Authors:
Cichon, S
Schmidt-Wolf, G
Schumacher, J
Muller, DJ
Hurter, M
Schulze, TG
Albus, M
Borrmann-Hassenbach, M
Franzek, E
Lanczik, M
Fritze, J
Kreiner, R
Weigelt, B
Minges, J
Lichtermann, D
Lerer, B
Kanyas, K
Strauch, K
Windemuth, C
Baur, MP
Wienker, TF
Maier, W
Rietschel, M
Propping, P
Nothen, MM
Citation: S. Cichon et al., A possible susceptibility locus for bipolar affective disorder in chromosomal region 10q25-q26, MOL PSYCHI, 6(3), 2001, pp. 342-349
Authors:
Wang, T
Franke, P
Neidt, H
Cichon, S
Knapp, M
Lichtermann, D
Maier, W
Propping, P
Nothen, MM
Citation: T. Wang et al., Association study of the low-activity allele of catechol-O-methyltransferase and alcoholism using a family-based approach, MOL PSYCHI, 6(1), 2001, pp. 109-111
Authors:
Jonsson, EG
Ivo, R
Forslund, K
Mattila-Evenden, M
Rylander, G
Cichon, S
Propping, P
Nothen, MM
Asberg, M
Sedvall, GC
Citation: Eg. Jonsson et al., No association between a promoter dopamine D-4 receptor gene variant and schizophrenia, AM J MED G, 105(6), 2001, pp. 525-528
Authors:
Schulze, TG
Muller, DJ
Krauss, H
Gross, M
Bauer, I
Fangerau-Lefevre, H
Illes, F
Ohlraun, S
Fimmers, R
Cichon, S
Held, T
Propping, P
Nothen, MM
Maier, W
Rietschell, M
Citation: Tg. Schulze et al., Brief research communication - Caught in the trio trap? Potential selection bias inherent to association studies using parent-offspring trios, AM J MED G, 105(4), 2001, pp. 351-353
Authors:
Hillmer, AM
Kruse, R
Betz, RC
Schumacher, J
Heyn, U
Propping, P
Nothen, MM
Cichon, S
Citation: Am. Hillmer et al., Variant 1859G -> A (Arg620Gln) of the "hairless" gene: Absence of association with papular atrichia or androgenetic alopecia, AM J HU GEN, 69(1), 2001, pp. 235-237
Authors:
Grunhage, F
Schulze, TG
Muller, DJ
Lanczik, M
Franzek, E
Albus, M
Borrmann-Hassenbach, M
Knapp, M
Cichon, S
Maier, W
Rietschel, M
Propping, P
Nothen, MM
Citation: F. Grunhage et al., Systematic screening for DNA sequence Variation in the coding region of the human dopamine transporter gene (DAT1), MOL PSYCHI, 5(3), 2000, pp. 275-282
Authors:
Vogt, IR
Shimron-Abarbanell, D
Neidt, H
Erdmann, J
Cichon, S
Schulze, TG
Muller, DJ
Maier, W
Albus, M
Borrmann-Hassenbach, M
Knapp, M
Rietschel, M
Propping, P
Nothen, MM
Citation: Ir. Vogt et al., Investigation of the human serotonin 6 (5-HT6) receptor gene in bipolar affective disorder and schizophrenia, AM J MED G, 96(2), 2000, pp. 217-221
Authors:
Cichon, S
Kruse, R
Hillmer, AM
Kukuk, G
Anker, M
Altland, K
Knapp, M
Propping, P
Nothen, MM
Citation: S. Cichon et al., A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family, BR J DERM, 143(4), 2000, pp. 811-814
Authors:
Betz, RC
Lee, YA
Bygum, A
Brandrup, F
Bernal, AI
Toribio, J
Alvarez, JI
Kukuk, GM
Ibsen, HHW
Rasmussen, HB
Wienker, TF
Reis, A
Propping, P
Kruse, R
Cichon, S
Nothen, MM
Citation: Rc. Betz et al., A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3, AM J HU GEN, 66(6), 2000, pp. 1979-1983
Authors:
Nothen, MM
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
Holler, T
Baur, MP
Rietschel, M
Propping, P
Citation: Mm. Nothen et al., Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families, MOL PSYCHI, 4(1), 1999, pp. 76-84
Authors:
Nothen, MM
Schulte-Korne, G
Grimm, T
Cichon, S
Vogt, IR
Muller-Myhsok, B
Propping, P
Remschmidt, H
Citation: Mm. Nothen et al., Genetic linkage analysis with dyslexia: Evidence for linkage of spelling disability to chromosome 15, EUR CHILD A, 8, 1999, pp. 56-59
Authors:
Craddock, N
Lendon, C
Cichon, S
Culverhouse, R
Detera-Wadleigh, S
Devon, R
Faraone, S
Foroud, T
Gejman, P
Leonard, S
McInnis, M
Owen, MJ
Riley, B
Armstrong, C
Barden, N
van Broeckhoven, C
Ewald, H
Folstein, S
Gerhard, D
Goldman, D
Gurling, H
Kelsoe, J
Levinson, D
Muir, W
Philippe, A
Pulver, A
Wildenauer, D
Citation: N. Craddock et al., Chromosome Workshop: Chromosomes 11, 14, and 15, AM J MED G, 88(3), 1999, pp. 244-254
Authors:
Stober, G
Hebebrand, J
Cichon, S
Bruss, M
Bonisch, H
Lehmkuhl, G
Poustka, F
Schmidt, M
Remschmidt, H
Propping, P
Nothen, MM
Citation: G. Stober et al., Tourette syndrome and the norepinephrine transporter gene: Results of a systematic mutation screening, AM J MED G, 88(2), 1999, pp. 158-163