PubRank

Irene Pichler

Author PubWeight™ 143.06‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Biological, clinical and population relevance of 95 loci for blood lipids. Nature 2010 28.21
2 Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nat Genet 2010 23.08
3 Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature 2010 20.01
4 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nat Genet 2010 17.89
5 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. Nat Genet 2008 12.32
6 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Nat Genet 2010 7.94
7 Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. Nat Genet 2011 3.40
8 Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. PLoS Genet 2012 3.21
9 Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis. Hum Mol Genet 2008 2.66
10 Large-scale replication and heterogeneity in Parkinson disease genetic loci. Neurology 2012 2.18
11 Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations. PLoS Genet 2012 1.79
12 Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: results of genome-wide association analyses including 4659 European individuals. Atherosclerosis 2009 1.78
13 Genetic determinants of circulating sphingolipid concentrations in European populations. PLoS Genet 2009 1.77
14 Linkage disequilibrium patterns and tagSNP transferability among European populations. Am J Hum Genet 2005 1.72
15 A genome-wide association search for type 2 diabetes genes in African Americans. PLoS One 2012 1.72
16 The genetic study of three population microisolates in South Tyrol (MICROS): study design and epidemiological perspectives. BMC Med Genet 2007 1.64
17 Genome-wide linkage analysis of serum creatinine in three isolated European populations. Kidney Int 2009 1.48
18 Exclusion of linkage to chromosome 14q in a large South Tyrolean family with Idiopathic Basal Ganglia Calcification (IBGC). Am J Med Genet B Neuropsychiatr Genet 2008 1.42
19 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. Circ Cardiovasc Genet 2009 1.35
20 Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels. Hum Mol Genet 2010 1.18
21 Involvement of proprotein convertase PCSK7 in the regulation of systemic iron homeostasis. Hepatology 2013 1.09
22 CLOCK gene variants associate with sleep duration in two independent populations. Biol Psychiatry 2010 1.06
23 Restless legs syndrome: epidemiological and clinicogenetic study in a South Tyrolean population isolate. Mov Disord 2006 0.94
24 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. Obesity (Silver Spring) 2009 0.93
25 A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants. J Med Genet 2012 0.90
26 Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster. Hum Mol Genet 2011 0.88
27 Genotyping human ancient mtDNA control and coding region polymorphisms with a multiplexed Single-Base-Extension assay: the singular maternal history of the Tyrolean Iceman. BMC Genet 2009 0.87
28 Profiling of Parkin-binding partners using tandem affinity purification. PLoS One 2013 0.84
29 Co-occurrence of restless legs syndrome and Parkin mutations in two families. Mov Disord 2006 0.82
30 Exome sequencing in a family with restless legs syndrome. Mov Disord 2012 0.78
31 Haplotype analysis of the 4p16.3 region in Portuguese families with Huntington's disease. Am J Med Genet B Neuropsychiatr Genet 2015 0.77
32 Genetic structure in contemporary South Tyrolean isolated populations revealed by analysis of Y-chromosome, mtDNA, and Alu polymorphisms. 2006. Hum Biol 2009 0.76
33 Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. PLoS Genet 2016 0.75
34 Update on the management of restless legs syndrome: existing and emerging treatment options. Nat Sci Sleep 2010 0.75
35 ParkScreen: a low-cost rapid linkage marker panel for Parkinson's disease. J Mol Neurosci 2009 0.75
36 Corrigendum: Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis. Nat Commun 2015 0.75