共 50 条
- [1] Next-Generation Sequencing in Intellectual Disability[J]. JOURNAL OF PEDIATRIC GENETICS, 2015, 4 (03) : 128 - 135Carvill, Gemma L.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Dept Pediat, Div Med Genet, Seattle, WA 98195 USA Univ Washington, Dept Pediat, Div Med Genet, Seattle, WA 98195 USAMefford, Heather C.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Dept Pediat, Div Med Genet, Seattle, WA 98195 USA Univ Washington, Dept Pediat, Div Med Genet, Seattle, WA 98195 USA
- [2] Applications of next-generation whole exome sequencing[J]. Journal of Neurology, 2014, 261 (6) : 1244 - 1246Harding K.E.论文数: 0 引用数: 0 h-index: 0机构: Department of Neurology, Institute of Psychological Medicine and Clinical Neuroscience, Cardiff University, Cardiff Department of Neurology, Institute of Psychological Medicine and Clinical Neuroscience, Cardiff University, CardiffRobertson N.P.论文数: 0 引用数: 0 h-index: 0机构: Department of Neurology, Institute of Psychological Medicine and Clinical Neuroscience, Cardiff University, Cardiff Department of Neurology, Institute of Psychological Medicine and Clinical Neuroscience, Cardiff University, Cardiff
- [3] Next-Generation Sequencing in Unexplained Intellectual Disability[J]. INDIAN JOURNAL OF PEDIATRICS, 2024, 91 (07): : 682 - 695Sandal, Sapna论文数: 0 引用数: 0 h-index: 0机构: Sir Ganga Ram Hosp, Inst Med Genet & Genom, New Delhi, India Sir Ganga Ram Hosp, Inst Med Genet & Genom, New Delhi, IndiaVerma, Ishwar Chander论文数: 0 引用数: 0 h-index: 0机构: Sir Ganga Ram Hosp, Inst Med Genet & Genom, New Delhi, India Sir Ganga Ram Hosp, Inst Med Genet & Genom, New Delhi, IndiaMahay, Sunita Bijarnia论文数: 0 引用数: 0 h-index: 0机构: Sir Ganga Ram Hosp, Inst Med Genet & Genom, New Delhi, India Sir Ganga Ram Hosp, Inst Med Genet & Genom, New Delhi, IndiaDubey, Sudhisha论文数: 0 引用数: 0 h-index: 0机构: Sir Ganga Ram Hosp, Inst Med Genet & Genom, New Delhi, India Sir Ganga Ram Hosp, Inst Med Genet & Genom, New Delhi, IndiaSabharwal, R. K.论文数: 0 引用数: 0 h-index: 0机构: Sir Ganga Ram Hosp, Dept Pediat Neurol, New Delhi, India Sir Ganga Ram Hosp, Inst Med Genet & Genom, New Delhi, IndiaKulshrestha, Samarth论文数: 0 引用数: 0 h-index: 0机构: Sir Ganga Ram Hosp, Inst Med Genet & Genom, New Delhi, India Sir Ganga Ram Hosp, Inst Med Genet & Genom, New Delhi, IndiaSaxena, Renu论文数: 0 引用数: 0 h-index: 0机构: Sir Ganga Ram Hosp, Inst Med Genet & Genom, New Delhi, India Sir Ganga Ram Hosp, Inst Med Genet & Genom, New Delhi, IndiaSuman, Praveen论文数: 0 引用数: 0 h-index: 0机构: Sir Ganga Ram Hosp, Dept Dev Pediat, New Delhi, India Sir Ganga Ram Hosp, Inst Med Genet & Genom, New Delhi, IndiaKumar, Praveen论文数: 0 引用数: 0 h-index: 0机构: Sir Ganga Ram Hosp, Dept Pediat Neurol, New Delhi, India Sir Ganga Ram Hosp, Inst Med Genet & Genom, New Delhi, IndiaPuri, Ratna Dua论文数: 0 引用数: 0 h-index: 0机构: Sir Ganga Ram Hosp, Inst Med Genet & Genom, New Delhi, India Sir Ganga Ram Hosp, Inst Med Genet & Genom, New Delhi, India
- [4] Medical exome sequencing vs whole exome sequencing in the diagnosis of intellectual disability[J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 228 - 228论文数: 引用数: h-index:机构:Keren, B.论文数: 0 引用数: 0 h-index: 0机构: Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, France Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, FranceMignot, C.论文数: 0 引用数: 0 h-index: 0机构: Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, France UPMC, Grp Rech Clin GRC Deficience Intellectuelle & Aut, Paris, France Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, FranceJulien, B.论文数: 0 引用数: 0 h-index: 0机构: Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, France Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, FranceEstrade, C.论文数: 0 引用数: 0 h-index: 0机构: Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, France Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, FranceKaragic, S.论文数: 0 引用数: 0 h-index: 0机构: Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, France Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, FranceLafitte, A.论文数: 0 引用数: 0 h-index: 0机构: Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, France Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, FranceLejeune, E.论文数: 0 引用数: 0 h-index: 0机构: Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, France Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, FranceMach, C.论文数: 0 引用数: 0 h-index: 0机构: Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, France Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, FranceOlin, V.论文数: 0 引用数: 0 h-index: 0机构: Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, France Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, FranceCourtin, T.论文数: 0 引用数: 0 h-index: 0机构: Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, France Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, FranceAfenjar, A.论文数: 0 引用数: 0 h-index: 0机构: Hop Armand Trousseau, APHP, Dept Genet, Paris, France Hop La Pitie Salpetriere, Ctr Reference Deficiences Intellectuelles Causes, Paris, France Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, FranceDoummar, D.论文数: 0 引用数: 0 h-index: 0机构: Hop Armand Trousseau, APHP, Serv Neuropediat, Paris, France Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, FranceMoutard, M.论文数: 0 引用数: 0 h-index: 0机构: Hop Armand Trousseau, APHP, Serv Neuropediat, Paris, France Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, Francede Villemeur, T. Billette论文数: 0 引用数: 0 h-index: 0机构: Hop Armand Trousseau, APHP, Serv Neuropediat, Paris, France Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, FranceNougues, M.论文数: 0 引用数: 0 h-index: 0机构: Hop Armand Trousseau, APHP, Serv Neuropediat, Paris, France Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, FranceValence, S.论文数: 0 引用数: 0 h-index: 0机构: Hop Armand Trousseau, APHP, Serv Neuropediat, Paris, France Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, FranceHeron, B.论文数: 0 引用数: 0 h-index: 0机构: Hop Armand Trousseau, APHP, Serv Neuropediat, Paris, France Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, FranceRodriguez-Levi, D.论文数: 0 引用数: 0 h-index: 0机构: Hop Armand Trousseau, APHP, Serv Neuropediat, Paris, France Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, FranceBurglen, L.论文数: 0 引用数: 0 h-index: 0机构: Hop Armand Trousseau, APHP, Dept Genet, Paris, France Hop Armand Trousseau, Ctr Reference Malformat & Malad Congenit Cervelet, Paris, France Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, FranceWhalen, S.论文数: 0 引用数: 0 h-index: 0机构: Hop Armand Trousseau, APHP, Dept Genet, Paris, France Hop Armand Trousseau, Ctr Reference Malformat & Malad Congenit Cervelet, Paris, France Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, FranceHaye, D.论文数: 0 引用数: 0 h-index: 0机构: Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, France Hop La Pitie Salpetriere, Ctr Reference Deficiences Intellectuelles Causes, Paris, France Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, FranceHeide, S.论文数: 0 引用数: 0 h-index: 0机构: Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, France UPMC, Grp Rech Clin GRC Deficience Intellectuelle & Aut, Paris, France Hop La Pitie Salpetriere, Ctr Reference Deficiences Intellectuelles Causes, Paris, France Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, FranceCharles, P.论文数: 0 引用数: 0 h-index: 0机构: Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, France UPMC, Grp Rech Clin GRC Deficience Intellectuelle & Aut, Paris, France Hop La Pitie Salpetriere, Ctr Reference Deficiences Intellectuelles Causes, Paris, France Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, FranceMarey, I.论文数: 0 引用数: 0 h-index: 0机构: Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, France UPMC, Grp Rech Clin GRC Deficience Intellectuelle & Aut, Paris, France Hop La Pitie Salpetriere, Ctr Reference Deficiences Intellectuelles Causes, Paris, France Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, FranceDepienne, C.论文数: 0 引用数: 0 h-index: 0机构: Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, France UPMC Univ Paris 06, Sorbonne Univ, Inst Cerveau & Moelle Epiniere, CNRS,UMR 7225,INSERM,U1127,ICM, Paris, France Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, FranceHeron, D.论文数: 0 引用数: 0 h-index: 0机构: Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, France UPMC, Grp Rech Clin GRC Deficience Intellectuelle & Aut, Paris, France Hop La Pitie Salpetriere, Ctr Reference Deficiences Intellectuelles Causes, Paris, France Hop La Pitie Salpetriere, APHP, Dept Genet, Paris, France
- [5] New Candidates for Autism/Intellectual Disability Identified by Whole-Exome Sequencing[J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2021, 22 (24)Bruno, Lucia Pia论文数: 0 引用数: 0 h-index: 0机构: Univ Siena, Med Genet, I-53100 Siena, Italy Univ Siena, Dept Med Biotechnol, Med Biotech Hub & Competence Ctr, I-53100 Siena, Italy Univ Siena, Med Genet, I-53100 Siena, ItalyDoddato, Gabriella论文数: 0 引用数: 0 h-index: 0机构: Univ Siena, Med Genet, I-53100 Siena, Italy Univ Siena, Dept Med Biotechnol, Med Biotech Hub & Competence Ctr, I-53100 Siena, Italy Univ Siena, Med Genet, I-53100 Siena, ItalyValentino, Floriana论文数: 0 引用数: 0 h-index: 0机构: Univ Siena, Med Genet, I-53100 Siena, Italy Univ Siena, Dept Med Biotechnol, Med Biotech Hub & Competence Ctr, I-53100 Siena, Italy Univ Siena, Med Genet, I-53100 Siena, Italy论文数: 引用数: h-index:机构:Tita, Rossella论文数: 0 引用数: 0 h-index: 0机构: Azienda Osped Univ Senese, Genet Med, I-53100 Siena, Italy Univ Siena, Med Genet, I-53100 Siena, Italy论文数: 引用数: h-index:机构:Bruttini, Mirella论文数: 0 引用数: 0 h-index: 0机构: Univ Siena, Med Genet, I-53100 Siena, Italy Azienda Osped Univ Senese, Genet Med, I-53100 Siena, Italy Univ Siena, Med Genet, I-53100 Siena, ItalyLo Rizzo, Caterina论文数: 0 引用数: 0 h-index: 0机构: Azienda Osped Univ Senese, Genet Med, I-53100 Siena, Italy Univ Siena, Med Genet, I-53100 Siena, ItalyMencarelli, Maria Antonietta论文数: 0 引用数: 0 h-index: 0机构: Azienda Osped Univ Senese, Genet Med, I-53100 Siena, Italy Univ Siena, Med Genet, I-53100 Siena, ItalyMari, Francesca论文数: 0 引用数: 0 h-index: 0机构: Univ Siena, Med Genet, I-53100 Siena, Italy Univ Siena, Dept Med Biotechnol, Med Biotech Hub & Competence Ctr, I-53100 Siena, Italy Azienda Osped Univ Senese, Genet Med, I-53100 Siena, Italy Univ Siena, Med Genet, I-53100 Siena, ItalyPinto, Anna Maria论文数: 0 引用数: 0 h-index: 0机构: Azienda Osped Univ Senese, Genet Med, I-53100 Siena, Italy Univ Siena, Med Genet, I-53100 Siena, Italy论文数: 引用数: h-index:机构:Fabbiani, Alessandra论文数: 0 引用数: 0 h-index: 0机构: Univ Siena, Med Genet, I-53100 Siena, Italy Univ Siena, Dept Med Biotechnol, Med Biotech Hub & Competence Ctr, I-53100 Siena, Italy Azienda Osped Univ Senese, Genet Med, I-53100 Siena, Italy Univ Siena, Med Genet, I-53100 Siena, ItalyLamacchia, Vittoria论文数: 0 引用数: 0 h-index: 0机构: Univ Siena, Med Genet, I-53100 Siena, Italy Univ Siena, Dept Med Biotechnol, Med Biotech Hub & Competence Ctr, I-53100 Siena, Italy Azienda Osped Univ Senese, Genet Med, I-53100 Siena, Italy Univ Siena, Med Genet, I-53100 Siena, ItalyCarrer, Anna论文数: 0 引用数: 0 h-index: 0机构: Univ Siena, Med Genet, I-53100 Siena, Italy Univ Siena, Dept Med Biotechnol, Med Biotech Hub & Competence Ctr, I-53100 Siena, Italy Azienda Osped Univ Senese, Genet Med, I-53100 Siena, Italy Univ Siena, Med Genet, I-53100 Siena, ItalyCaputo, Valentina论文数: 0 引用数: 0 h-index: 0机构: Univ Siena, Med Genet, I-53100 Siena, Italy Univ Siena, Dept Med Biotechnol, Med Biotech Hub & Competence Ctr, I-53100 Siena, Italy Azienda Osped Univ Senese, Genet Med, I-53100 Siena, Italy Univ Siena, Med Genet, I-53100 Siena, ItalyGranata, Stefania论文数: 0 引用数: 0 h-index: 0机构: Univ Siena, Med Genet, I-53100 Siena, Italy Univ Siena, Dept Med Biotechnol, Med Biotech Hub & Competence Ctr, I-53100 Siena, Italy Azienda Osped Univ Senese, Genet Med, I-53100 Siena, Italy Univ Siena, Med Genet, I-53100 Siena, ItalyBenetti, Elisa论文数: 0 引用数: 0 h-index: 0机构: Univ Siena, Dept Med Biotechnol, Med Biotech Hub & Competence Ctr, I-53100 Siena, Italy Univ Siena, Med Genet, I-53100 Siena, ItalyZguro, Kristina论文数: 0 引用数: 0 h-index: 0机构: Univ Siena, Dept Med Biotechnol, Med Biotech Hub & Competence Ctr, I-53100 Siena, Italy Univ Siena, Med Genet, I-53100 Siena, Italy论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Ariani, Francesca论文数: 0 引用数: 0 h-index: 0机构: Univ Siena, Med Genet, I-53100 Siena, Italy Univ Siena, Dept Med Biotechnol, Med Biotech Hub & Competence Ctr, I-53100 Siena, Italy Azienda Osped Univ Senese, Genet Med, I-53100 Siena, Italy Univ Siena, Med Genet, I-53100 Siena, Italy
- [6] Next-generation sequencing in X-linked intellectual disability[J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2015, 23 (11) : 1513 - 1518论文数: 引用数: h-index:机构:Grasshoff, Ute论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Inst Med Genet & Appl Genom, Tubingen, Germany Tech Univ Dresden, Inst Clin Genet, D-01307 Dresden, GermanyBeck-Woedl, Stefanie论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Inst Med Genet & Appl Genom, Tubingen, Germany Tech Univ Dresden, Inst Clin Genet, D-01307 Dresden, GermanyDufke, Claudia论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Inst Med Genet & Appl Genom, Tubingen, Germany Tech Univ Dresden, Inst Clin Genet, D-01307 Dresden, GermanyBauer, Claudia论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Inst Med Genet & Appl Genom, Tubingen, Germany Tech Univ Dresden, Inst Clin Genet, D-01307 Dresden, GermanyKehrer, Martin论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Inst Med Genet & Appl Genom, Tubingen, Germany Tech Univ Dresden, Inst Clin Genet, D-01307 Dresden, GermanyEvers, Christina论文数: 0 引用数: 0 h-index: 0机构: Heidelberg Univ, Inst Human Genet, Heidelberg, Germany Tech Univ Dresden, Inst Clin Genet, D-01307 Dresden, GermanyMoog, Ute论文数: 0 引用数: 0 h-index: 0机构: Heidelberg Univ, Inst Human Genet, Heidelberg, Germany Tech Univ Dresden, Inst Clin Genet, D-01307 Dresden, GermanyOehl-Jaschkowitz, Barbara论文数: 0 引用数: 0 h-index: 0机构: Practice Human Genet, Homburg, Saar, Germany Tech Univ Dresden, Inst Clin Genet, D-01307 Dresden, Germany论文数: 引用数: h-index:机构:Maiwald, Robert论文数: 0 引用数: 0 h-index: 0机构: Med Care Ctr, Monchengladbach, Germany Tech Univ Dresden, Inst Clin Genet, D-01307 Dresden, GermanyJung, Christine论文数: 0 引用数: 0 h-index: 0机构: Ctr Human Genet, Mannheim, Germany Tech Univ Dresden, Inst Clin Genet, D-01307 Dresden, GermanyKuechler, Alma论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Essen, Inst Human Genet, Essen, Germany Tech Univ Dresden, Inst Clin Genet, D-01307 Dresden, GermanySchulz, Solveig论文数: 0 引用数: 0 h-index: 0机构: Jena Univ Hosp, Ctr Human Genet, Jena, Germany Tech Univ Dresden, Inst Clin Genet, D-01307 Dresden, GermanyMeinecke, Peter论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Hamburg Eppendorf, Inst Human Genet, Hamburg, Germany Tech Univ Dresden, Inst Clin Genet, D-01307 Dresden, GermanySpranger, Stephanie论文数: 0 引用数: 0 h-index: 0机构: Practice Human Genet, Bremen, Germany Tech Univ Dresden, Inst Clin Genet, D-01307 Dresden, GermanyKohlhase, Juergen论文数: 0 引用数: 0 h-index: 0机构: Ctr Human Genet, Freiburg, Germany Tech Univ Dresden, Inst Clin Genet, D-01307 Dresden, GermanySeidel, Joerg论文数: 0 引用数: 0 h-index: 0机构: Practice Pediat, Jena, Germany Tech Univ Dresden, Inst Clin Genet, D-01307 Dresden, GermanyReif, Silke论文数: 0 引用数: 0 h-index: 0机构: Practice Med Genet, Dresden, Germany Tech Univ Dresden, Inst Clin Genet, D-01307 Dresden, GermanyRieger, Manuela论文数: 0 引用数: 0 h-index: 0机构: Practice Med Genet, Dresden, Germany Tech Univ Dresden, Inst Clin Genet, D-01307 Dresden, GermanyRiess, Angelika论文数: 0 引用数: 0 h-index: 0机构: Tech Univ Dresden, Inst Clin Genet, D-01307 Dresden, GermanySturm, Marc论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Inst Med Genet & Appl Genom, Tubingen, Germany Tech Univ Dresden, Inst Clin Genet, D-01307 Dresden, GermanyBickmann, Julia论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Inst Med Genet & Appl Genom, Tubingen, Germany Tech Univ Dresden, Inst Clin Genet, D-01307 Dresden, GermanySchroeder, Christopher论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Inst Med Genet & Appl Genom, Tubingen, Germany Tech Univ Dresden, Inst Clin Genet, D-01307 Dresden, GermanyDufke, Andreas论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Inst Med Genet & Appl Genom, Tubingen, Germany Tech Univ Dresden, Inst Clin Genet, D-01307 Dresden, GermanyRiess, Olaf论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Inst Med Genet & Appl Genom, Tubingen, Germany Tech Univ Dresden, Inst Clin Genet, D-01307 Dresden, GermanyBauer, Peter论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Inst Med Genet & Appl Genom, Tubingen, Germany Tech Univ Dresden, Inst Clin Genet, D-01307 Dresden, Germany
- [7] Next-generation sequencing in X-linked intellectual disability[J]. European Journal of Human Genetics, 2015, 23 : 1513 - 1518Andreas Tzschach论文数: 0 引用数: 0 h-index: 0机构: Institute of Clinical Genetics,Ute Grasshoff论文数: 0 引用数: 0 h-index: 0机构: Institute of Clinical Genetics,Stefanie Beck-Woedl论文数: 0 引用数: 0 h-index: 0机构: Institute of Clinical Genetics,Claudia Dufke论文数: 0 引用数: 0 h-index: 0机构: Institute of Clinical Genetics,Claudia Bauer论文数: 0 引用数: 0 h-index: 0机构: Institute of Clinical Genetics,Martin Kehrer论文数: 0 引用数: 0 h-index: 0机构: Institute of Clinical Genetics,Christina Evers论文数: 0 引用数: 0 h-index: 0机构: Institute of Clinical Genetics,Ute Moog论文数: 0 引用数: 0 h-index: 0机构: Institute of Clinical Genetics,Barbara Oehl-Jaschkowitz论文数: 0 引用数: 0 h-index: 0机构: Institute of Clinical Genetics,Nataliya Di Donato论文数: 0 引用数: 0 h-index: 0机构: Institute of Clinical Genetics,Robert Maiwald论文数: 0 引用数: 0 h-index: 0机构: Institute of Clinical Genetics,Christine Jung论文数: 0 引用数: 0 h-index: 0机构: Institute of Clinical Genetics,Alma Kuechler论文数: 0 引用数: 0 h-index: 0机构: Institute of Clinical Genetics,Solveig Schulz论文数: 0 引用数: 0 h-index: 0机构: Institute of Clinical Genetics,Peter Meinecke论文数: 0 引用数: 0 h-index: 0机构: Institute of Clinical Genetics,Stephanie Spranger论文数: 0 引用数: 0 h-index: 0机构: Institute of Clinical Genetics,Jürgen Kohlhase论文数: 0 引用数: 0 h-index: 0机构: Institute of Clinical Genetics,Jörg Seidel论文数: 0 引用数: 0 h-index: 0机构: Institute of Clinical Genetics,Silke Reif论文数: 0 引用数: 0 h-index: 0机构: Institute of Clinical Genetics,Manuela Rieger论文数: 0 引用数: 0 h-index: 0机构: Institute of Clinical Genetics,Angelika Riess论文数: 0 引用数: 0 h-index: 0机构: Institute of Clinical Genetics,Marc Sturm论文数: 0 引用数: 0 h-index: 0机构: Institute of Clinical Genetics,Julia Bickmann论文数: 0 引用数: 0 h-index: 0机构: Institute of Clinical Genetics,Christopher Schroeder论文数: 0 引用数: 0 h-index: 0机构: Institute of Clinical Genetics,Andreas Dufke论文数: 0 引用数: 0 h-index: 0机构: Institute of Clinical Genetics,Olaf Riess论文数: 0 引用数: 0 h-index: 0机构: Institute of Clinical Genetics,Peter Bauer论文数: 0 引用数: 0 h-index: 0机构: Institute of Clinical Genetics,
- [8] Combining Panel-Based Next-Generation Sequencing and Exome Sequencing for Genetic Liver Diseases[J]. JOURNAL OF PEDIATRICS, 2023, 258Chen, Chi -Bo论文数: 0 引用数: 0 h-index: 0机构: Natl Taiwan Univ, Coll Med, Dept Pediat, 17F, 8, Chung Shan South Rd, Taipei 100, Taiwan Childrens Hosp, 17F, 8, Chung Shan South Rd, Taipei 100, Taiwan Natl Taiwan Univ, Coll Med, Dept Pediat, 17F, 8, Chung Shan South Rd, Taipei 100, TaiwanHsu, Jacob Shujui论文数: 0 引用数: 0 h-index: 0机构: Natl Taiwan Univ, Coll Med, Grad Inst Med Genom & Prote, Taipei, Taiwan Natl Taiwan Univ, Coll Med, Dept Pediat, 17F, 8, Chung Shan South Rd, Taipei 100, TaiwanChen, Pei-Lung论文数: 0 引用数: 0 h-index: 0机构: Natl Taiwan Univ, Coll Med, Grad Inst Med Genom & Prote, Taipei, Taiwan Natl Taiwan Univ Hosp, Dept Med Genet, Taipei, Taiwan Natl Taiwan Univ, Coll Med & Hosp, Dept Internal Med, Taipei, Taiwan Natl Taiwan Univ, Coll Med, Dept Pediat, 17F, 8, Chung Shan South Rd, Taipei 100, TaiwanWu, Jia-Feng论文数: 0 引用数: 0 h-index: 0机构: Natl Taiwan Univ, Coll Med, Dept Pediat, 17F, 8, Chung Shan South Rd, Taipei 100, Taiwan Childrens Hosp, 17F, 8, Chung Shan South Rd, Taipei 100, Taiwan Natl Taiwan Univ, Coll Med, Dept Pediat, 17F, 8, Chung Shan South Rd, Taipei 100, TaiwanLi, Huei-Ying论文数: 0 引用数: 0 h-index: 0机构: Natl Taiwan Univ, Coll Med, Med Microbiome Ctr, Taipei, Taiwan Natl Taiwan Univ, Coll Med, Dept Pediat, 17F, 8, Chung Shan South Rd, Taipei 100, TaiwanLiou, Bang -Yu论文数: 0 引用数: 0 h-index: 0机构: Natl Taiwan Univ, Coll Med, Dept Pediat, 17F, 8, Chung Shan South Rd, Taipei 100, Taiwan Childrens Hosp, 17F, 8, Chung Shan South Rd, Taipei 100, Taiwan Natl Taiwan Univ, Coll Med, Dept Pediat, 17F, 8, Chung Shan South Rd, Taipei 100, TaiwanChang, Mei-Hwei论文数: 0 引用数: 0 h-index: 0机构: Natl Taiwan Univ, Coll Med, Dept Pediat, 17F, 8, Chung Shan South Rd, Taipei 100, Taiwan Childrens Hosp, 17F, 8, Chung Shan South Rd, Taipei 100, Taiwan Natl Taiwan Univ, Coll Med, Dept Pediat, 17F, 8, Chung Shan South Rd, Taipei 100, TaiwanNi, Yen-Hsuan论文数: 0 引用数: 0 h-index: 0机构: Natl Taiwan Univ, Coll Med, Dept Pediat, 17F, 8, Chung Shan South Rd, Taipei 100, Taiwan Childrens Hosp, 17F, 8, Chung Shan South Rd, Taipei 100, Taiwan Natl Taiwan Univ, Coll Med, Med Microbiome Ctr, Taipei, Taiwan Natl Taiwan Univ Hosp, Hepatitis Res Ctr, Taipei, Taiwan Natl Taiwan Univ, Coll Med, Dept Pediat, 17F, 8, Chung Shan South Rd, Taipei 100, TaiwanHwu, Wuh-Liang论文数: 0 引用数: 0 h-index: 0机构: Natl Taiwan Univ, Coll Med, Dept Pediat, 17F, 8, Chung Shan South Rd, Taipei 100, Taiwan Childrens Hosp, 17F, 8, Chung Shan South Rd, Taipei 100, Taiwan Natl Taiwan Univ, Coll Med, Grad Inst Med Genom & Prote, Taipei, Taiwan Natl Taiwan Univ, Coll Med, Dept Pediat, 17F, 8, Chung Shan South Rd, Taipei 100, TaiwanChien, Yin-Hsiu论文数: 0 引用数: 0 h-index: 0机构: Natl Taiwan Univ, Coll Med, Dept Pediat, 17F, 8, Chung Shan South Rd, Taipei 100, Taiwan Childrens Hosp, 17F, 8, Chung Shan South Rd, Taipei 100, Taiwan Natl Taiwan Univ, Coll Med, Grad Inst Med Genom & Prote, Taipei, Taiwan Natl Taiwan Univ, Coll Med, Dept Pediat, 17F, 8, Chung Shan South Rd, Taipei 100, TaiwanChou, Yen -Yin论文数: 0 引用数: 0 h-index: 0机构: Natl Cheng Kung Univ Hosp, Dept Pediat, Tainan, Taiwan Natl Taiwan Univ, Coll Med, Dept Pediat, 17F, 8, Chung Shan South Rd, Taipei 100, Taiwan论文数: 引用数: h-index:机构:Lee, Ni-Chung论文数: 0 引用数: 0 h-index: 0机构: Natl Taiwan Univ, Coll Med, Dept Pediat, 17F, 8, Chung Shan South Rd, Taipei 100, Taiwan Childrens Hosp, 17F, 8, Chung Shan South Rd, Taipei 100, Taiwan Natl Taiwan Univ, Coll Med, Dept Pediat, 17F, 8, Chung Shan South Rd, Taipei 100, TaiwanChen, Huey-Ling论文数: 0 引用数: 0 h-index: 0机构: Natl Taiwan Univ, Coll Med, Dept Pediat, 17F, 8, Chung Shan South Rd, Taipei 100, Taiwan Childrens Hosp, 17F, 8, Chung Shan South Rd, Taipei 100, Taiwan Natl Taiwan Univ Hosp, Hepatitis Res Ctr, Taipei, Taiwan Natl Taiwan Univ, Coll Med, Dept Med Educ & Bioeth, Taipei, Taiwan Natl Taiwan Univ, Coll Med, Dept Pediat, 17F, 8, Chung Shan South Rd, Taipei 100, Taiwan
- [9] Next-generation whole exome sequencing of glioblastoma with a primitive neuronal component[J]. BRAIN TUMOR PATHOLOGY, 2019, 36 (03) : 129 - 134Xu, Guiyan论文数: 0 引用数: 0 h-index: 0机构: North Shore Univ Hosp, Dept Pathol & Lab Med, Lake Success, NY 11042 USA Long Isl Jewish Med Ctr, Lake Success, NY 11042 USA North Shore Univ Hosp, Dept Pathol & Lab Med, Lake Success, NY 11042 USAZheng, Hongwu论文数: 0 引用数: 0 h-index: 0机构: Weill Cornell Med Coll, Dept Pathol & Lab Med, New York, NY 10065 USA North Shore Univ Hosp, Dept Pathol & Lab Med, Lake Success, NY 11042 USALi, Jian Yi论文数: 0 引用数: 0 h-index: 0机构: North Shore Univ Hosp, Dept Pathol & Lab Med, Lake Success, NY 11042 USA Long Isl Jewish Med Ctr, Lake Success, NY 11042 USA Donald & Barbara Zucker Sch Med Hofstra Northwell, Inst Canc, Northwell Hlth, Lake Success, Hempstead, NY 11549 USA North Shore Univ Hosp, Dept Pathol & Lab Med, Lake Success, NY 11042 USA
- [10] Next-generation whole exome sequencing of glioblastoma with a primitive neuronal component[J]. Brain Tumor Pathology, 2019, 36 : 129 - 134Guiyan Xu论文数: 0 引用数: 0 h-index: 0机构: North Shore University Hospital and Long Island Jewish Medical Center,Department of Pathology and Laboratory MedicineHongwu Zheng论文数: 0 引用数: 0 h-index: 0机构: North Shore University Hospital and Long Island Jewish Medical Center,Department of Pathology and Laboratory MedicineJian Yi Li论文数: 0 引用数: 0 h-index: 0机构: North Shore University Hospital and Long Island Jewish Medical Center,Department of Pathology and Laboratory Medicine