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- [21] Rare genetic susceptibility variants assessment in autism spectrum disorder: detection rate and practical useTRANSLATIONAL PSYCHIATRY, 2020, 10 (01)论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Cassinari, Kevin论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, UNIROUEN, INSERM, U1245,Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Rouen Univ Hosp, Dept Genet, Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Rouen Univ Hosp, Reference Ctr Dev Disorders, Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Normandie Univ, UNIROUEN, INSERM, U1245,Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Goldenberg, Alice论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, UNIROUEN, INSERM, U1245,Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Rouen Univ Hosp, Dept Genet, Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Rouen Univ Hosp, Reference Ctr Dev Disorders, Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Normandie Univ, UNIROUEN, INSERM, U1245,Normandy Ctr Genom & Personalized Med, F-76000 Rouen, FranceGuerrot, Anne-Marie论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, UNIROUEN, INSERM, U1245,Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Rouen Univ Hosp, Dept Genet, Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Rouen Univ Hosp, Reference Ctr Dev Disorders, Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Normandie Univ, UNIROUEN, INSERM, U1245,Normandy Ctr Genom & Personalized Med, F-76000 Rouen, FranceRichard, Anne-Claire论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, UNIROUEN, INSERM, U1245,Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Rouen Univ Hosp, Dept Genet, Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Rouen Univ Hosp, Reference Ctr Dev Disorders, Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Normandie Univ, UNIROUEN, INSERM, U1245,Normandy Ctr Genom & Personalized Med, F-76000 Rouen, FranceDrouin-Garraud, Valerie论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, UNIROUEN, INSERM, U1245,Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Rouen Univ Hosp, Dept Genet, Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Rouen Univ Hosp, Reference Ctr Dev Disorders, Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Normandie Univ, UNIROUEN, INSERM, U1245,Normandy Ctr Genom & Personalized Med, F-76000 Rouen, FranceBrehin, Anne-Claire论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, UNIROUEN, INSERM, U1245,Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Rouen Univ Hosp, Dept Genet, Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Rouen Univ Hosp, Reference Ctr Dev Disorders, Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Normandie Univ, UNIROUEN, INSERM, U1245,Normandy Ctr Genom & Personalized Med, F-76000 Rouen, FranceSoleimani, Maryam论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, UNIROUEN, INSERM, U1245,Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Rouen Univ Hosp, Dept Genet, Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Rouen Univ Hosp, Reference Ctr Dev Disorders, Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Normandie Univ, UNIROUEN, INSERM, U1245,Normandy Ctr Genom & Personalized Med, F-76000 Rouen, FranceTaton, Romain论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp Rouvray, Ctr Ressources Autisme Normandie Seine Eure, Sotteville Les Rouen, France Normandie Univ, UNIROUEN, INSERM, U1245,Normandy Ctr Genom & Personalized Med, F-76000 Rouen, FranceRotharmel, Maud论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp Rouvray, Dept Res, Sotteville Les Rouen, France Normandie Univ, UNIROUEN, INSERM, U1245,Normandy Ctr Genom & Personalized Med, F-76000 Rouen, FranceRosier, Antoine论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp Rouvray, Ctr Ressources Autisme Normandie Seine Eure, Sotteville Les Rouen, France Normandie Univ, UNIROUEN, INSERM, U1245,Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France论文数: 引用数: h-index:机构:Le Meur, Nathalie论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, UNIROUEN, INSERM, U1245,Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Rouen Univ Hosp, Dept Genet, Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Rouen Univ Hosp, Reference Ctr Dev Disorders, Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Normandie Univ, UNIROUEN, INSERM, U1245,Normandy Ctr Genom & Personalized Med, F-76000 Rouen, FranceJoly-Helas, Geraldine论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, UNIROUEN, INSERM, U1245,Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Rouen Univ Hosp, Dept Genet, Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Rouen Univ Hosp, Reference Ctr Dev Disorders, Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Normandie Univ, UNIROUEN, INSERM, U1245,Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Deleuze, Jean-Francois论文数: 0 引用数: 0 h-index: 0机构: Univ Paris Saclay, CNRGH, Inst Biol Francois Jacob, CEA, F-91057 Evry, France Normandie Univ, UNIROUEN, INSERM, U1245,Normandy Ctr Genom & Personalized Med, F-76000 Rouen, FranceOlaso, Robert论文数: 0 引用数: 0 h-index: 0机构: Univ Paris Saclay, CNRGH, Inst Biol Francois Jacob, CEA, F-91057 Evry, France Normandie Univ, UNIROUEN, INSERM, U1245,Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France论文数: 引用数: h-index:机构:Nicolas, Gael论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, UNIROUEN, INSERM, U1245,Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Rouen Univ Hosp, Dept Genet, Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Rouen Univ Hosp, Reference Ctr Dev Disorders, Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Normandie Univ, UNIROUEN, INSERM, U1245,Normandy Ctr Genom & Personalized Med, F-76000 Rouen, FranceGuillin, Olivier论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, UNIROUEN, INSERM, U1245,Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Rouen Univ Hosp, Dept Genet, Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Rouen Univ Hosp, Reference Ctr Dev Disorders, Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Ctr Hosp Rouvray, Dept Res, Sotteville Les Rouen, France Normandie Univ, UNIROUEN, INSERM, U1245,Normandy Ctr Genom & Personalized Med, F-76000 Rouen, FranceCampion, Dominique论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, UNIROUEN, INSERM, U1245,Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Rouen Univ Hosp, Dept Genet, Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Rouen Univ Hosp, Reference Ctr Dev Disorders, Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France Ctr Hosp Rouvray, Dept Res, Sotteville Les Rouen, France Normandie Univ, UNIROUEN, INSERM, U1245,Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France
- [22] Rare Pathogenic Variants Identified in Whole Exome Sequencing of Monozygotic Twins With Autism Spectrum DisorderPEDIATRIC NEUROLOGY, 2024, 158 : 113 - 123Anitha, Ayyappan论文数: 0 引用数: 0 h-index: 0机构: Inst Commun & Cognit Neurosci ICCONS, Dept Neurogenet, Palakkad 679523, Kerala, India Inst Commun & Cognit Neurosci ICCONS, Dept Neurogenet, Palakkad 679523, Kerala, IndiaBanerjee, Moinak论文数: 0 引用数: 0 h-index: 0机构: Rajiv Gandhi Ctr Biotechnol, Dept Neurobiol, Thiruvananthapuram, Kerala, India Inst Commun & Cognit Neurosci ICCONS, Dept Neurogenet, Palakkad 679523, Kerala, IndiaThanseem, Ismail论文数: 0 引用数: 0 h-index: 0机构: Inst Commun & Cognit Neurosci ICCONS, Dept Neurogenet, Palakkad 679523, Kerala, India Inst Commun & Cognit Neurosci ICCONS, Dept Neurogenet, Palakkad 679523, Kerala, IndiaPrakash, Anil论文数: 0 引用数: 0 h-index: 0机构: Rajiv Gandhi Ctr Biotechnol, Dept Neurobiol, Thiruvananthapuram, Kerala, India Inst Commun & Cognit Neurosci ICCONS, Dept Neurogenet, Palakkad 679523, Kerala, IndiaMelempatt, Nisha论文数: 0 引用数: 0 h-index: 0机构: ICCONS, Dept Audiol & Speech Language Pathol ASLP, Palakkad, Kerala, India Inst Commun & Cognit Neurosci ICCONS, Dept Neurogenet, Palakkad 679523, Kerala, IndiaSumitha, P. S.论文数: 0 引用数: 0 h-index: 0机构: Inst Commun & Cognit Neurosci ICCONS, Dept Neurogenet, Palakkad 679523, Kerala, India Inst Commun & Cognit Neurosci ICCONS, Dept Neurogenet, Palakkad 679523, Kerala, IndiaIype, Mary论文数: 0 引用数: 0 h-index: 0机构: ICCONS, Dept Neurol, Thiruvananthapuram, Kerala, India ICCONS, Dept Neurol, Shoranur, Kerala, India Govt Med Coll, Dept Pediat Neurol, Thiruvananthapuram, Kerala, India Inst Commun & Cognit Neurosci ICCONS, Dept Neurogenet, Palakkad 679523, Kerala, IndiaThomas, Sanjeev V.论文数: 0 引用数: 0 h-index: 0机构: ICCONS, Dept Neurol, Thiruvananthapuram, Kerala, India ICCONS, Dept Neurol, Shoranur, Kerala, India Inst Commun & Cognit Neurosci ICCONS, Dept Neurogenet, Palakkad 679523, Kerala, India
- [23] Association Analysis of Rare CNTN5 Variants With Autism Spectrum Disorder in a Japanese PopulationNEUROPSYCHOPHARMACOLOGY REPORTS, 2025, 45 (01)Hadi, Abdul Fuad论文数: 0 引用数: 0 h-index: 0机构: Niigata Univ, Sch Med, Dept Psychiat, Niigata, Japan Niigata Univ, Grad Sch Med & Dent Sci, Niigata, Japan Niigata Univ, Sch Med, Dept Psychiat, Niigata, JapanArta, Reza K.论文数: 0 引用数: 0 h-index: 0机构: Niigata Univ, Sch Med, Dept Psychiat, Niigata, Japan Niigata Univ, Grad Sch Med & Dent Sci, Niigata, Japan Niigata Univ, Sch Med, Dept Psychiat, Niigata, Japan论文数: 引用数: h-index:机构:Egawa, Jun论文数: 0 引用数: 0 h-index: 0机构: Niigata Univ, Sch Med, Dept Psychiat, Niigata, Japan Niigata Univ, Grad Sch Med & Dent Sci, Niigata, Japan Niigata Univ, Sch Med, Dept Psychiat, Niigata, JapanWatanabe, Yuichiro论文数: 0 引用数: 0 h-index: 0机构: Niigata Univ, Sch Med, Dept Psychiat, Niigata, Japan Niigata Univ, Grad Sch Med & Dent Sci, Niigata, Japan Uonuma Kikan Hosp, Dept Psychiat, Niigata, Japan Niigata Univ, Sch Med, Dept Psychiat, Niigata, JapanOzaki, Norio论文数: 0 引用数: 0 h-index: 0机构: Nagoya Univ, Grad Sch Med, Pathophysiol Mental Disorders, Nagoya, Aichi, Japan Niigata Univ, Sch Med, Dept Psychiat, Niigata, JapanSomeya, Toshiyuki论文数: 0 引用数: 0 h-index: 0机构: Niigata Univ, Sch Med, Dept Psychiat, Niigata, Japan Niigata Univ, Grad Sch Med & Dent Sci, Niigata, Japan Niigata Univ, Sch Med, Dept Psychiat, Niigata, Japan
- [24] Rare genetic susceptibility variants assessment in autism spectrum disorder: detection rate and practical useTranslational Psychiatry, 10Thomas Husson论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ,Department of ResearchFrançois Lecoquierre论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ,Department of ResearchKevin Cassinari论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ,Department of ResearchCamille Charbonnier论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ,Department of ResearchOlivier Quenez论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ,Department of ResearchAlice Goldenberg论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ,Department of ResearchAnne-Marie Guerrot论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ,Department of ResearchAnne-Claire Richard论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ,Department of ResearchValérie Drouin-Garraud论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ,Department of ResearchAnne-Claire Brehin论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ,Department of ResearchMaryam Soleimani论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ,Department of ResearchRomain Taton论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ,Department of ResearchMaud Rotharmel论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ,Department of ResearchAntoine Rosier论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ,Department of ResearchPascal Chambon论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ,Department of ResearchNathalie Le Meur论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ,Department of ResearchGéraldine Joly-Helas论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ,Department of ResearchPascale Saugier-Veber论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ,Department of ResearchAnne Boland论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ,Department of ResearchJean-François Deleuze论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ,Department of ResearchRobert Olaso论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ,Department of ResearchThierry Frebourg论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ,Department of ResearchGael Nicolas论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ,Department of ResearchOlivier Guillin论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ,Department of ResearchDominique Campion论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ,Department of Research
- [25] An integrative scoring approach for prioritization of rare autism spectrum disorder candidate variants from whole exome sequencing dataScientific Reports, 15 (1)Apurba Shil论文数: 0 引用数: 0 h-index: 0机构: Ben-Gurion University of the Negev,Department of Epidemiology, Biostatistics and Community Health Sciences, Faculty of Health Sciences Ben-Gurion University of the Negev,Department of Epidemiology, Biostatistics and Community Health Sciences, Faculty of Health SciencesNoa Arava论文数: 0 引用数: 0 h-index: 0机构: Ben-Gurion University of the Negev,Azrieli National Centre for Autism and Neurodevelopment Research Ben-Gurion University of the Negev,Department of Epidemiology, Biostatistics and Community Health Sciences, Faculty of Health SciencesNoam Levi论文数: 0 引用数: 0 h-index: 0机构: Ben-Gurion University of the Negev,Zlotowski Center for Neuroscience Ben-Gurion University of the Negev,Department of Epidemiology, Biostatistics and Community Health Sciences, Faculty of Health SciencesLiron Levine论文数: 0 引用数: 0 h-index: 0机构: Ben-Gurion University of the Negev,Azrieli National Centre for Autism and Neurodevelopment Research Ben-Gurion University of the Negev,Department of Epidemiology, Biostatistics and Community Health Sciences, Faculty of Health SciencesHava Golan论文数: 0 引用数: 0 h-index: 0机构: Ben-Gurion University of the Negev,Department of Epidemiology, Biostatistics and Community Health Sciences, Faculty of Health Sciences Ben-Gurion University of the Negev,Department of Epidemiology, Biostatistics and Community Health Sciences, Faculty of Health SciencesGal Meiri论文数: 0 引用数: 0 h-index: 0机构: Ben-Gurion University of the Negev,Azrieli National Centre for Autism and Neurodevelopment Research Ben-Gurion University of the Negev,Department of Epidemiology, Biostatistics and Community Health Sciences, Faculty of Health SciencesAnalya Michaelovski论文数: 0 引用数: 0 h-index: 0机构: Ben-Gurion University of the Negev,Zlotowski Center for Neuroscience Ben-Gurion University of the Negev,Department of Epidemiology, Biostatistics and Community Health Sciences, Faculty of Health SciencesYair Tsadaka论文数: 0 引用数: 0 h-index: 0机构: Ben-Gurion University of the Negev,Bioinformatics Core Facility Ben-Gurion University of the Negev,Department of Epidemiology, Biostatistics and Community Health Sciences, Faculty of Health SciencesAdi Aran论文数: 0 引用数: 0 h-index: 0机构: Ben-Gurion University of the Negev,Azrieli National Centre for Autism and Neurodevelopment Research Ben-Gurion University of the Negev,Department of Epidemiology, Biostatistics and Community Health Sciences, Faculty of Health SciencesIdan Menashe论文数: 0 引用数: 0 h-index: 0机构: Ben-Gurion University of the Negev,Zlotowski Center for Neuroscience Ben-Gurion University of the Negev,Department of Epidemiology, Biostatistics and Community Health Sciences, Faculty of Health Sciences
- [26] Comprehensive Analysis of Rare Variants of 101 Autism-Linked Genes in a Hungarian Cohort of Autism Spectrum Disorder PatientsFRONTIERS IN GENETICS, 2019, 10Balicza, Peter论文数: 0 引用数: 0 h-index: 0机构: Semmelweis Univ, Inst Genom Med & Rare Disorders, Budapest, Hungary Semmelweis Univ, Inst Genom Med & Rare Disorders, Budapest, HungaryVarga, Noemi Agnes论文数: 0 引用数: 0 h-index: 0机构: Semmelweis Univ, Inst Genom Med & Rare Disorders, Budapest, Hungary Semmelweis Univ, Inst Genom Med & Rare Disorders, Budapest, HungaryBolgar, Bence论文数: 0 引用数: 0 h-index: 0机构: Budapest Univ Technol & Econ, Fac Elect Engn & Informat, Budapest, Hungary Semmelweis Univ, Inst Genom Med & Rare Disorders, Budapest, HungaryPentelenyi, Klara论文数: 0 引用数: 0 h-index: 0机构: Semmelweis Univ, Inst Genom Med & Rare Disorders, Budapest, Hungary Semmelweis Univ, Inst Genom Med & Rare Disorders, Budapest, HungaryBencsik, Renata论文数: 0 引用数: 0 h-index: 0机构: Semmelweis Univ, Inst Genom Med & Rare Disorders, Budapest, Hungary Semmelweis Univ, Inst Genom Med & Rare Disorders, Budapest, HungaryGal, Aniko论文数: 0 引用数: 0 h-index: 0机构: Semmelweis Univ, Inst Genom Med & Rare Disorders, Budapest, Hungary Semmelweis Univ, Inst Genom Med & Rare Disorders, Budapest, HungaryGezsi, Andras论文数: 0 引用数: 0 h-index: 0机构: Budapest Univ Technol & Econ, Fac Elect Engn & Informat, Budapest, Hungary Semmelweis Univ, Inst Genom Med & Rare Disorders, Budapest, HungaryPrekop, Csilla论文数: 0 引用数: 0 h-index: 0机构: Vadaskert Fdn Childrens Mental Hlth, Budapest, Hungary Semmelweis Univ, Inst Genom Med & Rare Disorders, Budapest, HungaryMolnar, Viktor论文数: 0 引用数: 0 h-index: 0机构: Semmelweis Univ, Inst Genom Med & Rare Disorders, Budapest, Hungary Semmelweis Univ, Inst Genom Med & Rare Disorders, Budapest, HungaryMolnar, Maria Judit论文数: 0 引用数: 0 h-index: 0机构: Semmelweis Univ, Inst Genom Med & Rare Disorders, Budapest, Hungary Semmelweis Univ, Inst Genom Med & Rare Disorders, Budapest, Hungary
- [27] miRNA and lncRNA gene variants in Autism Spectrum DisorderEUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 258 - 259Marques, A. R.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Hlth Doutor Ricardo Jorge, Hlth Promot & Non Communicable Dis Prevent, Lisbon, Portugal Univ Lisbon, Fac Ciencias, BioISI, Lisbon, Portugal Natl Inst Hlth Doutor Ricardo Jorge, Hlth Promot & Non Communicable Dis Prevent, Lisbon, PortugalMartiniano, H.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Hlth Doutor Ricardo Jorge, Hlth Promot & Non Communicable Dis Prevent, Lisbon, Portugal Univ Lisbon, Fac Ciencias, BioISI, Lisbon, Portugal Univ Lisbon, Fac Ciencias, Dept Informat, Lisbon, Portugal Natl Inst Hlth Doutor Ricardo Jorge, Hlth Promot & Non Communicable Dis Prevent, Lisbon, PortugalSantos, J. X.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Hlth Doutor Ricardo Jorge, Hlth Promot & Non Communicable Dis Prevent, Lisbon, Portugal Univ Lisbon, Fac Ciencias, BioISI, Lisbon, Portugal Natl Inst Hlth Doutor Ricardo Jorge, Hlth Promot & Non Communicable Dis Prevent, Lisbon, PortugalVilela, J.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Hlth Doutor Ricardo Jorge, Hlth Promot & Non Communicable Dis Prevent, Lisbon, Portugal Univ Lisbon, Fac Ciencias, BioISI, Lisbon, Portugal Natl Inst Hlth Doutor Ricardo Jorge, Hlth Promot & Non Communicable Dis Prevent, Lisbon, PortugalAsif, M.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Hlth Doutor Ricardo Jorge, Hlth Promot & Non Communicable Dis Prevent, Lisbon, Portugal Univ Lisbon, Fac Ciencias, BioISI, Lisbon, Portugal Natl Inst Hlth Doutor Ricardo Jorge, Hlth Promot & Non Communicable Dis Prevent, Lisbon, PortugalOliveira, G.论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp Coimbra, Unidade Neurodesenvolvimento & Autismo UNDA, Ctr Invest & Formacao Clin, Serv Ctr Desenvolvimento Crianca,Hosp Pediat, Coimbra, Portugal Univ Coimbra, Unidade Neurodesenvolvimento & Autismo UNDA, Ctr Invest & Formacao Clin, Serv Ctr Desenvolvimento Crianca,Hosp Pediat, Coimbra, Portugal Univ Coimbra, Fac Med, Inst Biomed Imaging & Life Sci, Coimbra, Portugal Natl Inst Hlth Doutor Ricardo Jorge, Hlth Promot & Non Communicable Dis Prevent, Lisbon, PortugalRomao, L.论文数: 0 引用数: 0 h-index: 0机构: Univ Lisbon, Fac Ciencias, BioISI, Lisbon, Portugal Natl Inst Hlth Doutor Ricardo Jorge, Human Genet Dept, Lisbon, Portugal Natl Inst Hlth Doutor Ricardo Jorge, Hlth Promot & Non Communicable Dis Prevent, Lisbon, PortugalVicente, A. M.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Hlth Doutor Ricardo Jorge, Hlth Promot & Non Communicable Dis Prevent, Lisbon, Portugal Univ Lisbon, Fac Ciencias, BioISI, Lisbon, Portugal Inst Gulbenkian Ciencias, Oeiras, Portugal Natl Inst Hlth Doutor Ricardo Jorge, Hlth Promot & Non Communicable Dis Prevent, Lisbon, Portugal
- [28] Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variantsNATURE NEUROSCIENCE, 2019, 22 (12) : 1961 - +Satterstrom, F. Kyle论文数: 0 引用数: 0 h-index: 0机构: Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USA Broad Inst MIT & Harvard, Program Med & Populat Genet, Cambridge, MA 02142 USA Massachusetts Gen Hosp, Dept Med, Analyt & Translat Genet Unit, Boston, MA 02114 USA Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USAWalters, Raymond K.论文数: 0 引用数: 0 h-index: 0机构: Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USA Broad Inst MIT & Harvard, Program Med & Populat Genet, Cambridge, MA 02142 USA Massachusetts Gen Hosp, Dept Med, Analyt & Translat Genet Unit, Boston, MA 02114 USA Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USASingh, Tarjinder论文数: 0 引用数: 0 h-index: 0机构: Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USA Broad Inst MIT & Harvard, Program Med & Populat Genet, Cambridge, MA 02142 USA Massachusetts Gen Hosp, Dept Med, Analyt & Translat Genet Unit, Boston, MA 02114 USA Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USAWigdor, Emilie M.论文数: 0 引用数: 0 h-index: 0机构: Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USA Broad Inst MIT & Harvard, Program Med & Populat Genet, Cambridge, MA 02142 USA Massachusetts Gen Hosp, Dept Med, Analyt & Translat Genet Unit, Boston, MA 02114 USA Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USALescai, Francesco论文数: 0 引用数: 0 h-index: 0机构: Lundbeck Fdn Initiat Integrat Psychiat Res, iPSYCH, Aarhus, Denmark Aarhus Univ, Ctr Integrat Sequencing, iSEQ, Aarhus, Denmark Aarhus Univ, Dept Biomed Human Genet, Aarhus, Denmark Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USADemontis, Ditte论文数: 0 引用数: 0 h-index: 0机构: Lundbeck Fdn Initiat Integrat Psychiat Res, iPSYCH, Aarhus, Denmark Aarhus Univ, Ctr Integrat Sequencing, iSEQ, Aarhus, Denmark Aarhus Univ, Dept Biomed Human Genet, Aarhus, Denmark Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USAKosmicki, Jack A.论文数: 0 引用数: 0 h-index: 0机构: Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USA Broad Inst MIT & Harvard, Program Med & Populat Genet, Cambridge, MA 02142 USA Massachusetts Gen Hosp, Dept Med, Analyt & Translat Genet Unit, Boston, MA 02114 USA Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USAGrove, Jakob论文数: 0 引用数: 0 h-index: 0机构: Lundbeck Fdn Initiat Integrat Psychiat Res, iPSYCH, Aarhus, Denmark Aarhus Univ, Ctr Integrat Sequencing, iSEQ, Aarhus, Denmark Aarhus Univ, Dept Biomed Human Genet, Aarhus, Denmark Aarhus Univ, Bioinformat Res Ctr, Aarhus, Denmark Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USAStevens, Christine论文数: 0 引用数: 0 h-index: 0机构: Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USA Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USABybjerg-Grauholm, Jonas论文数: 0 引用数: 0 h-index: 0机构: Lundbeck Fdn Initiat Integrat Psychiat Res, iPSYCH, Aarhus, Denmark Statens Serum Inst, Dept Congenital Disorders, Ctr Neonatal Screening, Copenhagen, Denmark Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USABaekvad-Hansen, Marie论文数: 0 引用数: 0 h-index: 0机构: Lundbeck Fdn Initiat Integrat Psychiat Res, iPSYCH, Aarhus, Denmark Statens Serum Inst, Dept Congenital Disorders, Ctr Neonatal Screening, Copenhagen, Denmark Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USAPalmer, Duncan S.论文数: 0 引用数: 0 h-index: 0机构: Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USA Broad Inst MIT & Harvard, Program Med & Populat Genet, Cambridge, MA 02142 USA Massachusetts Gen Hosp, Dept Med, Analyt & Translat Genet Unit, Boston, MA 02114 USA Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USAMaller, Julian B.论文数: 0 引用数: 0 h-index: 0机构: Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USA Broad Inst MIT & Harvard, Program Med & Populat Genet, Cambridge, MA 02142 USA Massachusetts Gen Hosp, Dept Med, Analyt & Translat Genet Unit, Boston, MA 02114 USA Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USANordentoft, Merete论文数: 0 引用数: 0 h-index: 0机构: Lundbeck Fdn Initiat Integrat Psychiat Res, iPSYCH, Aarhus, Denmark Univ Copenhagen, Mental Hlth Ctr Copenhagen, Mental Hlth Serv Capital Reg Denmark, Copenhagen, Denmark Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USAMors, Ole论文数: 0 引用数: 0 h-index: 0机构: Lundbeck Fdn Initiat Integrat Psychiat Res, iPSYCH, Aarhus, Denmark Aarhus Univ Hosp, Psychosis Res Unit, Risskov, Denmark Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USARobinson, Elise B.论文数: 0 引用数: 0 h-index: 0机构: Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USA Broad Inst MIT & Harvard, Program Med & Populat Genet, Cambridge, MA 02142 USA Massachusetts Gen Hosp, Dept Med, Analyt & Translat Genet Unit, Boston, MA 02114 USA Harvard TH Chan Sch Publ Hlth, Dept Epidemiol, Boston, MA USA Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USAHougaard, David M.论文数: 0 引用数: 0 h-index: 0机构: Lundbeck Fdn Initiat Integrat Psychiat Res, iPSYCH, Aarhus, Denmark Statens Serum Inst, Dept Congenital Disorders, Ctr Neonatal Screening, Copenhagen, Denmark Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USAWerge, Thomas M.论文数: 0 引用数: 0 h-index: 0机构: Lundbeck Fdn Initiat Integrat Psychiat Res, iPSYCH, Aarhus, Denmark Mental Hlth Serv Copenhagen, Inst Biol Psychiat, Mental Hlth Ctr Sct, Roskilde, Denmark Univ Copenhagen, Dept Clin Med, Copenhagen, Denmark Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USAMortensen, Preben Bo论文数: 0 引用数: 0 h-index: 0机构: Lundbeck Fdn Initiat Integrat Psychiat Res, iPSYCH, Aarhus, Denmark Aarhus Univ, Ctr Integrat Sequencing, iSEQ, Aarhus, Denmark Aarhus Univ, Natl Ctr Register Based Res, Aarhus, Denmark Aarhus Univ, Ctr Integrated Register Based Res, Aarhus, Denmark Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USANeale, Benjamin M.论文数: 0 引用数: 0 h-index: 0机构: Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USA Broad Inst MIT & Harvard, Program Med & Populat Genet, Cambridge, MA 02142 USA Massachusetts Gen Hosp, Dept Med, Analyt & Translat Genet Unit, Boston, MA 02114 USA Harvard Med Sch, Dept Med, Boston, MA 02115 USA Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USABorglum, Anders D.论文数: 0 引用数: 0 h-index: 0机构: Lundbeck Fdn Initiat Integrat Psychiat Res, iPSYCH, Aarhus, Denmark Aarhus Univ, Ctr Integrat Sequencing, iSEQ, Aarhus, Denmark Aarhus Univ, Dept Biomed Human Genet, Aarhus, Denmark Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USADaly, Mark J.论文数: 0 引用数: 0 h-index: 0机构: Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USA Broad Inst MIT & Harvard, Program Med & Populat Genet, Cambridge, MA 02142 USA Massachusetts Gen Hosp, Dept Med, Analyt & Translat Genet Unit, Boston, MA 02114 USA Harvard Med Sch, Dept Med, Boston, MA 02115 USA Univ Helsinki, Inst Mol Med Finland, HiLIFE, Helsinki, Finland Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USA
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