부산대학교 도서관

Domenighetti, C; Sugier, P-E; Ashok, Kumar Sreelatha A; Schulte, C; Grover, S; Portugal, B; Lee, P-C; May, P; Bobbili, D; Radivojkov, Blagojevic M

NEUROLOGY. 103(3)

Domenighetti, C; Sugier, P-E; Sreelatha, AAK; Schulte, C; Grover, S; Mohamed, O; Portugal, B; May, P; Bobbili, DR; Radivojkov-Blagojevic, M

JOURNAL OF PARKINSONS DISEASE. 12(1):267-282

Domenighetti, C; Sugier, P-E; Sreelatha, AAK; Schulte, C; Grover, S; Mohamed, O; Portugal, B; May, P; Bobbili, DR; Radivojkov-Blagojevic, M

MOVEMENT DISORDERS. 37(4):857-864

Domenighetti, C; Douillard, V; Sugier, P-E; Sreelatha, AAK; Schulte, C; Grover, S; May, P; Bobbili, DR; Radivojkov-Blagojevic, M; Lichtner, P

MOVEMENT DISORDERS. 37(9):1929-1937

Grover, S; Kumar, Sreelatha AA; Pihlstrom, L; Domenighetti, C; Schulte, C; Sugier, P-E; Radivojkov-Blagojevic, M; Lichtner, P; Mohamed, O; Portugal, B

NEUROLOGY. 99(7):e698-e710

Sugier, Pierre-Emmanuel; Lucotte, Elise A; Bacq-Daian, Delphine; Boland-Augé, Anne; Olaso, Robert; Deleuze, Jean-François; Lesueur, Fabienne; Ostroumova, Evgenia; Kesminiene, Ausrele; de Vathaire, Florent; Guénel, Pascal; consortium, EPITHYR; Domenighetti, Cloé; Sreelatha, Ashwin Ashok Kumar; Schulte, Claudia; Grover, Sandeep; May, Patrick; Bobbili, Dheeraj R; Radivojkov-Blagojevic, Milena; Lichtner, Peter; Singleton, Andrew B; Hernandez, Dena Michelle Godwin; Edsall, Connor; Law, Matthew H; Mellick, George D; Zimprich, Alexander; Pirker, Walter; Rogaeva, Ekaterina; Lang, Anthony E; Koks, Sulev; Taba, Pille; Lesage, Suzanne; Brice, Alexis; Corvol, Jean-Christophe; Iles, Mark M; Chartier-Harlin, Marie-Christine; Mutez, Eugénie; Brockmann, Kathrin; Deutschländer, Angela B; Hadjigeorgiou, Georges M; Dardiotis, Efthimios; Stefanis, Leonidas; Simitsi, Athina Maria; Valente, Enza Maria; Petrucci, Simona; Brown, Kevin; Straniero, Letizia; Zecchinelli, Anna; Pezzoli, Gianni; Brighina, Laura; Ferrarese, Carlo; Annesi, Grazia; Quattrone, Andrea; Gagliardi, Monica; Matsuo, Hirotaka; Nakayama, Akiyoshi; Amos, Christopher; Hattori, Nobutaka; Nishioka, Kenya; Chung, Sun Ju; Kim, Yun Joong; Kolber, Pierre; van de Warrenburg, Bart P C; Bloem, Bastiaan R; Aasly, Jan; Toft, Mathias; Pihlstrøm, Lasse; McKay, James D; Guedes, Leonor Correia; Ferreira, Joaquim J; Bardien, Soraya; Carr, Jonathan; Tolosa, Eduardo; Ezquerra, Mario; Pastor, Pau; Diez-Fairen, Monica; Wirdefeldt, Karin; Pedersen, Nancy; Hung, Rayjean J; Ran, Caroline; Belin, Andrea C; Puschmann, Andreas; Rödström, Emil Ygland; Clarke, Carl E; Morrison, Karen E; Tan, Manuela; Krainc, Dimitri; Burbulla, Lena F; Farrer, Matt J; Karimi, Mojgan; Kruger, Rejko; Gasser, Thomas; Sharma, Manu; Genetics, Comprehensive Unbiased Risk Factor Assessment for; Disease, Environment in Parkinson's; Truong, Thérèse; Elbaz, Alexis

Mov Disord
Movement Disorders
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
Institut de Recerca Germans Trias i Pujol (IGTP)
Movement disorders 38 (2023): 604–615. doi:10.1002/mds.29337
info:cnr-pdr/source/autori:Sugier P-E; Lucotte E A.; Domenighetti C; Law M H.; Iles,M M.; Brown K; Amos C; McKay J D; Hung R J.; Karimi M; Bacq-Daian D; Boland-Auge A; Olaso R; Deleuze J-F; Lesueur F; Ostroumova E; Kesminiene A; de Vathaire F; Guenel P; Sreelatha Ashwin A K; Schulte C; Grover S; May P; Bobbili D R; Radivojkov-Blagojevic M; Lichtner P; Singleton A B; Hernandez D G; Edsall C; Mellick G D.; Zimprich A; Pirker W; Rogaeva E; Lang A E.; Koks S; Taba P; Lesage S; Brice A; Corvol J-C; Chartier-Harlin M-C; Mutez E; Brockmann K; Deutschlaender A B; Hadjigeorgiou G M; Dardiotis E; Stefanis L; Simitsi A M; Valente E M; Petrucci S; Straniero L; Zecchinelli A; Pezzoli G; Brighina L; Ferrarese C; Annesi G ; Quattrone A; Gagliardi M; Matsuo H; Nakayama A; Hattori N; Nishioka K; Chung S J; Kim Yun J; Kolber P; van de Warrenburg B P C.; Bloem B R.; Aasly J; Toft M; Pihlstrom L; Guedes L C; Ferreira J J; Bardien S; Carr J; Tolosa E; Ezquerra M; PastorP; Diez-Fairen M; Wirdefeldt K; Pedersen N; Ran C; Belin A C; Puschmann A; Roedstroem E Y; Clarke C E; Morrison K E; Tan M; Krainc D; Burbulla L F; Farrer M J; Kruger R; Gasser T; Sharma M; Truong T; Elbaz A/titolo:Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers/doi:10.1002%2Fmds.29337/rivista:Movement disorders/anno:2023/pagina_da:604/pagina_a:615/intervallo_pagine:604–615/volume:38
Movement disorders 38(4), 604-615 (2023). doi:10.1002/mds.29337
Movement Disorders, 38, 4, pp. 604-615
Sugier, PE, Lucotte, E A, Domenighetti, C, Law, M H, Iles, M M, Brown, K, Amos, C, McKay, J D, Hung, R J, Karimi, M, Bacq-Daian, D, Boland-Augé, A, Olaso, R, Deleuze, J, Lesueur, F, Ostroumova, E, Kesminiene, A, de Vathaire, F, Guénel, P, Sreelatha, A A K, Schulte, C, Grover, S, May, P, Bobbili, D R, Radivojkov-Blagojevic, M, Lichtner, P, Singleton, A B, Hernandez, D G, Edsall, C, Mellick, G D, Zimprich, A, Pirker, W, Rogaeva, E, Lang, A E, Koks, S, Taba, P, Lesage, S, Brice, A, Corvol, JC, Chartier-Harlin, MC, Mutez, E, Brockmann, K, Deutschländer, A B, Hadjigeorgiou, G M, Dardiotis, E, Stefanis, L, Simitsi, A M, Valente, E M, Petrucci, S, Morrison, K E, the EPITHYR consortium & the Comprehensive Unbiased Risk Factor Assessment for Genetics and Environment in Parkinson's Disease (Courage-PD) consortium 2023, 'Investigation of shared genetic risk factors between Parkinson's disease and cancers', Movement Disorders. https://doi.org/10.1002/mds.29337
Mov. Disord. 38, 604-615 (2023)

Liu H.; Dehestani M.; Blauwendraat C.; Makarious M. B.; Leonard H.; Kim J. J.; Schulte C.; Noyce A.; Jacobs B. M.; Foote I.; Sharma M.; Koks S.; Mellick G. D.; Pirker W.; Zimprich A.; Lang A. E.; Rogaeva E.; Taba P.; Brice A.; Chartier-Harlin M. -C.; Corvol J. -C.; Domenighetti C.; Elbaz A.; Lesage S.; Mutez E.; Sugier P. -E.; Sreelatha A. A. K.; Grover S.; Brockmann K.; Deutschlander A. B.; Gasser T.; Kruger J.; Lichtner P.; Radivojkov-Blagojevic M.; Dardiotis E.; Hadjigeorgiou G. M.; Simitsi A. M.; Stefanis L.; Annesi G.; Brighina L.; Ferrarese C.; Petrucci S.; Pezzoli G.; Quattrone A.; Straniero L.; Gagliardi M.; Valente E. M.; Zecchinelli A.; Hattori N.; Nakayama A.; Matsuo H.; Nishioka K.; Bobbili D.; Kruger R.; Landoulsi Z.; May P.; Pavelka L.; Bloem B. R.; van de Warrenburg B. P. C.; Aasly J.; Pihlstrom L.; Toft M.; Ferreira J. J.; Guedes L. C.; Bardien S.; Carr J.; Chung S. J.; Kim Y. J.; Diez-Fairen M.; Ezquerra M.; Pastor P.; Tolosa E.; Belin A. C.; Pedersen N. L.; Puschmann A.; Ran C.; Rodstrom E. Y.; Wirdefeldt K.; Clarke C. E.; Morrison K. E.; Tan M.; Edsall C.; Farrer M. J.; Krainc D.; Singleton A. B.; Burbulla L. F.; Hernandez D. G.; Nalls M.; Singleton A.; Bandres-Ciga S.

Ann Neurol
Annals of neurology 92(2), 270-278 (2022). doi:10.1002/ana.26416
Liu, H, Dehestani, M, Blauwendraat, C, Makarious, M B, Leonard, H, Kim, J J, Schulte, C, Noyce, A, Jacobs, B M, Foote, I, Sharma, M, Koks, S, Mellick, G D, Pirker, W, Zimprich, A, Lang, A E, Rogaeva, E, Taba, P, Brice, A, Chartier-Harlin, M C, Corvol, J C, Domenighetti, C, Elbaz, A, Lesage, S, Mutez, E, Sugier, P E, Sreelatha, A A K, Grover, S, Brockmann, K, Deutschländer, A B, Gasser, T, Krüger, J, Lichtner, P, Radivojkov-Blagojevic, M, Schulte, C, Sharma, M, Dardiotis, E, Hadjigeorgiou, G M, Simitsi, A M, Stefanis, L, Annesi, G, Brighina, L, Ferrarese, C, Petrucci, S, Pezzoli, G, Quattrone, A, Straniero, L, Gagliardi, M, Valente, E M, Zecchinelli, A, Morrison, K E & International Parkinson's Disease Genomics Consortium; Comprehensive Unbiased Risk Factor Assessment for Genetics and Environment in Parkinson's Disease Consortium 2022, 'Polygenic resilience modulates the penetrance of parkinson disease genetic risk factors', Annals of neurology, vol. 92, no. 2, pp. 270-278. https://doi.org/10.1002/ana.26416

Zied Landoulsi; Ashwin Ashok Kumar Sreelatha; Nicole Kuznetsov; Claudia Schulte; Dheeraj Reddy Bobbili; Ludovica Montanucci; Costin Leu; Lisa-Marie Niestroj; Emadeldin Hassanin; Cloé Domenighetti; Pierre-Emmanuel Sugier; Milena Radivojkov-Blagojevic; Peter Lichtner; Berta Portugal; Connor Edsall; Jens Kru□ger; Dena G Hernandez; Cornelis Blauwendraat; George D Mellick; Alexander Zimprich; Walter Pirker; Manuela Tan; Ekaterina Rogaeva; Anthony Lang; Sulev Koks; Pille Taba; Suzanne Lesage; Alexis Brice; Jean-Christophe Corvol; Marie-Christine Chartier-Harlin; Eugenie Mutez; Kathrin Brockmann; Angela B Deutschländer; Georges M Hadjigeorgiou; Efthimos Dardiotis; Leonidas Stefanis; Athina Maria Simitsi; Enza Maria Valente; Simona Petrucci; Letizia Straniero; Anna Zecchinelli; Gianni Pezzoli; Laura Brighina; Carlo Ferrarese; Grazia Annesi; Andrea Quattrone; Monica Gagliardi; Lena F Burbulla; Hirotaka Matsuo; Akiyoshi Nakayama; Nobutaka Hattori; Kenya Nishioka; Sun Ju Chung; Yun Joong Kim; Lukas Pavelka; Pierre Kolber; Bart PC van de Warrenburg; Bastiaan R Bloem; Andrew B. Singleton; Dan Vitale; Mathias Toft; Lasse Pihlstrom; Leonor Correia Guedes; Joaquim J Ferreira; Soraya Bardien; Jonathan Carr; Eduardo Tolosa; Mario Ezquerra; Pau Pastor; Karin Wirdefeldt; Nancy L Pedersen; Caroline Ran; Andrea C Belin; Andreas Puschmann; Carl E Clarke; Karen E Morrison; Dimitri Krainc; Matt J Farrer; Dennis Lal; Alexis Elbaz; Thomas Gasser; Rejko Krüger; Manu Sharma; Patrick May

medRxiv
Landoulsi, Z, Sreelatha, A A K, Kuznetsov, N, Schulte, C, Bobbili, D R, Montanucci, L, Leu, C, Niestroj, L-M, Hassanin, E, Domenighetti, C, Sugier, P-E, Radivojkov-Blagojevic, M, Lichtner, P, Portugal, B, Edsall, C, Kru Ger, J, Hernandez, D G, Blauwendraat, C, Mellick, G D, Zimprich, A, Pirker, W, Tan, M, Rogaeva, E, Lang, A, Koks, S, Taba, P, Lesage, S, Brice, A, Corvol, J-C, Chartier-Harlin, M-C, Mutez, E, Brockmann, K, Deutschländer, A B, Hadjigeorgiou, G M, Dardiotis, E, Stefanis, L, Simitsi, A M, Valente, E M, Petrucci, S, Straniero, L, Zecchinelli, A, Pezzoli, G, Brighina, L, Ferrarese, C, Annesi, G, Quattrone, A, Gagliardi, M, Burbulla, L F, Matsuo, H, Morrison, K E & Global Parkinson Genetics Program (GP2) 2025 'Genome-wide association study of copy number variations in Parkinson's disease'.

Škorić-Milosavljević, D.; Tadros, R.; Bosada, F.M.; Tessadori, F.; van Weerd, J.H.; Woudstra, O.I.; Tjong, F.V.Y.; Lahrouchi, N.; Bajolle, F.; Cordell, H.J.; Agopian, A.J.; Blue, G.M.; Barge-Schaapveld, D.; Gewillig, M.; Preuss, C.; Lodder, E.M.; Barnett, P.; Ilgun, A.; Beekman, L.; van Duijvenboden, K.; Bokenkamp, R.; Müller-Nurasyid, M.; Vliegen, H.W.; Konings, T.C.; van Melle, J.P.; van Dijk, A.P.J.; van Kimmenade, R.R.J.; Roos-Hesselink, J.W.; Sieswerda, G.T.; Meijboom, F.; Abdul-Khaliq, H.; Berger, F; Dittrich, S.; Hitz, M.P.; Moosmann, J.; Riede, F.T.; Schubert, S.; Galan, P.; Lathrop, M.; Munter, H.M.; Al-Chalabi, A.; Shaw, C.E.; Shaw, P.J.; Morrison, K.E.; Veldink, J.H.; van den Berg, L.H.; Evans, S.; Nobrega, M.A.; Aneas, I.; Radivojkov-Blagojević, M.; Meitinger, T.; Oechslin, E.; Mondal, T.; Bergin, L.; Smythe, J.F.; Altamirano-Diaz, L.; Lougheed, J.; Bouma, B.J.; Chaix, M.A.; Kline, J.; Bassett, A.S.; Andelfinger, G.; van der Palen, R.L.F.; Bouvagnet, P.; Clur, S.B.; Breckpot, J.; Kerstjens-Frederikse, W.S.; Winlaw, D.S.; Bauer, U.M.M.; Mital, S.; Goldmuntz, E.; Keavney, B.; Bonnet, D.; Mulder, B. J. M.; Tanck, M.W.T.; Bakkers, J.; Christoffels, V.M.; Boogerd, C.J.; Postma, A.V.; Bezzina, C.R.

Circ Res
KORA-Study Group 2022, 'Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries', Circulation Research, vol. 130, no. 2, pp. 166-180. https://doi.org/10.1161/CIRCRESAHA.120.317107
Circulation Research, 130, 2, pp. 166-180
Paediatrics Publications
Circ. Res. 130, 166-180 (2021)
KORA-Study Group 2022, 'Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries', Circulation research, vol. 130, no. 2, pp. 166-180. https://doi.org/10.1161/CIRCRESAHA.120.317107

Sugier, P.-E.; Lucotte, E.A.; Domenighetti, C.; Law, M.H.; Iles, M.M.; Brown, K.; Amos, C.; McKay, J.D.; Hung, R.J.; Karimi, M.; Bacq-Daian, D.; Boland-Augé, A.; Olaso, R.; Deleuze, J.-F.; Lesueur, F.; Ostroumova, E.; Kesminiene, A.; de Vathaire, F.; Guénel, P.; Sreelatha, A.A.K.; Schulte, C.; Grover, S.; May, P.; Bobbili, D.R.; Radivojkov-Blagojevic, M.; Lichtner, P.; Singleton, A.B.; Hernandez, D.G.; Edsall, C.; Mellick, G.D.; Zimprich, A.; Pirker, W.; Rogaeva, E.; Lang, A.E.; Koks, S.; Taba, P.; Lesage, S.; Brice, A.; Corvol, J.-C.; Chartier-Harlin, M.-C.; Mutez, E.; Brockmann, K.; Deutschländer, A.B.; Hadjigeorgiou, G.M.; Dardiotis, E.; Stefanis, L.; Simitsi, A.M.; Valente, E.M.; Petrucci, S.; Straniero, L.; Zecchinelli, A.; Pezzoli, G.; Brighina, L.; Ferrarese, C.; Annesi, G.; Quattrone, A.; Gagliardi, M.; Matsuo, H.; Nakayama, A.; Hattori, N.; Nishioka, K.; Chung, S.J.; Kim, Y.J.; Kolber, P.; van de Warrenburg, B.P.C.; Bloem, B.R.; Aasly, J.; Toft, M.; Pihlstrøm, L.; Guedes, L.C.; Ferreira, J.J.; Bardien, S.; Carr, J.; Tolosa, E.; Ezquerra, M.; Pastor, P.; Diez-Fairen, M.; Wirdefeldt, K.; Pedersen, N.; Ran, C.; Belin, A.C.; Puschmann, A.; Rödström, E.Y.; Clarke, C.E.; Morrison, K.E.; Tan, M.; Krainc, D.; Burbulla, L.F.; Farrer, M.J.; Kruger, R.; Gasser, T.; Sharma, M.; Truong, T.; Elbaz, A.; the EPITHYR consortium; the Comprehensive Unbiased Risk Factor Assessment for Genetics; Environment in Parkinson's Disease (Courage-PD) consortium

Lin, K; Pulit, SL; Van Rheenen, W; Shatunov, A; Dekker, AM; McLaughlin, RL; Diekstra, FP; Van Der Spek, RAA; Võsa, U; De Jong, S; Robinson, MR; Yang, J; Fogh, I; Van Doormaal, PT; Tazelaar, GHP; Koppers, M; Blokhuis, AM; Sproviero, W; Jones, AR; Kenna, KP; Van Eijk, KR; Harschnitz, O; Schellevis, RD; Brands, WJ; Medic, J; Menelaou, A; Vajda, A; Ticozzi, N; Rogelj, B; Vrabec, K; Ravnik-Glavač, M; Koritnik, B; Zidar, J; Leonardis, L; Grošelj, LD; Millecamps, S; Salachas, F; Meininger, V; De Carvalho, M; Pinto, S; Mora, JS; Rojas-García, R; Polak, M; Chandran, S; Colville, S; Swingler, R; Morrison, KE; Shaw, PJ; Hardy, J; Orrell, RW; Pittman, A; Sidle, K; Fratta, P; Malaspina, A; Topp, S; Petri, S; Abdulla, S; Drepper, C; Sendtner, M; Meyer, T; Ophoff, RA; Staats, KA; Wiedau-Pazos, M; Lomen-Hoerth, C; Van Deerlin, VM; Trojanowski, JQ; Elman, L; McCluskey, L; Basak, AN; Tunca, C; Hamzeiy, H; Parman, Y; Meitinger, T; Lichtner, P; Radivojkov-Blagojevic, M; Andres, CR; Maurel, C; Bensimon, G; Landwehrmeyer, B; Brice, A; Payan, CAM; Saker-Delye, S; Dürr, A; Wood, NW; Tittmann, L; Lieb, W; Franke, A; Rietschel, M; Cichon, S; Nöthen, MM; Amouyel, P; Tzourio, C; Dartigues, J-F; Uitterlinden, AG; Rivadeneira, F; Estrada, K; Hofman, A; Curtis, C; Blauw, HM; Van Der Kooi, AJ; De Visser, M; Goris, A; Weber, M; Shaw, CE; Smith, BN; Pansarasa, O; Cereda, C; Del Bo, R; Comi, GP; D'Alfonso, S; Bertolin, C; Sorarù, G; Mazzini, L; Pensato, V; Gellera, C; Tiloca, C; Ratti, A; Calvo, A; Moglia, C; Brunetti, M; Arcuti, S; Capozzo, R; Zecca, C; Lunetta, C; Penco, S; Riva, N; Padovani, A; Filosto, M; Muller, B; Stuit, RJ; Registry, P; Group, Slalom; Registry, S; Consortium, Fals Sequencing; Consortium, Slagen; Group, Nnipps Study; Blair, I; Zhang, K; McCann, EP; Fifita, JA; Nicholson, GA; Rowe, DB; Pamphlett, R; Kiernan, MC; Grosskreutz, J; Witte, OW; Ringer, T; Prell, T; Stubendorff, B; Kurth, I; Hübner, CA; Leigh, PN; Casale, F; Chio, A; Beghi, E; Pupillo, E; Tortelli, R; Logroscino, G; Powell, J; Ludolph, AC; Weishaupt, JH; Robberecht, W; Van Damme, P; Franke, L; Pers, TH; Brown, RH; Glass, JD; Landers, JE; Hardiman, O; Andersen, PM; Corcia, P; Vourc'H, P; Silani, V; Wray, NR; Visscher, PM; De Bakker, PIW; Van Es, MA; Pasterkamp, RJ; Lewis, CM; Breen, G; Al-Chalabi, A; Van Den Berg, LH; Veldink, JH

NATURE GENETICS
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Institut d’Investigació Biomèdica Sant Pau (IIB Sant Pau)
instname
van Rheenen, W, Shatunov, A, Dekker, A M, McLaughlin, R L, Diekstra, F P, Pulit, S L, van der Spek, R A A, Võsa, U, de Jong, S, Robinson, M R, Yang, J, Fogh, I, van Doormaal, P T, Tazelaar, G H P, Koppers, M, Blokhuis, A M, Sproviero, W, Jones, A R, Kenna, K P, van Eijk, K R, Harschnitz, O, Schellevis, R D, Brands, W J, Medic, J, Menelaou, A, Vajda, A, Ticozzi, N, Lin, K, Rogelj, B, Vrabec, K, Ravnik-Glavač, M, Koritnik, B, Zidar, J, Leonardis, L, Grošelj, L D, Millecamps, S, Salachas, F, Meininger, V, de Carvalho, M, Pinto, S, Fratta, P, Topp, S, Curtis, C, Shaw, C E, Smith, B N, Leigh, P N, Powell, J, Lewis, C M, Breen, G, Al-Chalabi, A 2016, ' Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis ', Nature Genetics, vol. 48, pp. 1043–1048 . https://doi.org/10.1038/ng.3622
Van Rheenen, W, Shatunov, A, Dekker, A M, Mclaughlin, R L, Diekstra, F P, Pulit, S L, Van Der Spek, R A A, Võsa, U, De Jong, S, Robinson, M R, Yang, J, Fogh, I, Van Doormaal, P T, Tazelaar, G H P, Koppers, M, Blokhuis, A M, Sproviero, W, Jones, A R, Kenna, K P, Van Eijk, K R, Harschnitz, O, Schellevis, R D, Brands, W J, Medic, J, Menelaou, A, Vajda, A, Ticozzi, N, Lin, K, Rogelj, B, Vrabec, K, Ravnik-glavač, M, Koritnik, B, Zidar, J, Leonardis, L, Grošelj, L D, Millecamps, S, Salachas, F, Meininger, V, De Carvalho, M, Pinto, S, Mora, J S, Rojas-garcía, R, Polak, M, Chandran, S, Colville, S, Swingler, R, Morrison, K E, Shaw, P J, Hardy, J, Orrell, R W, Pittman, A, Sidle, K, Fratta, P, Malaspina, A, Topp, S, Petri, S, Abdulla, S, Drepper, C, Sendtner, M, Meyer, T, Ophoff, R A, Staats, K A, Wiedau-pazos, M, Lomen-hoerth, C, Van Deerlin, V M, Trojanowski, J Q, Elman, L, Mccluskey, L, Basak, A N, Tunca, C, Hamzeiy, H, Parman, Y, Meitinger, T, Lichtner, P, Radivojkov-blagojevic, M, Andres, C R, Maurel, C, Bensimon, G, Landwehrmeyer, B, Brice, A, Payan, C A M, Saker-delye, S, Dürr, A, Wood, N W, Tittmann, L, Lieb, W, Franke, A, Rietschel, M, Cichon, S, Nöthen, M M, Amouyel, P, Tzourio, C, Dartigues, J, Uitterlinden, A G, Rivadeneira, F, Estrada, K, Hofman, A, Curtis, C, Blauw, H M, Van Der Kooi, A J, De Visser, M, Goris, A, Weber, M, Shaw, C E, Smith, B N, Pansarasa, O, Cereda, C, Del Bo, R, Comi, G P, D'alfonso, S, Bertolin, C, Sorarù, G, Mazzini, L, Pensato, V, Gellera, C, Tiloca, C, Ratti, A, Calvo, A, Moglia, C, Brunetti, M, Arcuti, S, Capozzo, R, Zecca, C, Lunetta, C, Penco, S, Riva, N, Padovani, A, Filosto, M, Muller, B, Stuit, R J, Blair, I, Zhang, K, Mccann, E P, Fifita, J A, Nicholson, G A, Rowe, D B, Pamphlett, R, Kiernan, M C, Grosskreutz, J, Witte, O W, Ringer, T, Prell, T, Stubendorff, B, Kurth, I, Hübner, C A, Leigh, P N, Casale, F, Chio, A, Beghi, E, Pupillo, E, Tortelli, R, Logroscino, G, Powell, J, Ludolph, A C, Weishaupt, J H, Robberecht, W, Van Damme, P, Franke, L, Pers, T H, Brown, R H, Glass, J D, Landers, J E, Hardiman, O, Andersen, P M, Corcia, P, Vourc'h, P, Silani, V, Wray, N R, Visscher, P M, De Bakker, P I W, Van Es, M A, Pasterkamp, R J, Lewis, C M, Breen, G, Al-chalabi, A, Van Den Berg, L H & Veldink, J H 2016, ' Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis ', Nature Genetics . https://doi.org/10.1038/ng.3622
Nat. Genet. 48, 1043-1048 (2016)
Nature Genetics

Domenighetti, C.; Douillard, V.; Sugier, P.-E.; Sreelatha, A.A.K.; Schulte, C.; Grover, S.; May, P.; Bobbili, D.R.; Radivojkov-Blagojevic, M.; Lichtner, P.; Singleton, A.B.; Hernandez, D.G.; Edsall, C.; Gourraud, P.-A.; Mellick, G.D.; Zimprich, A.; Pirker, W.; Rogaeva, E.; Lang, A.E.; Koks, S.; Taba, P.; Lesage, S.; Brice, A.; Corvol, J.-C.; Chartier-Harlin, M.-C.; Mutez, E.; Brockmann, K.; Deutschländer, A.B.; Hadjigeorgiou, G.M.; Dardiotis, E.; Stefanis, L.; Simitsi, A.M.; Valente, E.M.; Petrucci, S.; Duga, S.; Straniero, L.; Zecchinelli, A.; Pezzoli, G.; Brighina, L.; Ferrarese, C.; Annesi, G.; Quattrone, A.; Gagliardi, M.; Matsuo, H.; Nakayama, A.; Hattori, N.; Nishioka, K.; Chung, S.J.; Kim, Y.J.; Kolber, P.; van de Warrenburg, B.P.C.; Bloem, B.R.; Aasly, J.; Toft, M.; Pihlstrøm, L.; Correia Guedes, L.; Ferreira, J.J.; Bardien, S.; Carr, J.; Tolosa, E.; Ezquerra, M.; Pastor, P.; Diez-Fairen, M.; Wirdefeldt, K.; Pedersen, N.L.; Ran, C.; Belin, A.C.; Puschmann, A.; Ygland Rödström, E.; Clarke, C.E.; Morrison, K.E.; Tan, M.; KraincMD, D.; Burbulla, L.F.; Farrer, M.J.; Krüger, R.; Gasser, T.; Sharma, M.; Vince, N.; Elbaz, A.; Comprehensive Unbiased Risk Factor Assessment for Genetics; Environment in Parkinson's Disease (Courage-PD) Consortium

Grover, Sandeep; Ashwin, Ashok Kumar Sreelatha; Pihlstrom, Lasse; Domenighetti, Cloé; Schulte, Claudia; Sugier, Pierre-Emmanuel; Radivojkov-Blagojevic, Milena; Lichtner, Peter; Mohamed, Océane; Portugal, Berta; Landoulsi, Zied; May, Patrick; Bobbili, Dheeraj Reddy; Edsall, Connor; Bartusch, Felix; Hanussek, Maximilian; Krüger, Jens; Hernandez, Dena G.; Blauwendraat, Cornelis; Mellick, George D.; Zimprich, Alexander; Pirker, Walter; Tan, Manuela; Rogaeva, Ekaterina; Lang, Anthony; Koks, Sulev; Taba, Pille; Lesage, Suzanne; Brice, Alexis; Corvol, Jean-Christophe; Chartier-Harlin, Marie-Christine; Mutez, Eugenie; Brockmann, Kathrin; Deutschländer, Angela B.; Hadjigeorgiou, Georges M.; Dardiotis, Efthimos; Stefanis, Leonidas; Simitsi, Athina Maria; Valente, Enza Maria; Petrucci, Simona; Straniero, Letizia; Zecchinelli, Anna; Pezzoli, Gianni; Brighina, Laura; Ferrarese, Carlo; Annesi, Grazia; Quattrone, Andrea; Gagliardi, Monica; Burbulla, Lena F.; Matsuo, Hirotaka; Kawamura, Yusuke; Hattori, Nobutaka; Nishioka, Kenya; Chung, Sun Ju; Kim, Yun Joong; Pavelka, Lukas; van de Warrenburg, Bart P. C.; Bloem, Bastiaan R.; Singleton, Andrew B.; Aasly, Jan; Toft, Mathias; Guedes, Leonor Correia; Ferreira, Joaquim J.; Bardien, Soraya; Carr, Jonathan; Tolosa, Eduardo; Ezquerra, Mario; Pastor, Pau; Diez-Fairen, Monica; Wirdefeldt, Karin; Pedersen, Nancy L.; Ran, Caroline; Belin, Andrea C.; Puschmann, Andreas; Hellberg, Clara; Clarke, Carl E.; Morrison, Karen E.; Krainc, Dimitri; Farrer, Matt J.; Krüger, Rejko; Elbaz, Alexis; Gasser, Thomas; Sharma, Manu; of, On Behalf; Genetics, The Comprehensive Unbiased Risk Factor Assessment For; consortium, Environment In Parkinson Textquoterights Disease Courage-P. D.

van Rheenen, Wouter; Shatunov, Aleksey; Dekker, Annelot M; McLaughlin, Russell L; Diekstra, Frank P; Pulit, Sara L; van der Spek, Rick AA; Võsa, Urmo; de Jong, Simone; Robinson, Matthew R; Yang, Jian; Fogh, Isabella; van Doormaal, Perry Tc; Tazelaar, Gijs HP; Koppers, Max; Blokhuis, Anna M; Sproviero, William; Jones, Ashley R; Kenna, Kevin P; van Eijk, Kristel R; Harschnitz, Oliver; Schellevis, Raymond D; Brands, William J; Medic, Jelena; Menelaou, Androniki; Vajda, Alice; Ticozzi, Nicola; Lin, Kuang; Rogelj, Boris; Vrabec, Katarina; Ravnik-Glavač, Metka; Koritnik, Blaž; Zidar, Janez; Leonardis, Lea; Grošelj, Leja Dolenc; Millecamps, Stéphanie; Salachas, François; Meininger, Vincent; de Carvalho, Mamede; Pinto, Susana; Mora, Jesus S; Rojas-García, Ricardo; Polak, Meraida; Chandran, Siddharthan; Colville, Shuna; Swingler, Robert; Morrison, Karen E; Shaw, Pamela J; Hardy, John; Orrell, Richard W; Pittman, Alan; Sidle, Katie; Fratta, Pietro; Malaspina, Andrea; Topp, Simon; Petri, Susanne; Abdulla, Susanne; Drepper, Carsten; Sendtner, Michael; Meyer, Thomas; Ophoff, Roel A; Staats, Kim A; Wiedau-Pazos, Martina; Lomen-Hoerth, Catherine; Van Deerlin, Vivianna M; Trojanowski, John Q; Elman, Lauren; McCluskey, Leo; Basak, A Nazli; Tunca, Ceren; Hamzeiy, Hamid; Parman, Yesim; Meitinger, Thomas; Lichtner, Peter; Radivojkov-Blagojevic, Milena; Andres, Christian R; Maurel, Cindy; Bensimon, Gilbert; Landwehrmeyer, Bernhard; Brice, Alexis; Payan, Christine AM; Saker-Delye, Safaa; Dürr, Alexandra; Wood, Nicholas W; Tittmann, Lukas; Lieb, Wolfgang; Franke, Andre; Rietschel, Marcella; Cichon, Sven; Nöthen, Markus M; Amouyel, Philippe; Tzourio, Christophe; Dartigues, Jean-François; Uitterlinden, Andre G; Rivadeneira, Fernando; Estrada, Karol; Hofman, Albert; Curtis, Charles; Blauw, Hylke M

Nature genetics, vol 48, iss 9

Tadros R; Department of Clinical and Experimental Cardiology, Amsterdam UMC, University of Amsterdam, Heart Center, Amsterdam Cardiovascular Sciences, Meibergdreef 9, AZ Amsterdam, The Netherlands.; Department of Medicine, Cardiovascular Genetics Center, Montreal Heart Institute and Faculty of Medicine, Université de Montréal, 5000 Belanger, Montreal, QC, Canada.; Tan HL; Department of Clinical and Experimental Cardiology, Amsterdam UMC, University of Amsterdam, Heart Center, Amsterdam Cardiovascular Sciences, Meibergdreef 9, AZ Amsterdam, The Netherlands.; El Mathari S; Department of Clinical and Experimental Cardiology, Amsterdam UMC, University of Amsterdam, Heart Center, Amsterdam Cardiovascular Sciences, Meibergdreef 9, AZ Amsterdam, The Netherlands.; Kors JA; Department of Medical Informatics, Erasmus MC, University Medical Center Rotterdam, Doctor Molewaterplein 40, GD Rotterdam, The Netherlands.; Postema PG; Department of Clinical and Experimental Cardiology, Amsterdam UMC, University of Amsterdam, Heart Center, Amsterdam Cardiovascular Sciences, Meibergdreef 9, AZ Amsterdam, The Netherlands.; Lahrouchi N; Department of Clinical and Experimental Cardiology, Amsterdam UMC, University of Amsterdam, Heart Center, Amsterdam Cardiovascular Sciences, Meibergdreef 9, AZ Amsterdam, The Netherlands.; Beekman L; Department of Clinical and Experimental Cardiology, Amsterdam UMC, University of Amsterdam, Heart Center, Amsterdam Cardiovascular Sciences, Meibergdreef 9, AZ Amsterdam, The Netherlands.; Radivojkov-Blagojevic M; Institute of Human Genetics, Helmholtz Zentrum München, Ingolstädter Landstraße 1, Neuherberg, Germany.; Amin AS; Department of Clinical and Experimental Cardiology, Amsterdam UMC, University of Amsterdam, Heart Center, Amsterdam Cardiovascular Sciences, Meibergdreef 9, AZ Amsterdam, The Netherlands.; Meitinger T; Institute of Human Genetics, Helmholtz Zentrum München, Ingolstädter Landstraße 1, Neuherberg, Germany.; Institute of Human Genetics, Technical University of Munich, Trogerstraße 32, Munich, Germany.; Tanck MW; Department of Clinical Epidemiology, Biostatistics and Bioinformatics, Amsterdam UMC, University of Amsterdam, Meibergdreef 9, AZ Amsterdam, The Netherlands.; Wilde AA; Department of Clinical and Experimental Cardiology, Amsterdam UMC, University of Amsterdam, Heart Center, Amsterdam Cardiovascular Sciences, Meibergdreef 9, AZ Amsterdam, The Netherlands.; Princess Al-Jawhara Al-Brahim Centre of Excellence in Research of Hereditary Disorders, 7393 Al-Malae'b St, King Abdul Aziz University, Jeddah, Saudi Arabia.; Bezzina CR; Department of Clinical and Experimental Cardiology, Amsterdam UMC, University of Amsterdam, Heart Center, Amsterdam Cardiovascular Sciences, Meibergdreef 9, AZ Amsterdam, The Netherlands.

Publisher: Oxford University Press Country of Publication: England NLM ID: 8006263 Publication Model: Print Cited Medium: Internet ISSN: 1522-9645 (Electronic) Linking ISSN: 0195668X NLM ISO Abbreviation: Eur Heart J Subsets: MEDLINE

Kunze C; Institute of Virology, Helmholtz Center Munich, Neuherberg, 85764, Germany.; Börner K; Department of Infectious Diseases, Virology, University Hospital Heidelberg, Heidelberg, 69120, Germany.; BioQuant Center and Cluster of Excellence CellNetworks at Heidelberg University, Heidelberg, 69120, Germany.; German Center for Infection Research (DZIF), Partner site Heidelberg, Heidelberg, 69120, Germany.; Kienle E; Department of Infectious Diseases, Virology, University Hospital Heidelberg, Heidelberg, 69120, Germany.; BioQuant Center and Cluster of Excellence CellNetworks at Heidelberg University, Heidelberg, 69120, Germany.; Orschmann T; SCADEV, Institute of Developmental Genetics, Helmholtz Center Munich, Neuherberg, 85764, Germany.; Rusha E; Institute of Stem Cell Research, Helmholtz Center Munich, Neuherberg, 85764, Germany.; Schneider M; Institute of Virology, Helmholtz Center Munich, Neuherberg, 85764, Germany.; Radivojkov-Blagojevic M; Institute of Human Genetics, Helmholtz Center Munich, Neuherberg, 85764, Germany.; Drukker M; Institute of Stem Cell Research, Helmholtz Center Munich, Neuherberg, 85764, Germany.; Desbordes S; SCADEV, Institute of Developmental Genetics, Helmholtz Center Munich, Neuherberg, 85764, Germany.; Grimm D; Department of Infectious Diseases, Virology, University Hospital Heidelberg, Heidelberg, 69120, Germany.; BioQuant Center and Cluster of Excellence CellNetworks at Heidelberg University, Heidelberg, 69120, Germany.; German Center for Infection Research (DZIF), Partner site Heidelberg, Heidelberg, 69120, Germany.; Brack-Werner R; Institute of Virology, Helmholtz Center Munich, Neuherberg, 85764, Germany.

Publisher: Wiley-Liss Country of Publication: United States NLM ID: 8806785 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1098-1136 (Electronic) Linking ISSN: 08941491 NLM ISO Abbreviation: Glia Subsets: MEDLINE

Andlauer, Till F. M.; Buck, Dorothea; Antony, Gisela; Bayas, Antonios; Bechmann, Lukas; Berthele, Achim; Chan, Andrew; Gasperi, Christiane; Gold, Ralf; Graetz, Christiane; Haas, Juergen; Hecker, Michael; Infante-Duarte, Carmen; Knop, Matthias; Kuempfel, Tania; Limmroth, Volker; Linker, Ralf A.; Loleit, Verena; Luessi, Felix; Meuth, Sven G.; Muehlau, Mark; Nischwitz, Sandra; Paul, Friedemann; Puetz, Michael; Ruck, Tobias; Salmen, Anke; Stangel, Martin; Stellmann, Jan-Patrick; Stuerner, Klarissa H.; Tackenberg, Bjoern; Bergh, Florian Then; Tumani, Hayrettin; Warnke, Clemens; Weber, Frank; Wiendl, Heinz; Wildemann, Brigitte; Zettl, Uwe K.; Ziemann, Ulf; Zipp, Frauke; Arloth, Janine; Weber, Peter; Radivojkov-Blagojevic, Milena; Scheinhardt, Markus O.; Dankowski, Theresa; Bettecken, Thomas; Lichtner, Peter; Czamara, Darina; Carrillo-Roa, Tania; Binder, Elisabeth B.; Berger, Klaus; Bertram, Lars; Franke, Andre; Gieger, Christian; Herms, Stefan; Homuth, Georg; Ising, Marcus; Joeckel, Karl-Heinz; Kacprowski, Tim; Kloiber, Stefan; Laudes, Matthias; Lieb, Wolfgang; Lill, Christina M.; Lucae, Susanne; Meitinger, Thomas; Moebus, Susanne; Mueller-Nurasyid, Martina; Noethen, Markus M.; Petersmann, Astrid; Rawal, Rajesh; Schminke, Ulf; Strauch, Konstantin; Voelzke, Henry; Waldenberger, Melanie; Wellmann, Juergen; Porcu, Eleonora; Mulas, Antonella; Pitzalis, Maristella; Sidore, Carlo; Zara, Ilenia; Cucca, Francesco; Zoledziewska, Magdalena; Ziegler, Andreas; Hemmer, Bernhard; Mueller-Myhsok, Bertram

SCIENCE ADVANCES; JUN 2016, 2 6, pUNSP e1501678 12p.

Brunet T; Institute of Human Genetics, Faculty of Medicine, Technical University Munich, Munich, Germany.; Institute of Human Genetics, Helmholtz Zentrum München, Neuherberg, Germany.; Radivojkov-Blagojevic M; Institute of Human Genetics, Helmholtz Zentrum München, Neuherberg, Germany.; Lichtner P; Institute of Human Genetics, Helmholtz Zentrum München, Neuherberg, Germany.; Kraus V; Department of Pediatrics, Klinik für Kinder- und Jugendmedizin, München Klinik Schwabing und Harlaching, Klinikum Rechts der Isar der Technischen Universität Munich, Munich, Germany.; Meitinger T; Institute of Human Genetics, Faculty of Medicine, Technical University Munich, Munich, Germany.; Institute of Human Genetics, Helmholtz Zentrum München, Neuherberg, Germany.; Wagner M; Institute of Human Genetics, Faculty of Medicine, Technical University Munich, Munich, Germany.; Institute of Human Genetics, Helmholtz Zentrum München, Neuherberg, Germany.; Institute for Neurogenomics, Helmholtz Zentrum München, Neuherberg, Germany.

Publisher: Wiley Periodicals, Inc on behalf of American Neurological Association Country of Publication: United States NLM ID: 101623278 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2328-9503 (Electronic) Linking ISSN: 23289503 NLM ISO Abbreviation: Ann Clin Transl Neurol Subsets: MEDLINE

Domenighetti, C.; Sugier, P. E.; Sreelatha, A. AshokKumar; Schulte, C.; Grover, S.; Mohamed, O.; Portugal, B.; May, P.; Bobbili, D.; Radivojkov-Blagojevic, M.; Lichtner, P.; Kruger, R.; Gasser, T.; Sharma, M.; Elbaz, A.

MOVEMENT DISORDERS; SEP 2021, 36 pS71-pS72, 2p. Supplement: 1

Brunet, T.; Radivojkov-Blagojevic, M.; Lichtner, P.; Kraus, V.; Meitinger, T.; Wagner, M.

EUROPEAN JOURNAL OF HUMAN GENETICS; DEC 2020, 28 SUPPL 1, p358-p359, 2p. Supplement: 1