Priebe, Lutz
University of Bonn
6 papers on CoChat
Most cited papers
- Verified
Genome-wide association study reveals two new risk loci for bipolar disorder
Mühleisen, T. W., Leber, M., Schulze, T. G., Strohmaier, J., Degenhardt, F., Treutlein, J., Mattheisen, M., Forstner, A. J., Schumacher, J., Breuer, R., et al. (2014) · Nature Communications
Bipolar Disorder and TreatmentGenetic Associations and Epidemiology
Cited by 346
- Verified
Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder
Cichon, S., Mühleisen, T. W., Degenhardt, F. A., Mattheisen, M., Miró, X., Strohmaier, J., Steffens, M., Meesters, C., Herms, S., Weingarten, M., et al. (2011) · The American Journal of Human Genetics
Bipolar Disorder and TreatmentGenetic Associations and Epidemiology
Cited by 286
- Verified
The complement control-related genes CSMD1 and CSMD2 associate to schizophrenia
Håvik, B., Le Hellard, S., Rietschel, M., Lybæk, H., Djurovic, S., Mattheisen, M., Mühleisen, T. W., Degenhardt, F., Priebe, L., Maier, W., et al. (2011) · Biological Psychiatry
Schizophrenia research and treatmentGenetic Associations and Epidemiology
Cited by 168
- Verified
Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder
Priebe, L., Degenhardt, F. A., Herms, S., Haenisch, B., Mattheisen, M., Nieratschker, V, Weingarten, M., Witt, S., Breuer, R., Paul, T., et al. (2012) · Molecular Psychiatry
Bipolar Disorder and TreatmentGenomic variations and chromosomal abnormalities
Cited by 84
- Verified
DNA methylation signature in peripheral blood reveals distinct characteristics of human X chromosome numerical aberrations
Sharma, A., Jamil, M. A., Nuesgen, N., Schreiner, F., Priebe, L., Hoffmann, P., Herns, S., Nöthen, M. M., Fröhlich, H., Oldenburg, J., et al. (2015) · Clinical Epigenetics
Genetic and Clinical Aspects of Sex Determination and Chromosomal AbnormalitiesEpigenetics and DNA Methylation
Cited by 81
- Verified
Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder
Mühleisen, T. W., Mattheisen, M., Strohmaier, J., Degenhardt, F., Priebe, L., Schultz, C. C., Breuer, R., Meier, S., Hoffmann, P., Rivandeneira, F., et al. (2012) · Schizophrenia Research
Schizophrenia research and treatmentBipolar Disorder and Treatment
Cited by 80
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