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- [1] Incidental and secondary findings in trio exome sequencingGENES & DISEASES, 2024, 11 (04)Cohen, Camille论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp ntercommunal Poissy St Germain en Laye, Dept Genet, F-78300 Poissy, France Ctr Hosp ntercommunal Poissy St Germain en Laye, Dept Genet, F-78300 Poissy, FranceBellanger, Emeline论文数: 0 引用数: 0 h-index: 0机构: RHuMA, UMR BREED, INRA ENVA UVSQ, F-78180 Montigny le Bretonneux, France Ctr Hosp ntercommunal Poissy St Germain en Laye, Dept Genet, F-78300 Poissy, FranceMortreux, Jeremie论文数: 0 引用数: 0 h-index: 0机构: Lab Eurofins Biomnis, Serv Genet, F-69007 Lyon, France Ctr Hosp ntercommunal Poissy St Germain en Laye, Dept Genet, F-78300 Poissy, FranceRaymond, Laure论文数: 0 引用数: 0 h-index: 0机构: Lab Eurofins Biomnis, Serv Genet, F-69007 Lyon, France Ctr Hosp ntercommunal Poissy St Germain en Laye, Dept Genet, F-78300 Poissy, FranceVialard, Francois论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp ntercommunal Poissy St Germain en Laye, Dept Genet, F-78300 Poissy, France RHuMA, UMR BREED, INRA ENVA UVSQ, F-78180 Montigny le Bretonneux, France Ctr Hosp ntercommunal Poissy St Germain en Laye, Dept Genet, F-78300 Poissy, FranceDard, Rodolphe论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp ntercommunal Poissy St Germain en Laye, Dept Genet, F-78300 Poissy, France Ctr Hosp ntercommunal Poissy St Germain en Laye, Dept Genet, F-78300 Poissy, France
- [2] Exploring secondary findings in a Spanish cohort of 641 patients undergoing whole exome sequencingEUROPEAN JOURNAL OF HUMAN GENETICS, 2020, 28 (SUPPL 1) : 696 - 696Codina Sola, M.论文数: 0 引用数: 0 h-index: 0机构: Hosp Valle De Hebron, Barcelona, Spain Hosp Valle De Hebron, Barcelona, SpainRovira Moreno, E.论文数: 0 引用数: 0 h-index: 0机构: Hosp Valle De Hebron, Barcelona, Spain Hosp Valle De Hebron, Barcelona, SpainAbuli Vidal, A.论文数: 0 引用数: 0 h-index: 0机构: Hosp Valle De Hebron, Barcelona, Spain Hosp Valle De Hebron, Barcelona, SpainValenzuela Palafoll, I.论文数: 0 引用数: 0 h-index: 0机构: Hosp Valle De Hebron, Barcelona, Spain Hosp Valle De Hebron, Barcelona, SpainCueto Gonzalez, A.论文数: 0 引用数: 0 h-index: 0机构: Hosp Valle De Hebron, Barcelona, Spain Hosp Valle De Hebron, Barcelona, SpainLopez Grondona, F.论文数: 0 引用数: 0 h-index: 0机构: Hosp Valle De Hebron, Barcelona, Spain Hosp Valle De Hebron, Barcelona, SpainParamonov, I.论文数: 0 引用数: 0 h-index: 0机构: Hosp Valle De Hebron, Barcelona, Spain Hosp Valle De Hebron, Barcelona, SpainOurani, S.论文数: 0 引用数: 0 h-index: 0机构: Hosp Valle De Hebron, Barcelona, Spain Hosp Valle De Hebron, Barcelona, SpainSerra Juhe, C.论文数: 0 引用数: 0 h-index: 0机构: Hosp Valle De Hebron, Barcelona, Spain Hosp Valle De Hebron, Barcelona, SpainGarcia Arumi, E.论文数: 0 引用数: 0 h-index: 0机构: Hosp Valle De Hebron, Barcelona, Spain Hosp Valle De Hebron, Barcelona, SpainCusco Marti, I.论文数: 0 引用数: 0 h-index: 0机构: Hosp Valle De Hebron, Barcelona, Spain Hosp Valle De Hebron, Barcelona, SpainTizzano Ferrari, E.论文数: 0 引用数: 0 h-index: 0机构: Hosp Valle De Hebron, Barcelona, Spain Hosp Valle De Hebron, Barcelona, Spain
- [3] Incidental findings in clinical exome sequencingEUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 1811 - 1812Yntema, H. G.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, Netherlandsvan der Schoot, V.论文数: 0 引用数: 0 h-index: 0机构: Maastricht Univ, Med Ctr, Dept Clin Genet, Maastricht, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, NetherlandsHaer-Wigman, L.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, NetherlandsOerlemans, A. J. M.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Sci Ctr Qual Healthcare, Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, Netherlandsvan Koolwijk, M.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, NetherlandsTammer, F.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, NetherlandsArens, Y.论文数: 0 引用数: 0 h-index: 0机构: Maastricht Univ, Med Ctr, Dept Clin Genet, Maastricht, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, NetherlandsBrunner, H. G.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, Netherlands Maastricht Univ, Med Ctr, Dept Clin Genet, Maastricht, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, NetherlandsVissers, L. E. L. M.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, NetherlandsFeenstra, I.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, Netherlands
- [4] Secondary findings of exome sequencing in Russian patientsEUROPEAN JOURNAL OF HUMAN GENETICS, 2022, 30 (SUPPL 1) : 568 - 569Mironovich, Olga论文数: 0 引用数: 0 h-index: 0机构: Res Ctr Med Genet, Moscow, Russia Res Ctr Med Genet, Moscow, RussiaGundorova, Polina论文数: 0 引用数: 0 h-index: 0机构: Res Ctr Med Genet, Moscow, Russia Res Ctr Med Genet, Moscow, RussiaCherevatova, Tatyana论文数: 0 引用数: 0 h-index: 0机构: Res Ctr Med Genet, Moscow, Russia Res Ctr Med Genet, Moscow, RussiaOrlova, Anna论文数: 0 引用数: 0 h-index: 0机构: Res Ctr Med Genet, Moscow, Russia Res Ctr Med Genet, Moscow, RussiaZabnenkova, Viktoria论文数: 0 引用数: 0 h-index: 0机构: Res Ctr Med Genet, Moscow, Russia Res Ctr Med Genet, Moscow, RussiaChuhrova, Alena论文数: 0 引用数: 0 h-index: 0机构: Res Ctr Med Genet, Moscow, Russia Res Ctr Med Genet, Moscow, RussiaPoliakov, Aleksander论文数: 0 引用数: 0 h-index: 0机构: Res Ctr Med Genet, Moscow, Russia Res Ctr Med Genet, Moscow, RussiaRyzhkova, Oxana论文数: 0 引用数: 0 h-index: 0机构: Res Ctr Med Genet, Moscow, Russia Res Ctr Med Genet, Moscow, Russia
- [5] Patients' views on incidental findings from clinical exome sequencingAPPLIED AND TRANSLATIONAL GENOMICS, 2015, 4 : 38 - 43Clift, Kristin E.论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Biomed Eth Program, Rochester, MN USA Mayo Clin, Biomed Eth Program, Rochester, MN USAHalverson, Colin M. E.论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Biomed Eth Program, Rochester, MN USA Univ Chicago, Dept Anthropol, Chicago, IL 60637 USA Mayo Clin, Biomed Eth Program, Rochester, MN USAFiksdal, Alexander S.论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Biomed Eth Program, Rochester, MN USA Mayo Clin, Biomed Eth Program, Rochester, MN USAKumbamu, Ashok论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Biomed Eth Program, Rochester, MN USA Mayo Clin, Biomed Eth Program, Rochester, MN USASharp, Richard R.论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Biomed Eth Program, Rochester, MN USA Div Hlth Care Res & Policy, London, England Div Gen Internal Med, Zurich, Switzerland Mayo Clin, Biomed Eth Program, Rochester, MN USAMcCormick, Jennifer B.论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Biomed Eth Program, Rochester, MN USA Div Hlth Care Res & Policy, London, England Div Gen Internal Med, Zurich, Switzerland Mayo Clin, Biomed Eth Program, Rochester, MN USA
- [6] Review of secondary findings reported in the qGenomics patient cohort, analyzed by exome sequencingEUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 : 574 - 574Carreno, Marta论文数: 0 引用数: 0 h-index: 0机构: qGen, NGS Clin Dept, Esplugas de Llobregat, Spain qGen, NGS Clin Dept, Esplugas de Llobregat, SpainSegura-Puimedon, Maria论文数: 0 引用数: 0 h-index: 0机构: qGen, NGS Clin Dept, Esplugas de Llobregat, Spain qGen, NGS Clin Dept, Esplugas de Llobregat, SpainGarcia, Raquel论文数: 0 引用数: 0 h-index: 0机构: qGen, NGS Clin Dept, Esplugas de Llobregat, Spain qGen, NGS Clin Dept, Esplugas de Llobregat, SpainCarreno, Lidia论文数: 0 引用数: 0 h-index: 0机构: qGen, NGS Clin Dept, Esplugas de Llobregat, Spain qGen, NGS Clin Dept, Esplugas de Llobregat, SpainArjona, Cesar论文数: 0 引用数: 0 h-index: 0机构: qGen, NGS Clin Dept, Esplugas de Llobregat, Spain qGen, NGS Clin Dept, Esplugas de Llobregat, SpainNicolas, Hector San论文数: 0 引用数: 0 h-index: 0机构: qGen, NGS Clin Dept, Esplugas de Llobregat, Spain qGen, NGS Clin Dept, Esplugas de Llobregat, SpainSintas, Celia论文数: 0 引用数: 0 h-index: 0机构: qGen, NGS Clin Dept, Esplugas de Llobregat, Spain qGen, NGS Clin Dept, Esplugas de Llobregat, SpainVall, Monica论文数: 0 引用数: 0 h-index: 0机构: qGen, NGS Clin Dept, Esplugas de Llobregat, Spain qGen, NGS Clin Dept, Esplugas de Llobregat, SpainMarcos, Olaya Villa论文数: 0 引用数: 0 h-index: 0机构: qGen, NGS Clin Dept, Esplugas de Llobregat, Spain qGen, NGS Clin Dept, Esplugas de Llobregat, SpainVinas-Jornet, Marina论文数: 0 引用数: 0 h-index: 0机构: qGen, NGS Clin Dept, Esplugas de Llobregat, Spain qGen, NGS Clin Dept, Esplugas de Llobregat, SpainArmengol, Lluis论文数: 0 引用数: 0 h-index: 0机构: qGen, NGS Clin Dept, Esplugas de Llobregat, Spain qGen, NGS Clin Dept, Esplugas de Llobregat, Spain
- [7] Clinical and psychological implications of secondary and incidental findings in cancer susceptibility genes after exome sequencing in patients with rare disordersJOURNAL OF MEDICAL GENETICS, 2023, 60 (07) : 685 - 691Carrasco, Estela论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Hosp Univ, Med Oncol Dept, Hereditary Canc Genet Grp, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, Spain Autonomous Univ Barcelona, Dept Pediat Obstet & Gynecol Preventat Med & Publ, Barcelona, Spain Vall dHebron Inst Oncol VHIO, Hereditary Canc Genet Grp, Med Oncol, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, Spain Vall dHebron Hosp Univ, Med Oncol Dept, Hereditary Canc Genet Grp, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, SpainLopez-Fernandez, Adria论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Hosp Univ, Med Oncol Dept, Hereditary Canc Genet Grp, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, Spain Vall dHebron Inst Oncol VHIO, Hereditary Canc Genet Grp, Med Oncol, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, Spain Vall dHebron Hosp Univ, Med Oncol Dept, Hereditary Canc Genet Grp, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, SpainCodina-Sola, Marta论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Hosp Univ, Dept Clin & Mol Genet, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, Spain Vall dHebron Hosp Univ, Vall dHebron Inst Recerca VHIR, Med Genet Grp, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, Spain ERN ITHACA, European Reference Network Rare Congenital Malfor, Barcelona, Spain Vall dHebron Hosp Univ, Med Oncol Dept, Hereditary Canc Genet Grp, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, SpainValenzuela, Irene论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Hosp Univ, Dept Clin & Mol Genet, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, Spain Vall dHebron Hosp Univ, Vall dHebron Inst Recerca VHIR, Med Genet Grp, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, Spain ERN ITHACA, European Reference Network Rare Congenital Malfor, Barcelona, Spain Vall dHebron Hosp Univ, Med Oncol Dept, Hereditary Canc Genet Grp, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, SpainCueto-Gonzalez, Am论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Hosp Univ, Dept Clin & Mol Genet, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, Spain Vall dHebron Hosp Univ, Vall dHebron Inst Recerca VHIR, Med Genet Grp, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, Spain ERN ITHACA, European Reference Network Rare Congenital Malfor, Barcelona, Spain Vall dHebron Hosp Univ, Med Oncol Dept, Hereditary Canc Genet Grp, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, SpainVillacampa, Guillermo论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Inst Oncol VHIO, Oncol Data Sci ODysSey Grp, Vail dHebron Barcelona Hosp Campus, Barcelona 08035, Spain Vall dHebron Hosp Univ, Med Oncol Dept, Hereditary Canc Genet Grp, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, SpainNavarro, Victor论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Inst Oncol VHIO, Oncol Data Sci ODysSey Grp, Vail dHebron Barcelona Hosp Campus, Barcelona 08035, Spain Vall dHebron Hosp Univ, Med Oncol Dept, Hereditary Canc Genet Grp, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, SpainTorres-Esquius, Sara论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Inst Oncol VHIO, Hereditary Canc Genet Grp, Med Oncol, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, Spain Vall dHebron Hosp Univ, Med Oncol Dept, Hereditary Canc Genet Grp, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, SpainPalau, Dolors论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Hosp Univ, Dept Clin & Mol Genet, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, Spain ERN ITHACA, European Reference Network Rare Congenital Malfor, Barcelona, Spain Vall dHebron Hosp Univ, Med Oncol Dept, Hereditary Canc Genet Grp, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, SpainCruellas, Mara论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Hosp Univ, Med Oncol Dept, Hereditary Canc Genet Grp, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, Spain Vall dHebron Inst Oncol VHIO, Hereditary Canc Genet Grp, Med Oncol, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, Spain Vall dHebron Hosp Univ, Med Oncol Dept, Hereditary Canc Genet Grp, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, SpainTorres, Maite论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Hosp Univ, Med Oncol Dept, Hereditary Canc Genet Grp, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, Spain Vall dHebron Hosp Univ, Med Oncol Dept, Hereditary Canc Genet Grp, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, SpainPerez-Duenas, Belen论文数: 0 引用数: 0 h-index: 0机构: Univ Autonoma Barcelona, Vall dHebron Hosp Univ, Paediat Neurol Dept, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, Spain Inst Salud Carlos III, Ctr Invest Biomed Red Enfermedades Raras CIBERER, Barcelona, Spain Vall dHebron Hosp Univ, Med Oncol Dept, Hereditary Canc Genet Grp, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, SpainAbuli, Anna论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Hosp Univ, Dept Clin & Mol Genet, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, Spain Vall dHebron Hosp Univ, Vall dHebron Inst Recerca VHIR, Med Genet Grp, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, Spain ERN ITHACA, European Reference Network Rare Congenital Malfor, Barcelona, Spain Vall dHebron Hosp Univ, Med Oncol Dept, Hereditary Canc Genet Grp, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, SpainDiez, Orland论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Inst Oncol VHIO, Hereditary Canc Genet Grp, Med Oncol, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, Spain Vall dHebron Hosp Univ, Dept Clin & Mol Genet, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, Spain ERN ITHACA, European Reference Network Rare Congenital Malfor, Barcelona, Spain Vall dHebron Hosp Univ, Med Oncol Dept, Hereditary Canc Genet Grp, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, SpainSabado-Alvarez, Constantino论文数: 0 引用数: 0 h-index: 0机构: Dept Pediat Oncol & Hematol, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, Spain Vall dHebron Hosp Univ, Med Oncol Dept, Hereditary Canc Genet Grp, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, SpainGarcia-Arumi, Elena论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Hosp Univ, Dept Clin & Mol Genet, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, Spain Vall dHebron Hosp Univ, Vall dHebron Inst Recerca VHIR, Med Genet Grp, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, Spain ERN ITHACA, European Reference Network Rare Congenital Malfor, Barcelona, Spain Inst Salud Carlos III, Ctr Invest Biomed Red Enfermedades Raras CIBERER, Barcelona, Spain Vall dHebron Hosp Univ, Vall dHebron Inst Recerca VHIR, Res Grp Neuromuscular & Mitochondria Disorders, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, Spain Vall dHebron Hosp Univ, Med Oncol Dept, Hereditary Canc Genet Grp, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, SpainTizzano, Eduardo F.论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Hosp Univ, Dept Clin & Mol Genet, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, Spain Vall dHebron Hosp Univ, Vall dHebron Inst Recerca VHIR, Med Genet Grp, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, Spain ERN ITHACA, European Reference Network Rare Congenital Malfor, Barcelona, Spain Vall dHebron Hosp Univ, Med Oncol Dept, Hereditary Canc Genet Grp, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, SpainMoreno, Lucas论文数: 0 引用数: 0 h-index: 0机构: Dept Pediat Oncol & Hematol, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, Spain Vall dHebron Hosp Univ, Vall dHebron Inst Recerca VHIR, Childhood Canc & Blood Disorders Grp, Vall dHebron Barcelona Hosp Campus, Barcelona, Spain Vall dHebron Hosp Univ, Med Oncol Dept, Hereditary Canc Genet Grp, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, SpainBalmana, Judith论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Hosp Univ, Med Oncol Dept, Hereditary Canc Genet Grp, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, Spain Vall dHebron Inst Oncol VHIO, Hereditary Canc Genet Grp, Med Oncol, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, Spain GENTURIS, European Reference Network GENTURIS, Barcelona, Spain Vall dHebron Hosp Univ, Med Oncol Dept, Hereditary Canc Genet Grp, Vall dHebron Barcelona Hosp Campus, Barcelona 08035, Spain
- [8] Coping with incidental findings in cancer susceptibility genes after exome sequencing in paediatric patientsEUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 : 12 - 13Carrasco Lopez, Estela论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Inst Oncol, Hereditary Canc Genet Grp, Barcelona, Spain Vall dHebron Hosp, Med Oncol Dept, Barcelona, Spain Vall dHebron Inst Oncol, Hereditary Canc Genet Grp, Barcelona, SpainLopez-Fernandez, Adria论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Inst Oncol, Hereditary Canc Genet Grp, Barcelona, Spain Vall dHebron Hosp, Med Oncol Dept, Barcelona, Spain Vall dHebron Inst Oncol, Hereditary Canc Genet Grp, Barcelona, SpainCodina-Sola, Marta论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Hosp, Dept Clin & Mol Genet, Barcelona, Spain Vall dHebron Inst Oncol, Hereditary Canc Genet Grp, Barcelona, SpainTorres-Esquius, Sara论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Inst Oncol, Hereditary Canc Genet Grp, Barcelona, Spain Vall dHebron Inst Oncol, Hereditary Canc Genet Grp, Barcelona, SpainVillacampa, Guillermo论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Inst Oncol, Oncol Data Sci ODysSey Grp, Barcelona, Spain Vall dHebron Inst Oncol, Hereditary Canc Genet Grp, Barcelona, SpainNavarro, Victor论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Inst Oncol, Hereditary Canc Genet Grp, Barcelona, SpainValenzuela, Irene论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Inst Oncol, Hereditary Canc Genet Grp, Barcelona, SpainPerez Duenas, Belen论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Hosp, Neuropediatr Dept, Barcelona, Spain Vall dHebron Inst Oncol, Hereditary Canc Genet Grp, Barcelona, SpainMaria Cueto-Gonzalez, Anna论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Hosp, Dept Clin & Mol Genet, Barcelona, Spain Vall dHebron Inst Oncol, Hereditary Canc Genet Grp, Barcelona, SpainDiez Gibert, Orland论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Inst Oncol, Hereditary Canc Genet Grp, Barcelona, Spain Vall dHebron Hosp, Dept Clin & Mol Genet, Barcelona, Spain Vall dHebron Inst Oncol, Hereditary Canc Genet Grp, Barcelona, SpainTorres, Maite论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Inst Oncol, Hereditary Canc Genet Grp, Barcelona, Spain Vall dHebron Inst Oncol, Hereditary Canc Genet Grp, Barcelona, SpainPalau, Dolors论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Hosp, Dept Clin & Mol Genet, Barcelona, Spain Vall dHebron Inst Oncol, Hereditary Canc Genet Grp, Barcelona, SpainCruellas, Mara论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Inst Oncol, Hereditary Canc Genet Grp, Barcelona, Spain Vall dHebron Hosp, Med Oncol Dept, Barcelona, Spain Vall dHebron Inst Oncol, Hereditary Canc Genet Grp, Barcelona, SpainSabado, Constantino论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Hosp, Pediat Oncol & Hematol Dept, Barcelona, Spain Vall dHebron Inst Oncol, Hereditary Canc Genet Grp, Barcelona, SpainGarcia Arumi, Elena论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Hosp, Dept Clin & Mol Genet, Barcelona, Spain Vall dHebron Inst Oncol, Hereditary Canc Genet Grp, Barcelona, SpainTizzano, Eduardo论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Hosp, Dept Clin & Mol Genet, Barcelona, Spain Vall dHebron Inst Oncol, Hereditary Canc Genet Grp, Barcelona, SpainMoreno, Lucas论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Hosp, Pediat Oncol & Hematol Dept, Barcelona, Spain Vall dHebron Inst Oncol, Hereditary Canc Genet Grp, Barcelona, SpainBalmana, Judith论文数: 0 引用数: 0 h-index: 0机构: Vall dHebron Inst Oncol, Hereditary Canc Genet Grp, Barcelona, Spain Vall dHebron Hosp, Med Oncol Dept, Barcelona, Spain Vall dHebron Inst Oncol, Hereditary Canc Genet Grp, Barcelona, Spain
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