PubRank

Marcella Rietschel

Author PubWeight™ 359.82‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Large recurrent microdeletions associated with schizophrenia. Nature 2008 20.25
2 Identification of loci associated with schizophrenia by genome-wide association and follow-up. Nat Genet 2008 10.52
3 Common variants conferring risk of schizophrenia. Nature 2009 10.37
4 Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet 2013 8.02
5 A mega-analysis of genome-wide association studies for major depressive disorder. Mol Psychiatry 2012 6.34
6 Microduplications of 16p11.2 are associated with schizophrenia. Nat Genet 2009 6.13
7 City living and urban upbringing affect neural social stress processing in humans. Nature 2011 5.46
8 A genome-wide association study of alcohol dependence. Proc Natl Acad Sci U S A 2010 4.94
9 Disruption of the neurexin 1 gene is associated with schizophrenia. Hum Mol Genet 2008 4.78
10 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
11 Identification of common variants associated with human hippocampal and intracranial volumes. Nat Genet 2012 3.73
12 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
13 Genome-wide association study of alcohol dependence. Arch Gen Psychiatry 2009 3.08
14 High frequencies of de novo CNVs in bipolar disorder and schizophrenia. Neuron 2011 3.08
15 Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder. Am J Hum Genet 2003 3.02
16 Neural mechanisms of a genome-wide supported psychosis variant. Science 2009 2.88
17 Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. Am J Hum Genet 2011 2.71
18 Dissecting the phenotype in genome-wide association studies of psychiatric illness. Br J Psychiatry 2009 2.65
19 Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1. Nat Genet 2010 2.46
20 Genome-wide pharmacogenetics of antidepressant response in the GENDEP project. Am J Psychiatry 2010 2.41
21 Common variants at VRK2 and TCF4 conferring risk of schizophrenia. Hum Mol Genet 2011 2.21
22 The neuronal transporter gene SLC6A15 confers risk to major depression. Neuron 2011 2.02
23 Interacting effects of the dopamine transporter gene and psychosocial adversity on attention-deficit/hyperactivity disorder symptoms among 15-year-olds from a high-risk community sample. Arch Gen Psychiatry 2007 2.02
24 Support for association of schizophrenia with genetic variation in the 6p22.3 gene, dysbindin, in sib-pair families with linkage and in an additional sample of triad families. Am J Hum Genet 2002 1.99
25 Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort. J Psychiatr Res 2010 1.98
26 Adolescent impulsivity phenotypes characterized by distinct brain networks. Nat Neurosci 2012 1.98
27 Brain function in carriers of a genome-wide supported bipolar disorder variant. Arch Gen Psychiatry 2010 1.95
28 Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness. Am J Psychiatry 2011 1.94
29 The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. Brain Imaging Behav 2014 1.90
30 Common variants on 8p12 and 1q24.2 confer risk of schizophrenia. Nat Genet 2011 1.88
31 Genome-wide association study of suicide attempts in mood disorder patients. Am J Psychiatry 2010 1.85
32 Three circadian clock genes Per2, Arntl, and Npas2 contribute to winter depression. Ann Med 2007 1.77
33 Lower ventral striatal activation during reward anticipation in adolescent smokers. Am J Psychiatry 2011 1.70
34 Genetic variation in the PNPLA3 gene is associated with alcoholic liver injury in caucasians. Hepatology 2010 1.65
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 Risk taking and the adolescent reward system: a potential common link to substance abuse. Am J Psychiatry 2011 1.56
37 Catechol-O-methyltransferase Val158 Met genotype, parenting practices and adolescent alcohol use: testing the differential susceptibility hypothesis. J Child Psychol Psychiatry 2011 1.45
38 A genomewide linkage study on suicidality in major depressive disorder confirms evidence for linkage to 2p12. Am J Med Genet B Neuropsychiatr Genet 2010 1.44
39 No association between the serine racemase gene (SRR) and schizophrenia in a German case-control sample. Psychiatr Genet 2007 1.42
40 A genome-wide significant linkage for severe depression on chromosome 3: the depression network study. Am J Psychiatry 2011 1.41
41 Systematic analysis of glutamatergic neurotransmission genes in alcohol dependence and adolescent risky drinking behavior. Arch Gen Psychiatry 2008 1.39
42 Pharmacogenetics in psychiatry satellite meeting at the American College of Neuropsychopharmacology, 2000. Neuropsychopharmacology 2002 1.39
43 Impact of age at first drink on vulnerability to alcohol-related problems: testing the marker hypothesis in a prospective study of young adults. J Psychiatr Res 2009 1.37
44 Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster. Addict Biol 2011 1.37
45 Impact of psychosocial adversity on alcohol intake in young adults: moderation by the LL genotype of the serotonin transporter polymorphism. Biol Psychiatry 2009 1.37
46 The complement control-related genes CSMD1 and CSMD2 associate to schizophrenia. Biol Psychiatry 2011 1.36
47 Genetic predictors of response to antidepressants in the GENDEP project. Pharmacogenomics J 2009 1.35
48 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
49 Age at onset in bipolar I affective disorder: further evidence for three subgroups. Am J Psychiatry 2003 1.33
50 The power of sample size and homogenous sampling: association between the 5-HTTLPR serotonin transporter polymorphism and major depressive disorder. Biol Psychiatry 2005 1.31
51 Interaction between the 5-HTTLPR serotonin transporter polymorphism and environmental adversity for mood and anxiety psychopathology: evidence from a high-risk community sample of young adults. Int J Neuropsychopharmacol 2009 1.28
52 The DTNBP1 (dysbindin) gene contributes to schizophrenia, depending on family history of the disease. Am J Hum Genet 2003 1.26
53 At-risk variant in TCF7L2 for type II diabetes increases risk of schizophrenia. Biol Psychiatry 2011 1.26
54 Whole genome linkage scan of recurrent depressive disorder from the depression network study. Hum Mol Genet 2005 1.25
55 Moderation of antidepressant response by the serotonin transporter gene. Br J Psychiatry 2009 1.25
56 Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder. Nat Commun 2013 1.25
57 Cognitive state and connectivity effects of the genome-wide significant psychosis variant in ZNF804A. Neuroimage 2010 1.24
58 Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder. Schizophr Res 2012 1.24
59 Pharmacogenetics of tardive dyskinesia: combined analysis of 780 patients supports association with dopamine D3 receptor gene Ser9Gly polymorphism. Neuropsychopharmacology 2002 1.23
60 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
61 Genetic predictors of response to serotonergic and noradrenergic antidepressants in major depressive disorder: a genome-wide analysis of individual-level data and a meta-analysis. PLoS Med 2012 1.19
62 Prevalence of incompletely penetrant Huntington's disease alleles among individuals with major depressive disorder. Am J Psychiatry 2010 1.16
63 Impact of polymorphisms of cytochrome-P450 isoenzymes 2C9, 2C19 and 2D6 on plasma concentrations and clinical effects of antidepressants in a naturalistic clinical setting. Eur J Clin Pharmacol 2004 1.16
64 Effects of the circadian rhythm gene period 1 (per1) on psychosocial stress-induced alcohol drinking. Am J Psychiatry 2011 1.15
65 Common genetic variants and gene-expression changes associated with bipolar disorder are over-represented in brain signaling pathway genes. Biol Psychiatry 2012 1.15
66 What is familial about familial bipolar disorder? Resemblance among relatives across a broad spectrum of phenotypic characteristics. Arch Gen Psychiatry 2006 1.15
67 Genetic models of schizophrenia and bipolar disorder: overlapping inheritance or discrete genotypes? Eur Arch Psychiatry Clin Neurosci 2005 1.13
68 Differential efficacy of escitalopram and nortriptyline on dimensional measures of depression. Br J Psychiatry 2009 1.13
69 Association of the functional V158M catechol-O-methyl-transferase polymorphism with panic disorder in women. Int J Neuropsychopharmacol 2004 1.12
70 Adverse reactions to antidepressants. Br J Psychiatry 2009 1.12
71 Genome-wide association studies of alcohol dependence and substance use disorders. Curr Psychiatry Rep 2011 1.11
72 Sex-specific association between the 5-HTT gene-linked polymorphic region and basal cortisol secretion. Psychoneuroendocrinology 2009 1.10
73 Computer-assisted phenotype characterization for genetic research in psychiatry. Hum Hered 2004 1.10
74 Partial support for ZNF804A genotype-dependent alterations in prefrontal connectivity. Hum Brain Mapp 2011 1.09
75 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
76 Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. Arch Gen Psychiatry 2012 1.08
77 Linkage-disequilibrium-based binning affects the interpretation of GWASs. Am J Hum Genet 2012 1.07
78 An integrated genome research network for studying the genetics of alcohol addiction. Addict Biol 2010 1.07
79 Psychiatric comorbidity and functional impairment in a clinically referred sample of adults with attention-deficit/hyperactivity disorder (ADHD). Eur Arch Psychiatry Clin Neurosci 2007 1.06
80 Human NPY promoter variation rs16147:T>C as a moderator of prefrontal NPY gene expression and negative affect. Hum Mutat 2010 1.06
81 RASGRF2 regulates alcohol-induced reinforcement by influencing mesolimbic dopamine neuron activity and dopamine release. Proc Natl Acad Sci U S A 2012 1.06
82 Neural and cognitive correlates of the common and specific variance across externalizing problems in young adolescence. Am J Psychiatry 2014 1.05
83 Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5'-region are associated with bipolar affective disorder. Hum Mol Genet 2007 1.05
84 Implication of a rare deletion at distal 16p11.2 in schizophrenia. JAMA Psychiatry 2013 1.05
85 Subtype differences in adults with attention-deficit/hyperactivity disorder (ADHD) with regard to ADHD-symptoms, psychiatric comorbidity and psychosocial adjustment. Eur Psychiatry 2007 1.05
86 Genetic predictors of increase in suicidal ideation during antidepressant treatment in the GENDEP project. Neuropsychopharmacology 2009 1.04
87 New findings in the genetics of major psychoses. Dialogues Clin Neurosci 2010 1.04
88 Molecular genetic overlap in bipolar disorder, schizophrenia, and major depressive disorder. World J Biol Psychiatry 2012 1.04
89 DNA sequence variants of the FKBP5 gene are associated with unipolar depression. Int J Neuropsychopharmacol 2010 1.04
90 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
91 Melancholic, atypical and anxious depression subtypes and outcome of treatment with escitalopram and nortriptyline. J Affect Disord 2011 1.03
92 Determinants of early alcohol use in healthy adolescents: the differential contribution of neuroimaging and psychological factors. Neuropsychopharmacology 2011 1.03
93 From nature versus nurture, via nature and nurture, to gene x environment interaction in mental disorders. Eur Child Adolesc Psychiatry 2009 1.02
94 Interacting effects of CRHR1 gene and stressful life events on drinking initiation and progression among 19-year-olds. Int J Neuropsychopharmacol 2009 1.02
95 Genomewide association scan of suicidal thoughts and behaviour in major depression. PLoS One 2011 1.02
96 HPA-axis activity in alcoholism: examples for a gene-environment interaction. Addict Biol 2007 1.01
97 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
98 Familiality of symptom dimensions in depression. Arch Gen Psychiatry 2004 1.00
99 Association analysis of Neuregulin 1 candidate regions in schizophrenia and bipolar disorder. Neurosci Lett 2010 1.00
100 ZNF804A and cortical structure in schizophrenia: in vivo and postmortem studies. Schizophr Bull 2013 0.99
101 Further evidence for a functional role of the glutamate receptor gene GRM3 in schizophrenia. Eur Neuropsychopharmacol 2008 0.99
102 Early and delayed onset of response to antidepressants in individual trajectories of change during treatment of major depression: a secondary analysis of data from the Genome-Based Therapeutic Drugs for Depression (GENDEP) study. J Clin Psychiatry 2011 0.99
103 Longer telomere length in patients with schizophrenia. Schizophr Res 2013 0.98
104 A systems medicine research approach for studying alcohol addiction. Addict Biol 2013 0.98
105 The dichotomy of schizophrenia and affective disorders in extended pedigrees. Schizophr Res 2002 0.97
106 Association of a functional 1019C>G 5-HT1A receptor gene polymorphism with panic disorder with agoraphobia. Int J Neuropsychopharmacol 2004 0.97
107 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
108 Dissection of phenotype reveals possible association between schizophrenia and Glutamate Receptor Delta 1 (GRID1) gene promoter. Schizophr Res 2009 0.97
109 Body weight as a predictor of antidepressant efficacy in the GENDEP project. J Affect Disord 2009 0.96
110 The Depression Network (DeNT) Study: methodology and sociodemographic characteristics of the first 470 affected sibling pairs from a large multi-site linkage genetic study. BMC Psychiatry 2004 0.96
111 Convergent animal and human evidence suggests a role of PPM1A gene in response to antidepressants. Biol Psychiatry 2010 0.96
112 Meta-analysis and brain imaging data support the involvement of VRK2 (rs2312147) in schizophrenia susceptibility. Schizophr Res 2012 0.95
113 Variant GADL1 and response to lithium in bipolar I disorder. N Engl J Med 2014 0.95
114 Volition diminishes genetically mediated amygdala hyperreactivity. Neuroimage 2009 0.95
115 Role of FKBP5 in emotion processing: results on amygdala activity, connectivity and volume. Brain Struct Funct 2014 0.94
116 Investigation of the human serotonin receptor gene HTR3B in bipolar affective and schizophrenic patients. Am J Med Genet B Neuropsychiatr Genet 2004 0.94
117 Creating probabilistic maps of the face network in the adolescent brain: a multicentre functional MRI study. Hum Brain Mapp 2011 0.94
118 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
119 New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis. Int J Epidemiol 2015 0.93
120 Dissecting the genetic heterogeneity of depression through age at onset. Am J Med Genet B Neuropsychiatr Genet 2012 0.93
121 Reduction of the internal capsule in families affected with schizophrenia. Biol Psychiatry 2007 0.93
122 Serotonin transporter 5HTTLPR polymorphism and affective disorders: no evidence of association in a large European multicenter study. Eur J Hum Genet 2004 0.93
123 Application of high-frequency repetitive transcranial magnetic stimulation to the DLPFC alters human prefrontal-hippocampal functional interaction. J Neurosci 2013 0.92
124 Association of rs1006737 in CACNA1C with alterations in prefrontal activation and fronto-hippocampal connectivity. Hum Brain Mapp 2013 0.92
125 Premorbid adjustment in schizophrenia--an important aspect of phenotype definition. Schizophr Res 2007 0.91
126 D2 antidopaminergic modulation of frontal lobe function in healthy human subjects. Biol Psychiatry 2006 0.91
127 Suicidal ideation during treatment of depression with escitalopram and nortriptyline in genome-based therapeutic drugs for depression (GENDEP): a clinical trial. BMC Med 2009 0.91
128 Increased medial orbitofrontal and amygdala activation: evidence for a systems-level endophenotype of bipolar I disorder. Am J Psychiatry 2012 0.91
129 Copy number variants in German patients with schizophrenia. PLoS One 2013 0.91
130 Genetic differences in cytochrome P450 enzymes and antidepressant treatment response. J Psychopharmacol 2013 0.91
131 Reduced anxiety and depression-like behaviours in the circadian period mutant mouse afterhours. PLoS One 2012 0.91
132 A genome-wide supported variant in CACNA1C influences hippocampal activation during episodic memory encoding and retrieval. Eur Arch Psychiatry Clin Neurosci 2013 0.91
133 Genome-wide supported risk variant for bipolar disorder alters anatomical connectivity in the human brain. Neuroimage 2011 0.90
134 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
135 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
136 Association of major depression with rare functional variants in norepinephrine transporter and serotonin1A receptor genes. Am J Med Genet B Neuropsychiatr Genet 2009 0.90
137 Pathological amygdala activation during working memory performance: Evidence for a pathophysiological trait marker in bipolar affective disorder. Hum Brain Mapp 2010 0.90
138 Converging Evidence for Epistasis between ANK3 and Potassium Channel Gene KCNQ2 in Bipolar Disorder. Front Genet 2013 0.90
139 Replication study and meta-analysis in European samples supports association of the 3p21.1 locus with bipolar disorder. Biol Psychiatry 2012 0.89
140 Suicide attempts in schizophrenia and affective disorders with relation to some specific demographical and clinical characteristics. Eur Psychiatry 2005 0.89
141 αCaMKII autophosphorylation controls the establishment of alcohol drinking behavior. Neuropsychopharmacology 2013 0.89
142 Hippocampal function in healthy carriers of the CLU Alzheimer's disease risk variant. J Neurosci 2011 0.89
143 Association study of nonsynonymous single nucleotide polymorphisms in schizophrenia. Biol Psychiatry 2011 0.88
144 Genetic variation in the schizophrenia-risk gene neuregulin 1 correlates with brain activation and impaired speech production in a verbal fluency task in healthy individuals. Hum Brain Mapp 2009 0.88
145 Genetic relationships between suicide attempts, suicidal ideation and major psychiatric disorders: a genome-wide association and polygenic scoring study. Am J Med Genet B Neuropsychiatr Genet 2014 0.88
146 Prefrontal-temporal gray matter deficits in bipolar disorder patients with persecutory delusions. J Affect Disord 2010 0.88
147 Gene-based analysis of regionally enriched cortical genes in GWAS data sets of cognitive traits and psychiatric disorders. PLoS One 2012 0.88
148 COMT val158met polymorphism and neural pain processing. PLoS One 2012 0.88
149 Assessment of Response to Lithium Maintenance Treatment in Bipolar Disorder: A Consortium on Lithium Genetics (ConLiGen) Report. PLoS One 2013 0.88
150 An interaction between a neuropeptide Y gene polymorphism and early adversity modulates endocrine stress responses. Psychoneuroendocrinology 2011 0.88
151 Gene expression of neuregulin-1 isoforms in different brain regions of elderly schizophrenia patients. World J Biol Psychiatry 2010 0.88
152 Impact of schizophrenia-risk gene dysbindin 1 on brain activation in bilateral middle frontal gyrus during a working memory task in healthy individuals. Hum Brain Mapp 2010 0.88
153 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
154 No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samples. Biol Psychiatry 2005 0.88
155 CYP2C19 genotype predicts steady state escitalopram concentration in GENDEP. J Psychopharmacol 2011 0.87
156 Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking. Genet Epidemiol 2013 0.87
157 The G72/G30 gene locus in psychiatric disorders: a challenge to diagnostic boundaries? Schizophr Bull 2006 0.87
158 Altered reward processing in adolescents with prenatal exposure to maternal cigarette smoking. JAMA Psychiatry 2013 0.87
159 A putative high risk diplotype of the G72 gene is in healthy individuals associated with better performance in working memory functions and altered brain activity in the medial temporal lobe. Neuroimage 2009 0.87
160 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
161 Genetic variation in the schizophrenia-risk gene neuregulin1 correlates with differences in frontal brain activation in a working memory task in healthy individuals. Neuroimage 2008 0.87
162 Changes in body weight during pharmacological treatment of depression. Int J Neuropsychopharmacol 2010 0.87
163 The rate of consanguineous marriages among parents of schizophrenic patients in the Arab Bedouin population in Southern Israel. World J Biol Psychiatry 2009 0.86
164 Unipolar depression and hippocampal volume: impact of DNA sequence variants of the glucocorticoid receptor gene. Am J Med Genet B Neuropsychiatr Genet 2008 0.86
165 KCNJ6 is associated with adult alcohol dependence and involved in gene × early life stress interactions in adolescent alcohol drinking. Neuropsychopharmacology 2011 0.86
166 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
167 The effect of neurogranin on neural correlates of episodic memory encoding and retrieval. Schizophr Bull 2011 0.86
168 Genetic variation in the schizophrenia-risk gene neuregulin1 correlates with personality traits in healthy individuals. Eur Psychiatry 2008 0.85
169 Neuregulin 3 is associated with attention deficits in schizophrenia and bipolar disorder. Int J Neuropsychopharmacol 2012 0.85
170 A phenotypic structure and neural correlates of compulsive behaviors in adolescents. PLoS One 2013 0.85
171 The interaction between the dopamine transporter gene and age at onset in relation to tobacco and alcohol use among 19-year-olds. Addict Biol 2009 0.85
172 Genetic variation in G72 correlates with brain activation in the right middle temporal gyrus in a verbal fluency task in healthy individuals. Hum Brain Mapp 2011 0.85
173 Interactive effects of corticotropin-releasing hormone receptor 1 gene and childhood adversity on depressive symptoms in young adults: findings from a longitudinal study. Eur Neuropsychopharmacol 2012 0.85
174 Studies in humans and mice implicate neurocan in the etiology of mania. Am J Psychiatry 2012 0.85
175 BDNF Val 66 Met and 5-HTTLPR genotype moderate the impact of early psychosocial adversity on plasma brain-derived neurotrophic factor and depressive symptoms: a prospective study. Eur Neuropsychopharmacol 2012 0.85
176 Epigenetic alteration of the dopamine transporter gene in alcohol-dependent patients is associated with age. Addict Biol 2012 0.85
177 The schizophrenia risk gene ZNF804A influences the antipsychotic response of positive schizophrenia symptoms. Eur Arch Psychiatry Clin Neurosci 2011 0.84
178 A coding variant of the novel serotonin receptor subunit 5-HT3E influences sustained attention in schizophrenia patients. Eur Neuropsychopharmacol 2010 0.84
179 DAOA/G72 predicts the progression of prodromal syndromes to first episode psychosis. Eur Arch Psychiatry Clin Neurosci 2009 0.84
180 Can long-range microsatellite data be used to predict short-range linkage disequilibrium? Hum Mol Genet 2002 0.84
181 Genome-wide association analysis of age at onset and psychotic symptoms in bipolar disorder. Am J Med Genet B Neuropsychiatr Genet 2011 0.84
182 Multiple polymorphisms in genes of the adrenergic stress system confer vulnerability to alcohol abuse. Addict Biol 2010 0.84
183 Disturbed frontal gyrification within families affected with schizophrenia. J Psychiatr Res 2006 0.84
184 Glutamate receptor δ 1 (GRID1) genetic variation and brain structure in schizophrenia. J Psychiatr Res 2012 0.84
185 FTO, obesity and the adolescent brain. Hum Mol Genet 2012 0.83
186 Neural mechanisms of attention-deficit/hyperactivity disorder symptoms are stratified by MAOA genotype. Biol Psychiatry 2013 0.83
187 The hippocampus in families with schizophrenia in relation to obstetric complications. Schizophr Res 2008 0.83
188 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
189 New Genetic Findings in Schizophrenia: Is there Still Room for the Dopamine Hypothesis of Schizophrenia? Front Behav Neurosci 2010 0.83
190 The effect of Neuregulin 1 on neural correlates of episodic memory encoding and retrieval. Neuroimage 2009 0.83
191 Reduced cortical thickness is associated with the glutamatergic regulatory gene risk variant DAOA Arg30Lys in schizophrenia. Neuropsychopharmacology 2011 0.83
192 Functional polymorphism of the dopamine β-hydroxylase gene is associated with increased risk of disulfiram-induced adverse effects in alcohol-dependent patients. J Clin Psychopharmacol 2012 0.83
193 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
194 Investigation of linkage and association/linkage disequilibrium of HLA A-, DQA1-, DQB1-, and DRB1-alleles in 69 sib-pair- and 89 trio-families with schizophrenia. Am J Med Genet 2002 0.83
195 Induction and quantification of prefrontal cortical network plasticity using 5 Hz rTMS and fMRI. Hum Brain Mapp 2012 0.83
196 Association between a serotonin transporter length polymorphism and primary insomnia. Sleep 2010 0.83
197 Disturbed cortico-amygdalar functional connectivity as pathophysiological correlate of working memory deficits in bipolar affective disorder. Eur Arch Psychiatry Clin Neurosci 2014 0.82
198 No differences in ventral striatum responsivity between adolescents with a positive family history of alcoholism and controls. Addict Biol 2014 0.82
199 Functional serotonin 1A receptor variant influences treatment response to atypical antipsychotics in schizophrenia. Pharmacogenet Genomics 2009 0.82
200 The impact of a Dysbindin schizophrenia susceptibility variant on fiber tract integrity in healthy individuals: a TBSS-based diffusion tensor imaging study. Neuroimage 2011 0.82
201 Influence of 5-HT3 receptor subunit genes HTR3A, HTR3B, HTR3C, HTR3D and HTR3E on treatment response to antipsychotics in schizophrenia. Pharmacogenet Genomics 2009 0.82
202 Gene expression of NMDA receptor subunits in the cerebellum of elderly patients with schizophrenia. Eur Arch Psychiatry Clin Neurosci 2009 0.82
203 Common structural correlates of trait impulsiveness and perceptual reasoning in adolescence. Hum Brain Mapp 2011 0.82
204 Sex-specific role for adenylyl cyclase type 7 in alcohol dependence. Biol Psychiatry 2011 0.82
205 Dual association of a TRKA polymorphism with schizophrenia. Psychiatr Genet 2011 0.82
206 No influence of brain-derived neurotrophic factor (BDNF) polymorphisms on treatment response in a naturalistic sample of patients with major depression. Eur Arch Psychiatry Clin Neurosci 2012 0.82
207 Manual dexterity correlating with right lobule VI volume in right-handed 14-year-olds. Neuroimage 2011 0.81
208 The effects of a DTNBP1 gene variant on attention networks: an fMRI study. Behav Brain Funct 2010 0.81
209 Genetic variation in the G72 gene is associated with increased frontotemporal fiber tract integrity. Eur Arch Psychiatry Clin Neurosci 2014 0.81
210 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
211 Population pharmacokinetic analysis of mirtazapine. Eur J Clin Pharmacol 2004 0.81
212 Mitochondrial DNA HV lineage increases the susceptibility to schizophrenia among Israeli Arabs. Schizophr Res 2007 0.81
213 Association of tumor necrosis factor alpha gene -G308A polymorphism with schizophrenia. Schizophr Res 2003 0.81
214 Relation between cerebrospinal fluid, gray matter and white matter changes in families with schizophrenia. J Psychiatr Res 2005 0.81
215 Genetic variation in CYP2D6 impacts neural activation during cognitive tasks in humans. Neuroimage 2011 0.81
216 Association study between two variants in the DOPA decarboxylase gene in bipolar and unipolar affective disorder. Am J Med Genet 2002 0.81
217 Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patients. Schizophr Res 2011 0.81
218 No association between a common haplotype of the 6 and 10-repeat alleles in intron 8 and the 3'UTR of the DAT1 gene and adult attention deficit hyperactivity disorder. Psychiatr Genet 2007 0.81
219 The novel brain-specific tryptophan hydroxylase-2 gene in panic disorder. J Psychopharmacol 2006 0.81
220 Variation in GNB3 predicts response and adverse reactions to antidepressants. J Psychopharmacol 2010 0.80
221 Dopamine inactivation efficacy related to functional DAT1 and COMT variants influences motor response evaluation. PLoS One 2012 0.80
222 Genome-wide association data provide further support for an association between 5-HTTLPR and major depressive disorder. J Affect Disord 2012 0.80
223 Association between a polymorphism in the pseudoautosomal X-linked gene SYBL1 and bipolar affective disorder. Am J Med Genet 2002 0.80
224 The risk variant in ODZ4 for bipolar disorder impacts on amygdala activation during reward processing. Bipolar Disord 2013 0.80
225 Efficient strategy for detecting gene × gene joint action and its application in schizophrenia. Genet Epidemiol 2013 0.80
226 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
227 Bipolar polygenic loading and bipolar spectrum features in major depressive disorder. Bipolar Disord 2014 0.80
228 Genetics of emergent suicidality during antidepressive treatment--data from a naturalistic study on a large sample of inpatients with a major depressive episode. Eur Neuropsychopharmacol 2012 0.79
229 Stressful life events, cognitive symptoms of depression and response to antidepressants in GENDEP. J Affect Disord 2010 0.79
230 DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder. PLoS One 2012 0.79
231 History of suicide attempts among patients with depression in the GENDEP project. J Affect Disord 2009 0.79
232 Family history influences age of onset in bipolar I disorder in females but not in males. Am J Med Genet B Neuropsychiatr Genet 2005 0.79
233 Do you see what I see? Sex differences in the discrimination of facial emotions during adolescence. Emotion 2013 0.79
234 Polymorphisms in the glutamate transporter gene SLC1A1 and obsessive-compulsive symptoms induced by second-generation antipsychotic agents. Psychiatr Genet 2012 0.79
235 The impact of dystrobrevin-binding protein 1 (DTNBP1) on neural correlates of episodic memory encoding and retrieval. Hum Brain Mapp 2010 0.79
236 The effect of G72 genotype on neural correlates of memory encoding and retrieval. Neuroimage 2009 0.79
237 Genome-wide association analysis accounting for environmental factors through propensity-score matching: application to stressful live events in major depressive disorder. Am J Med Genet B Neuropsychiatr Genet 2013 0.79
238 Genetic association between the phospholipase A2 gene and unipolar affective disorder: a multicentre case-control study. Psychiatr Genet 2003 0.79
239 The methionine synthase polymorphism c.2756Aright curved arrow G (D919G) is relevant for disease-free longevity. Int J Mol Med 2005 0.78
240 Association study of a functional promoter polymorphism in the XBP1 gene and schizophrenia. Am J Med Genet B Neuropsychiatr Genet 2006 0.78
241 Genetics of chronic post-surgical pain: a crucial step toward personal pain medicine. Can J Anaesth 2014 0.78
242 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
243 Dimensions of manic symptoms in youth: psychosocial impairment and cognitive performance in the IMAGEN sample. J Child Psychol Psychiatry 2014 0.78
244 No evidence for an association between variants at the proline dehydrogenase locus and schizophrenia or bipolar affective disorder. Psychiatr Genet 2005 0.78
245 Sexual dysfunction during treatment with serotonergic and noradrenergic antidepressants: clinical description and the role of the 5-HTTLPR. World J Biol Psychiatry 2011 0.78
246 A summary statistic approach to sequence variation in noncoding regions of six schizophrenia-associated gene loci. Eur J Hum Genet 2006 0.78
247 Effect of the G72 (DAOA) putative risk haplotype on cognitive functions in healthy subjects. BMC Psychiatry 2009 0.78
248 No association between genetic variants at the GLYT2 gene and bipolar affective disorder and schizophrenia. Psychiatr Genet 2006 0.78
249 A genome-wide supported psychiatric risk variant in NCAN influences brain function and cognitive performance in healthy subjects. Hum Brain Mapp 2014 0.78
250 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
251 A functional variant in the neuropeptide S receptor 1 gene moderates the influence of urban upbringing on stress processing in the amygdala. Stress 2014 0.78
252 Gene expression of glutamate transporters SLC1A1, SLC1A3 and SLC1A6 in the cerebellar subregions of elderly schizophrenia patients and effects of antipsychotic treatment. World J Biol Psychiatry 2012 0.77
253 Association study between genetic variants at the VAMP2 and VAMP3 loci and bipolar affective disorder. Psychiatr Genet 2008 0.77
254 From gene to brain to behavior: schizophrenia-associated variation in AMBRA1 alters impulsivity-related traits. Eur J Neurosci 2013 0.77
255 Perceived stress has genetic influences distinct from neuroticism and depression. Behav Genet 2013 0.77
256 Functional connectivity analyses in imaging genetics: considerations on methods and data interpretation. PLoS One 2011 0.77
257 Exploring the role of drug-metabolising enzymes in antidepressant side effects. Psychopharmacology (Berl) 2015 0.77
258 No evidence for an involvement of copy number variation in ABCA13 in schizophrenia, bipolar disorder, or major depressive disorder. Psychiatr Genet 2013 0.77
259 A risk variant for alcoholism in the NMDA receptor affects amygdala activity during fear conditioning in humans. Biol Psychol 2013 0.77
260 Further evidence for age of onset being an indicator for severity in bipolar disorder. J Affect Disord 2002 0.77
261 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
262 A target sample of adolescents and reward processing: same neural and behavioral correlates engaged in common paradigms? Exp Brain Res 2012 0.77
263 Segment-wise genome-wide association analysis identifies a candidate region associated with schizophrenia in three independent samples. PLoS One 2012 0.77
264 Sex differences in symptom patterns of recurrent major depression in siblings. Depress Anxiety 2008 0.77
265 DRD4 exon 3 variants are not associated with symptomatology of major psychoses in a German population. Neurosci Lett 2004 0.76
266 Analysis of genome-wide significant bipolar disorder genes in borderline personality disorder. Psychiatr Genet 2014 0.76
267 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
268 No association between the D-aspartate oxidase locus and schizophrenia. Psychiatr Genet 2009 0.76
269 SCN1A affects brain structure and the neural activity of the aging brain. Biol Psychiatry 2012 0.76
270 Genetic variation at the synaptic vesicle gene SV2A is associated with schizophrenia. Schizophr Res 2012 0.76
271 Alterations of Glucocorticoid Receptor Gene Methylation in Externalizing Disorders During Childhood and Adolescence. Behav Genet 2015 0.76
272 Increased levels of glucocorticoid receptors and enhanced glucocorticoid receptor auto-regulation after hydrocortisone challenge in B-lymphoblastoids from patients with affective disorders. Psychoneuroendocrinology 2004 0.76
273 No association between genetic variants at the ASCT1 gene and schizophrenia or bipolar disorder in a German sample. Psychiatr Genet 2006 0.76
274 No association between genetic variants at the GRIN1 gene and bipolar disorder in a German sample. Psychiatr Genet 2006 0.76
275 Association between neuropeptide Y receptor Y2 promoter variant rs6857715 and major depressive disorder. Psychiatr Genet 2017 0.76
276 Functional outcome in major psychiatric disorders and associated clinical and psychosocial variables: A potential cross-diagnostic phenotype for further genetic investigations? World J Biol Psychiatry 2015 0.75
277 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
278 Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2. Psychiatr Genet 2016 0.75
279 Genome-wide association study of co-occurring anxiety in major depression. World J Biol Psychiatry 2013 0.75
280 Time-resolved influences of functional DAT1 and COMT variants on visual perception and post-processing. PLoS One 2012 0.75
281 The impact of genetics on psychiatric nosology. Am J Psychiatry 2006 0.75
282 Association study of the GRIA1 and CLINT1 (Epsin 4) genes in a German schizophrenia sample. Psychiatr Genet 2011 0.75
283 Investigation of tryptophan hydroxylase 2 (TPH2) in schizophrenia and in the response to antipsychotics. J Psychiatr Res 2012 0.75
284 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
285 No association between the serine racemase gene (SRR) and bipolar disorder in a German case-control sample. Psychiatr Genet 2007 0.75
286 Parents' attitudes toward genetic research in autism spectrum disorder. Psychiatr Genet 2016 0.75
287 Forum: The interplay of genes and environment in psychiatric disorders. Curr Opin Psychiatry 2008 0.75
288 No association between genetic variants at the DGCR2 gene and schizophrenia in a German sample. Psychiatr Genet 2009 0.75
289 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
290 The "DGPPN-Cohort": A national collaboration initiative by the German Association for Psychiatry and Psychotherapy (DGPPN) for establishing a large-scale cohort of psychiatric patients. Eur Arch Psychiatry Clin Neurosci 2013 0.75
291 Smoking behaviour: investigation of the coaction of environmental and genetic risk factors. Psychiatr Genet 2014 0.75
292 Shape changes in prefrontal, but not parieto-occipital regions: brains of schizophrenic patients come closer to a circle in coronal and sagittal view. Psychiatry Res 2004 0.75
293 Association study of 20 genetic variants at the (D)-amino acid oxidase gene in schizophrenia. Psychiatr Genet 2010 0.75
294 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
295 No evidence for association between NOTCH4 and schizophrenia in a large family-based and case-control association analysis. Psychiatr Genet 2006 0.75
296 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
297 Increase in Mental Disorders During the COVID-19 Pandemic-the Role of Occupational and Financial Strains. An Analysis of the German National Cohort (NAKO) Study. Dtsch Arztebl Int 2022 0.75
298 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
299 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
300 Abnormal neuroendocrine response to clomipramine in hereditary affective psychosis. Depress Anxiety 2009 0.75
301 Genetic predictors of antidepressant side effects: a grouped candidate gene approach in the Genome-Based Therapeutic Drugs for Depression (GENDEP) study. J Psychopharmacol 2014 0.75
302 Effect of copy number variant burden on Global Assessment of Functioning in schizophrenia. Psychiatr Genet 2016 0.75
303 Brief report: no association between premorbid adjustment in adult-onset schizophrenia and genetic variation in Dysbindin. J Autism Dev Disord 2008 0.75