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GENDER-SPECIFIC ASSOCIATION OF VARIANTS IN THE AKR1C1 GENE WITH DIMENSIONAL ANXIETY IN PATIENTS WITH PANIC DISORDER: ADDITIONAL EVIDENCE FOR THE IMPORTANCE OF NEUROSTEROIDS IN ANXIETY?
Published in:
Depression & Anxiety (1091-4269), 2014, v. 31, n. 10, p. 843, doi. 10.1002/da.22229
By:
- Quast, Carina;
- Reif, Andreas;
- Brückl, Tanja;
- Pfister, Hildegard;
- Weber, Heike;
- Mattheisen, Manuel;
- Cichon, Sven;
- Lang, Thomas;
- Hamm, Alfons;
- Fehm, Lydia;
- Ströhle, Andreas;
- Arolt, Volker;
- Domschke, Katharina;
- Kircher, Tilo;
- Wittchen, Hans‐Ulrich;
- Pauli, Paul;
- Gerlach, Alexander L.;
- Alpers, Georg W.;
- Deckert, Jürgen;
- Rupprecht, Rainer
Publication type:
Article
Neuregulin 3 is associated with attention deficits in schizophrenia and bipolar disorder.
Published in:
International Journal of Neuropsychopharmacology, 2013, v. 16, n. 3, p. 549, doi. 10.1017/S1461145712000697
By:
- Meier, Sandra;
- Strohmaier, Jana;
- Breuer, Rene;
- Mattheisen, Manuel;
- Degenhardt, Franziska;
- Mühleisen, Thomas W.;
- Schulze, Thomas G.;
- Nöthen, Markus M.;
- Cichon, Sven;
- Rietschel, Marcella;
- Wüst, Stefan
Publication type:
Article
Associations between antagonistic SNPs for neuropsychiatric disorders and human brain structure.
Published in:
Translational Psychiatry, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41398-024-03098-1
By:
- Federmann, Lydia M.;
- David, Friederike S.;
- Jockwitz, Christiane;
- Mühleisen, Thomas W.;
- Pelzer, Dominique I.;
- Nöthen, Markus M.;
- Caspers, Svenja;
- Amunts, Katrin;
- Goltermann, Janik;
- Andlauer, Till F. M.;
- Stein, Frederike;
- Brosch, Katharina;
- Kircher, Tilo;
- Cichon, Sven;
- Dannlowski, Udo;
- Sindermann, Lisa;
- Forstner, Andreas J.
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
Epigenetic alteration of the dopamine transporter gene in alcohol-dependent patients is associated with age.
Published in:
Addiction Biology, 2014, v. 19, n. 2, p. 305, doi. 10.1111/j.1369-1600.2012.00459.x
By:
- Nieratschker, Vanessa;
- Grosshans, Martin;
- Frank, Josef;
- Strohmaier, Jana;
- von der Goltz, Christoph;
- El‐Maarri, Osman;
- Witt, Stephanie H.;
- Cichon, Sven;
- Nöthen, Markus M.;
- Kiefer, Falk;
- Rietschel, Marcella
Publication type:
Article
Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster.
Published in:
Addiction Biology, 2012, v. 17, n. 1, p. 171, doi. 10.1111/j.1369-1600.2011.00395.x
By:
- Frank, Josef;
- Cichon, Sven;
- Treutlein, Jens;
- Ridinger, Monika;
- Mattheisen, Manuel;
- Hoffmann, Per;
- Herms, Stefan;
- Wodarz, Norbert;
- Soyka, Michael;
- Zill, Peter;
- Maier, Wolfgang;
- Mössner, Rainald;
- Gaebel, Wolfgang;
- Dahmen, Norbert;
- Scherbaum, Norbert;
- Schmäl, Christine;
- Steffens, Michael;
- Lucae, Susanne;
- Ising, Marcus;
- Müller-Myhsok, Bertram
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
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
Identification of pleiotropy at the gene level between psychiatric disorders and related traits.
Published in:
Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01530-4
By:
- Polushina, Tatiana;
- Banerjee, Niladri;
- Giddaluru, Sudheer;
- Bettella, Francesco;
- Espeseth, Thomas;
- Lundervold, Astri J.;
- Djurovic, Srdjan;
- Cichon, Sven;
- Hoffmann, Per;
- Nöthen, Markus M.;
- Steen, Vidar M.;
- Andreassen, Ole A.;
- Le Hellard, Stéphanie
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
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
Studying variability in human brain aging in a population-based German cohort—rationale and design of 1000BRAINS.
Published in:
Frontiers in Aging Neuroscience, 2014, v. 6, p. 1, doi. 10.3389/fnagi.2014.00149
By:
- Caspers, Svenja;
- Moebus, Susanne;
- Lux, Silke;
- Pundt, Noreen;
- Schütz, Holger;
- Mühleisen, Thomas W.;
- Gras, Vincent;
- Eickhoff, Simon B.;
- Romanzetti, Sandro;
- Stöcker, Tony;
- Stirnberg, Rüdiger;
- Kirlangic, Mehmet E.;
- Minnerop, Martina;
- Pieperhoff, Peter;
- Mödder, Ulrich;
- Das, Samir;
- Evans, Alan C.;
- Jöckel, Karl-Heinz;
- Erbel, Raimund;
- Cichon, Sven
Publication type:
Article
Studying variability in human brain aging in a population-based German cohort – Rationale and design of 1000BRAINS.
Published in:
Frontiers in Aging Neuroscience, 2014, v. 6, p. 1, doi. 10.3389/fnagi.2014.00149
By:
- Caspers, Svenja;
- Moebus, Susanne;
- Lux, Silke;
- Pundt, Noreen;
- Schütz, Holger;
- Mühleisen, Thomas W.;
- Gras, Vincent;
- Eickhoff, Simon B.;
- Romanzetti, Sandro;
- Stöcker, Tony;
- Stirnberg, Rüdiger;
- Kirlangic, Mehmet E.;
- Minnerop, Martina;
- Pieperhoff, Peter;
- Mödder, Ulrich;
- Das, Samir;
- Evans, Alan C.;
- Jöckel, Karl-Heinz;
- Erbel, Raimund;
- Cichon, Sven
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
Effects of copy number variations on brain structure and risk for psychiatric illness: Large‐scale studies from the ENIGMA working groups on CNVs.
Published in:
Human Brain Mapping, 2022, v. 43, n. 1, p. 300, doi. 10.1002/hbm.25354
By:
- Sønderby, Ida E.;
- Ching, Christopher R. K.;
- Thomopoulos, Sophia I.;
- van der Meer, Dennis;
- Sun, Daqiang;
- Villalon‐Reina, Julio E.;
- Agartz, Ingrid;
- Amunts, Katrin;
- Arango, Celso;
- Armstrong, Nicola J.;
- Ayesa‐Arriola, Rosa;
- Bakker, Geor;
- Bassett, Anne S.;
- Boomsma, Dorret I.;
- Bülow, Robin;
- Butcher, Nancy J.;
- Calhoun, Vince D.;
- Caspers, Svenja;
- Chow, Eva W. C.;
- Cichon, Sven
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
P3-196: A genome-wide association study for late-onset Alzheimer's disease using DNA pooling
Published in:
2008
By:
- Abraham, Richard;
- Georgieva, Lyudmila;
- Sims, Rebecca;
- Morgan, Angharad;
- Hollingworth, Paul;
- Lovestone, Simon;
- Brayne, Carol;
- Cichon, Sven;
- O'Donovan, Michael;
- Williams, Julie;
- Owen, Michael;
- Kirov, George
Publication type:
Abstract
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
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Article
Distinct Conditions Support a Novel Classification for Bradykinin-Mediated Angio-Oedema.
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Dermatology (10188665), 2015, v. 230, n. 4, p. 324, doi. 10.1159/000371814
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Publication type:
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Exploring the genetics of lithium response in bipolar disorders.
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International Journal of Bipolar Disorders, 2024, v. 12, n. 1, p. 1, doi. 10.1186/s40345-024-00341-y
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Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics.
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International Journal of Bipolar Disorders, 2018, v. 6, n. 1, p. 1, doi. 10.1186/s40345-018-0132-x
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Common and Rare Variant Analysis in Early-Onset Bipolar Disorder Vulnerability.
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PLoS ONE, 2014, v. 9, n. 8, p. 1, doi. 10.1371/journal.pone.0104326
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A Genetic Deconstruction of Neurocognitive Traits in Schizophrenia and Bipolar Disorder.
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PLoS ONE, 2013, v. 8, n. 12, p. 1, doi. 10.1371/journal.pone.0081052
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Enzymatic Assays for the Diagnosis of Bradykinin-Dependent Angioedema.
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PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0070140
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Copy Number Variants in German Patients with Schizophrenia.
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PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0064035
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Assessment of Response to Lithium Maintenance Treatment in Bipolar Disorder: A Consortium on Lithium Genetics (ConLiGen) Report.
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PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0065636
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A Genome-Wide Association Study Suggests Novel Loci Associated with a Schizophrenia-Related Brain-Based Phenotype.
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PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0064872
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Reduced Anxiety and Depression-Like Behaviours in the Circadian Period Mutant Mouse Afterhours.
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PLoS ONE, 2012, v. 7, n. 6, p. 1, doi. 10.1371/journal.pone.0038263
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Gene-Based Analysis of Regionally Enriched Cortical Genes in GWAS Data Sets of Cognitive Traits and Psychiatric Disorders.
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PLoS ONE, 2012, v. 7, n. 2, p. 1, doi. 10.1371/journal.pone.0031687
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- Rietschel, Marcella;
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- Werge, Thomas;
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Untersuchung genetischer Einflüsse auf Riechstörungen bei Patienten mit hereditärem Angioödem Typ 1 und 2.
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Journal der Deutschen Dermatologischen Gesellschaft, 2021, v. 19, n. 7, p. 1060, doi. 10.1111/ddg.14417_g
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- Förster‐Ruhrmann, Ulrike;
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- Cichon, Sven;
- Nöthen, Markus M.;
- Ellrich, André;
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- Maurer, Marcus;
- Magerl, Markus
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Analysis of genetic impact on smell impairment in patients with hereditary angioedema type 1 and 2.
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Journal der Deutschen Dermatologischen Gesellschaft, 2021, v. 19, n. 7, p. 1060, doi. 10.1111/ddg.14417
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- Förster‐Ruhrmann, Ulrike;
- Pierchalla, Greta;
- Stieber, Christiane;
- Heilmann‐Heimbach, Stefanie;
- Cichon, Sven;
- Nöthen, Markus M.;
- Ellrich, André;
- Olze, Heidi;
- Maurer, Marcus;
- Magerl, Markus
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Identification of mutations in the human hairless gene in two new families with congenital atrichia.
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Archives of Dermatological Research, 2007, v. 299, n. 3, p. 157, doi. 10.1007/s00403-007-0747-8
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- Betz, Regina C.;
- Indelman, Margarita;
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- Schreiner, Felix;
- Bauer, Ralf;
- Bergman, Reuven;
- Lentze, Michael J.;
- Nöthen, Markus M.;
- Cichon, Sven;
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No evidence for DUP25 in patients with panic disorder using a quantitative real-time PCR approach.
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Human Genetics, 2003, v. 114, n. 1, p. 115, doi. 10.1007/s00439-003-1022-5
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- Schumacher, Johannes;
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- Franke, Petra;
- Abou Jamra, Rami;
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- xFC;rgen#Deckert, J&;
- Nöthen, Markus M.;
- Cichon, Sven
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