Christian Fuchsberger

Author PubWeight™ 65.10‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Fast and accurate genotype imputation in genome-wide association studies through pre-phasing. Nat Genet 2012 11.29
2 The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits. PLoS Genet 2012 6.15
3 New loci associated with kidney function and chronic kidney disease. Nat Genet 2010 5.58
4 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. Nat Genet 2009 4.10
5 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. Circulation 2011 3.68
6 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. Nat Genet 2010 3.55
7 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
8 CUBN is a gene locus for albuminuria. J Am Soc Nephrol 2011 2.70
9 Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion. Nat Genet 2012 2.55
10 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
11 Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. Nat Genet 2013 1.72
12 Genome-wide association and functional follow-up reveals new loci for kidney function. PLoS Genet 2012 1.68
13 Genome-wide association analysis identifies multiple loci related to resting heart rate. Hum Mol Genet 2010 1.67
14 The genetic study of three population microisolates in South Tyrol (MICROS): study design and epidemiological perspectives. BMC Med Genet 2007 1.64
15 Genes predict village of origin in rural Europe. Eur J Hum Genet 2010 1.61
16 Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function. Hum Mol Genet 2012 1.14
17 Common genetic variation in the 3'-BCL11B gene desert is associated with carotid-femoral pulse wave velocity and excess cardiovascular disease risk: the AortaGen Consortium. Circ Cardiovasc Genet 2011 1.11
18 Drawing the history of the Hutterite population on a genetic landscape: inference from Y-chromosome and mtDNA genotypes. Eur J Hum Genet 2009 1.03
19 Heritability analysis of life span in a semi-isolated population followed across four centuries reveals the presence of pleiotropy between life span and reproduction. J Gerontol A Biol Sci Med Sci 2010 1.01
20 Proteomics profiling of microdissected low- and high-grade prostate tumors identifies Lamin A as a discriminatory biomarker. J Proteome Res 2010 1.00
21 Jenti: an efficient tool for mining complex inbred genealogies. Bioinformatics 2008 0.94
22 Anterior gradient 2 and 3--two prototype androgen-responsive genes transcriptionally upregulated by androgens and by oestrogens in prostate cancer cells. FEBS J 2013 0.94
23 Genotype imputation in genome-wide association studies. Curr Protoc Hum Genet 2013 0.90
24 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
25 Common variants in Mendelian kidney disease genes and their association with renal function. J Am Soc Nephrol 2013 0.82
26 Influence of blood sampling on protein profiling and pattern analysis using matrix-assisted laser desorption/ionisation mass spectrometry. BJU Int 2007 0.79
27 Copy number variation and association over T-cell receptor genes--influence of DNA source. Immunogenetics 2010 0.78
28 Linkage and association analysis of hyperthyrotropinaemia in an Alpine population reveal two novel loci on chromosomes 3q28-29 and 6q26-27. J Med Genet 2011 0.78
29 Fertility pattern and family structure in three Alpine settlements in South Tyrol (italy): marriage cohorts from 1750 to 1949. J Biosoc Sci 2009 0.76
30 Fine-mapping of restless legs locus 4 (RLS4) identifies a haplotype over the SPATS2L and KCTD18 genes. J Mol Neurosci 2012 0.75
31 Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function. Sci Rep 2017 0.75