Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Marcelo Bertalan"'
Autor:
Olsen, Line, Sparsø, Thomas, Weinsheimer, Shantel M, Dos Santos, Marcelo Bertalan Quintanilha, Mazin, Wiktor, Rosengren, Anders, Sanchez, Xabier Calle, Hoeffding, Louise K, Schmock, Henriette, Baekvad-Hansen, Marie, Bybjerg-Grauholm, Jonas, Daly, Mark J, Neale, Benjamin M, Pedersen, Marianne G, Agerbo, Esben, Mors, Ole, Børglum, Anders, Nordentoft, Merete, Hougaard, David M, Mortensen, Preben Bo, Geschwind, Daniel H, Pedersen, Carsten, Thompson, Wesley K, Werge, Thomas
Publikováno v:
In The Lancet Psychiatry July 2018 5(7):573-580
Autor:
Patricia T. Michie, Franziska Degenhardt, Brandon Wormley, Paola Giusti-Rodríguez, Mark J. Daly, Raquelle I. Mesholam-Gately, Ingrid Melle, Sibylle G. Schwab, Andrew McQuillin, Benjamin M. Neale, Joshua L. Roffman, Abraham Reichenberg, Pamela Sklar, Diana O. Perkins, Jennifer L. Moran, Donald W. Black, Per Hoffmann, A. Hofman, Hailiang Huang, John L. Waddington, Giulio Genovese, Aaron R. Wolen, Deborah L. Levy, David Curtis, Digby Quested, Carlos N. Pato, Nicholas John Craddock, Stephanie Williams, Kung Yee Liang, Zhouzhi Wang, Tracey L. Petryshen, Ann E. Pulver, Randy L. Buckner, Stephan Ripke, Roel A. Ophoff, Danielle Posthuma, Lili Milani, Jacques Mallet, Menachem Fromer, Christian R. Marshall, Jaana Suvisaari, Jana Strohmaier, Richard Bruggeman, Marcella Rietschel, Ayman H. Fanous, Andrew M. McIntosh, James T.R. Walters, Dimitris Dikeos, Panos Roussos, Veikko Salomaa, Aiden Corvin, Carin J. Meijer, Tiina Paunio, Assen Jablensky, Sarah E. Bergen, Nancy G. Buccola, Annelie Nordin, Wolfgang Maier, Srdjan Djurovic, Naomi R. Wray, Aniket Shetty, Joel Eriksson, Dan Rujescu, Jouko Lönnqvist, Brian Kelly, Wenting Wu, Alexander Richards, Frans Henskens, Rich Belliveau, Bryan J. Mowry, Elodie Drapeau, Andreas J. Forstner, Silviu Alin Bacanu, Jubao Duan, Tõnu Esko, Bernard Lerer, Carmel M. Loughland, Olli Pietiläinen, Michael Conlon O'Donovan, Shaun M. Purcell, Michael Gill, Thomas G. Schulze, Douglas S. Greer, Stephen W. Scherer, Eli A. Stahl, Markus M. Nöthen, Guiqing Cai, William M. Brandler, Kristin K. Nicodemus, Dominique Campion, David A. Collier, Farooq Amin, Joel N. Hirschhorn, Robin M. Murray, Timothy G. Dinan, Mark Reimers, Murray J. Cairns, Rodney J. Scott, Aarno Palotie, Robert Freedman, Nelson B. Freimer, Joshua R. Atkins, Gary Donohoe, Ann Olincy, Jonathan Sebat, Colm McDonald, Srinivas Thirumalai, John Powell, Jo Knight, Vahram Haroutunian, Dieter B. Wildenauer, Tim B. Bigdeli, Lieuwe de Haan, Peter Eichhammer, James J. Crowley, Lynn E. DeLisi, Ulrich Schall, Rolf Adolfsson, Marcelo Bertalan, Thomas Hansen, Eric Strengman, Michael Davidson, Dheeraj Malhotra, Manuel Mattheisen, Jeffrey A. Lieberman, Benedicto Crespo-Facorro, Stephanie Godard, Edward M. Scolnick, Jonathan Pimm, Bertram Müller-Myhsok, Qingqin Li, Michele T. Pato, Wiepke Cahn, Christos Pantelis, Ingrid Agartz, Brendan Bulik-Sullivan, Madhusudan Gujral, Martilias S. Farrell, Brady J. Maher, Laurent Essioux, Karin V Fuentes Fajarado, Andres Metspalu, Stephanie H. Witt, Patrick F. Sullivan, Mark Weiser, Younes Mokrab, Kai How Farh, Line Olsen, Dermot Walsh, Peter Holmans, Hugh Gurling, Joseph I. Friedman, Andrew Pocklington, Daniel P. Howrigan, Lude Franke, Tune H. Pers, Larry J. Seidman, Pablo V. Gejman, Dalila Pinto, Michael John Owen, Inez Myin-Germeys, Steven A. McCarroll, Wei Cheng, Jackie Goldstein, C. Robert Cloninger, Elliot S. Gershon, Deborah A. Nertney, Thomas Werge, Noa Carrera, Kieran C. Murphy, Rita M. Cantor, Ariel Darvasi, Mark Hansen, Annette M. Hartmann, Ole A. Andreassen, Bradley T. Webb, Henrik B. Rasmussen, David Cohen, Elvira Bramon, Erik G. Jönsson, Vaughan J. Carr, Pui Y. Lee, Masashi Ikeda, Daniele Merico, Danny Antaki, Brien P. Riley, Stefan Herms, Igor Nenadic, Bettina Konte, Kimberley D. Chambert, Jurgen Del Favero, George Kirov, Matthew C. Keller, Jacob Gratten, Douglas F. Levinson, Luba Kalaydjieva, Bhooma Thiruvahindrapuram, Alan R. Sanders, Sang-Yun Oh, Alkes L. Price, Vihra Milanova, Juha Veijola, Erik Söderman, Dragan M. Svrakic, David H. Kavanagh, Patrik K. E. Magnusson, Douglas Blackwood, Nakao Iwata, Jim van Os, Jeremy M. Silverman, Elena Parkhomenko, Kenneth L. Davis, Jing Qin Wu, Eadbhard O'Callaghan, Chris C. A. Spencer, Juha Karjalainen, Anna K. Kähler, Clement C. Zai, Nigel Williams, Joseph D. Buxbaum, Jin P. Szatkiewicz, Laura Nisenbaum, Sang Hong Lee, Yunjung Kim, Colm O'Dushlaine, René S. Kahn, Morten Mattingsdal, Inge Joa, Marian L. Hamshere, Frank Dudbridge, Ina Giegling, Sandra Meier, Derek W. Morris, Robert W. McCarley, Douglas M. Ruderfer, Paul Cormican, Lyudmila Georgieva, Sven Cichon, Josef Frank, Jianxin Shi, George N. Papadimitriou, Kenneth S. Kendler, Margot Albus, Enrico Domenici, Claudine Laurent, Francis A. O'Neill, Adam Savitz, Jordan W. Smoller, James L. Kennedy, Peter M. Visscher, Valentina Escott-Price, Christina M. Hultman, T. Scott Stroup, Elizabeth Bevilacqua, James A. Knowles, William Byerley, Paul A. Tooney, Madeline Alexander, Stanley V. Catts, David St Clair, Sophie E. Legge, Gerald Nestadt, Michelle S. Maile
Publikováno v:
Nature Genetics, 49(1), 27-35. Nature Publishing Group
BASE-Bielefeld Academic Search Engine
Marshall, Christian R; Howrigan, Daniel P; Merico, Daniele; Thiruvahindrapuram, Bhooma; Wu, Wenting; Greer, Douglas S; et al.(2017). Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.. Nature genetics, 49(1), 27-35. doi: 10.1038/ng.3725. Lawrence Berkeley National Laboratory: Retrieved from: http://www.escholarship.org/uc/item/7jq1c9p6
Nature genetics, 49(1), 27-35. Nature Publishing Group
Marshall, C R, Howrigan, D P, Merico, D, Thiruvahindrapuram, B, Wu, W, Greer, D S, Antaki, D, Shetty, A, Holmans, P A, Pinto, D, Gujral, M, Brandler, W M, Malhotra, D, Wang, Z, Fajarado, K V F, Maile, M S, Ripke, S, Agartz, I, Albus, M, Alexander, M, Amin, F, Atkins, J, Bacanu, S A, Belliveau, R A, Bergen, S E, Bertalan, M, Bevilacqua, E, Bigdeli, T B, Black, D W, Bruggeman, R, Buccola, N G, Buckner, R L, Bulik-Sullivan, B, Byerley, W, Cahn, W, Cai, G, Cairns, M J, Campion, D, Cantor, R M, Carr, V J, Carrera, N, Catts, S V, Chambert, K D, Cheng, W, Cloninger, C R, Cohen, D, Cormican, P, Craddock, N, Crespo-Facorro, B, Posthuma, D & Psychosis Endophenotypes International Consortium 2017, ' Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects ', Nature Genetics, vol. 49, no. 1, pp. 27-35 . https://doi.org/10.1038/ng.3725
Marshall, C R, Howrigan, D P, Merico, D, Thiruvahindrapuram, B, Wu, W, Greer, D S, Antaki, D, Shetty, A, Holmans, P A, Pinto, D, Gujral, M, Brandler, W M, Malhotra, D, Wang, Z, Fuentes Fajarado, K V, Maile, M S, Ripke, S, Agartz, I, Albus, M, Alexander, M, Amin, F, Atkins, J, Bacanu, S A, Belliveau, R A, Bergen, S E, Bertalan, M, Bevilacqua, E, Bigdeli, T B, Black, D W, Bruggeman, R, Buccola, N G, Buckner, R L, Bulik-Sullivan, B, Byerley, W, Cahn, W, Cai, G, Cairns, M J, Campion, D, Cantor, R M, Carr, V J, Carrera, N, Catts, S V, Chambert, K D, Cheng, W, Cloninger, C R, Cohen, D, Cormican, P, Craddock, N, Crespo-Facorro, B, Crowley, J J, Curtis, D, Davidson, M, Davis, K L, Degenhardt, F, Del Favero, J, DeLisi, L E, Dikeos, D, Dinan, T, Djurovic, S, Donohoe, G, Drapeau, E, Duan, J, Dudbridge, F, Eichhammer, P, Eriksson, J, Escott-Price, V, Essioux, L, Fanous, A H, Farh, K H, Farrell, M S, Frank, J, Franke, L, Freedman, R, Freimer, N B, Friedman, J I, Forstner, A J, Fromer, M, Genovese, G, Georgieva, L, Gershon, E S, Giegling, I, Giusti-Rodríguez, P, Godard, S, Goldstein, J I, Gratten, J, De Haan, L, Hamshere, M L, Hansen, M, Hansen, T, Haroutunian, V, Hartmann, A M, Henskens, F A, Herms, S, Hirschhorn, J N, Hoffmann, P, Hofman, A, Huang, H, Ikeda, M, Joa, I, Kähler, A K, Kahn, R S, Kalaydjieva, L, Karjalainen, J, Kavanagh, D, Keller, M C, Kelly, B J, Kennedy, J L, Kim, Y, Knowles, J A, Konte, B, Laurent, C, Lee, P, Lee, S H, Legge, S E, Lerer, B, Levy, D L, Liang, K Y, Lieberman, J, Lönnqvist, J, Loughland, C M, Magnusson, P K E, Maher, B S, Maier, W, Mallet, J, Mattheisen, M, Mattingsdal, M, McCarley, R W, McDonald, C, McIntosh, A M, Meier, S, Meijer, C J, Melle, I, Mesholam-Gately, R I, Metspalu, A, Michie, P T, Milani, L, Milanova, V, Mokrab, Y, Morris, D W, Müller-Myhsok, B, Murphy, K C, Murray, R M, Myin-Germeys, I, Nenadic, I, Nertney, D A, Nestadt, G, Nicodemus, K K, Nisenbaum, L, Nordin, A, O'Callaghan, E, O'Dushlaine, C, Oh, S Y, Olincy, A, Olsen, L, O'Neill, F A, Van Os, J, Pantelis, C, Papadimitriou, G N, Parkhomenko, E, Pato, M T, Paunio, T, Perkins, D O, Pers, T H, Pietiläinen, O, Pimm, J, Pocklington, A J, Powell, J, Price, A, Pulver, A E, Purcell, S M, Quested, D, Rasmussen, H B, Reichenberg, A, Reimers, M A, Richards, A L, Roffman, J L, Roussos, P, Ruderfer, D M, Salomaa, V, Sanders, A R, Savitz, A, Schall, U, Schulze, T G, Schwab, S G, Scolnick, E M, Scott, R J, Seidman, L J, Shi, J, Silverman, J M, Smoller, J W, Söderman, E, Spencer, C C A, Stahl, E A, Strengman, E, Strohmaier, J, Stroup, T S, Suvisaari, J, Svrakic, D M, Szatkiewicz, J P, Thirumalai, S, Tooney, P A, Veijola, J, Visscher, P M, Waddington, J, Walsh, D, Webb, B T, Weiser, M, Wildenauer, D B, Williams, N M, Williams, S, Witt, S H, Wolen, A R, Wormley, B K, Wray, N R, Wu, J Q, Zai, C C, Adolfsson, R, Andreassen, O A, Blackwood, D H R, Bramon, E, Buxbaum, J D, Cichon, S, Collier, D A, Corvin, A, Daly, M J, Darvasi, A, Domenici, E, Esko, T, Gejman, P V, Gill, M, Gurling, H, Hultman, C M, Iwata, N, Jablensky, A V, Jönsson, E G, Kendler, K S, Kirov, G, Knight, J, Levinson, D F, Li, Q S, McCarroll, S A, McQuillin, A, Moran, J L, Mowry, B J, Nöthen, M M, Ophoff, R A, Owen, M J, Palotie, A, Pato, C N, Petryshen, T L, Posthuma, D, Rietschel, M, Riley, B P, Rujescu, D, Sklar, P, St Clair, D, Walters, J T R, Werge, T, Sullivan, P F, O'Donovan, M C, Scherer, S W, Neale, B M & Sebat, J 2017, ' Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects ', Nature Genetics, vol. 49, no. 1, pp. 27-35 . https://doi.org/10.1038/ng.3725
NATURE GENETICS
Nature genetics
Marshall, C R, Howrigan, D P, Merico, D, Thiruvahindrapuram, B, Wu, W, Greer, D S, Antaki, D, Shetty, A, Holmans, P A, Pinto, D, Gujral, M, Brandler, W M, Malhotra, D, Wang, Z, Fajarado, K V F, Maile, M S, Ripke, S, Agartz, I, Albus, M, Alexander, M, Amin, F, Atkins, J, Bacanu, S-A, Belliveau, R A, Bergen, S E, Bertalan, M, Bevilacqua, E, Bigdeli, T B, Black, D W, Bruggeman, R, Buccola, N G, Buckner, R L, Bulik-Sullivan, B K, Byerley, W F, Cahn, W, Cai, G, Cairns, M J, Campion, D, Cantor, R M, Carr, V J, Carrera, N, Catts, S V, Chambert, K D, Cheng, W-T, Cloninger, C R, Cohen, D J, Cormican, P, McIntosh, A & Nicodemus, K & Blackwood, D H R 2017, ' Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects ', Nature Genetics, vol. 49, no. 1, pp. 27-35 . https://doi.org/10.1038/ng.3725
Nature Genetics
BASE-Bielefeld Academic Search Engine
Marshall, Christian R; Howrigan, Daniel P; Merico, Daniele; Thiruvahindrapuram, Bhooma; Wu, Wenting; Greer, Douglas S; et al.(2017). Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.. Nature genetics, 49(1), 27-35. doi: 10.1038/ng.3725. Lawrence Berkeley National Laboratory: Retrieved from: http://www.escholarship.org/uc/item/7jq1c9p6
Nature genetics, 49(1), 27-35. Nature Publishing Group
Marshall, C R, Howrigan, D P, Merico, D, Thiruvahindrapuram, B, Wu, W, Greer, D S, Antaki, D, Shetty, A, Holmans, P A, Pinto, D, Gujral, M, Brandler, W M, Malhotra, D, Wang, Z, Fajarado, K V F, Maile, M S, Ripke, S, Agartz, I, Albus, M, Alexander, M, Amin, F, Atkins, J, Bacanu, S A, Belliveau, R A, Bergen, S E, Bertalan, M, Bevilacqua, E, Bigdeli, T B, Black, D W, Bruggeman, R, Buccola, N G, Buckner, R L, Bulik-Sullivan, B, Byerley, W, Cahn, W, Cai, G, Cairns, M J, Campion, D, Cantor, R M, Carr, V J, Carrera, N, Catts, S V, Chambert, K D, Cheng, W, Cloninger, C R, Cohen, D, Cormican, P, Craddock, N, Crespo-Facorro, B, Posthuma, D & Psychosis Endophenotypes International Consortium 2017, ' Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects ', Nature Genetics, vol. 49, no. 1, pp. 27-35 . https://doi.org/10.1038/ng.3725
Marshall, C R, Howrigan, D P, Merico, D, Thiruvahindrapuram, B, Wu, W, Greer, D S, Antaki, D, Shetty, A, Holmans, P A, Pinto, D, Gujral, M, Brandler, W M, Malhotra, D, Wang, Z, Fuentes Fajarado, K V, Maile, M S, Ripke, S, Agartz, I, Albus, M, Alexander, M, Amin, F, Atkins, J, Bacanu, S A, Belliveau, R A, Bergen, S E, Bertalan, M, Bevilacqua, E, Bigdeli, T B, Black, D W, Bruggeman, R, Buccola, N G, Buckner, R L, Bulik-Sullivan, B, Byerley, W, Cahn, W, Cai, G, Cairns, M J, Campion, D, Cantor, R M, Carr, V J, Carrera, N, Catts, S V, Chambert, K D, Cheng, W, Cloninger, C R, Cohen, D, Cormican, P, Craddock, N, Crespo-Facorro, B, Crowley, J J, Curtis, D, Davidson, M, Davis, K L, Degenhardt, F, Del Favero, J, DeLisi, L E, Dikeos, D, Dinan, T, Djurovic, S, Donohoe, G, Drapeau, E, Duan, J, Dudbridge, F, Eichhammer, P, Eriksson, J, Escott-Price, V, Essioux, L, Fanous, A H, Farh, K H, Farrell, M S, Frank, J, Franke, L, Freedman, R, Freimer, N B, Friedman, J I, Forstner, A J, Fromer, M, Genovese, G, Georgieva, L, Gershon, E S, Giegling, I, Giusti-Rodríguez, P, Godard, S, Goldstein, J I, Gratten, J, De Haan, L, Hamshere, M L, Hansen, M, Hansen, T, Haroutunian, V, Hartmann, A M, Henskens, F A, Herms, S, Hirschhorn, J N, Hoffmann, P, Hofman, A, Huang, H, Ikeda, M, Joa, I, Kähler, A K, Kahn, R S, Kalaydjieva, L, Karjalainen, J, Kavanagh, D, Keller, M C, Kelly, B J, Kennedy, J L, Kim, Y, Knowles, J A, Konte, B, Laurent, C, Lee, P, Lee, S H, Legge, S E, Lerer, B, Levy, D L, Liang, K Y, Lieberman, J, Lönnqvist, J, Loughland, C M, Magnusson, P K E, Maher, B S, Maier, W, Mallet, J, Mattheisen, M, Mattingsdal, M, McCarley, R W, McDonald, C, McIntosh, A M, Meier, S, Meijer, C J, Melle, I, Mesholam-Gately, R I, Metspalu, A, Michie, P T, Milani, L, Milanova, V, Mokrab, Y, Morris, D W, Müller-Myhsok, B, Murphy, K C, Murray, R M, Myin-Germeys, I, Nenadic, I, Nertney, D A, Nestadt, G, Nicodemus, K K, Nisenbaum, L, Nordin, A, O'Callaghan, E, O'Dushlaine, C, Oh, S Y, Olincy, A, Olsen, L, O'Neill, F A, Van Os, J, Pantelis, C, Papadimitriou, G N, Parkhomenko, E, Pato, M T, Paunio, T, Perkins, D O, Pers, T H, Pietiläinen, O, Pimm, J, Pocklington, A J, Powell, J, Price, A, Pulver, A E, Purcell, S M, Quested, D, Rasmussen, H B, Reichenberg, A, Reimers, M A, Richards, A L, Roffman, J L, Roussos, P, Ruderfer, D M, Salomaa, V, Sanders, A R, Savitz, A, Schall, U, Schulze, T G, Schwab, S G, Scolnick, E M, Scott, R J, Seidman, L J, Shi, J, Silverman, J M, Smoller, J W, Söderman, E, Spencer, C C A, Stahl, E A, Strengman, E, Strohmaier, J, Stroup, T S, Suvisaari, J, Svrakic, D M, Szatkiewicz, J P, Thirumalai, S, Tooney, P A, Veijola, J, Visscher, P M, Waddington, J, Walsh, D, Webb, B T, Weiser, M, Wildenauer, D B, Williams, N M, Williams, S, Witt, S H, Wolen, A R, Wormley, B K, Wray, N R, Wu, J Q, Zai, C C, Adolfsson, R, Andreassen, O A, Blackwood, D H R, Bramon, E, Buxbaum, J D, Cichon, S, Collier, D A, Corvin, A, Daly, M J, Darvasi, A, Domenici, E, Esko, T, Gejman, P V, Gill, M, Gurling, H, Hultman, C M, Iwata, N, Jablensky, A V, Jönsson, E G, Kendler, K S, Kirov, G, Knight, J, Levinson, D F, Li, Q S, McCarroll, S A, McQuillin, A, Moran, J L, Mowry, B J, Nöthen, M M, Ophoff, R A, Owen, M J, Palotie, A, Pato, C N, Petryshen, T L, Posthuma, D, Rietschel, M, Riley, B P, Rujescu, D, Sklar, P, St Clair, D, Walters, J T R, Werge, T, Sullivan, P F, O'Donovan, M C, Scherer, S W, Neale, B M & Sebat, J 2017, ' Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects ', Nature Genetics, vol. 49, no. 1, pp. 27-35 . https://doi.org/10.1038/ng.3725
NATURE GENETICS
Nature genetics
Marshall, C R, Howrigan, D P, Merico, D, Thiruvahindrapuram, B, Wu, W, Greer, D S, Antaki, D, Shetty, A, Holmans, P A, Pinto, D, Gujral, M, Brandler, W M, Malhotra, D, Wang, Z, Fajarado, K V F, Maile, M S, Ripke, S, Agartz, I, Albus, M, Alexander, M, Amin, F, Atkins, J, Bacanu, S-A, Belliveau, R A, Bergen, S E, Bertalan, M, Bevilacqua, E, Bigdeli, T B, Black, D W, Bruggeman, R, Buccola, N G, Buckner, R L, Bulik-Sullivan, B K, Byerley, W F, Cahn, W, Cai, G, Cairns, M J, Campion, D, Cantor, R M, Carr, V J, Carrera, N, Catts, S V, Chambert, K D, Cheng, W-T, Cloninger, C R, Cohen, D J, Cormican, P, McIntosh, A & Nicodemus, K & Blackwood, D H R 2017, ' Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects ', Nature Genetics, vol. 49, no. 1, pp. 27-35 . https://doi.org/10.1038/ng.3725
Nature Genetics
Copy number variants (CNVs) have been strongly implicated in the genetic etiology of schizophrenia (SCZ). However, genome-wide investigation of the contribution of CNV to risk has been hampered by limited sample sizes. We sought to address this obsta
Autor:
Preben Bo Mortensen, Jonas Bybjerg-Grauholm, Marcelo Bertalan, Shantel Weinsheimer, David M. Hougaard, Thomas Sparsø, Carsten Bøcker Pedersen, Marie Bækvad-Hansen, Anna Starnawska, Thomas Werge, Christine Søholm Hansen, Alfonso Buil
Publikováno v:
European Neuropsychopharmacology. 29:S794-S795
Background Emerging evidence implicates altered DNA methylation in mental illness including autism, ADHD, bipolar disorder, major depressive disorder, anorexia and schizophrenia. However, it is unclear whether the DNA methylation changes observed to
Autor:
Preben Bo Mortensen, Alfonso Buil, Line Olsen, Carsten Bøcker Pedersen, Jonas Bybjerg-Grauholm, Wiktor Mazin, Christine Søholm Hansen, Shantel Weinsheimer, Marie Bækvad-Hansen, David M. Hougaard, Anna Starnawska, Mette Nyegaard, Marcelo Bertalan, Thomas Werge, Thomas Sparsø
Publikováno v:
Starnawska, A, Hansen, C S, Sparsø, T, Mazin, W, Olsen, L, Bertalan, M, Buil, A, Bybjerg-Grauholm, J, Bækvad-Hansen, M, Hougaard, D M, Mortensen, P B, Pedersen, C B, Nyegaard, M, Werge, T & Weinsheimer, S 2017, ' Differential DNA methylation at birth associated with mental disorder in individuals with 22q11.2 deletion syndrome ', Translational Psychiatry, vol. 7, e1221 . https://doi.org/10.1038/tp.2017.181
Starnawska, A, Hansen, C S, Sparsø, T, Mazin, W, Olsen, L, Bertalan, M, Buil, A, Bybjerg-Grauholm, J, Bækvad-Hansen, M, Hougaard, D M, Mortensen, P B, Pedersen, C B, Nyegaard, M, Werge, T & Weinsheimer, S 2017, ' Differential DNA methylation at birth associated with mental disorder in individuals with 22q11.2 deletion syndrome ', Translational Psychiatry, vol. 7, no. 8, 1221, pp. e1221 . https://doi.org/10.1038/tp.2017.181
Translational Psychiatry
Starnawska, A, Hansen, C S, Sparsø, T, Mazin, W, Olsen, L, Bertalan, M, Buil, A, Bybjerg-Grauholm, J, Bækvad-Hansen, M, Hougaard, D M, Mortensen, P B, Pedersen, C B, Nyegaard, M, Werge, T & Weinsheimer, S 2017, ' Differential DNA methylation at birth associated with mental disorder in individuals with 22q11.2 deletion syndrome ', Translational Psychiatry, vol. 7, no. 8, 1221, pp. e1221 . https://doi.org/10.1038/tp.2017.181
Translational Psychiatry
Individuals with 22q11.2 deletion syndrome (DS) have an increased risk of comorbid mental disorders including schizophrenia, attention deficit hyperactivity disorder, depression, as well as intellectual disability. Although most 22q11.2 deletion carr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b12cfcd13fd4a2e5ddcf4de31b612b98
https://curis.ku.dk/portal/da/publications/differential-dna-methylation-at-birth-associated-with-mental-disorder-in-individuals-with-22q112-deletion-syndrome(360a41f2-5177-4415-9074-95e98a914727).html
https://curis.ku.dk/portal/da/publications/differential-dna-methylation-at-birth-associated-with-mental-disorder-in-individuals-with-22q112-deletion-syndrome(360a41f2-5177-4415-9074-95e98a914727).html
Autor:
Adhemar Zerlotini Neto, Laurent Farinelli, Marcelo Bertalan, Michael Regulski, W. Richard McCombie, Renato Vicentini, Adriana Silva Hemerly, Clícia Grativol, Robert A. Martienssen, Felipe Rodrigues da Silva, Paulo Cavalcanti Gomes Ferreira
Publikováno v:
The Plant Journal. 79:162-172
Many economically important crops have large and complex genomes that hamper their sequencing by standard methods such as whole genome shotgun (WGS). Large tracts of methylated repeats occur in plant genomes that are interspersed by hypomethylated ge
Autor:
Thomas Hansen, Marcelo Bertalan, Sara Hougaard Pedersen, Rikke Elgaard Christensen, Inger Jansen-Olesen, Lisette J. A. Kogelman, Jes Olesen
Publikováno v:
Neuroscience. 350
The trigeminal ganglia (TG) subserving the head and the dorsal root ganglia (DRG) subserving the rest of the body are homologous handling sensory neurons. Differences exist, as a number of signaling substances cause headache but no pain in the rest o
Autor:
Aiden Corvin, Kenneth S. Kendler, Jouko Lönnqvist, Patricia T. Michie, Stephanie H. Witt, Annelie Nordin, Robin M. Murray, Benjamin M. Neale, Dermot Walsh, Peter Holmans, Richard A. Belliveau, Jacques Mallet, Matthew C. Keller, Hugh Gurling, Joseph I. Friedman, Giulio Genovese, Andrew Pocklington, Lieuwe de Haan, Marcelo Bertalan, Noa Carrera, Brian Kelly, Lude Franke, Carlos N. Pato, Inez Myin-Germeys, Brandon Wormley, Nicholas John Craddock, Sven Cichon, Manuel Mattheisen, Annette M. Hartmann, Ole A. Andreassen, Masashi Ikeda, Madhusudan Gujral, Edward M. Scolnick, Jeffrey A. Lieberman, Elodie Drapeau, Deborah A. Nertney, Richard Bruggeman, Bertram Müller-Myhsok, Raquelle I. Mesholam-Gately, Ingrid Melle, Jacob Gratten, Ingrid Agartz, Frans Henskens, Stephanie Godard, Andres Metspalu, Mark Weiser, Johan G. Eriksson, Christian R. Marshall, Preben Bo Mortensen, Tõnu Esko, Sarah E. Bergen, Ina Giegling, Carmel M. Loughland, Stephen W. Scherer, Panos Roussos, Colm McDonald, Douglas F. Levinson, David Cohen, Martilias S. Farrell, James J. Crowley, Sibylle G. Schwab, Stephanie Williams, Henrik B. Rasmussen, Wei Cheng, Ann Olincy, Anders D. Børglum, Andreas J. Forstner, Wenting Wu, Benedicto Crespo-Facorro, David J. Kavanagh, Aniket Shetty, Thomas Werge, Daniel P. Howrigan, Gary Donohoe, Stephan Ripke, Jo Knight, Michael Conlon O'Donovan, Erik Söderman, Luba Kalaydjieva, Silviu Alin Bacanu, Dragan M. Svrakic, Brion S. Maher, Alexander Richards, Digby Quested, Eadbhard O' Callaghan, René S. Kahn, Lili Milani, Karin V. Fuentes Fajarado, Mark Hansen, Douglas S. Greer, Sandra Meier, S. Hong Lee, Markus M. Nöthen, Brendan Bulik-Sullivan, Guiqing Cai, Lynn E. DeLisi, Thomas Hansen, Bernard Lerer, Jubao Duan, James T.R. Walters, Ulrich Schall, Ole Mors, Kai-How Farh, Randy L. Buckner, Andrew M. McIntosh, Kung-Yee Liang, Olli Pietiläinen, Colm O. Dushlaine, Paola Giusti-Rodríguez, Srdjan Djurovic, Jaana Suvisaari, Carin J. Meijer, Christos Pantelis, Peter Eichhammer, Nancy G. Buccola, Kristin K. Nicodemus, Phil Lee, Zhouzhi Wang, Dominique Campion, Rita M. Cantor, Ariel Darvasi, Christina M. Hultman, Dan Rujescu, Joshua R. Atkins, Naomi R. Wray, Michael Davidson, Michele T. Pato, Brien P. Riley, Tim B. Bigdeli, Patrik K. E. Magnusson, Aaron R. Wolen, Srinivas Thirumalai, Vahram Haroutunian, Joshua L. Roffman, Tiina Paunio, K Kähler Anna, Thomas G. Schulze, Assen Jablensky, Andrew McQuillin, Kimberley D. Chambert, John Powell, Douglas Blackwood, Ditte Demontis, Daniele Merico, Stefan Herms, Tune H. Pers, Bryan J. Mowry, Eric Strengman, Larry J. Seidman, Pablo V. Gejman, Laura Nisenbaum, Bettina Konte, Jennifer L. Moran, Donald W. Black, Michael Gill, Line Olsen, Aarno Palotie, Robert Freedman, Dalila Pinto, Abraham Reichenberg, Qingqin S. Li, Ann E. Pulver, Mark Reimers, Jurgen Del Favero, Murray J. Cairns, Patrick F. Sullivan, Deborah L. Levy, John L. Waddington, Menachem Fromer, Marcella Rietschel, Jonathan Sebat, Rolf Adolfsson, George Kirov, Veikko Salomaa, David Curtis, Rodney J. Scott, Jin P. Szatkiewicz, Jacqueline I. Goldstein, Tracey L. Petryshen, Nelson B. Freimer, Mads V. Hollegaard, Franziska Degenhardt, David M. Hougaard, Dimitris Dikeos, Pamela Sklar, Diana O. Perkins, Shaun Purcell, Yunjung Kim, Laurent Essioux, Dheeraj Malhotra, Wolfgang Maier, Eli A. Stahl, Per Hoffmann, David A. Collier, Farooq Amin, Juha Karjalainen, William M. Brandler, Clement C. Zai, A. Hofman, Nigel Williams, Hailiang Huang, Joseph D. Buxbaum, Danielle Posthuma, Kieran C. Murphy, Jonathan Pimm, Bradley T. Webb, Joel N. Hirschhorn, Elvira Bramon, Timothy G. Dinan, Jana Strohmaier, Wiepke Cahn, Erik G. Jönsson, F. Anthony O’ Neill, Dieter B. Wildenauer, Michael John Owen, Igor Nenadic, Vaughan J. Carr, Esben Agerbo, Younes Mokrab, Morten Mattingsdal, Elliot S. Gershon, Danny Antaki, Jim van Os, Bhooma Thiruvahindrapuram, Alan R. Sanders, Sang-Yun Oh, Alkes L. Price, Vihra Milanova, Juha Veijola, Chris C. A. Spencer, Nakao Iwata, Jeremy M. Silverman, Mark J. Daly, Elena Parkhomenko, Kenneth L. Davis, Jing Qin Wu, Robert W. McCarley, Steven A. McCarroll, Derek W. Morris, Douglas M. Ruderfer, Josef Frank, C. Robert Cloninger, George N. Papadimitriou, Paul Cormican, Lyudmila Georgieva, Enrico Domenici, Claudine Laurent, James L. Kennedy, Frank Dudbridge, Peter M. Visscher, Valentina Escott-Price, Inge Joa, Marian L. Hamshere, Jianxin Shi, Margot Albus, Jordan W. Smoller, Adam Savitz, T. Scott Stroup, Elizabeth Bevilacqua, James A. Knowles, William Byerley, Madeline Alexander, Stanley V. Catts, David St Clair, Sophie E. Legge, Roel A. Ophoff, Gerald Nestadt, Paul A. Tooney, Ayman H. Fanous
Genomic copy number variants (CNVs) have been strongly implicated in the etiology of schizophrenia (SCZ). However, apart from a small number of risk variants, elucidation of the CNV contribution to risk has been difficult due to the rarity of risk al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3587abb6cea4d0c8d5a64806bc3149f2
https://doi.org/10.1101/040493
https://doi.org/10.1101/040493
Autor:
Nicola Corton, Stephen D. Bentley, Ana Cerdeño-Tárraga, Andrew Barron, Jane Moore, Valerie R. Abratt, Craig Corton, Simon Houston, Sheila Patrick, Garry W. Blakely, Michael A. Quail, Julian Parkhill, Alexandra Bignell, Louise Clark, Marcelo Bertalan
Publikováno v:
Patrick, S, Blakely, G W, Houston, S, Moore, J, Abratt, V R, Bertalan, M, Cerdeño-Tárraga, A M, Quail, M A, Corton, N, Corton, C, Bignell, A, Barron, A, Clark, L, Bentley, S D & Parkhill, J 2010, ' Twenty-eight divergent polysaccharide loci specifying within-and amongst-strain capsule diversity in three strains of Bacteroides fragilis ', Microbiology, vol. 156, no. 11, pp. 3255-69 . https://doi.org/10.1099/mic.0.042978-0
Microbiology
Microbiology
Comparison of the complete genome sequence ofBacteroides fragilis638R, originally isolated in the USA, was made with two previously sequenced strains isolated in the UK (NCTC 9343) and Japan (YCH46). The presence of 10 loci containing genes associate
Autor:
Michael Bunce, Jing Zhao, Rasmus Nielsen, Paula F. Campos, M. Thomas P. Gilbert, Finn Cilius Nielsen, Yingrui Li, Anders Albrechtsen, Mads Bak, Eske Willerslev, Morten Rasmussen, Bjarne Grønnow, Ene Metspalu, Stinus Lindgreen, Tracey Pierre, Ramneek Gupta, Ludmila P. Osipova, Andrew Gledhill, Hanne Munkholm Kamp, Michael H. Crawford, Eline D. Lorenzen, Thomas Sicheritz-Pontén, Christian Bendixen, Toomas Kivisild, S. A. Fedorova, Richard Villems, Marcelo Bertalan, Minfeng Chen, Jakob Skou Pedersen, Andrew Wilson, Morten Meldgaard, Hao Zhang, Kasper Nielsen, Søren Brunak, Thomas Higham, Xiuqing Zhang, Silvana R. Tridico, Xiaosen Guo, Zhuo Li, Thomas Hansen, Jun Wang, Yong Wang, Mait Metspalu, Maanasa Raghavan, Jonas Binladen, Karsten Kristiansen, Anders Krogh, Niels Tommerup, Claus Andreasen, Ida Moltke, Ludovic Orlando, Christopher Bronk Ramsey
Publikováno v:
Rasmussen, M, Li, Y, Lindgren, S, Pedersen, J S, Anders, A, Moltke, I, Metspalu, M, Metspalu, E, Kivisild, T, Gupta, R, Bertalan, M, Nielsen, K, Gilbert, M T P, Wang, Y, Raghavan, M, Campos, P F, Munkholm Kamp, H, Wilson, A S, Gledhill, A, Tridico, S, Bunce, M, Lorenzen, E D, Binladen, J, Guo, X, Zhao, J, Xhang, X, Zhang, H, Li, Z, Chen, M, Orlando, L, Kristiansen, K, Bak, M, Tommerup, N, Bendixen, C, Pierre, T L, Morten, M, Andreasen, C, Feodorova, S, Osipova, L P, Highham, T F G, Ramsey, C B, Hansen, T O, Nielsen, F C, Crawford, M H, Søren, B, Sicheritz-Pontén, T, Villems, R, Nielsen, R, Krogh, A, Wang, J, Willerslev, E & Grønnow, B 2010, ' Ancient human genome sequence of an extinct Palaeo-Eskimo ', Nature, vol. 463, no. 7282, pp. 757-762 . https://doi.org/10.1038/nature08835
Rasmussen, M, Li, Y, Lindgreen, S, Pedersen, J S, Albrechtsen, A, Moltke, I, Metspalu, M, Metspalu, E, Kivisild, T, Gupta, R, Bertalan, M, Nielsen, K, Gilbert, T, Wang, Y, Raghavan, M, Campos, P, Kamp, H L M, Wilson, A S, Gledhill, A, Tridico, S, Bunce, M, Lorenzen, E, Binladen, J K M A, Guo, X, Zhao, J, Zhang, X, Zhang, H, Li, Z, Chen, M, Orlando, L A A, Kristiansen, K, Bak, M, Tommerup, N, Bendixen, C, Pierre, T L, Grønnow, B, Meldgaard, M, Andreasen, C, Fedorova, S A, Osipova, L P, Higham, T F G, Ramsey, C B, Hansen, T V O, Nielsen, F C, Crawford, M H, Brunak, S, Sicheritz-Pontén, T, Villems, R, Nielsen, R, Krogh, A, Wang, J & Willerslev, E 2010, ' Ancient human genome sequence of an extinct Palaeo-Eskimo ', Nature, vol. 463, no. 7282, pp. 757-762 . https://doi.org/10.1038/nature08835
Rasmussen, M, Li, Y, Lindgreen, S, Pedersen, J S, Albrechtsen, A, Moltke, I, Metspalu, M, Metspalu, E, Kivisild, T, Gupta, R, Bertalan, M, Nielsen, K, Gilbert, T, Wang, Y, Raghavan, M, Campos, P, Kamp, H L M, Wilson, A S, Gledhill, A, Tridico, S, Bunce, M, Lorenzen, E, Binladen, J K M A, Guo, X, Zhao, J, Zhang, X, Zhang, H, Li, Z, Chen, M, Orlando, L A A, Kristiansen, K, Bak, M, Tommerup, N, Bendixen, C, Pierre, T L, Grønnow, B, Meldgaard, M, Andreasen, C, Fedorova, S A, Osipova, L P, Higham, T F G, Ramsey, C B, Hansen, T V O, Nielsen, F C, Crawford, M H, Brunak, S, Sicheritz-Pontén, T, Villems, R, Nielsen, R, Krogh, A, Wang, J & Willerslev, E 2010, ' Ancient human genome sequence of an extinct Palaeo-Eskimo ', Nature, vol. 463, no. 7282, pp. 757-762 . https://doi.org/10.1038/nature08835
We report here the genome sequence of an ancient human. Obtained from approximately 4,000-year-old permafrost-preserved hair, the genome represents a male individual from the first known culture to settle in Greenland. Sequenced to an average depth o
Autor:
Johan H. Thygesen, Josef Parnas, Marcelo Bertalan, Sine Zambach, Pär Lundin, Laura Ferrero-Miliani, Thomas Hansen, Ditte Bjerre, Anders Rosengren, Thomas Werge, Henrik B. Rasmussen, Andres Ingason
Publikováno v:
Schizophrenia research. 169(1-3)
Formal thought disorder is a major feature of schizophrenia and other psychotic disorders. It is heritable, found in healthy relatives of patients with schizophrenia and other mental disorders but knowledge of specific genetic factors is lacking. The