Works matching AU Cichon, Sven

Results: 99

Efficient Strategy for Detecting Gene × Gene Joint Action and Its Application in Schizophrenia.

Published in:

Genetic Epidemiology, 2014, v. 38, n. 1, p. 60, doi. 10.1002/gepi.21779

By:

Won, Sungho;
Kwon, Min‐Seok;
Mattheisen, Manuel;
Park, Suyeon;
Park, Changsoon;
Kihara, Daisuke;
Cichon, Sven;
Ophoff, Roel;
Nöthen, Markus M.;
Rietschel, Marcella;
Baur, Max;
Uitterlinden, Andre G.;
Hofmann, A.;
Lange, Christoph

Publication type:

Article

Haplotype interaction analysis of unlinked regions.

Published in:

Genetic Epidemiology, 2005, v. 29, n. 4, p. 313, doi. 10.1002/gepi.20096

By:

Becker, Tim;
Schumacher, Johannes;
Cichon, Sven;
Baur, Max P.;
Knapp, Michael

Publication type:

Article

Recessive SERPING1 Variant Leads to Kinin–Kallikrein System Control Failure in a Consanguineous Brazilian Family with Hereditary Angioedema.

Published in:

Journal of Clinical Medicine, 2023, v. 12, n. 23, p. 7299, doi. 10.3390/jcm12237299

By:

Maia, Luana Sella Motta;
Burger, Bettina;
Ghannam, Arije;
Nunes, Fernanda Leonel;
Ferriani, Mariana Paes Leme;
Dias, Marina Mendonça;
Arruda, Luisa Karla;
Drouet, Christian;
Cichon, Sven

Publication type:

Article

Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorder.

Published in:

Translational Psychiatry, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41398-018-0175-x

By:

Hughes, Timothy;
Sønderby, Ida E.;
Polushina, Tatiana;
Hansson, Lars;
Holmgren, Asbjørn;
Athanasiu, Lavinia;
Melbø-Jørgensen, Christian;
Hassani, Sahar;
Hoeffding, Louise K.;
Herms, Stefan;
Bergen, Sarah E.;
Karlsson, Robert;
Song, Jie;
Rietschel, Marcella;
Nöthen, Markus M.;
Forstner, Andreas J.;
Hoffmann, Per;
Hultman, Christina M.;
Landén, Mikael;
Cichon, Sven

Publication type:

Article

Brief Report: No Association Between Premorbid Adjustment in Adult-Onset Schizophrenia and Genetic Variation in Dysbindin.

Published in:

Journal of Autism & Developmental Disorders, 2008, v. 38, n. 10, p. 1977, doi. 10.1007/s10803-008-0582-6

By:

Schirmbeck, Frederike;
Georgi, Alexander;
Strohmaier, Jana;
Schmael, Christine;
Boesshenz, Katja V.;
Mühleisen, Thomas W.;
Herms, Stefan;
Hoffmann, Per;
Jamra, Rami Abou;
Schumacher, Johannes;
Maier, Wolfgang;
Propping, Peter;
Nöthen, Markus M.;
Cichon, Sven;
Rietschel, Marcella;
Schulze, Thomas G.

Publication type:

Article

Integration of transcriptomic and cytoarchitectonic data implicates a role for MAOA and TAC1 in the limbic-cortical network.

Published in:

Brain Structure & Function, 2018, v. 223, n. 5, p. 2335, doi. 10.1007/s00429-018-1620-6

By:

Bludau, Sebastian;
Mühleisen, Thomas W.;
Eickhoff, Simon B.;
Hawrylycz, Michael J.;
Cichon, Sven;
Amunts, Katrin

Publication type:

Article

Genetics of structural connectivity and information processing in the brain.

Published in:

Brain Structure & Function, 2016, v. 221, n. 9, p. 4643, doi. 10.1007/s00429-016-1194-0

By:

Giddaluru, Sudheer;
Espeseth, Thomas;
Salami, Alireza;
Westlye, Lars;
Lundquist, Anders;
Christoforou, Andrea;
Cichon, Sven;
Adolfsson, Rolf;
Steen, Vidar;
Reinvang, Ivar;
Nilsson, Lars;
Hellard, Stéphanie;
Nyberg, Lars

Publication type:

Article

Efficacy and safety of exogenous ketone bodies for preventive treatment of migraine: A study protocol for a single-centred, randomised, placebo-controlled, double-blind crossover trial.

Published in:

2019

By:

Gross, Elena;
Putananickal, Niveditha;
Orsini, Anna-Lena;
Schmidt, Simone;
Vogt, Deborah R.;
Cichon, Sven;
Sandor, Peter;
Fischer, Dirk

Publication type:

journal article

Large recurrent microdeletions associated with schizophrenia.

Published in:

Nature, 2008, v. 455, n. 7210, p. 232, doi. 10.1038/nature07229

By:

Stefansson, Hreinn;
Rujescu, Dan;
Cichon, Sven;
Pietiläinen, Olli P. H.;
Ingason, Andres;
Steinberg, Stacy;
Fossdal, Ragnheidur;
Sigurdsson, Engilbert;
Sigmundsson, Thordur;
Buizer-Voskamp, Jacobine E.;
Hansen, Thomas;
Jakobsen, Klaus D.;
Muglia, Pierandrea;
Francks, Clyde;
Matthews, Paul M.;
Gylfason, Arnaldur;
Halldorsson, Bjarni V.;
Gudbjartsson, Daniel;
Thorgeirsson, Thorgeir E.;
Sigurdsson, Asgeir

Publication type:

Article

Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics.

Published in:

International Journal of Bipolar Disorders, 2018, v. 6, n. 1, p. 1, doi. 10.1186/s40345-018-0132-x

By:

Breuer, René;
Mattheisen, Manuel;
Frank, Josef;
Krumm, Bertram;
Treutlein, Jens;
Kassem, Layla;
Strohmaier, Jana;
Herms, Stefan;
Mühleisen, Thomas W.;
Degenhardt, Franziska;
Cichon, Sven;
Nöthen, Markus M.;
Karypis, George;
Kelsoe, John;
Greenwood, Tiffany;
Nievergelt, Caroline;
Shilling, Paul;
Shekhtman, Tatyana;
Edenberg, Howard;
Craig, David

Publication type:

Article

Imaging genetics of FOXP2 in dyslexia.

Published in:

European Journal of Human Genetics, 2012, v. 20, n. 6, p. 714, doi. 10.1038/ejhg.2012.31

By:

Wilcke, Arndt;
Jana Burkhardt, Carolin Ligges;
Alexander, Michael;
Wolf, Christiane;
Quente, Elfi;
Ahnert, Peter;
Hoffmann, Per;
Becker, Albert;
Müller-Myhsok, Bertram;
Cichon, Sven;
Boltze, Johannes;
Kirsten, Holger

Publication type:

Article

Imaging genetics of FOXP2 in dyslexia.

Published in:

European Journal of Human Genetics, 2012, v. 20, n. 2, p. 224, doi. 10.1038/ejhg.2011.160

By:

Wilcke, Arndt;
Ligges, Carolin;
Burkhardt, Jana;
Alexander, Michael;
Wolf, Christiane;
Quente, Elfi;
Ahnert, Peter;
Hoffmann, Per;
Becker, Albert;
Müller-Myhsok, Bertram;
Cichon, Sven;
Boltze, Johannes;
Kirsten, Holger

Publication type:

Article

A summary statistic approach to sequence variation in noncoding regions of six schizophrenia-associated gene loci.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 9, p. 1037, doi. 10.1038/sj.ejhg.5201664

By:

Winantea, Jane;
Hoang, My Ngo;
Ohlraun, Stefanie;
Rietschel, Marcella;
Cichon, Sven;
Propping, Peter;
Nöthen, Markus M.;
Freudenberg, Jan;
Freudenberg-Hua, Yun

Publication type:

Article

Genome-wide association study identifies five new schizophrenia loci.

Published in:

Nature Genetics, 2011, v. 43, n. 10, p. 969, doi. 10.1038/ng.940

By:

Ripke, Stephan;
Sanders, Alan R;
Kendler, Kenneth S;
Levinson, Douglas F;
Sklar, Pamela;
Holmans, Peter A;
Lin, Dan-Yu;
Duan, Jubao;
Ophoff, Roel A;
Andreassen, Ole A;
Scolnick, Edward;
Cichon, Sven;
St. Clair, David;
Corvin, Aiden;
Gurling, Hugh;
Werge, Thomas;
Rujescu, Dan;
Blackwood, Douglas H R;
Pato, Carlos N;
Malhotra, Anil K

Publication type:

Article

Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4.

Published in:

Nature Genetics, 2011, v. 43, n. 10, p. 977, doi. 10.1038/ng.943

By:

Sklar, Pamela;
Ripke, Stephan;
Scott, Laura J;
Andreassen, Ole A;
Cichon, Sven;
Craddock, Nick;
Edenberg, Howard J;
Nurnberger, John I;
Rietschel, Marcella;
Blackwood, Douglas;
Corvin, Aiden;
Flickinger, Matthew;
Guan, Weihua;
Mattingsdal, Morten;
McQuillin, Andrew;
Kwan, Phoenix;
Wienker, Thomas F;
Daly, Mark;
Dudbridge, Frank;
Holmans, Peter A

Publication type:

Article

Reply to 'Replication of association of 3p21.1 with susceptibility to bipolar disorder but not major depression'.

Published in:

2011

By:

McMahon, Francis J.;
Akula, Nirmala;
Cichon, Sven;
Detera-Wadleigh, Sevilla D.;
Edenberg, Howard;
Holsboer, Florian;
Nöthen, Markus M.;
Nurnberger, John I.;
Potash, James;
Preisig, Martin;
Rietschel, Marcella;
Schulze, Thomas G.

Publication type:

Letter

Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1.

Published in:

Nature Genetics, 2010, v. 42, n. 2, p. 128, doi. 10.1038/ng.523

By:

McMahon, Francis J.;
Akula, Nirmala;
Schulze, Thomas G.;
Muglia, Pierandrea;
Tozzi, Federica;
Detera-Wadleigh, Sevilla D.;
Steele, C. J. M.;
Breuer, René;
Strohmaier, Jana;
Wendland, Jens R.;
Mattheisen, Manuel;
Mühleisen, Thomas W.;
Maier, Wolfgang;
Nöthen, Markus M.;
Cichon, Sven;
Farmer, Anne;
Vincent, John B.;
Holsboer, Florian;
Preisig, Martin;
Rietschel, Marcella

Publication type:

Article

CLCN2 variants in idiopathic generalized epilepsy.

Published in:

2009

By:

Kleefuß-Lie, Ailing;
Friedl, Waltraut;
Cichon, Sven;
Haug, Karsten;
Warnstedt, Maike;
Alekov, Alexi;
Sander, Thomas;
Ramirez, Alfredo;
Poser, Barbara;
Maljevic, Snezana;
Hebeisen, Simon;
Kubisch, Christian;
Rebstock, Johannes;
Horvath, Steve;
Hallmann, Kerstin;
Dullinger, Jörn S.;
Rau, Birgit;
Haverkamp, Fritz;
Beyenburg, Stefan;
Schulz, Herbert

Publication type:

Letter

Corrigendum: Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis.

Published in:

2009

By:

Wen, Yaran;
Liu, Yang;
Xu, Yiming;
Zhao, Yiwei;
Hua, Rui;
Wang, Kaibo;
Sun, Miao;
Li, Yuanhong;
Yang, Sen;
Zhang, Xue-Jun;
Kruse, Roland;
Cichon, Sven;
Betz, Regina C;
Nöthen, Markus M;
van Steensel, Maurice A M;
van Geel, Michel;
Steijlen, Peter M;
Hohl, Daniel;
Huber, Marcel;
Dunnill, Giles S

Publication type:

Correction Notice

Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis.

Published in:

Nature Genetics, 2009, v. 41, n. 2, p. 228, doi. 10.1038/ng.276

By:

Yaran Wen;
Yang Liu;
Yiming Xu;
Yiwei Zhao;
Rui Hua;
Kaibo Wang;
Miao Sun;
Yuanhong Li;
Sen Yang;
Xue-Jun Zhang;
Kruse, Roland;
Cichon, Sven;
Betz, Regina C.;
Nöthen, Markus M.;
van Steensel, Maurice A. M.;
van Geel, Michel;
Steijlen, Peter M.;
Hohl, Daniel;
Huber, Marcel;
Dunnill, Giles S.

Publication type:

Article

Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin.

Published in:

2004

By:

Cichon, Sven;
Buervenich, Silvia;
Kirov, George;
Akula, Nirmala;
Dimitrova, Albena;
Green, Elaine;
Schumacher, Johannes;
Klopp, Norman;
Becker, Tim;
Ohlraun, Stephanie;
Schulze, Thomas G.;
Tullius, Monja;
Gross, Magdalena M.;
Jones, Lisa;
Krastev, Stefan;
Nikolov, Ivan;
Hamshere, Marian;
Jones, Ian;
Czerski, Piotr M.;
Leszczynska-Rodziewicz, Anna

Publication type:

Letter

Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin.

Published in:

Nature Genetics, 2003, v. 34, n. 2, p. 151, doi. 10.1038/ng1163

By:

Levy-Nissenbaum, Etgar;
Betz, Regina C;
Frydman, Moshe;
Simon, Michel;
Lahat, Hadas;
Bakhan, Tengiz;
Goldman, Boleslaw;
Bygum, Anette;
Pierick, Monika;
Hillmer, Axel M;
Jonca, Nathalie;
Toribio, Jaime;
Kruse, Roland;
Dewald, Georg;
Cichon, Sven;
Kubisch, Christian;
Guerrin, Marina;
Serre, Guy;
Nothen, Markus M

Publication type:

Article

Feasible and Successful: Genome-Wide Interaction Analysis Involving All 1.9 × 10 Pair-Wise Interaction Tests.

Published in:

Human Heredity, 2010, v. 69, n. 4, p. 268, doi. 10.1159/000295896

By:

Steffens, Michael;
Becker, Tim;
Sander, Thomas;
Fimmers, Rolf;
Herold, Christine;
Holler, Daniela A.;
Leu, Costin;
Herms, Stefan;
Cichon, Sven;
Bohn, Bastian;
Gerstner, Thomas;
Griebel, Michael;
Nöthen, Markus M.;
Wienker, Thomas F.;
Baur, Max P.

Publication type:

Article

Distinct Conditions Support a Novel Classification for Bradykinin-Mediated Angio-Oedema.

Published in:

Dermatology (10188665), 2015, v. 230, n. 4, p. 324, doi. 10.1159/000371814

By:

Dessart, Panteha;
Defendi, Federica;
Humeau, Hélène;
Nicolie, Brigitte;
Sarre, Marie-Elodie;
Charignon, Delphine;
Ponard, Denise;
Cichon, Sven;
Drouet, Christian;
Martin, Ludovic

Publication type:

Article

Altered Functional Subnetwork During Emotional Face Processing: A Potential Intermediate Phenotype for Schizophrenia.

Published in:

2016

By:

Hengyi Cao;
Bertolino, Alessandro;
Walter, Henrik;
Schneider, Michael;
Schafer, Axel;
Taurisano, Paolo;
Blasi, Giuseppe;
Haddad, Leila;
Grimm, Oliver;
Otto, Kristina;
Dixson, Luanna;
Erk, Susanne;
Mohnke, Sebastian;
Heinz, Andreas;
Romanczuk-Seiferth, Nina;
Muhleisen, Thomas W.;
Mattheisen, Manuel;
Witt, Stephanie H.;
Cichon, Sven;
Noethen, Markus

Publication type:

journal article

Striatal response to reward anticipation: evidence for a systems-level intermediate phenotype for schizophrenia.

Published in:

2014

By:

Grimm, Oliver;
Heinz, Andreas;
Walter, Henrik;
Kirsch, Peter;
Erk, Susanne;
Haddad, Leila;
Plichta, Michael M;
Romanczuk-Seiferth, Nina;
Pöhland, Lydia;
Mohnke, Sebastian;
Mühleisen, Thomas W;
Mattheisen, Manuel;
Witt, Stephanie H;
Schäfer, Axel;
Cichon, Sven;
Nöthen, Markus;
Rietschel, Marcella;
Tost, Heike;
Meyer-Lindenberg, Andreas

Publication type:

Journal Article

Striatal Response to Reward Anticipation.

Published in:

JAMA Psychiatry, 2014, v. 71, n. 5, p. 531, doi. 10.1001/jamapsychiatry.2014.9

By:

Grimm, Oliver;
Heinz, Andreas;
Walter, Henrik;
Kirsch, Peter;
Erk, Susanne;
Haddad, Leila;
Plichta, Michael M.;
Romanczuk-Seiferth, Nina;
Pöhland, Lydia;
Mohnke, Sebastian;
Mühleisen, Thomas W.;
Mattheisen, Manuel;
Witt, Stephanie H.;
Schäfer, Axel;
Cichon, Sven;
Nöthen, Markus;
Rietschel, Marcella;
Tost, Heike;
Meyer-Lindenberg, Andreas

Publication type:

Article

Implication of a rare deletion at distal 16p11.2 in schizophrenia.

Published in:

2013

By:

Guha, Saurav;
Rees, Elliott;
Darvasi, Ariel;
Ivanov, Dobril;
Ikeda, Masashi;
Bergen, Sarah E;
Magnusson, Patrik K;
Cormican, Paul;
Morris, Derek;
Gill, Michael;
Cichon, Sven;
Rosenfeld, Jeffrey A;
Lee, Annette;
Gregersen, Peter K;
Kane, John M;
Malhotra, Anil K;
Rietschel, Marcella;
Nöthen, Markus M;
Degenhardt, Franziska;
Priebe, Lutz

Publication type:

journal article

Implication of a Rare Deletion at Distal 16pll.2 in Schizophrenia.

Published in:

JAMA Psychiatry, 2013, v. 70, n. 3, p. 253, doi. 10.1001/2013.jamapsychiatry.71

By:

Guha, Saurav;
Rees, Elliott;
Darvasi, Ariel;
Ivanov, Dobril;
Ikeda, Masashi;
Bergen, Sarah E.;
Magnusson, Patrik K.;
Cormican, Paul;
Morris, Derek;
Gill, Michael;
Cichon, Sven;
Rosenfeld, Jeffrey A.;
Lee, Annette;
Gregersen, Peter K.;
Kane, John M.;
Malhotra, Anil K.;
Rietschel, Marcella;
NÖthen, Markus M.;
Degenhardt, Franziska;
Priebe, Lutz

Publication type:

Article

Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder.

Published in:

Translational Psychiatry, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41398-020-00906-2

By:

Yousaf, Afsheen;
Waltes, Regina;
Haslinger, Denise;
Klauck, Sabine M.;
Duketis, Eftichia;
Sachse, Michael;
Voran, Anette;
Biscaldi, Monica;
Schulte-Rüther, Martin;
Cichon, Sven;
Nöthen, Markus;
Ackermann, Jörg;
Koch, Ina;
Freitag, Christine M.;
Chiocchetti, Andreas G.

Publication type:

Article

SwissGenVar : A Platform for Clinical-Grade Interpretation of Genetic Variants to Foster Personalized Healthcare in Switzerland.

Published in:

Journal of Personalized Medicine, 2024, v. 14, n. 6, p. 648, doi. 10.3390/jpm14060648

By:

Kraemer, Dennis;
Terumalai, Dillenn;
Famiglietti, Maria Livia;
Filges, Isabel;
Joset, Pascal;
Koller, Samuel;
Maurer, Fabienne;
Meier, Stéphanie;
Nouspikel, Thierry;
Sanz, Javier;
Zweier, Christiane;
Abramowicz, Marc;
Berger, Wolfgang;
Cichon, Sven;
Schaller, André;
Superti-Furga, Andrea;
Barbié, Valérie;
Rauch, Anita

Publication type:

Article

Systematic Integration of Brain eQTL and GWAS Identifies ZNF323 as a Novel Schizophrenia Risk Gene and Suggests Recent Positive Selection Based on Compensatory Advantage on Pulmonary Function.

Published in:

Schizophrenia Bulletin, 2015, v. 41, n. 6, p. 1294, doi. 10.1093/schbul/sbv017

By:

Xiong-Jian Luo;
Mattheisen, Manuel;
Ming Li;
Liang Huang;
Rietschel, Marcella;
Børglum, Anders D.;
Als, Thomas D.;
van den Oord, Edwin J.;
Aberg, Karolina A.;
Mors, Ole;
Mortensen, Preben Bo;
Zhenwu Luo;
Degenhardt, Franziska;
Cichon, Sven;
Schulze, Thomas G.;
Nöthen, Markus M.;
Bing Su;
Zhongming Zhao;
Lin Gan;
Yao, Yong-Gang

Publication type:

Article

ZNF804A and Cortical Structure in Schizophrenia: In Vivo and Postmortem Studies.

Published in:

2014

By:

Schultz, Carl Christoph;
Nenadic, Igor;
Riley, Brien;
Vladimirov, Vladimir I.;
Wagner, Gerd;
Koch, Kathrin;
Schachtzabel, Claudia;
Mühleisen, Thomas W.;
Basmanav, Buket;
Nöthen, Markus M.;
Deufel, Thomas;
Kiehntopf, Michael;
Rietschel, Marcella;
Reichenbach, Jürgen R.;
Cichon, Sven;
Schlösser, Ralf G. M.;
Sauer, Heinrich

Publication type:

Journal Article

ZNF804A and Cortical Structure in Schizophrenia: In Vivo and Postmortem Studies.

Published in:

Schizophrenia Bulletin, 2014, v. 40, n. 3, p. 532, doi. 10.1093/schbul/sbt123

By:

Schultz, Carl Christoph;
Nenadic, Igor;
Riley, Brien;
Vladimirov, Vladimir I.;
Wagner, Gerd;
Koch, Kathrin;
Schachtzabel, Claudia;
Mühleisen, Thomas W.;
Basmanav, Buket;
Nöthen, Markus M.;
Deufel, Thomas;
Kiehntopf, Michael;
Rietschel, Marcella;
Reichenbach, Jürgen R.;
Cichon, Sven;
Schlösser, Ralf G. M.;
Sauer, Heinrich

Publication type:

Article

Genes and Schizophrenia: The G72/G30 Gene Locus in Psychiatric Disorders: A Challenge to Diagnostic Boundaries?

Published in:

Schizophrenia Bulletin, 2006, v. 32, n. 4, p. 599

By:

Abou Jamra, Rami;
Schmael, Christine;
Cichon, Sven;
Rietschel, Marcella;
Schumacher, Johannes;
Nöthen, Markus M.

Publication type:

Article

Untersuchung genetischer Einflüsse auf Riechstörungen bei Patienten mit hereditärem Angioödem Typ 1 und 2.

Published in:

Journal der Deutschen Dermatologischen Gesellschaft, 2021, v. 19, n. 7, p. 1060, doi. 10.1111/ddg.14417_g

By:

Förster‐Ruhrmann, Ulrike;
Pierchalla, Greta;
Stieber, Christiane;
Heilmann‐-Heimbach, Stefanie;
Cichon, Sven;
Nöthen, Markus M.;
Ellrich, André;
Olze, Heidi;
Maurer, Marcus;
Magerl, Markus

Publication type:

Article

Analysis of genetic impact on smell impairment in patients with hereditary angioedema type 1 and 2.

Published in:

Journal der Deutschen Dermatologischen Gesellschaft, 2021, v. 19, n. 7, p. 1060, doi. 10.1111/ddg.14417

By:

Förster‐Ruhrmann, Ulrike;
Pierchalla, Greta;
Stieber, Christiane;
Heilmann‐Heimbach, Stefanie;
Cichon, Sven;
Nöthen, Markus M.;
Ellrich, André;
Olze, Heidi;
Maurer, Marcus;
Magerl, Markus

Publication type:

Article

Identification of mutations in the human hairless gene in two new families with congenital atrichia.

Published in:

Archives of Dermatological Research, 2007, v. 299, n. 3, p. 157, doi. 10.1007/s00403-007-0747-8

By:

Betz, Regina C.;
Indelman, Margarita;
Pforr, Jana;
Schreiner, Felix;
Bauer, Ralf;
Bergman, Reuven;
Lentze, Michael J.;
Nöthen, Markus M.;
Cichon, Sven;
Sprecher, Eli

Publication type:

Article

A mega-analysis of genome-wide association studies for major depressive disorder.

Published in:

Molecular Psychiatry, 2013, v. 18, n. 4, p. 497, doi. 10.1038/mp.2012.21

By:

Ripke, Stephan;
Wray, Naomi R;
Lewis, Cathryn M;
Hamilton, Steven P;
Weissman, Myrna M;
Breen, Gerome;
Byrne, Enda M;
Blackwood, Douglas H R;
Boomsma, Dorret I;
Cichon, Sven;
Heath, Andrew C;
Holsboer, Florian;
Lucae, Susanne;
Madden, Pamela A F;
Martin, Nicholas G;
McGuffin, Peter;
Muglia, Pierandrea;
Noethen, Markus M;
Penninx, Brenda P;
Pergadia, Michele L

Publication type:

Article

Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5′-region are associated with bipolar affective disorder.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 1, p. 87

By:

Cichon, Sven;
Winge, Ingeborg;
Mattheisen, Manuel;
Georgi, Alexander;
Karpushova, Anna;
Freudenberg, Jan;
Freudenberg-Hua, Yun;
Babadjanova, Gulia;
Van Den Bogaert, Ann;
Abramova, Lilia I.;
Kapiletti, Sofia;
Knappskog, Per M.;
McKinney, Jeffrey;
Maier, Wolfgang;
Abou Jamra, Rami;
Schulze, Thomas G.;
Schumacher, Johannes;
Propping, Peter;
Rietschel, Marcella;
Haavik, Jan

Publication type:

Article

A genome screen for genes predisposing to bipolar affective disorder detects a new susceptibility locus on 8q.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 14, p. 1685, doi. 10.1093/hmg/11.14.1685

By:

Cichon, Sven;
Schumacher, Johannes;
Müller, Daniel J.;
Hürter, Martina;
Windemuth, Christine;
Strauch, Konstantin;
Hemmer, Susanne;
Schulze, Thomas G.;
Schmidt-Wolf, Gabriele;
Albus, Margot;
Borrmann-Hassenbach, Margitta;
Franzek, Ernst;
Lanczik, Mario;
Fritze, Jürgen;
Kreiner, Roland;
Reuner, Ulrike;
Weigelt, Bettina;
Minges, Jürgen;
Lichtermann, Dirk;
Lerer, Bernhard

Publication type:

Article

Can long-range microsatellite data be used to predict short-range linkage disequilibrium?

Published in:

Human Molecular Genetics, 2002, v. 11, n. 12, p. 1363, doi. 10.1093/hmg/11.12.1363

By:

Schulze, Thomas G.;
Chen, Yu-Sheng;
Akula, Nirmala;
Hennessy, Kathleen;
Badner, Judith A.;
McInnis, Melvin G.;
DePaulo, J. Raymond;
Schumacher, Johannes;
Cichon, Sven;
Propping, Peter;
Maier, Wolfgang;
Rietschel, Marcella;
Nöthen, Markus M.;
McMahon, Francis J.

Publication type:

Article

A genome screen for genes predisposingto bipolar affective disorder detects a new susceptibility locus on 8q.

Published in:

Human Molecular Genetics, 2001, v. 10, n. 25, p. 2933, doi. 10.1093/hmg/10.25.2933

By:

Cichon, Sven;
Schumacher, Johannes;
Müller, Daniel J.;
Windemuth, Christine;
Strauch, Konstantin;
Hemmer, Susanne;
Schulze, Thomas G.;
Schmidt-Wolf, Gabriele;
Albus, Margot;
Borrmann-Hassenbach, Margitta;
Franzek, Ernst;
Lanczik, Mario;
Fritze, Jürgen;
Kreiner, Roland;
Reuner, Ulrike;
Weigelt, Bettina;
Minges, Jürgen;
Lichtermann, Dirk;
Lerer, Bernhard;
Kanyas, Kyra

Publication type:

Article

Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 11, p. 1671, doi. 10.1093/hmg/7.11.1671

By:

Cichon, Sven;
Anker, Martina;
Vogt, Ina R.;
Rohleder, Hendrik;
Pützstück, Markus;
Hillmer, Axel;
Farooq, Sardar A.;
Al‐Dhafri, Khamis S.;
Ahmad, Mahmud;
Haque, Sayedul;
Rietschel, Marcella;
Propping, Peter;
Kruse, Roland;
Nöthen, Markus M.

Publication type:

Article

Human dopamine D4 receptor gene: frequent occurrence of a null allele and observation of homozygosity.

Published in:

Human Molecular Genetics, 1994, v. 3, n. 12, p. 2207

By:

Nöthen, Markus M.;
Cichon, Sven;
Hemmer, Susanne;
Hebebrand, Johannes;
Remschmidt, Helmut;
Lehmkuhl, Gerd;
Poustka, Fritz;
Schmidt, Martin;
Catalano, Marco;
Fimmers, Rolf;
Kömer, Judith;
Rletschel, Marcella;
Propping, Peter

Publication type:

Article

Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 2, p. 276, doi. 10.1002/ajmg.b.32402

By:

Bigdeli, Tim B.;
Ripke, Stephan;
Bacanu, Silviu‐Alin;
Lee, Sang Hong;
Wray, Naomi R.;
Gejman, Pablo V.;
Rietschel, Marcella;
Cichon, Sven;
St Clair, David;
Corvin, Aiden;
Kirov, George;
McQuillin, Andrew;
Gurling, Hugh;
Rujescu, Dan;
Andreassen, Ole A.;
Werge, Thomas;
Blackwood, Douglas H. R.;
Pato, Carlos N.;
Pato, Michele T.;
Malhotra, Anil K.

Publication type:

Article

MicroRNA hsa-miR-4717-5p regulates RGS2 and may be a risk factor for anxiety-related traits.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2015, v. 168B, n. 4, p. 296, doi. 10.1002/ajmg.b.32312

By:

Hommers, Leif;
Raab, Annette;
Bohl, Alexandra;
Weber, Heike;
Scholz, Claus‐Jürgen;
Erhardt, Angelika;
Binder, Elisabeth;
Arolt, Volker;
Gerlach, Alexander;
Gloster, Andrew;
Kalisch, Raffael;
Kircher, Tilo;
Lonsdorf, Tina;
Ströhle, Andreas;
Zwanzger, Peter;
Mattheisen, Manuel;
Cichon, Sven;
Lesch, Klaus‐Peter;
Domschke, Katharina;
Reif, Andreas

Publication type:

Article

Common Obesity Risk Alleles in Childhood Attention-Deficit/Hyperactivity Disorder.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2013, v. 162B, n. 4, p. 295, doi. 10.1002/ajmg.b.32144

By:

Albayrak, Özgür;
Pütter, Carolin;
Volckmar, Anna‐Lena;
Cichon, Sven;
Hoffmann, Per;
Nöthen, Markus M.;
Jöckel, Karl‐Heinz;
Schreiber, Stefan;
Wichmann, H‐Erich;
Faraone, Stephen V.;
Neale, Benjamin M.;
Herpertz‐Dahlmann, Beate;
Lehmkuhl, Gerd;
Sinzig, Judith;
Renner, Tobias J.;
Romanos, Marcel;
Warnke, Andreas;
Lesch, Klaus‐Peter;
Reif, Andreas;
Schimmelmann, Benno G.

Publication type:

Article

Hippocampal Function in Healthy Carriers of the CLU Alzheimer's Disease Risk Variant.

Published in:

Journal of Neuroscience, 2011, v. 31, n. 49, p. 18180, doi. 10.1523/JNEUROSCI.4960-11.2011

By:

Erk, Susanne;
Meyer-Lindenberg, Andreas;
von Boberfeld, Carola Opitz;
Esslinger, Christine;
Schnell, Knut;
Kirsch, Peter;
Mattheisen, Manuel;
Mühleisen, Thomas W.;
Cichon, Sven;
Witt, Stephanie H.;
Rietschel, Marcella;
Nöthen, Markus M.;
Walter, Henrik

Publication type:

Article

Genotype‐phenotype correlations in Brazilian patients with hereditary angioedema due to C1 inhibitor deficiency.

Published in:

2019

By:

Maia, Luana S. M.;
Moreno, Adriana S.;
Ferriani, Mariana P. L.;
Nunes, Fernanda Leonel;
Ferraro, Maria Fernanda;
Dias, Marina M.;
Roxo‐Junior, Persio;
Dias, Fabrício César;
Valle, Solange O. R.;
Levy, Soloni;
Alonso, Maria Luiza Oliva;
França, Alfeu T.;
Serpa, Faradiba Sarquis;
Motta, Antonio Abílio;
Maia, Felipe G. M.;
Aragon, Davi Casale;
Sarti, Willy;
Silva, Wilson Araújo;
Cichon, Sven;
Bork, Konrad

Publication type:

Letter to the Editor