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Burn, Lachlan [Author]; Faull, Jonathan [Author]; Kirilenko, Andrei [Author]; Laffan, Brigid [Author]; Landau, Jean-Pierre [Author]; Manuelides, Yannis [Author]; Micheler, Eva-Maria [Author]; Miles, David [Author]; Sandbu, Martin [Author]; Smoleńska, Agnieszka [Author]; Schlosser, Pierre [Author]; Zettelmeyer, Jeromin [Author] ; Allen, Franklin [Editor]; Carletti, Elena [Editor]; Gray, Joanna [Editor]; Gulati, Mitu [Editor] Europäische Kommission Exekutivagentur für Kleine und Mittlere UnternehmenThe changing geography of finance and regulation in EuropeView onlineSchließen
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Burn, LachlanCapital Markets Union and regulation of the EU’s capital marketsView onlineSchließen
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Published in: Capital Markets Law Journal
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Burn, Lachlan; Golden, JeffreyEditors’ NoteView onlineSchließen
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Published in: Capital Markets Law Journal
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Golden, Jeffrey; Burn, LachlanEditors’ NoteView onlineSchließen
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Published in: Capital Markets Law Journal
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Burn, Lachlan; Greene, EdwardEditors’ NoteView onlineSchließen
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Published in: Capital Markets Law Journal
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Burn, Lachlan; Greene, EdWhat are capital markets and what are they for?View onlineSchließen
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Published in: Capital Markets Law Journal
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Packman, Lachlan; Philippa, Bronson; Pivrikas, Almantas; Burn, Paul L.; Gentle, Ian R.Reconstructing the 3D Coordinates of Guest:Host OLED Blends with Single Atom ResolutionView onlineSchließen
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Published in: Small Methods
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Mallo, Neil; McAnally, Shaun; Jin, Hui; Babazadeh, Mohammad; Packman, Lachlan; Chu, Ronan; Burn, Paul L.; Gentle, Ian R.; Shaw, Paul E.The Effect of Fluorinated Benzothiadiazole-dicyanovinyl Acceptors on the Dielectric Constants of Organic Photovoltaic MaterialsView onlineSchließen
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Published in: ACS Applied Energy Materials
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Packman, Lachlan; Mallo, Neil; Raynor, Aaron; Gao, Mile; Babazadeh, Mohammad; Jin, Hui; Huang, David M.; Burn, Paul L.; Gentle, Ian R.; Shaw, Paul E.The impact of film deposition and annealing on the nanostructure and dielectric constant of organic semiconductor thin filmsView onlineSchließen
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Published in: Physical Chemistry Chemical Physics
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Aitken, Stuart; Firth, Helen V.; McRae, Jeremy; Halachev, Mihail; Kini, Usha; Parker, Michael J.; Lees, Melissa M.; Lachlan, Katherine; Sarkar, Ajoy; Joss, Shelagh; Splitt, Miranda; McKee, Shane; Németh, Andrea H.; Scott, Richard H.; Wright, Caroline F.; Marsh, Joseph A.; Hurles, Matthew E.; FitzPatrick, David R.; Fitzgerald, T.W.; Gerety, S.S.; Jones, W.D.; van Kogelenberg, M.; King, D.A.; McRae, J.; [...]Finding Diagnostically Useful Patterns in Quantitative Phenotypic DataView onlineSchließen
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Published in: The American Journal of Human Genetics
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Martin, Hilary C.; Gardner, Eugene J.; Samocha, Kaitlin E.; Kaplanis, Joanna; Akawi, Nadia; Sifrim, Alejandro; Eberhardt, Ruth Y.; Tavares, Ana Lisa Taylor; Neville, Matthew D. C.; Niemi, Mari E. K.; Gallone, Giuseppe; McRae, Jeremy; Borras, Silvia; Clark, Caroline; Dean, John; Miedzybrodzka, Zosia; Ross, Alison; Tennant, Stephen; Dabir, Tabib; Donnelly, Deirdre; Humphreys, Mervyn; Magee, Alex; McConnell, Vivienne; McKee, Shane; [...]The contribution of X-linked coding variation to severe developmental disordersView onlineSchließen
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Published in: Nature Communications
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Kaplanis, Joanna; Samocha, Kaitlin E.; Wiel, Laurens; Zhang, Zhancheng; Arvai, Kevin J.; Eberhardt, Ruth Y.; Gallone, Giuseppe; Lelieveld, Stefan H.; Martin, Hilary C.; McRae, Jeremy F.; Short, Patrick J.; Torene, Rebecca I.; de Boer, Elke; Danecek, Petr; Gardner, Eugene J.; Huang, Ni; Lord, Jenny; Martincorena, Iñigo; Pfundt, Rolph; Reijnders, Margot R. F.; Yeung, Alison; Yntema, Helger G.; Borras, Silvia; Clark, Caroline; [...]Evidence for 28 genetic disorders discovered by combining healthcare and research dataView onlineSchließen
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Published in: Nature
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Blok, Lot Snijders; Rousseau, Justine; Twist, Joanna; Ehresmann, Sophie; Takaku, Motoki; Venselaar, Hanka; Rodan, Lance H.; Nowak, Catherine B.; Douglas, Jessica; Swoboda, Kathryn J.; Steeves, Marcie A.; Sahai, Inderneel; Stumpel, Connie T. R. M.; Stegmann, Alexander P. A.; Wheeler, Patricia; Willing, Marcia; Fiala, Elise; Kochhar, Aaina; Gibson, William T.; Cohen, Ana S. A.; Agbahovbe, Ruky; Innes, A. Micheil; Au, P. Y. Billie; Rankin, Julia; [...]Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and languageView onlineSchließen
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Published in: Nature Communications
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Snijders Blok, Lot; Rousseau, Justine; Twist, Joanna; Ehresmann, Sophie; Takaku, Motoki; Venselaar, Hanka; Rodan, Lance H.; Nowak, Catherine B.; Douglas, Jessica; Swoboda, Kathryn J.; Steeves, Marcie A.; Sahai, Inderneel; Stumpel, Connie T. R. M.; Stegmann, Alexander P. A.; Wheeler, Patricia; Willing, Marcia; Fiala, Elise; Kochhar, Aaina; Gibson, William T.; Cohen, Ana S. A.; Agbahovbe, Ruky; Innes, A. Micheil; Au, P. Y. Billie; Rankin, Julia; [...]Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and languageView onlineSchließen
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Published in: Nature Communications
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O’Donnell-Luria, Anne H.; Pais, Lynn S.; Faundes, Víctor; Wood, Jordan C.; Sveden, Abigail; Luria, Victor; Abou Jamra, Rami; Accogli, Andrea; Amburgey, Kimberly; Anderlid, Britt Marie; Azzarello-Burri, Silvia; Basinger, Alice A.; Bianchini, Claudia; Bird, Lynne M.; Buchert, Rebecca; Carre, Wilfrid; Ceulemans, Sophia; Charles, Perrine; Cox, Helen; Culliton, Lisa; Currò, Aurora; Demurger, Florence; Dowling, James J.; Duban-Bedu, Benedicte; [...]Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and EpilepsyView onlineSchließen
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Published in: The American Journal of Human Genetics
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Snijders Blok, Lot; Rousseau, Justine; Twist, Joanna; Ehresmann, Sophie; Takaku, Motoki; Venselaar, Hanka; Rodan, Lance H.; Nowak, Catherine B.; Douglas, Jessica; Swoboda, Kathryn J.; Steeves, Marcie A.; Sahai, Inderneel; Stumpel, Connie T. R. M.; Stegmann, Alexander P. A.; Wheeler, Patricia; Willing, Marcia; Fiala, Elise; Kochhar, Aaina; Gibson, William T.; Cohen, Ana S. A.; Agbahovbe, Ruky; Innes, A. Micheil; Au, P. Y. Billie; Rankin, Julia; [...]CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and languageView onlineSchließen
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Published in: Nature Communications
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Faundes, Víctor; Newman, William G.; Bernardini, Laura; Canham, Natalie; Clayton-Smith, Jill; Dallapiccola, Bruno; Davies, Sally J.; Demos, Michelle K.; Goldman, Amy; Gill, Harinder; Horton, Rachel; Kerr, Bronwyn; Kumar, Dhavendra; Lehman, Anna; McKee, Shane; Morton, Jenny; Parker, Michael J.; Rankin, Julia; Robertson, Lisa; Temple, I. Karen; Banka, Siddharth; Adam, Shelin; du Souich, Christèle; Elliott, Alison M.; [...]Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental DisordersView onlineSchließen
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Published in: The American Journal of Human Genetics
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Sadleir, Lynette G.; Mountier, Emily I.; Gill, Deepak; Davis, Suzanne; Joshi, Charuta; DeVile, Catherine; Kurian, Manju A.; Mandelstam, Simone; Wirrell, Elaine; Nickels, Katherine C.; Murali, Hema R.; Carvill, Gemma; Myers, Candace T.; Mefford, Heather C.; Scheffer, Ingrid E.; Bevan, A. Paul; Dixit, Abhijit; Pridham, Abigail; Tivey, Adrian R.; Sarkar, Ajoy; Donaldson, Alan; Fryer, Alan; Sifrim, Alejandro; Henderson, Alex; [...]Not all SCN1A epileptic encephalopathies are Dravet syndrome : Early profound Thr226Met phenotype : Early profound Thr226Met phenotypeView onlineSchließen
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Published in: Neurology
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Gorman, Kathleen M.; Meyer, Esther; Grozeva, Detelina; Spinelli, Egidio; McTague, Amy; Sanchis-Juan, Alba; Carss, Keren J.; Bryant, Emily; Reich, Adi; Schneider, Amy L.; Pressler, Ronit M.; Simpson, Michael A.; Debelle, Geoff D.; Wassmer, Evangeline; Morton, Jenny; Sieciechowicz, Diana; Jan-Kamsteeg, Eric; Paciorkowski, Alex R.; King, Mary D.; Cross, J. Helen; Poduri, Annapurna; Mefford, Heather C.; Scheffer, Ingrid E.; Haack, Tobias B.; [...]Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-DyskinesiaView onlineSchließen
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Published in: The American Journal of Human Genetics