학술논문


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'학술논문' 에서 검색결과 878건 | 목록 1~20
Academic Journal
Auvin S; Service de Neurologie Pédiatrique, Hôpital Robert Debré, Paris, France.; Serraz B; Biocodex, Gentilly, France.; Lespinasse J; eXYSTAT, Malakoff, France.; Chancharme L; Biocodex Research Center, Compiègne, France.
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
Martin-Brevet, SandraRodríguez-Herreros, BorjaNielsen, Jared A.Moreau, ClaraModenato, ClaudiaMaillard, Anne M.Pain, AurélieRichetin, SoniaJønch, Aia E.Qureshi, Abid Y.Zürcher, Nicole R.Conus, PhilippeAddor, Marie ClaudeAndrieux, JorisArveiler, BenoîtBaujat, GenevièveSloan-Béna, FrédériqueBelfiore, MarcoBonneau, DominiqueBouquillon, SoniaBoute, OdileBrusco, AlfredoBusa, TiffanyCaberg, Jean HubertCampion, DominiqueColombert, VanessaCordier, Marie PierreDavid, AlbertDebray, François GuillaumeDelrue, Marie AngeDoco-Fenzy, MartineDunkhase-Heinl, UlrikeEdery, PatrickFagerberg, ChristinaFaivre, LaurenceForzano, FrancescaGenevieve, DavidGérard, MarionGiachino, DanielaGuichet, AgnèsGuillin, OlivierHéron, DelphineIsidor, BertrandJacquette, AuréliaJaillard, SylvieJournel, HubertKeren, BorisLacombe, DidierLebon, SébastienLe Caignec, CédricLemaître, Marie PierreLespinasse, JamesMathieu-Dramart, MichèleMercier, SandraMignot, CyrilMissirian, ChantalPetit, FlorencePilekær Sørensen, KristinaPinson, LucilePlessis, GhislainePrieur, FabienneRooryck-Thambo, CarolineRossi, MassimilianoSanlaville, DamienSchlott Kristiansen, BrittaSchluth-Bolard, CarolineTill, MarianneVan Haelst, MiekeVan Maldergem, LionelAlupay, HanaloreAaronson, BenjaminAckerman, SeanAnkenman, KatyAnwar, AyeshaAtwell, ConstanceBowe, AlexandraBeaudet, Arthur L.Benedetti, MartaBerg, JessicaBerman, JeffreyBerry, Leandra N.Bibb, Audrey L.Blaskey, LisaBrennan, JonathanBrewton, Christie M.Buckner, Randy L.Bukshpun, PolinaBurko, JordanCali, PhilCerban, BettinaChang, YishinCheong, MaxwellChow, VivianChu, ZiliChudnovskaya, DarinaCornew, LaurenDale, CorbyDell, JohnDempsey, Allison G.Deschamps, TrentEarl, RachelEdgar, JamesElgin, JennaOlson, Jennifer EndreEvans, Yolanda L.Findlay, AnneFischbach, Gerald D.Fisk, CharlieFregeau, BrieanaGaetz, BillGaetz, LeahGarza, SilviaGerdts, JenniferGlenn, OritGobuty, Sarah E.Golembski, RachelGreenup, MarionHeiken, KoryHines, KatherineHinkley, LeightonJackson, Frank I.Jenkins, JulianJeremy, Rita J.Johnson, KellyKanne, Stephen M.Kessler, SudhaKhan, Sarah Y.Ku, MatthewKuschner, EmilyLaakman, Anna L.Lam, PeterLasala, Morgan W.Lee, HanaLaGuerre, KevinLevy, SusanCavanagh, Alyss LianLlorens, Ashlie V.Campe, Katherine LoftusLuks, Tracy L.Marco, Elysa J.Martin, StephenMartin, Alastair J.Marzano, GabrielaMasson, ChristinaMcGovern, Kathleen E.McNally Keehn, RebeccaMiller, David T.Miller, Fiona K.Moss, Timothy J.Murray, RebeccaNagarajan, Srikantan S.Nowell, Kerri P.Owen, JuliaPaal, Andrea M.Packer, AlanPage, Patricia Z.Paul, Brianna M.Peters, AlanaPeterson, DanicaPoduri, AnnapurnaPojman, Nicholas J.Porche, KenProud, Monica B.Qasmieh, SabaRamocki, Melissa B.Reilly, BeauRoberts, Timothy P.L.Shaw, DennisSinha, TuhinSmith-Packard, BethannyGallagher, Anne SnowSwarnakar, VivekThieu, TonyTriantafallou, ChristinaVaughan, RogerWakahiro, MariWallace, ArianneWard, TraceyWenegrat, JuliaWolken, AnneChung, Wendy K.Sherr, Elliott H.Spiro, John E.Kherif, FerathBeckmann, Jacques S.Hadjikhani, NouchineReymond, AlexandreDraganski, BogdanJacquemont, Sébastien
Simons Variation in Individuals Project (VIP) Consortium & 16p11.2 European Consortium 2018, 'Quantifying the Effects of 16p11.2 Copy Number Variants on Brain Structure : A Multisite Genetic-First Study', Biological Psychiatry, vol. 84, no. 4, pp. 253-264. https://doi.org/10.1016/j.biopsych.2018.02.1176
Biological Psychiatry
Biological psychiatry, vol. 84, no. 4, pp. 253-264
16p11.2 European Consortium 2018, ' Quantifying the Effects of 16p11.2 Copy Number Variants on Brain Structure : A Multisite Genetic-First Study ', Biological Psychiatry, vol. 84, no. 4, pp. 253-264 . https://doi.org/10.1016/j.biopsych.2018.02.1176
Report
LHCb collaborationAaij, R.Adeva, B.Adinolfi, M.Affolder, A.Ajaltouni, Z.Akar, S.Albrecht, J.Alessio, F.Alexander, M.Ali, S.Alkhazov, G.Cartelle, P. AlvarezAlves Jr, A. A.Amato, S.Amerio, S.Amhis, Y.An, L.Anderlini, L.Anderson, J.Andreassen, R.Andreotti, M.Andrews, J. E.Appleby, R. B.Gutierrez, O. AquinesArchilli, F.Artamonov, A.Artuso, M.Aslanides, E.Auriemma, G.Baalouch, M.Bachmann, S.Back, J. J.Badalov, A.Baesso, C.Baldini, W.Barlow, R. J.Barschel, C.Barsuk, S.Barter, W.Batozskaya, V.Battista, V.Bay, A.Beaucourt, L.Beddow, J.Bedeschi, F.Bediaga, I.Belogurov, S.Belous, K.Belyaev, I.Ben-Haim, E.Bencivenni, G.Benson, S.Benton, J.Berezhnoy, A.Bernet, R.Bettler, M. -O.van Beuzekom, M.Bien, A.Bifani, S.Bird, T.Bizzeti, A.Bjørnstad, P. M.Blake, T.Blanc, F.Blouw, J.Blusk, S.Bocci, V.Bondar, A.Bondar, N.Bonivento, W.Borghi, S.Borgia, A.Borsato, M.Bowcock, T. J. V.Bowen, E.Bozzi, C.Brambach, T.Brand, J. van denBressieux, J.Brett, D.Britsch, M.Britton, T.Brodzicka, J.Brook, N. H.Brown, H.Bursche, A.Busetto, G.Buytaert, J.Cadeddu, S.Calabrese, R.Calvi, M.Gomez, M. CalvoCampana, P.Perez, D. CamporaCarbone, A.Carboni, G.Cardinale, R.Cardini, A.Carson, L.Akiba, K. CarvalhoCasse, G.Cassina, L.Garcia, L. CastilloCattaneo, M.Cauet, Ch.Cenci, R.Charles, M.Charpentier, Ph.Chefdeville, M.Chen, S.Cheung, S. -F.Chiapolini, N.Chrzaszcz, M.Ciba, K.Vidal, X. CidCiezarek, G.Clarke, P. E. L.Clemencic, M.Cliff, H. V.Closier, J.Coco, V.Cogan, J.Cogneras, E.Cojocariu, L.Collins, P.Comerma-Montells, A.Contu, A.Cook, A.Coombes, M.Coquereau, S.Corti, G.Corvo, M.Counts, I.Couturier, B.Cowan, G. A.Craik, D. C.Torres, M. CruzCunliffe, S.Currie, R.D'Ambrosio, C.Dalseno, J.David, P.David, P. N. Y.Davis, A.De Bruyn, K.De Capua, S.De Cian, M.De Miranda, J. M.De Paula, L.De Silva, W.De Simone, P.Decamp, D.Deckenhoff, M.Del Buono, L.Déléage, N.Derkach, D.Deschamps, O.Dettori, F.Di Canto, A.Dijkstra, H.Donleavy, S.Dordei, F.Dorigo, M.Suárez, A. DosilDossett, D.Dovbnya, A.Dreimanis, K.Dujany, G.Dupertuis, F.Durante, P.Dzhelyadin, R.Dziurda, A.Dzyuba, A.Easo, S.Egede, U.Egorychev, V.Eidelman, S.Eisenhardt, S.Eitschberger, U.Ekelhof, R.Eklund, L.Rifai, I. ElElsasser, Ch.Ely, S.Esen, S.Evans, H. -M.Evans, T.Falabella, A.Färber, C.Farinelli, C.Farley, N.Farry, S.Fay, RFFerguson, D.Albor, V. FernandezRodrigues, F. FerreiraFerro-Luzzi, M.Filippov, S.Fiore, M.Fiorini, M.Firlej, M.Fitzpatrick, C.Fiutowski, T.Fontana, M.Fontanelli, F.Forty, R.Francisco, O.Frank, M.Frei, C.Frosini, M.Fu, J.Furfaro, E.Torreira, A. GallasGalli, D.Gallorini, S.Gambetta, S.Gandelman, M.Gandini, P.Gao, Y.Pardiñas, J. GarcíaGarofoli, J.Tico, J. GarraGarrido, L.Gaspar, C.Gauld, R.Gavardi, L.Gavrilov, G.Geraci, A.Gersabeck, E.Gersabeck, M.Gershon, T.Ghez, Ph.Gianelle, A.Gianì, S.Gibson, V.Giubega, L.Gligorov, V. V.Göbel, C.Golubkov, D.Golutvin, A.Gomes, A.Gotti, C.Gándara, M. GrabalosaDiaz, R. GracianiCardoso, L. A. GranadoGraugés, E.Graziani, G.Grecu, A.Greening, E.Gregson, S.Griffith, P.Grillo, L.Grünberg, O.Gui, B.Gushchin, E.Guz, Yu.Gys, T.Hadjivasiliou, C.Haefeli, G.Haen, C.Haines, S. C.Hall, S.Hamilton, B.Hampson, T.Han, X.Hansmann-Menzemer, S.Harnew, N.Harnew, S. T.Harrison, J.He, J.Head, T.Heijne, V.Hennessy, K.Henrard, P.Henry, L.Morata, J. A. Hernandovan Herwijnen, E.Heß, M.Hicheur, A.Hill, D.Hoballah, M.Hombach, C.Hulsbergen, W.Hunt, P.Hussain, N.Hutchcroft, D.Hynds, D.Idzik, M.Ilten, P.Jacobsson, R.Jaeger, A.Jalocha, J.Jans, E.Jaton, P.Jawahery, A.Jing, F.John, M.Johnson, D.Jones, C. R.Joram, C.Jost, B.Jurik, N.Kandybei, S.Kanso, W.Karacson, M.Karbach, T. M.Karodia, S.Kelsey, M.Kenyon, I. R.Ketel, T.Khanji, B.Khurewathanakul, C.Klaver, S.Klimaszewski, K.Kochebina, O.Kolpin, M.Komarov, I.Koopman, R. F.Koppenburg, P.Korolev, M.Kozlinskiy, A.Kravchuk, L.Kreplin, K.Kreps, M.Krocker, G.Krokovny, P.Kruse, F.Kucewicz, W.Kucharczyk, M.Kudryavtsev, V.Kurek, K.Kvaratskheliya, T.La Thi, V. N.Lacarrere, D.Lafferty, G.Lai, A.Lambert, D.Lambert, R. W.Lanfranchi, G.Langenbruch, C.Langhans, B.Latham, T.Lazzeroni, C.Gac, R. Levan Leerdam, J.Lees, J. -P.Lefèvre, R.Leflat, A.Lefrançois, J.Leo, S.Leroy, O.Lesiak, T.Lespinasse, M.Leverington, B.Li, Y.Likhomanenko, T.Liles, M.Lindner, R.Linn, C.Lionetto, F.Liu, B.Lohn, S.Longstaff, I.Lopes, J. H.Lopez-March, N.Lowdon, P.Lu, H.Lucchesi, D.Luo, H.Lupato, A.Luppi, E.Lupton, O.Machefert, F.Machikhiliyan, I. V.Maciuc, F.Maev, O.Malde, S.Malinin, A.Manca, G.Mancinelli, G.Mapelli, A.Maratas, J.Marchand, J. F.Marconi, U.Benito, C. MarinMarino, P.Märki, R.Marks, J.Martellotti, G.Martens, A.Sánchez, A. MartínMartinelli, M.Santos, D. MartinezVidal, F. MartinezTostes, D. MartinsMassafferri, A.Matev, R.Mathe, Z.Matteuzzi, C.Mazurov, A.McCann, M.McCarthy, J.McNab, A.McNulty, R.McSkelly, B.Meadows, B.Meier, F.Meissner, M.Merk, M.Milanes, D. A.Minard, M. -N.Moggi, N.Rodriguez, J. MolinaMonteil, S.Morandin, M.Morawski, P.Mordà, A.Morello, M. J.Moron, J.Morris, A. -B.Mountain, R.Muheim, F.Müller, K.Mussini, M.Muster, B.Naik, P.Nakada, T.Nandakumar, R.Nasteva, I.Needham, M.Neri, N.Neubert, S.Neufeld, N.Neuner, M.Nguyen, A. D.Nguyen, T. D.Nguyen-Mau, C.Nicol, M.Niess, V.Niet, R.Nikitin, N.Nikodem, T.Novoselov, A.O'Hanlon, D. P.Oblakowska-Mucha, A.Obraztsov, V.Oggero, S.Ogilvy, S.Okhrimenko, O.Oldeman, R.Onderwater, C. J. G.Orlandea, M.Goicochea, J. M. OtaloraOwen, P.Oyanguren, A.Pal, B. K.Palano, A.Palombo, F.Palutan, M.Panman, J.Papanestis, A.Pappagallo, M.Pappalardo, L. L.Parkes, C.Parkinson, C. J.Passaleva, G.Patel, G. D.Patel, M.Patrignani, C.Pearce, A.Pellegrino, A.Altarelli, M. PepePerazzini, S.Perret, P.Perrin-Terrin, M.Pescatore, L.Pesen, E.Petridis, K.Petrolini, A.Olloqui, E. PicatostePietrzyk, B.Pilař, T.Pinci, D.Pistone, A.Playfer, S.Casasus, M. PloPolci, F.Poluektov, A.Polycarpo, E.Popov, A.Popov, D.Popovici, B.Potterat, C.Price, E.Prisciandaro, J.Pritchard, A.Prouve, C.Pugatch, V.Navarro, A. PuigPunzi, G.Qian, W.Rachwal, B.Rademacker, J. H.Rakotomiaramanana, B.Rama, M.Rangel, M. S.Raniuk, I.Rauschmayr, N.Raven, G.Reichert, S.Reid, M. M.Reis, A. C. dosRicciardi, S.Richards, S.Rihl, M.Rinnert, K.Molina, V. RivesRomero, D. A. RoaRobbe, P.Rodrigues, A. B.Rodrigues, E.Perez, P. RodriguezRoiser, S.Romanovsky, V.Vidal, A. RomeroRotondo, M.Rouvinet, J.Ruf, T.Ruiz, H.Valls, P. RuizSilva, J. J. SaboridoSagidova, N.Sail, P.Saitta, B.Guimaraes, V. SalustinoMayordomo, C. SanchezSedes, B. SanmartinSantacesaria, R.Rios, C. SantamarinaSantovetti, E.Sarti, A.Satriano, C.Satta, A.Saunders, D. M.Savrina, D.Schiller, M.Schindler, H.Schlupp, M.Schmelling, M.Schmidt, B.Schneider, O.Schopper, A.Schune, M. -H.Schwemmer, R.Sciascia, B.Sciubba, A.Semennikov, A.Sepp, I.Serra, N.Serrano, J.Sestini, L.Seyfert, P.Shapkin, M.Shapoval, I.Shcheglov, Y.Shears, T.Shekhtman, L.Shevchenko, V.Shires, A.Coutinho, R. SilvaSimi, G.Sirendi, M.Skidmore, N.Skwarnicki, T.Smith, N. A.Smith, E.Smith, J.Smith, M.Snoek, H.Sokoloff, M. D.Soler, F. J. P.Soomro, F.Souza, D.De Paula, B. SouzaSpaan, B.Sparkes, A.Spradlin, P.Sridharan, S.Stagni, F.Stahl, M.Stahl, S.Steinkamp, O.Stenyakin, O.Stevenson, S.Stoica, S.Stone, S.Storaci, B.Stracka, S.Straticiuc, M.Straumann, U.Stroili, R.Subbiah, V. K.Sun, L.Sutcliffe, W.Swientek, K.Swientek, S.Syropoulos, V.Szczekowski, M.Szczypka, P.Szumlak, T.T'Jampens, S.Teklishyn, M.Tellarini, G.Teubert, F.Thomas, C.Thomas, E.van Tilburg, J.Tisserand, V.Tobin, M.Tolk, S.Tomassetti, L.Tonelli, D.Topp-Joergensen, S.Torr, N.Tournefier, E.Tourneur, S.Tran, M. T.Tresch, M.Trisovic, A.Tsaregorodtsev, A.Tsopelas, P.Tuning, N.Garcia, M. UbedaUkleja, A.Ustyuzhanin, A.Uwer, U.Vagnoni, V.Valenti, G.Vallier, A.Gomez, R. VazquezRegueiro, P. VazquezSierra, C. VázquezVecchi, S.Velthuis, J. J.Veltri, M.Veneziano, G.Vesterinen, M.Viaud, B.Vieira, D.Diaz, M. VieitesVilasis-Cardona, X.Vollhardt, A.Volyanskyy, D.Voong, D.Vorobyev, A.Vorobyev, V.Voß, C.de Vries, J. A.Waldi, R.Wallace, C.Wallace, R.Walsh, J.Wandernoth, S.Wang, J.Ward, D. R.Watson, N. K.Websdale, D.Whitehead, M.Wicht, J.Wiedner, D.Wilkinson, G.Williams, M. P.Williams, M.Wilson, F. F.Wimberley, J.Wishahi, J.Wislicki, W.Witek, M.Wormser, G.Wotton, S. A.Wright, S.Wu, S.Wyllie, K.Xie, Y.Xing, Z.Xu, Z.Yang, Z.Yuan, X.Yushchenko, O.Zangoli, M.Zavertyaev, M.Zhang, L.Zhang, W. C.Zhang, Y.Zhelezov, A.Zhokhov, A.Zhong, L.Zvyagin, A.
JHEP 10(2014)088
Academic Journal
Modenato, C.Kumar, K.Moreau, C.Martin-Brevet, S.Huguet, G.Schramm, C.Jean-Louis, M.Martin, C.-O.Younis, N.Tamer, P.Douard, E.Thébault-Dagher, F.Côté, V.Charlebois, A.-R.Deguire, F.Maillard, A.M.Rodriguez-Herreros, B.Pain, A.Richetin, S.Addor, M.-C.Andrieux, J.Arveiler, B.Baujat, G.Sloan-Béna, F.Belfiore, M.Bonneau, D.Bouquillon, S.Boute, O.Brusco, A.Busa, T.CABERG, Jean-HubertCampion, D.Colombert, V.Cordier, M.-P.David, A.Debray, François-GuillaumeDelrue, M.-A.Doco-Fenzy, M.Dunkhase-Heinl, U.Edery, P.Fagerberg, C.Faivre, L.Forzano, F.Genevieve, D.Gérard, M.Giachino, D.Guichet, A.Guillin, O.Héron, D.Isidor, B.Jacquette, A.Jaillard, S.Journel, H.Keren, B.Lacombe, D.Lebon, S.Le Caignec, C.Lemaître, M.-P.Lespinasse, J.Mathieu-Dramart, M.Mercier, S.Mignot, C.Missirian, C.Petit, F.Pilekær Sørensen, K.Pinson, L.Plessis, G.Prieur, F.Raymond, A.Rooryck-Thambo, C.Rossi, M.Sanlaville, D.Schlott Kristiansen, B.Schluth-Bolard, C.Till, M.Van Haelst, M.Van Maldergem, L.Alupay, H.Aaronson, B.Ackerman, S.Ankenman, K.Anwar, A.Atwell, C.Bowe, A.Beaudet, A.L.Benedetti, M.Berg, J.Berman, J.Berry, L.N.Bibb, A.L.Blaskey, L.Brennan, J.Brewton, C.M.Buckner, R.Bukshpun, P.Burko, J.Cali, P.Cerban, B.Chang, Y.Cheong, M.Chow, V.Chu, Z.Chudnovskaya, D.Cornew, L.Dale, C.Dell, J.Dempsey, A.G.Deschamps, T.Earl, R.Edgar, J.Elgin, J.Olson, J.E.Evans, Y.L.Findlay, A.Fischbach, G.D.Fisk, C.Fregeau, B.Gaetz, B.Gaetz, L.Garza, S.Gerdts, J.Glenn, O.Gobuty, S.E.Golembski, R.Greenup, M.Heiken, K.Hines, K.Hinkley, L.Jackson, F.I.Jenkins, J.Jeremy, R.J.Johnson, K.Kanne, S.M.Kessler, S.Khan, S.Y.Ku, M.Kuschner, E.Laakman, A.L.Lam, P.Lasala, M.W.Lee, H.LaGuerre, K.Levy, S.Cavanagh, A.L.Llorens, A.V.Campe, K.L.Luks, T.L.Marco, E.J.Martin, S.Martin, A.J.Marzano, G.Masson, C.McGovern, K.E.Keehn, R.M.N.Miller, D.T.Miller, F.K.Moss, T.J.Murray, R.Nagarajan, S.S.Nowell, K.P.Owen, J.Paal, A.M.Packer, A.Page, P.Z.Paul, B.M.Peters, A.Peterson, D.Poduri, A.Pojman, N.J.Porche, K.Proud, M.B.Qasmieh, S.Ramocki, M.B.Reilly, B.Roberts, T.P.L.Shaw, D.Sinha, T.Smith-Packard, B.Gallagher, A.S.Swarnakar, V.Thieu, T.Triantafallou, C.Vaughan, R.Wakahiro, M.Wallace, A.Ward, T.Wenegrat, J.Wolken, A.Melie-Garcia, L.Kushan, L.Silva, A.I.van den Bree, M.B.M.Linden, D.E.J.Owen, M.J.Hall, J.Lippé, S.Chakravarty, M.Bzdok, D.Montreal Neurological Institute, McGill UniversityBearden, C.E.Draganski, B.Jacquemont, S.16p11.2 European ConsortiumSimons Searchlight Consortium
Transl Psychiatry
Translational Psychiatry, Vol 11, Iss 1, Pp 1-10 (2021)
16p11.2 European Consortium & Simons Searchlight Consortium 2021, 'Effects of eight neuropsychiatric copy number variants on human brain structure', Translational Psychiatry, vol. 11, no. 1, 399. https://doi.org/10.1038/s41398-021-01490-9
Translational Psychiatry
Translational psychiatry, vol. 11, no. 1, pp. 399
Modenato, C, Kumar, K, Moreau, C, Martin-Brevet, S, Huguet, G, Schramm, C, Jean-Louis, M, Martin, C O, Younis, N, Tamer, P, Douard, E, Thébault-Dagher, F, Côté, V, Charlebois, A R, Deguire, F, Maillard, A M, Rodriguez-Herreros, B, Pain, A, Richetin, S, 16p11.2 European Consortium, Simons Searchlight Consortium, Melie-Garcia, L, Kushan, L, Silva, A I, van den Bree, M B M, Linden, D E J, Owen, M J, Hall, J, Lippé, S, Chakravarty, M, Bzdok, D, Bearden, C E, Draganski, B, Jacquemont, S, Dunkhase-Heinl, U, Fagerberg, C, Pilekær Sørensen, K & Schlott Kristiansen, B 2021, ' Effects of eight neuropsychiatric copy number variants on human brain structure ', Translational Psychiatry, vol. 11, no. 1, 399 . https://doi.org/10.1038/s41398-021-01490-9
Translational Psychiatry, vol 11, iss 1
Academic Journal
Heiblig M; Hematology Department, Centre Hospitalier Lyon Sud, Pierre-Bénite, France.; Gourguechon C; Department of Hematology, Amiens University Hospital, Amiens, France.; Guilpain P; CEREMAST, the Department of Internal Medicine-Multi-organ Diseases, Saint-Eloi University Hospital, Montpellier University, Montpellier, France.; Bulai-Livideanu C; CEREMAST Toulouse, Dermatology Departmen, CHU de Toulouse, Toulouse, France.; Barete S; Sorbonne Université, APHP, Unité Fonctionnelle de Dermatologie, Groupe Hospitalier Pitié-Salpêtrière-C. Foix, Paris, France.; French Reference Center for Mastocytosis (CEREMAST), Necker-Enfants Malades University Hospital, APHP, Paris, France.; Chantran Y; Department of Biological Hematology, Pitié-Salpêtrière Hospital, DMU BioGem, AP-HP, Sorbonne University, Paris, France.; Department of Biological Immunology, Saint-Antoine Hospital, DMU BioGem, AP-HP, Sorbonne University, Paris, France.; Health Environmental Risk Assessment (HERA) Team, Centre of Research in Epidemiology and Statistics (CRESS), Inserm/INRAE, Faculty of Pharmacy, Université de Paris, Paris, France.; Agopian J; Association Française pour les Initiatives de Recherche sur le Mastocyte et les Mastocytoses (AFIRMM), Paris, France.; Brenet F; Centre de Recherche en Cancérologie de Marseille (CRCM) INSERM U1068, CNRS UMR7258, AMU U105, Département d'Onco-Hématologie-Immunologie, Institut Paoli-Calmettes, Marseille, France.; Dubreuil P; Centre de Recherche en Cancérologie de Marseille (CRCM) INSERM U1068, CNRS UMR7258, AMU U105, Département d'Onco-Hématologie-Immunologie, Institut Paoli-Calmettes, Marseille, France.; Lespinasse J; eXYSTAT, Malakoff, France.; Lemal R; Adult Clinical Hematology, Clermont-Ferrand University Hospital, INSERM CIC501, EA 7453-Université Clermont Auvergne, Clermont-Ferrand, France.; Tournilhac O; Adult Clinical Hematology, Clermont-Ferrand University Hospital, INSERM CIC501, EA 7453-Université Clermont Auvergne, Clermont-Ferrand, France.; Terriou L; INSERM, CHU Lille, Department of Internal Medicine and Clinical Immunology, U1286 - INFINITE - Institute for Translational Research in Inflammation, University Lille, Lille, France.; Launay D; INSERM, CHU Lille, Service de Médecine Interne et Immunologie Clinique, Centre de référence des maladies autoimmunes systémiques rares du Nord et Nord-Ouest de France (CeRAINO), U1286 - INFINITE - Institute for Translational Research in Inflammation, University Lille, Lille, France.; Bouillet L; Internal Medicine Department, Grenoble Alpes University Hospital, Univ. Grenoble Alpes, T-RAIG unit, CNRS, UMR 5525, VetAgro Sup, Grenoble INP, CHU Grenoble Alpes, TIMC, Grenoble, France.; Chatain C; Internal Medicine Department, Grenoble Alpes University Hospital, Univ. Grenoble Alpes, T-RAIG unit, CNRS, UMR 5525, VetAgro Sup, Grenoble INP, CHU Grenoble Alpes, TIMC, Grenoble, France.; Damaj G; Haematology Institute, Normandy University School of Medicine, Caen, France.; Ballul T; French Reference Center for Mastocytosis (CEREMAST), Necker-Enfants Malades University Hospital, APHP, Paris, France.; Imagine Institute, INSERM U1163, Necker-Enfants Malades University Hospital, Paris University, Paris, France.; Greco C; CEREMAST, the Department of Pain and Palliative Care Unit, Necker-Children's Hospital, AP-HP, Paris Centre University, Paris, France.; Polivka L; Haematology Institute, Normandy University School of Medicine, Caen, France.; Department of Dermatology, Reference Center for Genodermatoses (MAGEC), Necker Hospital for Sick Children, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris Cité University, Paris, France.; CEREMAST, the Department of Hematology, Necker-Children's Hospital, AP-HP, Paris Centre University, Paris, France.; Frenzel L; French Reference Center for Mastocytosis (CEREMAST), Necker-Enfants Malades University Hospital, APHP, Paris, France.; Imagine Institute, INSERM U1163, Necker-Enfants Malades University Hospital, Paris University, Paris, France.; Meni C; French Reference Center for Mastocytosis (CEREMAST), Necker-Enfants Malades University Hospital, APHP, Paris, France.; Bouktit H; French Reference Center for Mastocytosis (CEREMAST), Necker-Enfants Malades University Hospital, APHP, Paris, France.; Benabou D; French Reference Center for Mastocytosis (CEREMAST), Necker-Enfants Malades University Hospital, APHP, Paris, France.; Gaudy-Marqueste C; Dermatology and Skin Cancer, Department, Aix-Marseille University, APHM, Marseille, France.; Gousseff M; Department of Internal Medicine, Bretagne Atlantique Hospital, Vannes, France.; Le Mouel E; Department of Internal Medicine and Clinical Immunology, Rennes University Hospital, Rennes, France.; Neel A; CEREMAST, the Department of Internal Medicine, Hôtel-Dieu University Hospital, Nantes, France.; Ranta D; Department of Haematology, Nancy University Hospital, Nancy, France.; Jaussaud R; Department of Internal Medicine and Clinical Immunology, Vandoeuvre-lès-Nancy, France.; Molina TJ; Department of pathology, Necker-Children's Hospital, AP-HP, Paris Centre University, Paris, France.; Bruneau J; Imagine Institute, INSERM U1163, Necker-Enfants Malades University Hospital, Paris University, Paris, France.; Department of pathology, Necker-Children's Hospital, AP-HP, Paris Centre University, Paris, France.; Villarese P; Laboratory of Onco-Hematology, Necker Children's Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.; Lhermitte L; Laboratory of Onco-Hematology, Necker Children's Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.; CNRS, INSERM U1151, Institut Necker Enfants Malades (INEM), Université Paris Cité, Paris, France.; Maouche-Chrétien L; Imagine Institute, INSERM U1163, Necker-Enfants Malades University Hospital, Paris University, Paris, France.; Temple M; Hematology Laboratory, Assistance Publique-Hôpitaux de Paris, Cochin Hospital, Paris, France.; INSERM U1016, Université de Paris, Institut Cochin, Paris, France.; Kosmider O; Hematology Laboratory, Assistance Publique-Hôpitaux de Paris, Cochin Hospital, Paris, France.; INSERM U1016, Université de Paris, Institut Cochin, Paris, France.; Javier RM; Rheumatology Department, Competence Center for Rare Genetic Bone Disorders, University-Hospital of Strasbourg, Strasbourg, France.; Pelletier F; CEREMAST, the Department of Dermatology, Allergology Unit, University Hospital of Besançon, Besançon, France.; Castelain F; Unité Transversale Allergologie, Dermatologie, CHU Besançon - Université de Franche-Comté, EFS, INSERM, UMR RIGHT, Besançon, France.; Retornaz F; Unité de soins et de recherche en médecine interne et maladies infectieuses, European Hospital, Marseille, France.; Cabrera Q; Department of Haematology, Sud Reunion University Hospital, Saint Pierre, France.; Zunic P; Department of Haematology, Sud Reunion University Hospital, Saint Pierre, France.; Gourin MP; CEREMAST, the Department of Hematology, CHU Dupuytren, Limoges, France.; Wierzbicka-Hainaut E; CEREMAST, the Department of Dermatology, CHU de Poitiers, Poitiers, France.; Viallard JF; Department of Internal Medicine, Hôpital Haut-Lévêque, Université de BORDEAUX, Pessac, France.; Lavigne C; Department of Internal Medicine, Angers University Hospital, Angers, France.; Hoarau C; The Service d'Immunologie Clinique et d'Allergologie, Centre Hospitalier Régional Universitaire, Tours, France.; Durieu I; Internal Medicine Department, Centre Hospitalier Lyon Sud, Pierre-Bénite, France.; INSERM U1290, Université Lyon 1, Lyon, France.; Dimicoli-Salazar S; Department of Hematology, CHU de Bordeaux, Bordeaux, France.; Torregrosa-Diaz JM; Service d'hématologie Oncologique et Thérapie Cellulaire, CIC-1402, CHU de Poitiers, Poitiers, France.; Wemeau M; Department of Haematology, Hospital Centre of Roubaix, Roubaix, France.; Soria A; Department of Dermatology and Allergy, Tenon Hospital, Sorbonne University, Paris, France.; Arock M; Platform of Molecular Analysis for Mastocytosis and MCAD (CEREMAST), Department of Biological Hematology, Pitié-Salpêtrière Hospital, AP-HP, Paris Sorbonne University, Paris, France.; Bodemer C; Department of Dermatology, Reference Center for Genodermatoses (MAGEC), Necker Hospital for Sick Children, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris Cité University, Paris, France.; CEREMAST, the Department of Hematology, Necker-Children's Hospital, AP-HP, Paris Centre University, Paris, France.; Lortholary O; French Reference Center for Mastocytosis (CEREMAST), Necker-Enfants Malades University Hospital, APHP, Paris, France.; Hermine O; French Reference Center for Mastocytosis (CEREMAST), Necker-Enfants Malades University Hospital, APHP, Paris, France.; CEREMAST, the Department of Pain and Palliative Care Unit, Necker-Children's Hospital, AP-HP, Paris Centre University, Paris, France.; Rossignol J; French Reference Center for Mastocytosis (CEREMAST), Necker-Enfants Malades University Hospital, APHP, Paris, France.; Imagine Institute, INSERM U1163, Necker-Enfants Malades University Hospital, Paris University, Paris, France.
Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 7610369 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1096-8652 (Electronic) Linking ISSN: 03618609 NLM ISO Abbreviation: Am J Hematol Subsets: MEDLINE
Academic Journal
Billes A; CHU Amiens Picardie, Service de Génétique Clinique, Amiens, France.; CHU Amiens Picardie, Laboratoire de Génétique Constitutionnelle, Amiens, France.; Pujalte M; Service de Génétique, Groupement Hospitalier Est, Hospices Civils de Lyon, Bron, France.; Jedraszak G; CHU Amiens Picardie, Laboratoire de Génétique Constitutionnelle, Amiens, France.; CHU Amiens Picardie, Département de génétique, UR4666 HEMATIM, CURS, Université Picardie Jules Verne, Amiens, France.; Amsallem D; Service de Neuropédiatrie, CHU de Besançon, Besançon, France.; Boudry-Labis E; Institut de Génétique Médicale, Hôpital Jeanne de Flandre, Centre Hospitalier Universitaire de Lille, Lille, France.; Boute O; Génétique Clinique, Centre Hospitalier Universitaire de Lille, Hôpital Jeanne de Flandre, Lille, France.; Bouquillon S; Institut de Génétique Médicale, Hôpital Jeanne de Flandre, Centre Hospitalier Universitaire de Lille, Lille, France.; Brischoux-Boucher E; Centre de Génétique Humaine - CHU de Besançon, Université de Bourgogne-Franche-Comté, Besançon, France.; Callier P; Inserm UMR 1231 GAD Génétique des Anomalies du Développement, Université de Bourgogne, Dijon, France.; Unité Fonctionnelle Innovation diagnostique dans les maladies rares, laboratoire de génétique chromosomique et moléculaire, Plateau Technique de Biologie, CHU Dijon Bourgogne, Dijon, France.; Fédération Hospitalo-Universitaire Médecine Translationnelle et Anomalies du Développement (FHU TRANSLAD), CHU Dijon Bourgogne et Université de Bourgogne-Franche Comté, Dijon, France.; Coutton C; Service de Génétique, Génomique, et Procréation, Centre Hospitalier Universitaire Grenoble Alpes, La Tronche, France.; INSERM 1209, CNRS UMR 5309, Institut pour l'Avancée des Biosciences (IAB), Université Grenoble Alpes, Grenoble, France.; Denizet AA; Centre de Génétique Humaine - CHU de Besançon, Université de Bourgogne-Franche-Comté, Besançon, France.; Dieterich K; Université Grenoble Alpes, Inserm, U1216, CHU Grenoble Alpes, Medical Genetics, Grenoble Institute of Neurosciences, Grenoble, France.; CHU Grenoble, UM Génétique Chromosomique, Grenoble, France.; Kuentz P; Oncobiologie Génétique Bioinformatique, PCBio, CHU de Besançon, Besançon, France.; UFR Des Sciences de Santé, INSERM-Université de Bourgogne UMR1231 GAD 'Génétique des Anomalies du Développement', FHUTRANSLAD, Dijon, France.; Lespinasse J; Centre Hospitalier de Chambéry, Service de Cytogénétique, Chambéry, France.; Mazel B; Centre de Génétique et Centre de Référence Anomalies du Développement et Syndromes Malformatifs, FHUTRANSLAD - CHU Dijon Bourgogne, Dijon, France.; Morin G; CHU Amiens Picardie, Service de Génétique Clinique, Amiens, France.; Amram F; CHU Amiens Picardie, Service de Génétique Clinique, Amiens, France.; Pennamen P; CHU Bordeaux, Laboratoire de Génétique Biologique, Bordeaux, France.; Rio M; Université Paris Cité, Institut Imagine, Inserm U1163, Paris, France.; Service de Médecine Génomique des maladies rares, AP-HP, Centre Hôpital Necker-Enfants Malades, Paris, France.; Piard J; Centre de Génétique Humaine - CHU de Besançon, Université de Bourgogne-Franche-Comté, Besançon, France.; UMR 1231 GAD, Inserm, Université de Bourgogne Franche Comté, Dijon, France.; Putoux A; Hospices Civils de Lyon, Service de Génétique, Groupement Hospitalier Est, Bron, France.; Equipe GENDEV, Centre de Recherche en Neurosciences de Lyon, INSERM U1028 CNRS UMR5292, Université Claude Bernard Lyon 1, Lyon, France.; Rama M; Institut de Génétique Médicale, Hôpital Jeanne de Flandre, Centre Hospitalier Universitaire de Lille, Lille, France.; Roze-Guillaumey V; Oncobiologie Génétique Bioinformatique, PCBio, CHU de Besançon, Besançon, France.; Schluth-Bolard C; Service de Génétique, Groupement Hospitalier Est, Hospices Civils de Lyon, Bron, France.; Institute NeuroMyoGène, Laboratoire Physiopathologie et Génétique du Neurone et du Muscle, CNRS UMR 5261-INSERM U1315, Université de Lyon - Université Claude Bernard Lyon 1, Lyon, France.; Laboratoire de Diagnostic Génétique, Institut de Génétique Médicale d'Alsace, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.; Till M; Service de Génétique, Groupement Hospitalier Est, Hospices Civils de Lyon, Bron, France.; Trouvé C; Centre de Génétique Humaine - CHU de Besançon, Université de Bourgogne-Franche-Comté, Besançon, France.; Vieville G; Département de Génétique et Procréation, Hôpital Couple Enfant, CHU Grenoble-Alpes, Grenoble, France.; Rooryck C; CHU de Bordeaux, Service de Génétique Médicale, Bordeaux, France.; Univ. Bordeaux, Maladies Rares: Génétique et Métabolisme (MRGM), U 1211 INSERM, Bordeaux, France.; Sanlaville D; Service de Génétique, Groupement Hospitalier Est, Hospices Civils de Lyon, Bron, France.; Institute NeuroMyoGène, Laboratoire Physiopathologie et Génétique du Neurone et du Muscle, CNRS UMR 5261-INSERM U1315, Université de Lyon - Université Claude Bernard Lyon 1, Lyon, France.; Chatron N; Service de Génétique, Groupement Hospitalier Est, Hospices Civils de Lyon, Bron, France.; Institute NeuroMyoGène, Laboratoire Physiopathologie et Génétique du Neurone et du Muscle, CNRS UMR 5261-INSERM U1315, Université de Lyon - Université Claude Bernard Lyon 1, Lyon, France.
Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE
Conference
EUROPEAN JOURNAL OF HUMAN GENETICS
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Fundació Sant Joan de Déu
Academic Journal
Loviglio, M. NLeleu, M.Männik, K.Passeggeri, M.Giannuzzi, G.van der Werf, I.Waszak, S. M.Zazhytska, M.Roberts Caldeira, I.Gheldof, N.Migliavacca, E.Alfaiz, A. A.Hippolyte, L.Maillard, A. M.van Dijck, A.Kooy, R. F.Sanlaville, D.Rosenfeld, J. A.Shaffer, L. G.Andrieux, J.Marshall, C.Scherer, S. W.Shen, Y.Gusella, J. F.Thorsteinsdottir, U.Thorleifsson, G.Dermitzakis, E. T.Deplancke, B.Beckmann, J. S.Rougemont, J.Jacquemont, S.Reymond, A.Collaborators: Loviglio MNMännik Kvan der Werf IGiannuzzi GZazhytska MGheldof NMigliavacca EAlfaiz AARoberts Caldeira IHippolyte LMaillard AMFerrarini AButschi FNConrad BAddor MCBelfiore MRoetzer KDijck AVBlaumeiser BKooy FRoelens FDheedene AChiaie BDMenten BOostra ACaberg JHCarter MKellam BStavropoulos DJMarshall CScherer SWWeksberg RCytrynbaum CBassett ALowther CGillis JMacKay SBache IOusager LBSmerdel MPGraakjaer JKjaergaard SMetspalu AMathieu MBonneau DGuichet AParent PFérec CGerard MPlessis GLespinasse JMasurel AMarle NFaivre LCallier PLayet VMeur NLLe Goff CDuban Bedu BSukno SBoute OAndrieux JBlanchet PGeneviève DPuechberty JSchneider ALeheup BJonveaux PMercier SDavid ALe Caignec Cde Pontual LPipiras EJacquette AKeren BGilbert Dussardier BBilan FGoldenberg AChambon PToutain ATill MSanlaville DLeube BRoyer Pokora BGrabe HJSchmidt COSchurmann CHomuth GThorleifsson GThorsteinsdottir UBernardini LNovelli AMicale LMerla GZollino MMARI, FRANCESCARizzo CLRENIERI, ALESSANDRASilengo MVulto van Silfhout ATSchouten MPfundt Rde Leeuw NVansenne FMaas SMBarge Schaapveld DQKnegt ACStadheim BRodningen OHouge GPrice SHawkes LCampbell CKini UVogt JWalters RBlakemore AGusella JFShen YScott DBacino CATsuchiya KLadda RSell SAsamoah AHamati AIRosenfeld JAShaffer LGMitchell EHodge JCBeckmann JSJacquemont SReymond AEwans LJMowat DWalker JAmor DJEsch HVLeroy PBamforth JSBabu DIsidor BDiDonato NHackmann KPasseggeri MHaeringen AVSmith REllingwood SFarber DMPuri VZadeh NWeaver DDMiller MWilks TJorgez CJLafayette DJacquemont S.
Mol Psychiatry
Molecular Psychiatry, 22, 6, pp. 836-849
Molecular Psychiatry, Vol. 22, No 6 (2017) pp. 836-849
Molecular Psychiatry, vol. 22, no. 6, pp. 836-849
Molecular psychiatry
Ousager, L B & 2p15 Consortium 2017, ' Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes ', Molecular Psychiatry, vol. 22, no. 6, pp. 836-849 . https://doi.org/10.1038/mp.2016.84
Molecular Psychiatry
Conference
Proceedings of the fifteenth ACM symposium on Operating systems principles. :156-171
Academic Journal
Delinière A; National Reference Center for Inherited Arrhythmia Syndromes of Lyon (CERA), Cardiac Electrophysiology Unit, Louis Pradel Hospital, Institut de Cardiologie, Hospices Civils de Lyon, Bron, France; Université Claude Bernard Lyon 1, MeLiS, CNRS UMR 5284, Institut NeuroMyoGène, Lyon, France.; Mulatier C; Pediatric cardiology department, Louis Pradel Hospital, Hospices Civils de Lyon, Bron, France.; Cheillan D; Inborn Errors of Metabolism Unit, Biochemistry and Molecular Biology Department, Lyon University Hospital, Lyon, France.; Gheurbi F; Reference Center for Intellectual Disability from Rare Causes, Child Neurology Department, Woman Mother and Child Hospital, Hospices Civils de Lyon, Bron, France; Université Claude Bernard Lyon 1, Lyon Neuroscience Research Centre, Bron, France.; Buchy M; Reference Center for Intellectual Disability from Rare Causes, Child Neurology Department, Woman Mother and Child Hospital, Hospices Civils de Lyon, Bron, France; Université Claude Bernard Lyon 1, Lyon Neuroscience Research Centre, Bron, France.; Dufay N; Biological Resource Center, Hospices Civils de Lyon, Bron, France.; Moulin-Zinsch A; Pediatric cardiology department, Louis Pradel Hospital, Hospices Civils de Lyon, Bron, France.; Bertail-Galoin C; Pediatric cardiology department, Louis Pradel Hospital, Hospices Civils de Lyon, Bron, France.; Sabour M; Pediatric cardiology department, Louis Pradel Hospital, Hospices Civils de Lyon, Bron, France.; Aarab M; Pediatric cardiology department, Louis Pradel Hospital, Hospices Civils de Lyon, Bron, France.; Perouse de Montclos T; Pediatric cardiology department, Louis Pradel Hospital, Hospices Civils de Lyon, Bron, France.; Ouvrier-Buffet D; Pediatric cardiology department, Louis Pradel Hospital, Hospices Civils de Lyon, Bron, France.; Boisson A; Pediatric cardiology department, Louis Pradel Hospital, Hospices Civils de Lyon, Bron, France.; Stos B; UE3C (Unité d'Explorations des Cardiopathies Congénitales et de Cardiologie Pédiatrique), Paris, France.; Rharbaoui M; Pôle de Cardiologie, Clinique du Millénaire, Montpellier, France.; Remerand G; Department of Neonatology, Estaing Hospital, Clermont-Ferrand University Hospital, Clermont-Ferrand, France.; Barnerias C; Child Neurology Department, Necker-Enfants-Malades Hospital, Paris, France.; Brassier A; Reference Centre for Inherited Metabolic Diseases, Imagine Institute, Necker Enfants-Malades Hospital, Paris University Hospital, University of Paris Descartes, Paris, France.; Goldenberg A; Department of Genetics and Reference Center for Developmental Disorders, Rouen University Hospital, Rouen, France.; Roubertie A; Child Neurology Department, Montpellier University Hospital, Montpellier, France.; Lion-François L; Reference Center for Intellectual Disability from Rare Causes, Child Neurology Department, Woman Mother and Child Hospital, Hospices Civils de Lyon, Bron, France.; Marignier S; Reference Center for Intellectual Disability from Rare Causes, Child Neurology Department, Woman Mother and Child Hospital, Hospices Civils de Lyon, Bron, France.; De Lonlay P; Reference Centre for Inherited Metabolic Diseases, Imagine Institute, Necker Enfants-Malades Hospital, Paris University Hospital, University of Paris Descartes, Paris, France.; Mochel F; AP-HP, Pitié-Salpêtrière, University Hospital, Department of Medical Genetics, Reference Center for Adult Neurometabolic diseases and Adult Leukodystrophies, Paris, France.; Navarro V; Epilepsy Unit and Reference Center for Rare Epilepsies, ERN EpiCare, AP-HP, Pitié-Salpêtrière University Hospital, Paris Brain Institute and Sorbonne Université, Paris, France.; Lespinasse J; Genetic Department, Métropole Savoie Chambéry Hospital, Chambéry, France.; Lacombe D; Genetic Department, Bordeaux University Hospital, Bordeaux, France.; Touraine R; Saint Etienne University Hospital, Saint Etienne, France.; Rheims S; Université Claude Bernard Lyon 1, Lyon Neuroscience Research Centre, Bron, France; Department of Functional Neurology and Epileptology, Hospices Civils de Lyon, Bron, France.; des Portes V; Reference Center for Intellectual Disability from Rare Causes, Child Neurology Department, Woman Mother and Child Hospital, Hospices Civils de Lyon, Bron, France; Université Claude Bernard Lyon 1, Lyon Neuroscience Research Centre, Bron, France.; Chevalier P; National Reference Center for Inherited Arrhythmia Syndromes of Lyon (CERA), Cardiac Electrophysiology Unit, Louis Pradel Hospital, Institut de Cardiologie, Hospices Civils de Lyon, Bron, France; Université Claude Bernard Lyon 1, MeLiS, CNRS UMR 5284, Institut NeuroMyoGène, Lyon, France.; Curie A; Reference Center for Intellectual Disability from Rare Causes, Child Neurology Department, Woman Mother and Child Hospital, Hospices Civils de Lyon, Bron, France; Université Claude Bernard Lyon 1, Lyon Neuroscience Research Centre, Bron, France. Electronic address: aurore.curie@chu-lyon.fr.
Publisher: Elsevier Country of Publication: United States NLM ID: 101200317 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1556-3871 (Electronic) Linking ISSN: 15475271 NLM ISO Abbreviation: Heart Rhythm Subsets: MEDLINE
Academic Journal
Lowther, C.Mehrjouy, M.M.Collins, R.L.Bak, M.C.Dudchenko, O.Brand, H.Dong, Z.Rasmussen, M.B.Gu, H.Weisz, D.Nazaryan-Petersen, L.Fjorder, A.S.Mang, Y.Lind-Thomsen, A.Mendez, J.M.M.Calle, X.Chopra, A.Hansen, C.Bugge, M.Broekema, R.V.Varilo, T.Luukkonen, T.Engelen, J.Vianna-Morgante, A.M.Fonseca, A.C.S.Mazzeu, J.F.Dornelles-Wawruk, H.Abe, K.T.Vermeesch, J.R.Van Den Bogaert, K.Sismani, C.Aristidou, C.Evangelidou, P.Schinzel, A.A.Sanlaville, D.Schluth-Bolard, C.Kalscheuer, V.M.Wenzel, M.Kim, H.-G.Õunap, K.Roht, L.Midyan, S.Bonaglia, M.C.Lindstrand, A.Eisfeldt, J.Ottosson, J.Nilsson, D.Pettersson, M.Bastos, E.F.Rajcan-Separovic, E.Silan, F.Sheth, F.J.Novelli, A.Frengen, E.Fannemel, M.Strømme, P.Vokač, N.K.Daumer-Haas, C.Moretti-Ferreira, D.de Souza, D.H.Ramos-Arroyo, M.A.Igoa, M.M.Angelova, L.Kroisel, P.M.del Rey, G.Vieira, T.A.P.Lewis, S.Hao, W.Drabova, J.Havlovicova, M.Hancarova, M.Sedláček, Z.Vogel, I.Hjortshøj, T.D.Møller, R.S.Tümer, Z.Fagerberg, C.Ousager, L.B.Schönewolf-Greulich, B.Lauridsen, M.Piard, J.Pebrel-Richard, C.Jaillard, S.Ehmke, N.Stefanou, E.G.Marta, C.György, K.Dalal, A.Dutta, U.R.Shukla, R.Lonardo, F.Zuffardi, O.Houge, G.Misceo, D.Baig, S.M.Midro, A.Wawrusiewicz-Kurylonek, N.Carreira, I.M.Melo, J.B.Martinez, L.R.Guitart, M.Lovmar, L.Gullander, J.Hansson, K.B.M.de Almeida Esteves, C.Akkari, Y.Batanian, J.R.Li, X.Lespinasse, J.Silahtaroglu, A.Harding, C.H.Krogh, L.N.Taylor, J.Lehnert, K.Hill, R.Snell, R.G.Samson, C.A.Jacobsen, J.C.Levy, B.Clark, O.A.Toylu, A.Nur, B.Mihci, E.O’Keefe, K.Mohajeri-Stickels, K.Wilch, E.S.Kammin, T.Piña-Aguilar, R.E.Nalbandian, K.Temel, S.G.Sag, S.O.Turkgenc, B.Kamath, A.Ruiz-Herrera, A.Banka, S.Schilit, S.L.P.Currall, B.B.Yachelevich, N.Galloway, S.Chung, W.K.Raskin, S.Maya, I.Orenstein, N.Gilad, N.K.Flamenbaum, K.R.Hay, B.N.Morton, C.C.Liao, E.Choy, K.W.Gusella, J.F.Jacky, P.Aiden, E.L.Bache, I.Talkowski, M.E.Tommerup, N.da Cruz, A.D.Kulikowski, L.D.Novo Filho, G.M.Melaragno, M.I.Vazharova, R.V.Bradinova, I.Chitayat, D.Barisic, I.Mekkawy, M.M.Agnes, G.Pellestor, F.Dupont, C.Lebbar, A.Belaud-Rotureau, M.-A.Philippe, J.Pampanos, A.A.Kitsiou-Tzeli, S.Kardara, K.Kasturirangan, C.G.Kanakavalli, M.Kandukuri, L.R.Oruganti, V.P.Madon, P.F.Faradz, S.M.H.Giardino, D.Larizza, L.Recalcati, M.P.Dalpà, L.Sala, E.Kurahashi, H.Aleksiūnienė, B.Utkus, A.Ankathil, R.Tan, S.C.Kurpisz, M.Sousa, A.B.Travessa, A.M.R.Plaseska-Karanfilska, D.Abdulwahed, O.A.Zagorac, A.Bafalliu-Vidal, J.A.Lopez-Exposito, I.Soler-Sanchez, G.Vera-Carbonell, A.Kristoffersson, U.Filges, I.Charalsawadi, C.Aslanger, A.D.Cingöz, S.Dundar, M.Wolff, D.J.
Lowther, C, Mehrjouy, M M, Collins, R L, Bak, M C, Dudchenko, O, Brand, H, Dong, Z, Rasmussen, M B, Gu, H, Weisz, D, Nazaryan-Petersen, L, Fjorder, A S, Mang, Y, Lind-Thomsen, A, Mendez, J M M, Calle, X, Chopra, A, Hansen, C, Bugge, M, Broekema, R V, Varilo, T, Luukkonen, T, Engelen, J, Vianna-Morgante, A M, Fonseca, A C S, Mazzeu, J F, Dornelles-Wawruk, H, Abe, K T, Vermeesch, J R, Van Den Bogaert, K, Sismani, C, Aristidou, C, Evangelidou, P, Schinzel, A A, Sanlaville, D, Schluth-Bolard, C, Kalscheuer, V M, Wenzel, M, Kim, H-G, Õunap, K, Roht, L, Midyan, S, Bonaglia, M C, Lindstrand, A, Eisfeldt, J, Ottosson, J, Nilsson, D, Pettersson, M, Bastos, E F, Rajcan-Separovic, E, Silan, F, Sheth, F J, Novelli, A, Frengen, E, Fannemel, M, Strømme, P, Vokač, N K, Daumer-Haas, C, Moretti-Ferreira, D, de Souza, D H, Ramos-Arroyo, M A, Igoa, M M, Angelova, L, Kroisel, P M, del Rey, G, Vieira, T A P, Lewis, S, Hao, W, Drabova, J, Havlovicova, M, Hancarova, M, Sedláček, Z, Vogel, I, Hjortshøj, T D, Møller, R S, Tümer, Z, Fagerberg, C, Ousager, L B, Schönewolf-Greulich, B, Lauridsen, M, Piard, J, Pebrel-Richard, C, Jaillard, S, Ehmke, N, Stefanou, E G, Marta, C, György, K, Dalal, A, Dutta, U R, Shukla, R, Lonardo, F, Zuffardi, O, Houge, G, Misceo, D, Baig, S M, Midro, A, Wawrusiewicz-Kurylonek, N, Carreira, I M, Melo, J B, Martinez, L R, Guitart, M, Lovmar, L, Gullander, J, Hansson, K B M, de Almeida Esteves, C, Akkari, Y, Batanian, J R, Li, X, Lespinasse, J, Silahtaroglu, A, Harding, C H, Krogh, L N, Taylor, J, Lehnert, K, Hill, R, Snell, R G, Samson, C A, Jacobsen, J C, Levy, B, Clark, O A, Toylu, A, Nur, B, Mihci, E, O’Keefe, K, Mohajeri-Stickels, K, Wilch, E S, Kammin, T, Piña-Aguilar, R E, Nalbandian, K, Temel, S G, Sag, S O, Turkgenc, B, Kamath, A, Ruiz-Herrera, A, Banka, S, Schilit, S L P, Currall, B B, Yachelevich, N, Galloway, S, Chung, W K, Raskin, S, Maya, I, Orenstein, N, Gilad, N K, Flamenbaum, K R, Hay, B N, Morton, C C, Liao, E, Choy, K W, Gusella, J F, Jacky, P, Aiden, E L, Bache, I, Talkowski, M E, Tommerup, N, da Cruz, A D, Kulikowski, L D, Novo Filho, G M, Melaragno, M I, Vazharova, R V, Bradinova, I, Chitayat, D, Barisic, I, Mekkawy, M M, Agnes, G, Pellestor, F, Dupont, C, Lebbar, A, Belaud-Rotureau, M-A, Philippe, J, Pampanos, A A, Kitsiou-Tzeli, S, Kardara, K, Kasturirangan, C G, Kanakavalli, M, Kandukuri, L R, Oruganti, V P, Madon, P F, Faradz, S M H, Giardino, D, Larizza, L, Recalcati, M P, Dalpà, L, Sala, E, Kurahashi, H, Aleksiūnienė, B, Utkus, A, Ankathil, R, Tan, S C, Kurpisz, M, Sousa, A B, Travessa, A M R, Plaseska-Karanfilska, D, Abdulwahed, O A, Zagorac, A, Bafalliu-Vidal, J A, Lopez-Exposito, I, Soler-Sanchez, G, Vera-Carbonell, A, Kristoffersson, U, Filges, I, Charalsawadi, C, Aslanger, A D, Cingöz, S, Dundar, M & Wolff, D J 2022, 'Balanced chromosomal rearrangements offer insights into coding and noncoding genomic features associated with developmental disorders', medRxiv. https://doi.org/10.1101/2022.02.15.22270795
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