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1
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Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.
|
Nat Genet
|
2013
|
8.02
|
|
2
|
A mega-analysis of genome-wide association studies for major depressive disorder.
|
Mol Psychiatry
|
2012
|
6.34
|
|
3
|
Loss-of-function mutations in APOC3, triglycerides, and coronary disease.
|
N Engl J Med
|
2014
|
5.47
|
|
4
|
Phosphatase inhibitor-1-deficient mice are protected from catecholamine-induced arrhythmias and myocardial hypertrophy.
|
Cardiovasc Res
|
2008
|
1.42
|
|
5
|
Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression.
|
Biol Psychiatry
|
2010
|
1.39
|
|
6
|
The complement control-related genes CSMD1 and CSMD2 associate to schizophrenia.
|
Biol Psychiatry
|
2011
|
1.36
|
|
7
|
Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder.
|
Schizophr Res
|
2012
|
1.24
|
|
8
|
Implication of a rare deletion at distal 16p11.2 in schizophrenia.
|
JAMA Psychiatry
|
2013
|
1.05
|
|
9
|
Copy number variants in German patients with schizophrenia.
|
PLoS One
|
2013
|
0.91
|
|
10
|
Neuregulin 3 is associated with attention deficits in schizophrenia and bipolar disorder.
|
Int J Neuropsychopharmacol
|
2012
|
0.85
|
|
11
|
Females with de novo aberrations in PHF6: clinical overlap of Borjeson-Forssman-Lehmann with Coffin-Siris syndrome.
|
Am J Med Genet C Semin Med Genet
|
2014
|
0.84
|
|
12
|
De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL association.
|
Eur J Hum Genet
|
2013
|
0.84
|
|
13
|
Genome-wide CNV analysis in 221 unrelated patients and targeted high-throughput sequencing reveal novel causative candidate genes for colorectal adenomatous polyposis.
|
Int J Cancer
|
2014
|
0.84
|
|
14
|
A new face of Borjeson-Forssman-Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype.
|
J Med Genet
|
2013
|
0.82
|
|
15
|
Genome-wide association data provide further support for an association between 5-HTTLPR and major depressive disorder.
|
J Affect Disord
|
2012
|
0.80
|
|
16
|
Summaries from the XVIII World Congress of Psychiatric Genetics, Athens, Greece, 3-7 October 2010.
|
Psychiatr Genet
|
2011
|
0.78
|
|
17
|
Analysis of genome-wide significant bipolar disorder genes in borderline personality disorder.
|
Psychiatr Genet
|
2014
|
0.76
|
|
18
|
Genetic variation at the synaptic vesicle gene SV2A is associated with schizophrenia.
|
Schizophr Res
|
2012
|
0.76
|
|
19
|
Association between neuropeptide Y receptor Y2 promoter variant rs6857715 and major depressive disorder.
|
Psychiatr Genet
|
2017
|
0.76
|
|
20
|
Effect of copy number variant burden on Global Assessment of Functioning in schizophrenia.
|
Psychiatr Genet
|
2016
|
0.75
|
|
21
|
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
|
|
22
|
Smoking behaviour: investigation of the coaction of environmental and genetic risk factors.
|
Psychiatr Genet
|
2014
|
0.75
|
|
23
|
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
|