PubRank

Sven Cichon

Author PubWeight™ 274.87‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Large recurrent microdeletions associated with schizophrenia. Nature 2008 20.25
2 Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. Nature 2012 16.13
3 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nat Genet 2011 13.25
4 Identification of loci associated with schizophrenia by genome-wide association and follow-up. Nat Genet 2008 10.52
5 Common variants conferring risk of schizophrenia. Nature 2009 10.37
6 Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet 2013 8.02
7 A mega-analysis of genome-wide association studies for major depressive disorder. Mol Psychiatry 2012 6.34
8 Microduplications of 16p11.2 are associated with schizophrenia. Nat Genet 2009 6.13
9 Disruption of the neurexin 1 gene is associated with schizophrenia. Hum Mol Genet 2008 4.78
10 Genomewide association studies: history, rationale, and prospects for psychiatric disorders. Am J Psychiatry 2009 4.74
11 Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. Nat Genet 2009 4.38
12 Multiple independent loci at chromosome 15q25.1 affect smoking quantity: a meta-analysis and comparison with lung cancer and COPD. PLoS Genet 2010 3.91
13 Identification of common variants associated with human hippocampal and intracranial volumes. Nat Genet 2012 3.73
14 Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24. Nat Genet 2009 3.58
15 Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q. Am J Hum Genet 2005 3.24
16 High frequencies of de novo CNVs in bipolar disorder and schizophrenia. Neuron 2011 3.08
17 Genome-wide association study of alcohol dependence. Arch Gen Psychiatry 2009 3.08
18 Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder. Am J Hum Genet 2003 3.02
19 Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate. Nat Genet 2009 2.93
20 Neural mechanisms of a genome-wide supported psychosis variant. Science 2009 2.88
21 Single nucleotide variation analysis in 65 candidate genes for CNS disorders in a representative sample of the European population. Genome Res 2003 2.75
22 Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1. Nat Genet 2010 2.46
23 Common variants at VRK2 and TCF4 conferring risk of schizophrenia. Hum Mol Genet 2011 2.21
24 A genome-wide association study for late-onset Alzheimer's disease using DNA pooling. BMC Med Genomics 2008 2.20
25 Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci. Nat Genet 2012 2.15
26 The neuronal transporter gene SLC6A15 confers risk to major depression. Neuron 2011 2.02
27 Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort. J Psychiatr Res 2010 1.98
28 Brain function in carriers of a genome-wide supported bipolar disorder variant. Arch Gen Psychiatry 2010 1.95
29 Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness. Am J Psychiatry 2011 1.94
30 Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia. Am J Hum Genet 2005 1.94
31 The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. Brain Imaging Behav 2014 1.90
32 Common variants on 8p12 and 1q24.2 confer risk of schizophrenia. Nat Genet 2011 1.88
33 Genome-wide association study of suicide attempts in mood disorder patients. Am J Psychiatry 2010 1.85
34 Susceptibility variants for male-pattern baldness on chromosome 20p11. Nat Genet 2008 1.80
35 Evidence for a relationship between genetic variants at the brain-derived neurotrophic factor (BDNF) locus and major depression. Biol Psychiatry 2005 1.61
36 Mast cells increase vascular permeability by heparin-initiated bradykinin formation in vivo. Immunity 2011 1.46
37 No association between the serine racemase gene (SRR) and schizophrenia in a German case-control sample. Psychiatr Genet 2007 1.42
38 Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression. Biol Psychiatry 2010 1.39
39 Systematic analysis of glutamatergic neurotransmission genes in alcohol dependence and adolescent risky drinking behavior. Arch Gen Psychiatry 2008 1.39
40 Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster. Addict Biol 2011 1.37
41 The complement control-related genes CSMD1 and CSMD2 associate to schizophrenia. Biol Psychiatry 2011 1.36
42 Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia. Am J Hum Genet 2005 1.35
43 Association of mouse Dlg4 (PSD-95) gene deletion and human DLG4 gene variation with phenotypes relevant to autism spectrum disorders and Williams' syndrome. Am J Psychiatry 2010 1.34
44 Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis. Nat Genet 2009 1.31
45 Haplotype interaction analysis of unlinked regions. Genet Epidemiol 2005 1.27
46 CLCN2 variants in idiopathic generalized epilepsy. Nat Genet 2009 1.26
47 At-risk variant in TCF7L2 for type II diabetes increases risk of schizophrenia. Biol Psychiatry 2011 1.26
48 The DTNBP1 (dysbindin) gene contributes to schizophrenia, depending on family history of the disease. Am J Hum Genet 2003 1.26
49 Metabotropic glutamate receptor 3 (GRM3) gene variation is not associated with schizophrenia or bipolar affective disorder in the German population. Am J Med Genet 2002 1.25
50 Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder. Nat Commun 2013 1.25
51 Cognitive state and connectivity effects of the genome-wide significant psychosis variant in ZNF804A. Neuroimage 2010 1.24
52 Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder. Schizophr Res 2012 1.24
53 Genotype-phenotype studies in bipolar disorder showing association between the DAOA/G30 locus and persecutory delusions: a first step toward a molecular genetic classification of psychiatric phenotypes. Am J Psychiatry 2005 1.21
54 Effects of the circadian rhythm gene period 1 (per1) on psychosocial stress-induced alcohol drinking. Am J Psychiatry 2011 1.15
55 Common genetic variants and gene-expression changes associated with bipolar disorder are over-represented in brain signaling pathway genes. Biol Psychiatry 2012 1.15
56 Brain-derived neurotrophic factor gene (BDNF) variants and schizophrenia: an association study. Prog Neuropsychopharmacol Biol Psychiatry 2006 1.10
57 Genome-wide association study in German patients with attention deficit/hyperactivity disorder. Am J Med Genet B Neuropsychiatr Genet 2011 1.09
58 A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia. Hum Mol Genet 2010 1.08
59 Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. Arch Gen Psychiatry 2012 1.08
60 Linkage-disequilibrium-based binning affects the interpretation of GWASs. Am J Hum Genet 2012 1.07
61 Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin. Nat Genet 2003 1.07
62 Implication of a rare deletion at distal 16p11.2 in schizophrenia. JAMA Psychiatry 2013 1.05
63 Molecular genetic overlap in bipolar disorder, schizophrenia, and major depressive disorder. World J Biol Psychiatry 2012 1.04
64 New findings in the genetics of major psychoses. Dialogues Clin Neurosci 2010 1.04
65 The first genomewide interaction and locus-heterogeneity linkage scan in bipolar affective disorder: strong evidence of epistatic effects between loci on chromosomes 2q and 6q. Am J Hum Genet 2007 1.04
66 Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample. Am J Med Genet B Neuropsychiatr Genet 2012 1.00
67 Association analysis of Neuregulin 1 candidate regions in schizophrenia and bipolar disorder. Neurosci Lett 2010 1.00
68 ZNF804A and cortical structure in schizophrenia: in vivo and postmortem studies. Schizophr Bull 2013 0.99
69 The International Consortium on Lithium Genetics (ConLiGen): an initiative by the NIMH and IGSLI to study the genetic basis of response to lithium treatment. Neuropsychobiology 2010 0.98
70 The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations. Hum Mol Genet 2009 0.97
71 Imaging genetics of FOXP2 in dyslexia. Eur J Hum Genet 2011 0.97
72 Dissection of phenotype reveals possible association between schizophrenia and Glutamate Receptor Delta 1 (GRID1) gene promoter. Schizophr Res 2009 0.97
73 Identification of mutations in the human hairless gene in two new families with congenital atrichia. Arch Dermatol Res 2007 0.96
74 Meta-analysis and brain imaging data support the involvement of VRK2 (rs2312147) in schizophrenia susceptibility. Schizophr Res 2012 0.95
75 The opioid peptides enkephalin and beta-endorphin in alcohol dependence. Biol Psychiatry 2008 0.95
76 Volition diminishes genetically mediated amygdala hyperreactivity. Neuroimage 2009 0.95
77 Retraction for Dixson et al., Identification of gene ontologies linked to prefrontal-hippocampal functional coupling in the human brain. Proc Natl Acad Sci U S A 2014 0.94
78 New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis. Int J Epidemiol 2015 0.93
79 Genetic and functional abnormalities of the melatonin biosynthesis pathway in patients with bipolar disorder. Hum Mol Genet 2012 0.93
80 Feasible and successful: genome-wide interaction analysis involving all 1.9 x 10(11) pair-wise interaction tests. Hum Hered 2010 0.93
81 Monoamine related functional gene variants and relationships to monoamine metabolite concentrations in CSF of healthy volunteers. BMC Psychiatry 2004 0.93
82 G72 and its association with major depression and neuroticism in large population-based groups from Germany. Am J Psychiatry 2008 0.93
83 Copy number variants in German patients with schizophrenia. PLoS One 2013 0.91
84 Reduced anxiety and depression-like behaviours in the circadian period mutant mouse afterhours. PLoS One 2012 0.91
85 Converging Evidence for Epistasis between ANK3 and Potassium Channel Gene KCNQ2 in Bipolar Disorder. Front Genet 2013 0.90
86 Genomewide scan and fine-mapping linkage studies in four European samples with bipolar affective disorder suggest a new susceptibility locus on chromosome 1p35-p36 and provides further evidence of loci on chromosome 4q31 and 6q24. Am J Hum Genet 2005 0.90
87 Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin. Nat Genet 2004 0.90
88 Replication study and meta-analysis in European samples supports association of the 3p21.1 locus with bipolar disorder. Biol Psychiatry 2012 0.89
89 αCaMKII autophosphorylation controls the establishment of alcohol drinking behavior. Neuropsychopharmacology 2013 0.89
90 VEGF gene haplotypes are associated with sarcoidosis. Chest 2009 0.89
91 Hippocampal function in healthy carriers of the CLU Alzheimer's disease risk variant. J Neurosci 2011 0.89
92 Hereditary angioedema with normal C1 inhibitor gene in a family with affected women and men is associated with the p.Thr328Lys mutation in the F12 gene. J Allergy Clin Immunol 2007 0.89
93 Prediction of serotonin transporter promoter polymorphism genotypes from single nucleotide polymorphism arrays using machine learning methods. Psychiatr Genet 2012 0.89
94 Association study of nonsynonymous single nucleotide polymorphisms in schizophrenia. Biol Psychiatry 2011 0.88
95 Gene-based analysis of regionally enriched cortical genes in GWAS data sets of cognitive traits and psychiatric disorders. PLoS One 2012 0.88
96 No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samples. Biol Psychiatry 2005 0.88
97 Common obesity risk alleles in childhood attention-deficit/hyperactivity disorder. Am J Med Genet B Neuropsychiatr Genet 2013 0.88
98 Candidate gene analysis of the human natural killer-1 carbohydrate pathway and perineuronal nets in schizophrenia: B3GAT2 is associated with disease risk and cortical surface area. Biol Psychiatry 2010 0.88
99 Assessment of Response to Lithium Maintenance Treatment in Bipolar Disorder: A Consortium on Lithium Genetics (ConLiGen) Report. PLoS One 2013 0.88
100 The catechol-O-methyl transferase (COMT) gene and its potential association with schizophrenia: findings from a large German case-control and family-based sample. Schizophr Res 2010 0.87
101 Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking. Genet Epidemiol 2013 0.87
102 The G72/G30 gene locus in psychiatric disorders: a challenge to diagnostic boundaries? Schizophr Bull 2006 0.87
103 Dopamine D4 receptor gene (DRD4) variants and schizophrenia: meta-analyses. Schizophr Res 2003 0.86
104 Variation in P2RX7 candidate gene (rs2230912) is not associated with bipolar I disorder and unipolar major depression in four European samples. Am J Med Genet B Neuropsychiatr Genet 2009 0.86
105 Neuregulin 3 is associated with attention deficits in schizophrenia and bipolar disorder. Int J Neuropsychopharmacol 2012 0.85
106 Association between a promoter dopamine D2 receptor gene variant and the personality trait detachment. Biol Psychiatry 2003 0.85
107 Studies in humans and mice implicate neurocan in the etiology of mania. Am J Psychiatry 2012 0.85
108 Epigenetic alteration of the dopamine transporter gene in alcohol-dependent patients is associated with age. Addict Biol 2012 0.85
109 Marie Unna hereditary hypotrichosis: identification of a U2HR mutation in the family from the original 1925 report. J Am Acad Dermatol 2010 0.84
110 Genome-wide association analysis of age at onset and psychotic symptoms in bipolar disorder. Am J Med Genet B Neuropsychiatr Genet 2011 0.84
111 Can long-range microsatellite data be used to predict short-range linkage disequilibrium? Hum Mol Genet 2002 0.84
112 Glutamate receptor δ 1 (GRID1) genetic variation and brain structure in schizophrenia. J Psychiatr Res 2012 0.84
113 A reappraisal of the association between Dysbindin (DTNBP1) and schizophrenia in a large combined case-control and family-based sample of German ancestry. Schizophr Res 2010 0.83
114 Possible association between genetic variants at the GRIN1 gene and schizophrenia with lifetime history of depressive symptoms in a German sample. Psychiatr Genet 2007 0.83
115 Reduced cortical thickness is associated with the glutamatergic regulatory gene risk variant DAOA Arg30Lys in schizophrenia. Neuropsychopharmacology 2011 0.83
116 Investigation of the tryptophan hydroxylase 2 gene in bipolar I disorder in the Romanian population. Psychiatr Genet 2008 0.82
117 Dual association of a TRKA polymorphism with schizophrenia. Psychiatr Genet 2011 0.82
118 A new susceptibility locus for bipolar affective disorder in PAR1 on Xp22.3/Yp11.3. Am J Med Genet B Neuropsychiatr Genet 2010 0.81
119 TLR4, ATF-3 and IL8 inflammation mediator expression correlates with seizure frequency in human epileptic brain tissue. Seizure 2013 0.81
120 Association study between two variants in the DOPA decarboxylase gene in bipolar and unipolar affective disorder. Am J Med Genet 2002 0.81
121 A Genome-Wide Association Study Suggests Novel Loci Associated with a Schizophrenia-Related Brain-Based Phenotype. PLoS One 2013 0.81
122 Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patients. Schizophr Res 2011 0.81
123 Mood-incongruent psychosis in bipolar disorder: conditional linkage analysis shows genome-wide suggestive linkage at 1q32.3, 7p13 and 20q13.31. Bipolar Disord 2009 0.80
124 Association between a polymorphism in the pseudoautosomal X-linked gene SYBL1 and bipolar affective disorder. Am J Med Genet 2002 0.80
125 Genome-wide association data provide further support for an association between 5-HTTLPR and major depressive disorder. J Affect Disord 2012 0.80
126 Efficient strategy for detecting gene × gene joint action and its application in schizophrenia. Genet Epidemiol 2013 0.80
127 No association between a putative functional promoter variant in the dopamine beta-hydroxylase gene and schizophrenia. Psychiatr Genet 2003 0.79
128 Genetic association between the phospholipase A2 gene and unipolar affective disorder: a multicentre case-control study. Psychiatr Genet 2003 0.79
129 DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder. PLoS One 2012 0.79
130 Distinct conditions support a novel classification for bradykinin-mediated angio-oedema. Dermatology 2015 0.79
131 Promoter variants determine γ-aminobutyric acid homeostasis-related gene transcription in human epileptic hippocampi. J Neuropathol Exp Neurol 2011 0.78
132 A summary statistic approach to sequence variation in noncoding regions of six schizophrenia-associated gene loci. Eur J Hum Genet 2006 0.78
133 Association study between genetic variants at the PIP5K2A gene locus and schizophrenia and bipolar affective disorder. Am J Med Genet B Neuropsychiatr Genet 2006 0.78
134 No evidence for an association between variants at the proline dehydrogenase locus and schizophrenia or bipolar affective disorder. Psychiatr Genet 2005 0.78
135 European collaborative study of early-onset bipolar disorder: Evidence for genetic heterogeneity on 2q14 according to age at onset. Am J Med Genet B Neuropsychiatr Genet 2010 0.78
136 Association study of a functional promoter polymorphism in the XBP1 gene and schizophrenia. Am J Med Genet B Neuropsychiatr Genet 2006 0.78
137 No association between genetic variants at the GLYT2 gene and bipolar affective disorder and schizophrenia. Psychiatr Genet 2006 0.78
138 No evidence for an involvement of copy number variation in ABCA13 in schizophrenia, bipolar disorder, or major depressive disorder. Psychiatr Genet 2013 0.77
139 No evidence for an association between variants at the gamma-amino-n-butyric acid type A receptor beta2 locus and schizophrenia. Psychiatr Genet 2007 0.77
140 Segment-wise genome-wide association analysis identifies a candidate region associated with schizophrenia in three independent samples. PLoS One 2012 0.77
141 Enzymatic assays for the diagnosis of bradykinin-dependent angioedema. PLoS One 2013 0.77
142 Human metabotropic glutamate receptor 2 gene (GRM2): chromosomal sublocalization (3p21.1-p21.2) and genomic organization. Am J Med Genet 2002 0.77
143 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? Depress Anxiety 2014 0.77
144 Association study between genetic variants at the VAMP2 and VAMP3 loci and bipolar affective disorder. Psychiatr Genet 2008 0.77
145 Further evidence for age of onset being an indicator for severity in bipolar disorder. J Affect Disord 2002 0.77
146 Rs6295 promoter variants of the serotonin type 1A receptor are differentially activated by c-Jun in vitro and correlate to transcript levels in human epileptic brain tissue. Brain Res 2013 0.76
147 DRD4 exon 3 variants are not associated with symptomatology of major psychoses in a German population. Neurosci Lett 2004 0.76
148 Analysis of genome-wide significant bipolar disorder genes in borderline personality disorder. Psychiatr Genet 2014 0.76
149 No association between genetic variants at the GRIN1 gene and bipolar disorder in a German sample. Psychiatr Genet 2006 0.76
150 No association between genetic variants at the ASCT1 gene and schizophrenia or bipolar disorder in a German sample. Psychiatr Genet 2006 0.76
151 A systematic association mapping on chromosome 6q in bipolar affective disorder--evidence for the melanin-concentrating-hormone-receptor-2 gene as a risk factor for bipolar affective disorder. Am J Med Genet B Neuropsychiatr Genet 2010 0.76
152 No association between the D-aspartate oxidase locus and schizophrenia. Psychiatr Genet 2009 0.76
153 Genetic variation at the synaptic vesicle gene SV2A is associated with schizophrenia. Schizophr Res 2012 0.76
154 No evidence for DUP25 in patients with panic disorder using a quantitative real-time PCR approach. Hum Genet 2003 0.76
155 Association between neuropeptide Y receptor Y2 promoter variant rs6857715 and major depressive disorder. Psychiatr Genet 2017 0.76
156 Association study of the GRIA1 and CLINT1 (Epsin 4) genes in a German schizophrenia sample. Psychiatr Genet 2011 0.75
157 Linking single nucleotide polymorphisms. Pharmacogenetics 2002 0.75
158 Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2. Psychiatr Genet 2016 0.75
159 No association between the serine racemase gene (SRR) and bipolar disorder in a German case-control sample. Psychiatr Genet 2007 0.75
160 Levetiracetam resistance: Synaptic signatures & corresponding promoter SNPs in epileptic hippocampi. Neurobiol Dis 2013 0.75
161 Is there a phenotypic difference between probands in case-control versus family-based association studies? Am J Med Genet B Neuropsychiatr Genet 2003 0.75
162 Lack of genetic association between the phospholipase A2 gene and bipolar mood disorder in a European multicentre case-control study. Psychiatr Genet 2006 0.75
163 No association between genetic variants at the DGCR2 gene and schizophrenia in a German sample. Psychiatr Genet 2009 0.75
164 Family-based association studies of alpha-adrenergic receptor genes in chromosomal regions with linkage to bipolar affective disorder. Am J Med Genet B Neuropsychiatr Genet 2004 0.75
165 No evidence for association between NOTCH4 and schizophrenia in a large family-based and case-control association analysis. Psychiatr Genet 2006 0.75
166 Possible association of different G72/G30 SNPs with mood episodes and persecutory delusions in bipolar I Romanian patients. Prog Neuropsychopharmacol Biol Psychiatry 2010 0.75
167 Expert and self-assessment of lifetime symptoms and diagnosis of major depressive disorder in large-scale genetic studies in the general population: comparison of a clinical interview and a self-administered checklist. Psychiatr Genet 2017 0.75
168 Contact system activation in patients with HAE and normal C1 inhibitor function. Immunol Allergy Clin North Am 2013 0.75
169 Smoking behaviour: investigation of the coaction of environmental and genetic risk factors. Psychiatr Genet 2014 0.75
170 A common microdeletion affecting a hippocampus- and amygdala-specific isoform of tryptophan hydroxylase 2 is not associated with affective disorders. Bipolar Disord 2014 0.75
171 Effects of exogenous agmatine in human leukemia HMC-1 and HL-60 cells on proliferation, polyamine metabolism and cell cycle. Leuk Res 2011 0.75
172 Association study of 20 genetic variants at the (D)-amino acid oxidase gene in schizophrenia. Psychiatr Genet 2010 0.75
173 Brief report: no association between premorbid adjustment in adult-onset schizophrenia and genetic variation in Dysbindin. J Autism Dev Disord 2008 0.75
174 Systematic screening for mutations in the human N-methyl-D-aspartate receptor 1 gene in schizophrenic patients from the German population. Psychiatr Genet 2004 0.75