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No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopecia

Heilmann, S. ; Nyholt, D. R. ; Brockschmidt, F. F. ; Hillmer, A. M. ; Herold, C. ; Becker, T. ; Martin, N. G. ; Nöthen, M. M.

British Journal of Dermatology, July 2013, Vol.169(1), pp.222-224 [Peer Reviewed Journal]

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Schizophrenia: genetic tools for unraveling the nature of a complex disorder

Propping, P ; Nöthen, M M

Proceedings of the National Academy of Sciences of the United States of America, 15 August 1995, Vol.92(17), pp.7607-8 [Peer Reviewed Journal]

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Fine mapping of the human AR/EDA2R locus in androgenetic alopecia

Brockschmidt, F. F. ; Hillmer, A. M. ; Eigelshoven, S. ; Hanneken, S. ; Heilmann, S. ; Barth, S. ; Herold, C. ; Becker, T. ; Kruse, R. ; Nöthen, M. M.

British Journal of Dermatology, April 2010, Vol.162(4), pp.899-903 [Peer Reviewed Journal]

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First report of a FXII gene mutation in a Brazilian family with hereditary angio‐oedema with normal C1 inhibitor

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.

British Journal of Dermatology, October 2015, Vol.173(4), pp.1102-1104 [Peer Reviewed Journal]

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Functional analysis of splice site mutations in the human hairless (HR) gene using a minigene assay

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.

British Journal of Dermatology, November 2011, Vol.165(5), pp.1127-1132 [Peer Reviewed Journal]

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Investigation of variants of the aromatase gene (CYP19A1) in female pattern hair loss

Redler, S. ; Birch, M. P. ; Drichel, D. ; Dobson, K. ; Brockschmidt, F. F. ; Tazi‐Ahnini, R. ; Giehl, K. A. ; Kluck, N. ; Kruse, R. ; Lutz, G. ; Wolff, H. ; Becker, T. ; Nöthen, M. M. ; Messenger, A. G. ; Betz, R. C.

British Journal of Dermatology, September 2011, Vol.165(3), pp.703-705 [Peer Reviewed Journal]

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Evidence for a polygenic contribution to androgenetic alopecia

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.

British Journal of Dermatology, October 2013, Vol.169(4), pp.927-930 [Peer Reviewed Journal]

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Investigation of selected cytokine genes suggests that IL2RA and the TNF / LTA locus are risk factors for severe alopecia areata

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.

British Journal of Dermatology, December 2012, Vol.167(6), pp.1360-1365 [Peer Reviewed Journal]

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Investigation of the male pattern baldness major genetic susceptibility loci AR / EDA2R and 20p11 in female pattern hair loss

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.

British Journal of Dermatology, June 2012, Vol.166(6), pp.1314-1318 [Peer Reviewed Journal]

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Systematic mutation screening of KRT5 supports the hypothesis that Galli–Galli disease is a variant of Dowling–Degos disease

Hanneken, S. ; Rütten, A. ; Pasternack, S. M. ; Eigelshoven, S. ; El Shabrawi‐Caelen, L. ; Wenzel, J. ; Braun‐Falco, M. ; Ruzicka, T. ; Nöthen, M. M. ; Kruse, R. ; Betz, R. C.

British Journal of Dermatology, July 2010, Vol.163(1), pp.197-200 [Peer Reviewed Journal]

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The TRAF1/C5 locus confers risk for familial and severe alopecia areata

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.

British Journal of Dermatology, April 2010, Vol.162(4), pp.866-869 [Peer Reviewed Journal]

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Rare SHANK2 variants in schizophrenia

Peykov, S ; Berkel, S ; Degenhardt, F ; Rietschel, M ; Nöthen, M M ; Rappold, G A

Molecular psychiatry, December 2015, Vol.20(12), pp.1487-8 [Peer Reviewed Journal]

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Arzneimittelassoziierte Angioödeme
Drug-induced angioedema

Sachs, B. ; Meier, T. ; Nöthen, M. ; Stieber, C. ; Stingl, J.

Der Hautarzt, 2018, Vol.69(4), pp.298-305 [Peer Reviewed Journal]

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Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male‐pattern baldness

Brockschmidt, F. F. ; Heilmann, S. ; Ellis, J. A. ; Eigelshoven, S. ; Hanneken, S. ; Herold, C. ; Moebus, S. ; Alblas, M. A. ; Lippke, B. ; Kluck, N. ; Priebe, L. ; Degenhardt, F. A. ; Jamra, R. A. ; Meesters, C. ; Jöckel, K. ‐H. ; Erbel, R. ; Harrap, S. ; Schumacher, J. ; Fröhlich, H. ; Kruse, R. ; Hillmer, A. M. ; Becker, T. ; Nöthen, M. M.

British Journal of Dermatology, December 2011, Vol.165(6), pp.1293-1302 [Peer Reviewed Journal]

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15
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The oestrogen receptor 2 ( ESR 2 ) gene in female‐pattern hair loss: replication of association with rs10137185 in German patients

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. ; Messenger, A. G. ; Betz, R. C.

British Journal of Dermatology, April 2014, Vol.170(4), pp.982-985 [Peer Reviewed Journal]

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16
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A novel KRT86 mutation in a Turkish family with monilethrix, and identification of maternal mosaicism

Redler, S. ; Pasternack, S. M. ; Wolf, S. ; Stienen, D. ; Wenzel, J. ; Nöthen, M. M. ; Betz, R. C.

Clinical and Experimental Dermatology, October 2015, Vol.40(7), pp.781-785 [Peer Reviewed Journal]

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17
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Human complement component C8. Molecular basis of the beta-chain polymorphism

Dewald, G ; Hemmer, S ; Nöthen, M M

FEBS letters, 07 March 1994, Vol.340(3), pp.211-5 [Peer Reviewed Journal]

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18
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Caspase recruitment domain 15 gene haplotypes in sarcoidosis

Pabst, S ; Golebiewski, M ; Herms, S ; Karpushova, A ; Díaz-Lacava, A ; Walier, M ; Zimmer, S ; Cichon, S ; Wienker, T F ; Nöthen, M M ; Nickenig, G ; Meyer, R ; Skowasch, D ; Grohé, C

Tissue antigens, April 2011, Vol.77(4), pp.333-7 [Peer Reviewed Journal]

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Etiopathological aspects of achalasia: lessons learned with Hirschsprung's disease

Gockel, H. R. ; Gockel, I. ; Schimanski, C. C. ; Schier, F. ; Schumacher, J. ; Nöthen, M. M. ; Lang, H. ; Müller, M. ; Eckardt, A. J. ; Eckardt, V. F.

Diseases of the Esophagus, August 2012, Vol.25(6), pp.566-572 [Peer Reviewed Journal]

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20
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Homozygosity for a factor XII mutation in one female and one male patient with hereditary angio‐oedema

Grumach, A. S. ; Stieber, C. ; Veronez, C. L. ; Cagini, N. ; Constantino‐Silva, R. N. ; Cordeiro, E. ; Nöthen, M. M. ; Pesquero, J. B. ; Cichon, S.

Allergy, January 2016, Vol.71(1), pp.119-123 [Peer Reviewed Journal]

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21
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Effects of a genome-wide supported psychosis risk variant on neural activation during a theory-of-mind task

Walter, H ; Schnell, K ; Erk, S ; Arnold, C ; Kirsch, P ; Esslinger, C ; Mier, D ; Schmitgen, M M ; Rietschel, M ; Witt, S H ; Nöthen, M M ; Cichon, S ; Meyer-Lindenberg, A

Molecular psychiatry, April 2011, Vol.16(4), pp.462-70 [Peer Reviewed Journal]

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22
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Identifying bipolar disorder susceptibility loci in a densely affected pedigree

Collins, A L ; Kim, Y ; Szatkiewicz, J P ; Bloom, R J ; Hilliard, C E ; Quackenbush, C R ; Meier, S ; Rivas, F ; Mayoral, F ; Cichon, S ; Nöthen, M M ; Rietschel, M ; Sullivan, P F

Molecular psychiatry, December 2013, Vol.18(12), pp.1245-6 [Peer Reviewed Journal]

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23
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Identification of increased genetic risk scores for schizophrenia in treatment-resistant patients

Frank, J ; Lang, M ; Witt, S H ; Strohmaier, J ; Rujescu, D ; Cichon, S ; Degenhardt, F ; Nöthen, M M ; Collier, D A ; Ripke, S ; Naber, D ; Rietschel, M

Molecular psychiatry, July 2015, Vol.20(7), pp.913 [Peer Reviewed Journal]

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24
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Independent evidence for the selective influence of GABA(A) receptors on one component of the bipolar disorder phenotype

Breuer, R ; Hamshere, M L ; Strohmaier, J ; Mattheisen, M ; Degenhardt, F ; Meier, S ; Paul, T ; O'Donovan, M C ; Mühleisen, T W ; Schulze, T G ; Nöthen, M M ; Cichon, S ; Craddock, N ; Rietschel, M

Molecular psychiatry, June 2011, Vol.16(6), pp.587-9 [Peer Reviewed Journal]

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25
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First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children

Roeske, D ; Ludwig, K U ; Neuhoff, N ; Becker, J ; Bartling, J ; Bruder, J ; Brockschmidt, F F ; Warnke, A ; Remschmidt, H ; Hoffmann, P ; Müller-Myhsok, B ; Nöthen, M M ; Schulte-Körne, G

Molecular psychiatry, January 2011, Vol.16(1), pp.97-107 [Peer Reviewed Journal]

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Genetic risk for schizophrenia impacts Theory-of-Mind-related brain activation

Walter, H ; Schnell, K ; Erk, S ; Arnold, C ; Kirsch, P ; Esslinger, C ; Mier, D ; Schmitgen, M M ; Rietschel, M ; Witt, S H ; Noethen, M M ; Cichon, S ; Meyer-Lindenberg, A

Molecular psychiatry, April 2011, Vol.16(4), pp.353 [Peer Reviewed Journal]

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27
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Evidence for the involvement of ZNF804A in cognitive processes of relevance to reading and spelling

Becker, J ; Czamara, D ; Hoffmann, P ; Landerl, K ; Blomert, L ; Brandeis, D ; Vaessen, A ; Maurer, U ; Moll, K ; Ludwig, K U ; Müller-Myhsok, B ; Nöthen, M M ; Schulte-Körne, G ; Schumacher, J

Translational psychiatry, 10 July 2012, Vol.2, pp.e136 [Peer Reviewed Journal]

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28
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Immunoglobulin light-chain amyloidosis shares genetic susceptibility with multiple myeloma

Weinhold, N ; Försti, A ; Da Silva Filho, M I ; Nickel, J ; Campo, C ; Hoffmann, P ; Nöthen, M M ; Hose, D ; Goldschmidt, H ; Jauch, A ; Langer, C ; Hegenbart, U ; Schönland, S O ; Hemminki, K

Leukemia, November 2014, Vol.28(11), pp.2254-6 [Peer Reviewed Journal]

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29
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Functional impact of a recently identified quantitative trait locus for hippocampal volume with genome-wide support

Erk, S ; Meyer-Lindenberg, A ; Schmierer, P ; Grimm, O ; Tost, H ; Mühleisen, T ; Mattheisen, M ; Seiferth, N ; Cichon, S ; Rietschel, M ; Nöthen, M M ; Heinz, A ; Walter, H

Translational psychiatry, 23 July 2013, Vol.3, pp.e287 [Peer Reviewed Journal]

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30
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Identification of increased genetic risk scores for schizophrenia in treatment-resistant patients

Frank, J ; Lang, M ; Witt, S H ; Strohmaier, J ; Rujescu, D ; Cichon, S ; Degenhardt, F ; Nöthen, M M ; Collier, D A ; Ripke, S ; Naber, D ; Rietschel, M

Molecular psychiatry, February 2015, Vol.20(2), pp.150-1 [Peer Reviewed Journal]

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31
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Replication of association between a SLITRK1 haplotype and Tourette Syndrome in a large sample of families

Karagiannidis, I ; Rizzo, R ; Tarnok, Z ; Wolanczyk, T ; Hebebrand, J ; Nöthen, M M ; Lehmkuhl, G ; Farkas, L ; Nagy, P ; Barta, C ; Szymanska, U ; Panteloglou, G ; Miranda, D M ; Feng, Y ; Sandor, P ; Barr, C ; Paschou, P

Molecular psychiatry, July 2012, Vol.17(7), pp.665-8 [Peer Reviewed Journal]

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32
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Identification and functional characterization of rare SHANK2 variants in schizophrenia

Peykov, S ; Berkel, S ; Schoen, M ; Weiss, K ; Degenhardt, F ; Strohmaier, J ; Weiss, B ; Proepper, C ; Schratt, G ; Nöthen, M M ; Boeckers, T M ; Rietschel, M ; Rappold, G A

Molecular psychiatry, December 2015, Vol.20(12), pp.1489-98 [Peer Reviewed Journal]

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33
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Genetic Variation in Human 5‐HT Receptors: Potential Pathogenetic and Pharmacological Role a

Göthert, M. ; Propping, P. ; Bönisch, H. ; Brüss, M. ; Nöthen, M. M.

Annals of the New York Academy of Sciences, December 1998, Vol.861(1), pp.26-30 [Peer Reviewed Journal]

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Genetic variation in human 5-HT receptors: potential pathogenetic and pharmacological role

Göthert, M ; Propping, P ; Bönisch, H ; Brüss, M ; Nöthen, M M

Annals of the New York Academy of Sciences, 15 December 1998, Vol.861, pp.26-30 [Peer Reviewed Journal]

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35
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Replication of Functional Serotonin Receptor Type 3A and B Variants in Bipolar Affective Disorder: A European Multicenter Study

Hammer, C ; Cichon, S ; Mühleisen, T W ; Haenisch, B ; Degenhardt, F ; Breuer, R ; Witt, S H ; Strohmaier, J ; Oruc, L ; Rivas, F ; Babadjanova, G ; Grigoroiu-Serbanescu, M ; Röth, R ; Rappold, G ; Rietschel, M ; Nöthen, M M ; Niesler, B ; Mattheisen, Manuel ; Hauser, J

Hammer, C, S Cichon, T W Mühleisen, B Haenisch, F Degenhardt, M Mattheisen, R Breuer, et al. 2012. Replication of functional serotonin receptor type 3A and B variants in bipolar affective disorder: A European Multicenter Study. Translational Psychiatry 2(4): e103. [Peer Reviewed Journal]

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36
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Distribution of a novel mutation in the first exon of the human dopamine D4 receptor gene in psychotic patients

Catalano, M ; Nobile, M ; Novelli, E ; Nöthen, M M ; Smeraldi, E

Biological psychiatry, 01 October 1993, Vol.34(7), pp.459-64 [Peer Reviewed Journal]

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Single-strand conformation analysis (SSCA) of the dopamine D1 receptor gene (DRD1) reveals no significant mutation in patients with schizophrenia and manic depression

Cichon, S ; Nöthen, M M ; Rietschel, M ; Körner, J ; Propping, P

Biological psychiatry, 15 December 1994, Vol.36(12), pp.850-3 [Peer Reviewed Journal]

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38