| Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
|
1
|
Large recurrent microdeletions associated with schizophrenia.
|
Nature
|
2008
|
20.25
|
|
2
|
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease.
|
Nat Genet
|
2009
|
15.15
|
|
3
|
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.
|
Nat Genet
|
2011
|
13.25
|
|
4
|
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes.
|
Nat Genet
|
2012
|
11.09
|
|
5
|
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease.
|
Nat Genet
|
2011
|
9.23
|
|
6
|
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.
|
Nat Genet
|
2013
|
8.02
|
|
7
|
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.
|
Nat Genet
|
2014
|
4.13
|
|
8
|
Common variants at ten loci modulate the QT interval duration in the QTSCD Study.
|
Nat Genet
|
2009
|
4.10
|
|
9
|
Identification of common variants associated with human hippocampal and intracranial volumes.
|
Nat Genet
|
2012
|
3.73
|
|
10
|
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.
|
Nat Genet
|
2013
|
3.25
|
|
11
|
Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups.
|
PLoS Genet
|
2010
|
3.21
|
|
12
|
Genetic associations with valvular calcification and aortic stenosis.
|
N Engl J Med
|
2013
|
3.02
|
|
13
|
Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder.
|
Am J Hum Genet
|
2011
|
2.71
|
|
14
|
Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease.
|
PLoS One
|
2010
|
2.57
|
|
15
|
Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1.
|
Nat Genet
|
2010
|
2.46
|
|
16
|
The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data.
|
Brain Imaging Behav
|
2014
|
1.90
|
|
17
|
Susceptibility variants for male-pattern baldness on chromosome 20p11.
|
Nat Genet
|
2008
|
1.80
|
|
18
|
Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype.
|
Blood
|
2013
|
1.45
|
|
19
|
The complement control-related genes CSMD1 and CSMD2 associate to schizophrenia.
|
Biol Psychiatry
|
2011
|
1.36
|
|
20
|
Deletion of the Aspergillus fumigatus lysine biosynthesis gene lysF encoding homoaconitase leads to attenuated virulence in a low-dose mouse infection model of invasive aspergillosis.
|
Arch Microbiol
|
2004
|
1.28
|
|
21
|
Effect of CACNA1C rs1006737 on neural correlates of verbal fluency in healthy individuals.
|
Neuroimage
|
2009
|
1.25
|
|
22
|
Common variation at 10p12.31 near MLLT10 influences meningioma risk.
|
Nat Genet
|
2011
|
1.12
|
|
23
|
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
|
|
24
|
The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease.
|
J Alzheimers Dis
|
2012
|
1.02
|
|
25
|
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
|
|
26
|
Association analysis of Neuregulin 1 candidate regions in schizophrenia and bipolar disorder.
|
Neurosci Lett
|
2010
|
1.00
|
|
27
|
ZNF804A and cortical structure in schizophrenia: in vivo and postmortem studies.
|
Schizophr Bull
|
2013
|
0.99
|
|
28
|
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
|
|
29
|
Dissection of phenotype reveals possible association between schizophrenia and Glutamate Receptor Delta 1 (GRID1) gene promoter.
|
Schizophr Res
|
2009
|
0.97
|
|
30
|
Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall Study.
|
BMC Med Genet
|
2013
|
0.95
|
|
31
|
Inherited genetic susceptibility to monoclonal gammopathy of unknown significance.
|
Blood
|
2014
|
0.94
|
|
32
|
Genetic and functional abnormalities of the melatonin biosynthesis pathway in patients with bipolar disorder.
|
Hum Mol Genet
|
2012
|
0.93
|
|
33
|
Replication study and meta-analysis in European samples supports association of the 3p21.1 locus with bipolar disorder.
|
Biol Psychiatry
|
2012
|
0.89
|
|
34
|
Hippocampal function in healthy carriers of the CLU Alzheimer's disease risk variant.
|
J Neurosci
|
2011
|
0.89
|
|
35
|
Coronary artery calcification and its relationship to validated genetic variants for diabetes mellitus assessed in the Heinz Nixdorf recall cohort.
|
Arterioscler Thromb Vasc Biol
|
2010
|
0.88
|
|
36
|
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
|
|
37
|
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
|
|
38
|
Neuregulin 3 is associated with attention deficits in schizophrenia and bipolar disorder.
|
Int J Neuropsychopharmacol
|
2012
|
0.85
|
|
39
|
Studies in humans and mice implicate neurocan in the etiology of mania.
|
Am J Psychiatry
|
2012
|
0.85
|
|
40
|
Glutamate receptor δ 1 (GRID1) genetic variation and brain structure in schizophrenia.
|
J Psychiatr Res
|
2012
|
0.84
|
|
41
|
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
|
|
42
|
Reduced cortical thickness is associated with the glutamatergic regulatory gene risk variant DAOA Arg30Lys in schizophrenia.
|
Neuropsychopharmacology
|
2011
|
0.83
|
|
43
|
Investigation of the tryptophan hydroxylase 2 gene in bipolar I disorder in the Romanian population.
|
Psychiatr Genet
|
2008
|
0.82
|
|
44
|
DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder.
|
PLoS One
|
2012
|
0.79
|
|
45
|
Summaries from the XVIII World Congress of Psychiatric Genetics, Athens, Greece, 3-7 October 2010.
|
Psychiatr Genet
|
2011
|
0.78
|
|
46
|
Genetic variation at the synaptic vesicle gene SV2A is associated with schizophrenia.
|
Schizophr Res
|
2012
|
0.76
|
|
47
|
Selected summaries from the XVII World Congress of Psychiatric Genetics, San Diego, California, USA, 4-8 November 2009.
|
Psychiatr Genet
|
2010
|
0.75
|
|
48
|
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
|
|
49
|
Smoking behaviour: investigation of the coaction of environmental and genetic risk factors.
|
Psychiatr Genet
|
2014
|
0.75
|
|
50
|
Brief report: no association between premorbid adjustment in adult-onset schizophrenia and genetic variation in Dysbindin.
|
J Autism Dev Disord
|
2008
|
0.75
|