학술논문

발행년
-
(예 : 2010-2015)
'학술논문' 에서 검색결과 390건 | 목록 20~30
Academic Journal
Mesinovic, M.Wong, X.C.Peariasamy, K.M.Peariasamy, K.Wong, X.C.Rajahram, G.S.Rajahram, G.S.Citarella, B.W.Olliaro, P.Merson, L.Balan, V.Baruch, J.Carson, G.Citarella, B.W.Dagens, A.Dunning, J.Escher, M.Horby, P.Merson, L.Olliaro, P.L.Pritchard, M.G.Sigfrid, L.van Someren Greve, F.Greve, F.V.S.Clifton, L.Kartsonaki, C.Kartsonaki, C.Abdukahil, S.A.Qasim, E.A.Humaid, F.B.Sadat, M.Abdulkadir, N.N.Bakar, N.A.Kaleesvran, T.Wahab, S.A.Abe, R.Abel, L.Abrous, A.Angoulvant, F.Bachelet, D.Bartoli, M.Basmaci, R.Behilill, S.Beluze, M.Benkerrou, D.Bhavsar, K.Bompart, F.Bouadma, L.Bouscambert, M.Cervantes-Gonzalez, M.Chair, A.Coelho, A.Couffignal, C.Couffin-Cadiergues, S.Da Silveira, C.Debray, M.-P.Delmas, C.Deplanque, D.Descamps, D.Desvallées, M.Diallo, A.Da Silva, F.D.Diouf, A.Dorival, C.D’Ortenzio, E.Dubos, F.Duval, X.Eloy, P.Enouf, V.Esperou, H.Esposito-Farese, M.Etienne, M.Ettalhaoui, N.Gault, N.Gaymard, A.Ghosn, J.Gigante, T.Gilg, M.Gorenne, I.Guedj, J.Hoctin, A.Hoffmann, I.Houas, I.Hulot, J.-S.Jaafoura, S.Kafif, O.Kaguelidou, F.Kali, S.Khalil, A.Khan, C.Laribi, S.Le, M.Hingrat, Q.L.Mestre, S.L.Nagard, H.L.Lescure, F.-X.Levy, Y.Levy-Marchal, C.Lina, B.Lingas, G.Lucet, J.C.Malvy, D.Mercier, N.Meziane, A.Mouquet, H.Mullaert, J.Neant, N.Noret, M.Pages, J.Papadopoulos, A.Paul, C.Peiffer-Smadja, N.Petrov-Sanchez, V.Peytavin, G.Picone, O.Puéchal, O.Rosa-Calatrava, M.Rossignol, B.Rossignol, P.Roy, C.Schneider, M.Semaille, C.Mohammed, N.S.Tagherset, L.Tardivon, C.Tellier, M.-C.Téoulé, F.Terrier, O.Timsit, J.-F.Trioux, T.Tual, C.Tubiana, S.Werf, S.V.D.Vanel, N.Veislinger, A.Visseaux, B.Wiedemann, A.Yazdanpanah, Y.Absil, L.Bouziotis, J.Cornelis, S.Preiser, J.-C.Snacken, M.Acker, A.Mergler, B.Rizer, N.Smood, B.Sperry, A.Usman, A.Adachi, S.Adam, E.Deligiannis, I.Neb, H.Sonntagbauer, M.Zacharowski, K.Adriano, E.Aiello, M.Bonelli, P.Caminiti, C.Carlacci, F.Chetta, A.A.Economopoulos, G.Ferrari, C.Fogliazza, F.Garofalo, F.Maglietta, G.Majori, M.Mammi, P.Meschi, T.Mutti, C.Parducci, P.Patrizi, L.Pisi, R.Puntoni, M.Rampello, A.Ranza, E.Rausa, F.Rossi, S.Sacchelli, L.Ticinesi, A.Valzano, I.Adrião, D.Fonseca, T.Neto, R.Rios, A.L.Ageel, S.A.Ahmed, S.Alkhafajee, Q.Feely, N.Vajdovics, C.Ainscough, K.Bergin, H.Brickell, K.Doran, P.Downey, J.Feeney, L.Gallagher, P.Hays, L.Keane, H.Krawczyk, K.Lester-Grant, A.Mallon, P.McPartlan, E.Meaney, E.Molloy, B.Murphy, L.Reid, L.Smyth, M.Varghese, P.Vencken, S.Airlangga, E.Baird, J.K.Hamers, R.L.Pitaloka, A.Rahardjani, M.Shankar, A.Subekti, D.Suwarti, A.Aisa, T.Hashmi, J.Kuriakose, D.Narayanan, N.Hssain, A.A.Aliudin, J.Taleb, S.Villanueva, J.A.Tamlihat, Y.A.Bergeaud, D.Roze, B.Akimoto, T.Akmal, E.Burhan, E.Lolong, N.Rasmin, M.Alalqam, R.Clarke, J.Cullen, A.Curley, G.Doherty, H.Foley, C.McEvoy, N.Choileain, O.N.Stolz, E.Towers, M.Alberti, A.Hartman, A.Manetta, F.Mihelis, E.Narasimhan, M.Sarmiento, I.C.E.Varrone, M.Al-dabbous, T.Alfoudri, H.Corpuz, A.J.Shamsah, M.Alegesan, S.Bourke, J.Boylan, M.Casey, S.Daly, S.Donohue, S.Donohue, Y.Higgins, E.Kelly, C.Kernan, M.Laffey, J.G.Maxwell, M.McCarthy, A.McNicholas, B.Metwally, O.Leathlobhair, N.N.Ranjan, R.Ryan, M.Chia, J.S.Tawfik, H.Tuite, H.Alegre, C.Contreras, S.Ferrer-Roca, R.Riera, J.Alessi, M.Cortegiani, A.Ippolito, M.Spinuzza, E.Alex, B.Bach, B.Scott-Brown, J.Alexandre, K.Artaud-Macari, E.Devouge, E.F.Lemee, V.Al-Fares, A.Ali, A.Chatterjee, A.Finlayson, W.Gomez, K.Meta, R.Wright, N.Ali, I.Hayes, A.O’Sullivan, M.Whelan, B.Alidjnou, K.E.Bauer, J.Boyer-Besseyre, M.Chopin, M.-C.Engelmann, I.Faure, K.Favory, R.Jourdain, M.Mathieu, D.Nseir, S.Poissy, J.Preau, S.Remy, M.Stabler, S.Vuotto, F.Allavena, C.Bouchez, S.Guery, R.Turnier, P.L.Mear-Passard, C.Allou, N.Jabot, J.Lagrange, M.Alves, J.Cabral, S.Catarino, A.Marques, A.Martins, J.Silva, C.Alves, J.M.Barrigoto, C.Bento, L.Oliveira, J.Proença, L.Roberto, A.Rodeia, S.Ventura, S.Alves, R.Cabrita, J.A.Amaral, M.Borges, D.Garcês, R.C.Cardoso, F.Cardoso, F.Cardoso, S.Cascão, M.Casimiro, J.Damas, J.Dantas, J.Santo, C.E.Estevão, J.Faria, P.Fernandes, J.Fernandes, M.A.Ferrão, J.Ferraz, M.Ferreira, B.Germano, N.Guerreiro, D.Inácio, H.Isidoro, T.Lopes, D.Machado, S.Martins, A.Mesquita, A.Monteiro, A.Paulos, J.Pereira, R.Pimentel, C.Pires, C.Ramalho, J.Sequeira, T.Teixeira, J.Torre, M.Val-Flores, L.Vieira, C.Amira, N.Ashraf, M.Asyraf, A.Balakrishnan, M.Barnett, S.U.Basri, M.F.H.Bidin, F.N.Kamarudin, M.N.B.Chua, J.Fateena, H.Gani, Y.Ing, Y.S.Kamaluddin, M.A.A.Karpayah, P.Khoo, D.Krishnan, V.Lee, Y.L.Lim, K.C.Misnan, N.A.Muyandy, G.Norharizam, N.F.I.Pang, L.H.Ramli, A.A.Ravi, T.Selvarajoo, M.Sivam, K.Syahrin, S.Tan, K.K.Tan, Y.C.Thabit, A.A.M.Thangavelu, S.Thirumanickam, J.Thurai, S.R.T.Veeran, S.Wahid, N.A.Wong, Y.S.Xuan, K.P.Ammerlaan, H.Ampaw, P.McCarthy, A.Pharand, S.Sarfo-Mensah, S.Andini, R.Bertolino, L.Boccia, F.Durante-Mangoni, E.Florio, L.L.Gagliardi, M.Mele, F.Patauner, F.Andréjak, C.Joseph, C.Lion-Daolio, S.Moyet, J.Angheben, A.Ansart, S.Bodenes, L.Ferriere, N.Guellec, D.L’Her, E.Tromeur, C.Anthonidass, S.Tho, L.C.Eng, C.C.Ismail, N.Joe, O.Y.Kumar, G.Loon, L.C.Mohamed, N.N.E.Mohamed, T.J.Muh, N.Y.Othman, S.Z.Png, H.S.Senian, R.B.Shahidan, S.A.Taib, S.M.Tham, Z.D.Toh, J.Z.Y.Wahab, N.H.Xian, G.E.Yakop, S.R.B.M.Hing, N.Y.L.Zaynah, N.Antonelli, M.Carelli, S.Grieco, D.L.de Brito, C.A.A.Araujo, C.Braga, C.de Oliveira França, R.F.Fonseca, C.D.Freire, M.V.Martelli, C.T.Anwar, K.R.Apriyana, A.Dewayanti, S.Juzar, D.Marwali, E.M.Arabi, Y.Aragao, I.Silva, M.J.Arancibia, F.Fritz, R.Sepulveda, C.Zambrano, M.Arcadipane, A.Bianco, C.Martucci, G.Occhipinti, G.Panarello, G.Rossetti, M.Vitiello, C.Archambault, P.Arenz, L.Barnikel, M.Stecher, S.-S.Arlet, J.-B.Auvet, A.Cholley, B.Diehl, J.-L.Livrozet, M.Sanchez, O.Arnold-Day, C.Arora, L.Arora, R.Aryal, D.Attanyake, A.M.U.L.Dondorp, A.M.Haniffa, R.Kodippily, C.Madiha, H.Muvindi, H.Priyadarshani, G.D.D.Rashan, T.Shiekh, M.Darshana, B.P.S.R.S.Udayanga, P.G.I.Asaki, M.Asensio, A.Cantero, M.Ashley, E.A.Assie, J.B.Delacroix, I.Elharrar, B.Garrait, V.Maitre, T.Atique, A.Campisi, J.Chen, A.Cheng, M.P.Gu, Y.Hsu, J.M.-Y.Kaur, A.Lee, T.C.Solomon, J.Tabrizi, S.Auchabie, J.Courtois, R.Lemeur, A.Mazzoni, T.Aumaitre, H.Azemar, L.Castor-Alexandre, G.Manda, V.Azoulay, C.Carlier, N.Lachatre, M.Launay, O.Luong, L.Badr, C.Caraux-Paz, P.Diop, F.Jaafar, D.Richier, L.Baig, N.Baillie, J.K.Bak, E.Bakakos, A.Kalomoiri, S.Kyriakoulis, K.Myrodia, D.M.Prapa, S.Syrigos, K.Toki, M.Trontzas, I.Xynogalas, I.Bal, A.Silva, R.Bani-Sadr, F.Didier, K.Hentzien, M.Romaru, J.Barbalho, R.Castanheira, N.Cavalin, R.Custodio, P.Figueiredo-Mello, C.Ribeiro, A.F.Lanza, M.Malaque, C.M.S.Rego, C.M.Sztajnbok, J.Vidal, J.E.Barbosa, N.Y.Granado, R.C.-D.Wainstein, M.Barclay, W.S.Barrasa, H.Maynar, J.Tejada, S.Barrelet, A.Bedossa, A.Machado, M.Battaglini, D.Pelosi, P.Robba, C.Rincon, D.F.B.Chica, J.Montes, C.Dow, D.B.Garimella, N.Lovelace-Macon, L.West, T.E.Beane, A.Bee, K.H.Lee, B.H.Begum, H.Uyeki, T.M.Webb, S.Beishuizen, A.Brusse-Keizer, M.Cornet, A.D.Delsing, C.Haalboom, M.Klont, R.Lowik, M.Piersma, D.Palen, J.V.D.Valk, P.V.D.Veen, I.V.Vonkeman, H.Beljantsev, A.Maasikas, O.Mihnovit, V.Bellemare, D.Blier, C.Turgeon, A.F.Beltrame, A.Buonsenso, D.Beltrão, B.A.Porto, D.B.Benech, N.Conrad, A.Perpoint, T.Benjiman, L.E.Ong, J.Y.Suppiah, D.Tonnii, S.L.Wong, T.F.Bennett, S.Cassandra, B.Lemmink, G.Mechlin, M.Richardson, D.Berdal, J.-E.Prebensen, C.Bertoli, G.Cardellino, C.S.Cattaneo, P.Moro, L.Rodari, P.Rossanese, A.Bessis, S.Betz, A.Bevilcaqua, S.Goehringer, F.Guillaumot, A.Kimmoun, A.Lefèvre, B.Levy, B.Mattei, M.Rabaud, C.Saint-Gilles, M.Bezulier, K.Leone, M.Pastene, B.Bhatt, A.Echeverria-Villalobos, M.Fiorda, J.Gonzalez, A.McKeown, J.Periel, L.Satyapriya, S.Shi, H.Uribe, A.Singh, M.B.Dhanger, P.Kataria, A.Bisoffi, Z.Piubelli, C.Bissuel, F.Biston, P.Piagnerelli, M.Bitker, L.Bolze, P.-A.Mezidi, M.Yonis, H.Bitton, J.Jouvet, P.Blanco-Schweizer, P.Bloos, F.Blot, M.Buisson, M.Catherine, F.-X.Mahy, S.Piroth, L.Blumberg, L.Dryden, M.Jassat, W.Mudara, C.Bogaert, D.Russell, C.D.Boivin, A.-H.Nyamankolly, E.Bolaños, I.Calvache, J.A.Hernandez, D.Orozco-Chamorro, C.M.Perez, D.Bonfasius, A.Elyazar, I.Rabaa, M.Borie, R.Charpentier, C.Chenard, L.De Montmollin, E.Deconninck, L.Florence, A.-M.Goulenok, T.Jaquet, P.Lafhej, N.Fevre, L.L.LeGac, S.Letrou, S.Luton, D.Patrier, J.Piquard, V.Su, R.Wicky, P.H.Bosse, H.M.Brandenburger, T.Kindgen-Milles, D.Vasconcelos, M.K.Weil, K.Botelho-Nevers, E.Gagneux-Brunon, A.Trouillon, T.Bouchaud, O.Cordel, H.Dournon, N.Bouhmani, D.Tessier-Grenier, H.Bouhour, D.Bouisse, C.Sedillot, N.Bouiller, K.Chirouze, C.Pagadoy, M.Tissot, N.Vauchy, C.Bouillet, L.Epaulard, O.Hamidfar, R.Maréchal, M.L.Payen, J.-F.Terzi, N.Bounphiengsy, T.Douangdala, P.Bountthasavong, L.Praphasiri, V.Yiaye, T.Boureau, A.-S.Bousquet, A.Ficko, C.Gominet, M.Boxma, B.Wesselius, S.Bozza, F.A.Braconnier, A.Monteiro, F.B.Brazzi, L.Montrucchio, G.Sales, G.Breen, D.Browne, S.Curran, C.Flynn, D.Foley, J.Kelly, N.Kelsey, M.Manning, E.Sweeney, L.M.Brien, F.O.Callaghan, A.O.Stone, A.Breen, P.McEneany, V.Brewster, D.Burrell, A.Coles, J.Hammond, N.Martinez, F.E.McCanny, P.Miller, J.Peake, S.L.Neto, A.S.Udy, A.Williams, P.J.Yarad, E.Browne, A.Brozzi, N.Hernandez-Montfort, J.Buchtele, N.Roessler, B.Schwameis, M.Staudinger, T.Ullrich, R.Bugaeva, P.Butnaru, D.Fomin, V.Glybochko, P.Nekliudov, N.Svistunov, A.Timashev, P.S.Bustos, I.G.Caceres, E.Garcia-Gallo, E.Cely, L.M.Cabie, A.Campana, V.Pasquier, J.Sandrine, P.-F.Turmel, J.-M.Cadoz, C.Dinot, V.Gaci, R.Louis, G.Ouamara, N.Callahan, M.D’Orleans, C.C.Dong, A.Javidfar, J.Ragazzo, G.Shiban, N.Calligy, K.Cho, S.-M.Camões, J.Carqueja, I.Ferreira, S.Molinos, E.Campbell, P.Khan, I.Quraishi, M.Canepa, C.Castañeda, S.Horcajada, J.P.Villar, J.Cárcel, S.León, R.Cardoso, N.Lima, C.Lourenco, S.Ribeiro, M.I.Sousa, A.C.Carmoi, T.Lasry, S.Rapp, C.Carney, G.Carret, M.-C.Isnard, M.Jego, F.Peigne, V.Pierobon, C.Carrier, F.M.Carroll, I.Conway, E.Driscoll, A.Egan, S.Hinchion, R.Motherway, C.Pudota, S.Ryan, M.Tey, A.Carvalho, L.Dias, A.Casanova, M.-L.Bris, C.L.Falher, G.L.Oziol, E.Thill, B.Castro, I.Cidade, J.P.Povoa, P.Cavalli, G.G.Loforte, A.Cavayas, A.Duplaix, M.Williams, V.Ceccato, A.de Mendoza, D.Cerkovnik, S.Chakveatze, C.Diamantis, S.Flateau, C.Chaleunphon, B.Phoutthavong, S.Chan, A.Daneman, N.Kiiza, P.Rishu, A.Shadowitz, E.Chand, M.Auger, C.C.Cheret, A.Goujard, C.Hadri, N.Jaureguiberry, S.Chapplain, J.-M.Laine, F.Lesouhaitier, M.Revest, M.Tattevin, P.Thibault, V.Chas, J.Iñiguez, J.S.C.Chiarabini, T.Lefebvre, B.Chidambaram, S.K.Chua, H.J.Pathmanathan, M.D.Chiumello, D.Cho, H.J.Chommanam, D.Christy, N.Dubot-Pérès, A.Keomany, S.Letizia, A.Mayxay, M.Phonemixay, O.Sibounheuang, B.Vongsouvath, M.Chow, T.S.Ean, S.C.Kang, K.Y.Xian, L.S.Chow, Y.P.Herreros, J.M.C.Dominguez, C.I.Ciullo, A.Crump, J.Griffee, M.Kida, Y.Mone, M.Rosenberger, D.Stuart, A.Clarke, E.Costigan, E.Cregan, R.Greene, C.Lennon, J.McNally, P.Clohisey, S.Codan, C.Cody, C.Marshal, M.O’Halloran, S.Supic, D.Coles, M.Joseph, M.Loschner, A.L.Colin, G.Decours, R.Guimard, T.Collins, M.Elapavaluru, S.Colombo, S.M.Grasselli, G.Leone, M.Panigada, M.Pesenti, A.Zanella, A.Combs, P.Song, T.Connor, M.Dalton, J.Donohue, C.Gamble, C.Girvan, M.Halpin, S.Harrison, J.Jackson, C.Saviciute, E.Cooke, G.S.Sriskandan, S.Copland, M.Dechert, W.Reeve, B.Corley, A.Dalton, H.Forsyth, S.Fraser, J.F.Hinton, S.Bassi, G.L.Shrapnel, S.Suen, J.Y.Yerkovich, S.Corvaisier, G.Langelot-Richard, M.Lariviere, D.Cousse, S.Goubert, L.Langlois, V.Cristella, C.de Jong, M.Janes, V.Scicluna, B.Willigen, H.V.Croonen, S.de Vries, P.Hattem, J.V.Crowl, G.Kandel, C.Powis, J.Cruz, C.Dias, A.Leal, E.Santos, M.L.Maltez, F.Pinto, R.Póvoas, D.Torres, M.Csete, M.Poli, S.Quesada, L.Saba, I.Cummings, M.O’Donnell, M.Curlier, E.Fabre, I.Markowicz, S.Ouissa, R.Roger, P.-M.da Silva Filipe, A.McDonald, S.E.Palmarini, M.Robertson, D.L.Scott, J.T.Thomson, E.C.Dabaliz, A.-A.Elshazly, T.McCloskey, C.Dahly, D.de Loughry, G.Hakak, S.Murphy, A.Singh, P.Smyth, C.Daniel, C.Dankwa, E.A.Donnelly, C.A.D’Aragon, F.Lamontagne, F.Marquis, C.de Pinho Oliveira, A.I.Eira, C.Patrão, L.De Rosa, R.De Rose, C.Ricchiuto, A.Sinatti, D.Valentini, P.de Silva, T.Deacon, J.Joshi, S.Marino, D.Menkiti, O.Quinones-Cardona, V.Dean, D.Debard, A.Delobel, P.Martin-Blondel, G.Rafiq, M.Rousset, S.Sarton, B.DeCastro, N.Liegeon, G.Ponscarme, D.Defous, E.Geraud, E.Resseguier, A.-S.Delaveuve, E.Dunand, P.Jaud-Fischer, C.Delavigne, K.Delfos, N.M.Feltz, M.V.D.Dell’Amore, A.Demonchy, E.Michelanglei, C.Risso, K.Denis, E.Fraser, C.Higgins, R.Kelly, S.Kennon, K.Lee, J.Lee, J.Moore, S.Smith, S.Depuydt, P.Wong, C.Desai, M.Diaz, J.J.Diaz, P.Ferreira, I.Maia, A.R.Martins, N.Melo, L.Mendes, J.J.Diaz, R.Dieperink, W.Postma, D.F.Stienstra, Y.Voort, P.V.D.Dimet, J.Morlaes, L.G.Illes, H.-G.Loufti, B.Dishon, Y.Haber, D.Paul, M.Zahran, M.Djossou, F.Kpangon, A.Mergeay-Fabre, M.Docherty, A.B.Drake, T.Fairfield, C.J.Harrison, E.M.Knight, S.R.McLean, K.A.Norman, L.Pius, R.Shaw, C.A.Donnelly, M.Fahy, A.Kelly, Y.Mason, S.Tierney, P.Douglas, J.J.Sahraei, V.Douma, R.Downer, T.Gavin, A.Hennessy, M.Higgins, D.Kelly, A.Kosgei, C.Purcell, G.Downing, M.Sultana, A.Dubee, V.Ducancelle, A.Mahieu, R.Duculan, T.Dudman, S.Dyrhol-Riise, A.M.Skeie, L.G.Hesstvedt, L.Holter, J.C.Jenum, S.Granerud, B.K.Lind, A.Müller, F.Pettersen, F.O.Quist-Paulsen, E.Reikvam, D.H.Holten, A.R.Stiksrud, B.Tonby, K.Duggal, A.Houltham, S.King, A.Krishnan, S.Mehkri, O.Durham, L.Neumann, E.Dussol, B.Duthoit, J.Meybeck, A.Robineau, O.Senneville, E.Sanharawi, M.E.Ellerbroek, J.Enderle, I.Endo, T.Esperatti, M.Fuentes, N.Villoldo, A.Everding, A.G.Ferreira, B.Evers, M.Hoiting, O.Prinssen, A.Fabre, M.Faheem, A.Katz, K.Fakar, Z.Fatoni, A.Z.Fayed, M.Garcia, R.Fernandes, S.Reis, R.Sousa, M.Uva, M.S.Ferrand, F.-X.Guego, M.Nghi, A.Flament, T.Garot, D.Gissot, V.Lemaignen, A.Mankikian, J.Mercier, E.Plantier, L.Gandonniere, C.S.Fletcher, T.Morton, B.Flynn, B.Fontela, P.Foster, D.Foti, G.Giani, M.Fourn, E.Salvator, H.Zucman, D.Fowler, 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In: Scientific Reports. (Scientific Reports, December 2024, 14(1))
Academic Journal
Mammi P; From the Rehabilitation Medicine Unit, Medical, Geriatric and Rehabilitation Department, University Hospital of Parma, Parma, Italy (PM, ER, AR, DR, AC, SM, EG, RB); and Department of Medicine and Surgery, University of Parma, Parma, Italy (FR).; Ranza ERampello ARavanetti DCavaldonati AMoretti SGobbi ERodà FBrianti R
Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 8803677 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-7385 (Electronic) Linking ISSN: 08949115 NLM ISO Abbreviation: Am J Phys Med Rehabil Subsets: MEDLINE
Academic Journal
Schalk A; Institut de génétique médicale d'Alsace (IGMA), Laboratoire de Diagnostic Génétique, Hôpitaux universitaires de Strasbourg, Strasbourg, Alsace, France.; Cousin MA; Department of Quantitative Health Sciences Research, Mayo Clinic, Rochester, Minnesota, USA.; Center for Individualized Medicine, Mayo Clinic, Rochester, Minnesota, USA.; Dsouza NR; Bioinformatics Research and Development Laboratory, Genomics Sciences and Precision Medicine Center, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.; Challman TD; Autism & Developmental Medicine Institute, Geisinger-Lewistown Hospital, Lewistown, Pennsylvania, USA.; Wain KE; Autism & Developmental Medicine Institute, Geisinger-Lewistown Hospital, Lewistown, Pennsylvania, USA.; Powis Z; Department of Clinical Genomics, Ambry Genetics Corp, Aliso Viejo, California, USA.; Minks K; Department of Clinical Genomics, Ambry Genetics Corp, Aliso Viejo, California, USA.; Trimouille A; Service de Génétique Médicale, Centre de Référence Anomalies du Développement et Syndrome Malformatifs, Centre Hospitalier Universitaire de Bordeaux, Bordeaux, Aquitaine, France.; Maladies rares: Génétique et Métabolisme (MRGM), INSERM U1211, Université de Bordeaux Centre de Génomique Fonctionnelle de Bordeaux, Bordeaux, Nouvelle-Aquitaine, France.; Lasseaux E; Service de Génétique Médicale, Centre de Référence Anomalies du Développement et Syndrome Malformatifs, Centre Hospitalier Universitaire de Bordeaux, Bordeaux, Aquitaine, France.; Lacombe D; Service de Génétique Médicale, Centre de Référence Anomalies du Développement et Syndrome Malformatifs, Centre Hospitalier Universitaire de Bordeaux, Bordeaux, Aquitaine, France.; Maladies rares: Génétique et Métabolisme (MRGM), INSERM U1211, Université de Bordeaux Centre de Génomique Fonctionnelle de Bordeaux, Bordeaux, Nouvelle-Aquitaine, France.; Angelini C; Service de Génétique Médicale, Centre de Référence Anomalies du Développement et Syndrome Malformatifs, Centre Hospitalier Universitaire de Bordeaux, Bordeaux, Aquitaine, France.; Maladies rares: Génétique et Métabolisme (MRGM), INSERM U1211, Université de Bordeaux Centre de Génomique Fonctionnelle de Bordeaux, Bordeaux, Nouvelle-Aquitaine, France.; Michaud V; Service de Génétique Médicale, Centre de Référence Anomalies du Développement et Syndrome Malformatifs, Centre Hospitalier Universitaire de Bordeaux, Bordeaux, Aquitaine, France.; Maladies rares: Génétique et Métabolisme (MRGM), INSERM U1211, Université de Bordeaux Centre de Génomique Fonctionnelle de Bordeaux, Bordeaux, Nouvelle-Aquitaine, France.; Van-Gils J; Département de Génétique Médicale, Centre de Référence Anomalies du Développement et Syndrome Malformatifs, Centre Hospitalier Universitaire de Bordeaux, Bordeaux, Aquitaine, France.; Spataro N; Genetics Laboratory, UDIAT-Centre Diagnòstic, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí, Sabadell, Catalunya, Spain.; Ruiz A; Genetics Laboratory, UDIAT-Centre Diagnòstic, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí, Sabadell, Catalunya, Spain.; Gabau E; Paediatric Unit, Parc Tauli Foundation-UAB University Institute, Sabadell, Catalunya, Spain.; Stolerman E; 106 Gregor Mendel Cir, Greenwood Genetic Center Inc, Greenwood, South Carolina, USA.; Washington C; 106 Gregor Mendel Cir, Greenwood Genetic Center Inc, Greenwood, South Carolina, USA.; Louie R; 106 Gregor Mendel Cir, Greenwood Genetic Center Inc, Greenwood, South Carolina, USA.; Lanpher BC; Center for Individualized Medicine, Mayo Clinic, Rochester, Minnesota, USA.; Department of Clinical Genomics, Mayo Clinic, Rochester, Minnesota, USA.; Kemppainen JL; Center for Individualized Medicine, Mayo Clinic, Rochester, Minnesota, USA.; Department of Clinical Genomics, Mayo Clinic, Rochester, Minnesota, USA.; Innes M; Department of Medical Genetics and Alberta Children's Hospital Research Institute, University of Calgary Cumming School of Medicine, Calgary, Alberta, Canada.; Kooy F; Center Medical Genetics, University Hospital Antwerp, Antwerp, Belgium.; Meuwissen M; Center Medical Genetics, University Hospital Antwerp, Antwerp, Belgium.; Goldenberg A; Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics and Reference Center for Developmental Disorders, Centre Hospitalier Universitaire de Rouen, Rouen, Normandie, France.; Lecoquierre F; Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics and Reference Center for Developmental Disorders, Centre Hospitalier Universitaire de Rouen, Rouen, Normandie, France.; Vera G; Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics and Reference Center for Developmental Disorders, Centre Hospitalier Universitaire de Rouen, Rouen, Normandie, France.; Diderich KEM; Erasmus Medical Center Department of Clinical Genetics, Rotterdam, Netherlands.; Sheidley B; Division of Epilepsy and Clinical Neurophysiology, Department of Neurology, Boston Children's Hospital, Boston, Massachusetts, USA.; El Achkar CM; Division of Epilepsy and Clinical Neurophysiology, Department of Neurology, Boston Children's Hospital, Boston, Massachusetts, USA.; Park M; Division of Epilepsy and Clinical Neurophysiology, Department of Neurology, Boston Children's Hospital, Boston, Massachusetts, USA.; Hamdan FF; Division of Medical Genetics, Department of Pediatrics, Saint Justine Hospital, Montreal, Quebec, Canada.; Michaud JL; Division of Medical Genetics, Department of Pediatrics, Saint Justine Hospital, Montreal, Quebec, Canada.; Lewis AJ; Pediatric Neurology, Kaiser Permanente Santa Clara Medical Center, Santa Clara, California, USA.; Zweier C; Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.; Department of Human Genetics, Inselspital University Hospital Bern, Bern, BE, Switzerland.; Reis A; Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.; Wagner M; Institute of Human Genetics, Technische Universitat Munchen, Munchen, Bayern, Germany.; Institute of Neurogenomics, Helmholtz Zentrum Munchen Deutsches Forschungszentrum fur Umwelt und Gesundheit, Neuherberg, Bayern, Germany.; Weigand H; Division of Pediatric Neurology, Developmental Medicine and Social Pediatrics, Department of Pediatrics, Dr von Hauner Children's Hospital, Munich University Hospital (Ludwig Maximilians University), Munchen, Bayern, Germany.; Journel H; Service de Génétique Médicale, Hopital Chubert, Vannes, Bretagne, France.; Keren B; Département de Génétique et de Cytogénétique, Centre de Reference Déficience Intellectuelle de Causes Rares, GRC UPMC « Déficience Intellectuelle et Autisme », Hôpital Universitaire Pitié Salpêtrière, Paris, Île-de-France, France.; INSERM U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle Épinière, Paris, Île-de-France, France.; Passemard S; APHP, Hopital Universitaire Robert-Debre Departement de genetique, Paris, Île-de-France, France.; NeuroDiderot, UMR1141, INSERM, Paris, France.; Mignot C; Département de Génétique et de Cytogénétique, Centre de Reference Déficience Intellectuelle de Causes Rares, GRC UPMC « Déficience Intellectuelle et Autisme », Hôpital Universitaire Pitié Salpêtrière, Paris, Île-de-France, France.; INSERM U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle Épinière, Paris, Île-de-France, France.; van Gassen K; Department of Genetics, University Medical Centre Utrecht Center for Molecular Medicine, Utrecht, The Netherlands.; Brilstra EH; Department of Genetics, University Medical Centre Utrecht Center for Molecular Medicine, Utrecht, The Netherlands.; Itzikowitz G; Department of Paediatrics and Child Health, Red Cross War Memorial Children's Hospital, Rondebosch, Western Cape, South Africa.; O'Heir E; Center for Mendelian Genomics and Program in Medical and Population Genetics, Broad Institute for Genome Research, Cambridge, Massachusetts, USA.; Division of Genetics and Genomics, Boston Children's Hospital, Boston, Massachusetts, USA.; Allen J; Stanley Center for Psychiatric Research, Broad Institute Stanley Center for Psychiatric Research, Cambridge, Massachusetts, USA.; Donald KA; Department of Paediatrics and Child Health, Red Cross War Memorial Children's Hospital, Rondebosch, Western Cape, South Africa.; Neuroscience Institute, University of Cape Town, Rondebosch, Western Cape, South Africa.; Korf BR; Department of Genetics, The University of Alabama at Birmingham, Birmingham, Alabama, USA.; Skelton T; Department of Genetics, The University of Alabama at Birmingham, Birmingham, Alabama, USA.; Thompson M; Department of Genetics, The University of Alabama at Birmingham, Birmingham, Alabama, USA.; HudsonAlpha Institute, HudsonAlpha Institute for Biotechnology, Huntsville, Alabama, USA.; Robin NH; Department of Genetics, The University of Alabama at Birmingham, Birmingham, Alabama, USA.; Rudy NL; Department of Genetics, The University of Alabama at Birmingham, Birmingham, Alabama, USA.; Dobyns WB; Department of Pediatrics (Genetics) and Neurology, University of Washington, Seattle Children's Research Institute, Seattle, Washington, USA.; Foss K; Department of Pediatrics (Genetics) and Neurology, University of Washington, Seattle Children's Research Institute, Seattle, Washington, USA.; Zarate YA; Section of Genetics and Metabolism, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.; Bosanko KA; Section of Genetics and Metabolism, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.; Alembik Y; Institut de génétique médicale d'Alsace (IGMA), Service de Génétique Médicale, Hôpitaux universitaires de Strasbourg, Strasbourg, Alsace, France.; Durand B; Institut de génétique médicale d'Alsace (IGMA), Service de Génétique Médicale, Hôpitaux universitaires de Strasbourg, Strasbourg, Alsace, France.; Tran Mau-Them F; Institut de génétique médicale d'Alsace (IGMA), Laboratoire de Diagnostic Génétique, Hôpitaux universitaires de Strasbourg, Strasbourg, Alsace, France.; Ranza E; Medigenome, Swiss Institute of Medicine, Bern, Bern, Switzerland.; Blanc X; Medigenome, Swiss Institute of Medicine, Bern, Bern, Switzerland.; Antonarakis SE; Medigenome, Swiss Institute of Medicine, Bern, Bern, Switzerland.; McWalter K; GeneDx, GeneDx, Gaithersburg, Maryland, USA.; Torti E; GeneDx, GeneDx, Gaithersburg, Maryland, USA.; Millan F; GeneDx, GeneDx, Gaithersburg, Maryland, USA.; Dameron A; GeneDx, GeneDx, Gaithersburg, Maryland, USA.; Tokita M; GeneDx, GeneDx, Gaithersburg, Maryland, USA.; Zimmermann MT; Bioinformatics Research and Development Laboratory, Genomics Sciences and Precision Medicine Center, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.; Department of Biochemistry, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.; Klee EW; Department of Quantitative Health Sciences Research, Mayo Clinic, Rochester, Minnesota, USA.; Center for Individualized Medicine, Mayo Clinic, Rochester, Minnesota, USA.; Department of Clinical Genomics, Mayo Clinic, Rochester, Minnesota, USA.; Piton A; Neurogenetics and Translational Medecine, Institut of Genetics and Molecular and Cellular Biology, Illkirch-Grafenstaden, Grand Est, France piton@igbmc.fr.; Gerard B; Institut de génétique médicale d'Alsace (IGMA), Laboratoire de Diagnostic Génétique, Hôpitaux universitaires de Strasbourg, Strasbourg, Alsace, France.
Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE
Rodan LH; Division of Genetics and Genomics, Department of Pediatrics, Boston Children's Hospital, Boston, MA, USA.; Department of Neurology, Boston Children's Hospital, Boston, MA, USA.; Spillmann RC; Division of Medical Genetics, Department of Pediatrics, Duke Health, Durham, NC, USA.; Kurata HT; Department of Pharmacology, Alberta Diabetes Institute, University of Alberta, Edmonton, AB, Canada.; Lamothe SM; Department of Pharmacology, Alberta Diabetes Institute, University of Alberta, Edmonton, AB, Canada.; Maghera J; Department of Pharmacology, Alberta Diabetes Institute, University of Alberta, Edmonton, AB, Canada.; Jamra RA; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Alkelai A; Institute for Genomic Medicine, Columbia University Medical Center, New York, NY, USA.; Antonarakis SE; Medigenome, Swiss Institute of Genomic Medicine, Geneva, Switzerland.; Atallah I; Division of Genetic Medicine, Lausanne University Hospital, Lausanne, Switzerland.; Bar-Yosef O; Pediatric Neurology Unit, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel-Hahsomer, Israel.; Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.; Bilan F; CHU de Poitiers, Service de Génétique, EA3808 NEUVACOD, Poitiers, France.; Bjorgo K; Department of Medical Genetics, Oslo University Hospital, Oslo, Norway.; Blanc X; Medigenome, Swiss Institute of Genomic Medicine, Geneva, Switzerland.; Van Bogaert P; CHU d'Angers, Service de Pédiatrie, EA3808 NEUVACOD, Angers, France.; Bolkier Y; Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.; Pediatric Cardiology Unit, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel-Hahsomer, Israel.; Burrage LC; Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Christ BU; Department of Paediatrics and Child Health, Red Cross War Memorial Children's Hospital, University of Cape Town, Cape Town, SA, South Africa.; Granadillo JL; Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine in St. Louis, St. Louis, MO, USA.; Dickson P; Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine in St. Louis, St. Louis, MO, USA.; Donald KA; Department of Paediatrics and Child Health, Red Cross War Memorial Children's Hospital, University of Cape Town, Cape Town, SA, South Africa.; Dubourg C; Service de Génétique Moléculaire et Génomique, CHU, Rennes, France.; University of Rennes, CNRS, IGDR, UMR 6290, Rennes, France.; Eliyahu A; Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.; The Danek Gertner Insitute of Human Genetics, Sheba Medical Center, Tel-Hahsomer, Israel.; Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel-Hahsomer, Israel.; Emrick L; Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Engleman K; Center for Pediatric Genomic Medicine, Children's Mercy Hospital, Kansas City, MO, USA.; Gonfiantini MV; Rare Diseases and Medical Genetic Unit, IRCCS Bambino Gesù Children's Hospital, Rome, Italy.; Good JM; Pediatric Neurology, Lausanne University Hospital, Lausanne, Switzerland.; Kalser J; Pediatric Neurology, Lausanne University Hospital, Lausanne, Switzerland.; Kloeckner C; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Lachmeijer G; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; Macchiaiolo M; Rare Diseases and Medical Genetic Unit, IRCCS Bambino Gesù Children's Hospital, Rome, Italy.; Nicita F; Unit of Neuromuscular and Neurodegenerative Diseases, Department of Neurosciences and Neurorehabilitation, IRCCS Bambino Gesù Children's Hospital, Rome, Italy.; Odent S; Service de Génétique Clinique, Centre de référence 'Maladies Rares' Anomalies du développement CLAD-Ouest, Hôpital SUD, Échirolles, France.; O'Heir E; Division of Genetics and Genomics, Department of Pediatrics, Boston Children's Hospital, Boston, MA, USA.; Center for Mendelian Genomics and Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Ortiz-Gonzalez X; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Pacio-Miguez M; Instituto de Genética Médica y Molecular (INGEMM), Hospital Universitario La Paz, IdiPAZ, CIBERER, ISCIII, Madrid, Spain.; Palomares-Bralo M; Instituto de Genética Médica y Molecular (INGEMM), Hospital Universitario La Paz, IdiPAZ, CIBERER, ISCIII, Madrid, Spain.; Pena L; Cincinnati Children's Hospital and Medical Center Cincinnati, Cincinnati, OH, USA.; University of Cincinnati College of Medicine Cincinnati, Cincinnati, OH, USA.; Platzer K; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Quinodoz M; Institute of Molecular and Clinical Ophthalmology Basel (IOB), Basel, Switzerland.; Department of Ophthalmology, University of Basel, Basel, Switzerland.; Ranza E; Medigenome, Swiss Institute of Genomic Medicine, Geneva, Switzerland.; Rosenfeld JA; Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Roulet-Perez E; Pediatric Neurology, Lausanne University Hospital, Lausanne, Switzerland.; Santani A; Division of Genomic Diagnostics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.; Santos-Simarro F; Instituto de Genética Médica y Molecular (INGEMM), Hospital Universitario La Paz, IdiPAZ, CIBERER, ISCIII, Madrid, Spain.; Pode-Shakked B; Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.; Institute of Rare Diseases, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel-Hahsomer, Israel.; Skraban C; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Slaugh R; Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine in St. Louis, St. Louis, MO, USA.; Superti-Furga A; Pediatric Neurology, Lausanne University Hospital, Lausanne, Switzerland.; Thiffault I; Center for Pediatric Genomic Medicine, Children's Mercy Hospital, Kansas City, MO, USA.; van Jaabrsveld RH; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; Vincent M; Service de Génétique Médicale, CHU Nantes, France; Inserm, CNRS, Univ Nantes, l'institut du thorax, Nantes, France.; Wang HG; Cardiovascular Research Institute, Weill Cornell Medicine, New York, NY, USA.; Zacher P; The Saxon Epilepsy Center Kleinwachau, Radeberg, Germany.; Rush E; The Children's Mercy Hospital, Kansas City, MO, USA.; Department of Pediatrics University of Missouri-Kansas City, Kansas City, MO, USA.; Department of Internal Medicine, University of Kansas Medical Center, Kansas City, MO, USA.; Pitt GS; Cardiovascular Research Institute, Weill Cornell Medicine, New York, NY, USA.; Au PYB; Alberta Children's Hospital Research Institute, Department of Genetics, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.; Shashi V; Division of Medical Genetics, Department of Pediatrics, Duke Health, Durham, NC, USA. vandana.shashi@duke.edu.
Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: PubMed not MEDLINE; MEDLINE
Academic Journal
Ranza E; Service de médecine génomique des maladies rares, Hôpital Necker-Enfants Malades (AP-HP centre), Paris, France.; Service de Médecine génétique, Hôpitaux Universitaires de Genève, Genève, Switzerland.; Medigenome, Swiss Institute of Genomic Medicine, Geneva, Switzerland.; Le Gouez M; Service de Pédiatrie, Hôpital Necker-Enfants Malades (AP-HP), Paris, France.; Guimier A; Service de médecine génomique des maladies rares, Hôpital Necker-Enfants Malades (AP-HP centre), Paris, France.; Institut Imagine, Inserm U1163, Université de Paris, Paris, France.; Dunlop NK; Service de Chirurgie Viscérale, Urologique et de Transplantation pédiatrique, Hôpital Universitaire Necker-Enfants Malades (AP-HP et Université de Paris), Paris, France.; Beaudoin S; Service de Chirurgie Viscérale, Urologique et de Transplantation pédiatrique, Hôpital Universitaire Necker-Enfants Malades (AP-HP et Université de Paris), Paris, France.; Malan V; Service de médecine génomique des maladies rares, Hôpital Necker-Enfants Malades (AP-HP centre), Paris, France.; Michot C; Service de médecine génomique des maladies rares, Hôpital Necker-Enfants Malades (AP-HP centre), Paris, France.; Baujat G; Service de médecine génomique des maladies rares, Hôpital Necker-Enfants Malades (AP-HP centre), Paris, France.; Rio M; Service de médecine génomique des maladies rares, Hôpital Necker-Enfants Malades (AP-HP centre), Paris, France.; Cormier-Daire V; Service de médecine génomique des maladies rares, Hôpital Necker-Enfants Malades (AP-HP centre), Paris, France.; Institut Imagine, Inserm U1163, Université de Paris, Paris, France.; Abadie V; Service de Pédiatrie, Hôpital Necker-Enfants Malades (AP-HP), Paris, France.; Sarnacki S; Service de Chirurgie Viscérale, Urologique et de Transplantation pédiatrique, Hôpital Universitaire Necker-Enfants Malades (AP-HP et Université de Paris), Paris, France.; Delacourt C; Service de Pneumologie Pédiatrique, Hôpital Necker-Enfants Malades (AP-HP), Paris, France.; Lyonnet S; Service de médecine génomique des maladies rares, Hôpital Necker-Enfants Malades (AP-HP centre), Paris, France.; Institut Imagine, Inserm U1163, Université de Paris, Paris, France.; Attié-Bitach T; Service de médecine génomique des maladies rares, Hôpital Necker-Enfants Malades (AP-HP centre), Paris, France.; Institut Imagine, Inserm U1163, Université de Paris, Paris, France.; Pingault V; Service de médecine génomique des maladies rares, Hôpital Necker-Enfants Malades (AP-HP centre), Paris, France.; Institut Imagine, Inserm U1163, Université de Paris, Paris, France.; Rousseau V; Service de Chirurgie Viscérale, Urologique et de Transplantation pédiatrique, Hôpital Universitaire Necker-Enfants Malades (AP-HP et Université de Paris), Paris, France.; Amiel J; Service de médecine génomique des maladies rares, Hôpital Necker-Enfants Malades (AP-HP centre), Paris, France.; Institut Imagine, Inserm U1163, Université de Paris, Paris, France.
Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE
Academic Journal
Küry S; Nantes Université, CHU Nantes, Service de Génétique Médicale, Nantes, France; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France. Electronic address: sebastien.kury@chu-nantes.fr.; Zhang J; Hatherly Laboratories, The Institute of Biomedical and Clinical Sciences, College of Medicine and Health, University of Exeter, Exeter, United Kingdom; Department of Neurosurgery, Yale School of Medicine, Yale University, New Haven, CT; State Key Laboratory of Bio-Organic and Natural Products Chemistry, Research Center of Chemical Kinomics, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai, China.; Besnard T; Nantes Université, CHU Nantes, Service de Génétique Médicale, Nantes, France; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France.; Caro-Llopis A; Unidad de Genética, Hospital Universitario y Politécnico La Fe, Valencia, Spain.; Zeng X; Department of Genetics, Yale School of Medicine, Yale University, New Haven, CT.; Robert SM; Department of Genetics, Yale School of Medicine, Yale University, New Haven, CT.; Josiah SS; Hatherly Laboratories, The Institute of Biomedical and Clinical Sciences, College of Medicine and Health, University of Exeter, Exeter, United Kingdom.; Kiziltug E; Department of Genetics, Yale School of Medicine, Yale University, New Haven, CT.; Denommé-Pichon AS; Département de Biochimie et Génétique, Centre Hospitalier Universitaire Angers, Angers, France; UMR CNRS 6214, INSERM 1083, Université d'Angers, Angers, France.; Cogné B; Nantes Université, CHU Nantes, Service de Génétique Médicale, Nantes, France; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France.; Kundishora AJ; Department of Neurosurgery, Yale School of Medicine, Yale University, New Haven, CT.; Hao LT; Department of Neurosurgery, Yale School of Medicine, Yale University, New Haven, CT.; Li H; Departments of Human Genetics and Pediatrics, School of Medicine, Emory University, Atlanta, GA.; Stevenson RE; Greenwood Genetic Center, Greenwood, SC.; Louie RJ; Greenwood Genetic Center, Greenwood, SC.; Deb W; Nantes Université, CHU Nantes, Service de Génétique Médicale, Nantes, France; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France.; Torti E; GeneDx, Gaithersburg, MD.; Vignard V; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France.; McWalter K; GeneDx, Gaithersburg, MD.; Raymond FL; Department of Medical Genetics, Cambridge Institute for Medical Research, University of Cambridge, Biomedical Campus Cambridge, Cambridge, United Kingdom.; Rajabi F; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA.; Ranza E; Medigenome, Swiss Institute of Genomic Medicine, Geneva, Switzerland.; Grozeva D; Department of Medical Genetics, Cambridge Institute for Medical Research, University of Cambridge, Biomedical Campus Cambridge, Cambridge, United Kingdom; Centre for Trials Research, Cardiff University, Cardiff, United Kingdom.; Coury SA; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA.; Blanc X; Medigenome, Swiss Institute of Genomic Medicine, Geneva, Switzerland.; Brischoux-Boucher E; Centre de Génétique Humaine, CHU de Besançon, Université de Bourgogne Franche-Comté, Besançon, France.; Keren B; Department of Genetics, Centre de Référence Déficiences Intellectuelles de Causes Rares, Pitié-Salpêtrière Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.; Õunap K; Department of Clinical Genetics, Genetics and Personalized Medicine Clinic, Tartu University Hospital, Tartu, Estonia; Department of Clinical Genetics, Institute of Clinical Medicine, Faculty of Medicine, University of Tartu, Tartu, Estonia.; Reinson K; Department of Clinical Genetics, Genetics and Personalized Medicine Clinic, Tartu University Hospital, Tartu, Estonia; Department of Clinical Genetics, Institute of Clinical Medicine, Faculty of Medicine, University of Tartu, Tartu, Estonia.; Ilves P; Department of Clinical Genetics, Institute of Clinical Medicine, Faculty of Medicine, University of Tartu, Tartu, Estonia; Department of Radiology, Tartu University Hospital, Tartu, Estonia.; Wentzensen IM; GeneDx, Gaithersburg, MD.; Barr EE; Departments of Human Genetics and Pediatrics, School of Medicine, Emory University, Atlanta, GA.; Guihard SH; Department of Genetics, Centre de Référence Déficiences Intellectuelles de Causes Rares, Pitié-Salpêtrière Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France; Groupe de Recherche Clinique, Déficience Intellectuelle et Autisme, Sorbonne University, Paris, France.; Charles P; Department of Genetics, Centre de Référence Déficiences Intellectuelles de Causes Rares, Pitié-Salpêtrière Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.; Seaby EG; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA; Genomic Informatics Group, University of Southampton, Southampton, United Kingdom.; Monaghan KG; GeneDx, Gaithersburg, MD.; Rio M; Developmental Brain Disorders laboratory, INSERM UMR 1163, Imagine Institute, University of Paris, Paris, France; Department of Genetics, Centre de Référence Déficiences Intellectuelles de Causes Rares, Necker Enfants Malades Hospital, APHP, Paris, France.; van Bever Y; Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, the Netherlands.; van Slegtenhorst M; Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, the Netherlands.; Chung WK; Departments of Pediatrics and Medicine, Columbia University Irving Medical Center, Columbia University New York, NY.; Wilson A; Division of Clinical Genetics, Department of Pediatrics, Columbia University Vagelos College of Physicians and Surgeons and New York-Presbyterian Morgan Stanley Children's Hospital, New York, NY.; Quinquis D; Nantes Université, CHU Nantes, Service de Génétique Médicale, Nantes, France.; Bréhéret F; Nantes Université, CHU Nantes, Service de Génétique Médicale, Nantes, France.; Retterer K; GeneDx, Gaithersburg, MD.; Lindenbaum P; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France.; Scalais E; Division of Pediatric Neurology, Department of Pediatrics, Centre Hospitalier de Luxembourg, Luxembourg City, Luxembourg.; Rhodes L; GeneDx, Gaithersburg, MD.; Stouffs K; Neurogenetics Research Group, Reproduction and Genetics, Vrije Universiteit Brussel (VUB), Universitair Ziekenhuis Brussel (UZ Brussel), Laarbeeklaan, Brussels, Belgium.; Pereira EM; Division of Clinical Genetics, Department of Pediatrics, Columbia University Vagelos College of Physicians and Surgeons and New York-Presbyterian Morgan Stanley Children's Hospital, New York, NY.; Berger SM; Division of Clinical Genetics, Department of Pediatrics, Columbia University Vagelos College of Physicians and Surgeons and New York-Presbyterian Morgan Stanley Children's Hospital, New York, NY.; Milla SS; Department of Radiology and Imaging Sciences, School of Medicine, Emory University, Atlanta, GA.; Jaykumar AB; Department of Pharmacology, UT Southwestern Medical Center, Dallas, TX.; Cobb MH; Department of Pharmacology, UT Southwestern Medical Center, Dallas, TX.; Panchagnula S; Unidad de Genética, Hospital Universitario y Politécnico La Fe, Valencia, Spain.; Duy PQ; Department of Neurosurgery, Yale School of Medicine, Yale University, New Haven, CT.; Vincent M; Nantes Université, CHU Nantes, Service de Génétique Médicale, Nantes, France; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France.; Mercier S; Nantes Université, CHU Nantes, Service de Génétique Médicale, Nantes, France; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France.; Gilbert-Dussardier B; Service de Génétique, CHU Poitiers, Poitiers, France.; Le Guillou X; Service de Génétique, CHU Poitiers, Poitiers, France.; Audebert-Bellanger S; Génétique Médicale, CHRU Brest, Brest, France.; Odent S; Service de Génétique Clinique, ERN ITHACA, CHU Rennes, Rennes, France; Institut de Génétique et Développement de Rennes, IGDR UMR 6290 CNRS, INSERM, IGDR Univ Rennes, Rennes, France.; Schmitt S; Nantes Université, CHU Nantes, Service de Génétique Médicale, Nantes, France.; Boisseau P; Nantes Université, CHU Nantes, Service de Génétique Médicale, Nantes, France.; Bonneau D; Département de Biochimie et Génétique, Centre Hospitalier Universitaire Angers, Angers, France; UMR CNRS 6214, INSERM 1083, Université d'Angers, Angers, France.; Toutain A; Unité de Génétique Médicale, Centre Hospitalier Régional Universitaire de Tours, France; Unité Mixte de Recherche 1253, iBrain, Université de Tours, Institut National de la Santé et de la Recherche Médicale, Tours, France.; Colin E; Département de Biochimie et Génétique, Centre Hospitalier Universitaire Angers, Angers, France; UMR CNRS 6214, INSERM 1083, Université d'Angers, Angers, France.; Pasquier L; Service de Génétique Clinique, ERN ITHACA, CHU Rennes, Rennes, France; Institut de Génétique et Développement de Rennes, IGDR UMR 6290 CNRS, INSERM, IGDR Univ Rennes, Rennes, France.; Redon R; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France.; Bouman A; Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, the Netherlands.; Rosenfeld JA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX.; Friez MJ; Greenwood Genetic Center, Greenwood, SC.; Pérez-Peña H; Department of Pharmaceutical and Biological Chemistry, UCL School of Pharmacy, University College London, London, United Kingdom.; Akhtar Rizvi SR; Department of Pharmaceutical and Biological Chemistry, UCL School of Pharmacy, University College London, London, United Kingdom.; Haider S; Department of Pharmaceutical and Biological Chemistry, UCL School of Pharmacy, University College London, London, United Kingdom; Centre for Advanced Research Computing, University College London, London, United Kingdom.; Antonarakis SE; Medigenome, Swiss Institute of Genomic Medicine, Geneva, Switzerland; Department of Genetic Medicine and Development, University of Geneva, Geneva, Switzerland; iGE3, Institute of Genetics and Genomics of Geneva, University of Geneva, Geneva, Switzerland.; Schwartz CE; Greenwood Genetic Center, Greenwood, SC.; Martínez F; Unidad de Genética, Hospital Universitario y Politécnico La Fe, Valencia, Spain.; Bézieau S; Nantes Université, CHU Nantes, Service de Génétique Médicale, Nantes, France; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France.; Kahle KT; Department of Neurosurgery, Yale School of Medicine, Yale University, New Haven, CT; Department of Cellular and Molecular Physiology, Yale School of Medicine, Yale University, New Haven, CT; NIH-Yale Centers for Mendelian Genomics, Yale School of Medicine, Yale University, New Haven, CT; Yale Stem Cell Center, Yale School of Medicine, Yale University, New Haven, CT. Electronic address: kahle.kristopher@mgh.harvard.edu.; Isidor B; Nantes Université, CHU Nantes, Service de Génétique Médicale, Nantes, France; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France.
Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: MEDLINE
Academic Journal
Meuwissen M; Center for Medical Genetics, Faculty of Medicine and Health Sciences, Antwerp University Hospital, University of Antwerp, Edegem, Belgium.; Verstraeten A; Center for Medical Genetics, Faculty of Medicine and Health Sciences, Antwerp University Hospital, University of Antwerp, Edegem, Belgium.; Ranza E; Medigenome, Swiss Institute of Genomic Medicine, Geneva, Switzerland.; Iwaszkiewicz J; Molecular Modeling Group, Swiss Institute of Bioinformatics, Lausanne, Switzerland.; Bastiaansen M; Center for Medical Genetics, Faculty of Medicine and Health Sciences, Antwerp University Hospital, University of Antwerp, Edegem, Belgium.; Mateiu L; Center for Medical Genetics, Faculty of Medicine and Health Sciences, Antwerp University Hospital, University of Antwerp, Edegem, Belgium.; Nemegeer M; Center for Medical Genetics, Faculty of Medicine and Health Sciences, Antwerp University Hospital, University of Antwerp, Edegem, Belgium.; Meester JAN; Center for Medical Genetics, Faculty of Medicine and Health Sciences, Antwerp University Hospital, University of Antwerp, Edegem, Belgium.; Afenjar A; Centre de Référence Malformations et Maladies Congénitales du Cervelet et Déficiences Intellectuelles de Causes Rares, Département de Génétique et Embryologie Médicale, Hôpital Trousseau, Sorbonne Université, AP-HP, Paris, France.; Amaral M; HudsonAlpha Institute for Biotechnology, Huntsville, AL.; Ballhausen D; Pediatric Metabolic Unit, Pediatrics, Woman-Mother-Child Department, University of Lausanne and University Hospital of Lausanne, Lausanne, Switzerland.; Barnett S; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN.; Barth M; Biochemistry and Genetics Department, University Hospital of Angers, Angers, France.; Asselbergh B; Neuromics Support Facility, VIB Center for Molecular Neurology, VIB, Antwerp, Belgium; Department of Biomedical Sciences, Faculty of Pharmaceutical, Biomedical and Veterinary Sciences, University of Antwerp, Antwerp, Belgium.; Spaas K; Neuromics Support Facility, VIB Center for Molecular Neurology, VIB, Antwerp, Belgium; Department of Biomedical Sciences, Faculty of Pharmaceutical, Biomedical and Veterinary Sciences, University of Antwerp, Antwerp, Belgium.; Heeman B; Department of Biomedical Sciences, Faculty of Pharmaceutical, Biomedical and Veterinary Sciences, University of Antwerp, Antwerp, Belgium; Applied and Translational Neurogenomics, VIB Center for Molecular Neurology, VIB, Antwerp, Belgium.; Bassetti J; Division of Medical Genetics, Department of Pediatrics, Weill Cornell Medicine, New York, NY.; Blackburn P; Department of Pathology, St. Jude Children's Research Hospital, Memphis, TN.; Schaer M; Autism Brain & Behavior Laboratory, Department Psychiatry, Faculty of Medicine, University of Geneva, Geneva, Switzerland.; Blanc X; Medigenome, Swiss Institute of Genomic Medicine, Geneva, Switzerland.; Zoete V; Molecular Modeling Group, Swiss Institute of Bioinformatics, Lausanne, Switzerland; Ludwig Institute for Cancer Research, Department of Fundamental Oncology, Faculty of Biology and Medicine, Lausanne University, Epalinges, Lausanne, Switzerland.; Casas K; Medical Genetics, Sanford Broadway Clinic, Fargo, ND.; Courtin T; Department of Genetics, AP-HP, La Pitié-Salpêtrière Hospital, Sorbonne Université, Paris.; Doummar D; Neuropédiatrie, AP-HP, Hôpital d'enfants Armand Trousseau, Sorbonne Université, Paris.; Guerry F; Medigenome, Swiss Institute of Genomic Medicine, Geneva, Switzerland.; Keren B; Department of Genetics, AP-HP, La Pitié-Salpêtrière Hospital, Sorbonne Université, Paris.; Pappas J; NYU Langone Medical Center, New York, NY.; Rabin R; NYU Langone Medical Center, New York, NY.; Begtrup A; GeneDx, Gaithersburg, MD.; Shinawi M; Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine in St. Louis, St. Louis, MO.; Vulto-van Silfhout AT; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.; Kleefstra T; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.; Wagner M; Institute of Human Genetics, Technical University München, Munich, Germany; Institute for Neurogenomics, Helmholtz Zentrum München, Neuherberg, Germany.; Ziegler A; Biochemistry and Genetics Department, University Hospital of Angers, Angers, France.; Schaefer E; Service de Génétique Médicale, Institut de Génétique Médicale d'Alsace, Hopitaux Universitaires de Strasbourg, Strasbourg, France.; Gerard B; Laboratoires de Diagnostic Génétique, Institut de Génétique Médicale d'Alsace, Hopitaux Universitaires de Strasbourg, Strasbourg, France.; De Bie CI; Department of Clinical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; Holwerda SJB; Department of Clinical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; Abbot MA; Medical Genetics, Department of Pediatrics, University of Massachusetts Medical School-Baystate, Springfield, MA.; Antonarakis SE; Medigenome, Swiss Institute of Genomic Medicine, Geneva, Switzerland. Electronic address: stylianos.antonarakis@medigenome.ch.; Loeys B; Center for Medical Genetics, Faculty of Medicine and Health Sciences, Antwerp University Hospital, University of Antwerp, Edegem, Belgium; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands. Electronic address: bart.loeys@uantwerpen.be.
Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: MEDLINE
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