학술논문


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'학술논문' 에서 검색결과 56건 | 목록 1~20
Academic Journal
Sarah M. BrookerMaria NovelliRobert CoukosNeha PrakashWalaa A. KamelMarta Amengual‐GualMathieu AnheimGiulia BarciaTanya BardakjianFranciska BaurSteffen BerweckBigna K. BölsterliMelanie BruggerThomas CassiniNicolas ChatronBrian CornerHormos Salimi DafsariJean‐Madeleine de Sainte AgatheColin A. EllisKimberly M. EzellCendrine FoucardSteven J. FruchtMaria C. GarciaDeepak GillAnne GuimierRizwan HamidDamià Heine‐SuñerPeter HerkenrathMarie HullyIoannis U. IsaiasLouis JanuelChloe LaurencinTaylor LautAlinoe LavillaureixGaetan LescaMarion Lesieur‐SebellinLuca MagistrelliCecilia MarelliHeather C. MeffordBryce A. MendelsohnSaadet Mercimek‐AndrewsClaire MillerShekeeb S. MohammadFrancesca MorganteSirisha NandipatiThomas OpladenMahesh PadmanabanMicaela PauniGianni PezzoliAmelie PitonFrancis RamondGiulietta M. RiboldiChristelle Rougeot‐JungFernando Santos‐SimarroIngrid E. SchefferNaoual SerariChristine M. StahlAnn Stembridge KungSusana Tarongí SanchezChristel Thauvin‐RobinetMarianne TillChristine TranchantChristopher TroedsonThomas F. TropeaOlivier VanakkerPatricia VegaMaxi Leona WieseUdo WieshmannLaura J. WilliamsThomas WirthMichael ZechHans ZempelEmmanuel RozeVincenzo LeuzziSerena GalosiVictor S. C. FungGemma CarvillDimitri KraincElizabeth GerardNiccolò E. Mencacci
Ann Neurol
Academic Journal
Caroline NavaBenjamin CogneAmandine SantiniElsa LeitãoFrançois LecoquierreYuyang ChenSarah L. StentonThomas BesnardSolveig HeideSarah BaerAbhilasha JakharSonja NeuserBoris KerenAnne FaudetSylvie ForlaniMarie FaoucherKevin UguenKonrad PlatzerAlexandra AfenjarJean-Luc AlessandriStephanie AndresChloé AngeliniBernard AralBenoit ArveilerTania Attie-BitachMarion Aubert MuccaGuillaume BanneauTahsin Stefan BarakatGiulia BarciaStéphanie BaulacClaire BeneteauFouzia BenkerdouVirginie BernardStéphane BézieauDominique BonneauMarie-Noelle Bonnet-DupeyronSimon BoussionOdile BouteElise Brischoux-BoucherSamantha J. BryenJulien BurattiTiffany BusaAlmuth CaliebeYline CapriKévin CassinariRoseline CaumesCamille CenniPascal ChambonPerrine CharlesJohn ChristodoulouCindy ColsonSolène ConradAuriane CospainJuliette CoursimaultThomas CourtinMadeline CouseCharles CouttonIsabelle CreveauxAlissa M. D’GamaBenjamin DauriatJean-Madeleine de Sainte AgatheGiulia Del GobboAndrée Delahaye-DuriezJulian DelanneAnne-Sophie Denommé-PichonAnne Dieux-CoeslierLaura Do Souto FerreiraMartine Doco-FenzyStephan DrukewitzVéronique DubocChristèle DubourgYannis DuffourdDavid DymentSalima El ChehadehMonique ElmalehLaurence FaivreSamuel FennellyHanna FischerMélanie FradinCamille Galludec VaillantBenjamin GanneJamal GhoumidHimanshu GoelZeynep Gokce-SamarAlice GoldenbergRomain Gonfreville RobertSvetlana GorokhovaLouise GoujonVictoria GranierMathilde GrasJohn M. GreallyBianca GreitenPaul GueguenAnne-Marie GuerrotSaurav GuhaAnne GuimierTobias B. HaackHamza Hadj AbdallahYosra HallebRadu HarbuzMadeleine HarrisJulia HentschelBénédicte HéronMarc-Phillip HitzA. Micheil InnesVincent JadasLouis JanuelNolwenn Jean-MarçaisVaidehi JobanputraFlorence JobicLudmila JorneaCéline JostSophie JuliaFrank J. KaiserDaniel KaschtaSabine KayaPetra KettelerBochra KhadijaFabian KilpertCordula KnoppFlorian KraftIlona KreyMarilyn LackmyFanny LaffargueLaetitia LambertRyan LamontVincent LaugelSteven LaurieJulie L. LauzonLouis LebretonMarine LebrunMarine LegendreEric LeguernDaphné LehalleElodie LejeuneGaetan LescaMarion Lesieur-SebellinJonathan LevyAgnès LinglartStanislas LyonnetKevin LüthyAlan S. MaCorinne MachJean-Louis MandelLamisse Mansour-HendiliJulien MarcadierVictor MarinHenri MargotValentine MarquetAngèle MayJohannes A. MayrCatherine MeriddaVincent MichaudCaroline MichotGwenael NadeauSophie NaudionLaetitia NguyenMathilde NizonFrédérique NowakSylvie OdentValerie OlinIkeoluwa A. Osei-OwusuMatthew OsmondKatrin ÕunapLaurent PasquierSandrine PassemardMelissa PaulyOlivier PatatMarine PensecLaurence Perrin-SabourinFlorence PetitChristophe PhilippeMarc PlanesAnnapurna PoduriCéline PoirsierAntoine PouzetBradley PrinceClément ProuteauAurora PujolCaroline RacineMélanie RamaFrancis RamondKara RanguinMargaux RawayAndré ReisMathilde RenaudNicole RevencuAnne-Claire RichardLucile Riera-NavarroRocio RiusDiana RodriguezAgustí Rodriguez-PalmeroSophie RondeauAnnika Roser-UnruhChristelle Rougeot JungHana SafraouVéronique SatrePascale Saugier-VeberClément SauvestreElise SchaeferWanqing ShaoIna SchanzeJan-Ulrich SchlumpAgatha Schlüter MartinCaroline Schluth-BolardSarah SchuhmannChristopher SchröderMonisha SebastinSabine SigaudyMalte SpielmannMarta SpodenkiewiczLaura St ClairJulie SteffannRadka StoevaHarald SurowyMark A. TarnopolskyCalina TodosiAnnick ToutainFrédéric Tran Mau-ThemAstrid UnterlauftJulien Van-GilsClémence VanlerbergheGeorgia VasileiouGabriella VeraAndré VerdelAlain VerloesYoann VialCédric VignalMarie VincentCatherine Vincent-DelormeAline Vincent-DevulderAntonio VitobelloSacha WeberMarjolaine WillemsKhaoula Zaafrane-KhachnaouiPia ZacherLena ZeltnerAlban ZieglerWojciech P. GalejHélène DollfusChristel ThauvinKym M. BoycottPierre MarijonAlban LermineValérie MalanMarlène RioAlma KuechlerBertrand IsidorSéverine DrunatThomas SmolNicolas ChatronAmélie PitonGael NicolasMatias WagnerRami Abou JamraDelphine HéronCyril MignotPierre BlancAnne O’Donnell-LuriaNicola WhiffinCamille CharbonnierClément CharentonJulien ThevenonChristel Depienne
Nat Genet
Nature Genetics
Academic Journal
Dong LiQin WangAllan BayatMark R. BattigYijing ZhouDaniëlle G.M. BoschGijs van HaaftenLeslie GrangerAndrea K. PetersenLuis A. Pérez-JuradoGemma Aznar-LaínAnushree AnejaMiroslava HancarovaSarka BendovaMartin SchwarzRadka Kremlikova PourovaZdenek SedlacekBeth A. KeenaMichael E. MarchCuiping HouNora O’ConnorElizabeth J. BhojMargaret H. HarrGabrielle LemireKym M. BoycottMeghan TowneMegan LiMark TarnopolskyLauren BradyMichael J. ParkerHanna FaghfouryLea Kristin ParsleyEmanuele AgoliniMaria Lisa DenticiAntonio NovelliMeredith WrightRachel PalmquistKhanh LaiMarcello ScalaPasquale StrianoMichele IacominoFederico ZaraAnnina CooperTimothy J. MaarupMelissa BylerRobert Roger LebelTugce B. BalciRaymond LouieMichael LyonsJessica DouglasCatherine NowakAlexandra AfenjarJuliane HoyerBoris KerenSaskia M. MaasMahdi M. MotazackerJulian A. Martinez-AgostoAhna M. RabaniElizabeth M. McCormickMarni J. FalkSarah M. RuggieroIngo HelbigRikke S. MøllerLino TessarolloFrancesco Tomassoni ArdoriMary Ellen PalkoTzung-Chien HsiehPeter M. KrawitzMythily GanapathiBruce D. GelbVaidehi JobanputraAshley WilsonJohn GreallySébastien JacquemontKhadijé JiziAnge-Line BruelChloé QuelinVinod K. MisraErika ChickCorrado RomanoDonatella GrecoAlessia ArenaManuela MorleoVincenzo NigroRie SeyamaYuri UchiyamaNaomichi MatsumotoRyoji TairaKatsuya TashiroYasunari SakaiGökhan YigitBernd WollnikMichael WagnerBarbara KutscheAnna C.E. HurstMichelle L. ThompsonRyan SchmidtLinda RandolphRebecca C. SpillmannVandana ShashiEdward J. HigginbothamDawn CordeiroAmanda CarnevaleGregory CostainTayyaba KhanBenoît FunalotFrederic Tran Mau-ThemLuis Fernandez Garcia MoyaSixto García-MiñaúrMatthew OsmondLauren ChadNada QuerciaDiana CarrascoChumei LiAmarilis Sanchez-ValleMeghan KelleyMathilde NizonBrynjar O. JenssonPatrick SulemKari StefanssonSvetlana GorokhovaTiffany BusaMarlène RioHamza Hadj HabdallahMarion Lesieur-SebellinJeanne AmielVéronique PingaultSandra MercierMarie VincentChristophe PhilippeClemence Fatus-FauconnierKathryn FriendRebecca K. HalliganSunita BiswasJane RosserCheryl ShoubridgeMark CorbettChristopher BarnettJozef GeczKathleen LeppigAnne SlavotinekCarlo MarcelisRolph PfundtBert B.A. de VriesMarjon A. van SlegtenhorstAlice S. BrooksBenjamin CogneThomas RambaudZeynep TümerElaine H. ZackaiNaiara AkizuYuanquan SongHakon Hakonarson
The Journal of Clinical Investigation, Vol 134, Iss 1 (2024)
Academic Journal
Italian botanist (2022). doi:10.3897/italianbotanist.13.86403
info:cnr-pdr/source/autori:Fabrizio Bartolucci; Gianniantonio Domina; Sebastiano Andreatta; Carlo Argenti; Giovanni Astuti; Sandro Ballelli; Sergio Ballestrin; Enrico Banfi; Davide Barberis; Liliana Bernardo; Alessio Bertolli; Fabrizio Bonali; Federica Bonini; Thomas Bruschi; Giovanni Buccomino; Orazio Caldarella; Laura Cancellieri; Paolo Caputo; Fabio Conti; Antonietta Crisanti; Emanuele Del Guacchio; Francesco Falcinelli; Francesco Festi; Valentina Ferri; Goffredo Filibeck; Gabriele Galasso; Giovanni Gestri; Daniela Gigante; Leonardo Gubellini; Günter Gottschlich; Riccardo Guarino; Nicole Hofmann; Gergely Király; Paolo Laghi; Valerio Lazzeri; Michele Lonati; Fabio Luchino; Jacopo Lupoletti; Giacomo Mei; Marco Merli; Konrad Pagitz; Bruno Paura; Riccardo Pennesi; Enrico Vito Perrino; Antonio Pica; Brunello Pierini; Lorenzo Pinzani; Marco Pittarello; Safiya Praleskouskaya; Filippo Prosser; Francesco Roma-Marzio; Francesco Santi; Daniele Saiani; Anastasia Sebellin; Adriano Soldano; Tommaso Spilli; Adriano Stinca; Massimo Terzi; Manuel Tiburtini; Giulia Tomasi; Roberto Venanzoni; Lorenzo Lastrucci/titolo:Notulae to the Italian native vascular flora: 13/doi:10.3897%2Fitalianbotanist.13.86403/rivista:Italian botanist/anno:2022/pagina_da:/pagina_a:/intervallo_pagine:/volume
Italian Botanist, Vol 13, Iss, Pp 67-84 (2022)
Italian Botanist 13: 67-84
Academic Journal
Lesieur-Sebellin M; Fédération de Génétique et Médecine Génomique, Service de Médecine Génomique des Maladies Rares, APHP.Centre, Hôpital Necker-Enfants Malades, Paris, France.; Génétique des Troubles du Neurodéveloppement INSERM UMR_1163, Institut Imagine, Université Paris Cité, Paris, France.; Wigby K; Department of Genetics, Division of Genomic Medicine, UC Davis MIND Institute, Sacramento, California, USA.; Rady Children's Institute for Genomic Medicine, San Diego, California, USA.; Schaefer E; Service de Génétique Médicale, Institut de Génétique Médicale d'Alsace, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.; Gouronc A; Laboratoire de diagnostic génétique, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.; Chatron N; Service de Génétique, Hospices Civils de Lyon, Bron Cedex, France.; Laboratoire Physiopathologie et Génétique du Neurone et du Muscle, CNRS UMR 5261, Institut NeuroMyoGène, Lyon, France.; Poulat AL; 9Service de Neuropédiatrie, Hospices Civils de Lyon, Lyon, France.; Putoux A; Service de Génétique, Hospices Civils de Lyon, Lyon, France.; INSERM U1028, CNRS UMR5292, UCBL1, GENDEV Team, Neurosciences Research Center of Lyon, Lyon, France.; Goldenberg A; Inserm U1245, Univ Rouen Normandie, Normandie Univ, Rouen, France.; Department of Genetics and Reference Center for Developmental Disorders, CHU Rouen, Rouen, France.; Quibeuf M; Inserm U1245, Univ Rouen Normandie, Normandie Univ, Rouen, France.; Department of Genetics and Reference Center for Developmental Disorders, CHU Rouen, Rouen, France.; Chambon P; Inserm U1245, Univ Rouen Normandie, Normandie Univ, Rouen, France.; Department of Genetics and Reference Center for Developmental Disorders, CHU Rouen, Rouen, France.; Rondeau S; Fédération de Génétique et Médecine Génomique, Service de Médecine Génomique des Maladies Rares, APHP.Centre, Hôpital Necker-Enfants Malades, Paris, France.; Molecular Genetics Laboratory, Groupe hospitalier Necker Enfants malades, Assistance publique-Hôpitaux de Paris, Paris, France.; Barcia G; Fédération de Génétique et Médecine Génomique, Service de Médecine Génomique des Maladies Rares, APHP.Centre, Hôpital Necker-Enfants Malades, Paris, France.; Levy J; Département de Génétique, Hôpital Robert Debré, Paris, France.; Piard J; Centre de génétique Humaine, Centre Hospitalier Universitaire, Université de Franche-Comté, Besançon, France.; UMR 1231 GAD, Inserm, Université de Bourgogne, Dijon, France.; Kuentz P; Oncobiologie Génétique Bioinformatique, FHU-TRANSLAD et Institut GIMI, Université de Franche-Comté, CHU Besançon, Besancon, France.; INSERM UMR1231 GAD Génétique des Anomalies du Développement, Université de Bourgogne, Dijon, France.; Doco-Fenzy M; Service de génétique, CRMR anddirares, CHU de Reims, Reims, France.; CHU de Nantes, Service de génétique, Nantes, France.; Bednarek N; Service de génétique, CRMR anddirares, CHU de Reims, Reims, France.; Caumes R; Service de Génétique Clinique, Hôpital Jeanne de Flandre, Lille, France.; Bouquillon S; Institut de Génétique Médicale, Hôpital Jeanne de Flandre, Lille, France.; Le Caignec C; Service de Génétique Médicale, CHU Toulouse Purpan, Toulouse, France.; ToNIC, INSERM UMR1214, Toulouse, France.; Patat O; Service de Génétique Médicale, CHU Toulouse Purpan, Toulouse, France.; Khau Van Kien P; Génétique Médicale, Centre de Compétences Anomalies du Développement et Syndromes Malformatifs, Hôpital Carémeau-CHU de Nîmes, Nimes, France.; Chiesa J; UF de Cytogénétique et Génétique Médicale, Hôpital Carémeau, CHU Nîmes, Nîmes, France.; Delplancq G; Unité de Génétique Constitutionnelle, Service de Biologie, Centre Hospitalier de Versailles, Le Chesnay, France.; Bacrot S; Unité de Génétique Constitutionnelle, Service de Biologie, Centre Hospitalier de Versailles, Le Chesnay, France.; Brisset S; Unité de Génétique Constitutionnelle, Service de Biologie, Centre Hospitalier de Versailles, Le Chesnay, France.; Ginglinger E; Service de pédiatrie, Hôpitaux Civils de Colmar, Colmar, France.; Cantagrel V; Génétique des Troubles du Neurodéveloppement INSERM UMR_1163, Institut Imagine, Université Paris Cité, Paris, France.; Lenberg J; Rady Children's Institute for Genomic Medicine, San Diego, California, USA.; Friedman JR; Department of Neuroscience, Rady Children's Institute for Genomic Medicine, San Diego, California, USA.; Division of Neurology, Rady Children's Hospital San Diego, San Diego, California, USA.; Rio M; Fédération de Génétique et Médecine Génomique, Service de Médecine Génomique des Maladies Rares, APHP.Centre, Hôpital Necker-Enfants Malades, Paris, France.; Génétique des Troubles du Neurodéveloppement INSERM UMR_1163, Institut Imagine, Université Paris Cité, Paris, France.; Scheidecker S; Laboratoire de diagnostic génétique, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.; Malan V; Fédération de Génétique et Médecine Génomique, Service de Médecine Génomique des Maladies Rares, APHP.Centre, Hôpital Necker-Enfants Malades, Paris, France valerie.malan@aphp.fr.; Génétique des Troubles du Neurodéveloppement INSERM UMR_1163, Institut Imagine, Université Paris Cité, Paris, France.
Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE
Academic Journal
Massier M; Department of Genetics, Reims University Hospital, Reims, France.; Doco-Fenzy M; Department of Genetics, Reims University Hospital, Reims, France.; Department of Genetics, Nantes University Hospital, Nantes, France.; Egloff M; Department of Genetics, Poitiers University Hospital, Poitiers, France.; University of Poitiers, INSERM, LNEC, Department of Genetics, Poitiers University Hospital, Poitiers, France.; Le Guillou X; Department of Genetics, Poitiers University Hospital, Poitiers, France.; University of Poitiers, CNRS, LMA, Department of Genetics, Poitiers University Hospital, Poitiers, France.; Le Guyader G; Department of Genetics, Poitiers University Hospital, Poitiers, France.; Redon S; Department of Genetics, Brest University Hospital, Brest, France.; Intellectual Disability Reference Center, Department of Pediatrics, Brest University Hospital, Brest, France.; University of Brest, Inserm, EFS, UMR 1078, GGB, Brest, France.; Benech C; University of Brest, Inserm, EFS, UMR 1078, GGB, Brest, France.; Le Millier K; Department of Genetics, Brest University Hospital, Brest, France.; Uguen K; Department of Genetics, Brest University Hospital, Brest, France.; Intellectual Disability Reference Center, Department of Pediatrics, Brest University Hospital, Brest, France.; University of Brest, Inserm, EFS, UMR 1078, GGB, Brest, France.; Ropars J; Intellectual Disability Reference Center, Department of Pediatrics, Brest University Hospital, Brest, France.; Sacaze E; Intellectual Disability Reference Center, Department of Pediatrics, Brest University Hospital, Brest, France.; Audebert-Bellanger S; Department of Genetics, Brest University Hospital, Brest, France.; Intellectual Disability Reference Center, Department of Pediatrics, Brest University Hospital, Brest, France.; Apetrei A; University of Normandy, UNICAEN, RU7450 BioTARGen, Caen University Hospital, Department of Genetics, Reference Center for Developmental Disorders and Malformative Syndromes, Anddi-Rares Network, Caen, France.; Molin A; University of Normandy, UNICAEN, RU7450 BioTARGen, Caen University Hospital, Department of Genetics, Reference Center for Developmental Disorders and Malformative Syndromes, Anddi-Rares Network, Caen, France.; Gruchy N; University of Normandy, UNICAEN, RU7450 BioTARGen, Caen University Hospital, Department of Genetics, Reference Center for Developmental Disorders and Malformative Syndromes, Anddi-Rares Network, Caen, France.; Vincent-Devulder A; University of Normandy, UNICAEN, RU7450 BioTARGen, Caen University Hospital, Department of Genetics, Reference Center for Developmental Disorders and Malformative Syndromes, Anddi-Rares Network, Caen, France.; Spodenkiewicz M; Department of Genetics, Le Reunion University Hospital, St-Pierre, France.; Jacquin C; Department of Genetics, Reims University Hospital, Reims, France.; Loron G; Department of Neonatal Medicine and Pediatric Intensive Care, University of Reims Champagne-Ardenne, CReSTIC, Reims University Hospital, Reims, France.; Thibaud M; Department of Pediatrics, American Memorial Hospital, Reims, France.; Delplancq G; Constitutional Genetics Unit, Versailles Hospital, Le Chesnay, France.; Brisset S; Constitutional Genetics Unit, Versailles Hospital, Le Chesnay, France.; Lesieur-Sebellin M; Department of Genomic Medicine of Rare Disorders, Necker Hospital, APHP Center, University Paris Cité, Paris, France.; Malan V; Department of Genomic Medicine of Rare Disorders, Necker Hospital, APHP Center, University Paris Cité, Paris, France.; Romana S; Department of Genomic Medicine of Rare Disorders, Necker Hospital, APHP Center, University Paris Cité, Paris, France.; Rio M; Department of Genomic Medicine of Rare Disorders, Necker Hospital, APHP Center, University Paris Cité, Paris, France.; Marlin S; Department of Genomic Medicine of Rare Disorders, Necker Hospital, APHP Center, University Paris Cité, Paris, France.; Amiel J; Department of Genomic Medicine of Rare Disorders, Necker Hospital, APHP Center, University Paris Cité, Paris, France.; Marquet V; Department of Cytogenetics, Clinical Genetics and Reproductive Biology, Limoges University Hospital, Limoges, France.; Dauriat B; Department of Cytogenetics, Clinical Genetics and Reproductive Biology, Limoges University Hospital, Limoges, France.; Moradkhani K; Department of Genetics, Nantes University Hospital, Nantes, France.; Mercier S; Department of Genetics, Nantes University Hospital, Nantes, France.; Isidor B; Department of Genetics, Nantes University Hospital, Nantes, France.; Arpin S; Department of Genetics, Tours University Hospital, UMR 1253, iBrain, University of Tours, Inserm, Tours, France.; Pujalte M; Department of Genetics, Hospices Civils de Lyon, Lyon, France.; Jedraszak G; Constitutional Genetic Laboratory, University Hospital of Amiens & UR4666 HEMATIM, University of Picardie Jules Verne, Amiens, France.; Pebrel-Richard C; Cytogenetic Medical Department; UIC Cytogenetics of Rare Diseases and Reproduction (GRUIC ADERGEN), Rare Diseases Reference Center (CRMR): Developmental Anomalies and Malformative Syndromes in the Auvergne Region, Clermont-Ferrand University Hospital, Clermont-Ferrand, France.; Salaun G; Cytogenetic Medical Department; UIC Cytogenetics of Rare Diseases and Reproduction (GRUIC ADERGEN), Rare Diseases Reference Center (CRMR): Developmental Anomalies and Malformative Syndromes in the Auvergne Region, Clermont-Ferrand University Hospital, Clermont-Ferrand, France.; Laffargue F; Department of Medical Genetics, UIC ADDIR (GRIUC ADERGEN), Constitutive Reference Center CLAD South-East: Developmental anomalies and malformative syndromes, Clermont-Ferrand University Hospital, Clermont-Ferrand, France.; Boudjarane J; Medical Genetics Department, Timone Enfants University Hospital, Assistance Publique des Hôpitaux de Marseille, Marseille, France.; Missirian C; Medical Genetics Department, Timone Enfants University Hospital, Assistance Publique des Hôpitaux de Marseille, Marseille, France.; Chelloug N; Department of Medical Genetics, Toulouse University Hospital, Toulouse, France.; Toutain A; Department of Genetics, Tours University Hospital, UMR 1253, iBrain, University of Tours, Inserm, Tours, France.; Chiesa J; Department of Genetics, Nimes, University Hospital, Nimes University Hospital, Nimes, France.; Keren B; Department of Genetics, APHP Sorbonne University, Paris, France.; Mignot C; Department of Genetics, APHP Sorbonne University, Paris, France.; Gouy E; Department of Genetics, Hospices Civils de Lyon, Lyon, France.; Jaillard S; Department of Cytogenetics and Cell Biology, Rennes university hospital, Rennes, France.; Landais E; Department of Genetics, Reims University Hospital, Reims, France.; Poirsier C; Department of Genetics, Reims University Hospital, Reims, France.
Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE
Academic Journal
Cetica V; Neuroscience Department, Meyer Children's Hospital IRCCS, Florence, Italy.; Pisano T; Neuroscience Department, Meyer Children's Hospital IRCCS, Florence, Italy.; Lesca G; Université Lyon 1, Centre National de la Recherche Scientifique (CNRS), Institut National de la Santé et de la Recherche Médicale (INSERM), Physiopathologie et Génétique du Neurone et du Muscle, Institut NeuroMyoGène, Lyon, France.; Department of Genetics, University Hospitals of Lyon, Hospices Civils de Lyon, Lyon, France.; Marafi D; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Department of Pediatrics, Faculty of Medicine, Kuwait University, Safat, Kuwait.; Licchetta L; Istituto di Ricovero e Cura a Carattere Scientifico IRCCS, Istituto delle Scienze Neurologiche di Bologna, full member of the European Reference Network EpiCARE, Bologna, Italy.; Riccardi F; Aix-Marseille University, Institut National de la Santé et de la Recherche Médicale (INSERM), Marseille Medical Genetics, Marseille, France.; Centre Hospitalier Intercommunal Toulon - La Seyne sur Mer (CHITS), Hôpital Ste Musse, Service de Génétique Médicale, Toulon, France.; Mei D; Neuroscience Department, Meyer Children's Hospital IRCCS, Florence, Italy.; Chung HB; Department of Paediatrics and Adolescent Medicine, School of Clinical Medicine, Li Ka Shing (LKS) Faculty of Medicine, University of Hong Kong, Hong Kong, China.; Bayat A; Department of Drug Design and Pharmacology, University of Copenhagen, Copenhagen, Denmark.; Department of Regional Health Research, University of Southern Denmark, Odense, Denmark.; Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Center, Dianalund, Denmark.; Balasubramanian M; Department of Oncology and Metabolism, University of Sheffield, Sheffield, UK.; Sheffield Clinical Genetics Service, Sheffield Children's National Health Service (NHS) Foundation Trust, Sheffield, UK.; Lowenstein DH; Department of Neurology, University of California, San Francisco, California, USA.; Endzinienė M; Medical Academy, Lithuanian University of Health Sciences, Kaunas, Lithuania.; Alotaibi M; King Saud Medical City, Riyadh, Saudi Arabia.; Villeneuve N; Depatment of Pediatric Neurology, Assistance Publique-Hopitaux de Marseille (AP-HM), Hôpital de la Timone Enfants, Marseille, France.; Jacobs J; Alberta Children's Research Institute, Hodgekiss Brain Institute, Cumming School of Medicine, University of Calgary, Alberta, Canada.; Isidor B; Service de Génétique Médicale, Centre Hospitalier Universitaire de Nantes, Nantes, France.; Université de Nantes, Centre National de la Recherche Scientifique (CNRS), Institut National de la Santé et de la Recherche Médicale (INSERM), l'Institut du Thorax, Centre Hospitalier Universitaire de Nantes, Nantes, France.; Solazzi R; Department of Pediatric Neuroscience, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.; den Hollander NS; Department of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands.; Marjanovic D; Holbæk Hospital Medical Department, Holbæk, Denmark.; Rougeot-Jung C; Department of Pediatric Neurology, University Hospital of Lyon, Lyon, France.; Jung J; Department of Functional Neurology and Epileptology, Hospices Civils de Lyon, Université de Lyon, Lyon, France.; Lesieur-Sebellin M; Department of Genomic Medicine of Rare Disorders, Necker Hospital, University Paris Cité, Paris, France.; Accogli A; Division of Medical Genetics, Department of Specialized Medicine, McGill University Health Centre, Montreal, Quebec, Canada.; Department of Human Genetics, McGill University, Montreal, Quebec, Canada.; Salpietro V; Department of Neuromuscular Disorders, Queen Square Institute of Neurology, University College London, London, UK.; Saadi NW; College of Medicine, University of Baghdad, Baghdad, Iraq.; Children Welfare Teaching Hospital, Baghdad, Iraq.; Panagiotakaki E; Department of Functional Neurology and Epileptology, Hospices Civils de Lyon, Université de Lyon, Lyon, France.; Foiadelli T; Clinica Pediatrica, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico IRCCS Policlinico San Matteo, Pavia, Italy.; Department of Clinical, Surgical, Diagnostic, and Pediatric Sciences, University of Pavia, Pavia, Italy.; Redon S; Service de Génétique Médicale, Centre Hospitalier et Universitaire de Brest, Brest, France.; Université de Brest, Institut National de la Santé et de la Recherche Médicale (INSERM), Etablissement Français du Sang, UMR 1078, Brest, France.; Centre de Référence Déficiences Intellectuelles de Causes Rares, Brest, France.; Tsai MH; Department of Neurology, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan.; School of Medicine, Chang Gung University, Kaohsiung, Taiwan.; Bisulli F; Istituto di Ricovero e Cura a Carattere Scientifico IRCCS, Istituto delle Scienze Neurologiche di Bologna, full member of the European Reference Network EpiCARE, Bologna, Italy.; Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.; Hammer TB; Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Center, Dianalund, Denmark.; Lupski JR; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Texas Children's Hospital, Houston, Texas, USA.; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA.; Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.; Parrini E; Neuroscience Department, Meyer Children's Hospital IRCCS, Florence, Italy.; Guerrini R; Neuroscience Department, Meyer Children's Hospital IRCCS, Florence, Italy.; University of Florence, Florence, Italy.
Publisher: Blackwell Science Country of Publication: United States NLM ID: 2983306R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1528-1167 (Electronic) Linking ISSN: 00139580 NLM ISO Abbreviation: Epilepsia Subsets: MEDLINE
Academic Journal
Guillouet C; Laboratory of Embryology and Genetics of Malformations, INSERM UMR 1163, Institut Imagine, Université Paris Cité, Paris, France.; Agostini V; Laboratory of Embryology and Genetics of Malformations, INSERM UMR 1163, Institut Imagine, Université Paris Cité, Paris, France.; Baujat G; Service de Médecine Génomique des Maladies Rares, Necker-Enfants Malades Hospital, AP-HP, Paris, France.; Cocciadiferro D; Laboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children's Hospital, IRCCS, 00165 Rome, Italy.; Pippucci T; IRCCS Azienda Ospedaliero, Universitaria di Bologna, Bologna, Italy.; Lesieur-Sebellin M; Laboratory of Embryology and Genetics of Malformations, INSERM UMR 1163, Institut Imagine, Université Paris Cité, Paris, France.; Georget M; Laboratory of Embryology and Genetics of Malformations, INSERM UMR 1163, Institut Imagine, Université Paris Cité, Paris, France.; Schatz U; Institute of Human Genetics, Medical University Innsbruck, Innsbruck, Austria; Institute of Human Genetics, Technical University of Munich, Munich, Germany.; Fauth C; Institute of Human Genetics, Medical University Innsbruck, Innsbruck, Austria.; Louie RJ; Greenwood Genetic Center, Greenwood, SC, USA.; Rogers C; Greenwood Genetic Center, Greenwood, SC, USA.; Davis JM; Greenwood Genetic Center, Greenwood, SC, USA.; Konstantopoulou V; Department of Pediatrics and Adolescent Medicine, Austrian Newborn Screening, Medical University of Vienna, 1090 Vienna, Austria.; Mayr JA; University Children's Hospital, Salzburger Landeskliniken (SALK), Paracelsus Medical University, 5020 Salzburg, Austria.; Bouman A; Department of Clinical Genetics, Erasmus University Medical Center, Rotterdam, the Netherlands.; Wilke M; Department of Clinical Genetics, Erasmus University Medical Center, Rotterdam, the Netherlands.; VanNoy GE; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; England EM; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Park KL; Departments of Pediatrics and Neurology, University of Colorado School of Medicine, Aurora, CO, USA.; Brown K; University of Colorado Anschutz Medical Campus, Aurora, CO, USA.; Saenz M; University of Colorado Anschutz Medical Campus, Aurora, CO, USA.; Novelli A; Laboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children's Hospital, IRCCS, 00165 Rome, Italy.; Digilio MC; Medical Genetics, Translational Pediatrics and Clinical Genetics Research Area, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.; Mastromoro G; Department of Laboratory Science, Ospedale Isola Tiberina - Gemelli Isola, Rome, Italy.; Rongioletti MCA; Department of Laboratory Science, Ospedale Isola Tiberina - Gemelli Isola, Rome, Italy.; Piacentini G; Fetal and Neonatal Cardiology Unit, Ospedale Isola Tiberina - Gemelli Isola, Rome, Italy.; Kaiyrzhanov R; Department of Neuromuscular Diseases, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK; Department of Neurology, South Kazakhstan Medical Academy, Shymkent, Kazakhstan.; Guliyeva S; MediClub Hospital, Baku, Azerbaijan.; Hasanova L; Caspian International Hospital, Baku, Azerbaijan.; Shears D; Oxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.; Bhatnagar I; Oxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.; Stals K; Exeter Genomics Laboratory, Royal Devon University Healthcare NHS Foundation Trust, Exeter, UK.; Klaas O; Institute for Human Genetics, University Hospital Muenster, Muenster, Germany.; Horvath J; Institute for Human Genetics, University Hospital Muenster, Muenster, Germany.; Bouvagnet P; Département de Génétique, Laboratoire Eurofins Biomnis, 69007 Lyon, France; Centre Pluridisciplinaire de Diagnostic Prénatal, Hôpital MFME, CHU Martinique, Fort de France, France.; Witmer PD; McKusick-Nathans Department of Genetic Medicine, School of Medicine, Johns Hopkins University, Baltimore, MD, USA.; MacCarrick G; McKusick-Nathans Department of Genetic Medicine, School of Medicine, Johns Hopkins University, Baltimore, MD, USA.; Cisarova K; Division of Oncology, Department of Internal Medicine, Medical University of Graz, 8036 Graz, Austria.; Good JM; Division of Genetic Medicine, Lausanne University Hospital (CHUV) and University of Lausanne, Lausanne, Switzerland.; Gorokhova S; Aix Marseille University, INSERM, MMG, U 1251, 13005 Marseille, France; Department of Medical Genetics, Timone Children's Hospital, AP-HM, 13005 Marseille, France.; Boute O; University Lille, CHU Lille, ULR 7364 - RADEME - Maladies Rares du Développement Embryonnaire et du Métabolisme, 59000 Lille, France.; Smol T; University Lille, CHU Lille, ULR 7364 - RADEME - Maladies Rares du Développement Embryonnaire et du Métabolisme, 59000 Lille, France.; Bruel AL; INSERM UMR1231 Team GAD, University of Burgundy and Franche-Comté, 21000 Dijon, France; Functional Unit of Innovative Diagnosis for Rare Diseases, Dijon Bourgogne University Hospital, 21000 Dijon, France.; Patat O; Department of Medical Genetics, CHU Toulouse Purpan, Toulouse, France.; Broadbent JR; Rare Disease Discovery Group, Murdoch Children's Research Institute, Melbourne, VIC, Australia.; Tan TY; Rare Disease Discovery Group, Murdoch Children's Research Institute, Melbourne, VIC, Australia; Department of Paediatrics, University of Melbourne, Melbourne, VIC, Australia; Victorian Clinical Genetics Services, Melbourne, VIC, Australia.; Tan NB; Victorian Clinical Genetics Services, Melbourne, VIC, Australia.; Lyonnet S; Laboratory of Embryology and Genetics of Malformations, INSERM UMR 1163, Institut Imagine, Université Paris Cité, Paris, France; Service de Médecine Génomique des Maladies Rares, Necker-Enfants Malades Hospital, AP-HP, Paris, France.; Busa T; Department of Medical Genetics, Timone Children's Hospital, AP-HM, 13005 Marseille, France.; Graziano C; U.O. Genetica Medica, Azienda USL della Romagna, Ravenna, Italy.; Amiel J; Laboratory of Embryology and Genetics of Malformations, INSERM UMR 1163, Institut Imagine, Université Paris Cité, Paris, France; Service de Médecine Génomique des Maladies Rares, Necker-Enfants Malades Hospital, AP-HP, Paris, France.; Gordon CT; Laboratory of Embryology and Genetics of Malformations, INSERM UMR 1163, Institut Imagine, Université Paris Cité, Paris, France. Electronic address: chris.gordon@inserm.fr.
Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-6605 (Electronic) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE
Academic Journal
Sabeh P; Department of Genetics, CHU Sainte-Justine, Montréal, QC, Canada.; Dumas SA; Department of Anatomy, Physiology, and Genetics, Uniformed Services University of the Health Sciences, F. Edward Herbert School of Medicine, Bethesda, MD 20814, USA.; Maios C; Department of Neuroscience, Université de Montréal, CRCHUM, Montréal, QC, Canada.; Daghar H; Department of Neuroscience, Université de Montréal, CRCHUM, Montréal, QC, Canada.; Korzeniowski M; Department of Anatomy, Physiology, and Genetics, Uniformed Services University of the Health Sciences, F. Edward Herbert School of Medicine, Bethesda, MD 20814, USA.; Rousseau J; Department of Genetics, CHU Sainte-Justine, Montréal, QC, Canada.; Lines M; Department of Clinical and Metabolic Genetics, Alberta Children's Hospital, Calgary, AB, Canada.; Guerin A; Division of Medical Genetics, Department of Pediatrics, Queen's University, Kingston, ON, Canada.; Millichap JJ; Department of Neurology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.; Landsverk M; Sanford Research, Pediatrics and Rare Diseases Group, University of South Dakota Sanford School of Medicine, Sioux Falls, SD, USA.; Grebe T; Department of Genetics and Metabolism, Phoenix Children Hospital, Phoenix, AZ, USA.; Lindstrom K; BioMarin Pharmaceutical, Inc., 105 Digital Dr., Novato, CA 94949, USA.; Strober J; Department of Child Neurology, University of California, San Francisco, San Francisco, CA, USA.; Ait Mouhoub T; Department of Genetic, University Hospital Center of Reims, Reims, France.; Zweier C; Department of Human Genetics, Inselspital Bern, University of Bern, Bern, Switzerland.; Steinraths M; Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada.; Hebebrand M; Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.; Callewaert B; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.; Abou Jamra R; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Kautza-Lucht M; Institute of Human Genetics, University Hospital of Schleswig-Holstein, Kiel, Germany.; Wegler M; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Kruszka P; GeneDx, Gaithersburg, MD, USA.; Kumps C; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.; Banne E; The Genetic Institute, Wolfson Medical Center, Holon, Israel.; Waberski MB; Pediatric Specialists of Virginia, Fairfax, VA, USA.; Dieux A; Service de génétique clinique du CHU de Lille, Lille, France.; Raible S; Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Krantz I; Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Medne L; Division of Genomic Diagnostics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Pechter K; Division of Genomic Diagnostics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Villard L; Aix Marseille University, INSERM, Marseille Medical Genetics Center, MMG, Marseille, France; University of Florence, Florence, Italy.; Guerrini R; Neuroscience and Human Genetics Department, Meyer Children's Hospital IRCCS, Florence, Italy; University of Florence, Florence, Italy.; Bianchini C; Neuroscience and Human Genetics Department, Meyer Children's Hospital IRCCS, Florence, Italy; University of Florence, Florence, Italy.; Barba C; Neuroscience and Human Genetics Department, Meyer Children's Hospital IRCCS, Florence, Italy; University of Florence, Florence, Italy.; Mei D; Neuroscience and Human Genetics Department, Meyer Children's Hospital IRCCS, Florence, Italy.; Blanc X; Medigenome, Swiss Institute of Genomic Medicine, Geneva, Switzerland.; Kallay C; Réseau Hospitalier Neuchâtelois, Neuchâtel, Switzerland.; Ranza E; Medigenome, Swiss Institute of Genomic Medicine, Geneva, Switzerland.; Yang XR; Department of Medical Genetics, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.; O'Heir E; Center for Mendelian Genomics, Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Donald KA; Department of Paediatrics and Child Health, Red Cross War Memorial Children's Hospital, University of Cape Town, Rondebosch, South Africa.; Murugasen S; Department of Paediatrics and Child Health, Red Cross War Memorial Children's Hospital, University of Cape Town, Rondebosch, South Africa.; Bruwer Z; Department of Paediatrics and Child Health, Red Cross War Memorial Children's Hospital, University of Cape Town, Rondebosch, South Africa.; Calikoglu M; University of North Carolina, Department of Pediatrics, Division of Genetics and Metabolism, Chapel Hill, NC, USA.; Mathews JM; University of North Carolina, Department of Pediatrics, Division of Genetics and Metabolism, Chapel Hill, NC, USA.; Lesieur-Sebellin M; Service de médecine génomique des maladies rares, Necker Hospital, Paris, France.; Baujat G; University of North Carolina, Department of Pediatrics, Division of Genetics and Metabolism, Chapel Hill, NC, USA.; Derive N; Laboratoire de Biologie Médicale Multi-Sites SeqOIA, Paris, France.; Pierson TM; Departments of Pediatrics and of Neurology, Guerin Children's Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA; Board of Governors Regenerative Medicine Institute, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA.; Murrell JR; Department of Pathology and Laboratory Medicine, Children's Hospital of the University of Pennsylvania, Philadelphia, PA, USA.; Shillington A; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.; Ormieres C; Service de médecine génomique des maladies rares, Necker Hospital, Paris, France.; Rondeau S; Service de médecine génomique des maladies rares, Necker Hospital, Paris, France.; Reis A; Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.; Fernandez-Jaen A; Department of Pediatric Neurology, Hospital Universitario Quirónsalud, Madrid, Spain.; Au PYB; Department of Medical Genetics, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.; Sweetser DA; Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.; Briere LC; Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.; Couque N; Département de Génétique - UF de Génétique Moléculaire Hôpital Robert Debré, Paris, France.; Perrin L; Département de Génétique - UF de Génétique Moléculaire Hôpital Robert Debré, Paris, France.; Schymick J; Santa Clara Valley Medical Center, San Jose, CA, USA.; Gueguen P; Laboratoire de Biologie Médicale Multi-Sites SeqOIA, Paris, France.; Lefebvre M; UF de génétique clinique, Centre Hospitalier Régional d'Orléans, Orléans, France.; Van Andel M; Santa Clara Valley Medical Center, San Jose, CA, USA.; Juusola J; GeneDx, Gaithersburg, MD, USA.; Antonarakis SE; Medigenome, Swiss Institute of Genomic Medicine, Geneva, Switzerland.; Parker JA; Department of Neuroscience, Université de Montréal, CRCHUM, Montréal, QC, Canada.; Burnett BG; Department of Anatomy, Physiology, and Genetics, Uniformed Services University of the Health Sciences, F. Edward Herbert School of Medicine, Bethesda, MD 20814, USA. Electronic address: barrington.burnett@usuhs.edu.; Campeau PM; Department of Genetics, CHU Sainte-Justine, Montréal, QC, Canada. Electronic address: p.campeau@umontreal.ca.
Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-6605 (Electronic) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE
Academic Journal
Lesieur-Sebellin M; Service de Médecine Génomique des Maladies Rares, APHP-Centre, Hôpital Necker-Enfants Malades, Paris, France.; Faculté de Médecine, Sorbonne Université, Paris, France.; Till M; Laboratoire de Cytogénétique, service de Génétique, Hospices Civils de Lyon, Groupement Hospitalier Est, Bron, France.; Khau Van Kien P; UF de Cytogénétique et Génétique Médicale, Hôpital Caremeau, Nîmes, France.; Herve B; Département de Génétique, CHI Poissy Saint-Germain, Saint-Germain, France.; Université Paris-Saclay, UVSQ, INRAE, BREED, Jouy-en-Josas, France.; Bourgon N; Service d'Obstétrique et de Médecine Fœtale, APHP-Centre, Hôpital Necker-Enfants Malades, Paris, France.; Dupont C; Département de Génétique, Unité de Cytogénétique, Hôpital Robert Debré, APHP Nord, Paris, France.; Tabet AC; Département de Génétique, Unité de Cytogénétique, Hôpital Robert Debré, APHP Nord, Paris, France.; Génétique Humaine et Fonctions Cognitives, Institut Pasteur, UMR3571 CNRS, Université de Paris, Paris, France.; Barrois M; Maternité Port Royal, APHP Centre, Hôpital Cochin, Paris, France.; Coussement A; Service des Maladies Génétiques de système et d'organes, APHP-Centre, Hôpital Cochin, Paris, France.; Loeuillet L; Service de Médecine Génomique des Maladies Rares, APHP-Centre, Hôpital Necker-Enfants Malades, Paris, France.; Mousty E; Service de Gynécologie Obstétrique, Hôpital Caremeau, Nîmes, France.; Ea V; UF de Cytogénétique et Génétique Médicale, Hôpital Caremeau, Nîmes, France.; El Assal A; Département de Gynécologie Obstétrique, CHI Poissy Saint-Germain, Saint-Germain, France.; Mary L; Service d'Anatomie Pathologique, CHU Rennes, Rennes, France.; Service de Cytogénétique et Biologie Cellulaire, CHU Rennes, Rennes, France.; Jaillard S; Service de Cytogénétique et Biologie Cellulaire, CHU Rennes, Rennes, France.; INSERM, EHESP, IRSET, Université Rennes 1, Rennes, France.; Beneteau C; Service de Génétique Médicale, CHU Nantes, Nantes, France.; UF de Fœtopathologie et Génétique, CHU de Nantes, Nantes, France.; Le Vaillant C; Service de Gynécologie et Obstétrique, CHU Nantes, Nantes, France.; Coutton C; Service de Génétique, Génomique et Procréation, Hôpital Couple Enfant, CHU Grenoble Alpes, Grenoble, France.; Université Grenoble Alpes, INSERM U1209, CNRS UMR 5309, Institut pour l'Avancée des Biosciences, Equipe Génétique, Epigénétique et Thérapies de l'infertilité, Grenoble, France.; Devillard F; Service de Génétique, Génomique et Procréation, Hôpital Couple Enfant, CHU Grenoble Alpes, Grenoble, France.; Goumy C; Cytogénétique Médicale, CHU Clermont-Ferrand, CHU Estaing, Université Clermont Auvergne, INSERM, U1240 Imagerie Moléculaire et Stratégies Théranostiques, Clermont-Ferrand, France.; Delabaere A; Unité de Médecine Fœtale, CHU Estaing, Clermont-Ferrand, France.; Redon S; CHU Brest, Inserm, Université de Brest, Brest, France.; Laurent Y; Service de Gynécologie et Obstétrique, GHBS Lorient, Lorient, France.; Lamouroux A; Service de Génétique Clinique, CHU Montpellier, Université de Montpellier, Montpellier, France.; Service de Gynécologie Obstétrique, CHU Nîmes, Université de Montpellier, Nîmes, France.; Massardier J; Service de Gynécologie et Obstétrique, Hôpital Femme-Mère-Enfant, Hospices Civils de Lyon, Bron, France.; Turleau C; Service de Médecine Génomique des Maladies Rares, APHP-Centre, Hôpital Necker-Enfants Malades, Paris, France.; Sanlaville D; Laboratoire de Cytogénétique, service de Génétique, Hospices Civils de Lyon, Groupement Hospitalier Est, Bron, France.; Cantagrel V; Université de Paris, Institut Imagine, Laboratoire de génétique des troubles du neurodéveloppement, Paris, France.; Université de Paris, Paris, France.; Sonigo P; Service de Radiologie Pédiatrique, APHP-Centre, Hôpital Necker-Enfants Malades, Paris, France.; Vialard F; Département de Génétique, CHI Poissy Saint-Germain, Saint-Germain, France.; Université Paris-Saclay, UVSQ, INRAE, BREED, Jouy-en-Josas, France.; Salomon LJ; Service d'Obstétrique et de Médecine Fœtale, APHP-Centre, Hôpital Necker-Enfants Malades, Paris, France.; Université de Paris, Paris, France.; Malan V; Service de Médecine Génomique des Maladies Rares, APHP-Centre, Hôpital Necker-Enfants Malades, Paris, France.; Université de Paris, Institut Imagine, Laboratoire de génétique des troubles du neurodéveloppement, Paris, France.; Université de Paris, Paris, France.
Publisher: Wiley Country of Publication: England NLM ID: 8106540 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-0223 (Electronic) Linking ISSN: 01973851 NLM ISO Abbreviation: Prenat Diagn Subsets: MEDLINE
Academic Journal
Abadie, C.Abderrahmane, A.Abdous, O.Abel, C.Ackermann, O.Acquaviva, C.Ader, F.Adham, S.Adjaoud, D.Afenjar, A.Aladjidi, N.Alary, A.-S.Albarel, F.Albert, S.Allard, L.Allix, I.Alunni, V.Amado, I.F.Amouroux, C.André, N.Angelini, C.Anheim, M.Sanfelliz, I.A.Aparicio, T.Arfeuille, C.Arlet, J.-B.Arnaud, L.Arnaud, P.Arnold, G.Attie-Bitach, T.Aubert-Mucca, M.Audo, I.Audrezet, M.-P.Auroux, M.Auzanneau, C.Ayrignac, X.Ba, I.Bachelot, A.Bacq, D.Bacrot, S.Bader-Meunier, B.Baer, S.Baert-Desurmont, S.Bal-Theoleyre, L.Balogoun, R.Baltzinger, P.Banneau, G.Bar, C.Barbet, A.Barcia, G.Barjhoux, L.Barlier, A.Barlogis, V.Barritault, M.Barth, M.Barthod-Malat, A.Baudouin-Cornu, P.Baujat, G.Baurand, A.Bay, J.-O.Beau-Faller, M.Beaudoin, J.-C.Bellance, R.Bellanné-Chantelot, C.Bellera, C.Belot, A.Ben Abdeljelil, R.Ben Sghaier, R.Benadiba, J.Benard, S.Beneteau, C.Benistan, K.Benkerdou, F.Benkirane, M.Benoist, J.-F.Benusiglio, P.R.Bergès, C.Bergougnoux, A.Bernadach, M.Bernard, E.Bernard, V.Bernard, V.Beroug, D.Berrard, A.Bertherat, J.Berthet, P.Berthier, C.Bertholet-Thomas, A.Bertocchio, J.-P.Bertucci, F.Besse, C.Besse-Pinot, E.Bessis, D.Beuvain, P.Bezieau, S.Bidart, M.Bièche, I.Biehler, M.Bienvenu, T.Bilan, F.Billon, C.Binquet, C.Bismuth, E.Bizaoui, V.Blanc, P.Blanché, H.Blay, J.-Y.Bloch, A.Bloch, G.Bloch-Zupan, A.Bocquet, B.Boedec, M.Boileau, C.Boissinot, M.Boland, A.Bolze, P.-A.Bonadona, V.Bonastre, J.Bonello-Palot, N.Bonnard, A.-A.Borie, R.Botsen, D.Bouattour, M.Bouctot, M.Bouhours-Nouet, N.Bouligand, J.Bouras, A.Bourgeron, T.Bourges, J.-L.Bourrat, E.Boursier, G.Bousquet, G.Bousquet, P.-J.Boussion, S.Boutaud, L.Boutin, J.Bouvagnet, P.Bouvattier, C.Boyault, S.Brac de la Perriere, A.Brahmi, M.Brard, V.Brasseur, M.Brazzalotto, N.Brémond-Gignac, D.Briand-Suleau, A.Briet, C.Bringuier, P.-P.Bris, C.Brischoux-Boucher, E.Brochard, K.Broly, M.Brosseau, L.Bruel, A.-L.Brunelle, P.Bubien, V.Buecher, B.Buffet, A.Buisson, A.Burglen, L.Des Roziers, C.B.Burnichon, N.Busa, T.Cabart, M.Cabet, S.Caille-Benigni, C.Caillot, C.Calvin, C.Cambon-Thomsen, A.Cances, C.Cantan, A.Carausu, L.Carbasse, A.Carbonneil, C.Cariou, B.Caron, O.Carras, S.Cartalat, S.Cassinari, K.Castelle, M.Castéra, L.Castinetti, F.Catteau, J.Caumes, R.Caux, A.Cavaillé, M.Cavé, H.Caye-Eude, A.Cazeneuve, C.Celse, T.Celton, N.Cenni, C.Cévost, J.Chaabna, R.Chabrol, B.Challet, I.Chalumeau, C.Chambon, P.Chansavang, A.Chanson, J.-B.Chapelant, S.Charbit-Henrion, F.Charles, P.Charrière, S.Charron, P.Chassaing, N.Chatron, N.Chaumette, B.Chaussain, C.Chaussenot, A.Cheillan, D.Chenavier, O.Chesneau, B.Chevalier, L.-M.Chomienne, C.Chougnet, C.Christin-Maitre, S.Chuet, M.Clappier, E.Clet, J.Cloteau, M.Cluzeau, T.Cogan, G.Cogné, B.Cohen, A.Cohen, C.Cohen-Haguenauer, O.Cohen-Solal, M.Colas, C.Colin, E.Collet, C.Collin-Chavagnac, D.Colliou, E.Collonge-Rame, M.-A.Colmard, M.Coopman, S.Coppin, L.Coquan, E.Cormier-Daire, V.Corradini, N.Corsini, C.Cossée, M.Coste, T.Cotteret, S.Cottet, R.Coubes, C.Coulet, F.Couque, N.Couratier, P.Courbebaisse, M.Courbette, O.Courdier, C.Coursimault, J.Courtin, T.Courtois, L.Coury, F.Coutos-Thévenot, L.Coutton, C.Creveaux, I.Crickx, E.Crivelli, L.Cuggia, M.Cuisset, L.Curcio, H.Curie, A.Cusin, V.Da Costa, N.Da Cruz, L.Dahlen, E.Dardenne, A.Dauriat, B.Dausse, N.De Becdelièvre, A.De Fraipont, F.De La Cruz, E.De la Motte Rouge, T.De Montgolfier, S.De Pauw, A.De Reyniès, A.De Sainte Agathe, J.-M.De Tayrac, M.Defachelles, A.-S.Degaud, M.Deiller, C.Delabesse, E.Delachaux, L.Delahaye-Duriez, A.Deleuze, J.-F.Delhomelle, H.Delmas, C.Delnatte, C.Delorme, C.Delorme, R.Demeer, B.Demilly, C.Denizeau, P.Denjoy, I.Denommé-Pichon, A.-S.Depienne, C.Derive, N.Dervillé, F.Portes, V.D.Desguerre, I.Desnous, B.Desseignes, C.Devillard, F.Deville, M.Dewulf-Pasz, N.Dhaenens, C.-M.Dietrich, K.Dieux, A.Diop, M.Disse, E.Djaber, S.Cao, C.D.Dollfus, H.Domenach, L.Donadieu, J.Donadille, B.Dougé, A.Dreyfus, H.Drunat, S.Dubois-Laforgue, D.Dubourg, C.Dubucs, C.Dubus, J.-C.Duchmann, M.Ducray, F.Ducrotverdun, M.Duffaud, F.Duffourd, Y.Dufour, W.Duhil de Bénazé, G.Dulac, Y.Dunand, O.Dunoyer de Segonzac, D.Dupain, C.Duployez, N.Dupré, A.Dupré, A.Dupuis-Girod, S.Duquet, R.Durand, A.Durand, B.Durand-Zaleski, I.Durando, X.Durr, A.Eberst, L.Edery, P.Egloff, M.El Chehadeh, S.El Khattabi, L.Engel, C.Entresangle, M.Espérou, H.Esselin, F.Etancelin, P.Evrevin, C.Ewenczyk, C.Eychene, A.Eychenne, T.Ezaru, A.Fabry, V.Faivre, L.Faoucher, M.Faure, C.Fauré, J.Fauret-Amsellem, A.-L.Feigerlova, E.Feillet, F.Fenwarth, L.Férec, C.Fergelot, P.Ferrari, A.Ferraro-Peyret, C.Feugeas, J.-P.Fieschi, C.Fievet, A.Fila, M.Fillatre, R.Filser, M.Fin, B.Fiore, M.Firmin, N.Flandrin-Gresta, P.Flechon, A.Fournier, B.Fragny, C.Francois-Heude, M.-C.Francou, B.Frébourg, T.Fressart, V.Frétigny, M.Funalot, B.Fusaro, M.Gaignard, P.Gandjbakhch, E.Ganne, B.Garde, A.Gatinois, V.Gaucher, C.Gaudillat, L.Gaulard, P.Gauthier, L.Gay-Bellile, M.Geneste, D.Geneviève, D.Genin, E.Genoux, S.Geoerger, B.Geoffroy, V.Georget, M.Gérard, B.Gertych, W.Halem, S.G.Ghorab, K.Gille, R.Gillet, C.Gillibert-Yvert, M.Gilly, O.Gimenez-Roqueplo, A.-P.Giraud, S.Girerd, B.Girodon, F.Glazunova, O.Gobert, D.Goizet, C.Gokce-Samar, Z.Golmard, L.Gomez-Roca, C.Gonzales, E.Gorce, M.Gorenstein, M.-C.Gorrichon, K.Gottrand, F.Gouas, L.Gourdon, S.Gourdy, P.Gouronc, A.Goursaud, C.Gousse, G.Gouy, E.Goze-Martineau, O.Gozlan, D.Grabli, D.Gras, M.Grelet, M.Gressin, L.Grivel, N.Grotto, S.Grouthier, V.Grunenwald, S.Grunewald, O.Gueguen, P.Guérin, C.Guerrot, A.-M.Guey, S.Guffon, N.Guichet, A.Guièze, R.Guillaud-Bataille, M.Guillemin, F.Guillerm, E.Guillermin, Y.Guillet-Pichon, V.Guillou, I.Guimbaud, R.Guimier, A.Guissart, C.Guittet, E.Guy, N.Hadchouel, A.Abdallah, H.H.Hadj-Rabia, S.Hadjadj, S.Hage-Sleiman, M.Haioun, C.Halawi, S.Hamza, A.Hanau, P.Hanna, N.Harbuz, R.Hardy, G.Hauspie, C.Hayette, S.Heard, J.-M.Heiblig, M.Heide, S.Heidet, L.Henry, M.Hentgen, V.Héron, B.Héron, D.Hervé, D.Herzig, A.Hirsch, P.Hommais, A.Honnorat, J.Horta, E.Houdayer, C.Houillier, 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S.Marquant, E.Marquet, V.Marsili, L.Martin, A.Martinerie, L.Maruani, A.Marzin, P.Massard, C.Masson, E.Mathieu, F.Mathieu, M.Mathoulin-Pelissier, S.Matthieu, F.Mauras, M.Maureille, A.Mazel, B.Mazeres, M.Leer, A.M.Melki, I.Menassa, R.Méneret, A.Menjard, J.Mercier, A.Merieau, E.Merlin, M.-S.Merlio, J.-P.Meslier, C.Mesnard, L.Mestre-Godin, S.Metay, C.Meunier, S.Meyer, P.Michaud, V.Michel-Calemard, L.Mignot, C.Miguet, M.Millat, G.Mirault, T.Miron de l'Espinay, A.Molac, C.Molin, A.Mondet, J.Monin, F.Monin, P.Monneur, A.Monnot, S.Montani, D.Morel, E.Morel, G.Morel, V.Moretta, J.Morice-Picard, F.Morillon, L.Morin, C.Morin-Meschin, M.-E.Morlat, P.Moshous, D.Mouret-Fourme, E.Moussy, A.Moutton, S.Mouzat, K.Muletier, R.Muller, J.Muller, M.Nadaj-Pakleza, A.Nambot, S.Nathan, N.Nava, C.Nectoux, J.Netter, J.Neumann, F.Neveu, J.Nevière, Z.Nguyen, L.Niclass, T.Nicolas, G.Nicolas, L.Ningarhari, M.Nogues, C.Novello, C.Nowak, F.Odent, S.Odou, M.-F.Olaso, R.Otmani, S.Ovaert, C.Pacot, L.Pages, M.Paillard, 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In: The Lancet Regional Health - Europe. (The Lancet Regional Health - Europe, March 2025, 50)
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