Müller-Myhsok B - Search Results

1

The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders.

Chang H, Hoshina N, Zhang C, Ma Y, Cao H, Wang Y, Wu DD, Bergen SE, Landén M, Hultman CM, Preisig M, Kutalik Z, Castelao E, Grigoroiu-Serbanescu M, Forstner AJ, Strohmaier J, Hecker J, Schulze TG, Müller-Myhsok B, Reif A, Mitchell PB, Martin NG, Schofield PR, Cichon S, Nöthen MM; Swedish Bipolar Study Group; MooDS Bipolar Consortium; Walter H, Erk S, Heinz A, Amin N, van Duijn CM, Meyer-Lindenberg A, Tost H, Xiao X, Yamamoto T, Rietschel M, Li M. Chang H, et al. Mol Psychiatry. 2018 Feb;23(2):400-412. doi: 10.1038/mp.2016.231. Epub 2017 Jan 10. Mol Psychiatry. 2018. PMID: 28070120 Free PMC article.

2

Genetic linkage analysis with dyslexia: evidence for linkage of spelling disability to chromosome 15.

Nöthen MM, Schulte-Körne G, Grimm T, Cichon S, Vogt IR, Müller-Myhsok B, Propping P, Remschmidt H. Nöthen MM, et al. Eur Child Adolesc Psychiatry. 1999;8 Suppl 3:56-9. doi: 10.1007/pl00010696. Eur Child Adolesc Psychiatry. 1999. PMID: 10638372

3

P2RX7, a gene coding for a purinergic ligand-gated ion channel, is associated with major depressive disorder.

Lucae S, Salyakina D, Barden N, Harvey M, Gagné B, Labbé M, Binder EB, Uhr M, Paez-Pereda M, Sillaber I, Ising M, Brückl T, Lieb R, Holsboer F, Müller-Myhsok B. Lucae S, et al. Hum Mol Genet. 2006 Aug 15;15(16):2438-45. doi: 10.1093/hmg/ddl166. Epub 2006 Jul 5. Hum Mol Genet. 2006. PMID: 16822851

4

Polymorphisms in the angiotensin-converting enzyme gene are associated with unipolar depression, ACE activity and hypercortisolism.

Baghai TC, Binder EB, Schule C, Salyakina D, Eser D, Lucae S, Zwanzger P, Haberger C, Zill P, Ising M, Deiml T, Uhr M, Illig T, Wichmann HE, Modell S, Nothdurfter C, Holsboer F, Müller-Myhsok B, Möller HJ, Rupprecht R, Bondy B. Baghai TC, et al. Mol Psychiatry. 2006 Nov;11(11):1003-15. doi: 10.1038/sj.mp.4001884. Epub 2006 Aug 22. Mol Psychiatry. 2006. PMID: 16924268

5

A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia.

Anthoni H, Zucchelli M, Matsson H, Müller-Myhsok B, Fransson I, Schumacher J, Massinen S, Onkamo P, Warnke A, Griesemann H, Hoffmann P, Nopola-Hemmi J, Lyytinen H, Schulte-Körne G, Kere J, Nöthen MM, Peyrard-Janvid M. Anthoni H, et al. Hum Mol Genet. 2007 Mar 15;16(6):667-77. doi: 10.1093/hmg/ddm009. Epub 2007 Feb 19. Hum Mol Genet. 2007. PMID: 17309879

6

Further evidence for a susceptibility locus contributing to reading disability on chromosome 15q15-q21.

Schumacher J, König IR, Schröder T, Duell M, Plume E, Propping P, Warnke A, Libertus C, Ziegler A, Müller-Myhsok B, Schulte-Körne G, Nöthen MM. Schumacher J, et al. Psychiatr Genet. 2008 Jun;18(3):137-42. doi: 10.1097/YPG.0b013e3282fb7fc6. Psychiatr Genet. 2008. PMID: 18496212

7

Genome-wide association study of recurrent major depressive disorder in two European case-control cohorts.

Muglia P, Tozzi F, Galwey NW, Francks C, Upmanyu R, Kong XQ, Antoniades A, Domenici E, Perry J, Rothen S, Vandeleur CL, Mooser V, Waeber G, Vollenweider P, Preisig M, Lucae S, Müller-Myhsok B, Holsboer F, Middleton LT, Roses AD. Muglia P, et al. Mol Psychiatry. 2010 Jun;15(6):589-601. doi: 10.1038/mp.2008.131. Epub 2008 Dec 23. Mol Psychiatry. 2010. PMID: 19107115

8

Variations in tryptophan hydroxylase 2 linked to decreased serotonergic activity are associated with elevated risk for metabolic syndrome in depression.

Kloiber S, Kohli MA, Brueckl T, Ripke S, Ising M, Uhr M, Menke A, Unschuld PG, Horstmann S, Salyakina D, Muller-Myhsok B, Binder EB, Holsboer F, Lucae S. Kloiber S, et al. Mol Psychiatry. 2010 Jul;15(7):736-47. doi: 10.1038/mp.2008.142. Epub 2009 Jan 6. Mol Psychiatry. 2010. PMID: 19125159

9

Proteomic-based genotyping in a mouse model of trait anxiety exposes disease-relevant pathways.

Ditzen C, Varadarajulu J, Czibere L, Gonik M, Targosz BS, Hambsch B, Bettecken T, Kessler MS, Frank E, Bunck M, Teplytska L, Erhardt A, Holsboer F, Müller-Myhsok B, Landgraf R, Turck CW. Ditzen C, et al. Mol Psychiatry. 2010 Jul;15(7):702-11. doi: 10.1038/mp.2008.146. Epub 2009 Jan 13. Mol Psychiatry. 2010. PMID: 19139748

10

Further evidence for DYX1C1 as a susceptibility factor for dyslexia.

Dahdouh F, Anthoni H, Tapia-Páez I, Peyrard-Janvid M, Schulte-Körne G, Warnke A, Remschmidt H, Ziegler A, Kere J, Müller-Myhsok B, Nöthen MM, Schumacher J, Zucchelli M. Dahdouh F, et al. Psychiatr Genet. 2009 Apr;19(2):59-63. doi: 10.1097/YPG.0b013e32832080e1. Psychiatr Genet. 2009. PMID: 19240663

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