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Items where Author is "Lesch, Klaus-Peter"

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Number of items: 8.

2020

Elvsåshagen, Torbjørn and Bahrami, Shahram and van der Meer, Dennis and Agartz, Ingrid and Alnæs, Dag and Barch, Deanna M. and Baur-Streubel, Ramona and Bertolino, Alessandro and Beyer, Mona K. and Blasi, Giuseppe and Borgwardt, Stefan and Boye, Birgitte and Buitelaar, Jan and Bøen, Erlend and Celius, Elisabeth Gulowsen and Cervenka, Simon and Conzelmann, Annette and Coynel, David and Di Carlo, Pasquale and Djurovic, Srdjan and Eisenacher, Sarah and Espeseth, Thomas and Fatouros-Bergman, Helena and Flyckt, Lena and Franke, Barbara and Frei, Oleksandr and Gelao, Barbara and Harbo, Hanne Flinstad and Hartman, Catharina A. and Håberg, Asta and Heslenfeld, Dirk and Hoekstra, Pieter J. and Høgestøl, Einar A. and Jonassen, Rune and Jönsson, Erik G. and Karolinska Schizophrenia Project consortium, and Kirsch, Peter and Kłoszewska, Iwona and Lagerberg, Trine Vik and Landrø, Nils Inge and Le Hellard, Stephanie and Lesch, Klaus-Peter and Maglanoc, Luigi A. and Malt, Ulrik F. and Mecocci, Patrizia and Melle, Ingrid and Meyer-Lindenberg, Andreas and Moberget, Torgeir and Nordvik, Jan Egil and Nyberg, Lars and Connell, Kevin S. O' and Oosterlaan, Jaap and Papalino, Marco and Papassotiropoulos, Andreas and Pauli, Paul and Pergola, Giulio and Persson, Karin and de Quervain, Dominique and Reif, Andreas and Rokicki, Jaroslav and van Rooij, Daan and Shadrin, Alexey A. and Schmidt, André and Schwarz, Emanuel and Selbæk, Geir and Soininen, Hilkka and Sowa, Piotr and Steen, Vidar M. and Tsolaki, Magda and Vellas, Bruno and Wang, Lei and Westman, Eric and Ziegler, Georg C. and Zink, Mathias and Andreassen, Ole A. and Westlye, Lars T. and Kaufmann, Tobias. (2020) The genetic architecture of human brainstem structures and their involvement in common brain disorders. Nature Communications, 11 (1). p. 4016.

2019

Kaufmann, Tobias and van der Meer, Dennis and Doan, Nhat Trung and Schwarz, Emanuel and Lund, Martina J. and Agartz, Ingrid and Alnæs, Dag and Barch, Deanna M. and Baur-Streubel, Ramona and Bertolino, Alessandro and Bettella, Francesco and Beyer, Mona K. and Bøen, Erlend and Borgwardt, Stefan and Brandt, Christine L. and Buitelaar, Jan and Celius, Elisabeth G. and Cervenka, Simon and Conzelmann, Annette and Córdova-Palomera, Aldo and Dale, Anders M. and de Quervain, Dominique J. F. and Di Carlo, Pasquale and Djurovic, Srdjan and Dørum, Erlend S. and Eisenacher, Sarah and Elvsåshagen, Torbjørn and Espeseth, Thomas and Fatouros-Bergman, Helena and Flyckt, Lena and Franke, Barbara and Frei, Oleksandr and Haatveit, Beathe and Håberg, Asta K. and Harbo, Hanne F. and Hartman, Catharina A. and Heslenfeld, Dirk and Hoekstra, Pieter J. and Høgestøl, Einar A. and Jernigan, Terry L. and Jonassen, Rune and Jönsson, Erik G. and Karolinska Schizophrenia Project, and Kirsch, Peter and Kłoszewska, Iwona and Kolskår, Knut K. and Landrø, Nils Inge and Le Hellard, Stephanie and Lesch, Klaus-Peter and Lovestone, Simon and Lundervold, Arvid and Lundervold, Astri J. and Maglanoc, Luigi A. and Malt, Ulrik F. and Mecocci, Patrizia and Melle, Ingrid and Meyer-Lindenberg, Andreas and Moberget, Torgeir and Norbom, Linn B. and Nordvik, Jan Egil and Nyberg, Lars and Oosterlaan, Jaap and Papalino, Marco and Papassotiropoulos, Andreas and Pauli, Paul and Pergola, Giulio and Persson, Karin and Richard, Geneviève and Rokicki, Jaroslav and Sanders, Anne-Marthe and Selbæk, Geir and Shadrin, Alexey A. and Smeland, Olav B. and Soininen, Hilkka and Sowa, Piotr and Steen, Vidar M. and Tsolaki, Magda and Ulrichsen, Kristine M. and Vellas, Bruno and Wang, Lei and Westman, Eric and Ziegler, Georg C. and Zink, Mathias and Andreassen, Ole A. and Westlye, Lars T.. (2019) Common brain disorders are associated with heritable patterns of apparent aging of the brain. Nature Neuroscience, 22 (10). pp. 1617-1623.

Demontis, Ditte and Walters, Raymond K. and Martin, Joanna and Mattheisen, Manuel and Als, Thomas D. and Agerbo, Esben and Baldursson, Gísli and Belliveau, Rich and Bybjerg-Grauholm, Jonas and Bækvad-Hansen, Marie and Cerrato, Felecia and Chambert, Kimberly and Churchhouse, Claire and Dumont, Ashley and Eriksson, Nicholas and Gandal, Michael and Goldstein, Jacqueline I. and Grasby, Katrina L. and Grove, Jakob and Gudmundsson, Olafur O. and Hansen, Christine S. and Hauberg, Mads Engel and Hollegaard, Mads V. and Howrigan, Daniel P. and Huang, Hailiang and Maller, Julian B. and Martin, Alicia R. and Martin, Nicholas G. and Moran, Jennifer and Pallesen, Jonatan and Palmer, Duncan S. and Pedersen, Carsten Bøcker and Pedersen, Marianne Giørtz and Poterba, Timothy and Poulsen, Jesper Buchhave and Ripke, Stephan and Robinson, Elise B. and Satterstrom, F. Kyle and Stefansson, Hreinn and Stevens, Christine and Turley, Patrick and Walters, G. Bragi and Won, Hyejung and Wright, Margaret J. and Adhd Working Group of the Psychiatric Genomics Consortium, and Early Lifecourse, and Genetic Epidemiology Consortium, and Andreassen, Ole A. and Asherson, Philip and Burton, Christie L. and Boomsma, Dorret I. and Cormand, Bru and Dalsgaard, Søren and Franke, Barbara and Gelernter, Joel and Geschwind, Daniel and Hakonarson, Hakon and Haavik, Jan and Kranzler, Henry R. and Kuntsi, Jonna and Langley, Kate and Lesch, Klaus-Peter and Middeldorp, Christel and Reif, Andreas and Rohde, Luis Augusto and Roussos, Panos and Schachar, Russell and Sklar, Pamela and Sonuga-Barke, Edmund J. S. and Sullivan, Patrick F. and Thapar, Anita and Tung, Joyce Y. and Waldman, Irwin D. and Medland, Sarah E. and Stefansson, Kari and Nordentoft, Merete and Hougaard, David M. and Werge, Thomas and Mors, Ole and Mortensen, Preben Bo and Daly, Mark J. and Faraone, Stephen V. and Børglum, Anders D. and Neale, Benjamin M.. (2019) Discovery of the First Genome-Wide Significant Risk Loci for Attention Deficit/Hyperactivity Disorder. Nature Genetics, 51 (1). pp. 63-75.

2015

Hommers, Leif and Raab, Annette and Bohl, Alexandra and Weber, Heike and Scholz, Claus-Jürgen and Erhardt, Angelika and Binder, Elisabeth and Arolt, Volker and Gerlach, Alexander and Gloster, Andrew and Kalisch, Raffael and Kircher, Tilo and Lonsdorf, Tina and Ströhle, Andreas and Zwanzger, Peter and Mattheisen, Manuel and Cichon, Sven and Lesch, Klaus-Peter and Domschke, Katharina and Reif, Andreas and Lohse, Martin J. and Deckert, Jürgen. (2015) MicroRNA hsa-miR-4717-5p Regulates RGS2 and May Be a Risk Factor for Anxiety-Related Traits. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics , 168B (4). pp. 296-306.

2012

Williams, Nigel M. and Franke, Barbara and Mick, Eric and Anney, Richard J. L. and Freitag, Christine M. and Gill, Michael and Thapar, Anita and O'Donovan, Michael C. and Owen, Michael J. and Holmans, Peter and Kent, Lindsey and Middleton, Frank and Zhang-James, Yanli and Liu, Lu and Meyer, Jobst and Nguyen, Thuy Trang and Romanos, Jasmin and Romanos, Marcel and Seitz, Christiane and Renner, Tobias J. and Walitza, Susanne and Warnke, Andreas and Palmason, Haukur and Buitelaar, Jan and Rommelse, Nanda and Vasquez, Alejandro Arias and Hawi, Ziarih and Langley, Kate and Sergeant, Joseph and Steinhausen, Hans-Christoph and Roeyers, Herbert and Biederman, Joseph and Zaharieva, Irina and Hakonarson, Hakon and Elia, Josephine and Lionel, Anath C. and Crosbie, Jennifer and Marshall, Christian R. and Schachar, Russell and Scherer, Stephen W. and Todorov, Alexandre and Smalley, Susan L. and Loo, Sandra and Nelson, Stanley and Shtir, Corina and Asherson, Philip and Reif, Andreas and Lesch, Klaus-Peter and Faraone, Stephen V.. (2012) Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder. American journal of psychiatry, Vol. 169, H. 2. pp. 195-204.

Elia, Josephine and Glessner, Joseph T. and Wang, Kai and Takahashi, Nagahide and Shtir, Corina J. and Hadley, Dexter and Sleiman, Patrick M. A. and Zhang, Haitao and Kim, Cecilia E. and Robison, Reid and Lyon, Gholson J. and Flory, James H. and Bradfield, Jonathan P. and Imielinski, Marcin and Hou, Cuiping and Frackelton, Edward C. and Chiavacci, Rosetta M. and Sakurai, Takeshi and Rabin, Cara and Middleton, Frank A. and Thomas, Kelly A. and Garris, Maria and Mentch, Frank and Freitag, Christine M. and Steinhausen, Hans-Christoph and Todorov, Alexandre A. and Reif, Andreas and Rothenberger, Aribert and Franke, Barbara and Mick, Eric O. and Roeyers, Herbert and Buitelaar, Jan and Lesch, Klaus-Peter and Banaschewski, Tobias and Ebstein, Richard P. and Mulas, Fernando and Oades, Robert D. and Sergeant, Joseph and Sonuga-Barke, Edmund and Renner, Tobias J. and Romanos, Marcel and Romanos, Jasmin and Warnke, Andreas and Walitza, Susanne and Meyer, Jobst and Pálmason, Haukur and Seitz, Christiane and Loo, Sandra K. and Smalley, Susan L. and Biederman, Joseph and Kent, Lindsey and Asherson, Philip and Anney, Richard J. L. and Gaynor, J. William and Shaw, Philip and Devoto, Marcella and White, Peter S. and Grant, Struan F. A. and Buxbaum, Joseph D. and Rapoport, Judith L. and Williams, Nigel M. and Nelson, Stanley F. and Faraone, Stephen V. and Hakonarson, Hakon. (2012) Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder. Nature genetics, Vol. 44, H. 1. pp. 78-84.

2010

Neale, Benjamin M. and Medland, Sarah and Ripke, Stephan and Anney, Richard J. L. and Asherson, Philip and Buitelaar, Jan and Franke, Barbara and Gill, Michael and Kent, Lindsey and Holmans, Peter and Middleton, Frank and Thapar, Anita and Lesch, Klaus-Peter and Faraone, Stephen V. and Daly, Mark and Nguyen, Thuy Trang and Schäfer, Helmut and Steinhausen, Hans-Christoph and Reif, Andreas and Renner, Tobias J. and Romanos, Marcel and Romanos, Jasmin and Warnke, Andreas and Walitza, Susanne and Freitag, Christine and Meyer, Jobst and Palmason, Haukur and Rothenberger, Aribert and Hawi, Ziarih and Sergeant, Joseph and Roeyers, Herbert and Mick, Eric and Biederman, Joseph and Image II Consortium Group, . (2010) Case-control genome-wide association study of attention-deficit/hyperactivity disorder. Journal of the American Academy of Child and Adolescent Psychiatry, 49 (9). pp. 906-920.

Neale, Benjamin M. and Medland, Sarah E. and Ripke, Stephan and Asherson, Philip and Franke, Barbara and Lesch, Klaus-Peter and Faraone, Stephen V. and Nguyen, Thuy Trang and Schäfer, Helmut and Holmans, Peter and Daly, Mark and Steinhausen, Hans-Christoph and Freitag, Christine and Reif, Andreas and Renner, Tobias J. and Romanos, Marcel and Romanos, Jasmin and Walitza, Susanne and Warnke, Andreas and Meyer, Jobst and Palmason, Haukur and Buitelaar, Jan and Vasquez, Alejandro Arias and Lambregts-Rommelse, Nanda and Gill, Michael and Anney, Richard J. L. and Langely, Kate and O'Donovan, Michael and Williams, Nigel and Owen, Michael and Thapar, Anita and Kent, Lindsey and Sergeant, Joseph and Roeyers, Herbert and Mick, Eric and Biederman, Joseph and Doyle, Alysa and Smalley, Susan and Loo, Sandra and Hakonarson, Hakon and Elia, Josephine and Todorov, Alexandre and Miranda, Ana and Mulas, Fernando and Ebstein, Richard P. and Rothenberger, Aribert and Banaschewski, Tobias and Oades, Robert D. and Sonuga-Barke, Edmund and McGough, James and Nisenbaum, Laura and Middleton, Frank and Hu, Xiaolan and Nelson, Stan and Psychiatric Gwas Consortium: Adhd Subgroup, . (2010) Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder. Journal of the American Academy of Child and Adolescent Psychiatry, 49 (9). pp. 884-897.

This list was generated on Fri Mar 29 03:18:53 2024 CET.