PubRank

Stephan Ripke

Author PubWeight™ 141.22‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 GenABEL: an R library for genome-wide association analysis. Bioinformatics 2007 18.10
2 Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. Nature 2012 16.13
3 The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. Science 2010 9.61
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 Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs. Nat Genet 2012 5.78
7 Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease. Nat Genet 2011 5.58
8 Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. Nat Genet 2007 4.54
9 Seven new loci associated with age-related macular degeneration. Nat Genet 2013 3.81
10 A rare penetrant mutation in CFH confers high risk of age-related macular degeneration. Nat Genet 2011 3.55
11 Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC). Proc Natl Acad Sci U S A 2010 3.33
12 Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries. Cell 2012 3.21
13 Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder. J Am Acad Child Adolesc Psychiatry 2010 3.13
14 Improved detection of common variants associated with schizophrenia and bipolar disorder using pleiotropy-informed conditional false discovery rate. PLoS Genet 2013 2.68
15 Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders. Neuron 2013 2.45
16 Association of granulomatosis with polyangiitis (Wegener's) with HLA-DPB1*04 and SEMA6A gene variants: evidence from genome-wide analysis. Arthritis Rheum 2013 2.17
17 The neuronal transporter gene SLC6A15 confers risk to major depression. Neuron 2011 2.02
18 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. Hum Mol Genet 2011 1.98
19 Novel genetic risk markers for ulcerative colitis in the IL2/IL21 region are in epistasis with IL23R and suggest a common genetic background for ulcerative colitis and celiac disease. Am J Gastroenterol 2009 1.96
20 Case-control genome-wide association study of attention-deficit/hyperactivity disorder. J Am Acad Child Adolesc Psychiatry 2010 1.86
21 PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome. Nat Genet 2008 1.78
22 Genome-wide association study of coronary and aortic calcification implicates risk loci for coronary artery disease and myocardial infarction. Atherosclerosis 2013 1.69
23 Estimation of SNP heritability from dense genotype data. Am J Hum Genet 2013 1.64
24 Polymorphisms in the drug transporter gene ABCB1 predict antidepressant treatment response in depression. Neuron 2008 1.57
25 Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls. PLoS Genet 2013 1.53
26 Runs of homozygosity implicate autozygosity as a schizophrenia risk factor. PLoS Genet 2012 1.40
27 Correction: Improved Detection of Common Variants Associated with Schizophrenia and Bipolar Disorder Using Pleiotropy-Informed Conditional False Discovery Rate. PLoS Genet 2015 1.39
28 Associations of CFHR1-CFHR3 deletion and a CFH SNP to age-related macular degeneration are not independent. Nat Genet 2010 1.35
29 Rare, low-frequency, and common variants in the protein-coding sequence of biological candidate genes from GWASs contribute to risk of rheumatoid arthritis. Am J Hum Genet 2012 1.35
30 Association study of common genetic variants and HIV-1 acquisition in 6,300 infected cases and 7,200 controls. PLoS Pathog 2013 1.33
31 Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes. Ophthalmology 2012 1.16
32 Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms. Am J Psychiatry 2012 1.15
33 Fine-mapping classical HLA variation associated with durable host control of HIV-1 infection in African Americans. Hum Mol Genet 2012 1.14
34 Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: genome-wide association study of both common and rare variants. Am J Med Genet B Neuropsychiatr Genet 2013 1.11
35 High loading of polygenic risk for ADHD in children with comorbid aggression. Am J Psychiatry 2013 1.10
36 Genetic variation in soluble epoxide hydrolase (EPHX2) is associated with an increased risk of ischemic stroke in white Europeans. Stroke 2008 1.09
37 Genome-wide association study of multiplex schizophrenia pedigrees. Am J Psychiatry 2012 1.05
38 Association of a brain methylation site with clinical outcomes in depression does not replicate across populations. Am J Psychiatry 2015 1.05
39 Genetic markers within glutamate receptors associated with antidepressant treatment-emergent suicidal ideation. Am J Psychiatry 2008 1.00
40 Genetic schizophrenia risk variants jointly modulate total brain and white matter volume. Biol Psychiatry 2012 0.96
41 Investigation of the genetic association between quantitative measures of psychosis and schizophrenia: a polygenic risk score analysis. PLoS One 2012 0.95
42 New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis. Int J Epidemiol 2015 0.93
43 A recessive genetic model and runs of homozygosity in major depressive disorder. Am J Med Genet B Neuropsychiatr Genet 2014 0.91
44 Genetic variation in the lymphotoxin-alpha pathway and the risk of ischemic stroke in European populations. Stroke 2009 0.89
45 Polymorphisms in the GAD2 gene-region are associated with susceptibility for unipolar depression and with a risk factor for anxiety disorders. Am J Med Genet B Neuropsychiatr Genet 2009 0.87
46 A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation. Biol Psychiatry 2013 0.87
47 Altered reward processing in adolescents with prenatal exposure to maternal cigarette smoking. JAMA Psychiatry 2013 0.87
48 Polymorphisms in the angiotensin-converting enzyme gene region predict coping styles in healthy adults and depressed patients. Am J Med Genet B Neuropsychiatr Genet 2009 0.84
49 Resistance to antidepressant treatment is associated with polymorphisms in the leptin gene, decreased leptin mRNA expression, and decreased leptin serum levels. Eur Neuropsychopharmacol 2012 0.82
50 No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis. Hum Mol Genet 2013 0.80
51 Bipolar polygenic loading and bipolar spectrum features in major depressive disorder. Bipolar Disord 2014 0.80
52 Acute and chronic nicotine effects on behaviour and brain activation during intertemporal decision making. Addict Biol 2013 0.80
53 Gene-gene and gene-environment interactions in ulcerative colitis. Hum Genet 2013 0.79
54 A novel approach to detect cumulative genetic effects and genetic interactions in Crohn's disease. Inflamm Bowel Dis 2013 0.78
55 Non-random mating, parent-of-origin, and maternal-fetal incompatibility effects in schizophrenia. Schizophr Res 2012 0.76
56 Genetic risk variants for social anxiety. Am J Med Genet B Neuropsychiatr Genet 2017 0.75