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ArticlesPeer ReviewedFull Text
Common and rare variant analysis in early-onset bipolar disorder vulnerability
Author / Creator:Jamain, Stéphane ; Cichon, Sven ; Etain, Bruno ; Mühleisen, Thomas W ; Georgi, Alexander ; Zidane, Nora ; Chevallier, Lucie ; Deshommes, Jasmine ; Nicolas, Aude ; Henrion, Annabelle ; Degenhardt, Franziska ; Mattheisen, Manuel ; Priebe, Lutz ; Mathieu, Flavie ; Kahn, Jean-Pierre ; Henry, Chantal ; Boland, Anne ; Zelenika, Diana ; Gut, Ivo ; Heath, Simon ; Lathrop, Mark ; Maier, Wolfgang ; Albus, Margot ; Rietschel, Marcella ; Schulze, Thomas G ; McMahon, Francis J ; Kelsoe, John R ; Hamshere, Marian ; Craddock, Nicholas ; Nöthen, Markus M ; Bellivier, Frank ; Leboyer, Marion
Publisher:United States: Public Library of Science
Journal title:PloS one, 2014-08, Vol.9 (8), p.e104326-e104326
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Copy number variants in German patients with schizophrenia
Author / Creator:Priebe, Lutz ; Degenhardt, Franziska ; Strohmaier, Jana ; Breuer, René ; Herms, Stefan ; Witt, Stephanie H ; Hoffmann, Per ; Kulbida, Rebecca ; Mattheisen, Manuel ; Moebus, Susanne ; Meyer-Lindenberg, Andreas ; Walter, Henrik ; Mössner, Rainald ; Nenadic, Igor ; Sauer, Heinrich ; Rujescu, Dan ; Maier, Wolfgang ; Rietschel, Marcella ; Nöthen, Markus M ; Cichon, Sven
Publisher:United States: Public Library of Science
Journal title:PloS one, 2013-07, Vol.8 (7), p.e64035-e64035
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A Genome-Wide Association Study Suggests Novel Loci Associated with a Schizophrenia-Related Brain-Based Phenotype
Author / Creator:Hass, Johanna ; Walton, Esther ; Kirsten, Holger ; Liu, Jingyu ; Priebe, Lutz ; Wolf, Christiane ; Karbalai, Nazanin ; Gollub, Randy ; White, Tonya ; Roessner, Veit ; Müller, Kathrin U ; Paus, Tomas ; Smolka, Michael N ; Schumann, Gunter ; Scholz, Markus ; Cichon, Sven ; Calhoun, Vince ; Ehrlich, Stefan
Publisher:United States: Public Library of Science
Journal title:PloS one, 2013-06, Vol.8 (6), p.e64872-e64872
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Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia
Author / Creator:Forstner, Andreas J., MD ; Basmanav, F. Buket, MSc ; Mattheisen, Manuel, MD ; GROUP Investigators, MSc ; Böhmer, Anne C., PhD ; Hollegaard, Mads V., BAS ; Janson, Esther, MSc ; Strengman, Eric, MSc ; Priebe, Lutz, MD ; Degenhardt, Franziska, PhD ; Hoffmann, Per, MSc ; Herms, Stefan, MD ; Maier, Wolfgang, MD ; Mössner, Rainald, MD ; Rujescu, Dan, PhD ; Ophoff, Roel A., PhD ; Moebus, Susanne, MD, DMSc ; Mortensen, Preben B., MD, PhD ; Børglum, Anders D., MD, DSc ; Hougaard, David M., MSc ; Frank, Josef, PhD ; Witt, Stephanie H., MD ; Rietschel, Marcella, PhD ; Zimmer, Andreas, MD ; Nöthen, Markus M., PhD ; Miró, Xavier, PhD ; Cichon, Sven
Publisher:Ottawa, ON: Canadian Medical Association
Journal title:Journal of psychiatry & neuroscience, 2014-11, Vol.39 (6), p.386-396
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Genome-wide association study reveals two new risk loci for bipolar disorder
Author / Creator:Mühleisen, Thomas W. ; Leber, Markus ; Schulze, Thomas G. ; Strohmaier, Jana ; Degenhardt, Franziska ; Treutlein, Jens ; Mattheisen, Manuel ; Forstner, Andreas J. ; Schumacher, Johannes ; Breuer, René ; Meier, Sandra ; Herms, Stefan ; Hoffmann, Per ; Lacour, André ; Witt, Stephanie H. ; Reif, Andreas ; Müller-Myhsok, Bertram ; Lucae, Susanne ; Maier, Wolfgang ; Schwarz, Markus ; Vedder, Helmut ; Kammerer-Ciernioch, Jutta ; Pfennig, Andrea ; Bauer, Michael ; Hautzinger, Martin ; Moebus, Susanne ; Priebe, Lutz ; Czerski, Piotr M. ; Hauser, Joanna ; Lissowska, Jolanta ; Szeszenia-Dabrowska, Neonila ; Brennan, Paul ; McKay, James D. ; Wright, Adam ; Mitchell, Philip B. ; Fullerton, Janice M. ; Schofield, Peter R. ; Montgomery, Grant W. ; Medland, Sarah E. ; Gordon, Scott D. ; Martin, Nicholas G. ; Krasnow, Valery ; Chuchalin, Alexander ; Babadjanova, Gulja ; Pantelejeva, Galina ; Abramova, Lilia I. ; Tiganov, Alexander S. ; Polonikov, Alexey ; Khusnutdinova, Elza ; Alda, Martin ; Grof, Paul ; Rouleau, Guy A. ; Turecki, Gustavo ; Laprise, Catherine ; Rivas, Fabio ; Mayoral, Fermin ; Kogevinas, Manolis ; Grigoroiu-Serbanescu, Maria ; Propping, Peter ; Becker, Tim ; Rietschel, Marcella ; Nöthen, Markus M. ; Cichon, Sven
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2014-03, Vol.5 (1), p.3339, Article 3339
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Homozygosity mapping in 64 Syrian consanguineous families with non-specific intellectual disability reveals 11 novel loci and high heterogeneity
Author / Creator:Abou Jamra, R ; Wohlfart, Sigrun ; Zweier, Markus ; Uebe, Steffen ; Priebe, Lutz ; Ekici, Arif ; Giesebrecht, Susanne ; Abboud, Ahmad ; Al Khateeb, Mohammed Ayman ; Fakher, Mahmoud ; Hamdan, Saber ; Ismael, Amina ; Muhammad, Safia ; Nöthen, Markus M ; Schumacher, Johannes ; Reis, André
Publisher:Cham: Springer International Publishing
Journal title:European journal of human genetics : EJHG, 2011-11, Vol.19 (11), p.1161-1166
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DNA methylation signature in peripheral blood reveals distinct characteristics of human X chromosome numerical aberrations
Author / Creator:Sharma, Amit ; Jamil, Muhammad Ahmer ; Nuesgen, Nicole ; Schreiner, Felix ; Priebe, Lutz ; Hoffmann, Per ; Herns, Stefan ; Nöthen, Markus M ; Fröhlich, Holger ; Oldenburg, Johannes ; Woelfle, Joachim ; El-Maarri, Osman
Publisher:Germany: BioMed Central Ltd
Journal title:Clinical epigenetics, 2015-07, Vol.7 (1), p.76-76, Article 76
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Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder
Author / Creator:Priebe, L ; Degenhardt, F A ; Herms, S ; Haenisch, B ; Mattheisen, M ; Nieratschker, V ; Weingarten, M ; Witt, S ; Breuer, R ; Paul, T ; Alblas, M ; Moebus, S ; Lathrop, M ; Leboyer, M ; Schreiber, S ; Grigoroiu-Serbanescu, M ; Maier, W ; Propping, P ; Rietschel, M ; Nöthen, M M ; Cichon, S ; Mühleisen, T W
Publisher:London: Nature Publishing Group UK
Journal title:Molecular psychiatry, 2012-04, Vol.17 (4), p.421-432
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Autosomal-dominant non-syndromic anal atresia: sequencing of candidate genes, array-based molecular karyotyping, and review of the literature
Author / Creator:Schramm, Charlotte ; Draaken, Markus ; Tewes, Gabriel ; Bartels, Enrika ; Schmiedeke, Eberhard ; Märzheuser, Stefanie ; Grasshoff-Derr, Sabine ; Hosie, Stuart ; Holland-Cunz, Stefan ; Priebe, Lutz ; Kreiß-Nachtsheim, Martina ; Hoffmann, Per ; Aretz, Stefan ; Nöthen, Markus M. ; Reutter, Heiko ; Ludwig, Michael
Publisher:Berlin/Heidelberg: Springer-Verlag
Journal title:European journal of pediatrics, 2011-06, Vol.170 (6), p.741-746
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Homozygosity mapping in 64 Syrian consanguineous families with non-syndromic intellectual disability reveals 11 novel loci and high heterogeneity
Author / Creator:Abou Jamra, Rami ; Wohlfart, Sigrun ; Zweier, Markus ; Uebe, Steffen ; Priebe, Lutz ; Ekici, Arif B ; Giesebrecht, Susanne ; Abboud, Ahmad ; Al-Khateeb, Muhammad Ayman ; Fakher, Mahmoud ; Hamdan, Saber ; Ismael, Amina ; Muhammad, Safia ; Nöthen, Markus ; Schumacher, Johannes ; Reis, Andre
Publisher:Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2011-06
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A Genome-Wide Association Study Suggests Novel Loci Associated with a Schizophrenia-Related Brain-Based Phenotype. e64872
Author / Creator:Hass, Johanna ; Walton, Esther ; Kirsten, Holger ; Liu, Jingyu ; Priebe, Lutz ; Wolf, Christiane ; Karbalai, Nazanin ; Gollub, Randy ; White, Tonya ; Roessner, Veit
Journal title:PloS one, 2013-06, Vol.8 (6)
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ReportsFull Text
Investigation of the involvement of mir185 and its target genes in the development of schizophrenia
Author / Creator:Forstner, Andreas J ; Basmanav, F. Buket ; Mattheisen, Manuel ; Bohmer, Anne C ; Hollegaard, Mads V ; Janson, Esther ; Strengman, Eric ; Priebe, Lutz ; Degenhardt, Franziska ; Hoffmann, Per ; Herms, Stefan ; Maier, Wolfgang ; Mossner, Rainald ; Rujescu, Dan ; Ophoff, Roel A ; Moebus, Susanne ; Mortensen, Preben B ; Borglum, Anders D ; Hougaard, David M ; Frank, Josef ; Witt, Stephanie H ; Rietschel, Marcella ; Zimmer, Andreas ; Nothen, Markus M ; Miro, Xavier ; Cichon, Sven
Publisher:Joule Inc
Journal title:Journal of Psychiatry and Neuroscience, 2014, Vol.39 (6), p.386
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ReportsFull Text
Investigation of the involvement of mir185 and its target genes in the development of schizophrenia
Author / Creator:Forstner, Andreas J ; Basmanav, F. Buket ; Mattheisen, Manuel ; Bohmer, Anne C ; Hollegaard, Mads V ; Janson, Esther ; Strengman, Eric ; Priebe, Lutz ; Degenhardt, Franziska ; Hoffmann, Per ; Herms, Stefan ; Maier, Wolfgang ; Mossner, Rainald ; Rujescu, Dan ; Ophoff, Roel A ; Moebus, Susanne ; Mortensen, Preben B ; Borglum, Anders D ; Hougaard, David M ; Frank, Josef ; Witt, Stephanie H ; Rietschel, Marcella ; Zimmer, Andreas ; Nothen, Markus M ; Miro, Xavier ; Cichon, Sven
Publisher:Joule Inc
Journal title:Journal of Psychiatry and Neuroscience, 2014, Vol.39 (6), p.386
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ReportsFull Text
A Genome-Wide Association Study Suggests Novel Loci Associated with a Schizophrenia-Related Brain-Based Phenotype
Author / Creator:Hass, Johanna ; Walton, Esther ; Kirsten, Holger ; Liu, Jingyu ; Priebe, Lutz ; Wolf, Christiane ; Karbalai, Nazanin ; Gollub, Randy ; White, Tonya ; Roessner, Veit ; Müller, Kathrin U ; Paus, Tomas ; Smolka, Michael N ; Schumann, Gunter ; Scholz, Markus ; Cichon, Sven ; Calhoun, Vince ; Ehrlich, Stefan
Publisher:Public Library of Science
Journal title:PLoS ONE, 2013, Vol.8 (6), p.e64872
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ReportsFull Text
Copy Number Variants in German Patients with Schizophrenia
Author / Creator:Priebe, Lutz ; Degenhardt, Franziska ; Strohmaier, Jana ; Breuer, René ; Herms, Stefan ; Witt, Stephanie H ; Hoffmann, Per ; Kulbida, Rebecca ; Mattheisen, Manuel ; Moebus, Susanne ; Meyer-Lindenberg, Andreas ; Walter, Henrik ; Mössner, Rainald ; Nenadic, Igor ; Sauer, Heinrich ; Rujescu, Dan ; Maier, Wolfgang ; Rietschel, Marcella ; Nöthen, Markus M ; Cichon, Sven
Publisher:Public Library of Science
Journal title:PLoS ONE, 2013, Vol.8 (7), p.e64035
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Common and rare variant analysis in early-onset bipolar disorder vulnerability

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Copy number variants in German patients with schizophrenia

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A Genome-Wide Association Study Suggests Novel Loci Associated with a Schizophrenia-Related Brain-Based Phenotype

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Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia

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Genome-wide association study reveals two new risk loci for bipolar disorder

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Homozygosity mapping in 64 Syrian consanguineous families with non-specific intellectual disability reveals 11 novel loci and high heterogeneity

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DNA methylation signature in peripheral blood reveals distinct characteristics of human X chromosome numerical aberrations

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Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder

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Autosomal-dominant non-syndromic anal atresia: sequencing of candidate genes, array-based molecular karyotyping, and review of the literature

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Homozygosity mapping in 64 Syrian consanguineous families with non-syndromic intellectual disability reveals 11 novel loci and high heterogeneity

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A Genome-Wide Association Study Suggests Novel Loci Associated with a Schizophrenia-Related Brain-Based Phenotype. e64872

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Investigation of the involvement of mir185 and its target genes in the development of schizophrenia

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Investigation of the involvement of mir185 and its target genes in the development of schizophrenia

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A Genome-Wide Association Study Suggests Novel Loci Associated with a Schizophrenia-Related Brain-Based Phenotype

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Copy Number Variants in German Patients with Schizophrenia

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