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Tytuł :
Genetic architecture of subcortical brain structures in 38,851 individuals
Autorzy :
Satizabal, Claudia L.Aff1, Aff2, Aff3, Aff4
Adams, Hieab H. H.Aff5, Aff6, Aff7
Hibar, Derrek P.
White, Charles C.Aff9, Aff10
Knol, Maria J.
Stein, Jason L.Aff8, Aff11, Aff12
Scholz, MarkusAff13, Aff14
Sargurupremraj, Muralidharan
Jahanshad, Neda
Roshchupkin, Gennady V.Aff5, Aff6, Aff16
Smith, Albert V.Aff17, Aff18, Aff19
Bis, Joshua C.
Jian, Xueqiu
Luciano, Michelle
Hofer, EdithAff23, Aff24
Teumer, Alexander
van der Lee, Sven J.
Yang, JingyunAff26, Aff27
Yanek, Lisa R.
Lee, Tom V.
Li, Shuo
Hu, Yanhui
Koh, Jia Yu
Eicher, John D.
Desrivières, Sylvane
Arias-Vasquez, AlejandroAff35, Aff36, Aff37, Aff38
Chauhan, GaneshAff15, Aff39
Athanasiu, LaviniaAff40, Aff41
Rentería, Miguel E.
Kim, SungeunAff43, Aff44, Aff45
Hoehn, David
Armstrong, Nicola J.
Chen, Qiang
Holmes, Avram J.Aff49, Aff50
den Braber, AnoukAff51, Aff52, Aff53, Aff54
Kloszewska, Iwona
Andersson, MicaelAff56, Aff57
Espeseth, ThomasAff40, Aff58
Grimm, Oliver
Abramovic, Lucija
Alhusaini, SaudAff61, Aff62
Milaneschi, Yuri
Papmeyer, MartinaAff64, Aff65
Axelsson, Tomas
Ehrlich, StefanAff50, Aff67, Aff68
Roiz-Santiañez, RobertoAff69, Aff70, Aff71
Kraemer, Bernd
Håberg, Asta K.Aff73, Aff74
Jones, Hannah J.Aff75, Aff76, Aff77
Pike, G. BruceAff78, Aff79
Stein, Dan J.Aff80, Aff81
Stevens, Allison
Bralten, JanitaAff36, Aff38
Vernooij, Meike W.Aff5, Aff6
Harris, Tamara B.
Filippi, Irina
Witte, A. VeronicaAff84, Aff85
Guadalupe, TulioAff86, Aff87
Wittfeld, KatharinaAff88, Aff89
Mosley, Thomas H.
Becker, James T.Aff91, Aff92, Aff93
Doan, Nhat Trung
Hagenaars, Saskia P.
Saba, Yasaman
Cuellar-Partida, Gabriel
Amin, Najaf
Hilal, SaimaAff96, Aff97
Nho, KwangsikAff43, Aff44, Aff45
Mirza-Schreiber, NazaninAff46, Aff98
Arfanakis, KonstantinosAff26, Aff99, Aff100
Becker, Diane M.
Ames, DavidAff101, Aff102
Goldman, Aaron L.
Lee, Phil H.Aff50, Aff103, Aff104, Aff105, Aff106
Boomsma, Dorret I.Aff51, Aff52, Aff53, Aff107
Lovestone, SimonAff108, Aff109
Giddaluru, SudheerAff110, Aff111
Le Hellard, StephanieAff110, Aff111
Mattheisen, ManuelAff112, Aff113, Aff114, Aff115, Aff116
Bohlken, Marc M.
Kasperaviciute, DaliaAff117, Aff118
Schmaal, LianneAff119, Aff120
Lawrie, Stephen M.
Agartz, IngridAff41, Aff115, Aff121
Walton, EstherAff67, Aff122
Tordesillas-Gutierrez, DianaAff71, Aff123
Davies, Gareth E.
Shin, Jean
Ipser, Jonathan C.
Vinke, Louis N.
Hoogman, MartineAff36, Aff38
Jia, Tianye
Burkhardt, RalphAff14, Aff127
Klein, MariekeAff36, Aff38
Crivello, Fabrice
Janowitz, Deborah
Carmichael, Owen
Haukvik, Unn K.Aff40, Aff130
Aribisala, Benjamin S.Aff131, Aff132
Schmidt, Helena
Strike, Lachlan T.Aff95, Aff133
Cheng, Ching-YuAff32, Aff134
Risacher, Shannon L.Aff44, Aff45
Pütz, Benno
Fleischman, Debra A.Aff26, Aff27, Aff135
Assareh, Amelia A.
Mattay, Venkata S.Aff48, Aff137, Aff138
Buckner, Randy L.Aff50, Aff139
Mecocci, Patrizia
Dale, Anders M.Aff141, Aff142, Aff143, Aff144, Aff145
Cichon, SvenAff146, Aff147, Aff148
Boks, Marco P.
Matarin, MarAff117, Aff149, Aff150
Penninx, Brenda W. J. H.
Calhoun, Vince D.Aff151, Aff152, Aff153
Chakravarty, M. MallarAff154, Aff155
Marquand, Andre F.Aff38, Aff156
Macare, Christine
Kharabian Masouleh, ShahrzadAff84, Aff157
Oosterlaan, JaapAff158, Aff159
Amouyel, PhilippeAff160, Aff161, Aff162, Aff163
Hegenscheid, Katrin
Rotter, Jerome I.
Schork, Andrew J.Aff166, Aff167
Liewald, David C. M.
de Zubicaray, Greig I.Aff168, Aff169
Wong, Tien YinAff32, Aff170
Shen, Li
Sämann, Philipp G.
Brodaty, HenryAff136, Aff172
Roffman, Joshua L.
de Geus, Eco J. C.Aff51, Aff52, Aff53, Aff107
Tsolaki, Magda
Erk, Susanne
van Eijk, Kristel R.
Cavalleri, Gianpiero L.
van der Wee, Nic J. A.Aff177, Aff178
McIntosh, Andrew M.Aff22, Aff64
Gollub, Randy L.Aff50, Aff68, Aff103
Bulayeva, Kazima B.
Bernard, Manon
Richards, Jennifer S.Aff35, Aff38, Aff180
Himali, Jayandra J.Aff3, Aff4, Aff30
Loeffler, MarkusAff13, Aff14
Rommelse, NandaAff37, Aff38, Aff181
Hoffmann, WolfgangAff89, Aff182
Westlye, Lars T.Aff40, Aff41
Valdés Hernández, Maria C.Aff131, Aff183
Hansell, Narelle K.Aff95, Aff133
van Erp, Theo G. M.Aff184, Aff185
Wolf, Christiane
Kwok, John B. J.Aff187, Aff188, Aff189
Vellas, BrunoAff190, Aff191
Heinz, Andreas
Olde Loohuis, Loes M.
Delanty, NormanAff61, Aff194
Ho, Beng-Choon
Ching, Christopher R. K.Aff8, Aff196
Shumskaya, ElenaAff36, Aff38, Aff156
Singh, Baljeet
Hofman, AlbertAff5, Aff198
van der Meer, DennisAff40, Aff41, Aff199
Homuth, Georg
Psaty, Bruce M.Aff20, Aff201, Aff202, Aff203
Bastin, Mark E.Aff131, Aff183
Montgomery, Grant W.
Foroud, Tatiana M.Aff45, Aff205
Reppermund, SimoneAff136, Aff206
Hottenga, Jouke-JanAff51, Aff52, Aff53, Aff107
Simmons, AndrewAff207, Aff208, Aff209
Meyer-Lindenberg, Andreas
Cahn, Wiepke
Whelan, Christopher D.Aff8, Aff61
van Donkelaar, Marjolein M. J.Aff36, Aff38
Yang, Qiong
Hosten, Norbert
Green, Robert CAff103, Aff210
Thalamuthu, Anbupalam
Mohnke, Sebastian
Hulshoff Pol, Hilleke E.
Lin, HonghuangAff3, Aff211
Jack, Jr, Clifford R.
Schofield, Peter R.Aff188, Aff213
Mühleisen, Thomas W.Aff148, Aff214, Aff215
Maillard, Pauline
Potkin, Steven G.
Wen, Wei
Fletcher, Evan
Toga, Arthur W.
Gruber, Oliver
Huentelman, Matthew
Davey Smith, George
Launer, Lenore J.
Nyberg, LarsAff56, Aff57, Aff218
Jönsson, Erik G.Aff41, Aff115
Crespo-Facorro, BenedictoAff70, Aff71
Koen, NastassjaAff80, Aff81
Greve, Douglas N.Aff68, Aff219
Uitterlinden, André G.Aff5, Aff220
Weinberger, Daniel R.Aff48, Aff137, Aff221, Aff222, Aff223
Steen, Vidar M.Aff110, Aff111
Fedko, Iryna O.Aff51, Aff52, Aff107
Groenewold, Nynke A.
Niessen, Wiro J.Aff6, Aff16, Aff224
Toro, Roberto
Tzourio, Christophe
Longstreth, Jr, William T.Aff202, Aff227
Ikram, M. KamranAff5, Aff228
Smoller, Jordan W.Aff50, Aff103, Aff105, Aff106
van Tol, Marie-Jose
Sussmann, Jessika E.
Paus, TomasAff230, Aff231, Aff232
Lemaître, Hervé
Schroeter, Matthias L.Aff14, Aff84, Aff233
Mazoyer, Bernard
Andreassen, Ole A.Aff40, Aff41
Holsboer, FlorianAff46, Aff234
Depondt, Chantal
Veltman, Dick J.
Turner, Jessica A.Aff152, Aff153, Aff236
Pausova, Zdenka
Schumann, Gunter
van Rooij, DaanAff35, Aff38, Aff180
Djurovic, SrdjanAff110, Aff237
Deary, Ian J.
McMahon, Katie L.Aff168, Aff169
Müller-Myhsok, BertramAff46, Aff238, Aff239
Brouwer, Rachel M.
Soininen, HilkkaAff240, Aff241
Pandolfo, Massimo
Wassink, Thomas H.
Cheung, Joshua W.
Wolfers, ThomasAff36, Aff38
Martinot, Jean-Luc
Zwiers, Marcel P.Aff38, Aff156
Nauck, MatthiasAff242, Aff243
Melle, IngridAff40, Aff41
Martin, Nicholas G.
Kanai, RyotaAff244, Aff245, Aff246
Westman, Eric
Kahn, René S.Aff60, Aff248
Sisodiya, Sanjay M.Aff117, Aff118
White, TonyaAff6, Aff249
Saremi, Arvin
van Bokhoven, HansAff36, Aff38
Brunner, Han G.Aff36, Aff38, Aff250, Aff251
Völzke, HenryAff25, Aff243
Wright, Margaret J.Aff133, Aff252
van ‘t Ent, DennisAff51, Aff52, Aff53, Aff107
Nöthen, Markus M.Aff147, Aff253
Ophoff, Roel A.Aff193, Aff254
Buitelaar, Jan K.Aff35, Aff38, Aff181
Fernández, GuillénAff35, Aff38
Sachdev, Perminder S.Aff136, Aff255
Rietschel, Marcella
van Haren, Neeltje E. M.Aff60, Aff249
Fisher, Simon E.Aff38, Aff87
Beiser, Alexa S.Aff3, Aff4, Aff30
Francks, ClydeAff38, Aff87
Saykin, Andrew J.Aff44, Aff45, Aff205
Mather, Karen A.Aff136, Aff188
Romanczuk-Seiferth, Nina
Hartman, Catharina A.
DeStefano, Anita L.Aff3, Aff30
Heslenfeld, Dirk J.
Weiner, Michael W.Aff257, Aff258
Walter, Henrik
Hoekstra, Pieter J.
Nyquist, Paul A.
Franke, BarbaraAff36, Aff37, Aff38
Bennett, David A.Aff26, Aff27
Grabe, Hans J.Aff88, Aff89
Johnson, Andrew D.
Chen, ChristopherAff96, Aff97
van Duijn, Cornelia M.Aff5, Aff259
Lopez, Oscar L.Aff92, Aff93
Fornage, MyriamAff21, Aff260
Wardlaw, Joanna M.Aff22, Aff183, Aff261
Schmidt, Reinhold
DeCarli, Charles
De Jager, Philip L.Aff9, Aff10
Villringer, ArnoAff84, Aff85
Debette, StéphanieAff4, Aff15, Aff226
Gudnason, VilmundurAff18, Aff19
Medland, Sarah E.
Shulman, Joshua M.Aff29, Aff263, Aff264, Aff265
Thompson, Paul M.
Seshadri, SudhaAff3, Aff4
Ikram, M. ArfanAff5, Aff6
Pokaż więcej
Źródło :
Nature Genetics. 51(11):1624-1636
Czasopismo naukowe
Tytuł :
Re-annotation of 191 developmental and epileptic encephalopathy-associated genes unmasks de novo variants in SCN1A
Autorzy :
Steward, Charles A.Aff1, Aff2
Roovers, JolienAff3, Aff4
Suner, Marie-MartheAff2, Aff5
Gonzalez, Jose M.Aff2, Aff5
Uszczynska-Ratajczak, BarbaraAff6, Aff7, Aff8
Pervouchine, Dmitri
Fitzgerald, Stephen
Viola, MargaridaAff3, Aff4
Stamberger, HannahAff3, Aff4, Aff10
Hamdan, Fadi F.
Ceulemans, Berten
Leroy, Patricia
Nava, CarolineAff14, Aff15
Lepine, Anne
Tapanari, ElectraAff2, Aff5
Keiller, Don
Abbs, Stephen
Sanchis-Juan, Alba
Grozeva, Detelina
Rogers, Anthony S.
Diekhans, Mark
Guigó, RodericAff6, Aff7
Petryszak, Robert
Minassian, Berge A.Aff22, Aff23
Cavalleri, Gianpiero
Vitsios, Dimitrios
Petrovski, Slavé
Harrow, JenniferAff2, Aff5, Aff26
Flicek, Paul
Lucy Raymond, F.
Lench, Nicholas J.Aff1, Aff27
Jonghe, Peter DeAff3, Aff4, Aff10
Mudge, Jonathan M.Aff2, Aff5
Weckhuysen, SarahAff3, Aff4, Aff10
Sisodiya, Sanjay M.Aff28, Aff29
Frankish, AdamAff2, Aff5
Pokaż więcej
Źródło :
npj Genomic Medicine. 4(1)
Czasopismo naukowe
Tytuł :
Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2
Autorzy :
Corbett, Mark A.
Kroes, Thessa
Veneziano, Liana
Bennett, Mark F.Aff3, Aff4, Aff5
Florian, Rahel
Schneider, Amy L.
Coppola, Antonietta
Licchetta, LauraAff8, Aff9
Franceschetti, SilvanaAff10, Aff11
Suppa, AntonioAff12, Aff13
Wenger, Aaron
Mei, Davide
Pendziwiat, Manuela
Kaya, Sabine
Delledonne, Massimo
Straussberg, RachelAff18, Aff19
Xumerle, Luciano
Regan, Brigid
Crompton, DouglasAff5, Aff21
van Rootselaar, Anne-Fleur
Correll, Anthony
Catford, Rachael
Bisulli, FrancescaAff8, Aff9
Chakraborty, Shreyasee
Baldassari, Sara
Tinuper, PaoloAff8, Aff9
Barton, Kirston
Carswell, Shaun
Smith, MartinAff24, Aff25
Berardelli, AlfredoAff12, Aff13
Carroll, Renee
Gardner, Alison
Friend, Kathryn L.
Blatt, Ilan
Iacomino, Michele
Di Bonaventura, Carlo
Striano, Salvatore
Buratti, Julien
Keren, Boris
Nava, Caroline
Forlani, Sylvie
Rudolf, GabrielleAff31, Aff32, Aff33, Aff34, Aff35
Hirsch, Edouard
Leguern, EricAff29, Aff30
Labauge, Pierre
Balestrini, SimonaAff37, Aff38
Sander, Josemir W.Aff37, Aff38
Afawi, Zaid
Helbig, IngoAff39, Aff16
Ishiura, Hiroyuki
Tsuji, ShojiAff40, Aff41, Aff42
Sisodiya, Sanjay M.Aff37, Aff38
Casari, Giorgio
Sadleir, Lynette G.
van Coller, Riaan
Tijssen, Marina A. J.
Klein, Karl MartinAff47, Aff48, Aff49
van den Maagdenberg, Arn M. J. M.
Zara, Federico
Guerrini, Renzo
Berkovic, Samuel F.
Pippucci, Tommaso
Canafoglia, LauraAff10, Aff11
Bahlo, MelanieAff3, Aff4
Striano, PasqualeAff52, Aff53
Scheffer, Ingrid E.Aff5, Aff54
Brancati, FrancescoAff2, Aff55, Aff56
Depienne, ChristelAff6, Aff31, Aff35
Gecz, JozefAff1, Aff57
Pokaż więcej
Źródło :
Nature Communications. 10(1)
Czasopismo naukowe
Tytuł :
A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay
Autorzy :
Mucha, Bettina E.
Banka, Siddharth
Ajeawung, Norbert Fonya
Molidperee, Sirinart
Chen, Gary G.
Koenig, Mary Kay
Adejumo, Rhamat B.
Till, Marianne
Harbord, Michael
Perrier, Renee
Lemyre, Emmanuelle
Boucher, Renee-Myriam
Skotko, Brian G.
Waxler, Jessica L.
Thomas, Mary Ann
Hodge, Jennelle C.
Gecz, Jozef
Nicholl, Jillian
McGregor, Lesley
Linden, Tobias
Sisodiya, Sanjay M.Aff16, Aff17
Sanlaville, Damien
Cheung, Sau W.
Ernst, Carl
Campeau, Philippe M.
Pokaż więcej
Źródło :
Genetics in Medicine: Official journal of the American College of Medical Genetics and Genomics. 21(5):1058-1064
Czasopismo naukowe
Tytuł :
Correction: A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay
Autorzy :
Mucha, Bettina E.
Banka, Siddharth
Ajeawung, Norbert Fonya
Molidperee, Sirinart
Chen, Gary G.
Koenig, Mary Kay
Adejumo, Rhamat B.
Till, Marianne
Harbord, Michael
Perrier, Renee
Lemyre, Emmanuelle
Boucher, Renee-Myriam
Skotko, Brian G.
Waxler, Jessica L.
Thomas, Mary Ann
Hodge, Jennelle C.
Gecz, Jozef
Nicholl, Jillian
McGregor, Lesley
Linden, Tobias
Sisodiya, Sanjay M.Aff16, Aff17
Sanlaville, Damien
Cheung, Sau W.
Ernst, Carl
Campeau, Philippe M.
Pokaż więcej
Źródło :
Genetics in Medicine: Official journal of the American College of Medical Genetics and Genomics. 21(9):2159-2160
Czasopismo naukowe
Tytuł :
Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study
Autorzy :
May, Patrick
Girard, Simon
Harrer, Merle
Bobbili, Dheeraj R
Schubert, Julian
Wolking, Stefan
Becker, Felicitas
Lachance-Touchette, Pamela
Meloche, Caroline
Gravel, Micheline
Niturad, Cristina E
Knaus, Julia
De Kovel, Carolien
Toliat, Mohamad
Polvi, Anne
Iacomino, Michele
Guerrero-López, Rosa
Baulac, Stéphanie
Marini, Carla
Thiele, Holger
Altmüller, Janine
Jabbari, Kamel
Ruppert, Ann-Kathrin
Jurkowski, Wiktor
Lal, Dennis
Rusconi, Raffaella
Cestèle, Sandrine
Terragni, Benedetta
Coombs, Ian D
Reid, Christopher A
Striano, Pasquale
Caglayan, Hande
Siren, Auli
Everett, Kate
Møller, Rikke S
Hjalgrim, Helle
Muhle, Hiltrud
Helbig, Ingo
Kunz, Wolfram S
Weber, Yvonne G
Weckhuysen, Sarah
De Jonghe, Peter
Sisodiya, Sanjay M
Nabbout, Rima
Franceschetti, Silvana
Coppola, Antonietta
Vari, Maria S
Kasteleijn-Nolst Trenité, Dorothée
Baykan, Betul
Ozbek, Ugur
Bebek, Nerses
Klein, Karl M
Rosenow, Felix
Nguyen, Dang K
Dubeau, François
Carmant, Lionel
Lortie, Anne
Desbiens, Richard
Clément, Jean-François
Cieuta-Walti, Cécile
Sills, Graeme J
Auce, Pauls
Francis, Ben
Johnson, Michael R
Marson, Anthony G
Berghuis, Bianca
Sander, Josemir W
Avbersek, Andreja
McCormack, Mark
Cavalleri, Gianpiero L
Delanty, Norman
Depondt, Chantal
Krenn, Martin
Zimprich, Fritz
Peter, Sarah
Nikanorova, Marina
Kraaij, Robert
van Rooij, Jeroen
Balling, Rudi
Arfan Ikram, M
Uitterlinden, André G
Avanzini, Giuliano
Schorge, Stephanie
Petrou, Steven
Mantegazza, Massimo
Sander, Thomas
LeGuern, Eric
Serratosa, Jose M
Koeleman, Bobby P C
Palotie, Aarno
Lehesjoki, Anna-Elina
Nothnagel, Michael
Nürnberg, Peter
Maljevic, Snezana
Zara, Federico
Cossette, Patrick
Krause, Roland
Lerche, Holger
Ferlazzo, Edoardo
di Bonaventura, Carlo
La Neve, Angela
Tinuper, Paolo
Bisulli, Francesca
Vignoli, Aglaia
Capovilla, Giuseppe
Crichiutti, Giovanni
Gambardella, Antonio
Belcastro, Vincenzo
Bianchi, Amedeo
Yalçın, Destina
Dizdarer, Gulsen
Arslan, Kezban
Yapıcı, Zuhal
Kuşcu, Demet
Leu, Costin
Heggeli, Kristin
Willis, Joseph
Langley, Sarah R
Jorgensen, Andrea
Srivastava, Prashant
Rau, Sarah
Hengsbach, Christian
Sonsma, Anja C.M.
May, Patrick
Pokaż więcej
Źródło :
In The Lancet Neurology August 2018 17(8):699-708
Czasopismo naukowe
Tytuł :
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals
Autorzy :
Feng, Yen-Chen Anne
Howrigan, Daniel P.
Abbott, Liam E.
Tashman, Katherine
Cerrato, Felecia
Singh, Tarjinder
Heyne, Henrike
Byrnes, Andrea
Churchhouse, Claire
Watts, Nick
Solomonson, Matthew
Lal, Dennis
Heinzen, Erin L.
Dhindsa, Ryan S.
Stanley, Kate E.
Cavalleri, Gianpiero L.
Hakonarson, Hakon
Helbig, Ingo
Krause, Roland
May, Patrick
Weckhuysen, Sarah
Petrovski, Slavé
Kamalakaran, Sitharthan
Sisodiya, Sanjay M.
Cossette, Patrick
Cotsapas, Chris
De Jonghe, Peter
Dixon-Salazar, Tracy
Guerrini, Renzo
Kwan, Patrick
Marson, Anthony G.
Stewart, Randy
Depondt, Chantal
Dlugos, Dennis J.
Scheffer, Ingrid E.
Striano, Pasquale
Freyer, Catharine
McKenna, Kevin
Regan, Brigid M.
Bellows, Susannah T.
Leu, Costin
Bennett, Caitlin A.
Johns, Esther M.C.
Macdonald, Alexandra
Shilling, Hannah
Burgess, Rosemary
Weckhuysen, Dorien
Bahlo, Melanie
O’Brien, Terence J.
Todaro, Marian
Stamberger, Hannah
Andrade, Danielle M.
Sadoway, Tara R.
Mo, Kelly
Krestel, Heinz
Gallati, Sabina
Papacostas, Savvas S.
Kousiappa, Ioanna
Tanteles, George A.
Štěrbová, Katalin
Vlčková, Markéta
Sedláčková, Lucie
Laššuthová, Petra
Klein, Karl Martin
Rosenow, Felix
Reif, Philipp S.
Knake, Susanne
Kunz, Wolfram S.
Zsurka, Gábor
Elger, Christian E.
Bauer, Jürgen
Rademacher, Michael
Pendziwiat, Manuela
Muhle, Hiltrud
Rademacher, Annika
van Baalen, Andreas
von Spiczak, Sarah
Stephani, Ulrich
Afawi, Zaid
Korczyn, Amos D.
Kanaan, Moien
Canavati, Christina
Kurlemann, Gerhard
Müller-Schlüter, Karen
Kluger, Gerhard
Häusler, Martin
Blatt, Ilan
Lemke, Johannes R.
Krey, Ilona
Weber, Yvonne G.
Wolking, Stefan
Becker, Felicitas
Hengsbach, Christian
Rau, Sarah
Maisch, Ana F.
Steinhoff, Bernhard J.
Schulze-Bonhage, Andreas
Schubert-Bast, Susanne
Schreiber, Herbert
Borggräfe, Ingo
Schankin, Christoph J.
Mayer, Thomas
Korinthenberg, Rudolf
Brockmann, Knut
Kurlemann, Gerhard
Dennig, Dieter
Madeleyn, Rene
Kälviäinen, Reetta
Auvinen, Pia
Saarela, Anni
Linnankivi, Tarja
Lehesjoki, Anna-Elina
Rees, Mark I.
Chung, Seo-Kyung
Pickrell, William O.
Powell, Robert
Schneider, Natascha
Balestrini, Simona
Zagaglia, Sara
Braatz, Vera
Johnson, Michael R.
Auce, Pauls
Sills, Graeme J.
Baum, Larry W.
Sham, Pak C.
Cherny, Stacey S.
Lui, Colin H.T.
Barišić, Nina
Delanty, Norman
Doherty, Colin P.
Shukralla, Arif
McCormack, Mark
El-Naggar, Hany
Canafoglia, Laura
Franceschetti, Silvana
Castellotti, Barbara
Granata, Tiziana
Zara, Federico
Iacomino, Michele
Madia, Francesca
Vari, Maria Stella
Mancardi, Maria Margherita
Salpietro, Vincenzo
Bisulli, Francesca
Tinuper, Paolo
Licchetta, Laura
Pippucci, Tommaso
Stipa, Carlotta
Minardi, Raffaella
Gambardella, Antonio
Labate, Angelo
Annesi, Grazia
Manna, Lorella
Gagliardi, Monica
Parrini, Elena
Mei, Davide
Vetro, Annalisa
Bianchini, Claudia
Montomoli, Martino
Doccini, Viola
Marini, Carla
Suzuki, Toshimitsu
Inoue, Yushi
Yamakawa, Kazuhiro
Tumiene, Birute
Sadleir, Lynette G.
King, Chontelle
Mountier, Emily
Caglayan, S. Hande
Arslan, Mutluay
Yapıcı, Zuhal
Yis, Uluc
Topaloglu, Pınar
Kara, Bulent
Turkdogan, Dilsad
Gundogdu-Eken, Aslı
Bebek, Nerses
Uğur-İşeri, Sibel
Baykan, Betül
Salman, Barış
Haryanyan, Garen
Yücesan, Emrah
Kesim, Yeşim
Özkara, Çiğdem
Poduri, Annapurna
Shiedley, Beth R.
Shain, Catherine
Buono, Russell J.
Ferraro, Thomas N.
Sperling, Michael R.
Lo, Warren
Privitera, Michael
French, Jacqueline A.
Schachter, Steven
Kuzniecky, Ruben I.
Devinsky, Orrin
Hegde, Manu
Khankhanian, Pouya
Helbig, Katherine L.
Ellis, Colin A.
Spalletta, Gianfranco
Piras, Fabrizio
Piras, Federica
Gili, Tommaso
Ciullo, Valentina
Reif, Andreas
McQuillin, Andrew
Bass, Nick
McIntosh, Andrew
Blackwood, Douglas
Johnstone, Mandy
Palotie, Aarno
Pato, Michele T.
Pato, Carlos N.
Bromet, Evelyn J.
Carvalho, Celia Barreto
Achtyes, Eric D.
Azevedo, Maria Helena
Kotov, Roman
Lehrer, Douglas S.
Malaspina, Dolores
Marder, Stephen R.
Medeiros, Helena
Morley, Christopher P.
Perkins, Diana O.
Sobell, Janet L.
Buckley, Peter F.
Macciardi, Fabio
Rapaport, Mark H.
Knowles, James A.
Fanous, Ayman H.
McCarroll, Steven A.
Gupta, Namrata
Gabriel, Stacey B.
Daly, Mark J.
Lander, Eric S.
Lowenstein, Daniel H.
Goldstein, David B.
Lerche, Holger
Berkovic, Samuel F.
Neale, Benjamin M.
Pokaż więcej
Źródło :
In The American Journal of Human Genetics 1 August 2019 105(2):267-282
Czasopismo naukowe

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