Author Hoffmann, Per

1 to 19 of 19 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​.​
    ​Details  PMID  PMC  WoS 
  • 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 
    ​Details  DOI  PMID  PMC  WoS 
  • 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 
    ​Details  DOI  PMID  PMC  WoS 
  • 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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  • 2011 | Journal Article
    ​ ​SUMO1 as a candidate gene for non-syndromic cleft lip with or without cleft palate: No evidence for the involvement of common or rare variants in Central European patients​
    de Assis, N. A.; Nowak, S.; Ludwig, K. U.; Reutter, H.; Vollmer, J.; Hellmann, S. & Kluck, N. et al.​ (2011) 
    International Journal of Pediatric Otorhinolaryngology, 75(1) pp. 49​-52​.​ DOI: https://doi.org/10.1016/j.ijporl.2010.10.005 
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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
    ​ ​Resequencing of VAX1 in patients with nonsyndromic cleft lip with or without cleft palate​
    Nasser, E.; Mangold, E.; Tradowsky, D. C.; Fier, H.; Becker, J.; Boehmer, A. C. & Herberz, R. et al.​ (2012) 
    Birth Defects Research Part A Clinical and Molecular Teratology, 94(11) pp. 925​-933​.​ DOI: https://doi.org/10.1002/bdra.23078 
    ​Details  DOI  PMID  PMC  WoS 
  • 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 
    ​Details  DOI  PMID  PMC  WoS 
  • 2012 | Journal Article
    ​ ​Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder​
    Muehleisen, T. W.; Mattheisen, M.; Strohmaier, J.; Degenhardt, F. A.; Priebe, L.; Schultz, C. C. & Breuer, R. et al.​ (2012) 
    Schizophrenia Research, 138(1) pp. 69​-73​.​ DOI: https://doi.org/10.1016/j.schres.2012.03.007 
    ​Details  DOI  PMID  PMC  WoS 
  • 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 
    ​Details  DOI  PMID  PMC  WoS 
  • 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 
    ​Details  DOI 
  • 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 
    ​Details  DOI  PMID  PMC  WoS 
  • 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 
    ​Details  DOI 
  • 2018 | Journal Article | 
    ​ ​Analysis of the Influence of microRNAs in Lithium Response in Bipolar Disorder​
    Reinbold, C. S.; Forstner, A. J.; Hecker, J.; Fullerton, J. M.; Hoffmann, P.; Hou, L. & Heilbronner, U.  et al.​ (2018) 
    Frontiers in Psychiatry, 9.​ DOI: https://doi.org/10.3389/fpsyt.2018.00207 
    ​Details  DOI 
  • 2019 | Journal Article
    ​ ​T40. Alzheimer’s Disease DNA (Hydroxy)Methylome in the Brain and Blood: Evidence for OXT Methylation as a Preclinical Marker​
    Lardenoije, R.; Roubroeks, J.; Pishva, E.; Leber, M.; Wagner, H.; Iatrou, A. & Smith, A. et al.​ (2019) 
    Biological Psychiatry, 85(10) pp. S144​.​ DOI: https://doi.org/10.1016/j.biopsych.2019.03.363 
    ​Details  DOI 
  • 2019 | Journal Article | 
    ​ ​Methylomic profiling in trisomy 21 identifies cognition- and Alzheimer’s disease-related dysregulation​
    Haertle, L.; Müller, T.; Lardenoije, R.; Maierhofer, A.; Dittrich, M.; Riemens, R. J. M. & Stora, S. et al.​ (2019) 
    Clinical Epigenetics, 11(1).​ DOI: https://doi.org/10.1186/s13148-019-0787-x 
    ​Details  DOI 
  • 2019 | Journal Article | 
    ​ ​Alzheimer’s disease-associated (hydroxy)methylomic changes in the brain and blood​
    Lardenoije, R.; Roubroeks, J. A. Y.; Pishva, E.; Leber, M.; Wagner, H.; Iatrou, A. & Smith, A. R. et al.​ (2019) 
    Clinical Epigenetics, 11(1).​ DOI: https://doi.org/10.1186/s13148-019-0755-5 
    ​Details  DOI 
  • 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 
    ​Details  DOI 
  • 2021 | Journal Article | 
    ​ ​Combining schizophrenia and depression polygenic risk scores improves the genetic prediction of lithium response in bipolar disorder patients​
    Schubert, K. O.; Thalamuthu, A.; Amare, A. T.; Frank, J.; Streit, F.; Adl, M. & Akula, N. et al.​ (2021) 
    Translational Psychiatry, 11(1) art. 606​.​ DOI: https://doi.org/10.1038/s41398-021-01702-2 
    ​Details  DOI 

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