Zobrazeno 1 - 10
of 514
pro vyhledávání: '"Bearden, CE"'
Autor:
Gudbrandsen, M, Daly, E, Murphy, CM, Wichers, RH, Stoencheva, V, Perry, E, Andrews, D, Blackmore, CE, Rogdaki, M, Kushan, L, Bearden, CE, Murphy, DGM, Craig, MC, Ecker, C
Publikováno v:
Cerebral cortex (New York, N.Y. : 1991), vol 29, iss 8
22q11.2 Deletion Syndrome (22q11.2DS) is a genetic condition associated with a high prevalence of neuropsychiatric conditions that include autism spectrum disorder (ASD). While evidence suggests that clinical phenotypes represent distinct neurodevelo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::bbe222b85a60afaff5ee9af9cf54eecc
https://escholarship.org/uc/item/0v8706n1
https://escholarship.org/uc/item/0v8706n1
Autor:
Hibar, DP, Westlye, LT, Doan, NT, Jahanshad, N, Cheung, JW, Ching, CRK, Versace, A, Bilderbeck, AC, Uhlmann, A, Mwangi, B, Krämer, B, Overs, B, Hartberg, CB, Abe, C, Dima, D, Grotegerd, D, Sprooten, E, Ben, E, Jimenez, E, Howells, FM, Delvecchio, G, Temmingh, H, Starke, J, Almeida, JRC, Goikolea, JM, Houenou, J, Beard, LM, Rauer, L, Abramovic, L, Bonnin, M, Ponteduro, MF, Keil, M, Rive, MM, Yao, N, Yalin, N, Najt, P, Rosa, PG, Redlich, R, Trost, S, Hagenaars, S, Fears, SC, Alonso-Lana, S, Van Erp, TGM, Nickson, T, Chaim-Avancini, TM, Meier, TB, Elvsashagen, T, Haukvik, UK, Lee, WH, Schene, AH, Lloyd, AJ, Young, AH, Nugent, A, Dale, AM, Pfennig, A, McIntosh, AM, Lafer, B, Baune, BT, Ekman, CJ, Zarate, CA, Bearden, CE, Henry, C, Simhandl, C, McDonald, C, Bourne, C, Stein, DJ, Wolf, DH, Cannon, DM, Glahn, DC, Veltman, DJ, Pomarol-Clotet, E, Vieta, E, Canales-Rodriguez, EJ, Nery, FG
Publikováno v:
Hibar, DP; Westlye, LT; Doan, NT; Jahanshad, N; Cheung, JW; Ching, CRK; et al.(2018). Cortical abnormalities in bipolar disorder: An MRI analysis of 6503 individuals from the ENIGMA Bipolar Disorder Working Group. Molecular Psychiatry, 23(4), 932-942. doi: 10.1038/mp.2017.73. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/7k30h82r
© 2018 Macmillan Publishers Limited, part of Springer Nature. All rights reserved. Despite decades of research, the pathophysiology of bipolar disorder (BD) is still not well understood. Structural brain differences have been associated with BD, but
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::5c97c1dc0a9fd132044344abb3eb2778
http://www.escholarship.org/uc/item/7k30h82r
http://www.escholarship.org/uc/item/7k30h82r
Autor:
Guo, T, Repetto, GM, McDonald McGinn, DM, Chung, JH, Nomaru, H, Campbell, CL, Blonska, A, Bassett, AS, Chow, EWC, Mlynarski, EE, Swillen, A, Vermeesch, J, Devriendt, K, Gothelf, D, Carmel, M, Michaelovsky, E, Schneider, M, Eliez, S, Antonarakis, SE, Coleman, K, Tomita-Mitchell, A, Mitchell, ME, Digilio, MC, Dallapiccola, B, Marino, B, Philip, N, Busa, T, Kushan-Wells, L, Bearden, CE, Piotrowicz, M, Hawuła, W, Roberts, AE, Tassone, F, Simon, TJ, Van Duin, EDA, Van Amelsvoort, TA, Kates, WR, Zackai, E, Johnston, HR, Cutler, DJ, Agopian, AJ, Goldmuntz, E, Mitchell, LE, Wang, T, Emanuel, BS, Morrow, BE
Publikováno v:
Guo, T; Repetto, GM; McDonald McGinn, DM; Chung, JH; Nomaru, H; Campbell, CL; et al.(2017). Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3. Circulation: Cardiovascular Genetics, 10(5). doi: 10.1161/CIRCGENETICS.116.001690. UC Davis: Retrieved from: http://www.escholarship.org/uc/item/7hp1507k
© 2017 The Authors. Background - The 22q11.2 deletion syndrome (22q11.2DS; DiGeorge syndrome/velocardiofacial syndrome) occurs in 1 of 4000 live births, and 60% to 70% of affected individuals have congenital heart disease, ranging from mild to sever
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::e7bc9daed0c704ea95eb91352a5daaf0
http://www.escholarship.org/uc/item/7hp1507k
http://www.escholarship.org/uc/item/7hp1507k
Autor:
Gur, RE, Bassett, AS, McDonald-McGinn, DM, Bearden, CE, Chow, E, Emanuel, BS, Owen, M, Swillen, A, Van Den Bree, Marianne Bernadette, Vermeesch, J, Vorstman, JAS, Warren, S, Lehner, T, Morrow, B, Niarchou, Maria
Rare copy number variants contribute significantly to the risk for schizophrenia, with the\ud 22q11.2 locus consistently implicated. Individuals with the 22q11.2 deletion syndrome\ud (22q11DS) have an estimated 25-fold increased risk for schizophreni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::378ade628b1f785b1eee1e5e6075b020
Autor:
Hibar, Derrek, Westlye, Lars Tjelta, Doan, Nhat Trung, Jahanshad, Neda, Cheung, J. W., Ching, Christopher R K, Versace, Amelia, Bilderbeck, A, Uhlmann, Anne, Mwangi, B, Krämer, B, Overs, B, Hartberg, Cecilie Bhandari, Abé, Christoph, Dima, Danai, Grotegerd, Dominik, Sprooten, Emma, Bøen, Erlend, Jimenez, Enrique, Howells, Fleur M., Delvecchio, G, Temmingh, H, Starke, J, Almeida, JRC, Goikolea, JM, Houenou, J, Beard, Lauren M., Rauer, L, Abramovic, Lucija, Bonnin, M., Ponteduro, MF, Keil, M, Rive, MM, Yao, N, Yalin, N, Najt, P, Rosa, PG, Redlich, Ronny, Trost, S, Hagenaars, Saskia, Fears, SC, Alonso-Lana, S, Van Erp, TGM, Nickson, Thomas, Chaim-Avancini, TM, Meier, TB, Elvsåshagen, Torbjørn, Haukvik, Unn Kristin H., Lee, Who-Seung, Schene, AH, Lloyd, AJ, Young, AH, Nugent, Allison C, Dale, AM, Pfennig, Andrea, McIntosh, AM, Lafer, Beny, Baune, BT, Ekman, CJ, Zarate, CA, Bearden, CE, Henry, C, Simhandl, Christian, McDonald, C, Bourne, C, Stein, DJ, Wolf, DH, Cannon, DM, Glahn, DC, Veltman, DJ, Pomarol-Clotet, E, Vieta, E, Canales-Rodriguez, EJ, Nery, FG, Duran, FLS, Busatto, GF, Roberts, G, Pearlson, GD, Goodwin, GM, Kugel, H, Whalley, HC, Ruhe, HG, Soares, JC, Fullerton, JM, Rybakowski, JK, Savitz, Jonathan, Chaim, KT, Fatjo-Vilas, Mar, Soeiro-de-Souza, MG, Boks, MP, Zanetti, MV, Otaduy, MCG, Schaufelberger, MS, Alda, Martin, Ingvar, Martin, Phillips, ML, Kempton, MJ, Bauer, M, Landén, M, Lawrence, NS, Van Haren, NEM, Horn, NR, Freimer, NB, Gruber, Oliver, Schofield, PR, Mitchell, PB, Kahn, RS, Lenroot, R, Machado-Vieira, R, Ophoff, RA, Sarró, S, Frangou, Sophia, Satterthwaite, TD, Hajek, Tomas, Dannlowski, Udo, Malt, Ulrik Fredrik, Arolt, Volker, Gattaz, WF, Drevets, WC, Caseras, Xavier, Agartz, Ingrid, Thompson, PM, Andreassen, Ole Andreas
Publikováno v:
Hibar, Derrek Westlye, Lars Tjelta Doan, Nhat Trung Jahanshad, Neda Cheung, J. W. Ching, Christopher R K Versace, Amelia Bilderbeck, A Uhlmann, Anne Mwangi, B Krämer, B Overs, B Hartberg, Cecilie Bhandari Abé, Christoph Dima, Danai Grotegerd, Dominik Sprooten, Emma Bøen, Erlend Jimenez, Enrique Howells, Fleur M. Delvecchio, G Temmingh, H Starke, J Almeida, JRC Goikolea, JM Houenou, J Beard, Lauren M. Rauer, L Abramovic, Lucija Bonnin, M. Ponteduro, MF Keil, M Rive, MM Yao, N Yalin, N Najt, P Rosa, PG Redlich, Ronny Trost, S Hagenaars, Saskia Fears, SC Alonso-Lana, S Van Erp, TGM Nickson, Thomas Chaim-Avancini, TM Meier, TB Elvsåshagen, Torbjørn Haukvik, Unn Kristin H. Lee, Who-Seung Schene, AH Lloyd, AJ Young, AH Nugent, Allison C Dale, AM Pfennig, Andrea McIntosh, AM Lafer, Beny Baune, BT Ekman, CJ Zarate, CA Bearden, CE Henry, C Simhandl, Christian McDonald, C Bo
Molecular Psychiatry
Molecular Psychiatry
Externí odkaz:
http://hdl.handle.net/10852/64950
https://www.duo.uio.no/bitstream/handle/10852/64950/2/enigma%2Bcortical%2Bthick.pdf
https://www.duo.uio.no/bitstream/handle/10852/64950/2/enigma%2Bcortical%2Bthick.pdf
Autor:
Mathalon, Daniel, Jeffries, CD, Perkins, DO, Chandler, SD, Stark, T, Yeo, E, Addington, J, Bearden, CE, Cadenhead, KS, Cannon, TD, Cornblatt, BA
Publikováno v:
Mathalon, Daniel; Jeffries, CD; Perkins, DO; Chandler, SD; Stark, T; Yeo, E; et al.(2016). Insights into psychosis risk from leukocyte microRNA expression. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/5m22m4sz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::f2d26e3deb1c6448afb5ab2296f5ff6b
http://www.escholarship.org/uc/item/5m22m4sz
http://www.escholarship.org/uc/item/5m22m4sz
Autor:
Hibar, DP, Westlye, LT, van Erp, TGM, Rasmussen, J, Leonardo, CD, Faskowitz, J, Haukvik, UK, Hartberg, CB, Doan, NT, Agartz, I, Dale, AM, Gruber, O, Kraemer, B, Trost, S, Liberg, B, Abe, C, Ekman, CJ, Ingvar, M, Landen, M, Fears, SC, Freimer, NB, Bearden, CE, Sprooten, E, Glahn, DC, Pearlson, GD, Emsell, L, Kenney, J, Scanlon, C, McDonald, C, Cannon, DM, Almeida, J, Versace, A, Caseras, X, Lawrence, NS, Phillips, ML, Dima, D, Delvecchio, G, Frangou, S, Satterthwaite, TD, Wolf, D, Houenou, J, Henry, C, Malt, UF, Boen, E, Elvsashagen, T, Young, AH, Lloyd, AJ, Goodwin, GM, Mackay, CE, Bourne, C, Bilderbeck, A, Abramovic, L, Boks, MP, van Haren, NEM, Ophoff, RA, Kahn, RS, Bauer, M, Pfennig, A, Alda, M, Hajek, T, Mwangi, B, Soares, JC, Nickson, T, Dimitrova, R, Sussmann, JE, Hagenaars, S, Whalley, HC, McIntosh, AM, Thompson, PM, Andreassen, OA, Gen, CRCC, Gr, ENIGMABDW
Publikováno v:
Hibar, DP; Westlye, LT; van Erp, TGM; Rasmussen, J; Leonardo, CD; Faskowitz, J; et al.(2016). Subcortical volumetric abnormalities in bipolar disorder. MOLECULAR PSYCHIATRY, 21(12), 1710-1716. doi: 10.1038/mp.2015.227. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/21s2z3q6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::6b5490b11f8e874edac06563509c2825
http://www.escholarship.org/uc/item/21s2z3q6
http://www.escholarship.org/uc/item/21s2z3q6
Autor:
Chung, Y, Jacobson, A, He, G, van Erp, TGM, McEwen, S, Addington, J, Bearden, CE, Cadenhead, K, Cornblatt, B, Mathalon, DH, McGlashan, T, Perkins, D, Seidman, LJ, Tsuang, M, Walker, E, Woods, SW, Heinssen, R, Cannon, TD
Publikováno v:
Chung, Y; Jacobson, A; He, G; van Erp, TGM; McEwen, S; Addington, J; et al.(2015). Prodromal Symptom Severity Predicts Accelerated Gray Matter Reduction and Third Ventricle Expansion Among Clinically High Risk Youth Developing Psychotic Disorders.. Molecular neuropsychiatry, 1(1), 13-22. doi: 10.1159/000371887. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/6z7795jb
A recent prospective longitudinal neuroimaging study of 274 prodromal risk syndrome subjects revealed that those who later developed full-blown psychotic symptoms exhibited accelerated gray matter loss and third ventricle expansion around the time of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::237d0445aaeacf82447ee82a1582c0cf
http://www.escholarship.org/uc/item/6z7795jb
http://www.escholarship.org/uc/item/6z7795jb
Autor:
Thompson, PM, Stein, JL, Medland, SE, Hibar, DP, Vasquez, AA, Renteria, ME, Toro, R, Jahanshad, N, Schumann, G, Franke, B, Wright, MJ, Martin, NG, Agartz, I, Alda, M, Alhusaini, S, Almasy, L, Almeida, J, Alpert, K, Andreasen, NC, Andreassen, OA, Apostolova, LG, Appel, K, Armstrong, NJ, Aribisala, B, Bastin, ME, Bauer, M, Bearden, CE, Bergmann, Ø, Binder, EB, Blangero, J, Bockholt, HJ, Bøen, E, Bois, C, Boomsma, DI, Booth, T, Bowman, IJ, Bralten, J, Brouwer, RM, Brunner, HG, Brohawn, DG, Buckner, RL, Buitelaar, J, Bulayeva, K, Bustillo, JR, Calhoun, VD, Cannon, DM, Cantor, RM, Carless, MA, Caseras, X, Cavalleri, GL, Chakravarty, MM, Chang, KD, Ching, CRK, Christoforou, A, Cichon, S, Clark, VP, Conrod, P, Coppola, G, Crespo-Facorro, B, Curran, JE, Czisch, M, Deary, IJ, de Geus, EJC, den Braber, A, Delvecchio, G, Depondt, C, de Haan, L, de Zubicaray, GI, Dima, D, Dimitrova, R, Djurovic, S
Publikováno v:
Thompson, PM; Stein, JL; Medland, SE; Hibar, DP; Vasquez, AA; Renteria, ME; et al.(2014). The ENIGMA Consortium: Large-scale collaborative analyses of neuroimaging and genetic data. Brain Imaging and Behavior, 8(2), 153-182. doi: 10.1007/s11682-013-9269-5. UCLA: Retrieved from: http://www.escholarship.org/uc/item/6hv0g5jf
The Enhancing NeuroImaging Genetics through Meta-Analysis (ENIGMA) Consortium is a collaborative network of researchers working together on a range of large-scale studies that integrate data from 70 institutions worldwide. Organized into Working Grou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::6f94a03c004fed87ca7f91e2249f4643
http://www.escholarship.org/uc/item/6hv0g5jf
http://www.escholarship.org/uc/item/6hv0g5jf
Autor:
Acosta, MT, Bearden, CE, Castellanos, XF, Cutting, L, Elgersma, Ype, Gioia, G, Gutmann, DH, Lee, YS, Legius, E, Muenke, M, North, K, Parada, LF, Ratner, N, Hunter-Schaedle, K, Silva, AJ
Publikováno v:
American Journal of Medical Genetics Part A, 161A(1), 236-236. Wiley-Liss Inc.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::dc765dfbc6aa9ff0efa2db3291cd6452
https://pure.eur.nl/en/publications/60b565f3-f2a6-4705-a743-0d52056f92e1
https://pure.eur.nl/en/publications/60b565f3-f2a6-4705-a743-0d52056f92e1