Zobrazeno 1 - 10
of 123
pro vyhledávání: '"Schork, AJ"'
Autor:
Ferrari R, Wang Y, Vandrovcova J, Guelfi S, Witeolar A, Karch CM, Schork AJ, Fan CC, Brewer JB, International FTD-Genomics Consortium (IFGC), International Parkinson's Disease Genomics Consortium (IPDGC), International Genomics of Alzheimer's Project (IGAP), Momeni P, Schellenberg GD, Dillon WP, Sugrue LP, Hess CP, Yokoyama JS, Bonham LW, Rabinovici GD, Miller BL, Andreassen OA, Dale AM, Hardy J, Desikan RS, Collaborators: Ferrari R, Hernandez DG, Nalls MA, Rohrer JD, Ramasamy A, Kwok JBJ, Dobson-Stone C, Schofield PR, Halliday GM, Hodges JR, Piguet O, Bartley L, Thompson E, Haan E, Hernández I, Ruiz A, Boada M, Borroni B, Padovani A, Cruchaga C, Cairns NJ, Benussi L, Binetti G, Ghidoni R, Forloni G, Albani D, Galimberti D, Fenoglio C, Serpente M, Scarpini E, Clarimón J, Lleó A, Blesa R, Landqvist Waldö M, Nilsson C, Mackenzie IRA, Hsiung GYR, Mann DMA, Grafman J, Morris CM, Attems J, Griffiths TD, McKeith IG, Thomas AJ, Pietrini P, Huey ED, Wassermann EM, Baborie A, Jaros E, Tierney MC, Pastor P, Razquin C, Ortega-Cubero S, Alonso E, Perneczky R, Diehl-Schmid J, Alexopoulos P, Kurz A, Rainero I, Rubino E, Pinessi L, Rogaeva E, St George-Hyslop P, Rossi G, Tagliavini F, Giaccone G, Rowe JB, Schlachetzki JCM, Uphill J, Collinge J, Mead S, Danek A, Van Deerlin VM, Grossman M, Trojanowski JQ, van der Zee J, Cruts M, Van Broeckhoven C, Cappa SF, Leber I, Hannequin D, Golfier V, Vercelletto M, Brice A, Nacmias B, Sorbi S, Bagnoli S, Piaceri I, Nielsen JE, Hjermind LE, Riemenschneider M, Mayhaus M, Ibach B, Gasparoni G, Pichler S, Gu W, Rossor MN, Fox NC, Warren JD, Spillantini MG, Morris HR, Rizzu P, Heutink P, Snowden JS, Rollinson S, Richardson A, Gerhard A, Bruni AC, Maletta R, Frangipane F, Cupidi C, Bernardi L, Anfossi M, Gallo M, Conidi ME, Smirne N, Rademakers R, Baker M, Dickson DW, Graff-Radford NR, Petersen RC, Knopman D, Josephs KA, Boeve BF, Parisi JE, Seeley WW, Karydas AM, Rosen H, van Swieten JC, Dopper EG, Seelaar H, Pijnenburg YAL, Scheltens P, Logroscino G, Capozzo R, Novelli V, Puca AA, Franceschi M, Postiglione A, Milan G, Sorrentino P, Kristiansen M, Chiang HH, Graff C, Pasquier F, Rollin A, Deramecourt V, Lebouvier T, Kapogiannis D, Ferrucci L, Pickering-Brown S, Singleton AB, Momeni P.
Publikováno v:
Journal of Neurology, Neurosurgery and Psychiatry, 88(2), 152-164. BMJ Publishing Group
Journal of neurology, neurosurgery and psychiatry
The IFGC and IPDGC members 2017, ' Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases ', Journal of Neurology, Neurosurgery and Psychiatry, vol. 88, no. 2, pp. 152-164 . https://doi.org/10.1136/jnnp-2016-314411
Journal of neurology, neurosurgery and psychiatry
The IFGC and IPDGC members 2017, ' Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases ', Journal of Neurology, Neurosurgery and Psychiatry, vol. 88, no. 2, pp. 152-164 . https://doi.org/10.1136/jnnp-2016-314411
Background Clinical, pathological and genetic overlap between sporadic frontotemporal dementia (FTD), Alzheimer9s disease (AD) and Parkinson9s disease (PD) has been suggested; however, the relationship between these disorders is still not well unders
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6de072e936d260a1800fa6d632d00a31
https://europepmc.org/articles/PMC5237405/
https://europepmc.org/articles/PMC5237405/
Autor:
Witoelar, A, Jansen, IE, Wang, Y, Desikan, RS, Gibbs, JR, Blauwendraat, C, Thompson, WK, Hernandez, DG, Djurovic, S, Schork, AJ, Bettella, F, Ellinghaus, D, Franke, A, Lie, BA, McEvoy, LK, Karlsen, T, Lesage, S, Morris, HR, Brice, A, Wood, NW, Heutink, P, Hardy, J, Singleton, AB, Dale, AM, Gasser, T, Andreassen, OA, Sharma, M, Conso, IPDG, Amer, BECN, Co, UKBE
Publikováno v:
Witoelar, A; Jansen, IE; Wang, Y; Desikan, RS; Gibbs, JR; Blauwendraat, C; et al.(2017). Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases. JAMA NEUROLOGY, 74(7), 780-792. doi: 10.1001/jamaneurol.2017.0469. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/3dn2j864
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::a85ef1126755d80c028e0ccfffa4e41e
http://www.escholarship.org/uc/item/3dn2j864
http://www.escholarship.org/uc/item/3dn2j864
Autor:
Ferrari, R, Wang, Y, Vandrovcova, J, Guelfi, S, Witeolar, A, Karch, CM, Schork, AJ, Fan, CC, Brewer, JB, Momeni, P, Schellenberg, GD, Dillon, WP, Sugrue, LP, Hess, CP, Yokoyama, JS, Bonham, LW, Rabinovici, GD, Miller, BL, Andreassen, OA, Dale, AM, Hardy, J, Desikan, RS, Hernandez, DG, Nalls, MA, Rohrer, JD, Ramasamy, A, Kwok, JBJ, Dobson-Stone, C, Schofield, PR, Halliday, GM, Hodges, JR, Piguet, O, Bartley, L, Thompson, E, Haan, E, Hernández, I, Ruiz, A, Boada, M, Borroni, B, Padovani, A, Cruchaga, C, Cairns, NJ, Benussi, L, Binetti, G, Ghidoni, R, Forloni, G, Albani, D, Galimberti, D, Fenoglio, C, Serpente, M, Scarpini, E, Clarimón, J, Lleó, A, Blesa, R, Landqvist Waldö, M, Nilsson, K, Nilsson, C, Mackenzie, IRA, Hsiung, GYR, Mann, DMA, Grafman, J, Morris, CM, Attems, J, Griffiths, TD, McKeith, IG, Thomas, AJ, Pietrini, P, Huey, ED, Wassermann, EM, Baborie, A, Jaros, E, Tierney, MC, Pastor, P, Razquin, C, Ortega-Cubero, S, Alonso, E, Perneczky, R, Diehl-Schmid, J, Alexopoulos, P, Kurz, A, Rainero, I, Rubino, E, Pinessi, L, Rogaeva, E, St George-Hyslop, P, Rossi, G, Tagliavini, F, Giaccone, G, Rowe, JB, Schlachetzki, JCM, Uphill, J
Publikováno v:
Ferrari, R; Wang, Y; Vandrovcova, J; Guelfi, S; Witeolar, A; Karch, CM; et al.(2017). Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases. Journal of Neurology, Neurosurgery and Psychiatry, 88(2), 152-164. doi: 10.1136/jnnp-2016-314411. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/09r1w13w
© Published by the BMJ Publishing Group Limited. Background Clinical, pathological and genetic overlap between sporadic frontotemporal dementia (FTD), Alzheimer's disease (AD) and Parkinson's disease (PD) has been suggested; however, the relationshi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::086cc7303d093b4706c2268e4963bd64
http://www.escholarship.org/uc/item/09r1w13w
http://www.escholarship.org/uc/item/09r1w13w
Autor:
Srinivasan, S, Bettella, F, Mattingsdal, M, Wang, Y, Witoelar, A, Schork, AJ, Thompson, WK, Zuber, V, Winsvold, BS, Zwart, JA, Collier, DA, Desikan, RS, Melle, I, Werge, T, Dale, AM, Djurovic, S, Andreassen, OA
Publikováno v:
Srinivasan, S; Bettella, F; Mattingsdal, M; Wang, Y; Witoelar, A; Schork, AJ; et al.(2016). Genetic Markers of Human Evolution Are Enriched in Schizophrenia. Biological Psychiatry, 80(4), 284-292. doi: 10.1016/j.biopsych.2015.10.009. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/5615t7wn
© 2016 Society of Biological Psychiatry Background Why schizophrenia has accompanied humans throughout our history despite its negative effect on fitness remains an evolutionary enigma. It is proposed that schizophrenia is a by-product of the comple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::5efd755d12bf22af09ee0eaf7f5e9cd4
http://www.escholarship.org/uc/item/5615t7wn
http://www.escholarship.org/uc/item/5615t7wn
Autor:
Reppe, S, Wang, Y, Thompson, WK, McEvoy, LK, Schork, AJ, Zuber, V, LeBlanc, M, Bettella, F, Mills, IG, Desikan, RS, Djurovic, S, Gautvik, KM, Dale, AM, Andreassen, OA, Estrada, K, Styrkarsdottir, U, Evangelou, E, Hsu, YH, Duncan, EL, Ntzani, EE, Oei, L, Albagha, OME, Amin, N, Kemp, JP, Koller, DL, Li, G, Liu, CT, Minster, RL, Moayyeri, A, Vandenput, L, Willner, D, Xiao, SM, Yerges-Armstrong, LM, Zheng, HF, Alonso, N, Eriksson, J, Kammerer, CM, Kaptoge, SK, Leo, PJ, Thorleifsson, G, Wilson, SG, Wilson, JF, Aalto, V, Alen, M, Aragaki, AK, Aspelund, T, Center, JR, Dailiana, Z, Duggan, DJ, Garcia, M, Garcia-Giralt, N, Giroux, S, Hallmans, G, Hocking, LJ, Husted, LB, Jameson, KA, Khusainova, R, Kim, GS, Kooperberg, C, Koromila, T, Kruk, M, Laaksonen, M, Lacroix, AZ
Publikováno v:
Reppe, S; Wang, Y; Thompson, WK; McEvoy, LK; Schork, AJ; Zuber, V; et al.(2015). Genetic sharing with cardiovascular disease risk factors and diabetes reveals novel bone mineral density loci. PLoS ONE, 10(12). doi: 10.1371/journal.pone.0144531. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/1dx1t1xx
© 2015 Reppe et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are cre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::6e8a1a438fe15a4ec3d353f19b5c2042
http://hdl.handle.net/10044/1/32666
http://hdl.handle.net/10044/1/32666
Autor:
Chen, CH, Peng, Q, Schork, AJ, Lo, MT, Fan, CC, Wang, Y, Desikan, RS, Bettella, F, Hagler, DJ, Westlye, LT, Kremen, WS, Jernigan, TL, Le Hellard, S, Steen, VM, Espeseth, T, Huentelman, M, Håberg, AK, Agartz, I, Djurovic, S, Andreassen, OA, Schork, N, Dale, AM, McCabe, C, Chang, L, Akshoomoff, N, Newman, E, Ernst, T, Van Zijl, P, Kuperman, J, Murray, S, Bloss, C, Appelbaum, M, Gamst, A, Thompson, W, Bartsch, H, Weiner, M, Aisen, P, Petersen, R, Jack, CR, Jagust, W, Trojanowki, JQ, Toga, AW, Beckett, L, Green, RC, Saykin, AJ, Morris, J, Shaw, LM, Khachaturian, Z, Sorensen, G, Carrillo, M, Kuller, L, Raichle, M, Paul, S, Davies, P, Fillit, H, Hefti, F, Holtzman, D, Mesulman, MM, Potter, W, Snyder, PJ, Schwartz, A, Montine, T, Thomas, RG, Donohue, M, Walter, S, Gessert, D, Sather, T, Jiminez, G, Harvey, D, Bernstein, M, Fox, N, Thompson, P, Schuff, N, DeCarli, C, Borowski, B, Gunter, J, Senjem, M, Vemuri, P, Jones, D, Kantarci, K, Ward, C, Koeppe, RA, Foster, N, Reiman, EM
Publikováno v:
Chen, CH; Peng, Q; Schork, AJ; Lo, MT; Fan, CC; Wang, Y; et al.(2015). Large-scale genomics unveil polygenic architecture of human cortical surface area. Nature Communications, 6. doi: 10.1038/ncomms8549. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/6tt4q2xx
© 2015 Macmillan Publishers Limited. All rights reserved. Little is known about how genetic variation contributes to neuroanatomical variability, and whether particular genomic regions comprising genes or evolutionarily conserved elements are enrich
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::bcc50e51ad10b8f646ec880993fab615
http://www.escholarship.org/uc/item/6tt4q2xx
http://www.escholarship.org/uc/item/6tt4q2xx
Autor:
Hibar, DP, Stein, JL, Renteria, ME, Arias-Vasquez, A, Desrivières, S, Jahanshad, N, Toro, R, Wittfeld, K, Abramovic, L, Andersson, M, Aribisala, BS, Armstrong, NJ, Bernard, M, Bohlken, MM, Boks, MP, Bralten, J, Brown, AA, Mallar Chakravarty, M, Chen, Q, Ching, CRK, Cuellar-Partida, G, Den Braber, A, Giddaluru, S, Goldman, AL, Grimm, O, Guadalupe, T, Hass, J, Woldehawariat, G, Holmes, AJ, Hoogman, M, Janowitz, D, Jia, T, Kim, S, Klein, M, Kraemer, B, Lee, PH, Olde Loohuis, LM, Luciano, M, MacAre, C, Mather, KA, Mattheisen, M, Milaneschi, Y, Nho, K, Papmeyer, M, Ramasamy, A, Risacher, SL, Roiz-Santiañez, R, Rose, EJ, Salami, A, Sämann, PG, Schmaal, L, Schork, AJ, Shin, J, Strike, LT, Teumer, A, Van Donkelaar, MMJ, Van Eijk, KR, Walters, RK, Westlye, LT, Whelan, CD
Publikováno v:
Hibar, DP; Stein, JL; Renteria, ME; Arias-Vasquez, A; Desrivières, S; Jahanshad, N; et al.(2015). Common genetic variants influence human subcortical brain structures. Nature, 520(7546), 224-229. doi: 10.1038/nature14101. UC Davis: Retrieved from: http://www.escholarship.org/uc/item/5cp2c1bd
©2015 Macmillan Publishers Limited. All rights reserved. The highly complex structure of the human brain is strongly shaped by genetic influences. Subcortical brain regions form circuits with cortical areas to coordinate movement, learning, memory a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::6790a02e4bfadf14c66d092bbf771be1
http://www.escholarship.org/uc/item/5cp2c1bd
http://www.escholarship.org/uc/item/5cp2c1bd
Autor:
Andreassen, Ole Andreas, Desikan, RS, Wang, Yunpeng, Thompson, WK, Schork, AJ, Zuber, Verena, Doncheva, NT, Ellinghaus, E, Mattingsdal, Morten, Franke, A, Lie, BA, Mills, Ian Geoffrey, Aukrust, Pål, McEvoy, LK, Djurovic, Srdjan, Karlsen, TH, Dale, AM
Publikováno v:
e0123057
PLoS ONE
PLoS ONE
Epidemiological studies suggest a relationship between blood lipids and immune-mediated diseases, but the nature of these associations is not well understood. We used genome-wide association studies (GWAS) to investigate shared single nucleotide poly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0df0f1498069535893e6f05813101ff5
https://hdl.handle.net/1956/9839
https://hdl.handle.net/1956/9839
Autor:
Andreassen, OA, Harbo, HF, Wang, Y, Thompson, WK, Schork, AJ, Mattingsdal, M, Zuber, V, Bettella, F, Ripke, S, Kelsoe, JR, Kendler, KS, O'Donovan, MC, Sklar, P, Psychiatric Genomics Consortium (PGC) Bipolar Disorder and Schizophrenia Work Groups, International Multiple Sclerosis Genetics Consortium (IMSGC), McEvoy, LK, Desikan, RS, Lie, BA, Djurovic, S, Dale, AM
Publikováno v:
Molecular psychiatry, vol 20, iss 2
Converging evidence implicates immune abnormalities in schizophrenia (SCZ), and recent genome-wide association studies (GWAS) have identified immune-related single-nucleotide polymorphisms (SNPs) associated with SCZ. Using the conditional false disco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::ba1e6a9a05afb55f678d8b5f0f7cd23b
https://escholarship.org/uc/item/39p9n9q8
https://escholarship.org/uc/item/39p9n9q8