R. Breuer

发表

Common variants conferring risk of schizophrenia

Pall I. Olason, P. Matthews, H. Stefánsson, 2009, Nature.

Common variants at VRK2 and TCF4 conferring risk of schizophrenia.

H. Stefánsson, D. Rujescu, S. Cichon, 2011, Human molecular genetics.

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

Manuel A. R. Ferreira, John P. Rice, Edward G. Jones, 2011, Nature Genetics.

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Jianxin Shi, Susmita Datta, Aribert Rothenberger, 2013, Nature Genetics.

Variation in P2RX7 candidate gene (rs2230912) is not associated with bipolar I disorder and unipolar major depression in four European samples

Thomas W. Mühleisen, S. Cichon, T. Mühleisen, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

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

Thomas W. Mühleisen, S. Cichon, P. Muglia, 2009, Nature Genetics.

Genome-Wide Association-, Replication-, and Neuroimaging Study Implicates HOMER1 in the Etiology of Major Depression

S. Cichon, M. Rietschel, M. Nöthen, 2010, Biological Psychiatry.

Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder.

Thomas W. Mühleisen, H. Stefánsson, S. Cichon, 2011, American journal of human genetics.

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

Janice M. Fullerton, Thomas W. Mühleisen, S. Cichon, 2014, Nature Communications.

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

N. Wray, H. Stefánsson, S. Cichon, 2013, Molecular Psychiatry.

Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder

Laura J. Scott, Naomi R. Wray, Margaret A. Pericak-Vance, 2015, American journal of human genetics.

Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe

Thomas W. Mühleisen, A. Hofman, A. Uitterlinden, 2012, Molecular Psychiatry.

Genome-wide association of mood-incongruent psychotic bipolar disorder

S Cichon, T Schulze, S. Cichon, 2012, Translational Psychiatry.

Genome-wide association data provide further support for an association between 5-HTTLPR and major depressive disorder.

S. Cichon, M. Rietschel, M. Nöthen, 2013, Journal of affective disorders.

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

Daniel L. Koller, Pamela B. Mahon, Thomas W. Mühleisen, 2018, International Journal of Bipolar Disorders.

Genotype-phenotype association mining in bipolar disorder: market research meets complex genetics

Thomas W. Mühleisen, G. Karypis, S. Cichon, 2017, bioRxiv.

Susceptibility genes: GSTM1 and GSTM3 as genetic risk factors in bladder cancer

R. Breuer, E. Schnakenberg, W. Schloot, 2001, Cytogenetic and Genome Research.

Gender‐specific effects of NAT2 and GSTM1 in bladder cancer

R. Breuer, M. Lustig, E. Schnakenberg, 2000, Clinical genetics.

A reappraisal of the association between Dysbindin (DTNBP1) and schizophrenia in a large combined case-control and family-based sample of German ancestry

S. Cichon, T. Mühleisen, M. Rietschel, 2010 .

Bibliography of Ulrich Wolf

C. Tyler-Smith, P. Yen, K. Hirschhorn, 2001, Cytogenetic and Genome Research.

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

Janice M. Fullerton, Thomas W. Mühleisen, S. Cichon, 2015, Translational Psychiatry.

Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

Laura J. Scott, Naomi R. Wray, Margaret A. Pericak-Vance, 2015, Nature Neuroscience.

The Complement Control-Related Genes CSMD1 and CSMD2 Associate to Schizophrenia

Vidar M. Steen, Marcella Rietschel, Stephanie Le Hellard, 2011, Biological Psychiatry.

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

J. Sebat, D. Malhotra, Annette Lee, 2013, JAMA psychiatry.

A rare deletion at distal 16 p 11 . 2 is implicated in schizophrenia

Degenhardt, Dheeraj, Franziska, 2013 .

Common variant at 16p11.2 conferring risk of psychosis

M. Pirinen, H. Stefánsson, D. Rujescu, 2014, Molecular Psychiatry.

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

S. Cichon, M. Rietschel, M. Leboyer, 2012, Molecular Psychiatry.

Two variants in Ankyrin 3 (ANK3) are independent genetic risk factors for bipolar disorder

S. Cichon, M. Rietschel, J. Pearl, 2008, Molecular Psychiatry.

Expanding the range of ZNF804A variants conferring risk of psychosis

R A Ophoff, T Sigmundsson, Pall I. Olason, 2011, Molecular Psychiatry.

Copy Number Variants in German Patients with Schizophrenia

D. Rujescu, S. Cichon, M. Rietschel, 2013, PloS one.

Association between copy number variants in 16p11.2 and major depressive disorder in a German case–control sample

Thomas W. Mühleisen, S. Cichon, T. Mühleisen, 2012, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Neuregulin 3 is associated with attention deficits in schizophrenia and bipolar disorder.

Thomas W. Mühleisen, S. Cichon, T. Mühleisen, 2013, The international journal of neuropsychopharmacology.

Genome-wide significant association between a ‘negative mood delusions' dimension in bipolar disorder and genetic variation on chromosome 3q26.1

John P. Rice, Daniel L. Koller, Pamela B. Mahon, 2012, Translational Psychiatry.

Molecular genetic overlap in bipolar disorder, schizophrenia, and major depressive disorder

Thomas G Schulze, Francis J McMahon, Sven Cichon, 2014, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.

Gene-Based Analysis of Regionally Enriched Cortical Genes in GWAS Data Sets of Cognitive Traits and Psychiatric Disorders

Ole A. Andreassen, Vidar M. Steen, Manuel Mattheisen, 2012, PloS one.

Replication of functional serotonin receptor type 3A and B variants in bipolar affective disorder: a European multicenter study

S. Cichon, M. Rietschel, M. Nöthen, 2012, Translational Psychiatry.

Longer telomere length in patients with schizophrenia

M. Rietschel, M. Nöthen, R. Breuer, 2013, Schizophrenia Research.

Genetic Differences in the Immediate Transcriptome Response to Stress Predict Risk-Related Brain Function and Psychiatric Disorders

N. Wray, H. Stefánsson, S. Cichon, 2015, Neuron.

Studies in humans and mice implicate neurocan in the etiology of mania.

Thomas W. Mühleisen, S. Cichon, T. Mühleisen, 2012, The American journal of psychiatry.

Supporting evidence for LRRTM1 imprinting effects in schizophrenia

S. Cichon, M. Rietschel, R. Breuer, 2009, Molecular Psychiatry.

Dissection of phenotype reveals possible association between schizophrenia and Glutamate Receptor Delta 1 (GRID1) gene promoter

Thomas W. Mühleisen, S. Cichon, T. Mühleisen, 2009, Schizophrenia Research.

The catechol-O-methyl transferase (COMT) gene and its potential association with schizophrenia: Findings from a large German case-control and family-based sample

Thomas W. Mühleisen, S. Cichon, T. Mühleisen, 2010, Schizophrenia Research.

Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder

C. Gieger, A. Hofman, A. Uitterlinden, 2012, Schizophrenia Research.

Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patients

Manuel Mattheisen, Markus M. Nöthen, Sven Cichon, 2011, Schizophrenia Research.

Independent evidence for the selective influence of GABAA receptors on one component of the bipolar disorder phenotype

S. Cichon, N. Craddock, M. Hamshere, 2011, Molecular Psychiatry.

Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder (vol 88, pg 372, 2011)

H. Stefánsson, S. Cichon, S. Steinberg, 2011 .

A reappraisal of the association between Dysbindin (DTNBP1) and schizophrenia in a large combined case–control and family-based sample of German ancestry

Thomas W. Mühleisen, S. Cichon, T. Mühleisen, 2010, Schizophrenia Research.

Segment-Wise Genome-Wide Association Analysis Identifies a Candidate Region Associated with Schizophrenia in Three Independent Samples

S. Cichon, R. Ophoff, M. Rietschel, 2012, PloS one.

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

D. Ledbetter, J. Sutcliffe, D. Rujescu, 2014 .

The association between lower educational attainment and depression owing to shared genetic effects? Results in ~25 000 subjects

John P. Rice, Min A. Jhun, S. Bandinelli, 2015, Molecular Psychiatry.

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

D. Ledbetter, J. Sutcliffe, D. Rujescu, 2014 .

Molecular genetic overlap in bipolar disorder, schizophrenia, and major depressive disorder

M. Nalls, A. Singleton, S. Cichon, 2014, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.

Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder

Thomas W. Mühleisen, C. Gieger, D. Rujescu, 2012, Schizophrenia Research.

Common variants at VRK2 and TCF4 conferring risk of schizophrenia.

H. Stefánsson, D. Rujescu, S. Cichon, 2011, Human molecular genetics.

Common variant at 16p11.2 conferring risk of psychosis

M. Pirinen, H. Stefánsson, D. Rujescu, 2014, Molecular Psychiatry.

Neuregulin 3 is associated with attention deficits in schizophrenia and bipolar disorder.

Thomas W. Mühleisen, S. Cichon, M. Rietschel, 2013, International Journal of Neuropsychopharmacology.