The Effect of Accompanying In Situ Ductal Carcinoma on Accuracy of Measuring Malignant Breast Tumor Size Using B-Mode Ultrasonography and Real-Time Sonoelastography

por Soliman, A. A., Wojcinski, S., Degenhardt, F.
Publicado 2012

The biology of malignant breast tumors has an impact on the presentation in ultrasound: an analysis of 315 cases

por Wojcinski, S, Stefanidou, N, Hillemanns, P, Degenhardt, F
Publicado 2013

How genetics can help diagnosis and treatment in psychiatric conditions

por Chaumette, B., Laurent-Levinson, C., Almos, P., Degenhardt, F.
Publicado 2021

Rare SHANK2 variants in schizophrenia

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

Polygenic risk has an impact on the structural plasticity of hippocampal subfields during aerobic exercise combined with cognitive remediation in multi-episode schizophrenia

por Papiol, S, Popovic, D, Keeser, D, Hasan, A, Schneider-Axmann, T, Degenhardt, F, Rossner, M J, Bickeböller, H, Schmitt, A, Falkai, P, Malchow, B
Publicado 2017

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

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

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

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

385 Mechanisms by which cystic fibrosis transmembrane conductance regulator may influence SARS-CoV-2 infection

por Tedbury, P., Manfredi, C., Conway, J., Horwath, M., McCracken, C., Sorscher, A., Moreau, S., Wright, C., Edwards, C., Brewer, J., Guarner, J., De Wit, E., Williamson, B., Ong, Y., Roback, J., Alter, D., Degenhardt, F., Karlsen, T., Franke, A., Sarafianos, S., Sorscher, E., Hong, J., Ehrhardt, A.
Publicado 2022

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

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

Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder

por Forstner, A J, Hofmann, A, Maaser, A, Sumer, S, Khudayberdiev, S, Mühleisen, T W, Leber, M, Schulze, T G, Strohmaier, J, Degenhardt, F, Treutlein, J, Mattheisen, M, Schumacher, J, Breuer, R, Meier, S, Herms, S, Hoffmann, P, Lacour, A, Witt, S H, Reif, A, Müller-Myhsok, B, Lucae, S, Maier, W, Schwarz, M, Vedder, H, Kammerer-Ciernioch, J, Pfennig, A, Bauer, M, Hautzinger, M, Moebus, S, Priebe, L, Sivalingam, S, Verhaert, A, Schulz, H, Czerski, P M, Hauser, J, Lissowska, J, Szeszenia-Dabrowska, N, Brennan, P, McKay, J D, Wright, A, Mitchell, P B, Fullerton, J M, Schofield, P R, Montgomery, G W, Medland, S E, Gordon, S D, Martin, N G, Krasnov, V, Chuchalin, A, Babadjanova, G, Pantelejeva, G, Abramova, L I, Tiganov, A S, Polonikov, A, Khusnutdinova, E, Alda, M, Cruceanu, C, Rouleau, G A, Turecki, G, Laprise, C, Rivas, F, Mayoral, F, Kogevinas, M, Grigoroiu-Serbanescu, M, Propping, P, Becker, T, Rietschel, M, Cichon, S, Schratt, G, Nöthen, M M
Publicado 2015

Genetic effects influencing risk for major depressive disorder in China and Europe

por Bigdeli, T B, Ripke, S, Peterson, R E, Trzaskowski, M, Bacanu, S-A, Abdellaoui, A, Andlauer, T F M, Beekman, A T F, Berger, K, Blackwood, D H R, Boomsma, D I, Breen, G, Buttenschøn, H N, Byrne, E M, Cichon, S, Clarke, T-K, Couvy-Duchesne, B, Craddock, N, de Geus, E J C, Degenhardt, F, Dunn, E C, Edwards, A C, Fanous, A H, Forstner, A J, Frank, J, Gill, M, Gordon, S D, Grabe, H J, Hamilton, S P, Hardiman, O, Hayward, C, Heath, A C, Henders, A K, Herms, S, Hickie, I B, Hoffmann, P, Homuth, G, Hottenga, J-J, Ising, M, Jansen, R, Kloiber, S, Knowles, J A, Lang, M, Li, Q S, Lucae, S, MacIntyre, D J, Madden, P A F, Martin, N G, McGrath, P J, McGuffin, P, McIntosh, A M, Medland, S E, Mehta, D, Middeldorp, C M, Milaneschi, Y, Montgomery, G W, Mors, O, Müller-Myhsok, B, Nauck, M, Nyholt, D R, Nöthen, M M, Owen, M J, Penninx, B W J H, Pergadia, M L, Perlis, R H, Peyrot, W J, Porteous, D J, Potash, J B, Rice, J P, Rietschel, M, Riley, B P, Rivera, M, Schoevers, R, Schulze, T G, Shi, J, Shyn, S I, Smit, J H, Smoller, J W, Streit, F, Strohmaier, J, Teumer, A, Treutlein, J, Van der Auwera, S, van Grootheest, G, van Hemert, A M, Völzke, H, Webb, B T, Weissman, M M, Wellmann, J, Willemsen, G, Witt, S H, Levinson, D F, Lewis, C M, Wray, N R, Flint, J, Sullivan, P F, Kendler, K S
Publicado 2017

Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia

por Witt, S H, Streit, F, Jungkunz, M, Frank, J, Awasthi, S, Reinbold, C S, Treutlein, J, Degenhardt, F, Forstner, A J, Heilmann-Heimbach, S, Dietl, L, Schwarze, C E, Schendel, D, Strohmaier, J, Abdellaoui, A, Adolfsson, R, Air, T M, Akil, H, Alda, M, Alliey-Rodriguez, N, Andreassen, O A, Babadjanova, G, Bass, N J, Bauer, M, Baune, B T, Bellivier, F, Bergen, S, Bethell, A, Biernacka, J M, Blackwood, D H R, Boks, M P, Boomsma, D I, Børglum, A D, Borrmann-Hassenbach, M, Brennan, P, Budde, M, Buttenschøn, H N, Byrne, E M, Cervantes, P, Clarke, T-K, Craddock, N, Cruceanu, C, Curtis, D, Czerski, P M, Dannlowski, U, Davis, T, de Geus, E J C, Di Florio, A, Djurovic, S, Domenici, E, Edenberg, H J, Etain, B, Fischer, S B, Forty, L, Fraser, C, Frye, M A, Fullerton, J M, Gade, K, Gershon, E S, Giegling, I, Gordon, S D, Gordon-Smith, K, Grabe, H J, Green, E K, Greenwood, T A, Grigoroiu-Serbanescu, M, Guzman-Parra, J, Hall, L S, Hamshere, M, Hauser, J, Hautzinger, M, Heilbronner, U, Herms, S, Hitturlingappa, S, Hoffmann, P, Holmans, P, Hottenga, J-J, Jamain, S, Jones, I, Jones, L A, Juréus, A, Kahn, R S, Kammerer-Ciernioch, J, Kirov, G, Kittel-Schneider, S, Kloiber, S, Knott, S V, Kogevinas, M, Landén, M, Leber, M, Leboyer, M, Li, Q S, Lissowska, J, Lucae, S, Martin, N G, Mayoral-Cleries, F, McElroy, S L, McIntosh, A M, McKay, J D, McQuillin, A, Medland, S E, Middeldorp, C M, Milaneschi, Y, Mitchell, P B, Montgomery, G W, Morken, G, Mors, O, Mühleisen, T W, Müller-Myhsok, B, Myers, R M, Nievergelt, C M, Nurnberger, J I, O'Donovan, M C, Loohuis, L M O, Ophoff, R, Oruc, L, Owen, M J, Paciga, S A, Penninx, B W J H, Perry, A, Pfennig, A, Potash, J B, Preisig, M, Reif, A, Rivas, F, Rouleau, G A, Schofield, P R, Schulze, T G, Schwarz, M, Scott, L, Sinnamon, G C B, Stahl, E A, Strauss, J, Turecki, G, Van der Auwera, S, Vedder, H, Vincent, J B, Willemsen, G, Witt, C C, Wray, N R, Xi, H S, Tadic, A, Dahmen, N, Schott, B H, Cichon, S, Nöthen, M M, Ripke, S, Mobascher, A, Rujescu, D, Lieb, K, Roepke, S, Schmahl, C, Bohus, M, Rietschel, M
Publicado 2017