Author Herms, Stefan

1 to 20 of 21 Items

2009 | Journal Article
IRF6 gene variants in Central European patients with non-syndromic cleft lip with or without cleft palate
Birnbaum, S.; Ludwig, K. U.; Reutter, H.; Herms, S.; de Assis, N. A.; Diaz-Lacava, A. & Barth, S. et al. (2009)
European Journal Of Oral Sciences, 117(6) pp. 766-769.
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2009 | Journal Article
Transforming growth factor-beta receptor type 1 (TGFBR1) is not associated with non-syndromic cleft lip with or without cleft palate in patients of Central European descent
Reutter, H.; Birnbaum, S.; Mende, M.; de Assis, N. A.; Hoffmann, P.; Lacava, A. D. & Herms, S. et al. (2009)
International Journal of Pediatric Otorhinolaryngology, 73(10) pp. 1334-1338. DOI: https://doi.org/10.1016/j.ijporl.2009.06.004
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2009 | Journal Article
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, N. A.; Diaz-Lacava, A.; Herms, S. & Scheer, M. et al. (2009)
European Journal Of Oral Sciences, 117(2) pp. 200-203. DOI: https://doi.org/10.1111/j.1600-0722.2008.00604.x
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2009 | Journal Article
Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24
Birnbaum, S.; Ludwig, K. U.; Reutter, H.; Herms, S.; Steffens, M.; Rubini, M. & Baluardo, C. et al. (2009)
Nature Genetics, 41(4) pp. 473-477. DOI: https://doi.org/10.1038/ng.333
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2010 | Journal Article |
Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate
Mangold, E.; Ludwig, K. U.; Birnbaum, S.; Baluardo, C.; Ferrian, M.; Herms, S. & Reutter, H. et al. (2010)
Nature Genetics, 42(1) pp. 24-26. DOI: https://doi.org/10.1038/ng.506
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2010 | Journal Article
The catechol-O-methyl transferase (COMT) gene and its potential association with schizophrenia: Findings from a large German case-control and family-based sample
Nieratschker, V.; Frank, J.; Muehleisen, T. W.; Strohmaier, J.; Wendland, J. R.; Schumacher, J. & Treutlein, J. et al. (2010)
Schizophrenia Research, 122(1-3) pp. 24-30. DOI: https://doi.org/10.1016/j.schres.2010.06.018
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2011 | Journal Article
Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder (vol 88, pg 372, 2011)
Cichon, S.; Muehleisen, T. W.; Degenhardt, F. A.; Mattheisen, M.; Miro, X.; Strohmaier, J. & Steffens, M. et al. (2011)
The American Journal of Human Genetics, 88(3). DOI: https://doi.org/10.1016/j.ajhg.2011.03.001
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2012 | Journal Article
Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci
Ludwig, K. U.; Mangold, E.; Herms, S.; Nowak, S.; Reutter, H.; Paul, A. & Becker, J. et al. (2012)
Nature Genetics, 44(9) pp. 968-971. DOI: https://doi.org/10.1038/ng.2360
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2012 | Journal Article
Evaluating SKI as a candidate gene for non-syndromic cleft lip with or without cleft palate
Mangold, E.; Reutter, H.; Leon-Cachon, R. B. R.; Ludwig, K. U.; Herms, S.; Chacon-Camacho, O. & Ortiz-Lopez, R. et al. (2012)
European Journal Of Oral Sciences, 120(5) pp. 373-377. DOI: https://doi.org/10.1111/j.1600-0722.2012.00991.x
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2012 | Journal Article
Genetic variation at the synaptic vesicle gene SV2A is associated with schizophrenia
Mattheisen, M.; Muehleisen, T. W.; Strohmaier, J.; Treutlein, J.; Nenadic, I.; Alblas, M. & Meier, S. et al. (2012)
Schizophrenia Research, 141(2-3) pp. 262-265. DOI: https://doi.org/10.1016/j.schres.2012.08.027
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2012 | Journal Article
Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe
Rietschel, M.; Mattheisen, M.; Degenhardt, F. A.; Muehleisen, T. W.; Kirsch, P.; Esslinger, C. & Herms, S. et al. (2012)
Molecular Psychiatry, 17(9) pp. 906-917. DOI: https://doi.org/10.1038/mp.2011.80
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2013 | Journal Article | Letter Note
No evidence for an involvement of copy number variation in ABCA13 in schizophrenia, bipolar disorder, or major depressive disorder
Degenhardt, F. A.; Priebe, L.; Strohmaier, J.; Herms, S.; Hoffmann, P.; Mattheisen, M. & Moessner, R. et al. (2013)
Psychiatric Genetics, 23(1) pp. 45-+. DOI: https://doi.org/10.1097/YPG.0b013e328358645b
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2014 | Journal Article
SUCLG2 identified as both a determinator of CSF Aβ1–42 levels and an attenuator of cognitive decline in Alzheimer's disease
Ramirez, A.; van der Flier, W. M.; Herold, C.; Ramonet, D.; Heilmann, S.; Lewczuk, P. & Popp, J. et al. (2014)
Human Molecular Genetics, 23(24) pp. 6644-6658. DOI: https://doi.org/10.1093/hmg/ddu372
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2014 | Journal Article |
Genome-wide association study reveals two new risk loci for bipolar disorder
Muehleisen, T. W.; Leber, M.; Schulze, T. G.; Strohmaier, J.; Degenhardt, F. A.; Treutlein, J. & Mattheisen, M. et al. (2014)
Nature Communications, 5 art. 3339. DOI: https://doi.org/10.1038/ncomms4339
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2016 | Journal Article | Letter Note
Effect of copy number variant burden on Global Assessment of Functioning in schizophrenia
Heilbronner, U. ; Gade, K. ; Herms, S.; Strohmaier, J.; Lang, M.; Nöthen, M. M. & Rietschel, M. et al. (2016)
Psychiatric Genetics, 26(4) pp. 184-185. DOI: https://doi.org/10.1097/YPG.0000000000000135
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2018 | Journal Article
Shared genetic etiology between alcohol dependence and major depressive disorder
Foo, J. C.; Streit, F.; Treutlein, J.; Ripke, S.; Witt, S. H.; Strohmaier, J. & Degenhardt, F. et al. (2018)
Psychiatric Genetics, 28(4) pp. 66-70. DOI: https://doi.org/10.1097/YPG.0000000000000201
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2018 | Journal Article |
Detecting significant genotype–phenotype association rules in bipolar disorder: market research meets complex genetics
Breuer, R.; Mattheisen, M.; Frank, J.; Krumm, B.; Treutlein, J.; Kassem, L. & Strohmaier, J. et al. (2018)
International Journal of Bipolar Disorders, 6(1) art. 24. DOI: https://doi.org/10.1186/s40345-018-0132-x
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2019 | Journal Article
EFFECTS OF SCHIZOPHRENIA AND BIPOLAR POLYGENIC RISK SCORES ON AGE AT ONSET IN BIPOLAR DISORDER
Kalman, J.; Papiol, S. ; Heilbronner, U. ; Andlauer, T. F.; Anderson-Schmidt, H. ; Budde, M. & Gade, K. et al. (2019)
European Neuropsychopharmacology, 29 pp. S967. DOI: https://doi.org/10.1016/j.euroneuro.2017.08.331
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2019 | Journal Article
Leptin gene polymorphisms are associated with weight gain during lithium augmentation in patients with major depression
Bopp, S. K.; Heilbronner, U. ; Schlattmann, P.; Mühleisen, T. W.; Bschor, T.; Richter, C. & Steinacher, B. et al. (2019)
European Neuropsychopharmacology, 29(2) pp. 211-221. DOI: https://doi.org/10.1016/j.euroneuro.2018.12.006
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2021 | Journal Article |
Polygenic risk scores across the extended psychosis spectrum
Smigielski, L.; Papiol, S.; Theodoridou, A.; Heekeren, K.; Gerstenberg, M.; Wotruba, D. & Buechler, R. et al. (2021)
Translational Psychiatry, 11(1) art. 600. DOI: https://doi.org/10.1038/s41398-021-01720-0
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