Items where Author is "Maier, W."

2011

Papassotiropoulos, A. and Henke, K. and Stefanova, E. and Aerni, A. and Müller, A. and Demougin, P. and Vogler, C. and Sigmund, J. C. and Gschwind, L. and Huynh, K.-D. and Coluccia, D. and Mondadori, C. R. and Hänggi, J. and Buchmann, A. and Kostic, V. and Novakovic, I. and van den Bussche, H. and Kaduszkiewicz, H. and Weyerer, S. and Bickel, H. and Riedel-Heller, S. and Pentzek, M. and Wiese, B. and Dichgans, M. and Wagner, M. and Jessen, F. and Maier, W. and de Quervain, D. J.-F.. (2011) A genome-wide survey of human short-term memory. Molecular psychiatry, 16 (2). pp. 184-192.

Erhardt, A. and Czibere, L. and Roeske, D. and Lucae, S. and Unschuld, P. G. and Ripke, S. and Kohli, M. A. and Kloiber, S. and Ising, M. and Heck, A. and Ellgas, A. and Pfister, H. and Lieb, R. and Puetz, B. and Uhr, M. and Hohoff, C. and Maier, W. and Bandelow, B. and Domschke, K. and Jacob, C. and Deckert, J. and Landgraf, R. and Bettecken, T. and Keck, M. E. and Müller-Myhsok, B. and Holsboer, F. and Binder, E. B.. (2011) TMEM132D : a new candidate for anxiety phenotypes - evidence from human and mouse studies. Molecular Psychiatry, Vol. 16, H. 6. pp. 647-663.

Erhardt, A. and Czibere, L. and Roeske, D. and Lucae, S. and Unschuld, P. G. and Ripke, S. and Specht, M. and Kohli, M. A. and Kloiber, S. and Ising, M. and Heck, A. and Pfister, H. and Zimmermann, P. and Lieb, R. and Pütz, B. and Uhr, M. and Weber, P. and Deussing, J. M. and Gonik, M. and Bunck, M. and Kebler, M. S. and Frank, E. and Hohoff, C. and Domschke, K. and Krakowitzky, P. and Maier, W. and Bandelow, B. and Jacob, C. and Deckert, J. and Schreiber, S. and Strohmaier, J. and Nöthen, M. and Cichon, S. and Rietschel, M. and Bettecken, T. and Keck, M. E. and Landgraf, R. and Müller-Myhsok, B. and Holsboer, F. and Binder, E. B.. (2011) TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies. Molecular Psychiatry, 16 (6). pp. 647-663.

2010

Domschke, K. and Reif, A. and Weber, H. and Richter, J. and Hohoff, C. and Ohrmann, P. and Pedersen, A. and Bauer, J. and Suslow, T. and Kugel, H. and Heindel, W. and Baumann, C. and Klauke, B. and Jacob, C. and Maier, W. and Fritze, J. and Bandelow, B. and Krakowitzky, P. and Rothermundt, M. and Erhardt, A. and Binder, E. and Holsboer, F. and Gerlach, A. L. and Kircher, T. and Lang, T. and Alpers, G. W. and Ströhle, A. and Fehm, L. and Gloster, A. T. and Wittchen, H. -U. and Arolt, V. and Pauli, P. and Hamm, A. and Deckert, J.. (2010) Neuropeptide S Receptor Gene-Converging Evidence for a Role in Panic Disorder. Molecular Psychiatry, 16 (9). pp. 938-948.

2008

Erhardt, A. and Lucae, S. and Kern, N. and Unschuld, P. G. and Ising, M. and Lieb, R. and Uhr, M. and Hohoff, C. and Deckert, J. and Bandelow, B. and Maier, W. and Binder, E. B. and Müller-Myhsok, B. and Keck, M. E. and Holsboer, F.. (2008) Association of polymorphisms in the angiotensin-converting enzyme gene with syndromal panic attacks. Molecular Psychiatry, Vol. 13. pp. 242-243.

Keck, M. E. and Kern, N. and Erhardt, A. and Unschuld, P. G. and Ising, M. and Salyakina, D. and Müller, M. B. and Knorr, C. C. and Lieb, R. and Hohoff, C. and Krakowitzky, P. and Maier, W. and Bandelow, B. and Fritze, J. and Deckert, J. and Holsboer, F. and Müller-Myhsok, B. and Binder, E. B.. (2008) Combined effects of exonic polymorphisms in CRHR1 and AVPR1B genes in a case/control study for panic disorder. American journal of medical genetics. Part B, Neuropsychiatric genetics, Vol. 147B, H. 7. pp. 1196-1204.

2002

Kockler, M. and Nitardy, A. and Papassotiropoulos, A. and Ptok, U. and Maier, W. and Heun, R.. (2002) Physical disorders and causes of death in relatives of Alzheimer's disease patients. International journal of geriatric psychiatry, Vol. 17, H. 4. pp. 335-342.

2001

Heun, R. and Papassotiropoulos, A. and Jessen, F. and Maier, W. and Breitner, J. C.. (2001) A family study of Alzheimer disease and early- and late-onset depression in elderly patients. Archives of general psychiatry, Vol. 58, H. 2. pp. 190-196.

Kölsch, H. and Ptok, U. and Bagli, M. and Papassotiropoulos, A. and Schmitz, S. and Barkow, K. and Kockler, M. and Rao, M. L. and Maier, W. and Heun, R.. (2001) Gene polymorphisms of interleukin-1alpha influence the course of Alzheimer's disease. Annals of neurology, Vol. 49, H. 6. pp. 818-819.

Ptok, U. and Papassotiropoulos, A. and Maier, W. and Heun, R.. (2001) Seasonal distribution of births in patients with Alzheimer's disease and elderly depressive patients. European psychiatry, Vol. 16, H. 3. pp. 157-161.

Jessen, F. and Kucharski, C. and Fries, T. and Papassotiropoulos, A. and Hoenig, K. and Maier, W. and Heun, R.. (2001) Sensory gating deficit expressed by a disturbed suppression of the P50 event-related potential in patients with Alzheimer's disease. American journal of psychiatry, Vol. 158, H. 8. pp. 1319-1321.

2000

Papassotiropoulos, A. and Bagli, M. and Kurz, A. and Kornhuber, J. and Förstl, H. and Maier, W. and Pauls, J. and Lautenschlager, N. and Heun, R.. (2000) A genetic variation of cathepsin D is a major risk factor for Alzheimer's disease. Annals of neurology, Vol. 47, H. 3. pp. 399-403.

Ptok, U. and Papassotiropoulos, A. and Maier, W. and Heun, R.. (2000) Advanced parental age : a risk factor for Alzheimer's disease or depression in the elderly? International psychogeriatrics, Vol. 12, H. 4. pp. 445-451.

Majores, M. and Bagli, M. and Papassotiropoulos, A. and Schwab, S. G. and Jessen, F. and Rao, M. L. and Maier, W. and Heun, R.. (2000) Allelic association between the D10S1423 marker and Alzheimer's disease in a German population. Neuroscience letters, Vol. 289, H. 3. pp. 224-226.

Schulze, T. G. and Müller, D. J. and Krauss, H. and Scherk, H. and Ohlraun, S. and Syagailo, Y. V. and Windemuth, C. and Neidt, H. and Grässle, M. and Papassotiropoulos, A. and Heun, R. and Nöthen, M. M. and Maier, W. and Lesch, K. P. and Rietschel, M.. (2000) Association between a functional polymorphism in the monoamine oxidase A gene promoter and major depressive disorder. American journal of medical genetics, Vol. 96, no. 6. pp. 801-803.

Bagli, M. and Papassotiropoulos, A. and Knapp, M. and Jessen, F. and Luise Rao, M. and Maier, W. and Heun, R.. (2000) Association between an interleukin-6 promoter and 3' flanking region haplotype and reduced Alzheimer's disease risk in a German population. Neuroscience letters, Vol. 283, H. 2. pp. 109-112.

Papassotiropoulos, A. and Bagli, M. and Jessen, F. and Frahnert, C. and Rao, M. L. and Maier, W. and Heun, R.. (2000) Confirmation of the association between bleomycin hydrolase genotype and Alzheimer's disease. Molecular psychiatry, Vol. 5, H. 2. pp. 213-215.

Bagli, M. and Papassotiropoulos, A. and Jessen, F. and Rao, M. L. and Maier, W. and Heun, R.. (2000) Gene-gene interaction between interleukin-6 and alpha2-macroglobulin influences the risk for Alzheimer's disease. Annals of neurology, Vol. 47, H. 1. pp. 138-139.

Bagli, M. and Papassotiropoulos, A. and Jessen, F. and Schmitz, S. and Rao, M. L. and Maier, W. and Heun, R.. (2000) Identical distribution of the alpha 2-macroglobulin pentanucleotide deletion in subjects with Alzheimer disease and controls in a German population. American journal of medical genetics, Vol. 96, no. 6. pp. 775-777.

Papassotiropoulos, A. and Bagli, M. and Jessen, F. and Maier, W. and Förstl, H. and Kurz, A. and Heun, R.. (2000) Interaction of two genes possibly involved in the regulation of the amyloid precursor protein (APP) processing. Molecular psychiatry, Vol. 5, H. 3. pp. 240-241.

Papassotiropoulos, A. and Bagli, M. and Becker, K. and Jessen, F. and Maier, W. and Rao, M. L. and Ludwig, M. and Heun, R.. (2000) No association between an intronic biallelic polymorphism of the FE65 gene and Alzheimer's disease. International journal of molecular medicine, Vol. 6, H. 5. pp. 587-589.

Papassotiropoulos, A. and Lütjohann, D. and Bagli, M. and Locatelli, S. and Jessen, F. and Rao, M. L. and Maier, W. and Björkhem, I. and von Bergmann, K. and Heun, R.. (2000) Plasma 24S-hydroxycholesterol : a peripheral indicator of neuronal degeneration and potential state marker for Alzheimer's disease. NeuroReport, Vol. 11, H. 9. pp. 1959-1962.

1999

Papassotiropoulos, A. and Bagli, M. and Jessen, F. and Bayer, T. A. and Maier, W. and Rao, M. L. and Heun, R.. (1999) A genetic variation of the inflammatory cytokine interleukin-6 delays the initial onset and reduces the risk for sporadic Alzheimer's disease. Annals of neurology, Vol. 45, H. 5. pp. 666-668.

Kühn, K. U. and Meyer, K. and Nöthen, M. M. and Gänsicke, M. and Papassotiropoulos, A. and Maier, W.. (1999) Allelic variants of dopamine receptor D4 (DRD4) and serotonin receptor 5HT2c (HTR2c) and temperament factors : replication tests. American journal of medical genetics, Vol. 88, no. 2. pp. 168-172.

Schwab, S. G. and Bagli, M. and Papassotiropoulos, A. and Jessen, F. and Maier, W. and Rao, M. L. and Heun, R.. (1999) Alpha-1-antichymotrypsin gene polymorphism and risk for sporadic Alzheimer's disease in a German population. Dementia and Geriatric Cognitive Disorders, 10 (6). pp. 469-472.

Papassotiropoulos, A. and Bagli, M. and Feder, O. and Jessen, F. and Maier, W. and Rao, M. L. and Ludwig, M. and Schwab, S. G. and Heun, R.. (1999) Genetic polymorphism of cathepsin D is strongly associated with the risk for developing sporadic Alzheimer's disease. Neuroscience letters, Vol. 262, H. 3. pp. 171-174.

Bagli, M. and Papassotiropoulos, A. and Schwab, S. G. and Jessen, F. and Rao, M. L. and Maier, W. and Heun, R.. (1999) No association between an intronic polymorphism in the presenilin-1 gene and Alzheimer disease in a German population. Journal of the neurological sciences, Vol. 167, No. 1. pp. 34-36.

Papassotiropoulos, A. and Heun, R. and Maier, W.. (1999) The impact of dementia on the detection of depression in elderly subjects from the general population. Psychological medicine, Vol. 29, H. 1. pp. 113-120.

1997

Papassotiropoulos, A. and Heun, R. and Maier, W.. (1997) Age and cognitive impairment influence the performance of the General Health Questionnaire. Comprehensive psychiatry, Vol. 38, H. 6. pp. 335-340.