학술논문


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'학술논문' 에서 검색결과 408건 | 목록 1~20
Academic Journal
Gverdtsiteli S; Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, DK-2100 Copenhagen, Denmark.; Hammer TB; Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, DK-2100 Copenhagen, Denmark.; Hermann X; Resource Center for Rare Oral Diseases, Copenhagen University Hospital, Rigshospitalet, DK-2100 Copenhagen, Denmark.; Andersen NB; The Epilepsy Clinic, Department of Neurology, Copenhagen University Hospital, Rigshospitalet, DK-2100 Copenhagen, Denmark.; Ros-Pardo D; Molecular Modeling Group, Centro de Biologia Molecular Severo Ochoa (CBM, CSIC-UAM), E-28049 Madrid, Spain.; Marcos-Alcalde I; Molecular Modeling Group, Centro de Biologia Molecular Severo Ochoa (CBM, CSIC-UAM), E-28049 Madrid, Spain.; Gómez-Puertas P; Molecular Modeling Group, Centro de Biologia Molecular Severo Ochoa (CBM, CSIC-UAM), E-28049 Madrid, Spain.; Brook AH; Adelaide Dental School, The University of Adelaide, Adelaide, SA 5000, Australia.; Silahtaroglu A; Department of Cellular and Molecular Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Blegdamsvej 3, DK-2200 Copenhagen, Denmark.; Tümer Z; Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, DK-2100 Copenhagen, Denmark.; Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Blegdamsvej 3, DK-2200 Copenhagen, Denmark.
Publisher: MDPI Country of Publication: Switzerland NLM ID: 101551097 Publication Model: Electronic Cited Medium: Internet ISSN: 2073-4425 (Electronic) Linking ISSN: 20734425 NLM ISO Abbreviation: Genes (Basel) Subsets: MEDLINE
Academic Journal
物探装备 / Equipment for Geophysical Prospecting. 26(5):290-293
Academic Journal
Khachatryan, V.Sirunyan, A. M.Tumasyan, A.Adam, W.Asilar, E.Bergauer, T.Brandstetter, J.Brondolin, E.Dragicevic, M.Erö, J.Flechl, M.Friedl, M.Frühwirth, R.Ghete, V. M.Hartl, C.Hörmann, N.Hrubec, J.Jeitler, M.Knünz, V.König, A.Krammer, M.Krätschmer, I.Liko, D.Mikulec, I.Rabady, D.Rahbaran, B.Rohringer, H.Schieck, J.Schöfbeck, R.Strauss, J.Treberer-Treberspurg, W.Waltenberger, W.Wulz, C.-E.Mossolov, V.Shumeiko, N.Suarez Gonzalez, J.Alderweireldt, S.Cornelis, T.De Wolf, E. A.Janssen, X.Knutsson, A.Lauwers, J.Luyckx, S.Ochesanu, S.Rougny, R.Van De Klundert, M.Van Haevermaet, H.Van Mechelen, P.Van Remortel, N.Van Spilbeeck, A.Abu Zeid, S.Blekman, F.D’Hondt, J.Daci, N.De Bruyn, I.Deroover, K.Heracleous, N.Keaveney, J.Lowette, S.Moreels, L.Olbrechts, A.Python, Q.Strom, D.Tavernier, S.Van Doninck, W.Van Mulders, P.Van Onsem, G. P.Van Parijs, I.Barria, P.Caillol, C.Clerbaux, B.De Lentdecker, G.Delannoy, H.Dobur, D.Fasanella, G.Favart, L.Gay, A. P. R.Grebenyuk, A.Léonard, A.Mohammadi, A.Perniè, L.Randleconde, A.Reis, T.Seva, T.Thomas, L.Vander Velde, C.Vanlaer, P.Wang, J.Zenoni, F.Beernaert, K.Benucci, L.Cimmino, A.Crucy, S.Fagot, A.Garcia, G.Gul, M.Mccartin, J.Ocampo Rios, A. A.Poyraz, D.Ryckbosch, D.Salva, S.Sigamani, M.Strobbe, N.Thyssen, F.Tytgat, M.Van Driessche, W.Yazgan, E.Zaganidis, N.Basegmez, S.Beluffi, C.Bondu, O.Bruno, G.Castello, R.Caudron, A.Ceard, L.Da Silveira, G. G.Delaere, C.du Pree, T.Favart, D.Forthomme, L.Giammanco, A.Hollar, J.Jafari, A.Jez, P.Komm, M.Lemaitre, V.Mertens, A.Nuttens, C.Perrini, L.Pin, A.Piotrzkowski, K.Popov, A.Quertenmont, L.Selvaggi, M.Vidal Marono, M.Beliy, N.Caebergs, T.Hammad, G. H.Aldá Júnior, W. L.Alves, G. A.Brito, L.Correa Martins Junior, M.Dos Reis Martins, T.Hensel, C.Mora Herrera, C.Moraes, A.Pol, M. E.Rebello Teles, P.Belchior Batista Das Chagas, E.Carvalho, W.Chinellato, J.Custódio, A.Da Costa, E. M.De Jesus Damiao, D.De Oliveira Martins, C.Fonseca De Souza, S.Huertas Guativa, L. M.Malbouisson, H.Matos Figueiredo, D.Mundim, L.Nogima, H.Prado Da Silva, W. L.Santaolalla, J.Santoro, A.Sznajder, A.Tonelli Manganote, E. J.Vilela Pereira, A.Ahuja, S.Bernardes, C. A.Dogra, S.Fernandez Perez Tomei, T. R.Gregores, E. M.Mercadante, P. G.Novaes, S. F.Padula, Sandra S.Romero Abad, D.Ruiz Vargas, J. C.Aleksandrov, A.Genchev, V.Hadjiiska, R.Iaydjiev, P.Marinov, A.Piperov, S.Rodozov, M.Stoykova, S.Sultanov, G.Vutova, M.Dimitrov, A.Glushkov, I.Litov, L.Pavlov, B.Petkov, P.Ahmad, M.Bian, J. G.Chen, G. M.Chen, H. S.Chen, M.Cheng, T.Du, R.Jiang, C. H.Plestina, R.Romeo, F.Shaheen, S. M.Tao, J.Wang, C.Wang, Z.Asawatangtrakuldee, C.Ban, Y.Li, Q.Liu, S.Mao, Y.Qian, S. J.Wang, D.Xu, Z.Zhang, F.Zhang, L.Zou, W.Avila, C.Cabrera, A.Chaparro Sierra, L. F.Florez, C.Gomez, J. P.Gomez Moreno, B.Sanabria, J. C.Godinovic, N.Lelas, D.Polic, D.Puljak, I.Antunovic, Z.Kovac, M.Brigljevic, V.Kadija, K.Luetic, J.Sudic, L.Attikis, A.Mavromanolakis, G.Mousa, J.Nicolaou, C.Ptochos, F.Razis, P. A.Rykaczewski, H.Bodlak, M.Finger, M.Finger, Jr., M.Aly, R.Aly, S.Assran, Y.Elgammal, S.Ellithi Kamel, A.Lotfy, A.Mahmoud, M. A.Radi, A.Sayed, A.Calpas, B.Kadastik, M.Murumaa, M.Raidal, M.Tiko, A.Veelken, C.Eerola, P.Voutilainen, M.Härkönen, J.Karimäki, V.Kinnunen, R.Lampén, T.Lassila-Perini, K.Lehti, S.Lindén, T.Luukka, P.Mäenpää, T.Peltola, T.Tuominen, E.Tuominiemi, J.Tuovinen, E.Wendland, L.Talvitie, J.Tuuva, T.Besancon, M.Couderc, F.Dejardin, M.Denegri, D.Fabbro, B.Faure, J. L.Favaro, C.Ferri, F.Ganjour, S.Givernaud, A.Gras, P.Hamel de Monchenault, G.Jarry, P.Locci, E.Malcles, J.Rander, J.Rosowsky, A.Titov, M.Zghiche, A.Baffioni, S.Beaudette, F.Busson, P.Cadamuro, L.Chapon, E.Charlot, C.Dahms, T.Davignon, O.Filipovic, N.Florent, A.Granier de Cassagnac, R.Mastrolorenzo, L.Miné, P.Naranjo, I. N.Nguyen, M.Ochando, C.Ortona, G.Paganini, P.Regnard, S.Salerno, R.Sauvan, J. B.Sirois, Y.Strebler, T.Yilmaz, Y.Zabi, A.Agram, J.-L.Andrea, J.Aubin, A.Bloch, D.Brom, J.-M.Buttignol, M.Chabert, E. C.Chanon, N.Collard, C.Conte, E.Fontaine, J.-C.Gelé, D.Goerlach, U.Goetzmann, C.Le Bihan, A.-C.Merlin, J. A.Skovpen, K.Van Hove, P.Gadrat, S.Beauceron, S.Beaupere, N.Bernet, C.Boudoul, G.Bouvier, E.Brochet, S.Carrillo Montoya, C. A.Chasserat, J.Chierici, R.Contardo, D.Courbon, B.Depasse, P.El Mamouni, H.Fan, J.Fay, J.Gascon, S.Gouzevitch, M.Ille, B.Laktineh, I. B.Lethuillier, M.Mirabito, L.Pequegnot, A. L.Perries, S.Ruiz Alvarez, J. D.Sabes, D.Sgandurra, L.Sordini, V.Vander Donckt, M.Verdier, P.Viret, S.Xiao, H.Toriashvili, T.Tsamalaidze, Z.Autermann, C.Beranek, S.Edelhoff, M.Feld, L.Heister, A.Kiesel, M. K.Klein, K.Lipinski, M.Ostapchuk, A.Preuten, M.Raupach, F.Sammet, J.Schael, S.Schulte, J. F.Verlage, T.Weber, H.Wittmer, B.Zhukov, V.Ata, M.Brodski, M.Dietz-Laursonn, E.Duchardt, D.Endres, M.Erdmann, M.Erdweg, S.Esch, T.Fischer, R.Güth, A.Hebbeker, T.Heidemann, C.Hoepfner, K.Klingebiel, D.Knutzen, S.Kreuzer, P.Merschmeyer, M.Meyer, A.Millet, P.Olschewski, M.Padeken, K.Papacz, P.Pook, T.Radziej, M.Reithler, H.Rieger, M.Schmitz, S. A.Sonnenschein, L.Teyssier, D.Thüer, S.Cherepanov, V.Erdogan, Y.Flügge, G.Geenen, H.Geisler, M.Haj Ahmad, W.Hoehle, F.Kargoll, B.Kress, T.Kuessel, Y.Künsken, A.Lingemann, J.Nowack, A.Nugent, I. M.Pistone, C.Pooth, O.Stahl, A.Aldaya Martin, M.Asin, I.Bartosik, N.Behnke, O.Behrens, U.Bell, A. J.Borras, K.Burgmeier, A.Cakir, A.Calligaris, L.Campbell, A.Choudhury, S.Costanza, F.Diez Pardos, C.Dolinska, G.Dooling, S.Dorland, T.Eckerlin, G.Eckstein, D.Eichhorn, T.Flucke, G.Garay Garcia, J.Geiser, A.Gizhko, A.Gunnellini, P.Hauk, J.Hempel, M.Jung, H.Kalogeropoulos, A.Karacheban, O.Kasemann, M.Katsas, P.Kieseler, J.Kleinwort, C.Korol, I.Lange, W.Leonard, J.Lipka, K.Lobanov, A.Mankel, R.Marfin, I.Melzer-Pellmann, I.-A.Meyer, A. B.Mittag, G.Mnich, J.Mussgiller, A.Naumann-Emme, S.Nayak, A.Ntomari, E.Perrey, H.Pitzl, D.Placakyte, R.Raspereza, A.Ribeiro Cipriano, P. M.Roland, B.Sahin, M. Ö.Salfeld-Nebgen, J.Saxena, P.Schoerner-Sadenius, T.Schröder, M.Seitz, C.Spannagel, S.Wissing, C.Blobel, V.Centis Vignali, M.Draeger, A. R.Erfle, J.Garutti, E.Goebel, K.Gonzalez, D.Görner, M.Haller, J.Hoffmann, M.Höing, R. S.Junkes, A.Kirschenmann, H.Klanner, R.Kogler, R.Lapsien, T.Lenz, T.Marchesini, I.Marconi, D.Nowatschin, D.Ott, J.Peiffer, T.Perieanu, A.Pietsch, N.Poehlsen, J.Rathjens, D.Sander, C.Schettler, H.Schleper, P.Schlieckau, E.Schmidt, A.Seidel, M.Sola, V.Stadie, H.Steinbrück, G.Tholen, H.Troendle, D.Usai, E.Vanelderen, L.Vanhoefer, A.Akbiyik, M.Barth, C.Baus, C.Berger, J.Böser, C.Butz, E.Chwalek, T.Colombo, F.De Boer, W.Descroix, A.Dierlamm, A.Feindt, M.Frensch, F.Giffels, M.Gilbert, A.Hartmann, F.Husemann, U.Katkov, I.Kornmayer, A.Lobelle Pardo, P.Mozer, M. U.Müller, T.Müller, Th.Plagge, M.Quast, G.Rabbertz, K.Röcker, S.Roscher, F.Simonis, H. J.Stober, F. M.Ulrich, R.Wagner-Kuhr, J.Wayand, S.Weiler, T.Wöhrmann, C.Wolf, R.Anagnostou, G.Daskalakis, G.Geralis, T.Giakoumopoulou, V. A.Kyriakis, A.Loukas, D.Markou, A.Psallidas, A.Topsis-Giotis, I.Agapitos, A.Kesisoglou, S.Panagiotou, A.Saoulidou, N.Tziaferi, E.Evangelou, I.Flouris, G.Foudas, C.Kokkas, P.Loukas, N.Manthos, N.Papadopoulos, I.Paradas, E.Strologas, J.Bencze, G.Hajdu, C.Hazi, A.Hidas, P.Horvath, D.Sikler, F.Veszpremi, V.Vesztergombi, G.Zsigmond, A. J.Beni, N.Czellar, S.Karancsi, J.Molnar, J.Palinkas, J.Szillasi, Z.Bartók, M.Makovec, A.Raics, P.Trocsanyi, Z. L.Mal, P.Mandal, K.Sahoo, N.Swain, S. K.Bansal, S.Beri, S. B.Bhatnagar, V.Chawla, R.Gupta, R.Bhawandeep, U.Kalsi, A. K.Kaur, A.Kaur, M.Kumar, R.Mehta, A.Mittal, M.Nishu, N.Singh, J. B.Walia, G.Kumar, AshokKumar, ArunBhardwaj, A.Choudhary, B. C.Kumar, A.Malhotra, S.Naimuddin, M.Ranjan, K.Sharma, R.Sharma, V.Banerjee, S.Bhattacharya, S.Chatterjee, K.Dey, S.Dutta, S.Gomber, B.Jain, Sa.Jain, Sh.Khurana, R.Majumdar, N.Modak, A.Mondal, K.Mukherjee, S.Mukhopadhyay, S.Roy, A.Roy, D.Roy Chowdhury, S.Sarkar, S.Sharan, M.Abdulsalam, A.Dutta, D.Jha, V.Kumar, V.Mohanty, A. K.Pant, L. M.Shukla, P.Topkar, A.Aziz, T.Banerjee, S.Bhowmik, S.Chatterjee, R. M.Dewanjee, R. K.Dugad, S.Ganguly, S.Ghosh, S.Guchait, M.Gurtu, A.Kole, G.Kumar, S.Maity, M.Majumder, G.Mazumdar, K.Mohanty, G. B.Parida, B.Sudhakar, K.Sur, N.Sutar, B.Wickramage, N.Sharma, S.Bakhshiansohi, H.Behnamian, H.Etesami, S. M.Fahim, A.Goldouzian, R.Khakzad, M.Mohammadi Najafabadi, M.Naseri, M.Paktinat Mehdiabadi, S.Rezaei Hosseinabadi, F.Safarzadeh, B.Zeinali, M.Felcini, M.Grunewald, M.Abbrescia, M.Calabria, C.Caputo, C.Chhibra, S. S.Colaleo, A.Creanza, D.Cristella, L.De Filippis, N.De Palma, M.Fiore, L.Iaselli, G.Maggi, G.Maggi, M.Miniello, G.My, S.Nuzzo, S.Pompili, A.Pugliese, G.Radogna, R.Ranieri, A.Selvaggi, G.Sharma, A.Silvestris, L.Venditti, R.Verwilligen, P.Abbiendi, G.Battilana, C.Benvenuti, A. C.Bonacorsi, D.Braibant-Giacomelli, S.Brigliadori, L.Campanini, R.Capiluppi, P.Castro, A.Cavallo, F. R.Codispoti, G.Cuffiani, M.Dallavalle, G. M.Fabbri, F.Fanfani, A.Fasanella, D.Giacomelli, P.Grandi, C.Guiducci, L.Marcellini, S.Masetti, G.Montanari, A.Navarria, F. L.Perrotta, A.Rossi, A. M.Rovelli, T.Siroli, G. P.Tosi, N.Travaglini, R.Cappello, G.Chiorboli, M.Costa, S.Giordano, F.Potenza, R.Tricomi, A.Tuve, C.Barbagli, G.Ciulli, V.Civinini, C.D’Alessandro, R.Focardi, E.Gallo, E.Gonzi, S.Gori, V.Lenzi, P.Meschini, M.Paoletti, S.Sguazzoni, G.Tropiano, A.Viliani, L.Benussi, L.Bianco, S.Fabbri, F.Piccolo, D.Calvelli, V.Ferro, F.Lo Vetere, M.Robutti, E.Tosi, S.Dinardo, M. 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Henrike.Heyne@hpi.de.; Windreich Department of Artificial Intelligence and Human Health, Icahn School of Medicine at Mount Sinai, New York, NY, USA. Henrike.Heyne@hpi.de.; Finnish Institute for Molecular Medicine (FIMM), University of Helsinki, Helsinki, Finland. Henrike.Heyne@hpi.de.; Syrbe S; Heidelberg University, Medical Faculty of Heidelberg, Center for Child and Adolescent Medicine, Clinic 1, Division of Pediatric Epileptology, Heidelberg, Germany.
Publisher: Nature Publishing Group Specialist Journals Country of Publication: England NLM ID: 9607835 Publication Model: Print Cited Medium: Internet ISSN: 1476-5578 (Electronic) Linking ISSN: 13594184 NLM ISO Abbreviation: Mol Psychiatry Subsets: MEDLINE; In Process
Academic Journal
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Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE
Academic Journal
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Journal of High Energy Physics. June 2014 2014(6):1-43
Academic Journal
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Lemke JR; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany. johannes.lemke@medizin.uni-leipzig.de.; Center for Rare Diseases, University of Leipzig Medical Center, Leipzig, Germany. johannes.lemke@medizin.uni-leipzig.de.; Eoli A; Hasso Plattner Institute, Digital Engineering Faculty, University of Potsdam, Potsdam, Germany.; Windreich Department of Artificial Intelligence and Human Health, Icahn School of Medicine at Mount Sinai, New York, NY, USA.; Krey I; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Center for Rare Diseases, University of Leipzig Medical Center, Leipzig, Germany.; Popp B; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Strehlow V; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Wittekind DA; Department of Psychiatry and Psychotherapy, University of Leipzig Medical Center, Leipzig, Germany.; Institue for Laboratory Medicine, Clinical Chemistry and Molecular Diagnostics, University of Leipzig Medical Center, Leipzig, Germany.; Vuorinen AL; Institute for Molecular Medicine Finland, University of Helsinki, Helsinki, Finland.; Faculty of Social Sciences, Unit of Health Sciences, Tampere University, Tampere, Finland.; Aldhalaan HM; Department of Neuroscience Centre, King Faisal Specialist Hospital and Research Centre, Riyadh, Kingdom of Saudi Arabia.; Baer S; Department of Pediatric Neurology, University Hospitals of Strasbourg, Strasbourg, France.; de Saint Martin A; Department of Pediatric Neurology, University Hospitals of Strasbourg, Strasbourg, France.; Hammer TB; Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.; Department of Epilepsy Genetics and Personalized Medicine, The Danish Epilepsy Centre, Dianalund, Denmark.; Herman I; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Hornemann F; Department of Pediatrics, Klinikum Chemnitz, Chemnitz, Germany.; Ingebrigtsen T; National Centre for Epilepsy, Oslo University Hospital, Oslo, Norway.; Lederer D; Centre de Génétique Humaine, Institut de Pathologie et Génétique (IPG), Charleroi (Gosselies), Belgium.; Lesca G; Department of Medical Genetics, University Hospital of Lyon, Claude Bernard University Lyon 1, Lyon, France.; Marafie D; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Department of Pediatrics, Faculty of Medicine, Kuwait University, Safat, Kuwait.; Mathot M; Neuropediatric Unit, CHU UCL-Namur, Namur, Belgium.; Rosenfeld JA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Baylor Genetics Laboratory, Houston, TX, USA.; Møller RS; Department of Epilepsy Genetics and Personalized Medicine, The Danish Epilepsy Centre, Dianalund, Denmark.; Department of Regional Health Research, University of Southern Denmark, Odense, Denmark.; Schelhaas HJ; Department of Neurology, Stichting Epilepsie Instellingen Nederland, SEIN, Zwolle, The Netherlands.; Stillman C; Section of Child Neurology, Department of Pediatrics, University of Colorado, Aurora, CO, USA.; Orsini A; Section of Pediatric Neurology, Division of Pediatrics, Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.; Patel AD; Division of Pediatric Neurology, Nationwide Children's Hospital, Department of Pediatrics, The Ohio State College of Medicine, Columbus, OH, USA.; Piard J; Centre de Génétique Humaine, Centre Hospitalier Universitaire, Université de Franche-Comté, Besançon, France.; UMR 1231 GAD, Inserm, Université de Bourgogne, Dijon, France.; Veggiotti P; Neuroscience Research Center, Department of Biomedical and Clinical Sciences, University of Milan, Milan, Italy.; Pediatric Neurology Unit, Buzzi Children's Hospital, Milan, Italy.; Vlaskamp DRM; Department of Genetics and Department of Neurology, University Medical Center Groningen, Groningen, The Netherlands.; Weckhuysen S; VIB-Center for Molecular Neurology, VIB, Antwerp, Belgium.; Department of Neurology, University Hospital Antwerp, Antwerp, Belgium.; Faculty of Medicine and Health Science, University of Antwerp, Antwerp, Belgium.; Traynelis SF; Department of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, GA, USA.; Center for the Functional Evaluation of Rare Variants (CFERV), Emory University School of Medicine, Atlanta, GA, USA.; Benke TA; Section of Child Neurology, Department of Pediatrics, University of Colorado, Aurora, CO, USA.; Heyne HO; Hasso Plattner Institute, Digital Engineering Faculty, University of Potsdam, Potsdam, Germany. Henrike.Heyne@hpi.de.; Windreich Department of Artificial Intelligence and Human Health, Icahn School of Medicine at Mount Sinai, New York, NY, USA. Henrike.Heyne@hpi.de.; Finnish Institute for Molecular Medicine (FIMM), University of Helsinki, Helsinki, Finland. Henrike.Heyne@hpi.de.; Syrbe S; Heidelberg University, Medical Faculty of Heidelberg, Center for Child and Adolescent Medicine, Clinic 1, Division of Pediatric Epileptology, Heidelberg, Germany.
Publisher: Nature Publishing Group Specialist Journals Country of Publication: England NLM ID: 9607835 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5578 (Electronic) Linking ISSN: 13594184 NLM ISO Abbreviation: Mol Psychiatry Subsets: MEDLINE
Academic Journal
Andersen PF; Department of Clinical Genetics, Center of Diagnostics. Copenhagen University Hospital -Rigshospitalet, Copenhagen, Denmark. Electronic address: peter.foerster.andersen@regionh.dk.; Ek J; Department of Clinical Genetics, Center of Diagnostics. Copenhagen University Hospital -Rigshospitalet, Copenhagen, Denmark.; Karstensen HG; Department of Clinical Genetics, Center of Diagnostics. Copenhagen University Hospital -Rigshospitalet, Copenhagen, Denmark.; Bak M; Department of Clinical Genetics, Center of Diagnostics. Copenhagen University Hospital -Rigshospitalet, Copenhagen, Denmark.; Grønborg SW; Department of Clinical Genetics, Center of Diagnostics. Copenhagen University Hospital -Rigshospitalet, Copenhagen, Denmark; Department of Paediatrics and Adolescent Medicine, Center for Rare Diseases, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.; Hove HB; Department of Paediatrics and Adolescent Medicine, Center for Rare Diseases, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.; Diness B; Department of Clinical Genetics, Center of Diagnostics. Copenhagen University Hospital -Rigshospitalet, Copenhagen, Denmark; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.; Hjortshøj TD; Department of Clinical Genetics, Center of Diagnostics. Copenhagen University Hospital -Rigshospitalet, Copenhagen, Denmark.; Hammer TB; Department of Clinical Genetics, Center of Diagnostics. Copenhagen University Hospital -Rigshospitalet, Copenhagen, Denmark.; Høi-Hansen C; Department of Paediatrics and Adolescent Medicine, Center for Rare Diseases, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.; Schönewolf-Greulich B; Department of Clinical Genetics, Center of Diagnostics. Copenhagen University Hospital -Rigshospitalet, Copenhagen, Denmark.; Bisgaard AM; Department of Paediatrics and Adolescent Medicine, Center for Rare Diseases, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.; Duno M; Department of Clinical Genetics, Center of Diagnostics. Copenhagen University Hospital -Rigshospitalet, Copenhagen, Denmark.; Østergaard E; Department of Clinical Genetics, Center of Diagnostics. Copenhagen University Hospital -Rigshospitalet, Copenhagen, Denmark; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
Publisher: Elsevier Country of Publication: Netherlands NLM ID: 101247089 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1878-0849 (Electronic) Linking ISSN: 17697212 NLM ISO Abbreviation: Eur J Med Genet Subsets: MEDLINE
Academic Journal
Papagiannis A; Institut Jules Bordet, Hôpital Universitaire de Bruxelles (H.U.B), Université libre de Bruxelles (ULB), Brussels, Belgium.; Majjaj S; Institut Jules Bordet, Hôpital Universitaire de Bruxelles (H.U.B), Université libre de Bruxelles (ULB), Brussels, Belgium.; Duhoux FP; Department of Medical Oncology, Cliniques universitaires Saint-Luc and Institut de Recherche Expérimentale et Clinique (Pôle MIRO), Université catholique de Louvain, Brussels, Belgium.; Agostinetto E; Institut Jules Bordet, Hôpital Universitaire de Bruxelles (H.U.B), Université libre de Bruxelles (ULB), Brussels, Belgium.; Stanciu AM; Institut Jules Bordet, Hôpital Universitaire de Bruxelles (H.U.B), Université libre de Bruxelles (ULB), Brussels, Belgium.; Vanhulst T; Institut Jules Bordet, Hôpital Universitaire de Bruxelles (H.U.B), Université libre de Bruxelles (ULB), Brussels, Belgium.; Buisseret L; Institut Jules Bordet, Hôpital Universitaire de Bruxelles (H.U.B), Université libre de Bruxelles (ULB), Brussels, Belgium.; Larsimont D; Institut Jules Bordet, Hôpital Universitaire de Bruxelles (H.U.B), Université libre de Bruxelles (ULB), Brussels, Belgium.; Veys I; Institut Jules Bordet, Hôpital Universitaire de Bruxelles (H.U.B), Université libre de Bruxelles (ULB), Brussels, Belgium.; Paesmans M; Institut Jules Bordet, Hôpital Universitaire de Bruxelles (H.U.B), Université libre de Bruxelles (ULB), Brussels, Belgium.; Hammer TB; Centre Hospitalier Universitaire Brugmann, Brussels, Belgium.; Awada A; Institut Jules Bordet, Hôpital Universitaire de Bruxelles (H.U.B), Université libre de Bruxelles (ULB), Brussels, Belgium.; Ameye L; Institut Jules Bordet, Hôpital Universitaire de Bruxelles (H.U.B), Université libre de Bruxelles (ULB), Brussels, Belgium.; Rothe F; Institut Jules Bordet, Hôpital Universitaire de Bruxelles (H.U.B), Université libre de Bruxelles (ULB), Brussels, Belgium.; Madriles F; Rejuversen Senescence Therapeutics, Barcelona, Spain.; Cash TP; Rejuversen Senescence Therapeutics, Barcelona, Spain.; Salgado R; Department of Pathology, ZAS Hospitals, Antwerp, Belgium; Division of Research, Peter Mac Callum Cancer Centre, Melbourne, Australia.; Willard-Gallo K; Institut Jules Bordet, Hôpital Universitaire de Bruxelles (H.U.B), Université libre de Bruxelles (ULB), Brussels, Belgium.; Sotiriou C; Institut Jules Bordet, Hôpital Universitaire de Bruxelles (H.U.B), Université libre de Bruxelles (ULB), Brussels, Belgium.; Vuylsteke P; CHU UCL Namur Sainte-Elisabeth, Namur, Belgium.; Neven P; Universitaire Ziekenhuizen Leuven, Leuven, Belgium.; Ignatiadis M; Institut Jules Bordet, Hôpital Universitaire de Bruxelles (H.U.B), Université libre de Bruxelles (ULB), Brussels, Belgium. michail.ignatiadis@hubruxelles.be.
Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE
Academic Journal
Leitão E; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; Santini A; Univ Rouen Normandie, Normandie Univ, Inserm U1245 and CHU Rouen, Department of Genetics and Reference Center for Developmental Abnormalities, Rouen, France.; Cogne B; Nantes Université, CHU de Nantes, Service de Génétique médicale, Nantes, France.; Nantes Université, CHU de Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France.; Laboratoire SeqOIA, Paris, France.; Essid M; Genetics Department, Hospices Civils de Lyon, Lyon, France.; Pathophysiology and Genetics of Neuron and Muscle (PNMG), UCBL, CNRS UMR5261 - INSERM, U1315, Lyon, France.; GCS AURAGEN, Lyon, France.; Member of ERN EpiCARE.; Athanasiadou M; CNRS, Inserm, Université de Strasbourg, IGBMC UMR 7104- UMR-S 1258, Illkirch, France.; Department of Integrated Structural Biology, IGBMC, Illkirch, France.; LaFlamme CW; Center for Pediatric Neurological Disease Research, St. Jude Children's Research Hospital, Memphis, TN, USA.; Graduate School of Biomedical Sciences, St. Jude Children's Research Hospital, Memphis, Memphis, TN, USA.; Marijon P; Laboratoire SeqOIA, Paris, France.; Bernard V; GCS AURAGEN, Lyon, France.; Chatron N; Genetics Department, Hospices Civils de Lyon, Lyon, France.; Pathophysiology and Genetics of Neuron and Muscle (PNMG), UCBL, CNRS UMR5261 - INSERM, U1315, Lyon, France.; GCS AURAGEN, Lyon, France.; Barcia G; Assistance Publique - Hôpitaux de Paris (APHP), Service de Médecine Génomique des Maladies Rares, Hôpital Necker-Enfants malades, Paris, France.; Université Paris Cité, INSERM, IHU Imagine - Institut des maladies génétiques, Paris, France.; Laboratoire SeqOIA, Paris, France.; Member of ERN EpiCARE.; Keren B; Assistance Publique - Hôpitaux de Paris (APHP) Sorbonne Université, Département de Génétique, Hôpital Pitié-Salpêtrière, Paris, France.; Laboratoire SeqOIA, Paris, France.; Mignot C; Assistance Publique - Hôpitaux de Paris (APHP) Sorbonne Université, Département de Génétique, Hôpital Pitié-Salpêtrière, Paris, France.; Centre de Référence Déficiences Intellectuelles de Causes Rares, Paris, France.; Charles P; Assistance Publique - Hôpitaux de Paris (APHP) Sorbonne Université, Département de Génétique, Hôpital Pitié-Salpêtrière, Paris, France.; Besnard T; Nantes Université, CHU de Nantes, Service de Génétique médicale, Nantes, France.; Nantes Université, CHU de Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France.; de Sainte Agathe JM; Assistance Publique - Hôpitaux de Paris (APHP) Sorbonne Université, Département de Génétique, Hôpital Pitié-Salpêtrière, Paris, France.; Laboratoire SeqOIA, Paris, France.; Fuerte EPA; Center for Pediatric Neurological Disease Research, St. Jude Children's Research Hospital, Memphis, TN, USA.; Sengupta S; Center for Pediatric Neurological Disease Research, St. Jude Children's Research Hospital, Memphis, TN, USA.; Milh M; Service de Neurologie Pediatrique, AP-HM, Marseille, France.; Aix Marseille Univ, Inserm, INMED, U1249, Marseille, France.; Ramond F; Département de Génétique, Centre Hospitalier Universitaire de Saint-Etienne, Saint-Etienne, France.; Allan T; Epilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Victoria, Australia.; An I; Assistance Publique - Hôpitaux de Paris (APHP) Sorbonne Université, Département de Neurologie, Center of Reference for Rare Epilepsies, ERN EPICARE, Hôpital Pitié-Salpêtrière, Paris, France.; Araujo C; Department of Surgery and Anatomy, Ribeirão Preto Medical School, University of São Paulo, Ribeirao Preto, Brazil.; Arpin S; Service de Génétique, CHU de Tours, Tours, France.; Austin-Tse C; Broad Center for Mendelian Genomics, Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Auvin S; Assistance Publique - Hôpitaux de Paris (APHP), Département de Neuropédiatrie, Hôpital Robert-Debré, Paris, France.; Université Paris Cité, INSERM NeuroDiderot, Paris, France.; Member of ERN EpiCARE.; Baer S; Service de neuropédiatrie, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.; Member of ERN EpiCARE.; Bahi-Buisson N; Université Paris Cité, INSERM, IHU Imagine - Institut des maladies génétiques, Paris, France.; Bak M; Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, Denmark.; Barth M; Department of Medical Genetics, Angers University Hospital, Angers, France.; University of Angers, MitoLab, Unité MITOVASC, UMR CNRS 6015, INSERM U1083, SFR ICAT, University Hospital of Angers, Angers, France.; Baulac S; Sorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS, APHP, Hôpital de la Pitié Salpêtrière, Paris, France.; Weirauch NB; Service de Pédiatrie, CHU Reims, Reims, France.; Université Reims Champagne Ardenne (URCA), UFR médecine, Reims, France.; CReSTIC/EA 3804, URCA, Reims, France.; Begemann M; Institute for Human Genetics and Genomic Medicine, Medical Faculty, RWTH Aachen University Hospital, Aachen, Germany.; Bennett MF; Epilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Victoria, Australia.; Genetics and Gene Regulation Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.; Department of Medical Biology, The University of Melbourne, Parkville, Victoria, Australia.; Bensabath U; Assistance Publique - Hôpitaux de Paris (APHP) Sorbonne Université, Département de Génétique, Hôpital Pitié-Salpêtrière, Paris, France.; Bézieau S; Nantes Université, CHU de Nantes, Service de Génétique médicale, Nantes, France.; Nantes Université, CHU de Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France.; Bhouri R; Department of Ophthalmology, Centre Hospitalier Intercommunal de Créteil (CHIC), Créteil, France.; Biehler M; Laboratoire de Diagnostic Génétique, Nouvel Hôpital Civil, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.; Hammer TB; Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, Denmark.; Danish Epilepsy center, Dianalund, Denmark.; Bogoin J; Assistance Publique - Hôpitaux de Paris (APHP) Sorbonne Université, Département de Génétique, Hôpital Pitié-Salpêtrière, Paris, France.; Bonanno E; Assistance Publique - Hôpitaux de Paris (APHP) Sorbonne Université, Département de Génétique, Hôpital Pitié-Salpêtrière, Paris, France.; Boussion S; Univ. Lille, CHU Lille, ULR7364 - RADEME, Lille, France.; Bramswig NC; Centre of Medical Genetics, Department of Medical Genetics, University and University Hospital Münster, Münster, Germany.; Bris C; Department of Medical Genetics, Angers University Hospital, Angers, France.; University of Angers, MitoLab, Unité MITOVASC, UMR CNRS 6015, INSERM U1083, SFR ICAT, University Hospital of Angers, Angers, France.; Brosseau-Beauvir A; Center for Intellectual Disability Reference, Brest University Hospital, Brest, France.; Bruel AL; Université Bourgogne Europe, CHU Dijon Bourgogne, Laboratoire de Génomique Médicale, Centre Neomics, FHU-TRANSLAD, Centre de recherche Translationnelle en Médecine moléculaire - Inserm UMR1231 équipe GAD, Dijon, France.; Buratti J; Assistance Publique - Hôpitaux de Paris (APHP) Sorbonne Université, Département de Génétique, Hôpital Pitié-Salpêtrière, Paris, France.; Chambon P; Univ Rouen Normandie, Normandie Univ, Inserm U1245 and CHU Rouen, Department of Genetics and Reference Center for Developmental Abnormalities, Rouen, France.; Laboratoire SeqOIA, Paris, France.; Chemaly N; Université Paris Cité, INSERM, IHU Imagine - Institut des maladies génétiques, Paris, France.; Reference Center for Rare Epilepsies, Department of Pediatric Neurology, Necker Enfants Malades Hospital, Paris, France.; Member of ERN EpiCARE.; Chesneau B; Service de Génétique médicale, CHU Purpan, Toulouse, France.; Colin E; Department of Medical Genetics, Angers University Hospital, Angers, France.; University of Angers, MitoLab, Unité MITOVASC, UMR CNRS 6015, INSERM U1083, SFR ICAT, University Hospital of Angers, Angers, France.; Colmard M; Service de Neuropédiatrie, CHU Montpellier, Montpellier, France.; Conrad S; Nantes Université, CHU de Nantes, Service de Génétique médicale, Nantes, France.; Courtin T; Assistance Publique - Hôpitaux de Paris (APHP), Service de Médecine Génomique des Maladies Rares, Hôpital Necker-Enfants malades, Paris, France.; Université Paris Cité, INSERM, IHU Imagine - Institut des maladies génétiques, Paris, France.; Dang LT; Department of Pediatrics, Michigan Medicine, University of Michigan, Ann Arbor, USA.; de Saint Martin A; Service de neuropédiatrie, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.; Member of ERN EpiCARE.; de Vanssay de Blavous Legendre C; service de Pédiatrie, consultation de neurologie pédiatrique GHH Jacques Monod, Le Havre, France.; Denommé-Pichon AS; Université Bourgogne Europe, CHU Dijon Bourgogne, Laboratoire de Génomique Médicale, Centre Neomics, FHU-TRANSLAD, Centre de recherche Translationnelle en Médecine moléculaire - Inserm UMR1231 équipe GAD, Dijon, France.; DiTroia S; Broad Center for Mendelian Genomics, Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Doco-Fenzy M; UF de Génétique Clinique, CHU de Reims, Reims, France.; Université Reims Champagne Ardenne (URCA), UFR médecine, Reims, France.; Nantes Université, CHU de Nantes, Service de Génétique médicale, Nantes, France.; Dubourg C; Laboratoire de Génétique Moléculaire et Génomique, FHU GenOMedS, CHU Rennes, Rennes, France.; Univ Rennes, CNRS, INSERM, IGDR (Institut de Génétique et Développement de Rennes)-UMR 6290, ERL U1305, Rennes, France.; Laboratoire SeqOIA, Paris, France.; Dubucs C; Département de Pathologie, Institut Universitaire du Cancer Toulouse - Oncopole, Toulouse, France.; Ducreux S; Assistance Publique - Hôpitaux de Paris (APHP), Service de Médecine Génomique des Maladies Rares, Hôpital Necker-Enfants malades, Paris, France.; Laboratoire SeqOIA, Paris, France.; Dufour L; Assistance Publique - Hôpitaux de Paris (APHP), Département de Neuropédiatrie, Hôpital Robert-Debré, Paris, France.; Duquet R; Assistance Publique - Hôpitaux de Paris (APHP) Sorbonne Université, Département de Génétique, Hôpital Pitié-Salpêtrière, Paris, France.; Durand B; Service de génétique médicale, Institut de Génétique Médicale d'Alsace (IGMA), CHU Strasbourg, Strasbourg, France.; Chehadeh SE; Service de génétique médicale, Institut de Génétique Médicale d'Alsace (IGMA), CHU Strasbourg, Strasbourg, France.; Elbracht M; Institute for Human Genetics and Genomic Medicine, Medical Faculty, RWTH Aachen University Hospital, Aachen, Germany.; Faivre L; Université Bourgogne Europe, CHU Dijon Bourgogne, Inserm, CTM UMR1231, équipe GAD, FHU TRANSLAD, Centre de génétique, Centre de référence Anomalies du Développement et Syndromes Malformatifs, Centre de référence Déficiences Intellectuelles de Causes Rares et Centre de référence GénoPsy, Dijon, France.; Faoucher M; Laboratoire de Génétique Moléculaire et Génomique, FHU GenOMedS, CHU Rennes, Rennes, France.; Univ Rennes, CNRS, INSERM, IGDR (Institut de Génétique et Développement de Rennes)-UMR 6290, ERL U1305, Rennes, France.; Laboratoire SeqOIA, Paris, France.; GCS AURAGEN, Lyon, France.; Faudet A; Assistance Publique - Hôpitaux de Paris (APHP) Sorbonne Université, Département de Génétique, Hôpital Pitié-Salpêtrière, Paris, France.; Forlani S; Sorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS, APHP, Hôpital de la Pitié Salpêtrière, Paris, France.; Fradin M; Service de Génétique Clinique, Centre de Référence 'Anomalies du Développement et Syndromes Malformatifs' de l'Inter-région Ouest, FHU GenOMedS, CHU Rennes Hôpital Sud, Rennes, France.; Gaignard P; Laboratoire de Biochimie Site Bicêtre, Faculté de Pharmacie, Hôpitaux Universitaires Paris-Saclay, Centre de référence des Maladies Mitochondriales, Filière Filnemu, Paris, France.; Laboratoire SeqOIA, Paris, France.; Ganne B; Laboratoire de Génétique chromosomique, CHU de Montpellier, Montpellier, France.; Garde A; Université Bourgogne Europe, CHU Dijon Bourgogne, Centre de Référence maladies rares «Anomalies du Développement et syndromes malformatifs», Centre de Génétique, FHU-TRANSLAD, Dijon, France.; Géraud J; Neuropediatric Department, University Hospital Centre Toulouse, Toulouse, France.; Gill D; Kids Neuroscience Centre, Kids Research Institute, Sydney, NSW, Australia.; TY Nelson Department of Neurology and Neurosurgery, The Children's Hospital at Westmead, Sydney Children's Hospitals Network, Sydney, NSW, Australia.; Specialty of Child and Adolescent Health, University of Sydney, Sydney, NSW, Australia.; Goldenberg A; Univ Rouen Normandie, Normandie Univ, Inserm U1245 and CHU Rouen, Department of Genetics and Reference Center for Developmental Abnormalities, Rouen, France.; Grabli D; Sorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS, APHP, Hôpital de la Pitié Salpêtrière, Paris, France.; Assistance Publique - Hôpitaux de Paris (APHP) Sorbonne Université, Département de Neurologie, Center of Reference for Rare Epilepsies, ERN EPICARE, Hôpital Pitié-Salpêtrière, Paris, France.; Grisel C; Service de Pédiatrie, Centre Hospitalier Intercommunal de Créteil, Créteil, France.; Gueden S; Department of Pediatric Neurology, Angers University Hospital, Angers, France.; Gueguen P; Service de Génétique, CHU de Tours, Tours, France.; Université de Tours, INSERM, Imaging Brain & Neuropsychiatry iBraiN U1253, Tours, France.; Laboratoire SeqOIA, Paris, France.; Guerrot AM; Univ Rouen Normandie, Normandie Univ, Inserm U1245 and CHU Rouen, Department of Genetics and Reference Center for Developmental Abnormalities, Rouen, France.; Guichet A; Department of Medical Genetics, Angers University Hospital, Angers, France.; University of Angers, MitoLab, Unité MITOVASC, UMR CNRS 6015, INSERM U1083, SFR ICAT, University Hospital of Angers, Angers, France.; Härting N; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; Häusler MG; Division of Neuropediatrics and Social Pediatrics, Department of Pediatrics, University Hospital, Rheinisch-Westfälische Technische Hochschule Aachen, Aachen, Germany.; Heide S; Assistance Publique - Hôpitaux de Paris (APHP) Sorbonne Université, Département de Génétique, Hôpital Pitié-Salpêtrière, Paris, France.; Héron B; Assistance Publique - Hôpitaux de Paris (APHP) Sorbonne Université, Département de Neurologie Pédiatrique, Hôpital Armand Trousseau-La Roche Guyon, Fédération Hospitalo-Universitaire I2-D2, Paris, France.; Héron D; Assistance Publique - Hôpitaux de Paris (APHP) Sorbonne Université, Département de Génétique, Hôpital Pitié-Salpêtrière, Paris, France.; Centre de Référence Déficiences Intellectuelles de Causes Rares, Paris, France.; Heulin M; Service de Neuropédiatrie, Hôpital Jean-Verdier, Bondy, France.; Houdayer C; Department of Medical Genetics, Angers University Hospital, Angers, France.; University of Angers, MitoLab, Unité MITOVASC, UMR CNRS 6015, INSERM U1083, SFR ICAT, University Hospital of Angers, Angers, France.; Isidor B; Nantes Université, CHU de Nantes, Service de Génétique médicale, Nantes, France.; Jacquette A; consultation de génétique, CCMR ANDDI rare, centre hospitalier d'Alençon, Alençon, France.; Januel L; Genetics Department, Hospices Civils de Lyon, Lyon, France.; GCS AURAGEN, Lyon, France.; Jean-Marçais N; Service de Génétique Clinique, Centre de Référence 'Anomalies du Développement et Syndromes Malformatifs' de l'Inter-région Ouest, FHU GenOMedS, CHU Rennes Hôpital Sud, Rennes, France.; Jousselin K; Laboratoire SeqOIA, Paris, France.; Kaiser FJ; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; Kaya S; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; King C; Department of Paediatrics and Child Health, University of Otago, Wellington, New Zealand.; Konyukh M; Département de Génétique Médicale, Hôpital Henri Mondor, Assistance Publique des Hôpitaux de Paris, Créteil, France.; Laboratoire SeqOIA, Paris, France.; Kraft F; Institute for Human Genetics and Genomic Medicine, Medical Faculty, RWTH Aachen University Hospital, Aachen, Germany.; Krause J; Institute for Human Genetics and Genomic Medicine, Medical Faculty, RWTH Aachen University Hospital, Aachen, Germany.; Kirstetter R; Assistance Publique - Hôpitaux de Paris (APHP), Service de Médecine Génomique des Maladies Rares, Hôpital Necker-Enfants malades, Paris, France.; Université Paris Cité, INSERM, IHU Imagine - Institut des maladies génétiques, Paris, France.; Kuechler A; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; Kurth I; Institute for Human Genetics and Genomic Medicine, Medical Faculty, RWTH Aachen University Hospital, Aachen, Germany.; Labalme A; Genetics Department, Hospices Civils de Lyon, Lyon, France.; Laloy JS; Assistance Publique - Hôpitaux de Paris (APHP), Service de Médecine Génomique des Maladies Rares, Hôpital Necker-Enfants malades, Paris, France.; Laugel V; Service de neuropédiatrie, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.; Bricquir FL; Nantes Université, CHU de Nantes, Service de Pédiatrie, Nantes, France.; Lèbre AS; Laboratoire de Génétique, CHU de Reims, Reims, France.; Université Reims Champagne Ardenne (URCA), UFR médecine, Reims, France.; Université Paris Cité, Institute of Psychiatry and Neuroscience of Paris (IPNP), INSERM U1266, [Krebs team], Paris, France.; Lebrun M; Département de Génétique, Centre Hospitalier Universitaire de Saint-Etienne, Saint-Etienne, France.; GCS AURAGEN, Lyon, France.; Leguern E; Sorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS, APHP, Hôpital de la Pitié Salpêtrière, Paris, France.; Assistance Publique - Hôpitaux de Paris (APHP) Sorbonne Université, Département de Génétique, Hôpital Pitié-Salpêtrière, Paris, France.; Levy J; Assistance Publique - Hôpitaux de Paris (APHP), Département de Neuropédiatrie, Hôpital Robert-Debré, Paris, France.; Laboratoire SeqOIA, Paris, France.; Lieffering N; Department of Paediatrics and Child Health, University of Otago, Wellington, New Zealand.; Lyonnet S; Assistance Publique - Hôpitaux de Paris (APHP), Service de Médecine Génomique des Maladies Rares, Hôpital Necker-Enfants malades, Paris, France.; Université Paris Cité, INSERM, IHU Imagine - Institut des maladies génétiques, Paris, France.; Lüthy K; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; Macdonald S; Epilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Victoria, Australia.; Mansour-Hendili L; Laboratoire SeqOIA, Paris, France.; Maraval J; Université Bourgogne Europe, CHU Dijon Bourgogne, Inserm, CTM UMR1231, équipe GAD, FHU TRANSLAD, Centre de génétique, Centre de référence Anomalies du Développement et Syndromes Malformatifs, Centre de référence Déficiences Intellectuelles de Causes Rares et Centre de référence GénoPsy, Dijon, France.; Mattausch C; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; Messaoud O; Broad Center for Mendelian Genomics, Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Harvard Medical School, Boston, Boston, MA, USA.; Division of Genetics and Genomics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.; Center for Genomic Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.; Morel G; Service de Génétique, CHU (Centre Hospitalier Universitaire) de La Réunion, Saint-Denis, La Réunion, France.; Mortreux J; GCS AURAGEN, Lyon, France.; Munnich A; Université Paris Cité, INSERM, IHU Imagine - Institut des maladies génétiques, Paris, France.; Nabbout R; Université Paris Cité, INSERM, IHU Imagine - Institut des maladies génétiques, Paris, France.; Reference Center for Rare Epilepsies, Department of Pediatric Neurology, Necker Enfants Malades Hospital, Paris, France.; Member of ERN EpiCARE.; Nambot S; Université Bourgogne Europe, CHU Dijon Bourgogne, Centre de Référence maladies rares «Anomalies du Développement et syndromes malformatifs», Centre de Génétique, FHU-TRANSLAD, Dijon, France.; Navarro V; Assistance Publique - Hôpitaux de Paris (APHP) Sorbonne Université, Département de Neurologie, Center of Reference for Rare Epilepsies, ERN EPICARE, Hôpital Pitié-Salpêtrière, Paris, France.; Sorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS, APHP, Hôpital de la Pitié Salpêtrière, Paris, France.; Neale A; Broad Center for Mendelian Genomics, Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Nguyen L; Assistance Publique - Hôpitaux de Paris (APHP) Sorbonne Université, Département de Génétique, Hôpital Pitié-Salpêtrière, Paris, France.; Nizon M; Nantes Université, CHU de Nantes, Service de Génétique médicale, Nantes, France.; Nowak F; Health Technologies Institute, Inserm, Paris, France.; O'Leary MC; Broad Center for Mendelian Genomics, Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Odent S; Service de Génétique Clinique, Centre de Référence 'Anomalies du Développement et Syndromes Malformatifs' de l'Inter-région Ouest, FHU GenOMedS, CHU Rennes Hôpital Sud, Rennes, France.; Univ Rennes, CNRS, INSERM, IGDR (Institut de Génétique et Développement de Rennes)-UMR 6290, ERL U1305, Rennes, France.; Ojeda NM; Department of Neurosciences, University of California San Diego, La Jolla, CA, USA.; Rady Children's Institute for Genomic Medicine, San Diego, CA, USA.; Olin V; Assistance Publique - Hôpitaux de Paris (APHP) Sorbonne Université, Département de Génétique, Hôpital Pitié-Salpêtrière, Paris, France.; Õunap K; Department of Genetics and Personalized Medicine, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia.; Department of Clinical Genetics, Genetics and Personalized Medicine Clinic, Tartu University Hospital, Tartu, Estonia.; Pais LS; Broad Center for Mendelian Genomics, Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Paluch R; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; Panagiotakaki E; Department of Pediatric Epileptology, University Hospitals of Lyon (HCL), Lyon, France.; Member of ERN EpiCARE.; Patat O; Service de Génétique médicale, CHU Purpan, Toulouse, France.; Perrin-Sabourin L; Assistance Publique - Hôpitaux de Paris (APHP), Département de Neuropédiatrie, Hôpital Robert-Debré, Paris, France.; Petit F; Univ. Lille, CHU Lille, ULR7364 - RADEME, Lille, France.; Philippe C; Laboratoire de Génétique Médicale, CHR Metz-Thionville, Hôpital Mercy, Metz, France.; GCS AURAGEN, Lyon, France.; Piton A; Laboratoire de Diagnostic Génétique, Nouvel Hôpital Civil, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.; Institute of Genetics and Cellular and Molecular Biology (IGBMC), INSERM-U964, CNRS-UMR7104, University of Strasbourg, Illkirch, France.; GCS AURAGEN, Lyon, France.; Planes M; Medical Genetics Department, Brest University Hospital, Brest, France.; Poirsier C; UF de Génétique Clinique, CHU de Reims, Reims, France.; Pouzet A; Assistance Publique - Hôpitaux de Paris (APHP), Département de Neuropédiatrie, Hôpital Robert-Debré, Paris, France.; Prouteau C; Department of Medical Genetics, Angers University Hospital, Angers, France.; University of Angers, MitoLab, Unité MITOVASC, UMR CNRS 6015, INSERM U1083, SFR ICAT, University Hospital of Angers, Angers, France.; Quéméner-Redon S; Medical Genetics Department, Brest University Hospital, Brest, France.; Center for Intellectual Disability Reference, Brest University Hospital, Brest, France.; University of Brest, Inserm, EFS, UMR 1078, GGB, Brest, France.; Renaud M; Service de Génétique Clinique, CHRU Nancy, Vandoeuvre les Nancy, France.; Richard AC; Univ Rouen Normandie, Normandie Univ, Inserm U1245 and CHU Rouen, Department of Genetics and Reference Center for Developmental Abnormalities, Rouen, France.; Rio M; Assistance Publique - Hôpitaux de Paris (APHP), Service de Médecine Génomique des Maladies Rares, Hôpital Necker-Enfants malades, Paris, France.; Université Paris Cité, INSERM, IHU Imagine - Institut des maladies génétiques, Paris, France.; Rivier C; Department of Pediatrics, Hôpital Nord-Ouest, Villefranche sur Saône, France.; Robin-Renaldo F; Assistance Publique - Hôpitaux de Paris (APHP) Sorbonne Université, Département de Neurologie Pédiatrique, Hôpital Armand Trousseau-La Roche Guyon, Fédération Hospitalo-Universitaire I2-D2, Paris, France.; Rollier P; Service de Génétique Clinique, Centre de Référence 'Anomalies du Développement et Syndromes Malformatifs' de l'Inter-région Ouest, FHU GenOMedS, CHU Rennes Hôpital Sud, Rennes, France.; Univ Rennes, CNRS, INSERM, IGDR (Institut de Génétique et Développement de Rennes)-UMR 6290, ERL U1305, Rennes, France.; Rossi M; Genetics Department, Hospices Civils de Lyon, Lyon, France.; Roubertie A; Service de Neuropédiatrie, CHU Montpellier, Montpellier, France.; INM, INSERM U 1298, Montpellier, France.; Rupin M; Department of Pediatric Neurology, Angers University Hospital, Angers, France.; Saugier-Veber P; Univ Rouen Normandie, Normandie Univ, Inserm U1245 and CHU Rouen, Department of Genetics and Reference Center for Developmental Abnormalities, Rouen, France.; Laboratoire SeqOIA, Paris, France.; Saneto R; Neuroscience Institute, Norcliff Center for Integrative Brain Research, Division of Pediatric Neurology, Seattle Children's Hospital/University of Washington, Seattle, USA.; Sarrazin E; Caribbean Reference Center for Neuromuscular Diseases, University Hospital, Fort de France, Martinique, France.; Schaefer E; Service de génétique médicale, Institut de Génétique Médicale d'Alsace (IGMA), CHU Strasbourg, Strasbourg, France.; Schluth-Bolard C; Laboratoire de Diagnostic Génétique, Nouvel Hôpital Civil, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.; UMRS 1112, INSERM, Université de Strasbourg, Strasbourg, France.; GCS AURAGEN, Lyon, France.; Schneider A; Epilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Victoria, Australia.; Schumann I; Centre of Medical Genetics, Department of Medical Genetics, University and University Hospital Münster, Münster, Germany.; Institute of Human Genetics, Leipzig University Medical Center, Leipzig, Germany.; Seplyarskiy V; Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.; Brigham and Women's Hospital, Division of Genetics, Harvard Medical School, Boston, MA, USA.; Smol T; Univ. Lille, CHU Lille, ULR7364 - RADEME, Lille, France.; Laboratoire SeqOIA, Paris, France.; Sunyaev S; Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.; Brigham and Women's Hospital, Division of Genetics, Harvard Medical School, Boston, MA, USA.; Sperelakis-Beedham B; Université Paris Cité, INSERM, IHU Imagine - Institut des maladies génétiques, Paris, France.; Assistance Publique - Hôpitaux de Paris (APHP), Service de Médecine Génomique des Maladies Rares, Hôpital Necker-Enfants malades, Paris, France.; Laboratoire SeqOIA, Paris, France.; Stenton SL; Broad Center for Mendelian Genomics, Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Division of Genetics and Genomics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.; Stock F; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; Tharreau M; Department of Molecular Genetics and Cytogenomics, Rare and Autoinflammatory Genetic Diseases, CeRéMAIA, Arnaud de Villeneuve Hospital and University of Montpellier, Montpellier, France.; Torun D; Department of Medical Genetics, Gulhane Military Medical Academy, Ankara, Turkey.; Toulouse J; Department of Pediatric Epileptology, University Hospitals of Lyon (HCL), Lyon, France.; Member of ERN EpiCARE.; Thiyagarajah H; Epilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Victoria, Australia.; Valence S; Assistance Publique - Hôpitaux de Paris (APHP) Sorbonne Université, Département de Neurologie Pédiatrique, Hôpital Armand Trousseau-La Roche Guyon, Fédération Hospitalo-Universitaire I2-D2, Paris, France.; Valleix S; Assistance Publique - Hôpitaux de Paris (APHP), Paris City University, Genomic Medicine Department of systemic and organ diseases, Cochin hospital, Paris, France.; Villard L; Service de Génétique Médicale, AP-HM, Marseille, France.; Aix Marseille Univ, Inserm, INMED, U1249, Marseille, France.; Ville D; Department of Pediatric Neurology and Reference Center for Rare Children Epilepsy and Tuberous Sclerosis, Hôpital Femme Mere Enfant, Centre Hospitalier Universitaire de Lyon, Lyon, France.; Villeneuve N; Service de Neurologie Pediatrique, AP-HM, Marseille, France.; Member of ERN EpiCARE.; Vitobello A; Université Bourgogne Europe, CHU Dijon Bourgogne, Laboratoire de Génomique Médicale, Centre Neomics, FHU-TRANSLAD, Centre de recherche Translationnelle en Médecine moléculaire - Inserm UMR1231 équipe GAD, Dijon, France.; GCS AURAGEN, Lyon, France.; Waernessyckle A; Assistance Publique - Hôpitaux de Paris (APHP) Sorbonne Université, Département de Génétique, Hôpital Pitié-Salpêtrière, Paris, France.; Weber Y; Section of Epileptology, Department Neurology, Medical Faculty, University RWTH Aachen, Aachen, Germany.; Wieczorek D; Institute of Human Genetics, Medical Faculty and University Hospital Düsseldorf, Heinrich Heine University Düsseldorf, Düsseldorf,, Düsseldorf, Germany.; Witkowski T; Epilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Victoria, Australia.; Yadavilli M; Department of Neurosciences, University of California San Diego, La Jolla, CA, USA.; Rady Children's Institute for Genomic Medicine, San Diego, CA, USA.; Yammine T; Laboratoire de Génétique, CHU de Reims, Reims, France.; Zaafrane-Khachnaoui K; Université Côte d'Azur, Centre Hospitalier Universitaire de Nice, Inserm U1081, CNRS UMR7284, IRCAN, Nice, France.; Zaki MS; Clinical Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt.; Ziegler A; UF de Génétique Clinique, CHU de Reims, Reims, France.; Service de Génétique médicale, CHU Purpan, Toulouse, France.; GCS AURAGEN, Lyon, France.; Lermine A; Laboratoire SeqOIA, Paris, France.; Nicolas G; Univ Rouen Normandie, Normandie Univ, Inserm U1245 and CHU Rouen, Department of Genetics and Reference Center for Developmental Abnormalities, Rouen, France.; Laboratoire SeqOIA, Paris, France.; Gleeson JG; Department of Neurosciences, University of California San Diego, La Jolla, CA, USA.; Rady Children's Institute for Genomic Medicine, San Diego, CA, USA.; Sadleir LG; Department of Paediatrics and Child Health, University of Otago, Wellington, New Zealand.; Hildebrand MS; Epilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Victoria, Australia.; Neuroscience Group, Murdoch Children's Research Institute, Parkville, Victoria, Australia.; Scheffer IE; Epilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Victoria, Australia.; Department of Paediatrics, University of Melbourne, Royal Children's Hospital, Melbourne, Australia.; Florey Institute and Murdoch Children's Research Institute, Melbourne, Australia.; Whiffin N; Big Data Institute, University of Oxford, Oxford, UK.; Centre for Human Genetics, University of Oxford, Oxford, UK.; Broad Center for Mendelian Genomics, Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; O'Donnell-Luria A; Broad Center for Mendelian Genomics, Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Division of Genetics and Genomics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.; Center for Genomic Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.; Mefford HC; Center for Pediatric Neurological Disease Research, St. Jude Children's Research Hospital, Memphis, TN, USA.; Blanc P; Laboratoire SeqOIA, Paris, France.; Thevenon J; Service de Génétique, Génomique et Procréation, CHU Grenoble Alpes, Grenoble, France.; Université Grenoble Alpes, INSERM U 1209, CNRS UMR 5309, Institut for Advanced Biosciences, Grenoble, France.; GCS AURAGEN, Lyon, France.; Charbonnier C; Univ Rouen Normandie, Normandie Univ, Inserm U1245 and CHU Rouen, Department of Biostatistics and Reference Center for Developmental Abnormalities, Rouen, France.; Charenton C; CNRS, Inserm, Université de Strasbourg, IGBMC UMR 7104- UMR-S 1258, Illkirch, France.; Department of Integrated Structural Biology, IGBMC, Illkirch, France.; Depienne C; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; Laboratoire SeqOIA, Paris, France.; Lesca G; Genetics Department, Hospices Civils de Lyon, Lyon, France.; Pathophysiology and Genetics of Neuron and Muscle (PNMG), UCBL, CNRS UMR5261 - INSERM, U1315, Lyon, France.; GCS AURAGEN, Lyon, France.; Member of ERN EpiCARE.; Nava C; Sorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS, APHP, Hôpital de la Pitié Salpêtrière, Paris, France.; Assistance Publique - Hôpitaux de Paris (APHP) Sorbonne Université, Département de Génétique, Hôpital Pitié-Salpêtrière, Paris, France.; Laboratoire SeqOIA, Paris, France.
Country of Publication: United States NLM ID: 101767986 Publication Model: Electronic Cited Medium: Internet NLM ISO Abbreviation: medRxiv Subsets: PubMed not MEDLINE
Academic Journal
Cuccurullo C; Epilepsy Center, Department of Neuroscience, Reproductive and Odontostomatological Sciences, Federico II University of Naples, Naples, Italy.; Neurology and Stroke Unit, Ospedale del Mare Hospital, Naples, Italy.; Cerulli Irelli E; Department of Human Neurosciences, Sapienza University of Rome, Rome, Italy.; Ugga L; Department of Advanced Biomedical Sciences, University Federico II, Naples, Italy.; Riva A; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.; Medical Genetic Unit, Istituti di Ricovero e Cura a Carattere Scientifico Istituto Giannina Gaslini, Genoa, Italy.; D'Amico A; Department of Radiology, 'Tortorella' private hospital, Salerno, Italy.; Cabet S; Pediatric and Fetal Imaging, Hôpital Femme-Mère-Enfant, Hospices Civils de Lyon, Lyon, France.; Lesca G; Service de Génétique, Hospices Civils de Lyon, Bron, France.; Institut NeuroMyoGene, CNRS UMR5310, INSERM U1217, Université Claude Bernard Lyon 1, Lyon, France.; Bilo L; Epilepsy Center, Department of Neuroscience, Reproductive and Odontostomatological Sciences, Federico II University of Naples, Naples, Italy.; Zara F; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.; Medical Genetic Unit, Istituti di Ricovero e Cura a Carattere Scientifico Istituto Giannina Gaslini, Genoa, Italy.; Iliescu C; Department of Clinical Neurosciences, 'Carol Davila' University of Medicine and Pharmacy, Bucharest, Romania.; Barca D; Department of Pediatric Neurology, Expertise Center for Rare Diseases in Pediatric Neurology, member of the EpiCARE European Reference Network, 'Prof. Dr. Alex. Obregia' Clinical Hospital, Bucharest, Romania.; Fung F; Department of Pediatrics and Neurology, Children's Hospital of Philadelphia and University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.; Helbig K; Department of Pediatrics and Neurology, Children's Hospital of Philadelphia and University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.; Ortiz-Gonzalez X; Department of Pediatrics and Neurology, Children's Hospital of Philadelphia and University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.; Schelhaas HJ; Department of Neurology, Epilepsy Center Kempenhaeghe, Heeze, the Netherlands.; Willemsen MH; Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.; van der Linden I; Department of Neurology, Epilepsy Center Kempenhaeghe, Heeze, the Netherlands.; Canafoglia L; Integrated Diagnostics for Epilepsy, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.; Courage C; Folkhälsan Research Center, Helsinki, Finland.; Department of Biomedical and Clinical Science, University of Milan, Milan, Italy.; Gommaraschi S; Department of Biomedical and Clinical Science, University of Milan, Milan, Italy.; Gonzalez-Alegre P; Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Pennsylvania, Philadelphia, USA.; Bardakjian T; Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Pennsylvania, Philadelphia, USA.; Syrbe S; Division of Paediatric Epileptology, Center for Pediatrics and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany.; Schuler E; Division of Paediatric Epileptology, Center for Pediatrics and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany.; Lemke JR; Center for Rare Diseases, University of Leipzig Medical Center, Leipzig, Germany.; Vari S; Pediatric Neurology and Muscular Diseases Unit, Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, 'G. Gaslini' Institute, University of Genoa, Genoa, Italy.; Roende G; Department of Pediatrics and Adolescent Medicine, University Hospital Rigshopitalet, Copenhagen, Denmark.; Bak M; Department of Clinical Genetics, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.; Huq M; Department of Pediatrics, Wayne State University, Detroit, Michigan, USA.; Powis Z; Ambry Genetics, Department of Emerging Genetic Medicine, CGC 15 Argonaut, Aliso Viejo, California, USA.; Johannesen KM; Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Center, Dianalund, Denmark.; Hammer TB; Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Center, Dianalund, Denmark.; Møller RS; Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Center, Dianalund, Denmark.; Rabin R; Clinical Genetic Services, Department of Pediatrics, NYU Grossman School of Medicine, New York, New York, USA.; Pappas J; Clinical Genetic Services, Department of Pediatrics, NYU Grossman School of Medicine, New York, New York, USA.; Zupanc ML; Children's Health of Orange County, Orange, California, USA.; Zadeh N; Genetics Center and Division of Medical Genetics, Children's Hospital of Orange County, Orange, California, USA.; Cohen J; Department of Neurology, Kennedy Krieger Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.; Naidu S; Department of Neurogenetics, Kennedy Krieger Institute, Baltimore, Maryland, USA.; Krey I; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Saneto R; Department of Neurology, Seattle Children's Hospital, University of Washington, Seattle, Washington, USA.; Department of Pediatrics, Seattle Children's Hospital, University of Washington, Seattle, Washington, USA.; Thies J; Seattle Children's Research Institute, University of Washington, Seattle, Washington, USA.; Licchetta L; IRCCS, Istituto Delle Scienze Neurologiche di Bologna, full member of the EpiCARE European Reference Network, Bologna, Italy.; Tinuper P; IRCCS, Istituto Delle Scienze Neurologiche di Bologna, full member of the EpiCARE European Reference Network, Bologna, Italy.; Bisulli F; IRCCS, Istituto Delle Scienze Neurologiche di Bologna, full member of the EpiCARE European Reference Network, Bologna, Italy.; Minardi R; Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.; Bayat A; Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Center, Dianalund, Denmark.; Department of Regional Health Research, University of Southern Denmark, Odense, Denmark.; Villeneuve N; Pediatric Neurology Department, Timone Children Hospital, Marseille, France.; Molinari F; Biolab, PolitoBIOMedLab, Department of Electronics and Telecommunications, Politecnico di Torino, Turin, Italy.; Salimi Dafsari H; Department of Pediatrics, Faculty of Medicine, University of Cologne and University Hospital Cologne, Cologne, Germany.; Center for Molecular Medicine Cologne, University of Cologne, Cologne, Germany.; Max Planck Institute for Biology of Ageing, Cologne, Germany.; Cologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases, University of Cologne, Cologne, Germany.; Department of Paediatric Neurology, Evelina's Children Hospital, Guy's & St. Thomas' Hospital NHS Foundation Trust, London, UK.; Randall Division of Cell and Molecular Biophysics, Muscle Signaling Section, King's College London, London, UK.; Moller B; Department of Pediatrics, Faculty of Medicine, University of Cologne and University Hospital Cologne, Cologne, Germany.; Center for Molecular Medicine Cologne, University of Cologne, Cologne, Germany.; Le Roux M; Department of Pediatric Neurology and Neurosurgery, CHU, Angers, France.; Houdayer C; Service de Génétique Médicale, Université d'Angers, CHU d'Angers, Inserm, CNRS, MITOVASC, SFR ICAT, Angers, France.; Vecchi M; University of Padua, Padua, Italy.; Mammi I; Medical Genetics Unit, Mirano Hospital, Venice, Italy.; Fiorini E; Child Neuropsychiatry Unit, University Hospital of Verona, full member of the EpiCARE European Reference Network, Verona, Italy.; Center for Research on Epilepsy in Pediatric Age, University Hospital of Verona, Verona, Italy.; Proietti J; Child Neuropsychiatry Unit, University Hospital of Verona, full member of the EpiCARE European Reference Network, Verona, Italy.; Center for Research on Epilepsy in Pediatric Age, University Hospital of Verona, Verona, Italy.; Ferri S; Child Neuropsychiatry Unit, University Hospital of Verona, full member of the EpiCARE European Reference Network, Verona, Italy.; Cantalupo G; Child Neuropsychiatry Unit, University Hospital of Verona, full member of the EpiCARE European Reference Network, Verona, Italy.; Center for Research on Epilepsy in Pediatric Age, University Hospital of Verona, Verona, Italy.; Innovation Biomedicine Section, Department of Engineering for Innovation Medicine, University of Verona, Verona, Italy.; Battaglia DI; Pediatric Neurology Unit, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.; Università Cattolica del Sacro Cuore, Rome, Italy.; Gambardella ML; Pediatric Neurology Unit, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.; Contaldo I; Pediatric Neurology Unit, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.; Brogna C; Pediatric Neurology Unit, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.; Neuropsychiatric Unit, ASL Avellino, Avellino, Italy.; Trivisano M; Neurology, Epilepsy, and Movement Disorders, Bambino Gesù Children's Hospital, IRCCS, full member of the EpiCARE European Reference Network, Rome, Italy.; De Dominicis A; Child Neurology Unit, Buzzi Children's Hospital, Milan, Italy.; Bova SM; Child Neurology Unit, Buzzi Children's Hospital, Milan, Italy.; Gardella E; Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Center, Dianalund, Denmark.; Striano P; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.; Pediatric Neurology and Muscular Diseases Unit, Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, 'G. Gaslini' Institute, University of Genoa, Genoa, Italy.; Coppola A; Epilepsy Center, Department of Neuroscience, Reproductive and Odontostomatological Sciences, Federico II University of Naples, Naples, 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
Berkhemer, Olvert AFransen, Puck SSBeumer, Debbievan den Berg, Lucie ALingsma, Hester FYoo, Albert JSchonewille, Wouter JVos, Jan AlbertNederkoorn, Paul JWermer, Marieke JHvan Walderveen, Marianne AAStaals, JulieHofmeijer, Jeannettevan Oostayen, Jacques A.Lycklama à Nijeholt, Geert J.Boiten, JelisBrouwer, Patrick A.Emmer, Bart J.de Bruijn, Sebastiaan F.van Dijk, Lukas C.Kappelle, JaapLo, Rob Hvan Dijk, Ewoud J.de Vries, Joostde Kort, Paul L.M.van Rooij, Willem Jan J.van den Berg, Jan S.P.van Hasselt, Boudewijn A.A.M.Aerden, Leo A.M.Dallinga, René J.Visser, Marieke C.Bot, Joseph C.J.Vroomen, Patrick C.Eshghi, OmidSchreuder, Tobien H.C.M.L.Heijboer, Roel J.J.Keizer, KoosTielbeek, Alexander V.den Hertog, Heleen M.Gerrits, Dick G.van den Berg-Vos, Renske M.Karas, Giorgos B.Steyerberg, Ewout W.Flach, ZwennekeMarquering, Henk A.Sprengers, Marieke E.S.Jenniskens, Sjoerd F.M.Beenen, Ludo F.M.van den Berg, RenéKoudstaal, Peter J.van Zwam, Wim H.Roos, Yvo B.W.E.M.van der Lugt, Aadvan Oostenbrugge, Robert J.Majoie, Charles B.L.M.Dippel, Diederik W.J.Brown, Martin M.Liebig, ThomasStijnen, TheoAndersson, TommyMattle, HeinrichWahlgren, Nilsvan der Heijden, EstherGhannouti, NazihaFleitour, NadineHooijenga, ImkePuppels, CorinaPellikaan, WilmaGeerling, AnnetLindl-Velema, Annemiekevan Vemde, Ginade Ridder, AnsGreebe, Pautde Bont-Stikkelbroeck, Joséde Meris, JokeJanssen, KirstenStruijk, WillyLicher, SilvanBoodt, NikkiRos, AdriaanVenema, EsmeeSlokkers, IlseGanpat, Raymie-JayceMulder, MaximSaiedie, NawidHeshmatollah, AlisSchipperen, StefanieVinken, Stefanvan Boxtel, TiemenKoets, JeroenBoers, MerelSantos, EmilieBorst, JordiJansen, IvoKappelhof, ManonLucas, MaritGeuskens, RalphBarros, Renan SalesDobbe, RoelandCsizmadia, MarloesHill, MDGoyal, MDemchuk, AMMenon, BKEesa, MRyckborst, KJWright, MRKamal, NRAndersen, LRandhawa, PAStewart, TPatil, SMinhas, PAlmekhlafi, MMishra, SClement, FSajobi, TShuaib, AMontanera, WJRoy, DSilver, FLJovin, TGFrei, DFSapkota, BRempel, JLThornton, 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GeorgesLapergue, BertrandBourdain, FrédéricEvrard, SergeGraveleau, PhilippeDecroix, Jean PierreWang, AdrienSellal, FrançoisAhle, GuidoCarelli, GabrielaDugay, Marie-HélèneGaultier, ClaudeLebedinsky, Ariel PabloLita, LaviniaMusacchio, Raul MarianoRenglewicz-Destuynder, CatherineTournade, AlainVuillemet, FrançisMontoro, Francisco MacianMounayer, CharbelFaugeras, FredericGimenez, LaetitiaLabach, CatherineLautrette, GéraldineDenier, ChristianSaliou, GuillaumeChassin, OlivierDussaule, ClaireMelki, ElsaOzanne, AugustinPuccinelli, FrancescoSachet, MarinaSarov, MarianaBonneville, Jean-FrançoisMoulin, ThierryBiondi, AlessandraDe Bustos Medeiros, ElisabethVuillier, FabriceCourtheoux, PatrickViader, FaustoApoil-Brissard, MarionBataille, MathieuBonnet, Anne-LaureCogez, JulienTouze, EmmanuelLeclerc, XavierLeys, DidierAggour, MohamedAguettaz, PierreBodenant, MarieCordonnier, CharlotteDeplanque, DominiqueGirot, MarieHenon, HildeKalsoum, ErwahLucas, ChristianPruvo, Jean-PierreZuniga, PaoloArquizan, CarolineCostalat, VincentMachi, PaoloMourand, IsabelleRiquelme, CarlosBounolleau, PierreArteaga, CharlesFaivre, AnthonyBintner, MarcTournebize, PatriceCharlin, CyrilDarcel, FrançoiseGauthier-Lasalarie, PascaleJeremenko, MarciaMouton, ServaneZerlauth, Jean-BaptisteLamy, ChantalHervé, DeramondHassan, HosseiniGaston, AndréBarral, Francis-GuyGarnier, PierreBeaujeux, RémyWolff, ValérieHerbreteau, DenisDebiais, SéverineMurray, AliciaFord, GaryMuir, Keith WWhite, PhilipBrown, Martin MClifton, AndyFreeman, JanetFord, IanMarkus, HughWardlaw, JoannaMolyneux, AndyRobinson, ThompsonLewis, SteffNorrie, JohnRobertson, FergusPerry, RichardDixit, AnandCloud, GeoffreyClifton, AndrewMadigan, JeremyRoffe, ChristineNayak, SanjeevLobotesis, KyriakosSmith, CraigHerwadkar, AmitKandasamy, NagaGoddard, TonyBamford, JohnSubramanian, GaneshLenthall, RobLittleton, EdwardLamin, SalStorey, KelleyGhatala, RitaBanaras, AzraAeron-Thomas, JohnHazel, BathMaguire, HollyVeraque, EmeldaHarrison, LouiseKeshvara, 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In The Lancet Neurology January 2018 17(1):47-53
Academic Journal
Hildonen M; Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, 2100, Copenhagen, Denmark.; Ciolfi A; Molecular Genetics and Functional Genomics, Bambino Gesù Children's Hospital, IRCCS, 00146, Rome, Italy.; Ferilli M; Molecular Genetics and Functional Genomics, Bambino Gesù Children's Hospital, IRCCS, 00146, Rome, Italy.; Cappelletti C; Molecular Genetics and Functional Genomics, Bambino Gesù Children's Hospital, IRCCS, 00146, Rome, Italy.; Al Alam C; Department of Pediatric Neurology, American center for Psychiatry and Neurology, Abu Dhabi, UAE.; Department of Pediatric Neurology, Haykel Hospital, El Koura, Lebanon.; Amor DJ; Department of Paediatrics, University of Melbourne, Murdoch Children's Research Institute, Melbourne, Australia.; Barakat TS; Deparment of Clinical Genetics, Erasmus MC, 3000CA, Rotterdam, The Netherlands.; ENCORE Expertise Center for Neurodevelopmental Disorders, Erasmus MC, University Medical Center, 3000CA, Rotterdam, Netherlands.; Benoit V; IPG, Centre for Human Genetics, Charleroi, Belgium.; Birk OS; Genetics Institute, Soroka University Medical Center, Beer-Sheva, Israel.; Callewaert B; Center for Medical Genetics, Ghent University Hospital, 9000, Ghent, Belgium.; Department of Biomolecular Medicine, Ghent University, 9000, Ghent, Belgium.; Cazurro-Gutiérrez A; Paediatric Neurology Research Group, Vall d'Hebron Institut de Recerca, 08035, Barcelona, Spain.; Universitat Autònoma de Barcelona, 08193, Barcelona, Spain.; De Wachter M; Department of Child Neurology, Antwerp University Hospital, University of Antwerp, Edegem, Belgium.; Doco-Fenzy M; SFR CAP SANTE, Service de génétique CHU Reims, 51092, Reims, France.; CHU de Nantes, service de génétique médicale, 44000, Nantes, France.; Gómez-Puertas P; Molecular Modeling Group, Centro de Biología Molecular Severo Ochoa, CBMSO (CSIC-UAM), E-28049, Madrid, Spain.; Hammer TB; Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, 2100, Copenhagen, Denmark.; Department of Epilepsy Genetics and Personalized Treatment, Danish Epilepsy Centre, Dianalund, Denmark.; Jamra RA; Institute of Human Genetics, University of Leipzig Medical Center Leipzig, 04103, Leipzig, Germany.; Kaiyrzhanov R; Department of Neuromuscular Disorders, University College London Institute of Neurology, WC1N 3BG, London, UK.; Kameyama S; Department of Human Genetics, Yokohama City University Graduate School of Medicine, 236-0004, Yokohama, Japan.; Keren B; Department of Medical Genetics, Pitié-Salpêtrière Hospital, AP-HP.Sorbonne Université, 75013, Paris, France.; Kresge C; Rutgers New Jersey Medical School, Newark, NJ, USA.; Krey I; Institute of Human Genetics, University of Leipzig Medical Center Leipzig, 04103, Leipzig, Germany.; Lederer D; IPG, Centre for Human Genetics, Charleroi, Belgium.; Marcos-Alcalde I; Molecular Modeling Group, Centro de Biología Molecular Severo Ochoa, CBMSO (CSIC-UAM), E-28049, Madrid, Spain.; Maroofian R; Department of Neuromuscular Disorders, University College London Institute of Neurology, WC1N 3BG, London, UK.; Matsumoto N; Department of Human Genetics, Yokohama City University Graduate School of Medicine, 236-0004, Yokohama, Japan.; Mizuguchi T; Department of Human Genetics, Yokohama City University Graduate School of Medicine, 236-0004, Yokohama, Japan.; Moey LH; Department of Clinical Genetics, Penang Hospital, 10450, Georgetown, Malaysia.; Morgan A; Speech and Language, Murdoch Children's Research Institute, 3052, Melbourne, Australia.; Department of Audiology and Speech Pathology, 3052, Melbourne, Australia.; Munell F; Paediatric Neurology Research Group, Vall d'Hebron Institut de Recerca, 08035, Barcelona, Spain.; Universitat Autònoma de Barcelona, 08193, Barcelona, Spain.; Platzer K; Institute of Human Genetics, University of Leipzig Medical Center Leipzig, 04103, Leipzig, Germany.; Pletcher BA; Rutgers New Jersey Medical School, Newark, NJ, USA.; Ros-Pardo D; Molecular Modeling Group, Centro de Biología Molecular Severo Ochoa, CBMSO (CSIC-UAM), E-28049, Madrid, Spain.; Rumping L; Department of Medical Genetics, Antwerp University Hospital, University of Antwerp, 2650, Edegem, Belgium.; Szakszon K; University of Debrecen, Faculty of Medicine, Clinical Center, Institute of Paediatrics, 4032, Debrecen, Hungary.; Van Schil K; Department of Medical Genetics, Antwerp University Hospital, University of Antwerp, 2650, Edegem, Belgium.; Verdura E; Paediatric Neurology Research Group, Vall d'Hebron Institut de Recerca, 08035, Barcelona, Spain.; Vogt J; West Midlands Regional Genetics Service, Birmingham Women's and Children's Hospital, B15 2TG, Birmingham, UK.; Wassmer E; Neurology, Birmingham Women's and Children's Hospital, B4 6 NH, Birmingham, UK.; Institute of Health and Neurodevelopment, Aston University, B4 7ET, Birmingham, UK.; Zamani M; Center for Genomics and Systems Biology, Department of Biology, New York University, New York, NY, 10003, USA.; Narges Medical Genetics and Prenatal Diagnosis Laboratory, Kianpars, Ahvaz, Iran.; Tümer Z; Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, 2100, Copenhagen, Denmark. Zeynep.tumer@regionh.dk.; Department of Clinical Medicine, Faculty of Medicine and Health Sciences, University of Copenhagen, 2100, Copenhagen, Denmark. Zeynep.tumer@regionh.dk.; Tartaglia M; Molecular Genetics and Functional Genomics, Bambino Gesù Children's Hospital, IRCCS, 00146, Rome, Italy. marco.tartaglia@opbg.net.
Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE
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