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- [31] Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disordersMolecular Psychiatry, 2014, 19 : 872 - 879E M Kenny论文数: 0 引用数: 0 h-index: 0机构: Neuropsychiatric Genetics Research Group,Department of PsychiatryP Cormican论文数: 0 引用数: 0 h-index: 0机构: Neuropsychiatric Genetics Research Group,Department of PsychiatryS Furlong论文数: 0 引用数: 0 h-index: 0机构: Neuropsychiatric Genetics Research Group,Department of PsychiatryE Heron论文数: 0 引用数: 0 h-index: 0机构: Neuropsychiatric Genetics Research Group,Department of PsychiatryG Kenny论文数: 0 引用数: 0 h-index: 0机构: Neuropsychiatric Genetics Research Group,Department of PsychiatryC Fahey论文数: 0 引用数: 0 h-index: 0机构: Neuropsychiatric Genetics Research Group,Department of PsychiatryE Kelleher论文数: 0 引用数: 0 h-index: 0机构: Neuropsychiatric Genetics Research Group,Department of PsychiatryS Ennis论文数: 0 引用数: 0 h-index: 0机构: Neuropsychiatric Genetics Research Group,Department of PsychiatryD Tropea论文数: 0 引用数: 0 h-index: 0机构: Neuropsychiatric Genetics Research Group,Department of PsychiatryR Anney论文数: 0 引用数: 0 h-index: 0机构: Neuropsychiatric Genetics Research Group,Department of PsychiatryA P Corvin论文数: 0 引用数: 0 h-index: 0机构: Neuropsychiatric Genetics Research Group,Department of PsychiatryG Donohoe论文数: 0 引用数: 0 h-index: 0机构: Neuropsychiatric Genetics Research Group,Department of PsychiatryL Gallagher论文数: 0 引用数: 0 h-index: 0机构: Neuropsychiatric Genetics Research Group,Department of PsychiatryM Gill论文数: 0 引用数: 0 h-index: 0机构: Neuropsychiatric Genetics Research Group,Department of PsychiatryD W Morris论文数: 0 引用数: 0 h-index: 0机构: Neuropsychiatric Genetics Research Group,Department of Psychiatry
- [32] Excess of de novo variants in genes involved in chromatin remodelling in patients with marfanoid habitus and intellectual disabilityJOURNAL OF MEDICAL GENETICS, 2020, 57 (07) : 466 - 474Chevarin, Martin论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceDuffourd, Yannis论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, France CHU Dijon, FHU TRANSLAD, Dijon, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceA. Barnard, Rebecca论文数: 0 引用数: 0 h-index: 0机构: Oregon Hlth & Sci Univ, Dept Mol & Med Genet, Portland, OR 97201 USA Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceMoutton, Sebastien论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, France CHU Dijon, Ctr Genet, Dijon, France CHU Dijon, Ctr Reference Anomalies Dev & Syndromes Malformat, Dijon, France CHU Bordeaux, Ctr Reference Anomalies Dev & Syndromes Malformat, Bordeaux, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceLecoquierre, Francois论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceDaoud, Fatma论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceKuentz, Paul论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, France CHU Dijon, FHU TRANSLAD, Dijon, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceCabret, Caroline论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceThevenon, Julien论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, France CHU Dijon, Ctr Genet, Dijon, France CHU Dijon, Ctr Reference Anomalies Dev & Syndromes Malformat, Dijon, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceGautier, Elodie论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon, FHU TRANSLAD, Dijon, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceCallier, Patrick论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, France CHU Dijon, FHU TRANSLAD, Dijon, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceSt-Onge, Judith论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceJouan, Thibaud论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceLacombe, Didier论文数: 0 引用数: 0 h-index: 0机构: CHU Bordeaux, Ctr Reference Anomalies Dev & Syndromes Malformat, Bordeaux, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceDelrue, Marie Ange论文数: 0 引用数: 0 h-index: 0机构: CHU Bordeaux, Ctr Reference Anomalies Dev & Syndromes Malformat, Bordeaux, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceGoizet, Cyril论文数: 0 引用数: 0 h-index: 0机构: CHU Bordeaux, Ctr Reference Anomalies Dev & Syndromes Malformat, Bordeaux, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceMorice-Picard, Fanny论文数: 0 引用数: 0 h-index: 0机构: CHU Bordeaux, Ctr Reference Anomalies Dev & Syndromes Malformat, Bordeaux, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceVan-Gils, Julien论文数: 0 引用数: 0 h-index: 0机构: CHU Bordeaux, Ctr Reference Anomalies Dev & Syndromes Malformat, Bordeaux, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceMunnich, Arnold论文数: 0 引用数: 0 h-index: 0机构: Hop Necker Enfants Malad, AP HP, Dept Genet, IHU Imagine, Paris, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceLyonnet, Stanislas论文数: 0 引用数: 0 h-index: 0机构: Hop Necker Enfants Malad, AP HP, Dept Genet, IHU Imagine, Paris, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceCormier-Daire, Valerie论文数: 0 引用数: 0 h-index: 0机构: Hop Necker Enfants Malad, AP HP, Dept Genet, IHU Imagine, Paris, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceBaujat, Genevieve论文数: 0 引用数: 0 h-index: 0机构: Hop Necker Enfants Malad, AP HP, Dept Genet, IHU Imagine, Paris, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceHolder, Muriel论文数: 0 引用数: 0 h-index: 0机构: CHU Lille, Ctr Reference Anomalies Dev & Syndromes Malformat, Lille, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FrancePetit, Florence论文数: 0 引用数: 0 h-index: 0机构: CHU Lille, Ctr Reference Anomalies Dev & Syndromes Malformat, Lille, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceLeheup, Bruno论文数: 0 引用数: 0 h-index: 0机构: CHU Nancy, Ctr Reference Anomalies Dev & Syndromes Malformat, Nancy, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceOdent, Sylvie论文数: 0 引用数: 0 h-index: 0机构: CHU Rennes, Ctr Reference Anomalies Dev & Syndromes Malformat, Rennes, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceJouk, Pierre-Simon论文数: 0 引用数: 0 h-index: 0机构: CHU Grenoble, Ctr Reference Anomalies Dev & Syndromes Malformat, Grenoble, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceLopez, Gipsy论文数: 0 引用数: 0 h-index: 0机构: CHU Grenoble, Ctr Reference Anomalies Dev & Syndromes Malformat, Grenoble, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceGenevieve, David论文数: 0 引用数: 0 h-index: 0机构: CHU Montpellier, Ctr Reference Anomalies Dev & Syndromes Malformat, Montpellier, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceCollignon, Patrick论文数: 0 引用数: 0 h-index: 0机构: CHI Toulon, Ctr Reference Anomalies Dev & Syndromes Malformat, La Seyne Sur Mer, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceMartin-Coignard, Dominique论文数: 0 引用数: 0 h-index: 0机构: CH Le Mans, Ctr Competence Anomalies Dev & Syndromes Malforma, Le Mans, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceJacquette, Aurelia论文数: 0 引用数: 0 h-index: 0机构: AP HP, Dept Genet, Paris, France AP HP, Ctr Reference Deficiences Intellectuelles Causes, Paris, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FrancePerrin, Laurence论文数: 0 引用数: 0 h-index: 0机构: Hop Robert Debre, AP HP, Ctr Reference Anomalies Dev & Syndromes Malformat, Paris, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FrancePutoux, Audrey论文数: 0 引用数: 0 h-index: 0机构: Hosp Civils Lyon, Ctr Reference Anomalies Dev & Syndromes Malformat, Lyon, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceSarrazin, Elisabeth论文数: 0 引用数: 0 h-index: 0机构: CHU Ft France, Hop Pierre Zobda Quitman, Ctr Reference Caribeen Malad Rares Neurol & Neuro, La Martinique, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceAmarof, Khadija论文数: 0 引用数: 0 h-index: 0机构: CHU Ft France, Hop Pierre Zobda Quitman, Ctr Reference Caribeen Malad Rares Neurol & Neuro, La Martinique, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceMissotte, Isabelle论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp Terr, Serv Pediat, New Caledonia, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceCoubes, Christine论文数: 0 引用数: 0 h-index: 0机构: CHU Montpellier, Ctr Reference Anomalies Dev & Syndromes Malformat, Montpellier, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceJagadeesh, Sujatha论文数: 0 引用数: 0 h-index: 0机构: Mediscan, Geneomm Med Ctr, Chennai, Tamil Nadu, India Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceLapi, Elisabetta论文数: 0 引用数: 0 h-index: 0机构: Azienda Osped Univ Anna Meyer, Genet Med, Florence, Italy Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceDemurger, Florence论文数: 0 引用数: 0 h-index: 0机构: CH Vannes, Serv Pediat Genet, Vannes, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceGoldenberg, Alice论文数: 0 引用数: 0 h-index: 0机构: CHU Rouen, Ctr Reference Anomalies Dev & Syndromes Malformat, Rouen, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceDoco-Fenzy, Martine论文数: 0 引用数: 0 h-index: 0机构: CHU Reims, Ctr Reference Anomalies Dev & Syndromes Malformat, EA3801, Reims, France CHU Reims, Serv Genet, Reims, France UFR Med Reims, Reims, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceMignot, Cyril论文数: 0 引用数: 0 h-index: 0机构: AP HP, Dept Genet, Paris, France AP HP, Ctr Reference Deficiences Intellectuelles Causes, Paris, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceHeron, Delphine论文数: 0 引用数: 0 h-index: 0机构: AP HP, Dept Genet, Paris, France AP HP, Ctr Reference Deficiences Intellectuelles Causes, Paris, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceJean-Marcais, Nolwenn论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon, FHU TRANSLAD, Dijon, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceMasurel, Alice论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon, Ctr Genet, Dijon, France CHU Dijon, Ctr Reference Anomalies Dev & Syndromes Malformat, Dijon, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceEl Chehadeh, Salima论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon, Ctr Genet, Dijon, France CHU Dijon, Ctr Reference Anomalies Dev & Syndromes Malformat, Dijon, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceMarle, Nathalie论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, France CHU Dijon, FHU TRANSLAD, Dijon, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, FranceHuet, Frederic论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon, FHU TRANSLAD, Dijon, France CHU Dijon, Serv Pediat 1, Dijon, France Univ Bourgogne Franche Comte, UMR Lipides, Genet Anomalies Dev, INSERM,U1231,Nutr, Dijon, France
- [33] 'Sequencing of cardiomyopathy genes in patients with hypertrophic cardiomyopathy reveals enrichment for rare variants in the genes for arrhythmogenic right ventricular cardiomyopathy'EUROPEAN JOURNAL OF HUMAN GENETICS, 2022, 30 (SUPPL 1) : 192 - 192Salakhov, Ramil Rinatovich论文数: 0 引用数: 0 h-index: 0机构: Res Inst Med Genet, Tomsk, Russia Res Inst Med Genet, Tomsk, RussiaGolubenko, Maria V.论文数: 0 引用数: 0 h-index: 0机构: Res Inst Med Genet, Tomsk, Russia Res Inst Med Genet, Tomsk, RussiaZarubin, Alexey A.论文数: 0 引用数: 0 h-index: 0机构: Res Inst Med Genet, Tomsk, Russia Res Inst Med Genet, Tomsk, RussiaPavlyukova, Elena N.论文数: 0 引用数: 0 h-index: 0机构: Cardiol Res Inst, Tomsk, Russia Res Inst Med Genet, Tomsk, RussiaKanev, Alexander F.论文数: 0 引用数: 0 h-index: 0机构: Cardiol Res Inst, Tomsk, Russia Res Inst Med Genet, Tomsk, RussiaGlotov, Oleg S.论文数: 0 引用数: 0 h-index: 0机构: City Hosp 40, St Petersburg, Russia Res Inst Med Genet, Tomsk, RussiaAlaverdian, Diana A.论文数: 0 引用数: 0 h-index: 0机构: City Hosp 40, St Petersburg, Russia Res Inst Med Genet, Tomsk, RussiaTsay, Viktoriia V.论文数: 0 引用数: 0 h-index: 0机构: City Hosp 40, St Petersburg, Russia Res Inst Med Genet, Tomsk, RussiaValiakhmetov, Nail R.论文数: 0 引用数: 0 h-index: 0机构: Res Inst Med Genet, Tomsk, Russia Res Inst Med Genet, Tomsk, RussiaNazarenko, Maria S.论文数: 0 引用数: 0 h-index: 0机构: Res Inst Med Genet, Tomsk, Russia Res Inst Med Genet, Tomsk, Russia
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