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Systematic investigation of genetic variability in 111 human genes-implications for studying variable drug response.
Published in:
Pharmacogenomics Journal, 2005, v. 5, n. 3, p. 183, doi. 10.1038/sj.tpj.6500306
By:
- Freudenberg-Hua, Y.;
- Freudenberg, J.;
- Winantea, J.;
- Kluck, N.;
- Cichon, S.;
- Brüss, M.;
- Propping, P.;
- Nöthen, M. M.
Publication type:
Article
Large Deletions in the BRCA1 Gene are not Common in a Set of Familial German Breast Cancer Patients.
Published in:
1999
By:
- Maringa, M.;
- Uhlhaas, S.;
- Kreyer, E.;
- Friedl, W.;
- Propping, P.;
- Schmutzler, R.K.
Publication type:
Abstract
Dopamine D[sub 3] receptor variant and tardive dyskinesia.
Published in:
European Archives of Psychiatry & Clinical Neuroscience, 2000, v. 250, n. 1, p. 31, doi. 10.1007/PL00007536
By:
- Rietschel, M.;
- Krauss, H.;
- Müller, D. J.;
- Schulze, T. G.;
- Knapp, M.;
- Marwinski, K.;
- Maroldt, A. -O.;
- Paus, S.;
- Grünhage, F.;
- Propping, P.;
- Maier, W.;
- Held, T.;
- Nöthen, M. M.
Publication type:
Article
Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder.
Published in:
Molecular Psychiatry, 2012, v. 17, n. 4, p. 421, doi. 10.1038/mp.2011.8
By:
- Priebe, L;
- Degenhardt, F A;
- Herms, S;
- Haenisch, B;
- Mattheisen, M;
- Nieratschker, V;
- Weingarten, M;
- Witt, S;
- Breuer, R;
- Paul, T;
- Alblas, M;
- Moebus, S;
- Lathrop, M;
- Leboyer, M;
- Schreiber, S;
- Grigoroiu-Serbanescu, M;
- Maier, W;
- Propping, P;
- Rietschel, M;
- Nöthen, M M
Publication type:
Article
Two variants in Ankyrin 3 (ANK3) are independent genetic risk factors for bipolar disorder.
Published in:
Molecular Psychiatry, 2009, v. 14, n. 5, p. 487, doi. 10.1038/mp.2008.134
By:
- Schulze, T. G.;
- Detera-Wadleigh, S. D.;
- Akula, N.;
- Gupta, A.;
- Kassem, L.;
- Steele, J.;
- Pearl, J.;
- Strohmaier, J.;
- Breuer, R.;
- Schwarz, M.;
- Propping, P.;
- Nöthen, M. M.;
- Cichon, S.;
- Schumacher, J.;
- Rietschel, M.;
- McMahon, F. J.
Publication type:
Article
Genetic variation of the FAT gene at 4q35 is associated with bipolar affective disorder.
Published in:
Molecular Psychiatry, 2008, v. 13, n. 3, p. 277, doi. 10.1038/sj.mp.4002111
By:
- Abou Jamra, R.;
- Becker, T.;
- Georgi, A.;
- Feulner, T.;
- Schumacher, J.;
- Stromaier, J.;
- Schirmbeck, F.;
- Schulze, T. G.;
- Propping, P.;
- Rietschel, M.;
- Nöthen, M. M.;
- Cichon, S.
Publication type:
Article
A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder.
Published in:
Molecular Psychiatry, 2008, v. 13, n. 2, p. 197, doi. 10.1038/sj.mp.4002012
By:
- Baum, A. E.;
- Akula, N.;
- Cabanero, M.;
- Cardona, I.;
- Corona, W.;
- Klemens, B.;
- Schulze, T. G.;
- Cichon, S.;
- Rietschel, M.;
- Nöthen, M. M.;
- Georgi, A.;
- Schumacher, J.;
- Schwarz, M.;
- Jamra, R. Abou;
- Höfels, S.;
- Propping, P.;
- Satagopan, J.;
- Detera-Wadleigh, S. D.;
- Hardy, J.;
- McMahon, F. J.
Publication type:
Article
Coexisting somatic promoter hypermethylation and pathogenic MLH1 germline mutation in Lynch syndrome.
Published in:
Journal of Pathology, 2008, v. 214, n. 1, p. 10, doi. 10.1002/path.2263
By:
- Rahner, N;
- Friedrichs, N;
- Steinke, V;
- Aretz, S;
- Friedl, W;
- Buettner, R;
- Mangold, E;
- Propping, P;
- Walldorf, C
Publication type:
Article
Low platelet MAO activity and schizophrenia: sex differences.
Published in:
Acta Psychiatrica Scandinavica, 1981, v. 64, n. 2, p. 167, doi. 10.1111/j.1600-0447.1981.tb00771.x
By:
- Gattaz, W. F.;
- Kasper, S.;
- Propping, P.;
- Friedl, W.;
- Beckmann, H.
Publication type:
Article
Genetic Variation in Human 5-HT Receptors: Potential Pathogenetic and Pharmacological Role<sup>a</sup>.
Published in:
Annals of the New York Academy of Sciences, 1998, v. 861, n. 1, p. 26, doi. 10.1111/j.1749-6632.1998.tb10169.x
By:
- GÖTHERT, M.;
- PROPPING, P.;
- BÖNISCH, H.;
- BRÜSS, M.;
- NÖTHEN, M. M.
Publication type:
Article
Plasma DBH, Platelet MAO and Proteins of Red Blood Cell Membranes in Individuals with Variants of the Normal EEG.
Published in:
Neuropsychobiology, 1979, v. 5, n. 6, p. 309, doi. 10.1159/000117696
By:
- Propping, P.;
- Friedl, W.;
- Nebel, B.;
- Feige, A.
Publication type:
Article
Erblich bedingte gastrointestinale Tumorerkrankungen.
Published in:
Der Internist, 1999, v. 40, n. 5, p. 502, doi. 10.1007/s001080050364
By:
- Jungck, M.;
- Friedl, W.;
- Propping, P.
Publication type:
Article
Interrelationship and Familiality of Dyslexia Related Quantitative Measures.
Published in:
Annals of Human Genetics, 2007, v. 71, n. 2, p. 160, doi. 10.1111/j.1469-1809.2006.00312.x
By:
- Schulte-Körne, G.;
- Ziegler, A.;
- Deimel, W.;
- Schumacher, J.;
- Plume, E.;
- Bachmann, C.;
- Kleensang, A.;
- Propping, P.;
- Nöthen, M. M.;
- Warnke, A.;
- Remschmidt, H.;
- König, I. R.
Publication type:
Article
Prodynorphin gene promotor polymorphism and temporal lobe epilepsy.
Published in:
2003
By:
- Tilgen N;
- Rebstock J;
- Horvath S;
- Propping P;
- Elger CE;
- Heils A;
- Stögmann E;
- Baumgartner C;
- Zimprich F
Publication type:
Journal Article
Frequency of Hereditary Non-Polyposis Colorectal Cancer among Unselected Patients with Colorectal Cancer in Germany.
Published in:
Digestion, 2006, v. 74, n. 1, p. 58, doi. 10.1159/000096868
By:
- Lamberti, C.;
- Mangold, E.;
- Pagenstecher, C.;
- Jungck, M.;
- Schwering, D.;
- Bollman, M.;
- Vogel, J.;
- Kindermann, D.;
- Nikorowitsch, R.;
- Friedrichs, N.;
- Schneider, B.;
- Houshdaran, F.;
- Schmidt-Wolf, I. G. H.;
- Friedl, W.;
- Propping, P.;
- Sauerbruch, T.;
- Büttner, R.;
- Matthiak, M.
Publication type:
Article
An association study of a neurotrophic3 (NT-3) gene polymorphism with schizophrenia.
Published in:
Acta Psychiatrica Scandinavica, 1995, v. 92, n. 6, p. 425, doi. 10.1111/j.1600-0447.1995.tb09607.x
By:
- Dawson, E.;
- Powell, J. F.;
- Sham, P. C.;
- Nöthen, M.;
- Crocq, M.-A.;
- Propping, P.;
- Körner, J.;
- Rietschel, M.;
- Os, J.;
- Wright, P.;
- Murray, R. M.;
- Gill, M.
Publication type:
Article
Clinical evidence for genomic imprinting in bipolar I disorder.
Published in:
Acta Psychiatrica Scandinavica, 1995, v. 92, n. 5, p. 365, doi. 10.1111/j.1600-0447.1995.tb09598.x
By:
- Grigoroiu-Serbanescu, M.;
- Nothen, M.;
- Propping, P.;
- Poustka, F.;
- Magureanu, S.;
- Vasilescu, R.;
- Marinescu, E.;
- Ardelean, V.
Publication type:
Article
A similarity-based method for genome-wide prediction of disease-relevant human genes.
Published in:
Bioinformatics, 2002, v. 18, p. S110, doi. 10.1093/bioinformatics/18.suppl_2.S110
By:
- Freudenberg, J.;
- Propping, P.
Publication type:
Article
Muir-Torre syndrome: clinical features and molecular genetic analysis.
Published in:
British Journal of Dermatology, 1997, v. 136, n. 6, p. 913, doi. 10.1111/j.1365-2133.1997.tb03933.x
By:
- Esche, C.;
- Kruse, R.;
- Lamberti, C.;
- Friedl, W.;
- Propping, P.;
- Lehmann, P.;
- Ruzicka, T.
Publication type:
Article
Die genetische Revolution.
Published in:
Der Internist, 2004, v. 45, n. 1, p. S6, doi. 10.1007/s00108-004-1218-3
By:
- Propping, P.;
- Aretz, S.
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
Genetic linkage analysis with dyslexia: evidence for linkage of spelling disability to chromosome 15.
Published in:
1999
By:
- Nöthen MM;
- Schulte-Körne G;
- Grimm T;
- Cichon S;
- Vogt IR;
- Müller-Myhsok B;
- Propping P;
- Remschmidt H
Publication type:
Journal Article
A family-based and case–control association study of trace amine receptor genes on chromosome 6q23 in bipolar affective disorder.
Published in:
2005
By:
- Jamra, R. Abou;
- Sircar, I.;
- Becker, T.;
- Freudenberg-Hua, Y.;
- Ohlraun, S.;
- Freudenberg, J.;
- Brockschmidt, F.;
- Schulze, T. G.;
- Gross, M.;
- Spira, F.;
- Deschner, M.;
- Schmäl, C.;
- Maier, W.;
- Propping, P.;
- Rietschel, M.;
- Cichon, S.;
- Nöthen, M. M.;
- Schumacher, J.
Publication type:
Letter
Investigation of the DAOA/G30 locus in panic disorder.
Published in:
Molecular Psychiatry, 2005, v. 10, n. 5, p. 428, doi. 10.1038/sj.mp.4001598
By:
- Schumacher, J.;
- Jamra, R. Abou;
- Becker, T.;
- Klopp, N.;
- Franke, P.;
- Jacob, C.;
- Sand, P.;
- Fritze, J.;
- Ohlraun, S.;
- Schulze, T. G.;
- Rietschel, M.;
- Illig, T.;
- Propping, P.;
- Cichon, S.;
- Deckert, J.;
- Nöthen, M. M.
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
No association between dopamine D4 receptor gene variants and Novelty Seeking.
Published in:
Molecular Psychiatry, 2002, v. 7, n. 1, p. 18
By:
- Johnson, E.G.;
- Ivo, R.;
- Gustavsson, J.P.;
- Geijer, T.;
- Forslund, K.;
- Mattila-Evenden, M.;
- Rylander, G.;
- Cichon, S.;
- Propping, P.;
- Bergman, H.;
- Asberg, M.;
- Nothen, M.M.
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
Description of the Genetic Analysis Workshop 10 bipolar disorder linkage data sets.
Published in:
Genetic Epidemiology, 1997, v. 14, n. 6, p. 563, doi. 10.1002/(SICI)1098-2272(1997)14:6<563::AID-GEPI2>3.0.CO;2-0
By:
- Goldin, L.R.;
- Gershon, E.S.;
- Berrettini, W.H.;
- Stine, O.C.;
- DePaulo, R.;
- McMahon, F.;
- Meyers, D.;
- Nothen, M.;
- Propping, P.;
- Cichon, S.;
- Fimmers, R.;
- Baur, M.;
- Albus, M.;
- Franzek, E.;
- Kreiner, R.;
- Maier, W.;
- Rietschel, M.;
- Baron, M.;
- Knowles, J.;
- Gilliam, C.
Publication type:
Article
MSH6 mutation in Muir-Torre syndrome: could this be a rare finding?
Published in:
British Journal of Dermatology, 2007, v. 156, n. 1, p. 158, doi. 10.1111/j.1365-2133.2006.07607.x
By:
- Mangold, E.;
- Rahner, N.;
- Friedrichs, N.;
- Buettner, R.;
- Pagenstecher, C.;
- Aretz, S.;
- Friedl, W.;
- Ruzicka, T.;
- Propping, P.;
- Rütten, A.;
- Kruse, R.
Publication type:
Article
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
Ziele und Grenzen der Quantifizierung genetischer Risiken.
Published in:
Medizinische Genetik, 2011, v. 23, n. 3, p. 385, doi. 10.1007/s11825-011-0296-6
By:
- Cremer, T.;
- Propping, P.
Publication type:
Article
Wechsel in der Schriftleitung.
Published in:
Medizinische Genetik, 2007, v. 19, n. 4, p. 389, doi. 10.1007/s11825-007-0065-8
By:
- Propping, P.
Publication type:
Article
Daten zur Geschichte der Deutschen Gesellschaft für Humangenetik.
Published in:
Medizinische Genetik, 2007, v. 19, n. 1, p. 18, doi. 10.1007/s11825-006-0002-2
By:
- Propping, P.
Publication type:
Article
Familiärer Darmkrebs.
Published in:
Medizinische Genetik, 2007, v. 19, n. 2, p. 216, doi. 10.1007/s11825-007-0015-5
By:
- Friedl, W.;
- Propping, P.
Publication type:
Article
Das goldene Zeitalter der Humangenetik geht weiter.
Published in:
Medizinische Genetik, 2007, v. 19, n. 1, p. 3, doi. 10.1007/s11825-007-0004-8
By:
- Propping, P.
Publication type:
Article
Linkage analyses of chromosomal region 18p11-q12 in dyslexia.
Published in:
Journal of Neural Transmission, 2006, v. 113, n. 3, p. 417, doi. 10.1007/s00702-005-0336-y
By:
- Schumacher, J.;
- König, I. R.;
- Plume, E.;
- Propping, P.;
- Warnke, A.;
- Manthey, M.;
- Duell, M.;
- Kleensang, A.;
- Repsilber, D.;
- Preis, M.;
- Remschmidt, H.;
- Ziegler, A.;
- Nöthen, M. M.;
- Schulte-Körne, G.
Publication type:
Article

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