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Results: 1-23 |
Results: 23
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
Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle inrippling muscle disease
Authors: Betz, RC Schoser, BGH Kasper, D Ricker, K Ramirez, A Stein, V Torbergsen, T Lee, YA Nothen, MM Wienker, TF Malin, JP Propping, P Reis, A Mortier, W Jentsch, TJ Vorgerd, M Kubisch, C
Citation: Rc. Betz et al., Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle inrippling muscle disease, NAT GENET, 28(3), 2001, pp. 218-219
Linkage analysis of asthma and atopy including models with genomic imprinting
Authors: Strauch, K Bogdanow, M Fimmers, R Baur, MP Wienker, TF
Citation: K. Strauch et al., Linkage analysis of asthma and atopy including models with genomic imprinting, GENET EPID, 21, 2001, pp. S204-S209
Assignment of PGL3 to chromosome 1 (q21-q23) in a family with autosomal dominant non-chromaffin paraganglioma
Authors: Niemann, S Becker-Follmann, J Nurnberg, G Ruschendorf, F Sieweke, N Hugens-Penzel, M Traupe, H Wienker, TF Reis, A Muller, U
Citation: S. Niemann et al., Assignment of PGL3 to chromosome 1 (q21-q23) in a family with autosomal dominant non-chromaffin paraganglioma, AM J MED G, 98(1), 2001, pp. 32-36
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
Genome search for susceptibility loci of common idiopathic generalised epilepsies
Authors: Sander, T Schulz, H Saar, K Gennaro, E Riggio, MC Bianchi, A Zara, F Luna, D Bulteau, C Kaminska, A Ville, D Cieuta, C Picard, F Prud'homme, JF Bate, L Sundquist, A Gardiner, RM Janssen, GAMAJ de Haan, GJ Kasteleijn-Nolst-Trenite, DGA Bader, A Lindhout, D Riess, O Wienker, TF Janz, D Reis, A
Citation: T. Sander et al., Genome search for susceptibility loci of common idiopathic generalised epilepsies, HUM MOL GEN, 9(10), 2000, pp. 1465-1472
hKCNN3 which maps to chromosome 1q21 is not the causative gene in periodiccatatonia, a familial subtype of schizophrenia
Authors: Stober, G Meyer, J Nanda, I Wienker, TF Saar, K Jatzke, S Schmid, M Lesch, KP Beckmann, H
Citation: G. Stober et al., hKCNN3 which maps to chromosome 1q21 is not the causative gene in periodiccatatonia, a familial subtype of schizophrenia, EUR ARCH PS, 250(4), 2000, pp. 163-168
Linkage and family-based association study of schizophrenia and the synapsin III locus that maps to chromosome 22q13
Authors: Stober, G Meyer, J Nanda, I Wienker, TF Saar, K Knapp, M Jatzke, S Schmid, M Lesch, KP Beckmann, H
Citation: G. Stober et al., Linkage and family-based association study of schizophrenia and the synapsin III locus that maps to chromosome 22q13, AM J MED G, 96(3), 2000, pp. 392-397
ADULT syndrome allelic to limb mammary syndrome (LMS)?
Authors: Propping, P Friedl, W Wienker, TF Uhlhaas, S Zerres, K
Citation: P. Propping et al., ADULT syndrome allelic to limb mammary syndrome (LMS)?, AM J MED G, 90(2), 2000, pp. 179-182
Pharmacogenetics of clozapine response
Authors: Schumacher, J Schulze, TG Wienker, TF Rietschel, M Nothen, MM
Citation: J. Schumacher et al., Pharmacogenetics of clozapine response, LANCET, 356(9228), 2000, pp. 506-507
A European study on the genetics of mite sensitization
Authors: Kurz, T Strauch, K Heinzmann, A Braun, S Jung, M Ruschendorf, F Moffatt, MF Cookson, WOCM Inacio, F Ruffilli, A Nordskov-Hansen, G Peltre, G Forster, J Kuehr, J Reis, A Wienker, TF Deichmann, KA
Citation: T. Kurz et al., A European study on the genetics of mite sensitization, J ALLERG CL, 106(5), 2000, pp. 925-932
Splitting schizophrenia: Periodic catatonia-susceptibility locus on chromosome 15q15
Authors: Stober, G Saar, K Ruschendorf, F Meyer, J Nurnberg, G Jatzke, S Franzek, E Reis, A Lesch, KP Wienker, TF Beckmann, H
Citation: G. Stober et al., Splitting schizophrenia: Periodic catatonia-susceptibility locus on chromosome 15q15, AM J HU GEN, 67(5), 2000, pp. 1201-1207
Genomewide scan in German families reveals evidence for a novel psoriasis-susceptibility locus on chromosome 19p13
Authors: Lee, YA Ruschendorf, F Windemuth, C Schmitt-Egenolf, M Stadelmann, A Nurnberg, G Stander, M Wienker, TF Reis, A Traupe, H
Citation: Ya. Lee et al., Genomewide scan in German families reveals evidence for a novel psoriasis-susceptibility locus on chromosome 19p13, AM J HU GEN, 67(4), 2000, pp. 1020-1024
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
Parametric and nonparametric multipoint linkage analysis with imprinting and two-locus-trait models: Application to mite sensitization
Authors: Strauch, K Fimmers, R Kurz, T Deichmann, KA Wienker, TF Baur, MP
Citation: K. Strauch et al., Parametric and nonparametric multipoint linkage analysis with imprinting and two-locus-trait models: Application to mite sensitization, AM J HU GEN, 66(6), 2000, pp. 1945-1957
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
Linkage analysis with adequate modeling of a parent-of-origin effect
Authors: Strauch, K Fimmers, R Windemuth, C Hahn, A Wienker, TF Baur, MP
Citation: K. Strauch et al., Linkage analysis with adequate modeling of a parent-of-origin effect, GENET EPID, 17, 1999, pp. S331-S336
Linkage analysis in alcohol dependence
Authors: Windemuth, C Hahn, A Strauch, K Baur, MP Wienker, TF
Citation: C. Windemuth et al., Linkage analysis in alcohol dependence, GENET EPID, 17, 1999, pp. S403-S407
Evaluation of a putative major susceptibility locus for juvenile myoclonicepilepsy on chromosome 15q14
Authors: Sander, T Schulz, H Vieira-Saeker, AMM Bianchi, AM Sailer, U Bauer, G Scaramelli, A Wienker, TF Saar, K Reis, A Janz, D Epplen, JT Riess, O
Citation: T. Sander et al., Evaluation of a putative major susceptibility locus for juvenile myoclonicepilepsy on chromosome 15q14, AM J MED G, 88(2), 1999, pp. 182-187
Promoter polymorphism at -238 of the tumor necrosis factor alpha gene is not associated with early onset psoriasis when tested by the transmission disequilibrium test
Authors: Jacob, N Ruschendorf, F Schmitt-Egenolf, M Hennies, HC Friedl, G Stander, M Wienker, TF Reis, A Traupe, H
Citation: N. Jacob et al., Promoter polymorphism at -238 of the tumor necrosis factor alpha gene is not associated with early onset psoriasis when tested by the transmission disequilibrium test, J INVES DER, 112(4), 1999, pp. 514-515
Diaphragmatic spinal muscular atrophy with respiratory distress is heterogeneous, and one form is linked to chromosome 11q13-q21
Authors: Grohmann, K Wienker, TF Saar, K Rudnik-Schoneborn, S Stoltenburg-Didinger, G Rossi, R Novelli, G Nurnberg, G Pfeufer, A Wirth, B Reis, A Zerres, K Hubner, C
Citation: K. Grohmann et al., Diaphragmatic spinal muscular atrophy with respiratory distress is heterogeneous, and one form is linked to chromosome 11q13-q21, AM J HU GEN, 65(5), 1999, pp. 1459-1462
Investigation of a family with autosomal dominant dilated cardiomyopathy defines a novel locus on chromosome 2q14-q22
Authors: Jung, M Poepping, I Perrot, A Ellmer, AE Wienker, TF Dietz, R Reis, A Osterziel, KJ
Citation: M. Jung et al., Investigation of a family with autosomal dominant dilated cardiomyopathy defines a novel locus on chromosome 2q14-q22, AM J HU GEN, 65(4), 1999, pp. 1068-1077
Limb mammary syndrome: A new genetic disorder with mammary hypoplasia, ectrodactyly, and other hand/foot anomalies maps to human chromosome 3q27
Authors: van Bokhoven, H Jung, M Smits, APT van Beersum, S Ruschendorf, F van Steensel, M Veenstra, M Tuerlings, JHAM Mariman, ECM Brunner, HG Wienker, TF Reis, A Ropers, HH Hamel, BCJ
Citation: H. Van Bokhoven et al., Limb mammary syndrome: A new genetic disorder with mammary hypoplasia, ectrodactyly, and other hand/foot anomalies maps to human chromosome 3q27, AM J HU GEN, 64(2), 1999, pp. 538-546
Risultati: 1-23 |