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Page 1
Exome sequencing in large, multiplex bipolar disorder families from Cuba.
Maaser A, Forstner AJ, Strohmaier J, Hecker J, Ludwig KU, Sivalingam S, Streit F, Degenhardt F, Witt SH, Reinbold CS, Koller AC, Raff R, Heilmann-Heimbach S, Fischer SB; Bipolar Disorder Working Group of the Psychiatric Genomics Consortium; Herms S, Hoffmann P, Thiele H, Nürnberg P, Löhlein Fier H, Orozco-Díaz G, Carmenate-Naranjo D, Proenza-Barzaga N, Auburger GWJ, Andlauer TFM, Cichon S, Marcheco-Teruel B, Mors O, Rietschel M, Nöthen MM. Maaser A, et al. Among authors: herms s. PLoS One. 2018 Oct 31;13(10):e0205895. doi: 10.1371/journal.pone.0205895. eCollection 2018. PLoS One. 2018. PMID: 30379966 Free PMC article.
Brief report: no association between premorbid adjustment in adult-onset schizophrenia and genetic variation in Dysbindin.
Schirmbeck F, Georgi A, Strohmaier J, Schmael C, Boesshenz KV, Mühleisen TW, Herms S, Hoffmann P, Jamra RA, Schumacher J, Maier W, Propping P, Nöthen MM, Cichon S, Rietschel M, Schulze TG. Schirmbeck F, et al. Among authors: herms s. J Autism Dev Disord. 2008 Nov;38(10):1977-81. doi: 10.1007/s10803-008-0582-6. Epub 2008 May 13. J Autism Dev Disord. 2008. PMID: 18473158
Susceptibility variants for male-pattern baldness on chromosome 20p11.
Hillmer AM, Brockschmidt FF, Hanneken S, Eigelshoven S, Steffens M, Flaquer A, Herms S, Becker T, Kortüm AK, Nyholt DR, Zhao ZZ, Montgomery GW, Martin NG, Mühleisen TW, Alblas MA, Moebus S, Jöckel KH, Bröcker-Preuss M, Erbel R, Reinartz R, Betz RC, Cichon S, Propping P, Baur MP, Wienker TF, Kruse R, Nöthen MM. Hillmer AM, et al. Among authors: herms s. Nat Genet. 2008 Nov;40(11):1279-81. doi: 10.1038/ng.228. Epub 2008 Oct 12. Nat Genet. 2008. PMID: 18849994
Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24.
Birnbaum S, Ludwig KU, Reutter H, Herms S, Steffens M, Rubini M, Baluardo C, Ferrian M, Almeida de Assis N, Alblas MA, Barth S, Freudenberg J, Lauster C, Schmidt G, Scheer M, Braumann B, Bergé SJ, Reich RH, Schiefke F, Hemprich A, Pötzsch S, Steegers-Theunissen RP, Pötzsch B, Moebus S, Horsthemke B, Kramer FJ, Wienker TF, Mossey PA, Propping P, Cichon S, Hoffmann P, Knapp M, Nöthen MM, Mangold E. Birnbaum S, et al. Among authors: herms s. Nat Genet. 2009 Apr;41(4):473-7. doi: 10.1038/ng.333. Epub 2009 Mar 8. Nat Genet. 2009. PMID: 19270707
Further evidence for the involvement of MYH9 in the etiology of non-syndromic cleft lip with or without cleft palate.
Birnbaum S, Reutter H, Mende M, de Assis NA, Diaz-Lacava A, Herms S, Scheer M, Lauster C, Braumann B, Schmidt G, Martini M, Hemprich A, Pötzsch S, Knapp M, Nöthen MM, Kramer FJ, Mangold E. Birnbaum S, et al. Among authors: herms s. Eur J Oral Sci. 2009 Apr;117(2):200-3. doi: 10.1111/j.1600-0722.2008.00604.x. Eur J Oral Sci. 2009. PMID: 19320731
Variation in P2RX7 candidate gene (rs2230912) is not associated with bipolar I disorder and unipolar major depression in four European samples.
Grigoroiu-Serbanescu M, Herms S, Mühleisen TW, Georgi A, Diaconu CC, Strohmaier J, Czerski P, Hauser J, Leszczynska-Rodziewicz A, Jamra RA, Babadjanova G, Tiganov A, Krasnov V, Kapiletti S, Neagu AI, Vollmer J, Breuer R, Rietschel M, Nöthen MM, Cichon S, Propping P, Nöthen MM, Cichon S. Grigoroiu-Serbanescu M, et al. Among authors: herms s. Am J Med Genet B Neuropsychiatr Genet. 2009 Oct 5;150B(7):1017-21. doi: 10.1002/ajmg.b.30952. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 19330776
Dissection of phenotype reveals possible association between schizophrenia and Glutamate Receptor Delta 1 (GRID1) gene promoter.
Treutlein J, Mühleisen TW, Frank J, Mattheisen M, Herms S, Ludwig KU, Treutlein T, Schmael C, Strohmaier J, Bösshenz KV, Breuer R, Paul T, Witt SH, Schulze TG, Schlösser RG, Nenadic I, Sauer H, Becker T, Maier W, Cichon S, Nöthen MM, Rietschel M. Treutlein J, et al. Among authors: herms s. Schizophr Res. 2009 Jun;111(1-3):123-30. doi: 10.1016/j.schres.2009.03.011. Epub 2009 Apr 5. Schizophr Res. 2009. PMID: 19346103
The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations.
Schumacher J, Laje G, Abou Jamra R, Becker T, Mühleisen TW, Vasilescu C, Mattheisen M, Herms S, Hoffmann P, Hillmer AM, Georgi A, Herold C, Schulze TG, Propping P, Rietschel M, McMahon FJ, Nöthen MM, Cichon S. Schumacher J, et al. Among authors: herms s. Hum Mol Genet. 2009 Jul 15;18(14):2719-27. doi: 10.1093/hmg/ddp204. Epub 2009 May 4. Hum Mol Genet. 2009. PMID: 19414483 Free PMC article.
233 results