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Angiotensin-converting enzyme (ACE) gene polymorphisms and familial occurrence of sarcoidosis.
Published in:
2001
By:
- Schürmann, M.;
- Reichel, P.;
- Müller-Myhsok, B.;
- Dieringer, T.;
- Wurm, K.;
- Schlaak, M.;
- Müller-Quernheim, J.;
- Schwinger, E.;
- Schürmann, M;
- Müller-Myhsok, B;
- Müller-Quernheim, J
Publication type:
journal article
Is there relatedness between maternal lines of Type 1 diabetic patients?
Published in:
Diabetologia, 2003, v. 46, n. 3, p. 441, doi. 10.1007/s00125-003-1048-1
By:
- Klöting, I.;
- Poetsch, M.;
- Müller-Myhsok, B.;
- Rjasanowski, I.;
- Kerner, W.;
- Klöting, N.
Publication type:
Article
Single-nucleotide polymorphisms in HLA- and non-HLA genes associated with the development of antibodies to interferon-β therapy in multiple sclerosis patients.
Published in:
Pharmacogenomics Journal, 2012, v. 12, n. 3, p. 238, doi. 10.1038/tpj.2011.14
By:
- Weber, F;
- Cepok, S;
- Wolf, C;
- Berthele, A;
- Uhr, M;
- Bettecken, Th;
- Buck, D;
- Hartung, H P;
- Holsboer, F;
- Müller-Myhsok, B;
- Hemmer, B
Publication type:
Article
Genetic Relationship Between Depression and Body Mass Index.
Published in:
European Psychiatry, 2015, v. 30, p. 710, doi. 10.1016/S0924-9338(15)30560-5
By:
- Rivera, M.;
- Locke, A.E.;
- Corre, T.;
- Czamara, D.;
- Wolf, C.;
- Ching-Lopez, A.;
- Milaneschi, Y.;
- Kloiber, S.;
- Boomsma, D.I.;
- Müller-Myhsok, B.;
- Penninx, B.W.J.H.;
- Preisig, M.;
- Farmer, A.E.;
- Lewis, C.M.;
- Breen, G.;
- McGuffin, P.
Publication type:
Article
Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation.
Published in:
Cephalalgia, 2008, v. 28, n. 4, p. 403, doi. 10.1111/j.1468-2982.2008.01540.x
By:
- Freilinger, T.;
- Bohe, M.;
- Wegener, B.;
- Müller-Myhsok, B.;
- Dichgans, M.;
- Knoblauch, H.
Publication type:
Article
Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility.
Published in:
Molecular Psychiatry, 2014, v. 19, n. 4, p. 527, doi. 10.1038/mp.2013.73
By:
- Li, M;
- Luo, X-j;
- Rietschel, M;
- Lewis, C M;
- Mattheisen, M;
- Müller-Myhsok, B;
- Jamain, S;
- Leboyer, M;
- Landén, M;
- Thompson, P M;
- Cichon, S;
- Nöthen, M M;
- Schulze, T G;
- Sullivan, P F;
- Bergen, S E;
- Donohoe, G;
- Morris, D W;
- Hargreaves, A;
- Gill, M;
- Corvin, A
Publication type:
Article
Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility.
Published in:
Molecular Psychiatry, 2014, v. 19, n. 4, p. 452, doi. 10.1038/mp.2013.37
By:
- Li, M;
- Luo, X-j;
- Rietschel, M;
- Lewis, C M;
- Mattheisen, M;
- Müller-Myhsok, B;
- Jamain, S;
- Leboyer, M;
- Landén, M;
- Thompson, P M;
- Cichon, S;
- Nöthen, M M;
- Schulze, T G;
- Sullivan, P F;
- Bergen, S E;
- Donohoe, G;
- Morris, D W;
- Hargreaves, A;
- Gill, M;
- Corvin, A
Publication type:
Article
A K<sub>ATP</sub> channel gene effect on sleep duration: from genome-wide association studies to function in Drosophila.
Published in:
Molecular Psychiatry, 2013, v. 18, n. 1, p. 122, doi. 10.1038/mp.2011.142
By:
- Allebrandt, K V;
- Amin, N;
- Müller-Myhsok, B;
- Esko, T;
- Teder-Laving, M;
- Azevedo, R V D M;
- Hayward, C;
- van Mill, J;
- Vogelzangs, N;
- Green, E W;
- Melville, S A;
- Lichtner, P;
- Wichmann, H-E;
- Oostra, B A;
- Janssens, A C J W;
- Campbell, H;
- Wilson, J F;
- Hicks, A A;
- Pramstaller, P P;
- Dogas, Z
Publication type:
Article
First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children.
Published in:
Molecular Psychiatry, 2011, v. 16, n. 1, p. 97, doi. 10.1038/mp.2009.102
By:
- 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.
Publication type:
Article
Proteomic-based genotyping in a mouse model of trait anxiety exposes disease-relevant pathways.
Published in:
Molecular Psychiatry, 2010, v. 15, n. 7, p. 702, doi. 10.1038/mp.2008.146
By:
- Ditzen, C.;
- Varadarajulu, J.;
- Czibere, L.;
- Gonik, M.;
- Targosz, B. S.;
- Hambsch, B.;
- Bettecken, T.;
- Keßler, M. S.;
- Frank, E.;
- Bunck, M.;
- Teplytska, L.;
- Erhardt, A.;
- Holsboer, F.;
- Müller-Myhsok, B.;
- Landgraf, R.;
- Turck, C. W.
Publication type:
Article
Genome-wide association study of recurrent major depressive disorder in two European case–control cohorts.
Published in:
Molecular Psychiatry, 2010, v. 15, n. 6, p. 589, doi. 10.1038/mp.2008.131
By:
- Muglia, P.;
- Tozzi, F.;
- Galwey, N. W.;
- Francks, C.;
- Upmanyu, R.;
- Kong, X. Q.;
- Antoniades, A.;
- Domenici, E.;
- Perry, J.;
- Rothen, S.;
- Vandeleur, C. L.;
- Mooser, V.;
- Waeber, G.;
- Vollenweider, P.;
- Preisig, M.;
- Lucae, S.;
- Müller-Myhsok, B.;
- Holsboer, F.;
- Middleton, L. T.;
- Roses, A. D.
Publication type:
Article
Supporting evidence for LRRTM1 imprinting effects in schizophrenia.
Published in:
2009
By:
- Ludwig, K. U.;
- Mattheisen, M.;
- Mühleisen, T. W.;
- Roeske, D.;
- Schmäl, C.;
- Breuer, R.;
- Schulte-Körne, G.;
- Müller-Myhsok, B.;
- Nöthen, M. M.;
- Hoffmann, P.;
- Rietschel, M.;
- Cichon, S.
Publication type:
Letter
Evidence for associations between PDE4D polymorphisms and a subtype of neuroticism.
Published in:
Molecular Psychiatry, 2008, v. 13, n. 9, p. 831, doi. 10.1038/mp.2008.2
By:
- Heck, A;
- Lieb, R;
- Unschuld, P G;
- Ellgas, A;
- Pfister, H;
- Lucae, S;
- Erhardt, A;
- Himmerich, H;
- Horstmann, S;
- Kloiber, S;
- Ripke, S;
- Müller-Myhsok, B;
- Bettecken, T;
- Uhr, M;
- Holsboer, F;
- Ising, M
Publication type:
Article
Association of polymorphisms in the angiotensin-converting enzyme gene with syndromal panic attacks.
Published in:
2008
By:
- Erhardt, A.;
- Lucae, S.;
- Kern, N.;
- Unschuld, P. G.;
- Ising, M.;
- Lieb, R.;
- Uhr, M.;
- Hohoff, C.;
- Deckert, J.;
- Bandelow, B.;
- Maier, W.;
- Binder, E. B.;
- Müller-Myhsok, B.;
- Keck, M. E.;
- Holsboer, F.
Publication type:
Letter
Investigation of 17 candidate genes for personality traits confirms effects of the HTR2A gene on novelty seeking.
Published in:
Genes, Brain & Behavior, 2009, v. 8, n. 4, p. 464, doi. 10.1111/j.1601-183X.2009.00494.x
By:
- Heck, A.;
- Lieb, R.;
- Ellgas, A.;
- Pfister, H.;
- Lucae, S.;
- Roeske, D.;
- Pütz, B.;
- Müller-Myhsok, B.;
- Uhr, M.;
- Holsboer, F.;
- Ising, M.
Publication type:
Article
Relevance ofex vivoblood lymphocyte assay forin vivolymphocyte function.
Published in:
Clinical & Experimental Immunology, 2005, v. 139, n. 1, p. 127, doi. 10.1111/j.1365-2249.2005.02667.x
By:
- Brattig, N. W.;
- Timmann, C.;
- Abraha, R. S.;
- Lepping, B.;
- Müller-Myhsok, B.;
- Horstmann, R. D.
Publication type:
Article
Discriminating metastasised from non-metastasised seminoma based on transcriptional changes in primary tumours using NGS.
Published in:
2014
By:
- Ruf, C G;
- Schmelz, H-U;
- Port, M;
- Wagner, W;
- Matthies, C;
- Müller-Myhsok, B;
- Meineke, V;
- Abend, M
Publication type:
journal article
Discriminating metastasised from non-metastasised seminoma based on transcriptional changes in primary tumours using NGS.
Published in:
British Journal of Cancer, 2014, v. 110, n. 11, p. 2738, doi. 10.1038/bjc.2014.134
By:
- Ruf, C G;
- Schmelz, H-U;
- Port, M;
- Wagner, W;
- Matthies, C;
- Müller-Myhsok, B;
- Meineke, V;
- Abend, M
Publication type:
Article
More CLEC16A gene variants associated with multiple sclerosis.
Published in:
Acta Neurologica Scandinavica, 2011, v. 123, n. 6, p. 400, doi. 10.1111/j.1600-0404.2010.01421.x
By:
- Nischwitz, S.;
- Cepok, S.;
- Kroner, A.;
- Wolf, C.;
- Knop, M.;
- Müller-Sarnowski, F.;
- Pfister, H.;
- Rieckmann, P.;
- Hemmer, B.;
- Ising, M.;
- Uhr, M.;
- Bettecken, T.;
- Holsboer, F.;
- Müller-Myhsok, B.;
- Weber, F.
Publication type:
Article
Association of human leucocyte-DR and DQ antigens in coeliac disease: A family study.
Published in:
Journal of Gastroenterology & Hepatology, 2000, v. 15, n. 7, p. 771, doi. 10.1046/j.1440-1746.2000.02227.x
By:
- Agrawal, S;
- Gupta, A;
- Yachha, Sk;
- Müller-Myhsok, B;
- Mehrotra, P;
- Agarwal, Ss
Publication type:
Article
Risk conferring genes in multiple sclerosis
Published in:
FEBS Letters, 2011, v. 585, n. 23, p. 3789, doi. 10.1016/j.febslet.2011.03.037
By:
- Nischwitz, S.;
- Müller-Myhsok, B.;
- Weber, F.
Publication type:
Article
Linkage analysis and genetic models in dyslexia - considerations pertaining to discrete trait analysis and quantitative trait analyses.
Published in:
European Child & Adolescent Psychiatry, 1999, v. 8, p. S040, doi. 10.1007/pl00010692
By:
- Müller-Myhsok, B.;
- Grimm, T.
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
Linkage analysis and genetic models in dyslexia -- considerations pertaining to discrete trait analysis and quantitative trait analyses.
Published in:
1999
By:
- Müller-Myhsok B;
- Grimm T
Publication type:
Journal Article
Polymorphisms in the angiotensin-converting enzyme gene are associated with unipolar depression, ACE activity and hypercortisolism.
Published in:
Molecular Psychiatry, 2006, v. 11, n. 11, p. 1003, doi. 10.1038/sj.mp.4001884
By:
- Baghai, T. C.;
- Binder, E. B.;
- Schule, C.;
- Salyakina, D.;
- Eser, D.;
- Lucae, S.;
- Zwanzger, P.;
- Haberger, C.;
- Zill, P.;
- Ising, M.;
- Deiml, T.;
- Uhr, M.;
- Illig, T.;
- Wichmann, H.-E.;
- Modell, S.;
- Nothdurfter, C.;
- Holsboer, F.;
- Müller-Myhsok, B.;
- Möller, H.-J.;
- Rupprecht, R.
Publication type:
Article
Somatization in major depression - clinical features and genetic associations.
Published in:
Acta Psychiatrica Scandinavica, 2011, v. 124, n. 4, p. 317, doi. 10.1111/j.1600-0447.2011.01743.x
By:
- Klengel, T.;
- Heck, A.;
- Pfister, H.;
- Brückl, T.;
- Hennings, J. M.;
- Menke, A.;
- Czamara, D.;
- Müller‐Myhsok, B.;
- Ising, M.
Publication type:
Article

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