نتائج البحث - HJ Möller
- يعرض 1 - 6 نتائج من 6
-
1
SNP and haplotype analysis of a novel tryptophan hydroxylase isoform (TPH2) gene provide evidence for association with major depression حسب P Zill, Thomas C. Baghai, Peter Zwanzger, Cornelius Schüle, D Eser, Rainer Rupprecht, HJ Möller, B Bondy, Manfred Ackenheil
منشور في 2004Artigo -
2
Effects of Alprazolam on Cholecystokinin-Tetrapeptide-Induced Panic and Hypothalamic–Pituitary–Adrenal-Axis Activity: A Placebo-Controlled Study حسب Peter Zwanzger, Daniela Eser, Sue A. Aicher, Cornelius Schüle, Thomas C. Baghai, Frank Padberg, Robin Ella, HJ Möller, Rainer Rupprecht
منشور في 2002Artigo -
3
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia حسب Clyde Francks, Shinji Maegawa, Juha Laurén, Brett S. Abrahams, Antonio Velayos‐Baeza, Sarah E. Medland, Stefano Colella, Matthias Groszer, E Z McAuley, Tara M. Caffrey, Tõnis Timmusk, Priit Pruunsild, Indrek Koppel, Penelope A. Lind, N Matsumoto-Itaba, Jérôme Nicod, Lan Xiong, Ridha Joober, Wolfgang Enard, Benjamin H. Krinsky, Eiji Nanba, A.J. Richardson, Brien P. Riley, Nicholas G. Martin, Stephen M. Strittmatter, HJ Möller, Dan Rujescu, David St Clair, Pierandrea Muglia, Johannes L. Roos, Simon E. Fisher, Richard Wade‐Martins, Guy A. Rouleau, John Stein, Maria Karayiorgou, Dan Geschwind, Jiannis Ragoussis, Kenneth S. Kendler, Matti S. Airaksinen, Mitsuo Oshimura, Lynn E. DeLisi, Anthony P. Monaco
منشور في 2007Artigo -
4
Copy number variations of chromosome 16p13.1 region associated with schizophrenia حسب Andrés Ingason, Dan Rujescu, Sven Cichon, Engilbert Sigurðsson, Thordur Sigmundsson, Olli Pietiläinen, Jacobine E. Buizer‐Voskamp, E Strengman, Clyde Francks, Pierandrea Muglia, Arnaldur Gylfason, Ómar Gústafsson, Pall I. Olason, Stacy Steinberg, Thomas Hansen, Klaus D. Jakobsen, Henrik B. Rasmussen, Ina Giegling, HJ Möller, A. Hartmann, Caroline Crombie, G. T. Fraser, Nicholas Walker, Jouko Lönnqvist, Jaana Suvisaari, Annamari Tuulio‐Henriksson, Elvira Bramon, Lambertus A. Kiemeney, Barbara Franke, Robin Murray, Evangelos Vassos, Timothea Toulopoulou, Thomas W. Mühleisen, Sarah Tosato, Mirella Ruggeri, Srdjan Djurovic, Ole A. Andreassen, Z Zhang, Thomas Werge, Roel A. Ophoff, Marcella Rietschel, Markus M. Nöthen, Hannes Pétursson, Hreinn Stefánsson, L. Peltonen, David Collier, Hreinn Stefánsson, David M. St. Clair
منشور في 2009Artigo -
5
Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2 حسب Michael O’Donovan, Nadine Norton, Hywel Williams, T Peirce, Valentina Moskvina, Ivan Nikolov, Marian L. Hamshere, Liam Carroll, L. Georgieva, Sarah Dwyer, Peter Holmans, Jonathan Marchini, Chris C. A. Spencer, Bryan Howie, H. T. T. Leung, Ina Giegling, Annette M. Hartmann, HJ Möller, Derek W. Morris, Yongyong Shi, Guofang Feng, Per Hoffmann, Peter Propping, Catalina Vasilescu, W. Maier, Marcella Rietschel, Stanley Zammit, J Schumacher, Emma M. Quinn, Thomas G. Schulze, Nakao Iwata, Masashi Ikeda, Ariel Darvasi, Sagiv Shifman, Lin He, Jubao Duan, Alan R. Sanders, Douglas F. Levinson, Rolf Adolfsson, Urban Ösby, Lars Terenius, Erik G. Jönsson, Sven Cichon, Markus M. Nöthen, Michael Gill, Aiden Corvin, Dan Rujescu, Pablo V. Gejman, George Kirov, Nick Craddock, Nigel Williams, Michael J. Owen
منشور في 2008Artigo -
6
Expanding the range of ZNF804A variants conferring risk of psychosis حسب Stacy Steinberg, Ole Mors, Anders D. Børglum, Ómar Gústafsson, Thomas Werge, Preben Bo Mortensen, Ole A. Andreassen, Engilbert Sigurðsson, Thorgeir E. Thorgeirsson, Yvonne Böttcher, Pall I. Olason, Roel A. Ophoff, Sven Cichon, Iris H Gudjonsdottir, Olli Pietiläinen, Mette Nyegaard, Annamari Tuulio‐Henriksson, Andrés Ingason, Thomas Hansen, Lavinia Athanasiu, Jaana Suvisaari, Jouko Lönnqvist, Tiina Paunio, Annette M. Hartmann, Gesche Jürgens, Merete Nordentoft, David M. Hougaard, B Nørgaard‐Pedersen, René Breuer, HJ Möller, Ina Giegling, Birte Glenthøj, Henrik Berg Rasmussen, Manuel Mattheisen, István Bitter, János Réthelyi, Thordur Sigmundsson, Ragnheiður Fossdal, Unnur Þorsteinsdóttir, Mirella Ruggeri, Sarah Tosato, E Strengman, Lambertus A. Kiemeney, Ingrid Melle, Srdjan Djurovic, Л. И. Абрамова, В. Г. Каледа, Muriel Walshe, Elvira Bramon, Evangelos Vassos, Tao Li, G. T. Fraser, Nicholas Walker, T. Toulopoulou, Joeng Lim Yoon, Nelson B. Freimer, Rita M. Cantor, Robin Murray, Augustine Kong, В. Е. Голимбет, Erik G. Jönsson, Lars Terenius, Ingrid Agartz, Hannes Pétursson, Markus M. Nöthen, Marcella Rietschel, Leena Peltonen, Dan Rujescu, David Collier, Hreinn Stefánsson, David St Clair, Kāri Stefánsson
منشور في 2010Artigo
أدوات البحث:
موضوعات ذات صلة
Psychiatry
Biology
Gene
Genetics
Psychology
Schizophrenia (object-oriented programming)
Receptor
Allele
Genetic association
Genotype
Medicine
Psychosis
SNP
Single-nucleotide polymorphism
Alprazolam
Alternative medicine
Anesthesia
Anxiety
Anxiety disorder
Candidate gene
Central nervous system
Cholecystokinin
Chromosome
Composite material
Copy-number variation
Endocrinology
Fibroblast growth factor
Fibroblast growth factor receptor 2
Forebrain
Genome