Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Article
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De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophreniaRees, Elliott ; Han, Jun ; Morgan, Joanne ; Carrera, Noa ; Escott-Price, Valentina ; Pocklington, Andrew J ; Duffield, Madeleine ; Hall, Lynsey S ; Legge, Sophie E ; Pardiñas, Antonio F ; Richards, Alexander L ; Roth, Julian ; Lezheiko, Tatyana ; Kondratyev, Nikolay ; Kaleda, Vasilii ; Golimbet, Vera ; Parellada, Mara ; González-Peñas, Javier ; Arango, Celso ; Gawlik, Micha ; Kirov, George ; Walters, James T R ; Holmans, Peter ; O'Donovan, Michael C ; Owen, Michael JNature neuroscience, 2020-02, Vol.23 (2), p.179-184 [Peer Reviewed Journal]United States: Nature Publishing GroupFull text available |
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2 |
Material Type: Article
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Antipsychotics in routine treatment are minor contributors to QT prolongation compared to genetics and ageHommers, Leif ; Scherf-Clavel, Maike ; Stempel, Roberta ; Roth, Julian ; Falter, Matthias ; Deckert, Jürgen ; Mattheisen, Manuel ; Unterecker, Stefan ; Gawlik, MichaJournal of psychopharmacology (Oxford), 2021-09, Vol.35 (9), p.1127-1133 [Peer Reviewed Journal]London, England: SAGE PublicationsFull text available |
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3 |
Material Type: Article
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Use of Complementary and Alternative Medicine in Patients with Primary Immunodeficiency: a Multicentric Analysis of 101 PatientsHarasim, Anna S. ; Krone, Manuel ; Tony, Hans-Peter ; Gawlik, Micha ; Witte, Torsten ; Joos, Stefanie ; Gernert, Michael ; Schmalzing, Marc ; Morbach, Henner ; Schwaneck, Eva C.Journal of clinical immunology, 2021-04, Vol.41 (3), p.585-594 [Peer Reviewed Journal]New York: Springer USFull text available |
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4 |
Material Type: Article
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The role of Pannexin gene variants in schizophrenia: systematic analysis of phenotypesGawlik, Micha ; Wagner, Martin ; Pfuhlmann, Bruno ; Stöber, GeraldEuropean archives of psychiatry and clinical neuroscience, 2016-08, Vol.266 (5), p.433-437 [Peer Reviewed Journal]Berlin/Heidelberg: Springer Berlin HeidelbergFull text available |
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5 |
Material Type: Article
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Is Ankyrin a genetic risk factor for psychiatric phenotypes?Gella, Alejandro ; Segura, Mònica ; Durany, Núria ; Pfuhlmann, Bruno ; Stöber, Gerald ; Gawlik, MichaBMC psychiatry, 2011-06, Vol.11 (1), p.103-103, Article 103 [Peer Reviewed Journal]England: BioMed Central LtdFull text available |
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6 |
Material Type: Article
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The DAOA/G30 locus and affective disorders: haplotype based association study in a polydiagnostic approachGawlik, Micha ; Wehner, Ingeborg ; Mende, Meinhard ; Jung, Sven ; Pfuhlmann, Bruno ; Knapp, Michael ; Stöber, GeraldBMC psychiatry, 2010-07, Vol.10 (1), p.59-59, Article 59 [Peer Reviewed Journal]England: BioMed Central LtdFull text available |
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7 |
Material Type: Article
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Is FKBP5 a genetic marker of affective psychosis? A case control study and analysis of disease related traitsGawlik, Micha ; Moller-Ehrlich, Kerstin ; Mende, Meinhard ; Jovnerovski, Michael ; Jung, Sven ; Jabs, Burkhard ; Knapp, Michael ; Stoeber, GeraldBMC psychiatry, 2006-11, Vol.6 (1), p.52-52, Article 52 [Peer Reviewed Journal]England: BioMed Central LtdFull text available |
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8 |
Material Type: Article
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ZDHHC8 as a candidate gene for schizophrenia: analysis of a putative functional intronic marker in case-control and family-based association studiesFaul, Thomas ; Gawlik, Micha ; Bauer, Martin ; Jung, Sven ; Pfuhlmann, Bruno ; Jabs, Burkhard ; Knapp, Michael ; Stöber, GeraldBMC psychiatry, 2005-10, Vol.5 (1), p.35-35 [Peer Reviewed Journal]England: BioMed Central LtdFull text available |
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9 |
Material Type: Article
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Wernicke-Kleist-Leonhard phenotypes of endogenous psychoses: a review of their validityFoucher, Jack R. ; Gawlik, Micha ; Roth, Julian N. ; de Crespin de Billy, Clément ; Jeanjean, Ludovic C. ; Obrecht, Alexandre ; Mainberger, Olivier ; Clauss, Julie M. E. ; Elowe, Julien ; Weibel, Sébastien ; Schorr, Benoit ; Cetkovich, Marcelo ; Morra, Carlos ; Rebok, Federico ; Ban, Thomas A. ; Bollmann, Barbara ; Roser, Mathilde M. ; Hanke, Markus S. ; Jabs, Burkhard E. ; Franzek, Ernst J. ; Berna, Fabrice ; Pfuhlmann, BrunoDialogues in clinical neuroscience, 2020-03, Vol.22 (1), p.37-49France: Taylor & FrancisFull text available |
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10 |
Material Type: Article
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Systematic mutation analysis of KIAA0767 and KIAA1646 in chromosome 22q-linked periodic catatoniaStöber, Gerald ; Kohlmann, Bernd ; Iekiera, Markus ; Rubie, Claudia ; Gawlik, Micha ; Möller-Ehrlich, Kerstin ; Meitinger, Thomas ; Bettecken, ThomasBMC psychiatry, 2005-10, Vol.5 (1), p.36-36, Article 36 [Peer Reviewed Journal]England: BioMed Central LtdFull text available |