Manuel Mattheisen

  1. 2009
  2. Published

    Genome-wide linkage scan of nonsyndromic orofacial clefting in 91 families of central European origin. / Mangold, Elisabeth; Reutter, Heiko; Birnbaum, Stefanie; Walier, Maja; Mattheisen, Manuel; Henschke, Henning; Lauster, Carola; Schmidt, Gül; Schiefke, Franziska; Reich, Rudolf H; Scheer, Martin; Hemprich, Alexander; Martini, Markus; Braumann, Bert; Krimmel, Michael; Opitz, Charlotte; Lenz, Jan-Hendrik; Kramer, Franz-Josef; Wienker, Thomas F; Nöthen, Markus M; Diaz Lacava, Amalia.

    In: American Journal of Medical Genetics. Part A, Vol. 149A, No. 12, 12.2009, p. 2680-94.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  3. Published

    Supporting evidence for LRRTM1 imprinting effects in schizophrenia. / Ludwig, K U; Mattheisen, Manuel; Mühleisen, T W; Roeske, D; Schmäl, C; Breuer, R; Schulte-Körne, G; Müller-Myhsok, B; Nöthen, M M; Hoffmann, P; Rietschel, M; Cichon, S.

    In: Molecular Psychiatry, Vol. 14, No. 8, 08.2009, p. 743-5.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  4. Published

    A novel locus for arterial hypertension on chromosome 1p36 maps to a metabolic syndrome trait cluster in the Sorbs, a Slavic population isolate in Germany. / Hoffmann, Katrin; Planitz, Christian; Rüschendorf, Franz; Müller-Myhsok, Bertram; Stassen, Hans H; Lucke, Barbara; Mattheisen, Manuel; Stumvoll, Michael; Bochmann, Rolf; Zschornack, Martin; Wienker, Thomas F; Nürnberg, Peter; Reis, André; Luft, Friedrich C; Lindner, Tom H.

    In: Journal of Hypertension, Vol. 27, No. 5, 05.2009, p. 983-90.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  5. 2008
  6. Published

    Inferential testing for linkage with GENEHUNTER-MODSCORE : the impact of the pedigree structure on the null distribution of multipoint MOD scores. / Mattheisen, Manuel; Dietter, Johannes; Knapp, Michael; Baur, Max P; Strauch, Konstantin.

    In: Genetic Epidemiology, Vol. 32, No. 1, 01.2008, p. 73-83.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  7. Published

    Brain-specific tryptophan hydroxylase 2 (TPH2) : a functional Pro206Ser substitution and variation in the 5'-region are associated with bipolar affective disorder. / Cichon, Sven; Winge, Ingeborg; Mattheisen, Manuel; Georgi, Alexander; Karpushova, Anna; Freudenberg, Jan; Freudenberg-Hua, Yun; Babadjanova, Gulia; Van Den Bogaert, Ann; Abramova, Lilia I; Kapiletti, Sofia; Knappskog, Per M; McKinney, Jeffrey; Maier, Wolfgang; Jamra, Rami Abou; Schulze, Thomas G; Schumacher, Johannes; Propping, Peter; Rietschel, Marcella; Haavik, Jan; Nöthen, Markus M.

    In: Human Molecular Genetics, Vol. 17, No. 1, 01.01.2008, p. 87-97.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  8. 2007
  9. Published

    Explorative two-locus linkage analysis suggests a multiplicative interaction between the 7q32 and 16p13 myoclonic seizures-related photosensitivity loci. / Pinto, Dalila; Kasteleijn-Nolst Trenité, Dorothée G A; Cordell, Heather J; Mattheisen, Manuel; Strauch, Konstantin; Lindhout, Dick; Koeleman, Bobby P C.

    In: Genetic Epidemiology, Vol. 31, No. 1, 01.2007, p. 42-50.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  10. Published

    A German genome-wide linkage scan for type 2 diabetes supports the existence of a metabolic syndrome locus on chromosome 1p36.13 and a type 2 diabetes locus on chromosome 16p12.2. / Hoffmann, K; Mattheisen, Manuel; Dahm, S; Nürnberg, P; Roe, C; Johnson, J; Cox, N J; Wichmann, H E; Wienker, T F; Schulze, J; Schwarz, P E; Lindner, T H.

    In: Diabetologia, Vol. 50, No. 7, 07.2007, p. 1418-22.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  11. Published

    Linkage analysis using sex-specific recombination fractions with GENEHUNTER-MODSCORE. / Dietter, Johannes; Mattheisen, Manuel; Fürst, Robert; Rüschendorf, Franz; Wienker, Thomas F; Strauch, Konstantin.

    In: Bioinformatics (Online), Vol. 23, No. 1, 01.01.2007, p. 64-70.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  12. 2005
  13. Published

    Genetic dissection of photosensitivity and its relation to idiopathic generalized epilepsy. / Tauer, Ulrike; Lorenz, Susanne; Lenzen, Kirsten P; Heils, Armin; Muhle, Hiltrud; Gresch, Meike; Neubauer, Bernd A; Waltz, Stephan; Rudolf, Gabrielle; Mattheisen, Manuel; Strauch, Konstantin; Nürnberg, Peter; Schmitz, Bettina; Stephani, Ulrich; Sander, Thomas.

    In: Annals of Neurology, Vol. 57, No. 6, 06.2005, p. 866-73.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  14. Published

    High factor VIII levels in venous thromboembolism show linkage to imprinted loci on chromosomes 5 and 11. / Berger, Mario; Mattheisen, Manuel; Kulle, Bettina; Schmidt, Henriette; Oldenburg, Johannes; Bickeböller, Heike; Walter, Ulrich; Lindner, Tom H; Strauch, Konstantin; Schambeck, Christian M.

    In: Blood, Vol. 105, No. 2, 15.01.2005, p. 638-44.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

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