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Items where Division is "03 Faculty of Medicine > Departement Biomedizin > Department of Biomedicine, University Hospital Basel > Human Genetics (Cichon)"

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Number of items at this level: 12.

2018

Reinbold, Céline S.. Application of bioinformatics tools for better interpretation of psychiatric GWAS through integration of biological information. 2018, Doctoral Thesis, University of Basel, Faculty of Psychology.

2015

Basmanav, F. Buket and Forstner, Andreas J. and Fier, Heide and Herms, Stefan and Meier, Sandra and Degenhardt, Franziska and Hoffmann, Per and Barth, Sandra and Fricker, Nadine and Strohmaier, Jana and Witt, Stephanie H. and Ludwig, Michael and Schmael, Christine and Moebus, Susanne and Maier, Wolfgang and Mössner, Rainald and Rujescu, Dan and Rietschel, Marcella and Lange, Christoph and Nöthen, Markus M. and Cichon, Sven. (2015) Investigation of the Role of TCF4 Rare Sequence Variants in Schizophrenia. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 168B (5). pp. 354-362.

Buch, Stephan and Stickel, Felix and Trépo, Eric and Way, Michael and Herrmann, Alexander and Nischalke, Hans Dieter and Brosch, Mario and Rosendahl, Jonas and Berg, Thomas and Ridinger, Monika and Rietschel, Marcella and McQuillin, Andrew and Frank, Josef and Kiefer, Falk and Schreiber, Stefan and Lieb, Wolfgang and Soyka, Michael and Semmo, Nasser and Aigner, Elmar and Datz, Christian and Schmelz, Renate and Brückner, Stefan and Zeissig, Sebastian and Stephan, Anna-Magdalena and Wodarz, Norbert and Devière, Jacques and Clumeck, Nicolas and Sarrazin, Christoph and Lammert, Frank and Gustot, Thierry and Deltenre, Pierre and Völzke, Henry and Lerch, Markus M. and Mayerle, Julia and Eyer, Florian and Schafmayer, Clemens and Cichon, Sven and Nöthen, Markus M. and Nothnagel, Michael and Ellinghaus, David and Huse, Klaus and Franke, Andre and Zopf, Steffen and Hellerbrand, Claus and Moreno, Christophe and Franchimont, Denis and Morgan, Marsha Y. and Hampe, Jochen. (2015) A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis. Nature Genetics, 47 (12). pp. 1443-1448.

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.

Johnson, Michael R. and Behmoaras, Jacques and Bottolo, Leonardo and Krishnan, Michelle L. and Pernhorst, Katharina and Meza Santoscoy, Paola L. and Rossetti, Tiziana and Speed, Doug and Srivastava, Prashant K. and Chadeau-Hyam, Marc and Hajji, Nabil and Dabrowska, Dabrowska and Rotival, Maxime and Razzaghi, Banafsheh and Kovac, Stjepana and Wanisch, Klaus and Grillo, Federico W. and Slaviero, Anna and Langley, Sarah R. and Shkura, Kirill and Roncon, Paolo and De, Tisham and Mattheisen, Manuel and Niehusmann, Pitt and O'Brien, Terence J. and Petrovski, Slave and von Lehe, Marec and Hoffmann, Per and Eriksson, Johan and Coffey, Alison J. and Cichon, Sven and Walker, Matthew and Simonato, Michele and Danis, Bénédicte and Mazzuferi, Manuela and Foerch, Patrik and Schoch, Susanne and De Paola, Vincenzo and Kaminski, Rafal M. and Cunliffe, Vincent T. and Becker, Albert J. and Petretto, Enrico. (2015) Systems genetics identifies Sestrin 3 as a regulator of a proconvulsant gene network in human epileptic hippocampus. Nature Communications, 6. p. 6031.

Juraeva, Dilafruz and Treutlein, Jens and Scholz, Henrike and Frank, Josef and Degenhardt, Franziska and Cichon, Sven and Ridinger, Monika and Mattheisen, Manuel and Witt, Stephanie H. and Lang, Maren and Sommer, Wolfgang H. and Hoffmann, Per and Herms, Stefan and Wodarz, Norbert and Soyka, Michael and Zill, Peter and Maier, Wolfgang and Jünger, Elisabeth and Gaebel, Wolfgang and Dahmen, Norbert and Scherbaum, Norbert and Schmäl, Christine and Steffens, Michael and Lucae, Susanne and Ising, Marcus and Smolka, Michael N. and Zimmermann, Ulrich S. and Müller-Myhsok, Bertram and Nöthen, Markus M. and Mann, Karl and Kiefer, Falk and Spanagel, Rainer and Brors, Benedikt and Rietschel, Marcella. (2015) XRCC5 as a Risk Gene for Alcohol Dependence: Evidence from a Genome-Wide Gene-Set-Based Analysis and Follow-up Studies in Drosophila and Humans. Neuropsychopharmacology, 40 (2). pp. 361-371.

Lee, S. Hong and Byrne, Enda M. and Hultman, Christina M. and Kähler, Anna and Vinkhuyzen, Anna AE and Ripke, Stephan and Andreassen, Ole A. and Frisell, Thomas and Gusev, Alexander and Hu, Xinli and Karlsson, Robert and Mantzioris, Vasilis X. and McGrath, John J. and Mehta, Divya and Stahl, Eli A. and Zhao, Qiongyi and Kendler, Kenneth S. and Sullivan, Patrick F. and Price, Alkes L. and O'Donovan, Michael and Okada, Yukinori and Mowry, Bryan J. and Raychaudhuri, Soumya and Wray, Naomi R. and Schizophrenia Working Group of the Psychiatric Genomics, Consortium and Rheumatoid Arthritis Consortium, International. (2015) New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis. International Journal of Epidemiology, 44 (5). pp. 1706-1721.

Libin, Alexander V. and Scholten, Joel and Schladen, Manon Maitland and Danford, Ellen and Shara, Nawar and Penk, Walter and Grafman, Jordan and Resnik, Linda and Bruner, Dwan and Cichon, Samantha and Philmon, Miriam and Tsai, Brenda and Blackman, Marc and Dromerick, Alexander. (2015) Executive functioning in TBI from rehabilitation to social reintegration: COMPASS (goal,) a randomized controlled trial (grant: 1I01RX000637-01A3 by the VA ORD RR&D, 2013-2016). Military Medical Research, 2. p. 32.

Luo, Xiong-Jian and Mattheisen, Manuel and Li, Ming and Huang, Liang and Rietschel, Marcella and Børglum, Anders D. and Als, Thomas D. and van den Oord, Edwin J. and Aberg, Karolina A. and Mors, Ole and Mortensen, Preben Bo and Luo, Zhenwu and Degenhardt, Franziska and Cichon, Sven and Schulze, Thomas G. and Nöthen, Markus M. and iPSYCH-GEMS, SCZ working group and MooDS, SCZ Consortium and Su, Bing and Zhao, Zhongming and Gan, Lin and Yao, Yong-Gang. (2015) Systematic Integration of Brain eQTL and GWAS Identifies ZNF323 as a Novel Schizophrenia Risk Gene and Suggests Recent Positive Selection Based on Compensatory Advantage on Pulmonary Function. Schizophrenia Bulletin, 41 (6). pp. 1294-1308.

Mansi, M. and Zanichelli, A. and Coerezza, A. and Suffritti, C. and Wu, M. A. and Vacchini, R. and Stieber, C. and Cichon, S. and Cicardi, M.. (2015) Presentation, diagnosis and treatment of angioedema without wheals: a retrospective analysis of a cohort of 1058 patients. Journal of Internal Medicine, 277 (5). pp. 585-593.

Nenadic, I. and Maitra, R. and Basmanav, F. B. and Schultz, C. C. and Lorenz, C. and Schachtzabel, C. and Smesny, S. and Nöthen, M. M. and Cichon, S. and Reichenbach, J. R. and Sauer, H. and Schlösser, R. G. M. and Gaser, C.. (2015) ZNF804A genetic variation (rs1344706) affects brain grey but not white matter in schizophrenia and healthy subjects. Psychological Medicine, 45 (1). pp. 143-152.

Paternoster, Lavinia and Standl, Marie and Waage, Johannes and Baurecht, Hansjörg and Hotze, Melanie and Strachan, David P. and Curtin, John A. and Bønnelykke, Klaus and Tian, Chao and Takahashi, Atsushi and Esparza-Gordillo, Jorge and Alves, Alexessander Couto and Thyssen, Jacob P. and den Dekker, Herman T. and Ferreira, Manuel A. and Altmaier, Elisabeth and Sleiman, Patrick M. and Xiao, Feng Li and Gonzalez, Juan R. and Marenholz, Ingo and Kalb, Birgit and Pino-Yanes, Maria and Xu, Cheng Jian and Carstensen, Lisbeth and Groen-Blokhuis, Maria M. and Venturini, Cristina and Pennell, Craig E. and Barton, Sheila J. and Levin, Arbet M. and Curjuric, Ivan and Bustamante, Mariona and Kreiner-Møller, Eskil and Lockett, Gabrielle A. and Bacelis, Jonas and Bunyavanich, Supinda and Myers, Rachel A. and Matanovic, Anja and Kumar, Ashish and Tung, Joyce Y and Hirota, Tomomitsu and Kubo, Michiaki and McArdle, Wendy L. and Henderson, A. John and Kemp, John P. and Zheng, Jie and Smith, George Davey and Rüschendorf, Franz and Bauerfeind, Anja and Lee-Kirsch, Min Ae and Arnold, Andreas and Homuth, Georg and Schmidt, Carsten O. and Mangold, Elisabeth and Cichon, Sven and Keil, Thomas and Rodríguez, Elke and Peters, Annette and Franke, Andre and Lieb, Wolfgang and Novak, Natalija and Fölster-Holst, Regina and Horikoshi, Momoko and Pekkanen, Juha and Sebert, Sylvain and Husemoen, Lise L. and Grarup, Niels and de Jongste, Johan C. and Rivadeneira, Fernando and Hofman, Albert and Jaddoe, Vincent W. V. and Pasmans, Suzanne G. M. A. and Elbert, Niels J. and Uitterlinden, André G. and Marks, Guy B. and Thompson, Philip J. and Matheson, Melanie C. and Robertson, Colin F. and Australian Asthma Genetics, Consortium (AAGC) and Ried, Janina S. and Li, Jin and Zuo, Xian Bo and Zheng, Xiao Dong and Yin, Xian Yong Yin and Sun, Liang Dan and McAleer, Maeve A. and O'Regan, Grainne M. and Fahy, Caoimhe M. R. and Campbell, Linda E. and Macek, Milan and Kurek, Michael and Hu, Donglei and Eng, Celeste and Postma, Dirkje S. and Feenstra, Bjarke and Geller, Frank and Hottenga, Jouke Jan and Middeldorp, Christel M. and Hysi, Pirro and Bataille, Veronique and Spector, Tim and Tiesler, Carla M. T. and Thiering, Elisabeth and Pahukasahasram, Badri and Yang, James J. and Imboden, Madea and Huntsman, Scott and Vilor-Tejedor, Natàlia and Relton, Caroline L. and Myhre, Ronny and Nystad, Wenche and Custovic, Adnan and Weiss, Scott T. and Meyers, Deborah A. and Soderhall, Cilla and Melén, Erik and Ober, Carole and Raby, Benjamin A. and Simpson, Angela and Jacobsson, Bo and Holloway, John W. and Bisgaard, Hans and Sunyer, Jordi and Probst-Hensch, Nicole M. and Williams, L. Keoki and Godfrey, Keith M. and Wang, Carol A. and Boomsma, Dorret I. and Melbye, Mads and Koppelman, Gerard H. and Jarvis, Deborah and McLean, W. H. Irwin and Irvine, Alan D. and Zhang, Xue Jun and Hakonarson, Hakon and Gieger, Christian and Burchard, Esteban G. and Martin, Nicholas G. and Duijts, Liesbeth and Linneberg, Allan and Jarvelin, Marjo-Riitta and Noethen, Markus M. and Lau, Susanne and Hübner, Norbert and Lee, Young-Ae and Tamari, Mayum and Hinds, David A. and Glass, Daniel and Brown, Sara J. and Heinrich, Joachim and Evans, David M. and Weidinger, Stephan and EArly Genetics, and Lifecourse Epidemiology (EAGLE) Eczema Consortium, . (2015) Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis. Nature Genetics, 47 (12). pp. 1449-1456.

This list was generated on Fri Sep 21 03:58:07 2018 CEST.