P; Ottawa Hospital Research Institute and Department of Medicine, University of Ottawa, Ottawa, Ontario, Canada.; Tsao MS; University Health Network, Toronto, Ontario, Canada.; Ugo F; Mesothelioma Unit (FG) & Department of Integrated Activities Research and Innovation (FU), SS. Antonio e Biagio C. Arrigo Hospital, Alessandria, Italy.; El-Osta H; Merck & Co, Inc., Rahway, New Jersey.; Gargiulo P; Clinical Trials Unit, Istituto Nazionalei Tumori Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Fondazione G. Pascale, Napoli, Italy.; Gaudreau PO; Canadian Cancer Trials Group, Kingston, Ontario, Canada.; Tu D; Canadian Cancer Trials Group, Kingston, Ontario, Canada.; Sederias J; Canadian Cancer Trials Group, Kingston, Ontario, Canada.; Brown-Walker P; Canadian Cancer Trials Group, Kingston, Ontario, Canada.; Perrone F; Clinical Trials Unit, Istituto Nazionalei Tumori Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Fondazione G. Pascale, Napoli, Italy.; Seymour L; Canadian Cancer Trials Group, Kingston, Ontario, Canada.; Laurie SA; Ottawa Hospital Research Institute and Department of Medicine, University of Ottawa, Ottawa, Ontario, Canada.

Publisher: Elsevier Country of Publication: United States NLM ID: 101274235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1556-1380 (Electronic) Linking ISSN: 15560864 NLM ISO Abbreviation: J Thorac Oncol Subsets: MEDLINE

Chen X; Data Science Platform, Imagine Institute, Université Paris Cité, Inserm UMR 1163, Paris, France.; Inserm, Centre de Recherche des Cordeliers, Sorbonne Université, Université Paris Cité, Paris, France.; HeKA, Inria Paris, Paris, France.; Wang J; Data Science Platform, Imagine Institute, Université Paris Cité, Inserm UMR 1163, Paris, France.; Faviez C; Inserm, Centre de Recherche des Cordeliers, Sorbonne Université, Université Paris Cité, Paris, France.; HeKA, Inria Paris, Paris, France.; Université Paris Cité, Paris, France.; Wang X; Inserm, Centre de Recherche des Cordeliers, Sorbonne Université, Université Paris Cité, Paris, France.; HeKA, Inria Paris, Paris, France.; Vincent M; Data Science Platform, Imagine Institute, Université Paris Cité, Inserm UMR 1163, Paris, France.; Tsopra R; Inserm, Centre de Recherche des Cordeliers, Sorbonne Université, Université Paris Cité, Paris, France.; HeKA, Inria Paris, Paris, France.; Hôpital Necker-Enfants Malades, Département d'informatique médicale, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.; Burgun A; Inserm, Centre de Recherche des Cordeliers, Sorbonne Université, Université Paris Cité, Paris, France.; HeKA, Inria Paris, Paris, France.; Université Paris Cité, Paris, France.; Hôpital Necker-Enfants Malades, Département d'informatique médicale, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.; Garcelon N; Data Science Platform, Imagine Institute, Université Paris Cité, Inserm UMR 1163, Paris, France.; Inserm, Centre de Recherche des Cordeliers, Sorbonne Université, Université Paris Cité, Paris, France.; HeKA, Inria Paris, Paris, France.

Publisher: IOS Press Country of Publication: Netherlands NLM ID: 9214582 Publication Model: Print Cited Medium: Internet ISSN: 1879-8365 (Electronic) Linking ISSN: 09269630 NLM ISO Abbreviation: Stud Health Technol Inform Subsets: MEDLINE