Works by Heilmann, S.


Results: 18
    1
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    3

    Genome-wide association study of pathological gambling.

    Published in:
    European Psychiatry, 2016, v. 36, p. 38, doi. 10.1016/j.eurpsy.2016.04.001
    By:
    • Lang, M.;
    • Leménager, T.;
    • Streit, F.;
    • Fauth-Bühler, M.;
    • Frank, J.;
    • Juraeva, D.;
    • Witt, S.H.;
    • Degenhardt, F.;
    • Hofmann, A.;
    • Heilmann-Heimbach, S.;
    • Kiefer, F.;
    • Brors, B.;
    • Grabe, H.-J.;
    • John, U.;
    • Bischof, A.;
    • Bischof, G.;
    • Völker, U.;
    • Homuth, G.;
    • Beutel, M.;
    • Lind, P.A.
    Publication type:
    Article
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    8

    Clinical presentation of qualitative olfactory dysfunction.

    Published in:
    European Archives of Oto-Rhino-Laryngology, 2004, v. 261, n. 7, p. 411, doi. 10.1007/s00405-003-0703-y
    By:
    • Frasnelli, J.;
    • Landis, B. N.;
    • Heilmann, S.;
    • Hauswald, B.;
    • Hüttenbrink, K. B.;
    • Lacroix, J. S.;
    • Leopold, D. A.;
    • Hummel, T.
    Publication type:
    Article
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    OPPI BRIEFS: N-ISOHEXYL-N-METHYLAMINE.

    Published in:
    Organic Preparations & Procedures International, 1973, v. 5, n. 4, p. 195, doi. 10.1080/00304947309355566
    By:
    • Wawzonek, S.;
    • Heilmann, S. M.
    Publication type:
    Article
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    Evidence for a polygenic contribution to androgenetic alopecia.

    Published in:
    British Journal of Dermatology, 2013, v. 169, n. 4, p. 927, doi. 10.1111/bjd.12443
    By:
    • 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.
    Publication type:
    Article
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    Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness.

    Published in:
    British Journal of Dermatology, 2011, v. 165, n. 6, p. 1293, doi. 10.1111/j.1365-2133.2011.10708.x
    By:
    • 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.
    Publication type:
    Article
    16
    17

    Contribution of Rare and Potentially Functionally Relevant Sequence Variants in Schizophrenia Risk‐Locus Xq28,distal.

    Published in:
    American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2025, v. 198, n. 3, p. 1, doi. 10.1002/ajmg.b.33011
    By:
    • Claus, I.;
    • Sivalingam, S.;
    • Koller, A. C.;
    • Weiß, A.;
    • Mathey, C. M.;
    • Sindermann, L.;
    • Klein, D.;
    • Henschel, L.;
    • Ludwig, K. U.;
    • Hoffmann, P.;
    • Heimbach, A.;
    • Heilmann‐Heimbach, S.;
    • Vedder, H.;
    • Kammerer‐Ciernioch, J.;
    • Stürmer, T.;
    • Streit, F.;
    • Maaser‐Hecker, A.;
    • Nenadić, I.;
    • Baune, B. T.;
    • Hartmann, A. M.
    Publication type:
    Article
    18

    MiRNA-149 as a Candidate for Facial Clefting and Neural Crest Cell Migration.

    Published in:
    Journal of Dental Research, 2022, v. 101, n. 3, p. 323, doi. 10.1177/00220345211038203
    By:
    • Stüssel, L.G.;
    • Hollstein, R.;
    • Laugsch, M.;
    • Hochfeld, L.M.;
    • Welzenbach, J.;
    • Schröder, J.;
    • Thieme, F.;
    • Ishorst, N.;
    • Romero, R. Olmos;
    • Weinhold, L.;
    • Hess, T.;
    • Gehlen, J.;
    • Mostowska, A.;
    • Heilmann-Heimbach, S.;
    • Mangold, E.;
    • Rada-Iglesias, A.;
    • Knapp, M.;
    • Schaaf, C.P.;
    • Ludwig, K.U.
    Publication type:
    Article