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P01-42 - G72/G30 candidate gene for bipolar I disorder is not associated with psychosis in the Romanian population
Published in:
2010
By:
- Grigoroiu-Serbanescu, M.;
- Herms, S.;
- Diaconu, C.C.;
- Bleotu, C.;
- Neagu, A.I.;
- Abou Jamra, R.;
- Gherghel, M.;
- Sima, D.;
- Dan, I.A.;
- Prelipceanu, D.;
- Nöthen, M.M.;
- Cichon, S.
Publication type:
Abstract
Morbus Galli-Galli.
Published in:
Der Hautarzt, 2011, v. 62, n. 11, p. 842, doi. 10.1007/s00105-011-2222-x
By:
- Hanneken, S.;
- Rütten, A.;
- Eigelshoven, S.;
- Braun-Falco, M.;
- Pasternack, S.M.;
- Ruzicka, T.;
- Nöthen, M.M.;
- Betz, R.C.;
- Kruse, R.
Publication type:
Article
Genetic linkage analysis with dyslexia: Evidence for linkage of spelling disability to chromosome 15.
Published in:
European Child & Adolescent Psychiatry, 1999, v. 8, p. S056
By:
- Nöthen, M.M.;
- Schulte-Körne, G.;
- Grimm, T.;
- Cichon, S.;
- Vogt, I.R.;
- Müller-Myhsok, B.;
- Propping, P.;
- Remschmidt, H.
Publication type:
Article
Examination of G72 and D-amino-acid oxidase as genetic risk factors for schizophrenia and bipolar affective disorder.
Published in:
Molecular Psychiatry, 2004, v. 9, n. 2, p. 203, doi. 10.1038/sj.mp.4001421
By:
- Schumacher, J.;
- Jamra, R. Abon;
- Freudenberg, J.;
- Becker, T.;
- Ohlraun, S.;
- Otte, A.C.J.;
- Tullius, M.;
- Kovalenko, S.;
- van den Bogaert, A.;
- Maier, W.;
- Rietschel, M.;
- Propping, P.;
- Nöthen, M.M.;
- Cichon, S.
Publication type:
Article
Association study of the low-activity allele of catechol-O- methyltransferase and alcoholism using a family-based approach.
Published in:
Molecular Psychiatry, 2001, v. 6, n. 1, p. 109, doi. 10.1038/sj.mp.4000803
By:
- Wang, T.;
- Franke, P.;
- Neidt, H.;
- Cichon, S.;
- Knapp, M.;
- Lichtermann, D.;
- Maier, W.;
- Propping, P.;
- Nöthen, M.M.
Publication type:
Article
Systematic screening for DNA sequence variation in the coding region of the human dopamine transporter gene (DAT1).
Published in:
Molecular Psychiatry, 2000, v. 5, n. 3, p. 275
By:
- Grünhage, F.;
- Schulze, T.G.;
- Müller, D.J.;
- Lanczik, M.;
- Franzek, E.;
- Albus, M.;
- Borrmann-Hassenbach, M.;
- Knapp, M.;
- Cichon, S.;
- Maier, W.;
- Rietschel, M.;
- Propping, P.;
- Nöthen, M.M.
Publication type:
Article
Strauch et al reply.
Published in:
Molecular Psychiatry, 2000, v. 5, n. 2, p. 126, doi. 10.1038/sj.mp.4000668
By:
- Strauch, K.;
- Fimmers, R.;
- Wienker, T.F.;
- Baur, M.P.;
- Cichon, S.;
- Propping, P.;
- Nöthen, M.M.
Publication type:
Article
DRD4 exon III VNTR polymorphism-susceptibility factor for heroin dependence? Results of a case-control and a family-based association approach.
Published in:
Molecular Psychiatry, 2000, v. 5, n. 1, p. 101, doi. 10.1038/sj.mp.4000583
By:
- Franke, P.;
- Nöthen, M.M.;
- Wang, T.;
- Knapp, M.;
- Lichtermann, D.;
- Neidt, H.;
- Sandler, T.;
- Propping, P.;
- Maier, W.
Publication type:
Article
Polymorphisms in the dopamine D2 receptor gene and their relationships to striatal dopamine receptor density of healthy volunteers.
Published in:
Molecular Psychiatry, 1999, v. 4, n. 3, p. 290
By:
- Jönsson, E.G.;
- Nöthen, M.M.;
- Grünhage, F.;
- Farde, L.;
- Nakashima, Y.;
- Propping, P.;
- Sedvall, G.C.
Publication type:
Article
Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families.
Published in:
Molecular Psychiatry, 1999, v. 4, n. 1, p. 76
By:
- Nöthen, M.M.;
- Cichon, S.;
- Rohleder, H.;
- Hemmer, S.;
- Franzek, E.;
- Fritze, J.;
- Albus, M.;
- Borrmann-Hassenbach, M.;
- Kreiner, R.;
- Weigelt, B.;
- Minges, J.;
- Lichtermann, D.;
- Maier, W.;
- Craddock, N.;
- Fimmers, R.;
- Höller, T.;
- Baur, M.P.;
- Roetschel, M.;
- Propping, P.
Publication type:
Article
Systematic mutation screening and association study of the A1 and A2a adenosine receptor genes in panic disorder suggest a contribution of the A2a gene to the development of disease.
Published in:
Molecular Psychiatry, 1998, v. 3, n. 1, p. 81, doi. 10.1038/sj.mp.4000345
By:
- Deckert, J.;
- Nöthen, M.M.;
- Franke, P.;
- Delmo, C.;
- Fritze, J.;
- Knapp, M.;
- Maier, W.;
- Beckmann, H.;
- Propping, P.
Publication type:
Article
De novo Partial Trisomy 18p and Partial Monosomy 18q in a Patient with Anorectal Malformation.
Published in:
Cytogenetic & Genome Research, 2011, v. 134, n. 3, p. 243, doi. 10.1159/000328833
By:
- Bartels, E.;
- Draaken, M.;
- Kazmierczak, B.;
- Spranger, S.;
- Schramm, C.;
- Baudisch, F.;
- Nöthen, M.M.;
- Schmiedeke, E.;
- Ludwig, M.;
- Reutter, H.
Publication type:
Article
First report of a FXII gene mutation in a Brazilian family with hereditary angio-oedema with normal C1 inhibitor.
Published in:
British Journal of Dermatology, 2015, v. 173, n. 4, p. 1102, doi. 10.1111/bjd.13791
By:
- Stieber, C.;
- Grumach, A.S.;
- Cordeiro, E.;
- Constantino ‐ Silva, R.N.;
- Barth, S.;
- Hoffmann, P.;
- Pesquero, J.B.;
- Renné, T.;
- Nöthen, M.M.;
- Cichon, S.
Publication type:
Article
The oestrogen receptor 2 ( ESR2) gene in female-pattern hair loss: replication of association with rs10137185 in German patients.
Published in:
British Journal of Dermatology, 2014, v. 170, n. 4, p. 982, doi. 10.1111/bjd.12756
By:
- Redler, S.;
- Birch, P.;
- Drichel, D.;
- Hofmann, P.;
- Dobson, K.;
- Böhmer, A.C.;
- Becker, J.;
- Giehl, K.A.;
- Tazi‐Ahnini, R.;
- Kruse, R.;
- Wolff, H.;
- Miesel, A.;
- Fischer, T.;
- Böhm, M.;
- Nuwayhid, R.;
- Garcia Bartels, N.;
- Lutz, G.;
- Becker, T.;
- Blume‐Peytavi, U.;
- Nöthen, M.M.
Publication type:
Article
Evidence for a polygenic contribution to androgenetic alopecia.
Published in:
British Journal of Dermatology, 2013, v. 169, n. 4, p. 927, doi. 10.1111/bjd.12443
By:
- Heilmann, S.;
- Brockschmidt, F.F.;
- Hillmer, A.M.;
- Hanneken, S.;
- Eigelshoven, S.;
- Ludwig, K.U.;
- Herold, C.;
- Mangold, E.;
- Becker, T.;
- Kruse, R.;
- Knapp, M.;
- Nöthen, M.M.
Publication type:
Article
No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopecia.
Published in:
British Journal of Dermatology, 2013, v. 169, n. 1, p. 222, doi. 10.1111/bjd.12292
By:
- Heilmann, S.;
- Nyholt, D.R.;
- Brockschmidt, F.F.;
- Hillmer, A.M.;
- Herold, C.;
- Becker, T.;
- Martin, N.G.;
- Nöthen, M.M.;
- Bataille, V.;
- Dedoussis, G.;
- Deloukas, P.;
- den Heijer, M.;
- Dimitriou, M.;
- Eigelshoven, S.;
- Eriksson, N.;
- Geller, F.;
- Glass, D.;
- Hanneken, S.;
- Heath, A.C.;
- Hinds, D.A.
Publication type:
Article
Investigation of selected cytokine genes suggests that IL2RA and the TNF/ LTA locus are risk factors for severe alopecia areata.
Published in:
British Journal of Dermatology, 2012, v. 167, n. 6, p. 1360, doi. 10.1111/bjd.12004
By:
- Redler, S.;
- Albert, F.;
- Brockschmidt, F.F.;
- Herold, C.;
- Hanneken, S.;
- Eigelshoven, S.;
- Giehl, K.A.;
- Kruse, R.;
- Lutz, G.;
- Wolff, H.;
- Blaumeiser, B.;
- Böhm, M.;
- Becker, T.;
- Nöthen, M.M.;
- Betz, R.C.
Publication type:
Article
Investigation of the male pattern baldness major genetic susceptibility loci AR/ EDA2R and 20p11 in female pattern hair loss.
Published in:
British Journal of Dermatology, 2012, v. 166, n. 6, p. 1314, doi. 10.1111/j.1365-2133.2012.10877.x
By:
- Redler, S.;
- Brockschmidt, F.F.;
- Tazi-Ahnini, R.;
- Drichel, D.;
- Birch, M.P.;
- Dobson, K.;
- Giehl, K.A.;
- Herms, S.;
- Refke, M.;
- Kluck, N.;
- Kruse, R.;
- Lutz, G.;
- Wolff, H.;
- Böhm, M.;
- Becker, T.;
- Nöthen, M.M.;
- Messenger, A.G.;
- Betz, R.C.
Publication type:
Article
Functional analysis of splice site mutations in the human hairless ( HR) gene using a minigene assay.
Published in:
British Journal of Dermatology, 2011, v. 165, n. 5, p. 1127, doi. 10.1111/j.1365-2133.2011.10495.x
By:
- Refke, M.;
- Pasternack, S.M.;
- Fiebig, B.;
- Wenzel, S.;
- Ishorst, N.;
- Ludwig, M.;
- Nöthen, M.M.;
- Seyger, M.M.;
- Hamel, B.C.;
- Betz, R.C.
Publication type:
Article
The TRAF1/C5 locus confers risk for familial and severe alopecia areata.
Published in:
British Journal of Dermatology, 2010, v. 162, n. 4, p. 866, doi. 10.1111/j.1365-2133.2009.09598.x
By:
- Redler, S.;
- Brockschmidt, F.F.;
- Forstbauer, L.;
- Giehl, K.A.;
- Herold, C.;
- Eigelshoven, S.;
- Hanneken, S.;
- De Weert, J.;
- Lutz, G.;
- Wolff, H.;
- Kruse, R.;
- Blaumeiser, B.;
- Böhm, M.;
- Becker, T.;
- Nöthen, M.M.;
- Betz, R.C.
Publication type:
Article
Fine mapping of the human AR/EDA2R locus in androgenetic alopecia.
Published in:
2010
By:
- Brockschmidt, F.F.;
- Hillmer, A.M.;
- Eigelshoven, S.;
- Hanneken, S.;
- Heilmann, S.;
- Barth, S.;
- Herold, C.;
- Becker, T.;
- Kruse, R.;
- Nöthen, M.M.
Publication type:
Letter
The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach.
Published in:
British Journal of Dermatology, 2002, v. 146, n. 4, p. 601, doi. 10.1046/j.1365-2133.2002.04766.x
By:
- Hillmer, A.M.;
- Kruse, R.;
- Macciardi, F.;
- Heyn, U.;
- Betz, R.C.;
- Ruzicka, T.;
- Propping, P.;
- Nöthen, M.M.;
- Cichon, S.
Publication type:
Article
A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family.
Published in:
British Journal of Dermatology, 2000, v. 143, n. 4, p. 811, doi. 10.1046/j.1365-2133.2000.03781.x
By:
- Cichon, S.;
- Kruse, R.;
- Hillmer, A.M.;
- Kukuk, G.;
- Anker, M.;
- Altland, K.;
- Knapp, M.;
- Propping, P.;
- Nöthen, M.M.
Publication type:
Article
Genetik der androgenetischen Alopezie.
Published in:
Medizinische Genetik, 2009, v. 21, n. 4, p. 511, doi. 10.1007/s11825-009-0197-0
By:
- Brockschmidt, F.F.;
- Hillmer, A.M.;
- Kruse, R.;
- Nöthen, M.M.
Publication type:
Article
Multifaktorielle Krankheiten.
Published in:
Medizinische Genetik, 2007, v. 19, n. 3, p. 293, doi. 10.1007/s11825-007-0042-2
By:
- Nöthen, M.M.
Publication type:
Article
Genetik der Alopecia areata.
Published in:
Medizinische Genetik, 2007, v. 19, n. 3, p. 356, doi. 10.1007/s11825-007-0035-1
By:
- Betz, R.C.;
- Hillmer, A.M.;
- Nöthen, M.M.
Publication type:
Article

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