Rare SHANK2 variants in schizophrenia

por Peykov, S, Berkel, S, Degenhardt, F, Rietschel, M, Nöthen, M M, Rappold, G A
Publicado 2015

Systematic investigation of a potential epidemiological and genetic association between male androgenetic alopecia and COVID‐19

por Henne, S. K., Hochfeld, L. M., Maj, C., Nöthen, M. M., Heilmann‐Heimbach, S.
Publicado 2021

072 Covid-19 and male androgenetic alopecia: Systematic investigation of a potential epidemiological and genetic association

por Henne, S.K., Hochfeld, L.M., Maj, C., Nöthen, M.M., Heilmann-Heimbach, S.
Publicado 2021

Identification of increased genetic risk scores for schizophrenia in treatment-resistant patients

por Frank, J, Lang, M, Witt, S H, Strohmaier, J, Rujescu, D, Cichon, S, Degenhardt, F, Nöthen, M M, Collier, D A, Ripke, S, Naber, D, Rietschel, M
Publicado 2015

Functional impact of a recently identified quantitative trait locus for hippocampal volume with genome-wide support

por Erk, S, Meyer-Lindenberg, A, Schmierer, P, Grimm, O, Tost, H, Mühleisen, T, Mattheisen, M, Seiferth, N, Cichon, S, Rietschel, M, Nöthen, M M, Heinz, A, Walter, H
Publicado 2013

Identification and functional characterization of rare SHANK2 variants in schizophrenia

por Peykov, S, Berkel, S, Schoen, M, Weiss, K, Degenhardt, F, Strohmaier, J, Weiss, B, Proepper, C, Schratt, G, Nöthen, M M, Boeckers, T M, Rietschel, M, Rappold, G A
Publicado 2015

Transcriptome-wide analysis of filarial extract-primed human monocytes reveal changes in LPS-induced PTX3 expression levels

por Buerfent, B. C., Gölz, L., Hofmann, A., Rühl, H., Stamminger, W., Fricker, N., Hess, T., Oldenburg, J., Nöthen, M. M., Schumacher, J., Hübner, M. P., Hoerauf, A.
Publicado 2019

Evidence for the involvement of ZNF804A in cognitive processes of relevance to reading and spelling

por Becker, J, Czamara, D, Hoffmann, P, Landerl, K, Blomert, L, Brandeis, D, Vaessen, A, Maurer, U, Moll, K, Ludwig, K U, Müller-Myhsok, B, Nöthen, M M, Schulte-Körne, G, Schumacher, J
Publicado 2012

Genome-wide significant association between a ‘negative mood delusions' dimension in bipolar disorder and genetic variation on chromosome 3q26.1

por Meier, S, Mattheisen, M, Vassos, E, Strohmaier, J, Treutlein, J, Josef, F, Breuer, R, Degenhardt, F, Mühleisen, T W, Müller-Myhsok, B, Steffens, M, Schmael, C, McMahon, F J, Nöthen, M M, Cichon, S, Schulze, T G, Rietschel, M
Publicado 2012

Investigation of manic and euthymic episodes identifies state- and trait-specific gene expression and STAB1 as a new candidate gene for bipolar disorder

por Witt, S H, Juraeva, D, Sticht, C, Strohmaier, J, Meier, S, Treutlein, J, Dukal, H, Frank, J, Lang, M, Deuschle, M, Schulze, T G, Degenhardt, F, Mattheisen, M, Brors, B, Cichon, S, Nöthen, M M, Witt, C C, Rietschel, M
Publicado 2014

Replication of functional serotonin receptor type 3A and B variants in bipolar affective disorder: a European multicenter study

por Hammer, C, Cichon, S, Mühleisen, T W, Haenisch, B, Degenhardt, F, Mattheisen, M, Breuer, R, Witt, S H, Strohmaier, J, Oruc, L, Rivas, F, Babadjanova, G, Grigoroiu-Serbanescu, M, Hauser, J, Röth, R, Rappold, G, Rietschel, M, Nöthen, M M, Niesler, B
Publicado 2012

A common variant in Myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults

por Ludwig, K U, Sämann, P, Alexander, M, Becker, J, Bruder, J, Moll, K, Spieler, D, Czisch, M, Warnke, A, Docherty, S J, Davis, O S P, Plomin, R, Nöthen, M M, Landerl, K, Müller-Myhsok, B, Hoffmann, P, Schumacher, J, Schulte-Körne, G, Czamara, D
Publicado 2013

Functional neuroimaging effects of recently discovered genetic risk loci for schizophrenia and polygenic risk profile in five RDoC subdomains

por Erk, S, Mohnke, S, Ripke, S, Lett, T A, Veer, I M, Wackerhagen, C, Grimm, O, Romanczuk-Seiferth, N, Degenhardt, F, Tost, H, Mattheisen, M, Mühleisen, T W, Charlet, K, Skarabis, N, Kiefer, F, Cichon, S, Witt, S H, Nöthen, M M, Rietschel, M, Heinz, A, Meyer-Lindenberg, A, Walter, H
Publicado 2017

Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci

por Børglum, A D, Demontis, D, Grove, J, Pallesen, J, Hollegaard, M V, Pedersen, C B, Hedemand, A, Mattheisen, M, Uitterlinden, A, Nyegaard, M, Ørntoft, T, Wiuf, C, Didriksen, M, Nordentoft, M, Nöthen, M M, Rietschel, M, Ophoff, R A, Cichon, S, Yolken, R H, Hougaard, D M, Mortensen, P B, Mors, O
Publicado 2014

MORC1 exhibits cross-species differential methylation in association with early life stress as well as genome-wide association with MDD

por Nieratschker, V, Massart, R, Gilles, M, Luoni, A, Suderman, M J, Krumm, B, Meier, S, Witt, S H, Nöthen, M M, Suomi, S J, Peus, V, Scharnholz, B, Dukal, H, Hohmeyer, C, Wolf, I A-C, Cirulli, F, Gass, P, Sütterlin, M W, Filsinger, B, Laucht, M, Riva, M A, Rietschel, M, Deuschle, M, Szyf, M
Publicado 2014

Duplications in RB1CC1 are associated with schizophrenia; identification in large European sample sets

por Degenhardt, F, Priebe, L, Meier, S, Lennertz, L, Streit, F, Witt, S H, Hofmann, A, Becker, T, Mössner, R, Maier, W, Nenadic, I, Sauer, H, Mattheisen, M, Buizer-Voskamp, J, Ophoff, R A, Rujescu, D, Giegling, I, Ingason, A, Wagner, M, Delobel, B, Andrieux, J, Meyer-Lindenberg, A, Heinz, A, Walter, H, Moebus, S, Corvin, A, Rietschel, M, Nöthen, M M, Cichon, S
Publicado 2013

Genetic markers associated with abstinence length in alcohol-dependent subjects treated with acamprosate

por Karpyak, V M, Biernacka, J M, Geske, J R, Jenkins, G D, Cunningham, J M, Rüegg, J, Kononenko, O, Leontovich, A A, Abulseoud, O A, Hall-Flavin, D K, Loukianova, L L, Schneekloth, T D, Skime, M K, Frank, J, Nöthen, M M, Rietschel, M, Kiefer, F, Mann, K F, Weinshilboum, R M, Frye, M A, Choi, D S
Publicado 2014

Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder

por Jarick, I, Volckmar, A-L, Pütter, C, Pechlivanis, S, Nguyen, T T, Dauvermann, M R, Beck, S, Albayrak, Ö, Scherag, S, Gilsbach, S, Cichon, S, Hoffmann, P, Degenhardt, F, Nöthen, M M, Schreiber, S, Wichmann, H-E, Jöckel, K-H, Heinrich, J, Tiesler, C M T, Faraone, S V, Walitza, S, Sinzig, J, Freitag, C, Meyer, J, Herpertz-Dahlmann, B, Lehmkuhl, G, Renner, T J, Warnke, A, Romanos, M, Lesch, K-P, Reif, A, Schimmelmann, B G, Hebebrand, J, Scherag, A, Hinney, A
Publicado 2014

A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1

por Vijayakrishnan, J, Kumar, R, Henrion, M Y R, Moorman, A V, Rachakonda, P S, Hosen, I, da Silva Filho, M I, Holroyd, A, Dobbins, S E, Koehler, R, Thomsen, H, Irving, J A, Allan, J M, Lightfoot, T, Roman, E, Kinsey, S E, Sheridan, E, Thompson, P D, Hoffmann, P, Nöthen, M M, Heilmann-Heimbach, S, Jöckel, K H, Greaves, M, Harrison, C J, Bartram, C R, Schrappe, M, Stanulla, M, Hemminki, K, Houlston, R S
Publicado 2017

Genome-wide significant risk factors for Alzheimer's disease: role in progression to dementia due to Alzheimer's disease among subjects with mild cognitive impairment

por Lacour, A, Espinosa, A, Louwersheimer, E, Heilmann, S, Hernández, I, Wolfsgruber, S, Fernández, V, Wagner, H, Rosende-Roca, M, Mauleón, A, Moreno-Grau, S, Vargas, L, Pijnenburg, Y A L, Koene, T, Rodríguez-Gómez, O, Ortega, G, Ruiz, S, Holstege, H, Sotolongo-Grau, O, Kornhuber, J, Peters, O, Frölich, L, Hüll, M, Rüther, E, Wiltfang, J, Scherer, M, Riedel-Heller, S, Alegret, M, Nöthen, M M, Scheltens, P, Wagner, M, Tárraga, L, Jessen, F, Boada, M, Maier, W, van der Flier, W M, Becker, T, Ramirez, A, Ruiz, A
Publicado 2017