Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Bettina Weigelt"'
Autor:
Peter Propping, Martina Hürter, Johannes Schumacher, Max P. Baur, Marcella Rietschel, Jürgen Minges, Konstantin Strauch, Bettina Weigelt, Daniel J. Müller, Thomas F. Wienker, M. Lanczik, Susanne Hemmer, Christine Windemuth, Markus M. Nöthen, R. Kreiner, Sven Cichon, Gabriele Schmidt-Wolf, Wolfgang Maier, Thomas G. Schulze, Margitta Borrmann-Hassenbach, B. Lerer, Kyra Kanyas, Jürgen Fritze, Dirk Lichtermann, Ernst Franzek, Ulrike Reuner, Margot Albus
Publikováno v:
Human molecular genetics
Bipolar affective disorder (BPAD), also known as manic depressive illness, is a severe psychiatric disorder characterized by episodes of mania and depression. It has a lifetime prevalence of approximately 1% in all human populations. In order to iden
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1662e706bde5faf1790d0b1a701a2712
https://doi.org/10.1093/hmg/10.25.2933
https://doi.org/10.1093/hmg/10.25.2933
Autor:
Peter Propping, Michael Knapp, Ernst Franzek, Hongzu Ren, Markus M. Nöthen, Jürgen Deckert, Gary L. Stiles, Marcella Rietschel, Margot Albus, Helmut Beckmann, Bettina Weigelt, Wolfgang Maier
Publikováno v:
American Journal of Medical Genetics. 81:18-23
In the present study we sought to identify genetic variation in the adenosine A1 receptor (A1AR) gene on chromosome 1q31-32.1, which through alteration of protein function or level of expression might contribute to the genetic predisposition to bipol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11896dc4895eccf3f1d4397aa9717d28
https://doi.org/10.1002/(sici)1096-8628(19980207)81:1<18::aid-ajmg4>3.0.co
https://doi.org/10.1002/(sici)1096-8628(19980207)81:1<18::aid-ajmg4>3.0.co
Autor:
Martina Hürter, Gabriele Schmidt-Wolf, Ernst Franzek, Bettina Weigelt, Wolfgang Maier, Markus M. Nöthen, B. Lerer, R. Kreiner, Thomas G. Schulze, Peter Propping, Kyra Kanyas, Jürgen Fritze, Marcella Rietschel, Christine Windemuth, Daniel J. Müller, Margot Albus, Thomas F. Wienker, Johannes Schumacher, M. Lanczik, Max P. Baur, Margitta Borrmann-Hassenbach, Jürgen Minges, Dirk Lichtermann, Konstantin Strauch, Sven Cichon
Publikováno v:
Molecular psychiatry
In an attempt to identify susceptibility loci for bipolar affective disorder, we are currently conducting a systematic genome screen with highly polymorphic microsatellite markers at an average marker spacing of 10 cM in a series of 75 families, comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0c56027fbab6a137db79b99d582b212
https://pubmed.ncbi.nlm.nih.gov/11326307
https://pubmed.ncbi.nlm.nih.gov/11326307
Autor:
Jürgen Fritze, Bettina Weigelt, Ernst Franzek, Susanne Hemmer, Markus M. Nöthen, Peter Propping, Dirk Lichtermann, H. Rohleder, Max P. Baur, Margitta Borrmann-Hassenbach, Margot Albus, Marcella Rietschel, Nicholas John Craddock, R. Kreiner, Rolf Fimmers, Tobias Höller, Jürgen Minges, Wolfgang Maier, Sven Cichon
Publikováno v:
Molecular psychiatry. 4(1)
Previously reported linkage of bipolar affective disorder to DNA markers on chromosome 18 was reexamined in a large sample of German bipolar families. Twenty-three short tandem repeat markers were investigated in 57 families containing 103 individual
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d1f7df97dc5ff2e2294417bce6c317c
https://pubmed.ncbi.nlm.nih.gov/10822335
https://pubmed.ncbi.nlm.nih.gov/10822335
Autor:
Monsheel S. Sodhi, David A. Collier, Robin M. Murray, N Davies, Margot Albus, Maria Arranz, Jeanette Erdmann, Markus M. Nöthen, Ernst Franzek, Daphne Shimron-Abarbanell, Robert Kerwin, Bettina Weigelt, Marcella Rietschel, Wolfgang Maier, George Kirov, Iman Abusaad, Pak C. Sham, David Ball, Peter Propping
Publikováno v:
Neuroscience letters. 224(2)
The aim of this study was to investigate the possible involvement of genetic variation in serotonin receptors in the aetiology of bipolar affective disorder. The 5-HT2A receptor gene was systematically screened for genetic variants by single strand c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0dc42eb71f633df9140c69d9f9ac1bdf
https://pubmed.ncbi.nlm.nih.gov/9086465
https://pubmed.ncbi.nlm.nih.gov/9086465
Autor:
D.B. Wildenauer, Bettina Weigelt, Wolfgang Maier, Marcella Rietschel, Peter Propping, Gerald Stöber, Roland Schroers, Markus M. Nöthen, Margot Albus, J. Körner, Sven Cichon, Rolf Fimmers, Ernst Franzek
Publikováno v:
American journal of medical genetics. 67(4)
A possible dysregulation of dopaminergic neurotransmission has been implicated in a variety of neuropsychiatric diseases. In the present study we systematically searched for the presence of mutations in the 5′-flanking region of the dopamine D1 rec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39fa2744f88376f82530681972ee9488
https://pubmed.ncbi.nlm.nih.gov/8837716
https://pubmed.ncbi.nlm.nih.gov/8837716
Autor:
J. Komer, Bettina Weigelt, Rolf Fimmers, Sven Cichon, Nicholas John Craddock, Wolfgang Maier, Ernst Franzek, Dirk Lichtermann, Markus M. Nöthen, Peter Propping, R. Rietschel, Margot Albus
Publikováno v:
Biological Psychiatry. 39:615
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::204d709fefcb94c5a490d24ea2d31481
https://doi.org/10.1016/0006-3223(96)84336-8
https://doi.org/10.1016/0006-3223(96)84336-8
Autor:
Ernst Franzek, B. Lerer, Peter Propping, W. Maier, M. M. Nöthen, Bettina Weigelt, Susanne Hemmer, Margot Albus, Rolf Fimmers, Sven Cichon, M. Rietschel
Publikováno v:
Psychiatric Genetics. 6:146
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2c6fee629033560eba389014d042bef
https://doi.org/10.1097/00041444-199623000-00033
https://doi.org/10.1097/00041444-199623000-00033