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Results: 1-19 |
Results: 19
A possible susceptibility locus for bipolar affective disorder in chromosomal region 10q25-q26
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
Association study of the low-activity allele of catechol-O-methyltransferase and alcoholism using a family-based approach
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
No association between a promoter dopamine D-4 receptor gene variant and schizophrenia
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
Brief research communication - Caught in the trio trap? Potential selection bias inherent to association studies using parent-offspring trios
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
Clozapine and weight gain
Authors: Theisen, FM Cichon, S Linden, A Martin, M Remschmidt, H Hebebrand, J
Citation: Fm. Theisen et al., Clozapine and weight gain, AM J PSYCHI, 158(5), 2001, pp. 816-816
Variant 1859G -> A (Arg620Gln) of the "hairless" gene: Absence of association with papular atrichia or androgenetic alopecia
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
Systematic screening for DNA sequence Variation in the coding region of the human dopamine transporter gene (DAT1)
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
Analysis of parental-origin effects in linkage data - Reply
Authors: Strauch, K Fimmers, R Wienker, TF Baur, MP Cichon, S Propping, P Nothen, MM
Citation: K. Strauch et al., Analysis of parental-origin effects in linkage data - Reply, MOL PSYCHI, 5(2), 2000, pp. 126-127
Pharmacogenetics of schizophrenia
Authors: Cichon, S Nothen, MM Rietschel, M Propping, P
Citation: S. Cichon et al., Pharmacogenetics of schizophrenia, AM J MED G, 97(1), 2000, pp. 98-106
Investigation of the human serotonin 6 (5-HT6) receptor gene in bipolar affective disorder and schizophrenia
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
Settling the score on hairless - Reply
Authors: Cichon, S Kruse, R Nothen, MM
Citation: S. Cichon et al., Settling the score on hairless - Reply, J INVES DER, 115(4), 2000, pp. 763-764
A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
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
Localization of a gene for syndactyly type 1 to chromosome 2q34-q36
Authors: Bosse, K Betz, RC Lee, YA Wienker, TF Reis, A Kleen, H Propping, P Cichon, S Nothen, MM
Citation: K. Bosse et al., Localization of a gene for syndactyly type 1 to chromosome 2q34-q36, AM J HU GEN, 67(2), 2000, pp. 492-497
A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3
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
Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families
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
Genetic linkage analysis with dyslexia: Evidence for linkage of spelling disability to chromosome 15
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
Chromosome Workshop: Chromosomes 11, 14, and 15
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
Tourette syndrome and the norepinephrine transporter gene: Results of a systematic mutation screening
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
Novel hairless mutations in two kindreds with autosomal recessive papular atrichia
Authors: Kruse, R Cichon, S Anker, M Hillmer, AM Barros-Nunez, P Cantu, JM Leal, E Weinlich, G Schmuth, M Fritsch, P Ruzicka, T Propping, P Nothen, MM
Citation: R. Kruse et al., Novel hairless mutations in two kindreds with autosomal recessive papular atrichia, J INVES DER, 113(6), 1999, pp. 954-959
Risultati: 1-19 |