This section provides links to selected publications, published both online and in print.
Publications are listed in chronological order, the first being the most recent.
Grandjean J, Desrosiers-Gregoire G, Anckaerts C, Angeles-Valdez D, Ayad F, Barrière DA, Blockx I, Bortel A, Broadwater M, Cardoso BM, Célestine M, Chavez-Negrete JE, Choi S, Christiaen E, Clavijo P, Colon-Perez L, Cramer S, Daniele T, Dempsey E, Diao Y, Doelemeyer A, Dopfel D, Dvořáková L, Falfán-Melgoza C, Fernandes FF, Fowler CF, Fuentes-Ibañez A, Garin CM, Gelderman E, Golden CEM, Guo CCG, Henckens MJAG, Hennessy LA, Herman P, Hofwijks N, Horien C, Ionescu TM, Jones J, Kaesser J, Kim E, Lambers H, Lazari A, Lee SH, Lillywhite A, Liu Y, Liu YY, López-Castro A, López-Gil X, Ma Z, MacNicol E, Madularu D, Mandino F, Marciano S, McAuslan MJ, McCunn P, McIntosh A, Meng X, Meyer-Baese L, Missault S, Moro F, Naessens DMP, Nava-Gomez LJ, Nonaka H, Ortiz JJ, Paasonen J, Peeters LM, Pereira M, Perez PD, Pompilus M, Prior M, Rakhmatullin R, Reimann HM, Reinwald J, Del Rio RT, Rivera-Olvera A, Ruiz-Pérez D, Russo G, Rutten TJ, Ryoke R, Sack M, Salvan P, Sanganahalli BG, Schroeter A, Seewoo BJ, Selingue E, Seuwen A, Shi B, Sirmpilatze N, Smith JAB, Smith C, Sobczak F, Stenroos PJ, Straathof M, Strobelt S, Sumiyoshi A, Takahashi K, Torres-García ME, Tudela R, van den Berg M, van der Marel K, et al.
Ciani O, Manyara AM, Davies P, Stewart D, Weir CJ, Young AE, Blazeby J, Butcher NJ, Bujkiewicz S, Chan AW, Dawoud D, Offringa M, Ouwens M, Hróbjartssson A, Amstutz A, Bertolaccini L, Bruno VD, Devane D, Faria CDCM, Gilbert PB, Harris R, Lassere M, Marinelli L, Markham S, Powers JH, Rezaei Y, Richert L, Schwendicke F, Tereshchenko LG, Thoma A, Turan A, Worrall A, Christensen R, Collins GS, Ross JS, Taylor RS.
Calvert C, Carruthers J, Denny C, Donaghy J, Hopcroft LEM, Hopkins L, Goulding A, Lindsay L, McLaughlin T, Moore E, Taylor B, Loane M, Dolk H, Morris J, Auyeung B, Bhaskaran K, Gibbons CL, Katikireddi SV, O'Leary M, McAllister D, Shi T, Simpson CR, Robertson C, Sheikh A, Stock SJ, Wood R.
Sharma SD, Reddy BK, Pal R, Ritakari TE, Cooper JD, Selvaraj BT, Kind PC, Chandran S, Wyllie DJA, Chattarji S.
Mbizvo GK, Schnier C, Simpson CR, Duncan SE, Chin RFM.
Mazzone PP, Hogg KM, Weir CJ, Stephen J, Bhattacharya S, Chin RFM.
Strafford H, Lacey AS, Hollinghurst J, Akbari A, Watkins A, Paterson J, Jennings D, Lyons RA, Powell HR, Kerr MP, Chin RW, Pickrell WO.
Besag FMC, Vasey MJ, Chin RFM.
Li BZ, Sumera A, Booker SA, McCullagh EA.
Leyhausen J, Schäfer T, Gurr C, Berg LM, Seelemeyer H, Pretzsch CM, Loth E, Oakley B, Buitelaar JK, Beckmann CF, Floris DL, Charman T, Bourgeron T, Banaschewski T, Jones EJH, Tillmann J, Chatham C; EU-AIMS LEAP Group; Murphy DG, Ecker C.
Davies FCJ, Marshall GF, Pegram E, Gadd D, Abbott CM.
Kontaxi C, Ivanova D, Davenport EC, Kind PC, Cousin MA.
Mbizvo GK, Schnier C, Ramsay J, Duncan SE, Chin RF.
Cresswell K, Anderson S, Montgomery C, Weir CJ, Atter M, Williams R.
Louros SR, Seo SS, Maio B, Martinez-Gonzalez C, Gonzalez-Lozano MA, Muscas M, Verity NC, Wills JC, Li KW, Nolan MF, Osterweil EK.
Yong K, Chin RFM, Shetty J, Hogg K, Burgess K, Lindsay M, McLellan A, Stone J, KamathTallur K; Edinburgh Paediatric FND Study Group.
Hocking LJ, Andrews C, Armstrong C, Ansari M, Baty D, Berg J, Bradley T, Clark C, Diamond A, Doherty J, Lampe A, McGowan R, Moore DJ, O'Sullivan D, Purvis A, Santoyo-Lopez J, Westwood P, Abbott M, Williams N; Scottish Genomes Partnership; Aitman TJ, Miedzybrodzka Z.
Wright CF, Campbell P, Eberhardt RY, Aitken S, Perrett D, Brent S, Danecek P, Gardner EJ, Chundru VK, Lindsay SJ, Andrews K, Hampstead J, Kaplanis J, Samocha KE, Middleton A, Foreman J, Hobson RJ, Parker MJ, Martin HC, FitzPatrick DR, Hurles ME, Firth HV; DDD Study.
Ford A, De Togni G, Erikainen S, Filipe AM, Pickersgill M, Sturdy S, Swallow J, Young I.
Yang Y, Booker SA, Clegg JM, Quintana-Urzainqui I, Sumera A, Kozic Z, Dando O, Martin Lorenzo S, Herault Y, Kind PC, Price DJ, Pratt T.
Stewart E, Pearce A, Given J, Gilbert R, Brophy S, Cookson R, Hardelid P, Harron KL, Leyland A, Wood R, Dundas R.
Kozar-Gillan N, Velichkova A, Kanatouris G, Eshed-Eisenbach Y, Steel G, Jaegle M, Aunin E, Peles E, Torsney C, Meijer DN.
Oblong LM, Llera A, Mei T, Haak K, Isakoglou C, Floris DL, Durston S, Moessnang C, Banaschewski T, Baron-Cohen S, Loth E, Dell'Acqua F, Charman T, Murphy DGM, Ecker C, Buitelaar JK, Beckmann CF; EU-AIMS LEAP Group; Forde NJ.
Speyer LG, Auyeung B, Murray AL.
Gospodinova KO, Olsen D, Kaas M, Anderson SM, Phillips J, Walker RM, Bermingham ML, Payne AL, Giannopoulos P, Pandya D, Spires-Jones TL, Abbott CM, Porteous DJ, Glerup S, Evans KL.
Chalkiadaki K, Hooshmandi M, Lach G, Statoulla E, Simbriger K, Amorim IS, Kouloulia S, Zafeiri M, Pothos P, Bonneil É, Gantois I, Popic J, Kim SH, Wong C, Cao R, Komiyama NH, Atlasi Y, Jafarnejad SM, Khoutorsky A, Gkogkas CG.
Schnier C, Chin RF.
Powers S, Likhite S, Gadalla KK, Miranda CJ, Huffenberger AJ, Dennys C, Foust KD, Morales P, Pierson CR, Rinaldi F, Perry S, Bolon B, Wein N, Cobb S, Kaspar BK, Meyer KC.
Blumrich EM, Nicholson-Fish JC, Pronot M, Davenport EC, Kurian D, Cole A, Smillie KJ, Cousin MA.
Needham N, Campbell IH, Grossi H, Kamenska I, Rigby BP, Simpson SA, McIntosh E, Bahuguna P, Meadowcroft B, Creasy F, Mitchell-Grigorjeva M, Norrie J, Thompson G, Gibbs MC, McLellan A, Fisher C, Moses T, Burgess K, Brown R, Thrippleton MJ, Campbell H, Smith DJ.
Joensuu M, Syed P, Saber SH, Lanoue V, Wallis TP, Rae J, Blum A, Gormal RS, Small C, Sanders S, Jiang A, Mahrhold S, Krez N, Cousin MA, Cooper-White R, Cooper-White JJ, Collins BM, Parton RG, Balistreri G, Rummel A, Meunier FA.
Gillespie DC, Flewitt BI, Sacripante R, Burns V, Young L, Chin RF, Duncan SE.
De Vas MG, Boulet F, Joshi SS, Garstang MG, Khan TN, Atla G, Parry D, Moore D, Cebola I, Zhang S, Cui W, Lampe AK, Lam WW; Genomics England Research Consortium; Ferrer J, Pradeepa MM, Atanur SS.
Bonnycastle K, Dobson KL, Blumrich EM, Gajbhiye A, Davenport EC, Pronot M, Steinruecke M, Trost M, Gonzalez-Sulser A, Cousin MA.
Bacon M, Appleton R, Bangalore H, Brand C, Browning J, Chin RF, Mahal S, Saranga Estevan S, McHale K, McLellan A, Milne N, Pujar S, Rao T, Short S, Warriner S, Yoong M.
Gillespie DC, Duncan SE, Flewitt BI, Sacripante R, Chin RF.
Martyn Pickersgill
Oberndorfer M, Henery PM, Dundas R, Leyland AH, Paranjothy S, Stock SJ, Wood R, Nelson SM, Kearns R, Pearce A.
Woodfield J, Chin RFM, van Schooneveld MMJ, van den Heuvel M, Bastin ME, Braun KPJ.
Kubota M, Hadley LV, Schaeffner S, Könen T, Meaney JA, Morey CC, Auyeung B, Moriguchi Y, Karbach J, Chevalier N.
Gillespie-Smith K, McConachie D, Ballantyne C, Auyeung B, Goodall K.
Berg LM, Gurr C, Leyhausen J, Seelemeyer H, Bletsch A, Schaefer T, Pretzsch CM, Oakley B, Loth E, Floris DL, Buitelaar JK, Beckmann CF, Banaschewski T, Charman T, Jones EJH, Tillmann J, Chatham CH, Bourgeron T; EU-AIMS LEAP Group; Murphy DG, Ecker C.
Kontaxi C, Kim N, Cousin MA.
Mbizvo GK, Bennett KH, Simpson CR, Duncan SE, Chin RFM, Larner AJ.
Bulovaite E, Qiu Z, Kratschke M, Zgraj A, Fricker DG, Tuck EJ, Gokhale R, Koniaris B, Jami SA, Merino-Serrais P, Husi E, Mendive-Tapia L, Vendrell M, O'Dell TJ, DeFelipe J, Komiyama NH, Holtmaat A, Fransén E, Grant SGN.
McKechanie AG, Lawrie SM, Whalley HC, Stanfield AC.
Clayton EL, Bonnycastle K, Isaacs AM, Cousin MA, Schorge S.
Calvert C, Carruthers J, Denny C, Donaghy J, Hillman S, Hopcroft LEM, Hopkins L, Goulding A, Lindsay L, McLaughlin T, Moore E, Pan J, Taylor B, Almaghrabi F, Auyeung B, Bhaskaran K, Gibbons CL, Katikireddi SV, McCowan C, Murray J, O'Leary M, Ritchie LD, Shah SA, Simpson CR, Robertson C, Sheikh A, Stock SJ, Wood R.
Speyer LG, Eisner M, Ribeaud D, Luciano M, Auyeung B, Murray AL.
Buller-Peralta I, Maicas-Royo J, Lu Z, Till SM, Wood ER, Kind PC, Escudero J, Gonzalez-Sulser A.
Wagstyl K, Whitaker K, Raznahan A, Seidlitz J, Vértes PE, Foldes S, Humphreys Z, Hu W, Mo J, Likeman M, Davies S, Lenge M, Cohen NT, Tang Y, Wang S, Ripart M, Chari A, Tisdall M, Bargallo N, Conde-Blanco E, Pariente JC, Pascual-Diaz S, Delgado-Martínez I, Pérez-Enríquez C, Lagorio I, Abela E, Mullatti N, O'Muircheartaigh J, Vecchiato K, Liu Y, Caligiuri M, Sinclair B, Vivash L, Willard A, Kandasamy J, McLellan A, Sokol D, Semmelroch M, Kloster A, Opheim G, Yasuda C, Zhang K, Hamandi K, Barba C, Guerrini R, Gaillard WD, You X, Wang I, González-Ortiz S, Severino M, Striano P, Tortora D, Kalviainen R, Gambardella A, Labate A, Desmond P, Lui E, O'Brien T, Shetty J, Jackson G, Duncan JS, Winston GP, Pinborg L, Cendes F, Cross JH, Baldeweg T, Adler S.
Mei T, Forde NJ, Floris DL, Dell'Acqua F, Stones R, Ilioska I, Durston S, Moessnang C, Banaschewski T, Holt RJ, Baron-Cohen S, Rausch A, Loth E, Oakley B, Charman T, Ecker C, Murphy DGM; EU-AIMS LEAP group; Beckmann CF, Llera A, Buitelaar JK.
Rudan I, Millington T, Antal K, Grange Z, Fenton L, Sullivan C, Buelo A, Wood R, Woolford L, Swann OV, Murray JLK, Cullen LA, Moore E, Haider F, Almaghrabi F, McMenamin J, Agrawal U, Shah SA, Kerr S, Simpson CR, Katikireddi SV, Ritchie SLD, Robertson C, Sheikh SA.
Bethlehem RAI, Seidlitz J, White SR, Vogel JW, Anderson KM, Adamson C, Adler S, Alexopoulos GS, Anagnostou E, Areces-Gonzalez A, Astle DE, Auyeung B, Ayub M, Bae J, Ball G, Baron-Cohen S, Beare R, Bedford SA, Benegal V, Beyer F, Blangero J, Blesa Cábez M, Boardman JP, Borzage M, Bosch-Bayard JF, Bourke N, Calhoun VD, Chakravarty MM, Chen C, Chertavian C, Chetelat G, Chong YS, Cole JH, Corvin A, Costantino M, Courchesne E, Crivello F, Cropley VL, Crosbie J, Crossley N, Delarue M, Delorme R, Desrivieres S, Devenyi GA, Di Biase MA, Dolan R, Donald KA, Donohoe G, Dunlop K, Edwards AD, Elison JT, Ellis CT, Elman JA, Eyler L, Fair DA, Feczko E, Fletcher PC, Fonagy P, Franz CE, Galan-Garcia L, Gholipour A, Giedd J, Gilmore JH, Glahn DC, Goodyer IM, Grant PE, Groenewold NA, Gunning FM, Gur RE, Gur RC, Hammill CF, Hansson O, Hedden T, Heinz A, Henson RN, Heuer K, Hoare J, Holla B, Holmes AJ, Holt R, Huang H, Im K, Ipser J, Jack CR Jr, Jackowski AP, Jia T, Johnson KA, Jones PB, Jones DT, Kahn RS, Karlsson H, Karlsson L, Kawashima R, Kelley EA, Kern S, Kim KW, Kitzbichler MG, Kremen WS, Lalonde F, Landeau B, et al.
Garcia-Font N, Mitchell-Heggs R, Saxena K, Gabbert C, Taylor G, Mastroberadino G, Spooner PA, Gobbo F, Dabrowska JK, Chattarji S, Kind PC, Schultz SR, Morris RGM.
Wright D, Kenny A, Eley S, McKechanie AG, Stanfield AC.
Zlatic SA, Duong D, Gadalla KKE, Murage B, Ping L, Shah R, Fink JJ, Khwaja O, Swanson LC, Sahin M, Rayaprolu S, Kumar P, Rangaraju S, Bird A, Tarquinio D, Carpenter R, Cobb S, Faundez V.
T.M Yates, A. Lain, J. Campbell, D.R. FitzPatrick, T.I. Simpson.
Till SM, Hickson RDL, Kind PC.
Stevering CH, Lamberink HJ, Woodfield J, van Schooneveld M, Otte WM, Chin RFM, Bastin ME, Geleijns K, Braun KPJ.
Rodriguez A, Tuck C, Dozier MF, Lewis SC, Eldridge S, Jackson T, Murray A, Weir CJ.
Imoto Y, Raychaudhuri S, Ma Y, Fenske P, Sandoval E, Itoh K, Blumrich EM, Matsubayashi HT, Mamer L, Zarebidaki F, Söhl-Kielczynski B, Trimbuch T, Nayak S, Iwasa JH, Liu J, Wu B, Ha T, Inoue T, Jorgensen EM, Cousin MA, Rosenmund C, Watanabe S
Kenny A, Wright D, Stanfield AC.
Alusi G, Berry-Kravis E, Nelson D, Orefice LL, Booker SA.
Pan N, Auyeung B, Wang X, Lin LZ, Li HL, Zhan XL, Jin CK, Jing J, Li XH.
Wang X, Auyeung B, Pan N, Lin LZ, Chen Q, Chen JJ, Liu SY, Dai MX, Gong JH, Li XH, Jing J.
Seo SS, Louros SR, Anstey N, Gonzalez-Lozano MA, Harper CB, Verity NC, Dando O, Thomson SR, Darnell JC, Kind PC, Li KW, Osterweil EK.
Asiminas A, Booker SA, Dando OR, Kozic Z, Arkell D, Inkpen FH, Sumera A, Akyel I, Kind PC, Wood ER.
Vandrey B, Armstrong J, Brown CM, Garden DLF, Nolan MF.
Bonnycastle K, Kind PC, Cousin MA.
Anstey NJ, Kapgal V, Tiwari S, Watson TC, Toft AKH, Dando OR, Inkpen FH, Baxter PS, Kozić Z, Jackson AD, He X, Nawaz MS, Kayenaat A, Bhattacharya A, Wyllie DJA, Chattarji S, Wood ER, Hardt O, Kind PC.
McTaggart S, MacColl G, Gronkowski K, Wood R, Leach JP, Bennie M.
Spitzer H, Ripart M, Whitaker K, D'Arco F, Mankad K, Chen AA, Napolitano A, De Palma L, De Benedictis A, Foldes S, Humphreys Z, Zhang K, Hu W, Mo J, Likeman M, Davies S, Güttler C, Lenge M, Cohen NT, Tang Y, Wang S, Chari A, Tisdall M, Bargallo N, Conde-Blanco E, Pariente JC, Pascual-Diaz S, Delgado-Martínez I, Pérez-Enríquez C, Lagorio I, Abela E, Mullatti N, O'Muircheartaigh J, Vecchiato K, Liu Y, Caligiuri ME, Sinclair B, Vivash L, Willard A, Kandasamy J, McLellan A, Sokol D, Semmelroch M, Kloster AG, Opheim G, Ribeiro L, Yasuda C, Rossi-Espagnet C, Hamandi K, Tietze A, Barba C, Guerrini R, Gaillard WD, You X, Wang I, González-Ortiz S, Severino M, Striano P, Tortora D, Kälviäinen R, Gambardella A, Labate A, Desmond P, Lui E, O'Brien T, Shetty J, Jackson G, Duncan JS, Winston GP, Pinborg LH, Cendes F, Theis FJ, Shinohara RT, Cross JH, Baldeweg T, Adler S, Wagstyl K.
Wyllie DJA, Bowie D.
Dooley N, Ruigrok A, Holt R, Allison C, Tsompanidis A, Waldman J, Auyeung B, Lombardo MV, Baron-Cohen S.
Kwok J, Hall HA, Murray AL, Lombardo MV, Auyeung B.
Cohen NT, You X, Krishnamurthy M, Sepeta LN, Zhang A, Oluigbo C, Whitehead MT, Gholipour T, Baldeweg T, Wagstyl K, Adler S, Gaillard WD; Multi-Centre Epilepsy Lesion Detection (MELD) Project.
Gonzalez-Sulser A.
Haddow K, Kind PC, Hardingham GE.
Walsh C, Mitchell L, Hrozanova M, Kotoulas SC, Derry C, Morrison I, Riha RL
Looden T, Floris DL, Llera A, Chauvin RJ, Charman T, Banaschewski T, Murphy D, Marquand AF, Buitelaar JK, Beckmann CF; AIMS-2-TRIALS group.
Speyer LG, Neaves S, Hall HA, Hemani G, Lombardo MV, Murray AL, Auyeung B, Luciano M.
Wason JMS, Dimairo M, Biggs K, Bowden S, Brown J, Flight L, Hall J, Jaki T, Lowe R, Pallmann P, Pilling MA, Snowdon C, Sydes MR, Villar SS, Weir CJ, Wilson N, Yap C, Hancock H, Maier R.
Owen Pickrell W, Guelfucci F, Martin M, Holland R, Chin RFM..
Abdullateef S, Jordan B, Rae V, McLellan A, Escudero J, Nenadovic V, Lo T.
Garcés P, Baumeister S, Mason L, Chatham CH, Holiga S, Dukart J, Jones EJH, Banaschewski T, Baron-Cohen S, Bölte S, Buitelaar JK, Durston S, Oranje B, Persico AM, Beckmann CF, Bougeron T, Dell'Acqua F, Ecker C, Moessnang C, Charman T, Tillmann J, Murphy DGM, Johnson M, Loth E, Brandeis D, Hipp JF; EU-AIMS LEAP group authorship.
Magdalena Navarro Torres Arpi, T. Ian Simpson
Tian T, Yuan Y, Mitra S, Gyongy I, Nolan MF.
Tennant SA, Clark H, Hawes I, Tam WK, Hua J, Yang W, Gerlei KZ, Wood ER, Nolan MF.
Eaton C, Yong K, Walter V, Mbizvo GK, Rhodes S, Chin RF.
Ivanova D, Cousin MA.
McQuaid F, Mulholland R, Sangpang Rai Y, Agrawal U, Bedford H, Cameron JC, Gibbons C, Roy P, Sheikh A, Shi T, Simpson CR, Tait J, Tessier E, Turner S, Villacampa Ortega J, White J, Wood R.
Yokoi N, Fukata Y, Okatsu K, Yamagata A, Liu Y, Sanbo M, Miyazaki Y, Goto T, Abe M, Kassai H, Sakimura K, Meijer D, Hirabayashi M, Fukai S, Fukata M.
Watkins JC, Evans RH, Bayés À, Booker SA, Gibb A, Mabb AM, Mayer M, Mellor JR, Molnár E, Niu L, Ortega A, Pankratov Y, Ramos-Vicente D, Rodríguez-Campuzano A, Rodríguez-Moreno A, Wang LY, Wang YT, Wollmuth L, Wyllie DJA, Zhuo M, Frenguelli BG..
Pickersgill M.
Muscas M, Seo SS, Louros SR, Osterweil EK.
Bernal J, Valdés-Hernández MDC, Escudero J, Heye AK, Sakka E, Armitage PA, Makin S, Touyz RM, Wardlaw JM, Thrippleton MJ.
Perkins EM, Burr K, Banerjee P, Mehta AR, Dando O, Selvaraj BT, Suminaite D, Nanda J, Henstridge CM, Gillingwater TH, Hardingham GE, Wyllie DJA, Chandran S, Livesey MR.
Hutchison M, Buxton G, Brand C, McLellan A, Shetty J.
Kafantaris E, Piper I, Lo TM, Escudero J.
Kind PC, Bird A.
Harden J, Black R, Pickersgill M, Shetty J, McLellan A, Brand C, Small M, McDonnell J, Clarke L, Chin RF.
Mulholland RH, Vasileiou E, Simpson CR, Robertson C, Ritchie LD, Agrawal U, Woolhouse M, Murray JL, Stagg HR, Docherty AB, McCowan C, Wood R, Stock SJ, Sheikh A.
Booker SA, Sumera A, Kind PC, Wyllie DJA.
Ivanova D, Dobson KL, Gajbhiye A, Davenport EC, Hacker D, Ultanir SK, Trost M, Cousin MA.
Fernandes G, Mishra PK, Nawaz MS, Donlin-Asp PG, Rahman MM, Hazra A, Kedia S, Kayenaat A, Songara D, Wyllie DJA, Schuman EM, Kind PC, Chattarji S.
Agrawal U, Katikireddi SV, McCowan C, Mulholland RH, Azcoaga-Lorenzo A, Amele S, Fagbamigbe AF, Vasileiou E, Grange Z, Shi T, Kerr S, Moore E, Murray JLK, Shah SA, Ritchie L, O'Reilly D, Stock SJ, Beggs J, Chuter A, Torabi F, Akbari A, Bedston S, McMenamin J, Wood R, Tang RSM, de Lusignan S, Hobbs FDR, Woolhouse M, Simpson CR, Robertson C, Sheikh A.
Harper CB, Smillie KJ.
Gerlei KZ, Brown CM, Sürmeli G, Nolan MF.
Huggins CJ, Escudero J, Parra MA, Scally B, Anghinah R, Vitória Lacerda de Araújo A, Basile LF, Abasolo D.
Symonds JD, Elliott KS, Shetty J, Armstrong M, Brunklaus A, Cutcutache I, Diver LA, Dorris L, Gardiner S, Jollands A, Joss S, Kirkpatrick M, McLellan A, MacLeod S, O'Regan M, Page M, Pilley E, Pilz DT, Stephen E, Stewart K, Ashrafian H, Knight JC, Zuberi SM.
Shah ASV, Gribben C, Bishop J, Hanlon P, Caldwell D, Wood R, Reid M, McMenamin J, Goldberg D, Stockton D, Hutchinson S, Robertson C, McKeigue PM, Colhoun HM, McAllister DA.
Mitchell C, Chatterton Dickson L, Ramsay A, Mesalles-Naranjo O, Leonard P, Brand C, Mclellan A, Shetty J.
Milosevic I, Cousin MA.
Siegel-Ramsay JE, Romaniuk L, Whalley HC, Roberts N, Branigan H, Stanfield AC, Lawrie SM, Dauvermann MR.
Bengani H, Grozeva D, Moyon L, Bhatia S, Louros SR, Hope J, Jackson A, Prendergast JG, Owen LJ, Naville M, Rainger J, Grimes G, Halachev M, Murphy LC, Spasic-Boskovic O, van Heyningen V, Kind P, Abbott CM, Osterweil E, Raymond FL, Roest Crollius H, FitzPatrick DR.
Bertelsen N, Landi I, Bethlehem RAI, Seidlitz J, Busuoli EM, Mandelli V, Satta E, Trakoshis S, Auyeung B, Kundu P, Loth E, Dumas G, Baumeister S, Beckmann CF, Bölte S, Bourgeron T, Charman T, Durston S, Ecker C, Holt RJ, Johnson MH, Jones EJH, Mason L, Meyer-Lindenberg A, Moessnang C, Oldehinkel M, Persico AM, Tillmann J, Williams SCR, Spooren W, Murphy DGM, Buitelaar JK; EU-AIMS LEAP group, Baron-Cohen S, Lai MC, Lombardo MV.
Cabrera FE, Sánchez-Núñez P, Vaccaro G, Peláez JI, Escudero J.
Horner AE, Norris RH, McLaren-Jones R, Alexander L, Komiyama NH, Grant SGN, Nithianantharajah J, Kopanitsa MV.
Speyer LG, Hall HA, Ushakova A, Murray AL, Luciano M, Auyeung B.
Speyer LG, Hall HA, Ushakova A, Murray AL, Luciano M, Auyeung B.
Hristova K, Martinez-Gonzalez C, Watson TC, Codadu NK, Hashemi K, Kind PC, Nolan MF, Gonzalez-Sulser A.
Marshall GF, Gonzalez-Sulser A, Abbott CM.
Cousin MA, Smillie KJ.
Booker SA, Wyllie DJA.
George C, Felix SA, McLellan A, Shetty J, Middleton J, Chin RF, Poveda B, Brand C, Small M, Verity K.
Smillie KJ, Cousin MA, Gordon SL.
Hall HA, Speyer LG, Murray AL, Auyeung B.
Bonnycastle K, Davenport EC, Cousin MA.
Subrahmanyam R, Dwivedi D, Rashid Z, Bonnycastle K, Cousin MA, Chattarji S.
Oliveira LS, Sumera A, Booker SA
Smith-Hicks C, Wright D, Kenny A, Stowe RC, McCormack M, Stanfield AC, Holder JL Jr.
Nobili L, de Weerd A, Rubboli G, Beniczky S, Derry C, Eriksson S, Halasz P, Högl B, Santamaria J, Khatami R, Ryvlin P, Rémi J, Tinuper P, Bassetti C, Manni R, Koutroumanidis M, Vignatelli L.
Harper CB, Blumrich EM, Cousin MA.
Cousin MA.
Martin HC, Gardner EJ, Samocha KE, Kaplanis J, Akawi N, Sifrim A, Eberhardt RY, Tavares ALT, Neville MDC, Niemi MEK, Gallone G, McRae J; Deciphering Developmental Disorders Study, Wright CF, FitzPatrick DR, Firth HV, Hurles ME.
Marson A, Burnside G, Appleton R, Smith D, Leach JP, Sills G, Tudur-Smith C, Plumpton C, Hughes DA, Williamson P, Baker GA, Balabanova S, Taylor C, Brown R, Hindley D, Howell S, Maguire M, Mohanraj R, Smith PE; SANAD II collaborators.
Marson A, Burnside G, Appleton R, Smith D, Leach JP, Sills G, Tudur-Smith C, Plumpton C, Hughes DA, Williamson P, Baker GA, Balabanova S, Taylor C, Brown R, Hindley D, Howell S, Maguire M, Mohanraj R, Smith PE; SANAD II collaborators.
UK Children’s Epilepsy Surgery Collaboration
Cizeron M, Qiu Z, Koniaris B, Gokhale R, Komiyama NH, Fransén E, Grant SGN.
Brotherstone R, McLellan A, Graham C, Fisher K.
Schnier C, Duncan S, Wilkinson T, Mbizvo GK, Chin RFM.
Mastro TL, Preza A, Basu S, Chattarji S, Till SM, Kind PC, Kennedy MB.
Rannikmäe K, Ngoh K, Bush K, Al-Shahi Salman R, Doubal F, Flaig R, Henshall DE, Hutchison A, Nolan J, Osborne S, Samarasekera N, Schnier C, Whiteley W, Wilkinson T, Wilson K, Woodfield R, Zhang Q, Allen N, Sudlow CLM.
Urquhart DS, Hill EA, Hill LE, Carruthers E, McLellan AE, Chin R, Shetty J.
Harper CB, Small C, Davenport EC, Low DW, Smillie KJ, Martínez-Mármol R, Meunier FA, Cousin MA.
Bernal J, Valdés-Hernández MDC, Escudero J, Viksne L, Heye AK, Armitage PA, Makin S, Touyz RM, Wardlaw JM.
Kafantaris E, Piper I, Lo TM, Escudero J.
Digard BG, Sorace A, Stanfield A, Fletcher-Watson S.
Abu-Akel A, Philip RCM, Lawrie SM, Johnstone EC, Stanfield AC.
Zhu F, Collins MO, Harmse J, Choudhary JS, Grant SGN, Komiyama NH.
Brown R, Lam AD, Gonzalez-Sulser A, Ying A, Jones M, Chou RC, Tzioras M, Jordan CY, Jedrasiak-Cape I, Hemonnot AL, Abou Jaoude M, Cole AJ, Cash SS, Saito T, Saido T, Ribchester RR, Hashemi K, Oren I.
Goldstein LH, Robinson EJ, Mellers JDC, Stone J, Carson A, Reuber M, Medford N, McCrone P, Murray J, Richardson MP, Pilecka I, Eastwood C, Moore M, Mosweu I, Perdue I, Landau S, Chalder T; CODES study group.
Kubota M, Hadley LV, Schaeffner S, Könen T, Meaney JA, Auyeung B, Morey CC, Karbach J, Chevalier N.
Das Sharma S, Pal R, Reddy BK, Selvaraj BT, Raj N, Samaga KK, Srinivasan DJ, Ornelas L, Sareen D, Livesey MR, Bassell GJ, Svendsen CN, Kind PC, Chandran S, Chattarji S, Wyllie DJA.
Ivanova D, Imig C, Camacho M, Reinhold A, Guhathakurta D, Montenegro-Venegas C, Cousin MA, Gundelfinger ED, Rosenmund C, Cooper B, Fejtova A.
Mewasingh LD, Chin RFM, Scott RC.
Cobb SR.
Rossini PM, Di Iorio R, Vecchio F, Anfossi M, Babiloni C, Bozzali M, Bruni AC, Cappa SF, Escudero J, Fraga FJ, Giannakopoulos P, Guntekin B, Logroscino G, Marra C, Miraglia F, Panza F, Tecchio F, Pascual-Leone A, Dubois B.
Duman M, Vaquié A, Nocera G, Heller M, Stumpe M, Siva Sankar D, Dengjel J, Meijer D, Yamaguchi T, Matthias P, Zeis T, Schaeren-Wiemers N, Hayoz A, Ruff S, Jacob C.
Procyshyn TL, Lombardo MV, Lai MC, Auyeung B, Crockford SK, Deakin J, Soubramanian S, Sule A, Baron-Cohen S, Bethlehem RAI.
Morrish P, Duncan S, Cock H.
Weir CJ, Heazell AEP, Whyte S, Norman JE.
Ensor H, Weir CJ.
Kaplanis J, Samocha KE, Wiel L, Zhang Z, Arvai KJ, Eberhardt RY, Gallone G, Lelieveld SH, Martin HC, McRae JF, Short PJ, Torene RI, de Boer E, Danecek P, Gardner EJ, Huang N, Lord J, Martincorena I, Pfundt R, Reijnders MRF, Yeung A, Yntema HG; Deciphering Developmental Disorders Study, Vissers LELM, Juusola J, Wright CF, Brunner HG, Firth HV, FitzPatrick DR, Barrett JC, Hurles ME, Gilissen C, Retterer K.
Jin X, Auyeung B, Chevalier N.
Eley SEA, McKechanie AG, Campbell S, Stanfield AC.
Vandrey B, Garden DLF, Ambrozova V, McClure C, Nolan MF, Ainge JA.
Baron-Cohen S, Tsompanidis A, Auyeung B, Nørgaard-Pedersen B, Hougaard DM, Abdallah M, Cohen A, Pohl A.
Gerlei K, Passlack J, Hawes I, Vandrey B, Stevens H, Papastathopoulos I, Nolan MF.
Mbizvo GK, Derry C, Davenport R.
Hunter MB, Yoong M, Sumpter RE, Verity K, Shetty J, McLellan A, Chin RFM.
Velasco-Estevez M, Gadalla KKE, Liñan-Barba N, Cobb S, Dev KK, Sheridan GK.
Booker SA, Simões de Oliveira L, Anstey NJ, Kozic Z, Dando OR, Jackson AD, Baxter PS, Isom LL, Sherman DL, Hardingham GE, Brophy PJ, Wyllie DJA, Kind PC.
Pastoll H, Garden DL, Papastathopoulos I, Sürmeli G, Nolan MF.
Edirisooriya M, Dykiert D, Auyeung B.
McAdam RL, Morton A, Gordon SL, Alterman JF, Khvorova A, Cousin MA, Smillie KJ.
Hulme H, Meikle LM, Strittmatter N, van der Hooft JJJ, Swales J, Bragg RA, Villar VH, Ormsby MJ, Barnes S, Brown SL, Dexter A, Kamat MT, Komen JC, Walker D, Milling S, Osterweil EK, MacDonald AS, Schofield CJ, Tardito S, Bunch J, Douce G, Edgar JM, Edrada-Ebel R, Goodwin RJA, Burchmore R, Wall DM.
Broer T, Pickersgill M, Cunningham-Burley S.
Symonds JD, Moloney TC, Lang B, McLellan A, O'Regan ME, MacLeod S, Jollands A, Vincent A, Kirkpatrick M, Brunklaus A, Shetty J, Dorris L, Forbes K, Abu-Arafeh I, Andrew J, Brink P, Callaghan M, Cruden J, Findlay C, Grattan R, MacDonnell J, McKnight J, Morrison CA, Nairn L, Pilley E, Stephen E, Thomsen S, Webb A, Wilson M, Zuberi SM.
Parker RA, Weir CJ.
Smith KM, Escudero J.
Hume DA, Caruso M, Ferrari-Cestari M, Summers KM, Pridans C, Irvine KM.
Yong XLH, Cousin MA, Anggono V.
Hall HA, Speyer LG, Murray AL, Auyeung B.
Benke TA, Kind PC.
Goldstein LH, Robinson EJ, Mellers JDC, Stone J, Carson A, Chalder T, Reuber M, Eastwood C, Landau S, McCrone P, Moore M, Mosweu I, Murray J, Perdue I, Pilecka I, Richardson MP, Medford N; CODES Study Group; CODES study group.
Davies FCJ, Hope JE, McLachlan F, Marshall GF, Kaminioti-Dumont L, Qarkaxhija V, Nunez F, Dando O, Smith C, Wood E, MacDonald J, Hardt O, Abbott CM.
Murray AL, Caye A, McKenzie K, Auyeung B, Murray G, Ribeaud D, Freeston M, Eisner M.
Gonzalez-Sulser A.
Wong H, Hooper AWM, Niibori Y, Lee SJ, Hategan LA, Zhang L, Karumuthil-Melethil S, Till SM, Kind PC, Danos O, Bruder JT, Hampson DR.
Baksh RA, Abrahams S, Bertlich M, Cameron R, Jany S, Dorrian T, Baron-Cohen S, Allison C, Smith P, MacPherson SE, Auyeung B.
Bush SJ, McCulloch MEB, Lisowski ZM, Muriuki C, Clark EL, Young R, Pridans C, Prendergast JGD, Summers KM, Hume DA.
Nobili L, de Weerd A, Rubboli G, Beniczky S, Derry C, Eriksson S, Halasz P, Högl B, Santamaria J, Khatami R, Ryvlin P, Rémi J, Tinuper P, Bassetti C, Manni R, Koutroumanidis M, Vignatelli L.
Bennett KH, Pujar SS, Martinos MM, Clark CA, Yoong M, Scott RC, Chin RFM.
Stephen J, Weir CJ, Chin RF.
Mbizvo GK, Bennett KH, Schnier C, Simpson CR, Duncan SE, Chin RFM.
Dimairo M, Pallmann P, Wason J, Todd S, Jaki T, Julious SA, Mander AP, Weir CJ, Koenig F, Walton MK, Nicholl JP, Coates E, Biggs K, Hamasaki T, Proschan MA, Scott JA, Ando Y, Hind D, Altman DG; ACE Consensus Group.
Kwok J, Hall HA, Murray AL, Auyeung B.
Bauermeister S, Orton C, Thompson S, Barker RA, Bauermeister JR, Ben-Shlomo Y, Brayne C, Burn D, Campbell A, Calvin C, Chandran S, Chaturvedi N, Chêne G, Chessell IP, Corbett A, Davis DHJ, Denis M, Dufouil C, Elliott P, Fox N, Hill D, Hofer SM, Hu MT, Jindra C, Kee F, Kim CH, Kim C, Kivimaki M, Koychev I, Lawson RA, Linden GJ, Lyons RA, Mackay C, Matthews PM, McGuiness B, Middleton L, Moody C, Moore K, Na DL, O'Brien JT, Ourselin S, Paranjothy S, Park KS, Porteous DJ, Richards M, Ritchie CW, Rohrer JD, Rossor MN, Rowe JB, Scahill R, Schnier C, Schott JM, Seo SW, South M, Steptoe M, Tabrizi SJ, Tales A, Tillin T, Timpson NJ, Toga AW, Visser PJ, Wade-Martins R, Wilkinson T, Williams J, Wong A, Gallacher JEJ.
McKechanie AG, Lawrie SM, Stanfield AC.
Schnier C, Wilkinson T, Akbari A, Orton C, Sleegers K, Gallacher J, Lyons RA, Sudlow C.
Idigo NJ, Soares DC, Abbott CM.
Crow YJ, Shetty J, Livingston JH.
Mbizvo GK, Schnier C, Simpson CR, Duncan SE, Chin RFM.
Babiloni C, Blinowska K, Bonanni L, Cichocki A, De Haan W, Del Percio C, Dubois B, Escudero J, Fernández A, Frisoni G, Guntekin B, Hajos M, Hampel H, Ifeachor E, Kilborn K, Kumar S, Johnsen K, Johannsson M, Jeong J, LeBeau F, Lizio R, Lopes da Silva F, Maestú F, McGeown WJ, McKeith I, Moretti DV, Nobili F, Olichney J, Onofrj M, Palop JJ, Rowan M, Stocchi F, Struzik ZM, Tanila H, Teipel S, Taylor JP, Weiergräber M, Yener G, Young-Pearse T, Drinkenburg WH, Randall F.
Popkirov S, Stone J, Derry CP.
Surana S, Kumar R, Pitt M, Hafner P, Mclellan A, Davidson J, Prabakhar P, Vincent A, Hacohen Y, Wright S.
Booker SA, Domanski APF, Dando OR, Jackson AD, Isaac JTR, Hardingham GE, Wyllie DJA, Kind PC.
McKechanie AG, Campbell S, Eley SEA, Stanfield AC.
Domanski APF, Booker SA, Wyllie DJA, Isaac JTR, Kind PC.
Goldstein LH, Robinson EJ, Reuber M, Chalder T, Callaghan H, Eastwood C, Landau S, McCrone P, Medford N, Mellers JDC, Moore M, Mosweu I, Murray J, Perdue I, Pilecka I, Richardson MP, Carson A, Stone J; CODES Study Group.
Nakajima R, Takao K, Hattori S, Shoji H, Komiyama NH, Grant SGN, Miyakawa T.
Kashiwagi Y, Higashi T, Obashi K, Sato Y, Komiyama NH, Grant SGN, Okabe S.
Das Sharma S, Pal R, Reddy BK, Selvaraj BT, Raj N, Samaga KK, Srinivasan DJ, Ornelas L, Sareen D, Livesey MR, Bassell GJ, Svendsen CN, Kind PC, Chandran S, Chattarji S, Wyllie DJA.
Brown SSG, Whalley HC, Kind PC, Stanfield AC.
Turko P, Groberman K, Browa F, Cobb S, Vida I.
Ibáñez-Molina AJ, Iglesias-Parro S, Escudero J.
Mbizvo GK, Lentell IC, Leen C, Roddie H, Derry CP, Duncan SE, Rannikmäe K.
Mbizvo GK, Bennett K, Simpson CR, Duncan SE, Chin RFM.
Vasistha NA, Johnstone M, Barton SK, Mayerl SE, Thangaraj Selvaraj B, Thomson PA, Dando O, Grünewald E, Alloza C, Bastin ME, Livesey MR, Economides K, Magnani D, Makedonopolou P, Burr K, Story DJ, Blackwood DHR, Wyllie DJA, McIntosh AM, Millar JK, Ffrench-Constant C, Hardingham GE, Lawrie SM, Chandran S.
McKechanie AG, Barnicoat A, Trender-Gerhard I, Allison M, Stanfield AC.
Train S, Kydonaki K, Rattray J, Stephen J, Weir CJ, Walsh TS.
Marwick KFM, Hansen KB, Skehel PA, Hardingham GE, Wyllie DJA.
Marwick KFM, Hansen KB, Skehel PA, Hardingham GE, Wyllie DJA.
Strehlow V, Heyne HO, Vlaskamp DRM, Marwick KFM, Rudolf G, de Bellescize J, Biskup S, Brilstra EH, Brouwer OF, Callenbach PMC, Hentschel J, Hirsch E, Kind PC, Mignot C, Platzer K, Rump P, Skehel PA, Wyllie DJA, Hardingham GE, van Ravenswaaij-Arts CMA, Lesca G, Lemke JR; GRIN2A study group.
Popkirov S, Nicholson TR, Bloem BR, Cock HR, Derry CP, Duncan R, Dworetzky BA, Edwards MJ, Espay AJ, Hallett M, Lang AE, Leach JP, Lehn A, McGonigal A, Morgante F, Perez DL, Reuber M, Richardson MP, Smith P, Stamelou M, Tijssen MAJ, Tinazzi M, Carson AJ, Stone J.
Wheeler GM, Mander AP, Bedding A, Brock K, Cornelius V, Grieve AP, Jaki T, Love SB, Odondi L, Weir CJ, Yap C, Bond SJ.
Wilkinson T, Schnier C, Bush K, Rannikmäe K, Henshall DE, Lerpiniere C, Allen NE, Flaig R, Russ TC, Bathgate D, Pal S, O'Brien JT, Sudlow CLM; Dementias Platform UK and UK Biobank.
Magnani D, Chandran S, Wyllie DJA, Livesey MR.
Symonds JD, Zuberi SM, Stewart K, McLellan A, O'Regan M, MacLeod S, Jollands A, Joss S, Kirkpatrick M, Brunklaus A, Pilz DT, Shetty J, Dorris L, Abu-Arafeh I, Andrew J, Brink P, Callaghan M, Cruden J, Diver LA, Findlay C, Gardiner S, Grattan R, Lang B, MacDonnell J, McKnight J, Morrison CA, Nairn L, Slean MM, Stephen E, Webb A, Vincent A, Wilson M.
Booker SA, Simões de Oliveira L, Anstey NJ, Kozic Z, Dando OR, Jackson AD, Baxter PS, Isom LL, Sherman DL, Hardingham GE, Brophy PJ, Wyllie DJA, Kind PC.
Martinos MM, Pujar S, O'Reilly H, de Haan M, Neville BGR, Scott RC, Chin RFM.
Muscas M, Louros SR, Osterweil EK.
Munro DAD, Wineberg Y, Tarnick J, Vink CS, Li Z, Pridans C, Dzierzak E, Kalisky T, Hohenstein P, Davies JA.
Hunter MB, Yoong M, Sumpter RE, Verity K, Shetty J, McLellan A, Jones J, Quigley A, Tallur KK, Chin RFM.
Lord J, Gallone G, Short PJ, McRae JF, Ironfield H, Wynn EH, Gerety SS, He L, Kerr B, Johnson DS, McCann E, Kinning E, Flinter F, Temple IK, Clayton-Smith J, McEntagart M, Lynch SA, Joss S, Douzgou S, Dabir T, Clowes V, McConnell VPM, Lam W, Wright CF, FitzPatrick DR, Firth HV, Barrett JC, Hurles ME;
Deciphering Developmental Disorders study.
Stanfield AC, McKechanie AG, Lawrie SM, Johnstone EC, Owens DGC.
Chin RF.
Johnstone M, Vasistha NA, Barbu MC, Dando O, Burr K, Christopher E, Glen S, Robert C, Fetit R, Macleod KG, Livesey MR, Clair DS, Blackwood DHR, Millar K, Carragher NO, Hardingham GE, Wyllie DJA, Johnstone EC, Whalley HC, McIntosh AM, Lawrie SM, Chandran S.
Myland M, Buysse B, Tsong W, Power GS, Nordli D, Chin RFM.
Demarest S, Pestana-Knight EM, Olson HE, Downs J, Marsh ED, Kaufmann WE, Partridge CA, Leonard H, Gwadry-Sridhar F, Frame KE, Cross JH, Chin RFM, Parikh S, Panzer A, Weisenberg J, Utley K, Jaksha A, Amin S, Khwaja O, Devinsky O, Neul JL, Percy AK, Benke TA.
Booth DG, Beckett AJ, Prior IA, Meijer D.
Asiminas A, Jackson AD, Louros SR, Till SM, Spano T, Dando O, Bear MF, Chattarji S, Hardingham GE, Osterweil EK, Wyllie DJA, Wood ER, Kind PC.
Cheung G, Cousin MA.
Kokotos AC, Harper CB, Marland JRK, Smillie KJ, Cousin MA, Gordon SL.
Tangwiriyasakul C, Premoli I, Spyrou L, Chin RF, Escudero J, Richardson MP.
Ostrowski PJ, Zachariou A, Loveday C, Beleza-Meireles A, Bertoli M, Dean J, Douglas AGL, Ellis I, Foster A, Graham JM, Hague J, Hilhorst-Hofstee Y, Hoffer M, Johnson D, Josifova D, Kant SG, Kini U, Lachlan K, Lam W, Lees M, Lynch S, Maitz S, McKee S, Metcalfe K, Nathanson K, Ockeloen CW, Parker MJ, Pierson TM, Rahikkala E, Sanchez-Lara PA, Spano A, Van Maldergem L, Cole T, Douzgou S, Tatton-Brown K.
Nabbout R, Arzimanoglou A, Chin RFM, Grinspan Z, Speechley K, Camfield P.
Marwick KFM, Skehel PA, Hardingham GE, Wyllie DJA.
Hume DA, Irvine KM, Pridans C.
Chin RFM.
McLachlan F, Sires AM, Abbott CM.
Chanaday NL, Cousin MA, Milosevic I, Watanabe S, Morgan JR.
Hansen CH, Warner P, Walker A, Parker RA, Whitaker L, Critchley HOD, Weir CJ.
Mbizvo GK, Bennett K, Simpson CR, Duncan SE, Chin RFM.
Kokotos AC, Peltier J, Davenport EC, Trost M, Cousin MA.
Pallmann P, Bedding AW, Choodari-Oskooei B, Dimairo M, Flight L, Hampson LV, Holmes J, Mander AP, Odondi L, Sydes MR, Villar SS, Wason JMS, Weir CJ, Wheeler GM, Yap C, Jaki T.
Al-Timemy AH, Bugmann G, Escudero J.
Chin RFM.
Azami H, Escudero J.
Zhu F, Cizeron M, Qiu Z, Benavides-Piccione R, Kopanitsa MV, Skene NG, Koniaris B, DeFelipe J, Fransén E, Komiyama NH, Grant SGN.
O'Neill N, McLaughlin C, Komiyama N, Sylantyev S.
Hendriksen RGF, Vles JSH, Aalbers MW, Chin RFM, Hendriksen JGM.
Selvaraj BT, Livesey MR, Zhao C, Gregory JM, James OT, Cleary EM, Chouhan AK, Gane AB, Perkins EM, Dando O, Lillico SG, Lee YB, Nishimura AL, Poreci U, Thankamony S, Pray M, Vasistha NA, Magnani D, Borooah S, Burr K, Story D, McCampbell A, Shaw CE, Kind PC, Aitman TJ, Whitelaw CBA, Wilmut I, Smith C, Miles GB, Hardingham GE, Wyllie DJA, Chandran S.
Kopanitsa MV, Gou G, Afinowi NO, Bayés À, Grant SGN, Komiyama NH.
Tho-Calvi SC, Thompson D, Saunders D, Agrawal S, Basu A, Chitre M, Chow G, Gibbon F, Hart A, Tallur KK, Kirkham F, Kneen R, McCullagh H, Mewasingh L, Vassallo G, Vijayakumar K, Wraige E, Yeo TH, Ganesan V; British Paediatric Neurology Association Moyamoya Study group.
Azami H, Escudero J.
Yoong M, Hunter M, Stephen J, Quigley A, Jones J, Shetty J, McLellan A, Bastin ME, Chin RFM.
Fernández A, Al-Timemy AH, Ferre F, Rubio G, Escudero J.
Weir CJ, Butcher I, Assi V, Lewis SC, Murray GD, Langhorne P, Brady MC.
Dimairo M, Coates E, Pallmann P, Todd S, Julious SA, Jaki T, Wason J, Mander AP, Weir CJ, Koenig F, Walton MK, Biggs K, Nicholl J, Hamasaki T, Proschan MA, Scott JA, Ando Y, Hind D, Altman DG.
Al-Qazzaz NK, Ali SHBM, Ahmad SA, Islam MS, Escudero J.
Coba MP, Ramaker MJ, Ho EV, Thompson SL, Komiyama NH, Grant SGN, Knowles JA, Dulawa SC.
Horner AE, McLaughlin CL, Afinowi NO, Bussey TJ, Saksida LM, Komiyama NH, Grant SGN, Kopanitsa MV.
Tillmann J, Ashwood K, Absoud M, Bölte S, Bonnet-Brilhault F, Buitelaar JK, Calderoni S, Calvo R, Canal-Bedia R, Canitano R, De Bildt A, Gomot M, Hoekstra PJ, Kaale A, McConachie H, Murphy DG, Narzisi A, Oosterling I, Pejovic-Milovancevic M, Persico AM, Puig O, Roeyers H, Rommelse N, Sacco R, Scandurra V, Stanfield AC, Zander E, Charman T.
Ebied A, Kinney-Lang E, Spyrou L, Escudero J.
Saxena K, Webster J, Hallas-Potts A, Mackenzie R, Spooner PA, Thomson D, Kind P, Chattarji S, Morris RGM.
Wilkinson T, Ly A, Schnier C, Rannikmäe K, Bush K, Brayne C, Quinn TJ, Sudlow CLM; UK Biobank Neurodegenerative Outcomes Group and Dementias Platform UK.
Garden DLF, Oostland M, Jelitai M, Rinaldi A, Duguid I, Nolan MF.
Wilson P, Wood R, Lykke K, Hauskov Graungaard A, Ertmann RK, Andersen MK, Haavet OR, Lagerløv P, Abildsnes E, Dahli MP, Mäkelä M, Varinen A, Hietanen M.
Malcolm R, Ecks S, Pickersgill M.
Martinos MM, Pujar S, Gillberg C, Cortina-Borja M, Neville BGR, De Haan M, Scott RC, Chin RFM.
Pujar SS, Martinos MM, Cortina-Borja M, Chong WKK, De Haan M, Gillberg C, Neville BG, Scott RC, Chin RF; North London Epilepsy Research Network.
Perkins EM, Clarkson YL, Suminaite D, Lyndon AR, Tanaka K, Rothstein JD, Skehel PA, Wyllie DJA, Jackson M.
Jammeh EA, Carroll CB, Pearson SW, Escudero J, Anastasiou A, Zhao P, Chenore T, Zajicek J, Ifeachor E.
Hagerman R, Jacquemont S, Berry-Kravis E, Des Portes V, Stanfield A, Koumaras B, Rosenkranz G, Murgia A, Wolf C, Apostol G, von Raison F.
Liu YH, Moratal D, Escudero J, Huang HP.
Tinson D, Crockford C, Gharooni S, Russell H, Zoeller S, Leavy Y, Lloyd R, Duncan S.
Wyllie DJA.
Booker SA, Loreth D, Gee AL, Watanabe M, Kind PC, Wyllie DJA, Kulik Á, Vida I.
Aaberg KM, Bakken IJ, Lossius MI, Lund Søraas C, Tallur KK, Stoltenberg C, Chin R, Surén P.
Goffin J, MacKenzie SA, Tallur KK, Kaliaperumal C.
Tennant SA, Fischer L, Garden DLF, Gerlei KZ, Martinez-Gonzalez C, McClure C, Wood ER, Nolan MF.
Grylls E, Kinsky M, Baggott A, Wabnitz C, McLellan A.
Baker K, Gordon SL, Melland H, Bumbak F, Scott DJ, Jiang TJ, Owen D, Turner BJ, Boyd SG, Rossi M, Al-Raqad M, Elpeleg O, Peck D, Mancini GMS, Wilke M, Zollino M, Marangi G, Weigand H, Borggraefe I, Haack T, Stark Z, Sadedin S; Broad Center for Mendelian Genomics, Tan TY, Jiang Y, Gibbs RA, Ellingwood S, Amaral M, Kelley W, Kurian MA, Cousin MA, Raymond FL.
Kinney-Lang E, Spyrou L, Ebied A, Chin RFM, Escudero J.
Reid LEM, Pretsch U, Jones MC, Lone NI, Weir CJ, Morrison Z.
Jaarsma D, Blot FGC, Wu B, Venkatesan S, Voogd J, Meijer D, Ruigrok TJH, Gao Z, Schonewille M, De Zeeuw CI.
McKay S, Ryan TJ, McQueen J, Indersmitten T, Marwick KFM, Hasel P, Kopanitsa MV, Baxter PS, Martel MA, Kind PC, Wyllie DJA, O'Dell TJ, Grant SGN, Hardingham GE, Komiyama NH.
Pujades-Rodriguez M, Assi V, Gonzalez-Izquierdo A, Wilkinson T, Schnier C, Sudlow C, Hemingway H, Whiteley WN.
Chin RFM, Stephen J, Weir CJ, Wood R.
Cousin MA, Gordon SL, Smillie KJ.
Authors
Hendriksen RGF, Vies JSH, Aalbers MW, Chin RFM, Hendriksen JGM. Eur J Paediatr Neurol. 2017 Dec.
Description
In a Dutch-Scottish collaboration study with questionnaires directed to an international population, this study suggests that almost one in thirteen children with Duchenne have epilepsy and that other brain-related comorbidities were higher if both conditions co-existed. However, the study may have been biased because there was not a universal response so future studies are needed to determine true incidence.
Authors
Martinos MM, Pujar S, Gillberg C, Cortina-Borja M, Neville BGR, De Haan M, Scott RC, Chin RFM. Dev Med Child Neurol. 2017 Dec.
Description
Having established the first study focused on prolonged seizures in children, Chin and colleagues followed this unique cohort for 8 years after their initial episode of prolonged seizures to determine behavioural outcomes. Just over a quarter had a behavioural/psychiatric disorder (including ADHD and autism spectrum disorders) with those who had epilepsy at the time of the prolonged seizures being more severely affected. Repeated episodes of prolonged seizures or having had previous seizures before the initial episode increases the risk for subsequent problems.
Authors
Leach JP, Smith PE, Craig J, Bagary M, Cavanagh D, Duncan S, Kelso ARC, Marson AG, McCorry D, Nashef L, Nelson-Piercy C, Northridge R, Sieradzan K, Thangaratinam S, Walker M, Winterbottom J, Reuber M. Seizure. 2017 Aug; 50:67-72.
Description
This paper summarises findings of a multidisciplinary meeting with representation from a wide group of professional bodies aimed at producing the best epilepsy pregnancy care to reduce mortality in expectant mothers with epilepsy, and reduce problems in their children. The authors identified Golden Moments of opportunities for improving outcomes, Key Groups to making change, and aimed to have these improvements in place by 2020.
Authors
Nicholson-Fish JC, Smillie KJ, Cousin MA. J Neurosci Methods. 2016 Jun; 266: 1-10.
Description
Having previously shown that abnormalities in activity-dependent bulk endocytosis may be implicated as a cause for epilepsy, and a potential target for development of novel antiepileptic drugs, the authors provide a new method to monitor the endocytosis mode.
Authors
Smith K, Absalo D, Escudero J. PLoS One. 2017 Oct; 12(10).
Description
There is evidence of interconnectivity of different parts of the brain, with varying degrees of network connectivity. How to measure these networks using imaging and EEG techniques, and how networks are involved in normal learning and behaviour as well as in diseases of the brain are a major research focus in laboratories worldwide. In this paper, the authors provide new evidence of the importance of considering a large number of edges in EEG connectivity network research.
Authors
Al-Qazzaz NK, Ali SHBM, Ahmad SA, Islam MS, Escudero J. Med Biol Eng Comput. 2017 Nov.
Description
EEGs are often used primarily for diagnosis and monitoring treatment of seizures. However, there is increasing use of EEG in identifying problems in learning and behaviour. Dr Escudero and colleagues demonstrate novel analytical methods of EEGs that may help in distinguishing between patients with stroke related cognitive problems and those with vascular dementia.
Authors
Bethlehem RAI, Lombardo MV, Lai MC, Auyeung B, Crockford SK, Deakin J, Soubramanian S, Sule A, Kundu P, Voon V, Baron-Cohen S. Transl Psychiatry. 2017 Apr; 7(4).
Description
The cause for gender differences in the incidence of different types of epilepsy and associated comorbidity is often unclear. This paper demonstrates that the naturally occurring hormone oxytocin affects brain connectivity in women. This may contribute to the differences in subsets of people with neurological conditions, including epilepsy.
Authors
Chadwick A, Van Rossum MC, Nolan MF. Elife. 2016 Dec; 5.
Description
Abnormalities in the function of specific brain cells, interneurons, are a possible cause for seizures in people with epilepsy. Learning problems are common in people with epilepsy, independent of seizure control, but the mechanism for these problems are unclear. In this study, Matt Nolan and colleagues demonstrate a mechanism of encoding information through interneuron-dependent brain rhythms.
Authors
Sherman S, Harden J, Cattanach D, Cameron ST. J Fam Plann Reprod Health Care. 2017 Oct; 43(4).
Description
Data on a doctoral project being supervised by MMEC’s Jeni Harden, one of the authors of this paper, show children with epilepsy often have limited knowledge about epilepsy. Publicly readily available information about epilepsy, aside from written information, specifically designed with children with mind are sparse. The current study shows that an animated film on early medical abortion might be valuable in providing information for women considering this procedure. Extrapolating from this, an animation film about epilepsy could be helpful in providing children with much needed information about the disease.
Authors
Clark D, King A, Sharpe K, Connelly G, Elliott L, Macpherson LMD, McMahon AD, Milligan I, Wilson P, Conway DI, Wood R. Public Health. 2017 Sep; 150.
Description
Dr Wood and colleagues demonstrate the strong potential of linking Scotland’s routine administrative social, education and health data to investigate the health outcomes of school aged children. By extending their method they propose to be able to include information on children who are not in public funded schooling.
Authors
Aaberg KM, Surén P, Søraas CL, Bakken IJ, Lossius MI, Stoltenberg C, Chin R. Epilepsia. 2017 Sep.
Description
In one of the first published studies to use the new ILAE classification scheme for epilepsy, and apply it to the largest validated and phenotyped epilepsy cohorts identified from a birth cohort worldwide, the Norway-UK researchers show: (1) the new classification allows for a greater precision in diagnoses which may help with prognosis, treatment and trying to find causes but as this requires detailed investigative results, may result in more epilepsies being unclassifiable pending results/availability of tests. (2) Despite advances in technology, the cause of epilepsy still remains unknown in most children.
Authors
Reijnders MRF, Ansor NM, Kousi M, Yue WW, Tan PL, Clarkson K, Clayton-Smith J, Corning K, Jones JR, Lam WWK, Mancini GMS, Marcelis C, Mohammed S, Pfundt R, Roifman M, Cohn R, Chitayat D; Deciphering Developmental Disorders Study, Millard TH, Katsanis N, Brunner HG, Banka S. Am J Hum Genet. 2017 Sep; 101(3).
Description
Dr Lam and colleagues through an international collaborative study reveals the role of mutations in RAC1 gene in neurodevelopmental disorders
Authors
Harper CB, Mancini GMS, van Slegtenhorst M, Cousin MA. Neurobiol Dis. 2017 Sep; 108.
Description
MMEC Pre-clinical lead Mike Cousin and his team reveal a form of severe intellectual disability and epilepsy found in a single patient was caused by a mutation in the SYP gene. They went on to show that this mutation specifically affected movement of a key protein for neuron communication – synaptobrevin II. They showed that this defect was also seen with other human mutations in SYP, this time from X-linked intellectual disability. Therefore correcting the altered movement of synaptobrevin II may be a potential avenue for therapeutic intervention in both epilepsy and intellectual disability.
Authors
Murray AL, Booth T, Auyeung B, McKenzie K, Kuenssberg R. Assessment. 2017 Sep; 1073191117733548.
Description
Autism is a common comorbidity in epilepsy and those on the milder end of the spectrum can be difficult to identify. Thus, screening methods for autism are important. This study confirms that a novel screening instrument (AQ-10) which determines who would benefit from more detailed testing, is not biased against females. Nonetheless the authors suggest one item to be replaced.
Authors
Thomson SR, Seo SS, Barnes SA, Louros SR, Muscas M, Dando O, Kirby C, Wyllie DJA, Hardingham GE, Kind PC, Osterweil EK. Neuron. 2017 Aug; 95(3).
Description
Fragile X syndrome (FXS) is the most common form of inherited X-linked intellectual disability, with patients often displaying epilepsy. FXS is thought to be caused by excessive synthesis of specific types of proteins controlled by FMRP, which is mutated in FXS. . The Osterweil group showed common FXS symptoms (including seizures) can be reversed in a model system by activating a pathway dependent on the neurotransmitter acetylcholine. Interestingly proteins for this pathway are increased in FXS, showing that enhancement of specific proteins may be beneficial preventing FXS symptoms, including seizures.
Authors
Corbett MA, Turner SJ, Gardner A, Silver J, Stankovich J, Leventer RJ, Derry CP, Carroll R, Ha T, Scheffer IE, Bahlo M, Jackson GD, Mackey DA, Berkovic SF, Gecz J. Eur J Med Genet. 2017 Aug; 60(8).
Description
Chris Derry from MMEC and colleagues discover mutations in COL18A1 gene in four sisters. These sisters display Lennox-Gastaut type severe refractory epilepsy and abnormality in the formation of the front of the brain. This finding is novel since it identifies a genetic, inherited cause for Lennox Gastatut Syndrome. Previously this genetic mutation was usually found in another neurological disorder therefore this study expands the types of diseases/conditions that occur due to abnormalities in COL18A1.
Authors
Wood R. Dev Med Child Neurol. 2017 Aug; 59(8).
Description
Dr. Wood comments on an original article by Glinianaia et al. on “Predicting the prevalence of cerebral palsy by severity level in children aged 3 to 15 years across England and Wales by 2020” Dr. Wood emphasises that the key message arising from the paper by Glinianaia et al. is that, austerity and service cuts notwithstanding, the need for robust, integrated services for children (and their families) with complex needs is unlikely to diminish in the short to medium term. Regardless of advances in prevention, there will always be children with significant impairment and disability, and how we collectively organize and deliver services to meet their needs will remain a measure of our society.
Authors
Leach JP, Smith PE, Craig J, Bagary M, Cavanagh D, Duncan S, Kelso ARC, Marson AG, McCorry D, Nashef L, Nelson-Piercy C, Northridge R, Sieradzan K, Thangaratinam S, Walker M, Winterbottom J, Reuber M. Seizure. 2017 Aug; 50.
Description
Susan Duncan, head of the adult epilepsy service in Edinburgh, and other members of the UK wide epilepsy mortality group put forward suggestions to optimise pregnancy care in women with epilepsy. The aim is to reduce maternal mortality and morbidity in children exposed to anti-epileptic medication whilst they are in the womb.
Authors
Siddiqui A, Cuttini M, Wood R, Velebil P, Delnord M, Zile I, Barros H, Gissler M, Hindori-Mohangoo AD, Blondel B, Zeitlin J; Euro-Peristat Scientific Committee. Paediatr Perinat Epidemiol. 2017 Jul; 31(4).
Description
The APGAR Score, usually given at 1 minute, 5 minutes, and 10 minutes after birth is often used to predict mortality within the first month of life. Furthermore lower scores are associated with long term health problems in children who survive past the first month of life. Dr. Wood and colleagues show that there is a large variation in APGAR scoring amongst countries, likely due to national scoring practices, makes the APGAR score an unsuitable indicator for comparing health in the newborn across countries.
Authors
Aaberg KM, Gunnes N, Bakken IJ, Lund Søraas C, Berntsen A, Magnus P, Lossius MI, Stoltenberg C, Chin R, Surén P. Pediatrics. 2017 May;139(5).
Description
In the second of a series of papers from a collaboration between the Norwegian Institute of Public Health and the University of Edinburgh, the researchers provide up to date information on the incidence of childhood epilepsy. The importance, strength and merits of analysing data collected routinely in clinical practice, often referred to as “Big Data” is increasingly being recognised. This paper demonstrates the importance of the validation of epilepsy diagnoses in such data, since a third of children can be erroneously coded as having epilepsy when they do not. The now validated epilepsy cohort is part of a much larger birth cohort and will allow the researchers to examine the development of children with epilepsy compared to those without, the prenatal and postnatal factors that lead to an increased risk for epilepsy and related neurodevelopmental problems, and factors that improve outcomes.
Authors
Pujar SS, Seunarine KK, Martinos MM, Neville BG, Scott RC, Chin RF, Clark CA. Epilepsia. 2017 May;58(5):772-780.
Description
Febrile seizures occur in 3 per 100 children between the ages of 6 months to 5 years. They generally last less than 5 minutes but can go on for longer than 30 minutes. These longer seizures, prolonged febrile seizures, are thought to cause brain damage. In this study of a unique group of children with prolonged febrile seizures, researchers from UCL and the University of Edinburgh report findings that suggest prolonged febrile seizures can interfere with usual development of how different parts of the brain connect with each other but adopts to this within 8 years through changes in the microstructure and organisation of the connective tracts of the brain.
Authors
Davies FC, Hope JE, McLachlan F, Nunez F, Doig J, Bengani H, Smith C, Abbott CM.
Description
Mutations in the gene EF1A2 have recently been found to give rise to neurodevelopmental disorders. In pre-clinical studies, the researchers produced mice with the mutation G70S (the most frequently occurring mutation in humans) in the eEF1A2 gene some of which have seizures and sudden death. They conclude that the abnormal protein formed due to this gene mutation is essentially non-functional, suggesting this disorder results from loss of normal eEF1A2 function
Authors
Currie SP, Luz LL, Booker SA, Wyllie DJ, Kind PC, Daw MI. Epilepsia. 2017 Apr;58(4):597-607.
Description
Developmental concerns and or problems can exist prior to the onset of seizures. Why cognitive and behavioural problems occur in a high proportion of people with epilepsy is unclear. This study shows that in an experimental model of a specific type of epilepsy, childhood absence epilepsy, there are changes in the way that the brain is usually connected PRIOR to the onset of seizures.
Authors
Cousin MA. J Physiol. 2017 Feb 15;595(4):1005-1006.
Description
Synaptic vesicles (SVs) store neurotransmitter inside brain cells and during neuronal activity are triggered to release their contents to evoke neuronal communication. This short commentary article highlighted our growing understanding that not all SVs are created equal, and that there are different populations that mediate different types of neurotransmission. This may be important for neurotransmitter release during epilepsy, and identifying which SVs are responsible may allow excessive neurotransmission to be limited.
Authors
Luz LL, Currie SP, Daw MI. PLoS One. 2017 Feb 8;12(2):e0171897.
Description
Preclinical, non-human studies are important to increase understanding of and development of treatments for epilepsy. Brain cells are constantly being formed and lost in the living brain with those that remain forming connections between them. This study shows the way that brain cells communicate with each other in experimental studies of brain slices in specialised preparations changes over time. Thus, in experiments using this technique, this has to be borne in mind.
Authors
Smith K, Escudero J. J Neurosci Methods. 2017 Jan 30;276:1-12.
Description
EEGs have traditionally been used to help in the diagnosis and treatment of epilepsy. There is increasing interest in using EEG to develop networks to enhance our understanding of how the brain is connected and how it works. This paper provides insight into the complex ways that brain networks are organised.
Authors
Gonzalez-Sulser A, Nolan MF. Nat Neurosci. 2016 Dec 27;20(1):1-2.
Description
Grid-firing fields of neurons in the entorhinal cortex are thought to require inputs encoding running speed. Glutamatergic projections from the medial septum may be one of the inputs that provide these speed signals.
Authors
Iniesta RR, Paciarotti I, Davidson I, McKenzie JM, Brand C, Chin RF, Brougham MF, Wilson DC. Br J Nutr. 2016 Dec;116(11):1926-1934.
Description
This study showed that in Scotland, children with cancer are at no higher risk of having low Vitamin D levels compared to children in the general Scottish population. However, in both groups, low levels are common. Older children with cancer, or those who are overweight or not taking vitamin D supplements are more likely to have low levels. The study collaborators in oncology, gastroenterology and neurology services at the Royal Hospital for Sick Children in Edinburgh recommended that supplementation and monitoring should implemented. Vitamin D levels in the “healthy” control group of children were obtained through a parallel study funded by the Roald Dahl Marvellous Children’s Charity, examining Vitamin D levels in Scottish children with epilepsy versus those without.
Authors
Chadwick A, van Rossum MC, Nolan MF. Elife. 2016 Dec 8;5.
Description
The brain electrical activity varies throughout the day and even at the same time period, there can be marked variation of electrical activity within different parts of the brain. These electrical activities have a rhythm and are described as oscillations. Maintenance of these oscillations are linked to learning and if they become abnormal could be associated with development of seizures. In this paper, the authors report on how the medial septum of the brain (a potential target for novel epilepsy treatments) influences oscillations.
Authors
Lai MC, Lombardo MV, Ruigrok AN, Chakrabarti B, Auyeung B, Szatmari P, Happé F, Baron-Cohen S; MRC AIMS Consortium. Autism. 2016 Nov 29.
Description
The co-occurrence of epilepsy and autism is common. From a study carried out by a consortium of researchers, Dr. Auyeung and colleagues investigated if and how people with autism “camouflage” their social communication difficulties. They found that the degree of camouflaging was not significantly influenced by age or IQ. On average, women with autism had higher camouflaging scores than men with autism with substantial variability in both groups. Greater camouflaging was associated with more depressive symptoms in men.
Authors
Murray AL, Allison C, Smith PL, Baron-Cohen S, Booth T, Auyeung B. Autism Res. 2016 Nov 28.
Description
There are more than 40 different types of epilepsy, and there are many autism spectrum conditions (ASC). This study addresses the possibility of misdiagnosis or underdiagnosis using the AQ-10, a screening test for ASC recommended by the National Institute of Clinical Excellence. Dr. Auyeung and colleagues show that some items were biased towards males and others to females but overall there was no bias. This supports the continued use of AQ-10 as a screening test, but caution should be exercised when interpreting responses to individual items.
Authors
Ruth R. Shah, Justyna Cholewa-Waclaw, Faith C.J. Davies, Katie M. Paton, Ronan Chaligne, Edith Heard, Catherine M. Abbott, Adrian P. Bird. Wellcome Open Res. 2016 Nov 15; 1: 13.
Description
There is increasing evidence of the role of genetic abnormalities in diseases of the nervous system, including epilepsy. Identification of a genetic abnormality is insufficient on its own and more work is needed to understand the changes in function that result from this event and thus the changes in biology in humans. Understanding this can be highly beneficial with prognostication and development of therapies. In this paper, Prof Abbott and colleagues show how a novel technique CRISPR/Cas 9 can be used to introduce genetic abnormalities in human brain cells. This is usually a very difficult process for brain cells that are grown in dishes. This new work opens up potential to study the mechanism of human brain diseases including Rett Syndrome and EEF1A2 disorder.
Authors
Shipston-Sharman O, Solanka L, Nolan MF. J Physiol. 2016 Nov 15;594(22):6547-6557.
Description
Seizures arise because of an imbalance between excitatory and inhibitory mechanisms in the brain. In this paper, the authors discuss evidence for continuous attractor network models that account for grid firing by synaptic interactions between excitatory and inhibitory cells.
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Aaberg KM, Bakken IJ, Lossius MI, Lund Soraas C, Haberg SE, Stoltenberg C, Suren P, Chin R. Pediatrics. 2016 Aug;138(3).
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Authors
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Description
The detection of spikes on EEGs is an important part of the diagnosis and treatment of epilepsy. Seizure detection devices rely on automated detection of such spikes but if there are irregularities in the trace from movement or other artefacts, this can be difficult or impossible. The authors report their discovery of a novel method of detecting spikes and announce the free availability of the code.
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Ramsden HL, Sürmeli G, McDonagh SG, Nolan MF. PLOS Computational Biology. 2015 Jan;11(1).
Reilly C, Atkinson P, Das KB, Chin RF, Aylett SE, Burch V, Gillberg C, Scott RC, Neville BG. Epilepsy Behav. 2015 Jan;42:86-92.
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